4104 Closed Entry-Level Biotechnology & Life Science Job Postings
This list includes jobs asking for Associates, Bachelors or Masters degrees and is available in three formats: chronological, alphabetical and geographical. We also keep records of all the old jobs we have posted that are no longer open: Entry-level History
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| Job Information | Description | Date Added | |
| 1 | Precision Medical Group Frederick, MD Repair Technician & Facilities Maintenance - Laboratory & Cold Storage (Fridge) HS diploma or equivalent Exp: 0-1 year(s) |
Our Bio-repository facility (similar to a warehouse) is hiring an entry level technician! You will monitor and report on all environmental storage units, performing preventive maintenance, repairing refrigeration equipment and monitoring systems. What the day-to-day will look like (in accordance with standard operating procedures, SOPs): Inspection and Repair; refrigeration, lab equipment, central monitoring system and emergency generator. Perform weekly inspections of emergency generators. Performing all inspections of refrigeration equipment which consists of a 15 point inspection of critical systems, including; oil level, compressor operation, electrical demand, temperature sensor calibration, etc. Performing performance qualifications of all refrigeration equipment. Reviewing equipment failures and evaluating potential causes with little supervision. etc. | 6/24/2020 |
| 2 | Nuvasive Aliso Viejo, CA Manufacturing Technician HS diploma or equivalent Exp: 1+ year(s) |
Job Description: Align, fit, and assemble component parts, using hand tools, power tools, fixtures, and templates. Analyze and record test results per acceptance test criteria, and prepare written testing documentation. Organize work areas. Install electrical and electronic parts and hardware in housings or assemblies, using soldering equipment and hand tools. Read blueprints, schematics, diagrams, manufacturing instructions, and work orders to determine methods and sequences of assembly. Repair, rework, and calibrate assemblies and systems to meet operational specifications and tolerances. etc. | 6/16/2020 |
| 3 | PAR Pharmaceutical Chestnut Ridge, NY Quality Technician II AA/AS Exp: 1-2 year(s) |
Responsible for laboratory and equipment cleanliness, routine physical and chemical testing per SOPs, and, with guidance, detects and participates in OOS/OOT and other investigations. Provides critical infrastructure support and receives, stocks and inventories reagents and supplies. Orders, receives and maintains controlled reference standards and samples. Works with metrology to perform routine daily instrument calibrations and maintenance. Communicates with the supervisor on a daily basis regarding the lab operations. Uses computer/lab software to enter the data. Understands and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. etc. | 6/17/2020 |
| 4 | Perrigo Minneapolis, MN QC Chemist II - 1st Shift BS/BA Exp: 1-2 year(s) |
Ensures the Quality and Compliance of raw materials and products by performing analytical testing on samples relative to the release of Perrigo materials and product, according to cGMP requirements. etc. | 6/17/2020 |
| 5 | Contract Pharmacal Corp Hauppauge, NY TECH; QA METROLOGY (Entry Level) BS/BA in sciences/engineering Exp: Entry Level |
The QA Metrology, Technician has primary responsibility for administering Laboratory computer programs such as Empower, managing the calibration and maintenance program for all laboratory equipment including related documentation such as SOPs and log books, and support the Data Integrity program. Complete all aspect of the company’s laboratory equipment and instrumentation program including; implementation, validation, periodic verification and calibration, perform basic troubleshoot etc. | 6/8/2020 |
| 6 | CRISPR Theraputics Cambridge, MA Research Associate II/Senior Research Associate, Editing Technologies - Cellular Biology MS in biology Exp: 1 year research experience |
Implement multiplexed gene editing strategies for next-generation CRISPR-based therapies. Engineer mammalian cells with CRISPR/Cas9, and perform downstream molecular and cellular analysis. Culture mammalian primary cells and cells lines, and introduce plasmid DNA, mRNA, gRNA and Cas9 RNP by appropriate methods, including cationic lipid-based transfection and electroporation. | 5/30/2020 |
| 7 | Cellink Boston, MA Technical Support Specialist BS in mechanical, software, or electrical engineering Exp: 0-3 years |
Provide high level technical support to CELLINK customers for a wide range of products. Diagnose, troubleshoot and resolve hardware and software questions from customers and create trouble tickets for hardware and software issues. Remotely interface, troubleshoot, diagnose and repair customer equipment supporting end customers, Application Specialist Team and distributors worldwide. | 5/30/2020 |
| 8 | Baxter Round Lake, IL Quality Lab Associate I BS/BA in biological sciences Exp: 0-2 years |
Conduct biological, chemical and physical analyses on pharmaceutical products (biologic and drugs) and medical devices through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs Conduct critical biological, physical analyses on raw materials, initial, in-process and final products, and samples collected from environmental monitoring programs at Baxter manufacturing facilities | 5/31/2020 |
| 9 | Masy Bioservices Pepperell, MA Calibration Field Technician II HS diploma/AS/AA Exp: 1-3 year(s) |
Perform routine calibration and preventive maintenance of Masy and customer equipment. Calibration may include temperature, relative humidity, CO2, voltage, pressure, time, rotation, etc. following documented procedures using precision standards. Calibrations will be performed in-house and at customer sites. Create, modify and execute calibration procedures and calibration certificates. Perform testing to support the quality management system and report, troubleshoot and make recommendations about quality issues relating to calibration. Assist in filing, data entry and general record keeping. etc. | 6/2/2020 |
| 10 | Masy Bioservices Pepperell, MA Quality Associate I HS diploma or equivalent Exp: 1+ year(s) |
This position provides day to day support assisting in areas such as GMP, ISO 9001 and ISO 17025 compliance and the company’s quality system. Duties include quality assurance and control activities in technical, systems, operations and service areas. This position may require frequent interaction with multiple departments. Works under general supervision of management or team lead. Duties/responsibilities: Actively participate in Masy’s QMS to maintain GMP compliance, ISO 9001 certification and ISO 17025 accreditation consisting of two or more of the following areas: Perform quality review of calibration certificates before release to customers. etc. | 6/2/2020 |
| 11 | Akoya Marlborough, MA Scientist, Applications MS in a life science Exp: 1-2 year(s) |
Akoya Biosciences is seeking an experienced immunohistochemist to join our Applications group in Marlborough, MA, which is responsible for developing new multiplexed immunohistochemistry methods and running exploratory and validation studies, using Akoya’s Phenoptics multiplexed immunofluorescence platform. Phenoptics enables staining of up to 9 colors, utilizing OPAL detection reagents and Vectra multispectral imaging instruments, providing unparalleled cell-level and architectural-level tissue analysis capabilities. The Applications group is a dynamic team that engages with important strategic collaborators in academia and in the pharmaceutical industry to help facilitate adoption of the Phenoptics platform and to develop new applications. etc. | 5/27/2020 |
| 12 | AliveCor Mountain View, CA Hardware Test Engineer BS in electrical engineering or related Exp: 1-5 year(s) |
AliveCor, the creator of the Kardia Mobile ECG app, seeks a Hardware Test Engineer to join an exciting start-up that is changing the face of mobile health. As the Hardware Test Engineer, you will be a crucial member of hardware R&D team responsible for ensuring that AliveCor products perform as intended and meet/exceed customer expectations. You will work closely with our Quality, Regulatory, Software Engineering, Product Management, and Creative teams to ensure new products perform as intended while fully documenting the verification process. You will also work with our manufacturing team to implement and support manufacturing test fixtures. etc. | 5/27/2020 |
| 13 | American Regent Columbus, OH QC Microbiologist I BS in microbiology, biology, or other life science Exp: 1 year |
This position in the Microbiology Laboratory will be primarily responsible for performing the microbiological testing for in-process as well as monitoring of controlled manufacturing facilities and utility systems. essential Duties and Responsibilities: Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time. Ensure all work is performed and documented in accordance with existing company policies, procedures, and Current Good Manufacturing Practices, health and safety requirements. Plan daily workload to meet requirements. etc. | 5/27/2020 |
| 14 | Brooks South Plainfield, NJ Associate Customer Support Scientist I BS/BA in biological sciences Exp: Entry Level |
The specific focus is on the Gene Synthesis and Cloning/Mutagenesis services. They advocate the client’s perspective to ensure excellent customer service. They enjoy interacting with people daily via phone, email or live chat. They work within our systems to identify the cause of an issue and can effectively address questions or concerns. When customers have ambiguous questions, they can provide meaningful responses. | 5/24/2020 |
| 15 | Brooks South Plainfield, NJ Product Marketing Associate BS/BA in business, marketing or life sciences Exp: 1-2 years in biotech/life sciences |
Gather and review product market trends and competitive landscape to identify target markets and develop lead generation strategies. Support generating opportunities through new services or service differentiation by representing the voice of the customer. Create and maintain competitive matrix and fine-tune service offerings and forecasts accordingly | 5/24/2020 |
| 16 | Brooks South Plainfield, NJ Associate Customer Support Scientist BS/BA in life sciences or business admin Exp: Entry Level |
The Associate Scientist I, Project Management position in Molecular Genetics is a non-bench role that works closely with customers and the lab in order to effectively manage the customer interaction with GENEWIZ. Provide consultation and troubleshooting for the molecular biology services including: PCR and sequencing applications, DNA, RNA, cDNA applications, Gene synthesis | 5/24/2020 |
| 17 | Brooks South Plainfield, NJ Associate Scientist I BS/BA in biological sciences Exp: 1+ years in lab |
Prepare amplified template libraries for high-throughput sequencing. Carry out DNA sequencing on next-generation DNA analyzers. Perform routine maintenance of DNA analyzers and related equipment. Check inventory and replenish consumable sequencing supplies. Communicate with customers by phone and e-mail in a friendly and professional manner | 5/24/2020 |
| 18 | BD Baltimiore, MD Quality Document Management Specialist I BS/BA Exp: No experience Necessary |
This position supports the Release Control function for the Prepared Media plant. The position requires the timely entry of various forms of data to meet production and quality goals. Requires review of records and data for completeness and GMP compliance. Associate will perform final release of products. Metrics tracking and reporting may be required. | 5/24/2020 |
| 19 | BD Baltimiore, MD Scientist I BS/BA in life sciences/engineering Exp: 1-4 years in lab work |
This person will be responsible for assisting in the design, development, integration and qualification of assays and/or specimen processing workflows on automateddiagnosticssystems.The successful candidate may also be expected to provide support in execution of clinical studies to validate performance of the assays andassemble relevant information in support of regulatory submissions. | 5/24/2020 |
| 20 | BD San Jose, CA Supplier Quality Engineer BS/BA in related field Exp: No experience Necessary |
The Quality Engineer is primarily responsible for reviewing and assessing Quality Notifications, Complaints, Deviation/Waivers and other cGMP activities for the assigned product lines in the instrument plant. The QM Engineer I oversees QC operations within the instrument plant and assuring documentation and procedures are followed, updated and maintained as required by internal Quality Policies and related FDA/GMP guidelines. The QM Engineer I conducts complaint investigations, assists in the investigation of manufacturing issues and provides data and input on technical issues and projects. | 5/24/2020 |
| 21 | BD Cayey, PR Quality Technician BS/BA in life/medical sciences Exp: 1-3 years in lab |
The Quality Control (QC) Technician is responsible for performing QC final testing of products, as well as, conducting raw material, stability, complaint, and special investigation testing. Is also responsible for ensuring all testing are performed correctly and results are reported promptly. Perform testing for Bactec product line. Report results on data forms. Perform physical, chemical and microbiological testing to raw materials, finished products and the record results. | 5/24/2020 |
| 22 | BD Sandy, UT Quality Control Inspector HS Diploma/GED Exp: 1 year in mechanical inspection |
The Quality Control Inspector will measure key quality characteristics on various molded plastic components and mold steel components. Enter data into computer for analysis and prepare graphs and charts for data analysis. Assist engineering in product design verification, process qualifications, and validations. Measure key quality characteristics on various molded plastic components and mold steel components. | 5/24/2020 |
| 23 | 10x Genomics Pleasanton, CA Research Associate 2-Molecular Biology/Product Development MS in molecular biology, genetics, analytical chemistry, or related Exp: 1+ year(s) |
We are seeking an outstanding Research Associate to join the Product Development team to support the development and commercial launch of new products. This is a unique cross-disciplinary position that will work closely with a variety of groups including Molecular Biology, Chemistry, Microfluidics, QC, and Manufacturing, to develop and validate novel reagents for the rapid expansion of 10x product lines. Candidates must have a broad working knowledge of molecular biology and be able to apply that knowledge creatively and independently in a fast-paced work environment. The successful applicant will have exceptional attention to detail and the ability to meticulously execute and analyze highly complex experiments. Previous industry experience is essential. etc. | 5/13/2020 |
| 24 | BioFire Salt Lake City, UT BioReagents Formulator - Day Actively enrolled in 2 year degree Exp: 1+ years in lab |
This is a full-time non-exempt position. Responsible for manufacturing and formulation of all BioReagents products and sub-assemblies including FilmArray. Operates production equipment and performs duties under compliance of cGMP manufacturing. Weighs, measures, and checks raw materials to assure that manufactured batches, lots, buffers and sub-assemblies contain the proper reagents and qualities. Has knowledge of commonly used concepts, practices, and procedures including PCR, real-time PCR, and use of fluorescence based nucleic acid detection techniques. | 5/16/2020 |
| 25 | BioFire Salt Lake City, UT Instrument Manufacturing Technician I / Trainee HS Diploma Exp: 0+ years |
Utilizing attention to detail, the Instrument Production Technician I operates production equipment and assembles instrument components using fine motor dexterity. Responsible for performing a wide variety of electronic or electro-mechanical assembly operations on sub-assembly components. | 5/16/2020 |
| 26 | BioFire Salt Lake City, UT Financial Analyst I BS/BA in accounting, finance, information systems Exp: 1+ years in accounting |
This position assists with financial variance analysis, compiles data for reporting, and assists with models for trending and forecasting. Perform all work in compliance with company policy and within the guidelines of BioFire Diagnostics’ Quality System. Monitor revenue transaction to ensure proper coding of transactions. Maintains sales and installed base reports and dashboards. | 5/16/2020 |
| 27 | BioFire Salt Lake City, UT Inventory Control Analyst I HS Diploma/GED Exp: 1+ years in warehouse |
Position will provide quick response to supply chain, quality, and production teams’ to resolve variances. Takes daily proactive measures to ensure a high degree of inventory accuracy. When necessary, will monitor internal MES and ERP queues, will identify and document queue errors, will analyze errors for root cause, and will resolve errors with appropriate action. | 5/16/2020 |
| 28 | BioMarin Brisbane, CA Pharmacovigilance Associate II BS in life scineces Exp: 1year in pharmacovigilance |
Participates in activities related to,and processing of Adverse Events for BioMarin post marketed products and investigational products. Accountable for accurate data capture for individual case safety reports. Responsible for narrative creation for individual case safety reports. Perform quality review (as appropriate) | 5/17/2020 |
| 29 | BioMarin Novato, CA QC Technician (TEMPORARY) Assocates in sciences Exp: 0-2 years in lab |
The QC In-Process (QCIP) Technician is responsible for supporting microbiological and analytical test methods on in-process intermediates and varying stages of drug products, under supervision and within Current Good Manufacturing Practices (cGMP) guidelines, to support further manufacturing of commercial and clinical therapeutics. | 5/17/2020 |
| 30 | BioMarin Novato, CA Manufacturing Associate (TEMPORARY) BS/BA in sciences or engineering Exp: 0-2 years in biotech |
Understanding of process theory and equipment operation. Ability to learn biopharmaceutical manufacturing processes including mammalian cell culture, depth filtration, tangential flow filtration, column chromatography, protein purification and formulation of bulk drug substance. Support initiatives for process optimization | 5/17/2020 |
| 31 | Baxter Round Lake, IL Engineer II BS in engineering Exp: 1-3 years |
With supervision, lead projects within Baxter’s change control management process, from initiation through closure. Change Owners assign and prepare impact assessments, develop change plans, write and execute engineering studies, while working closely with manufacturing plants, quality, regulatory, purchasing, and various scientific/technical groups. | 5/3/2020 |
| 32 | BD Sumter, SC Micro Lab Technician HS Diploma/GED Exp: 0-1 years in clean room experience |
Performs testing that assures the sterility of BD product, in addition performs environmental monitoring of manufacturing areas to ensure that product integrity. Familiarity with Microbiology techniques, equipment and good laboratory practices, including a working in clean room atmosphere is preferred. Duties will include collection test samples, media preparation, verification/calibration of equipment, upkeep of various laboratory databases, routine housekeeping, and providing support to special projects. | 5/3/2020 |
| 33 | BD Sumter, SC Validation Technician HS Diploma/GED, Associates Preferred Exp: 1 year in quality |
Support the Compliance group by performing various tests, collecting data and being the QA floor representative relating to validation / process characterization projects. Reports directly to a Quality Manager. Conduct experiments and collect data for use in analysis of quality cost, process capability, etc. Perform measurements using precision equipment with accuracy to .0001” | 5/3/2020 |
| 34 | BD Columbus, NE Product Line Coordinator BS/BA in business admin, management, industrial tech Exp: 1-3 years in manufacturing |
The Product Line Coordinator is responsible for all production management and supervisory activities and to support the Unit Manager in setting and achieving overall business objectives for all product lines including compliance to cost, quality, safety, human resource and regulatory plans and requirements. Administer plant policies (safety, attendance, disciplinary actions). Responsible for training of new employees including new operator orientation, ITR's, and appropriate counseling/coaching. | 5/3/2020 |
| 35 | BD Columbus, NE Small Gauge Packroom Operator - B shift HS Diploma/GED Exp: 0 years required |
Run auto inspection machines and assist in Changeovers, and trouble-shooting machines in the Cannula Department. Perform 100% Inspect Qc checks, and check material into SAP . Support the activities of the department as necessary to meet objectives. The nature of these jobs requires flexibility and adaptability as condition change. Assist QC Manufacturing Representative and /or QC Technician in performing machine and process capability studies, etc. | 5/3/2020 |
| 36 | BD Baltimore, MD QM Associate Scientist BS/BA in biological sciences Exp: 1-2 years |
Responsible for Microbiology Quality Control testing in peptone manufacturing, raw material products, Tissue Culture Testing, Dyes & Stains testing and Final DCM testing as required. The QM Associate Scientist is required to perform testing of various Microorganisms in a Biosafety Level II and TB Laboratory with strict adherence to safety policies. | 5/3/2020 |
| 37 | Upsher-Smith Maple Grove, MN Quality Inspector I HS diploma or equivalent Exp: 0-2+ years |
The Quality Inspector I inspects and samples incoming raw materials manufactured outside of the company, packaging components and labeling materials, per sampling requirements. Completes all relevant SAP transactions to document inspection and sample consumption. Submits samples to laboratory. Inspects all labeling components for correctness against the approved proofmaster. (eg., text, barcodes and revision date). Applies appropriate stickers (e.g., RD, reject and hold) as necessary. Initiates data packets for incoming materials, if applicable. Receives laboratory samples from production by performing the appropriate SAP transactions. etc. | 5/6/2020 |
| 38 | Viant Brimfield, MA Machinist HS diploma or equivalent Exp: 6-12 months |
The primary purpose of this job is to set up, operate, and maintain CNC equipment to manufacture precision parts. Accountabilities & Responsibilities: Adheres to Viant’s Values and all safety, environmental, security and quality requirements including, but not limited to: Quality Management Systems (QMS), Safety, Environmental and Security Management Systems, U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements. Operates and sets up CNC shop equipment with minimal assistance. Accountable for meeting cycle time and yield expectations. etc. | 5/6/2020 |
| 39 | Viant Westfield, PA Machine Operator - Part Time HS diploma or equivalent Exp: Not necessary |
This position ensures that assigned machines/equipment produce product at or above department standards. Responsible to produce, assemble, inspect and pack all parts as per the work instructions for each assigned task or machine. Maintain all required paperwork and documentation to Good Manufacturing Practice (GMP) and ISO 13485 standards. Main Job Duties/Responsibilities: ATTENDANCE IS PARAMOUNT. All associates are required to report to work on time and when scheduled. Operate machines maintaining productivity, efficiency and product quality. etc. | 5/6/2020 |
| 40 | Viant Grand Rapids, MI Manufacturing Operator 1 - ALL SHIFTS HS diploma or equivalent Exp: 6-12 months |
Under the direction of the area Supervisor, responsible for production work according to specifications and established policies, procedures, practices and standards. Main Job Duties/Responsibilities: Follows all Good Manufacturing Practices (GMP’s) and Standard Operating Procedures (SOP’s) as defined by Viant policies, practices and procedures to insure that FDA and ISO regulations and quality standards are met. Assembles components. May be required to operate packaging machine. Barsealing/Traysealing. Boxes products and applies labeling materials. etc. | 5/6/2020 |
| 41 | Viant Indianapolis, IN Manufacturing Team Member - Deburr Department HS diploma or equivalent Exp: Not necessary |
The primary purpose of this role is to perform assembly and inspection operations over a range of products and processes. Will support both cyclical and non-cyclical work, independently preparing work to be accomplished by studying manufacturing process instructions and quality work instructions, gathering parts, tools, and materials as required. May train other team members in assembly operations. Job Description Details: Adheres to Viant Medical’s Core Beliefs, Behavioral Based Safety process and Quality Policy. Sets up equipment needed for assembly/inspection as per Manufacturing Process Instructions (MPI’s) and Quality Work Instructions (QWI’s). Understands own tasks and how they relate to others in their team. Works under minimal Supervision. Will follow Standard Work where applicable. Understands overall production flow within their department. May perform significant non-cyclic work for the department. etc. | 5/6/2020 |
| 42 | Stryker Casper, WY JR Sales Associate BS/BA Exp: 1+ year(s) |
What you will do: Increasing Joint Replacement sales through assisting the sales teams and building own accounts by means of working with existing customers as well as identify new customers in order to grow their territory. Communicating with current and new Joint Replacement customer accounts regarding a variety of topics including product updates, changes to product portfolio and educational programs. etc. | 4/29/2020 |
| 43 | Stryker Davie, FL Quality Assurance Technician HS diploma Exp: 1-2 year(s) |
Job Description: Maintain certification to inspect a minimum of one business units products and Incoming Inspection equipment. Perform incoming inspection on components and Electro/mechanical products per company/regulatory specifications. Work from engineering schematics or blueprints to perform accurate checks and tests. Comply be required to comply with documentation and regulatory procedures and policies. etc. | 4/29/2020 |
| 44 | Stryker , GA PCBA Manufacturing Engineer, Advanced Operations BS/BA in engineering Exp: 1-2 year(s) |
Be a PCBA Manufacturing Engineer in one of the most exciting and successful areas at Stryker Robotics. Be part of the development and introduction of new products and work extensively with Product Development, Quality and Manufacturing Operations to take a product from design concept through production ramp up. etc. | 4/29/2020 |
| 45 | Stryker , TN PCBA Manufacturing Engineer, Advanced Operations BS/BA in engineering Exp: 1-2 year(s) |
Be a PCBA Manufacturing Engineer in one of the most exciting and successful areas at Stryker Robotics. Be part of the development and introduction of new products and work extensively with Product Development, Quality and Manufacturing Operations to take a product from design concept through production ramp up. Specific responsibilities of the PCBA Manufacturing Engineer include, but are not limited to, the following: Develop processes for the manufacture of PCBAs. etc. | 4/29/2020 |
| 46 | Stryker , MI Trauma Sales Associate-Detroit BS/BA Exp: 1+ year(s) |
You will get exposure to the proven winning Stryker Trauma culture that delivers Industry leading results in all market segments. You will receive best-in-class formal Trauma training on product portfolio and selling skills which includes on-the-job training in the operating room. You’ll become an expert on surgical procedures by observing well-over 300 cases in your first year. etc. | 4/29/2020 |
| 47 | Stryker Fort Lauderdale, FL PCBA Manufacturing Engineer, Advanced Operations BS/BA in engineering Exp: 1-2 year(s) |
Be a PCBA Manufacturing Engineer in one of the most exciting and successful areas at Stryker Robotics. Be part of the development and introduction of new products and work extensively with Product Development, Quality and Manufacturing Operations to take a product from design concept through production ramp up. Specific responsibilities of the PCBA Manufacturing Engineer include, but are not limited to, the following: Develop processes for the manufacture of PCBAs. etc. | 4/29/2020 |
| 48 | Tempus Chicago, IL Clinical Molecular Technologist (Sunday-Wednesday with Shift Diff.) MS in a medical, physical, or biological science Exp: Not necessary for MS candidates |
What you’ll do: Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Utilize automation and robotics to standardize the discovery pipeline from sample acquisition to sequencing output. Maintain quality metrics and data generation for next-generation sequencing platforms. Work to maintain CLIA/CAP compliance in a novel field. etc. | 4/29/2020 |
| 49 | Tempus Chicago, IL Clinical Molecular Technologist MS in a medical, physical, or biological science Exp: Not necessary for MS candidates |
What you’ll do: Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Utilize automation and robotics to standardize the discovery pipeline from sample acquisition to sequencing output. Maintain quality metrics and data generation for next-generation sequencing platforms. Work to maintain CLIA/CAP compliance in a novel field. etc. | 4/29/2020 |
| 50 | Tempus Chicago, IL Molecular Technologist, Infectious Disease BS/MS in a medical, physical, or biological science Exp: 1 year |
What you’ll do: Work in a cutting-edge clinical laboratory to provide high-quality molecular test data with rapid turnaround times. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform molecular techniques, which might include quantitative PCR, next-generation sequencing, nucleic acid extraction, DNA/RNA quantification and qualification, NGS library preparation, probe hybridization, probe/library capture, library cleanup and quantification, loading sequencing libraries onto the Illumina Nextseq, HiSeq4000, and Novaseq. etc. | 4/29/2020 |
| 51 | Tempus Chicago, IL Laboratory Supervisor, Molecular Infectious Disease BS in a chemical, physical, biological or other laboratory science Exp: 1 year |
What You’ll Do: Provide daily oversight of a cutting-edge molecular workflow to provide high-quality next-generation sequencing data with rapid turnaround times. Monitor laboratory processes to ensure that acceptable levels of analytic performance are maintained, to include review of quality control, instrument and equipment maintenance, and other quality assurance activities. Assure all remedial actions are taken whenever test systems deviate from the laboratory's established performance specifications. etc. | 4/29/2020 |
| 52 | Tempus Chicago, IL Account Associate BS in biology, other life science, business, or marketing Exp: 0-2 years |
Responsibilities: Building and maintaining relationships with physicians and office staff to drive clinical orders in the community. Building and maintaining relationships with pathology departments to ensure smooth specimen sendouts - tissue procurement. Maintain a regular cadence of touch points (in person, emailing value adds) with certain targeted accounts (ie 3 x month per physician). Coordinating Medical Affairs report review with physicians after clinical orders. etc. | 4/29/2020 |
| 53 | Tempus Atlanta, GA Research Laboratory Assistant AS/BS in a biological science Exp: 1 year |
Responsibilities and Duties: A team player helping to construct, implement, and manage multiple tasks. Receives shipments/specimens from couriers, inventories specimens, and documents the receipt of the samples in accordance with laboratory standard operating procedures. Properly identifies specimens that do not follow the proper submission criteria described in the Specimen Processing SOP, and properly documents and reports any issues to team lead, Laboratory Operations and Project Manager for follow up. Ensures the proper handling of specimens in accordance with assigned SOPs including, but not limited to, proper data entry, specimen handling, storage and aliquoting of the specimens. etc. | 4/29/2020 |
| 54 | Tempus Atlanta, GA Research Associate (AKESOgen) BS in a biological science Exp: 1+ year(s) |
Responsibilities and Duties: A team player helping to construct, implement, and manage multiple experiments. Run automated Nucleic Acid instrumentation, real time PCR, DNA/RNA spectrometer, and genetic scanners. Maintains a clean, safe, and organized lab. Document and maintain records systematically such that they can be easily obtained when needed. Ensure the accuracy of the information before filing. Assist the team leads and scientists in related function. etc. | 4/29/2020 |
| 55 | AMPAC Fine Chemicals Rancho Cordova, CA Analytical Scientist I BS in chemistry or related Exp: 1-3 years in method development/transfer |
Candidate will develop and validate methods; provide analytical support to the research and development group to meet project goals; select appropriate methods and techniques in performing experiments; collaborate with analytical personnel to help develop routine analytical methods; work cross functionally to achieve target goals and proactively seek out potential solutions to issues. Candidate will also assist in creating method validation and/or qualification protocols and reports as well as analytical methods;perform all lab work that will support method validation, transfer, and qualification; perform qualification of primary and secondary reference material to be used as analytical standards. | 4/18/2020 |
| 56 | AMPAC Fine Chemicals Rancho Cordova, CA Operations Technician 1 HS Diploma/GED Exp: 1-4 years in chemical processing plant |
Operations Technician I will perform multiple duties related to the production of chemicals using a series if chemical processes in a batch type or continuous process chemical plant. These duties require careful observation and recording of data during all steps of the process. Assists in assigning tasks to other technicians, monitors performance of personnel, ensures that personnel follow all departmental and AFC policies and procedures, interacts with other personnel of other disciplines, participates in training fellow employees, conveys and logs status of processes, facilities, and personnel to the Crew Chief. Performs a variety of assignments in order to control process and equipment, both manually and with computers. Weigh, measure, and charge into chemical processing equipment a wide variety of chemicals. Operates all process equipment per operating instructions and procedures. | 4/18/2020 |
| 57 | AMRI Albany, NY Research Scientist I BS/BA or MS in chemistry or related Exp: 0-5 years in medical chemistry |
The Research Scientist I is expected to demonstrate expertise in both the theoretical and practical aspects of organic chemistry. Purify synthesized chemicals to an appropriate degree. The scientist will be able to use the full range of chromatographic, crystallization, and distillation techniques. Analyze and identify compounds using a good range of modern separation and spectroscopic techniques. This will include interpretation of TLC, HPLC, polarimetry, IR, and NMR spectra of moderate complexity. | 4/18/2020 |
| 58 | AMRI Springfield, MO Pilot Plant Technician HS Diploma/GED, BS/BA in chemistry preferred Exp: 0-2 years |
Set up and operate equipment to prescribed instructions to perform various unit operations such as reactions, filtrations, distillations, drying, milling, etc on raw materials and various stages of chemical processing. Follow and document per batch sheet instructions to produce products according to all current Good Manufacturing Procedure guidelines as required. | 4/18/2020 |
| 59 | AMRI Grafton, WI QUALITY CONTROL ANALYST I BS/BA in chemistry or natural sciences Exp: 1-3 years in QC lab |
Conduct testing using approved analytical methods. Apply established laboratory methods or techniques to analysis, develop solutions to problems. Contribute to technical reports by providing detailed experimental write-ups. Maintain up-to-date laboratory records in accordance with company guidelines. Clearly document research and results in laboratory notebooks so that others can readily reproduce work. | 4/18/2020 |
| 60 | AMRI Albany, NY Research Scientist I (Small Scale Manufacturing) BS in chemistry or related Exp: 0-2 years |
Adapt internal or customer supplied procedures to cGMP production operations. Manufacture batches of API, under cGMP protocols, for use in human clinical trials. Manage all aspects of a cGMP manufacturing campaign, including batch record review, safety evaluations, material procurement, equipment ordering/set-up/cleaning and project execution. | 4/18/2020 |
| 61 | AMRI Lebanon, NJ Quality Control Analyst I BS/BA in engineering Exp: 0-2 years |
Assist with developing and validating test methods based on relevant ISO, ASTM standards and or client requirements. Independently perform tests per ISO, ASTM, and/or client requirements. Perform testing within the specified test plan and/or SOP for each test. Monitor projects for conformance with applicable SOPs and test specifications. | 4/18/2020 |
| 62 | ARL Bio Pharma Oklahoma City, OK Chemist I-Analytical BS/BA in chemistry or related Exp: 0-2 years industrial experience |
Under general supervision, the Chemist I is responsible for utilizing established methods and standard lab equipment/instrumentation (HPLC, IC) to qualitatively and quantitatively analyze routine pharmaceutical substances and formulations. This is a safety sensitive position as defined by state and federal laws that will require working with hazardous materials and/or handling medicine | 4/18/2020 |
| 63 | AnaptysBio San Diego, CA Research Associate II MS/MA in molecular biology or related Exp: 0-2 years |
This position is responsible for cloning and expressing antigens, antibodies and their variants for our antibody discovery programs. Perform cloning methods, PCR methodologies, and vector and primer design. Perform PCR, DNA mini-, midi-, maxi-prepping procedures. Prepare and process samples for next generation sequencing. | 4/18/2020 |
| 64 | Ardelyx Fremont, CA Quality Assurance Specialist I-III BS/BA or higher in sciences Exp: 1-7 years in manufacturing |
The QA Specialist I-III will provide QA support for Quality Operations and Quality System management. Working in a fast -paced pharmaceutical environment with a broad scope of responsibilities, the candidate will be able to bring many different skills to the job, with a focus on QA activities. The position requires diverse skill sets and will provide the opportunity to challenge an individual’s abilities to perform batch records review, data review and product dispositions, to implement sound Quality System improvements and manage QA procedures, assess GMP suppliers and service providers, and perform QA oversight of contract manufacturers. | 4/19/2020 |
| 65 | Ardelyx Fremont, CA QA Specialist I - III BS in technical discipline/science/engineering Exp: 1-7 years in quality environment |
This role will be responsible for QA oversight of all GxP Computer Systems Validation. The incumbent, working with the functional teams must ensure that all GxP regulated systems are purchased, audited, installed and maintained based on industry best practices (e.g. GAMP5) and regulatory requirements (e.g. 21CFR Part 11 and relevant FDA Guidance). The position plans and organizes all QA activities for computer system validation projects. | 4/19/2020 |
| 66 | Pyramid Laboratories Costa Mesa, CA Manufacturing Technician No degree required Exp: 1+ year(s) |
Under general supervision, perform various manufacturing related activities for a GMP compliant Fill/Finish operation applying standard practices, techniques and procedures. Able to assist in the preparation of reports, records, etc., for assigned tasks. PRINCIPAL DUTIES: Familiar with related GMP procedures and requirements, as directly related to the position. Ensure that appropriate procedures and processes are utilized without unauthorized modifications. etc. | 4/21/2020 |
| 67 | PAR Pharmaceutical Rochester, MI Quality Technician I, Chemistry HS diploma or equivalent Exp: 0-1 year(s) |
Responsible for laboratory and equipment cleanliness, routine physical testing per SOPs, and for receiving, stocking and inventorying reagents and supplies. Works with metrology to perform routine daily instrument calibrations and maintenance. Disposes of laboratory materials in accordance with EH&S, DEA and biohazard procedures. Communicates with the supervisor on a daily basis regarding the lab operations. Uses computer/lab software to enter the data. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. ROLE AND RESPONSIBILITIES: General Lab Support: Maintains the cleanliness of glassware by operating glassware washers or hand washing. Maintains laboratory and instrumentation organization and cleanliness. etc. | 4/15/2020 |
| 68 | Paraxel Durham, NC Software Developer BS in computer science or related Exp: 1 year |
Parexel is hiring an Associate Software Engineer to play a key role in the implementation of COTS applications as well as design, development, testing and maintenance of the clinical applications. The Associate Software Engineer will be expected to provide a solution to business requirements with offering functional design and implementation. Associate Software Engineer also collaborates with peers, product owner, Scrum master to deliver releases in agile development practice. etc. | 4/15/2020 |
| 69 | New England Peptide Gardner, MA Lab Assistant Unspecified Exp: 0-1 year(s) |
NEP is seeking a highly motivated individual interested in a career in the Biotech/Pharmaceutical industry. Local candidates only. No experience necessary, we will train! Working alongside other Peptide Scientists and Technicians, the Lab Assistant will help support the production process. Job duties may include: Weighing of Amino Acids. Stocking Chemicals. etc. | 4/15/2020 |
| 70 | New England Peptide Gardner, MA Lab Assistant (Night Shift) Unspecified Exp: 0-1 year(s) |
NEP is seeking a highly motivated individual interested in a career in the Biotech/Pharmaceutical industry. Local candidates only. No experience necessary, we will train! Working alongside other Peptide Scientists and Technicians, the Lab Assistant will help support the production process. Job duties may include: Weighing of Amino Acids. Stocking Chemicals. etc. | 4/15/2020 |
| 71 | New England Peptide Gardner, MA Lab Technician BS in biology, chemistry, or related Exp: 1 year |
NEP is seeking a qualified individual interested in a career in the Biotech/Pharmaceutical industry. Working alongside other peptide scientists, the Lab Technician will be responsible for synthesizing, analyzing and purifying peptides. This is an excellent opportunity to get practical, hands on experience at a thriving biotech company. etc. | 4/15/2020 |
| 72 | New England Peptide Gardner, MA Lab Technician (Night Shift) BS in biology, chemistry, or related Exp: 2 year |
NEP is seeking a qualified individual interested in a career in the Biotech/Pharmaceutical industry. Working alongside other peptide scientists, the Lab Technician will be responsible for synthesizing, analyzing and purifying peptides. This is an excellent opportunity to get practical, hands on experience at a thriving biotech company. etc. | 4/15/2020 |
| 73 | Personalis Menlo Park, CA Business Development Associate BS in a life science Exp: 1-2 year(s) |
The Business Development Associate will be primarily responsible for developing and nurturing a pipeline of immuno-oncology and targeted therapy prospects in small to mid-size biotech/pharma globally. The Business Development Associate manages inquiries by phone and/or web, identifies target accounts decision makers, sets up appointments for corporate field sales and reports results on each. Will be required to proactively initiate and manage cold call activities into a target list of accounts, warm calls from trade show and other incoming lead sources. The Business Development Associate must be able to identify and qualify opportunities, build trust and credibility, deliver a clear and compelling message, uncover initiatives and gain commitment from prospect to engage with Personalis. etc. | 4/15/2020 |
| 74 | Pharmaron Germantown, MD Associate Bioanalytical Scientist, Large Molecule Bioanalysis BS/MS in related field Exp: 0-1+ year(s) |
This position is responsible for carrying out sample analysis and data processing within stated timeframes and in accordance with Standard Operating Procedures (SOPs) and Company Policies. Contributes to the laboratory and equipment maintenance to ensure efficient operations. Essential Functions: Perform serological and cell-based LBA assays (ELISA/ECL) using plate readers, MSD and flow cytometry. Basic operation and routine maintenance of general laboratory equipment. Participate in day-to-day operation of the Laboratory, the analysis of samples and associated duties. Responsible for handling and processing of biological samples including competent handling and pipetting technique. etc. | 4/15/2020 |
| 75 | Adare Pharmaceuticals Vandalia, OH Regulatory Affairs Specialist ll BS/BA Exp: 1 year in regulatory affiars |
Provide diverse regulatory support to the Regulatory Affairs Department as outlined in essential duties and responsibilities below. Assesses change control documentation and technical documents for incorporation of the information into regulatory submissions. Prepares regulatory submissions for annual reports and assists as necessary with preparation of new regulatory submissions and amendments. Demonstrates an understanding of health authority reporting obligations throughout annual report preparation and seeks guidance when needed to address complex changes. | 4/4/2020 |
| 76 | NanoString Bothell, WA Manufacturing Research Associate I BS in molecular biology, biochemistry, or related Exp: 0-2 years |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to operate equipment, perform SOPs, navigate Document Control systems, ERP systems, etc. This position is Non-Exempt. etc. | 4/7/2020 |
| 77 | Notal Vision Manassas, VA Field Service Engineer BS in electronics, engineering, or related Exp: 1-3 year(s) |
The Field Service Engineer, under supervision and direction of the Director, Operations & Business Performance, installs, calibrates, tests, repairs, upgrades and performs preventative maintenance on specified Notal Vision imaging devices at customer sites and the company’s Headquarters. Deep acumen in of ophthalmic imaging devices is required to understand, assess and act on the needs of the customers and to mitigate loss of testing. ROLES AND RESPONSIBILITIES: Responsibilities of the Field Service Engineer include but are not limited to the following: Provide technical support for imaging devices in multiple care and support settings. etc. | 4/7/2020 |
| 78 | Nuvasive Memphis, TN Associate Engineer, Quality BS in an engineering discipline Exp: 0-2 years |
This role is responsible for the, implementation, and improvement of overall quality systems. The Associate Quality Engineer will participate in Design Control activities and provide guidance to engineering on successful creation and maintenance of design history files during new product introductions. The Associate Quality Engineer may work closely with suppliers or contractors, including auditing, developing inspection/testing plans, performing risk analysis. Lead the development of adequate inspection criteria. Identify the need for custom gauging for NuVasive and suppliers. Identify and qualify equipment required to perform inspection. Support transfer of design to internal or contract manufacturing, including establishment of inspection plans both at NuVasive and at the supplier. Evaluate product and process changes for qualification and validation requirements and assist in change implementations. etc. | 4/8/2020 |
| 79 | Nuvasive Aliso Viejo, CA Clean Room Technician Unspecified Exp: 1+ year(s) |
This role ensures that production is not contaminated by following strict clean room guidelines. Duties include knowing and following all clean room protocols, keeping work areas organized, and maintaining equipment. Key Responsibilities: Follow clean room procedures. Follow production schedule. Follow Instructions. Read drawings and Work Orders. Collect materials required. Assemble mechanical sub- and final assemblies according to QSR’s, Manufacturing Instructions (MIs), and other applicable company procedures. etc. | 4/8/2020 |
| 80 | Nuvasive Memphis, TN Quality Technician Unspecified Exp: 1-3 year(s) |
The Quality Technician is responsible for performing on-site calibration activities and managing a calibration program. Primary duties include performing calibrations utilizing advanced inspection equipment such as a supermic or vision systems, generating controlled documents required to maintain compliance to standards for performing calibrations, contacting vendors for requesting return or calibrations of custom / functional gauging. Review/analyze data and documentation for Quality managed systems. An understanding of industry standard and advanced inspection equipment is necessary to perform essential job duties. etc. | 4/8/2020 |
| 81 | Nuvasive West Carrollton, OH Production Associate - 2nd Shift HS diploma or equivalent Exp: <1 year |
The Associate Post Processing Technician is responsible for the finishing/assembly operations to ensure quality products are produced. The Post Processing Technician helps in driving best practices and creates open communication across all teams to foster a collaborative, high functioning culture. Understand setup and final assembly instructions. Process product through laser marking process with high accuracy and attention to detail. Follow standard applications in order to achieve dimensional integrity and required finish characteristics. Follow the router protocol to ensure the product moves through channels efficiently and GDP is correct prior to moving the product to the next area. Work from quality review and corrective work documents to repair or rework parts. etc. | 4/8/2020 |
| 82 | Nuvasive Memphis, TN Associate Sterile Processing Tech HS diploma or equivalent Exp: 1+ year(s) |
Initiates, maintains, and compiles records associated with ordering, receiving, storing, issuing, and shipping materials, supplies, and equipment by performing the following duties: Compares nomenclature, stock numbers, and other listed information on packing slips to verify the accuracy of purchase orders and shipping orders. Compiles data from sources such as contracts, purchase orders, invoices, requisitions, and accounting reports and writes, types, or enters information into computer to maintain inventory, purchasing, shipping, and other records. Verifies inventory computations against physical count of stock and adjusts errors and reports documenting reasons for discrepancies with proposed corrective action. Compiles and maintains manual or computerized records such as material inventory, in-process production reports, and status of material locations. etc. | 4/8/2020 |
| 83 | Nuvasive West Carrollton, OH Production Associate HS diploma or equivalent Exp: 1-2 year(s) |
The Post Processing Technician is responsible for the finishing/assembly operations to ensure quality products are produced. The Post Processing Technician helps in driving best practices and creates open communication across all teams to foster a collaborative, high functioning culture. Understand setup and final assembly instructions. Process product through laser marking process with high accuracy and attention to detail. Follow standard applications in order to achieve dimensional integrity and required finish characteristics. Follow the router protocol to ensure the product moves through channels efficiently and GDP is correct prior to moving the product to the next area. Work from quality review and corrective work documents to repair or rework parts. etc. | 4/8/2020 |
| 84 | Nuvasive Aliso Viejo, CA Manufacturing Technician Unspecified Exp: 1+ year(s) |
Job Description: Align, fit, and assemble component parts, using hand tools, power tools, fixtures, and templates. Analyze and record test results per acceptance test criteria, and prepare written testing documentation. Organize work areas. Install electrical and electronic parts and hardware in housings or assemblies, using soldering equipment and hand tools. Read blueprints, schematics, diagrams, manufacturing instructions, and work orders to determine methods and sequences of assembly. Repair, rework, and calibrate assemblies and systems to meet operational specifications and tolerances. Test performance of electromechanical assemblies, using test instruments such as oscilloscopes, and electronic voltmeters. etc. | 4/8/2020 |
| 85 | PAR Pharmaceutical Chestnut Ridge, NY Quality Associate l HS diploma or equivalent Exp: 0-1 year(s) |
The Quality Associate I, Operations is responsible for actively participating in “on the floor” Quality activities during product manufacturing and/or packaging. Quality activities include product sampling and inspection, area clearance to confirm process readiness, and non-conforming event support to resolve in-process issues. Communicates to multiple departments and supervision to provide timely process and issue updates. Identifies and escalates issues or problems to appropriate supervision. Participates as a team member on cross-functional teams. Participates in reviews and structured processes for continuous improvement. etc. | 4/8/2020 |
| 86 | Adare Pharmaceuticals Vandalia, OH Quality Assurance Technician (Night Shift) BS in chemical/biological sciences Exp: 0-2 years in pharma |
This position is responsible for providing quality support to the manufacturing floor, auditing batch production documentation, dispositioning intermediates and equipment after cleaning, performing in process checks, reviewing and approving incident reports, revise quality documents (e.g. SOP, protocols, methods), and ensuring adherence to cGMP. | 4/4/2020 |
| 87 | 10xGenomics Pleasanton, CA Research Associate – Sequencing Core BS/BA in biology/biochemistry or related Exp: 1-3 years in lab, qPCR, auto liquid handling systems |
We are seeking an experienced, collaborative and adaptable individual to join our 10X sequencing core team. The candidate will have a strong background in nucleic acid quantification and NGS workflows.Quantitation and QC of incoming sequencing libraries. Operate epMotion and other automated liquid handlers | 3/28/2020 |
| 88 | 10xGenomics Pleasanton, CA Research Associate – Protein Engineering BS in biological sciences Exp: 1+ years in industry |
We are seeking a skilled and enthusiastic protein engineer at a Research Associate level to join the Protein Engineering Group. The candidate will be expected to work on a variety of protein engineering projects to optimize and generate differentiated enzymatic leads. Participate in protein engineering efforts to optimize various enzymes used in 10x Genomics products. Protein expression of various enzymes, preferably nucleic acid modifying enzymes. | 3/28/2020 |
| 89 | 10xGenomics Pleasanton, CA Production Associate 1 BS or MS in biological sciences, chemistry, or engineering Exp: 1+ years in lab or QC of life science products |
Execute production operations according to defined procedures and ensure the integrity and quality of products. Operate liquid handling robotic system and complex manufacturing equipment for production biochemistry under supervision. Perform formulation and dispensing of reagent consumables and assemble into final kit configurations. Process work orders accurately using an ERP system in a timely manner | 3/28/2020 |
| 90 | 10xGenomics Pleasanton, CA Process Engineer MS in life sciences/ engineering Exp: 1-3 years in lab |
10x is looking for an outstanding Process Engineer to join the Process Development team. This is a key position for the commercialization of consumable products associated with Next Generation Sequencing chemistries. This person will be responsible for developing and integrating process control and yield optimization solutions for complex reagent manufacturing workflows and identifying process to function relationships. | 3/28/2020 |
| 91 | 4G Clinical Wellesley, MA Project Coordinator BS/BA in business administration or equal Exp: 0-2 years |
The Project Coordinator is an administrative professional who works with the Client Services Lead to ensure a project’s success. Monitor and communicate project status to team members. Organize and plan meetings. Communicate timeline changes and information to team | 3/28/2020 |
| 92 | A2 Biotherapeutics Aqoura Hills, CA Research Associate MS in life sciences Exp: 1+ years in lab |
The Drug Discovery team is seeking a highly motivated individual with experience in cell and molecular biology. Molecular cloning, including construct generation and DNA/RNA preparations. Mammalian cell culture maintenance and cell-based assays. Design, execution, documentation and presentation of experiments | 3/28/2020 |
| 93 | A2 Biotherapeutics Aqoura Hills, CA Research Associate MS in life sciences Exp: 1+ years in lab |
The Drug Discovery team is seeking a highly motivated individual with experience in cell and molecular biology. The successful candidate will join us at our research facility in Agoura Hills, CA and work on cutting edge science in a dynamic, fast-paced and team-oriented environment. Purification and biochemical characterization of recombinant proteins. Mammalian cell culture maintenance and cell-based assays | 3/28/2020 |
| 94 | WCG Clinical Eden Prairie, MN Associate Project Manager BS/BA in realted Exp: 1 year in admin for client facing projects |
The Associate Project Manager, at our Eden Prairie, MN office location, is responsible for the oversight of the more complex day-to-day administration and organization of client projects (working closely with the Project Manager) to ensure that projects are delivered on time, within budget and according to the agreed upon scope of work. | 3/29/2020 |
| 95 | Aurolife Pharma Dayton, NJ Warehouse Associate HS Diploma/GED Exp: 1 year in pharma warehouse |
It is the Warehouse Associate's responsibility to ensure that all cGMP material received (for example API, Excipients, & Packaging & Printing Components) are properly , accounted, stored and recorded as per cGMP requirements and standard procedures and to make sure all the ERP entries will be completed on time. 1. Receive materials and conform the information in the packing slip and issued P.O. 2. Store API, Excipient, Packaging and Printed components and other inventory controlled items on qualified location in the warehouse | 3/29/2020 |
| 96 | Aurolife Pharma Lawrenceville, NJ Associate Chemist II BS in chemistry Exp: 1-3 years in pharma/analytical testing |
Chemist will perform a variety of QC testing to assess the strength, identity and purity of test samples and/or materials. Incumbent will work as a member of team to effectively plan and QC analytical testing using established (official and/or in-house) test procedures. The incumbent may execute 95% - 100% of their work at the bench level. | 3/29/2020 |
| 97 | Acumed New York, NY Sales Associate - NYC BS in business/medical field Exp: 0-3 years in sales |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. Continuously assesses the customer base to identify new business opportunities and develops a targeted sales strategy for each identified opportunity proactively ensuring all leads are followed up on appropriately. | 3/29/2020 |
| 98 | Acumed Hillsboro, OR Quality Assurance Technician 1 (Swing Shift) HS Diploma/GED Exp: 6-12 months in related |
The Quality Assurance Technician 1 (QAT) inspects in-process and finished materials and products, purchased or manufactured, to the required drawing or print specification, inspection plan or other controlling document. Documents out of specification situations by initiating nonconformance reports (NCMRs). Tests, inspects, or measures products, materials, and/or processes to evaluate conformance with specifications. | 3/29/2020 |
| 99 | MRIGlobal Kansas City, MO Associate Scientist, In Vivo MS Exp: Not necessary for MS candidates |
MRIGlobal’s Global Health and Security (GHS) Operations, Medical Countermeasures (MCM) Division is looking for an experienced Junior Scientist at our Kansas City headquarters. The Associate Scientist will provide technical project leadership and technical guidance to junior staff. The primary responsibilities of the position are: Serve as a Study Coordinator/Study Director for studies conducted in MCM (i.e. including Toxicology, Animal Health, and Biological and Chemical containment) and as a resource on animal models. Serve as a point of contact for clients and represent MRIGlobal. Provide technical guidance and direction to ensure the group meets and achieves project milestones. Provides leadership and training to technical staff on procedures and instrumentation. Helps to establish a course of action to accomplish a specific project or goal; plans proper assignments of personnel and appropriate allocation of resources; determines schedule of events; communicates expectations about tasks and deadlines; develops contingency plans. etc. | 4/1/2020 |
| 100 | MRIGlobal Kansas City, MO Electrical Engineer MS Exp: Not necessary for MS candidates |
MRIGlobal has an exciting full-time opportunity for an Associate Electrical Engineer in our Intelligence, Surveillance, and Reconnaissance Division located in Kansas City, MO. In this unique opportunity, the selected candidate will work with other engineering and technical disciplines in the design, prototyping, and testing of custom systems to meet customer requirements. Furthermore, the selected candidate will: Design a broad range of analog and digital circuits. Design and layout custom circuit boards to meet challenging packaging and performance requirements. Design, layout, and assemble control and power distribution panels for custom systems. etc. | 4/1/2020 |
| 101 | Merck KGaA Sheboygan Falls, WI Associate Production Scientist BS/BA in chemistry, biochemistry, chemical engineering or related Exp: Not necessary for BS/BA candidates |
Manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. Safely perform operations to meet quality expectations. Ensure quality throughout the process. Assure you are adequately trained to perform tasks/assignments. Perform routine assays, processes and/or unit operations. Complete the volume of work required to achieve group/departmental goals and meet deadlines. Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal). etc. | 4/1/2020 |
| 102 | Mirati Therapeutics San Diego, CA Clinical Trial Associate BS in a scientific or healthcare field Exp: 1-3 year(s) |
We are seeking a highly motivated individual to join Mirati Therapeutics as a Clinical Trial Associate (CTA) within the Clinical Science/Operation Teams, reporting into a Director of Clinical Science. The CTA will interact with Clinical Science/Operation teams and collaborate effectively with CROs and vendors. The CTA supports the timely conduct of clinical studies according to protocols, Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and all applicable regulations governing the conduct of clinical trials. etc. | 4/1/2020 |
| 103 | Molecular Templates Austin, TX Manufacturing Associate - GMP Upstream (2nd Shift) AS in a life science or engineering Exp: 1+ year(s) |
Molecular Templates is seeking an energetic and highly motivated professional to support upstream processing of therapeutic proteins. This position will perform functions related to production and GMP manufacturing operations, including execution of protein fermentation steps. Equipment, facility, process and people will be prepared to deliver quality ETBs, the next generation of immunotoxins, to patients in clinical trials. The Manufacturing Associate will provide on-the-floor execution to bioprocessing unit operations requiring attention to detail, working in a team environment and interest in learning about bioprocessing operations. The Manufacturing Associate will be responsible for adhering to Standard Operating Procedure (SOP) guidelines, Good Manufacturing Practices and all safety requirements in a state-of-the-art biologics manufacturing facility. etc. | 4/1/2020 |
| 104 | Molecular Templates Austin, TX Manufacturing Associate - GMP Upstream (1st Shift) AS in a life science or engineering Exp: 1+ year(s) |
Molecular Templates is seeking an energetic and highly motivated professional to support upstream processing of therapeutic proteins. This position will perform functions related to production and GMP manufacturing operations, including execution of protein fermentation steps. Equipment, facility, process and people will be prepared to deliver quality ETBs, the next generation of immunotoxins, to patients in clinical trials. The Manufacturing Associate will provide on-the-floor execution to bioprocessing unit operations requiring attention to detail, working in a team environment and interest in learning about bioprocessing operations. The Manufacturing Associate will be responsible for adhering to Standard Operating Procedure (SOP) guidelines, Good Manufacturing Practices and all safety requirements in a state-of-the-art biologics manufacturing facility. etc. | 4/1/2020 |
| 105 | Molecular Templates Austin, TX Manufacturing Associate - GMP Downstream (2nd Shift) AS in a life science or engineering Exp: 1+ year(s) |
Molecular Templates is seeking an energetic and highly motivated professional to support downstream processing of therapeutic proteins. This position will perform functions related to production and GMP manufacturing operations, including execution of protein purification steps. Equipment, facility, process and people will be prepared to deliver quality ETBs, the next generation of immunotoxins, to patients in clinical trials. The Manufacturing Associate will provide on-the-floor execution to bioprocessing unit operations requiring attention to detail, working in a team environment and interest in learning about bioprocessing operations. The Manufacturing Associate will be responsible for adhering to Standard Operating Procedure (SOP) guidelines, Good Manufacturing Practices and all safety requirements in a state-of-the-art biologics manufacturing facility. etc. | 4/1/2020 |
| 106 | Molecular Templates Austin, TX Manufacturing Associate - GMP Downstream (1st Shift) AS in a life science or engineering Exp: 1+ year(s) |
Molecular Templates is seeking an energetic and highly motivated professional to support downstream processing of therapeutic proteins. This position will perform functions related to production and GMP manufacturing operations, including execution of protein purification steps. Equipment, facility, process and people will be prepared to deliver quality ETBs, the next generation of immunotoxins, to patients in clinical trials. The Manufacturing Associate will provide on-the-floor execution to bioprocessing unit operations requiring attention to detail, working in a team environment and interest in learning about bioprocessing operations. The Manufacturing Associate will be responsible for adhering to Standard Operating Procedure (SOP) guidelines, Good Manufacturing Practices and all safety requirements in a state-of-the-art biologics manufacturing facility. etc. | 4/1/2020 |
| 107 | Molecular Templates Jersey City, NJ Clinical Trial Assistant BS in a life science Exp: 1+ year(s) |
Molecular Templates is seeking a highly-motivated and skilled professional to assist the Clinical Operations team. The Clinical Trial Assistant will provide support through maintenance of clinical trial studies. This includes establishing and maintaining the trial master file structure for all ongoing studies, providing coordination of supplies and inventory, coordinating meetings and preparing materials and ongoing general administrative support. This position requires excellent technical, analytical, time management and organizational skills, along with adherence to written and verbal instructions and accurate and timely completion of documentation. This position requires excellent organizational, time management and multi-tasking skills, along with the ability to follow standard operating procedures and manage competing priorities. etc. | 4/1/2020 |
| 108 | Wake Research Las Vegas, NV Clinical Research Patient Recruiter HS Diploma/GED Exp: 0-2 years |
The Clinical Research Patient Recruiter will engage in community resources to identify, pre-screen and schedule subjects based on assigned studies by demonstrating a knowledge of study requirements and schedules. They are also responsible for maintaining a working knowledge of all actively-enrolling and upcoming trials. Engage in community resources, including but not limited to, social media, support groups and educational events. | 3/21/2020 |
| 109 | WuXi AppTech St. Paul , MN Associate Chemistry Specialist BS/BA Exp: 0 years |
The Associate Chemistry Specialist will perform a variety of testing preparation techniques, including sample preparations/extractions, reagent preparation procedures and solvent exchange. The position will also include performing a variety of routine benchtop and analytical analysis. Extract test samples using soxhlet, submersion, and fluid path techniques. Perform benchtop testing, including pH, non-volatile residue, USP wet chemistry, and other entry level techniques. | 3/21/2020 |
| 110 | Lifecore Biomedical Chaska, MN Machine Operator I HS diploma or equivalent Exp: 6+ months |
The Machine Operator I is responsible for the setup and operation of standard packaging machinery in the packaging department. This includes working with and monitoring other packaging personnel to complete equipment set up and operation required by the department schedule. Machine Operators must comply with regulatory requirements, Good Manufacturing Practices (GMP), Standard Operating Procedures (SOP), and Manufacturing Process Records (MPR). They will perform all processes as required to fill, label, print, tray seal, pouch, final package, and inspect any Lifecore product; document completed work during packaging of final product; continually practice proper precautions and procedures when working with equipment and handling chemicals; etc. | 3/24/2020 |
| 111 | Lifecore Biomedical Chaska, MN QC Microbiologist I BS in microbiology, biology, or related science Exp: 0-2 years |
This individual will ensure accurate, reproducible, and timely QC testing in support of manufacturing; support development, validation and stability studies on an as-needed basis; participate in methods improvements within the laboratory. They will perform testing on in-process product, final product, and raw materials for routine testing, validation testing, and stability testing; communicate results through appropriate documentation and batch records, statistical analysis and trending; acquire and maintain cleanroom and gowning qualification; participate in rotation to provide weekend and holiday coverage; perform instrument maintenance; identify and report equipment and method failures; identify areas for continuous improvement. etc. | 3/24/2020 |
| 112 | Matinas Biopharma Bridgewater, NJ Clinical Manufacturing Technician AS/AA Exp: 0-1 year(s) |
The Clinical Manufacturing Technician, LNC Manufacturing is responsible for the safe and compliant manufacture of clinical drug products as well as maintaining the manufacturing area in a clean, well supplied, and orderly state. The Clinical Manufacturing Operator, LNC Manufacturing Will Be Specifically Responsible For: Manufacturing of Clinical Supply Batches. Packaging and Labeling of Clinical Supply Batches. Following area Standard Operating Procedures. Cleaning of the Clinical Manufacturing Facilities and Equipment. etc. | 3/25/2020 |
| 113 | LabCorp Burlington, NC Technologist (1st Shift) BA/BS in biology, chemistry, medical technology, or related Exp: 0-1+ year(s) |
We are seeking a Technologist to join our Reference Microbiology lab team in Burlington, NC! Performs tests and analyses according to established testing procedures in designated technical department. Assays performed in the in our department utilize a variety of scientific techniques, including Performs tests and analyses according to established procedures in designated technical department. Position may perform various techniques including EIA, IFA, and other non-automated and automated procedures. Open to entry level and senior level technologist's candidates as well as Technicians with an associates in Medical Laboratory Technology or Biotechnology. etc. | 3/25/2020 |
| 114 | LabCorp Winston-Salem, NC Medical Lab Technician - Float AS/AA in a laboratory science or medical technology Exp: 1 year |
Are you looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference? Are you an experienced Medical Lab Professional or desire to start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technician in Winston Salem, NC. In this position, you will work in a fast paced, customer focused, and challenging environment. etc. | 3/25/2020 |
| 115 | LabCorp Burlington, NC Technologist (2nd Shift) BA/BS in biology, chemistry, medical technology, or related Exp: 0-1+ year(s) |
Are you looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference? Are you an experienced Medical Lab Professional or desire to start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in our Molecular Microbiology lab. In this position, you will work in a fast paced, customer focused, and challenging environment. Assays performed in the Molecular Microbiology area include Qualitative and Quantitative PCR, with the overall goal of providing results that can be used for the diagnosis and management of a wide range of infections using real-time PCR detection of nucleic acid. We are currently looking for someone who has or is looking to gain experience in PCR testing for this entry level Molecular Microbiology position. etc. | 3/25/2020 |
| 116 | LabCorp Charlotte, NC ASCP Certified Medical Technician BA/BS in a laboratory science or medical technology Exp: 1 year |
Responsibilities: This is a clerical and processing position with no testing involved. Determine the acceptability of specimens for testing according to established criteria. Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. Monitor, operate and troubleshoot instrumentation. Demonstrate the ability to make technical decisions regarding testing and problem solving. etc. | 3/25/2020 |
| 117 | LabCorp Burlington, NC Specimen Processing Specialist HS diploma or equivalent Exp: 1 year |
Job Duties/Responsibilities: Prepare laboratory specimens for analysis and testing. Spin samples, pour urine tubes, and create frozen samples. Unpack and route specimen to their respective staging areas. Accurately identify and label specimens. Pack and ship specimen to proper testing facilities. Properly prepare and store excess specimen samples. Process all necessary paperwork to process and submit specimen. etc. | 3/25/2020 |
| 118 | LabCorp Houston, TX Technician AS/AA in a laboratory science or medical technology Exp: 1 year |
Are you looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference? Are you an experienced Medical Lab Professional or desire to start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technician in Houston, TX. In this position, you will work in a fast paced, customer focused, and challenging environment. The shift for this position will be Tuesday- Saturday 6 am to 2:30 pm. etc. | 3/25/2020 |
| 119 | Invitae San Francisco, CA DNA Extraction Technician BS in a clinical laboratory science or related Exp: 1+ year(s) |
We're looking for passionate laboratory technicians who will support high complexity laboratory testing on patient specimens across various assays and platforms. This role will be performing quality control and quality assurance procedures while complying with all applicable local, state and federal laboratory requirements. The work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask and be flexible with tasks and schedules, and the ability to work independently in a team environment. This role requires on-site work at our San Francisco location as well as ability to work overtime and off-schedule days as needed. etc. | 3/17/2020 |
| 120 | Invitae San Francisco, CA Data Analyst, Lab Operations unspecified Exp: 1+ year(s) |
We are seeking a data analyst to join our team. Responsibilities will include monitoring our product pipeline using custom software tools with the goal of assuring samples move through smoothly. Candidates should have experience with UNIX. They are expected to take initiative to automate tasks and troubleshoot the production process through detail-oriented analysis. An important part of this job is to be able to clearly communicate technical findings to non-technical teammates. | 3/17/2020 |
| 121 | Jounce Therapeutics Cambridge, MA Clinical Trial Associate (CTA) BS/BA Exp: 1+ year(s) |
The successful candidate will assist with daily clinical trial execution activities and assist in the coordination of documentation associated with the conduct of investigational clinical studies in accordance with Food and Drug Administration (FDA) Regulations, Good Clinical Practice (GCP), and company standard operating policies and procedures. Responsibilities: Key support role to senior Clinical Operations staff; ensures that delegated components of clinical trials are executed to expected and specified quality standards. Responsible for study laboratory sample management, including tracking and vendor management support. Collect trial information and disseminate it to the internal project team, the CRO, and other stakeholders. Schedule and coordinate study meetings, materials and agendas; recording and disseminating decisions and actions. etc. | 3/17/2020 |
| 122 | Celgene Seattle, WA Research Associate, Viral Vector Process Analytics BS/MS in molecular biology, biochemistry, bioengineering or related Exp: 1-3 year(s) |
The Research Associate will join an analytical team in the viral vector process development group. The Research Associate will perform assays to quantify and characterize adeno-associated virus vector (AAV) and lentiviral vector. AAV and lentiviral vector deliver the genetic information used to re-engage a patient’s own immune system to cure cancer. These viral vectors are key intermediates in Bristol Meyers Squibb CAR-T and TCR cell therapy drug products. Responsibilities: Perform molecular and cell-based analytical assays, process data, review and report results, and follow established laboratory protocols. Maintain accurate and detailed documentation in laboratory notebook. etc. | 3/17/2020 |
| 123 | Celgene Bothell, WA Facilities Compliance Associate I BS/BA Exp: 0-2 years |
The Associate will support Facilities compliance by overseeing GxP documentation including creation and revision of Standard Operating Practices (SOPs) and associated Work Instructions (WIN). The Associate will be responsible in performing F&E related deviation investigations and CAPA. DUTIES AND RESPONSIBILITIES: Key Responsibilities: Responsible for adherence to all Operating Procedures, protocols, policies, regulatory requirements, GMP, and safety guidelines. Responsible for maintaining all required records and adherence to established guidelines for quality control procedures, GMP’s, and safety. Participate in the development and revisions to the Facilities & Engineering training program. etc. | 3/17/2020 |
| 124 | Celgene Seattle, WA Research Associate, Viral Vector Process Development BS in bioengineering, chemical engineering, virology, or related Exp: 0-2 years |
The Research Associate will join our viral vector process development group supporting process development, production and characterization of AAV vectors, which are key intermediates in the generation of multiple T-cell derived drug products. The candidate will support AAV programs and advance our capabilities in vector production. Responsibilities: Hands-on experimental work in the development and optimization of upstream (cell culture and transfection conditions) and downstream (clarification, tangential flow filtration, chromatography) unit operations for viral vector production. Support the process development program for AAV vector manufacturing platforms. etc. | 3/17/2020 |
| 125 | Celgene Seattle, WA Process Engineer I/Senior Research Associate, Process Science and Technology MS in bioengineering, chemical engineering, or related Exp: 1+ year(s) |
BMS company is seeking enthusiastic, self-driven individuals to join its innovation-focused, multi-disciplinary team focused on advancing new, enabling technologies. This development role will be part of a team of associates, engineers, and scientists that develop next-generation processes and technologies for manufacturing adoptive T-cell therapies. The positions will require experimental design, experimental execution, data analysis, drafting of technical reports, and presentation of results. etc. | 3/17/2020 |
| 126 | Celgene Seattle, WA Research Associate, Product Sciences BS in immunology or related Exp: 0-2 years |
The Cell Therapy Product Sciences department is seeking a Research Associate to support the development of early stage CAR T and engineered TCR cell products. The Product Sciences Team is responsible for developing and executing mechanism of action and characterization studies to support the development of gene-engineered T cell therapies. The primary focus of the Product Sciences Research Associate role will be to build CAR T cell product and process understanding in support of pipeline projects. Successful candidates will have a strong foundation in immunology and/or human T cell biology and experience with implementation and optimization of a broad range of in vitro cell-based and molecular assays. etc. | 3/17/2020 |
| 127 | Just-Evotec Biologics Redmond, WA Associate Scientist, Functional Biocharacterization BS in biochemistry, molecular biology, chemical engineering, or related Exp: 0-5 years |
Just is seeking a motivated and creative Associate Scientist who desires a significant opportunity to improve worldwide access to biotherapeutics. In this position, you will work with a multidisciplinary team for the analytical and functional biocharacterization of large molecule therapeutics and analysis of process impurities. Experience with ELISA binding assays, DNA extraction, and PCR preferred. Additional experience with cell-based and ligand-receptor binding assays, as well as high-throughput methods and liquid handling robotics beneficial. The successful candidate has strong written and verbal communication skills and is interested in ways to improve technology. etc. | 3/17/2020 |
| 128 | Just-Evotec Biologics Redmond, WA Associate Scientist, High Throughput Analytical BS in biochemistry, molecular biology, chemical engineering, or related Exp: 0-5 years |
Just is seeking a motivated and creative Associate Scientist, who desires a significant opportunity to improve worldwide access to biotherapeutics. We are looking for a motivated scientist to join a fast-paced, collaborative, and multidisciplinary team. As a member of the High Throughput Analytical group, you will support process development through application of H/UPLC and CE methodologies. Additional experience with other analytical techniques as well liquid handling robotics is a plus. The ideal candidate has strong written and verbal communications skills and works well independently and in teams. etc. | 3/17/2020 |
| 129 | Just-Evotec Biologics Seattle, WA Associate Scientist, Protein Expression BS Exp: 0-5 years |
Just is seeking a motivated and creative researcher who desires a significant opportunity to improve worldwide access to biotherapeutics. In this position, you will work as a member of a small but highly experienced and innovative team to develop cell lines for the purpose of manufacturing biologic therapeutics. The successful candidate will have experience with cell culture as well as a strong foundation in cell and molecular biology. Experience in cell line development, cell culture automation, and expression vector design, is a plus. The candidate must possess strong written and verbal communication skills, strong organizational skills, a desire to learn new scientific concepts, and an ability to work directly with scientific staff across multiple disciplines. etc. | 3/17/2020 |
| 130 | LakePharma Hayward, CA Scientist II/Senior Scientist I, Antibody Engineering MS in molecular biology, biochemistry, chemical engineering or related Exp: No experience necessary |
We are rapidly growing and seeking a talented individual to join our Antibody Center Department, specialized in antibody engineering. The candidate will be part of the Antibody Engineering Group, responsible for phage library construction and screening, new antibody discovery and affinity maturation, as well as the companion biochemical assays. Essential Duties and Responsibilities: Work on various projects for our clients that involve the discovery of novel antibodies or engineering of existing antibodies to improve their functional activities. etc. | 3/18/2020 |
| 131 | LakePharma Worcester, MA Lab Assistant/Associate Scientist I AS/BS in biology or related Exp: 0-3 year(s) |
We are rapidly growing and seeking a talented individual(s) to join our Molecular Biology Team as an Associate Scientist. The employee will be responsible for executing projects within the laboratory, writing study/research plans, and summarizing data to clients and colleagues via technical reports. The position requires a drive to provide outstanding customer service by maintaining regular communications with clients, meeting or exceeding quality and timeline expectations. etc. | 3/18/2020 |
| 132 | Veracyte South San Francisco, CA Clinical Lab Scientist BS or MS in biological sciences/technology Exp: 1 year in molecular diagnostic testing |
The Veracyte Clinical Laboratory continues to grow! We are seeking a new Clinical Laboratory Scientist (CLS) to perform cutting-edge diagnostic testing on patient specimens in our collaborative, high-energy work environment. S/he will accurately perform molecular genetic testing, using a variety of molecular biological techniques including expression microarray analysis. | 3/14/2020 |
| 133 | Vero Biotech Atlanta, GA Quality Assurance Associate (Biotech) BS/BA in sciences Exp: 1-3 years in FDA/cGMP environment |
Responsible for ensuring that the quality of products being manufactured meet the prescribed quality levels. Performs Quality Assurance activities including review of manufacturing and quality inspection documentation. Monitors the quality system including records and results from processes and procedures to ensure product Quality and compliance. Ensuring manufacturing and quality documentation is accurate, maintained, and reflects GMP, procedural and regulatory requirements. | 3/14/2020 |
| 134 | Viant Grand Rapids, MI Technical Operator 1 - 1st Shift HS Diploma/GED Exp: 1 year in manufacturing |
Under the director of the area Supervisor, responsible for production work according to specifications and established policies, procedures, practices and standards. Assembles components. May be required to operate packaging machine. Performs bar sealing/tray sealing duties | 3/16/2020 |
| 135 | Viant San Antonio, TX Quality Engineer III MS in engineering Exp: 0-5 years |
The Quality function oversees the development of quality standards and protocols for quality assurance testing models. Quality assists in the design and implementation of policies and procedures for testing and evaluating the precision and accuracy of products and/or equipment. Interact with customers and provide support for Engineering, Quality Systems and Process engineering. | 3/16/2020 |
| 136 | Viant Elkhorn, WI OPERATOR - Entry Level HS Diploma/GED Exp: 1 year in manufacturing |
This position ensures that assigned machines/equipment produce product at or above department standards. Responsible to produce, assemble, inspect and pack all parts as per the work instructions for each assigned task or machine. Maintain all required paperwork and documentation to Good Manufacturing Practice (GMP) and ISO 13485:2016 standards. | 3/16/2020 |
| 137 | Homology Medicines Bedford, MA Research Associate, Analytical Development BA/BS in a biological science Exp: 0-2+ years |
The role of Analytical Development Research Associate is to aid in developing and refining analytical methods to characterize AAV vector products. The individual in this role will be a highly-skilled, talented and motivated researcher who will focus on the analysis of research/development-grade vector samples using multiple AAV-specific analytical methods. This individual will participate in conducting, optimizing and qualifying molecular and bioanalytical assays such as cell-based infectivity, potency, and immunoassay. We seek candidates with proven ability to work independently after initial training and collaboratively to achieve optimized project plans, with the ultimate goal to deliver products that transform the lives of patients. etc. | 3/9/2020 |
| 138 | Hovione East Windsor, NJ Process Technician - Drug Product Continuous Manufacturing BS in chemical or other engineering Exp: 1-2 year(s) |
The Process Technician will support the installation and qualification of a GMP continuous tablet manufacturing line, highly automated, with Process Analytical Technology enabled control. This position will also support the development and manufacturing activities for drug product and formulation development projects. Main responsibilities: Work in a GMP environment area, executing chemical and physical operations following approved written instructions and in accordance with cGMPs and EHS regulations. Clean/verify proper cleaning of equipment and production areas according with cGMPs. Adhere to the necessary gowning requirements and in alignment with the various room classifications. Ensure that performed activities are recorded in applicable documentation. etc. | 3/9/2020 |
| 139 | Idexx Worthington, OH Medical Lab Technician - Parasitology - temporary HS diploma/AS/BS Exp: 1+ year(s) |
You will be using automated analyzers, microscopes and other laboratory diagnostic tools to perform analyses and tests that diagnose animal illnesses, injuries and diseases in support of veterinarian animal treatment. You will be responsible for setting up and running lab tests, and reading and releasing results according to SOPs (Standard Operating Procedures). You can expect to specialize in one or more of the following areas: Parasitology: Examining samples to identify parasites, utilizing fecal flotation and various microscopic techniques. etc. | 3/9/2020 |
| 140 | Immatics Houston, TX Research Associate - CMC - PD BS in biology, biochemistry, biotechnology, or related Exp: 1-2 year(s) |
The primary purpose of the Research Associate I position is to perform complex, highly specialized and time sensitive technical cell manipulation and/or perform analytical tests to characterize and assess the functionality of final products. Overall Responsibilities: Perform cell growth and manipulation procedures such as cell enrichment, cell evaluation and sorting, cell culture, cellular product cryopreservation, cell product thaw/wash. Perform accurate calculations to determine cell viability, dilutions and cell concentrations. Responsible for aseptic handling of reagents and products and characterization of cells by molecular assays, flowcytometry and functional assays. etc. | 3/9/2020 |
| 141 | Immucor Waukesha, WI Laboratory Technician - Filling HS diploma or equivalent Exp: 6-24 months |
We are looking to hire a Filling Laboratory Technician. This role is responsible for performing tasks and functions associated with the filling of production. In addition, you must perform routine upkeep and maintenance of the lab including recording temperatures, cleaning, and disposal of contaminated waste. If you’ve got the necessary skills and experience to excel in this position, we want to hear from you. Apply today! Responsibilities: As the Filling Laboratory Technician, your responsibility will be to accurately complete paperwork with minimal corrections and timely entry of time and materials into ERP when required. etc. | 3/9/2020 |
| 142 | Integer Brooklyn Park, MN Manufacturing Team Member 1-1 HS diploma or equivalent Exp: 0-2 years |
The primary purpose of this position is to develop competency in and performance basic assembly and/or inspection operations at Integer. The incumbent is expected to follow written procedures to meet production and quality requirements. 1. Adheres to Integer's Values, Behavioral Based Safety process and Integer Associate Quality Policy. 2. Sets up equipment needed for assembly/inspection as per Manufacturing Process Instructions (MPI's) and Quality Work Instructions (QWI's). 3. Understands own tasks and how they relate to others on their team. Works under close Supervision where duties are clearly defined. Will follow Standard Work where applicable. | 3/10/2020 |
| 143 | Integer Salem, MA Associate Machine Operator - MCE 2nd Shift HS diploma or equivalent Exp: 0-1 year(s) |
The primary purpose of this job is to operate and monitor machines routinely used in the production of the organization's product. May be involved in the basic set-up, calibration and maintenance of equipment and/or perform finish operations. Key Accountabilities and Responsibilities: 1. Adheres to Integer Values and all safety and quality requirements. 2. Operates machinery used in the manufacture of products with close supervision. 3. May be involved in the basic set-up and/or calibration of equipment. etc. | 3/10/2020 |
| 144 | Integer Salem, MA Associate Machine Operator - Subassembly Weekend Days HS diploma or equivalent Exp: 0-1 year(s) |
The primary purpose of this job is to operate and monitor machines routinely used in the production of the organization's product. May be involved in the basic set-up, calibration and maintenance of equipment and/or perform finish operations. Key Accountabilities and Responsibilities: 1. Adheres to Integer Values and all safety and quality requirements. 2. Operates machinery used in the manufacture of products with close supervision. 3. May be involved in the basic set-up and/or calibration of equipment. etc. | 3/10/2020 |
| 145 | Integer Trenton, NJ Assembler Operations 1 - 1st Shift HS diploma or equivalent Exp: 1 year |
Assembler has the general responsibility of assembly and production of components. Position Requirements: Assemble products per assembly process specifications. Conduct product testing under supervision of engineers. Maintain all log books and lot control information per standard operating procedures. Fully trained assembler will have the following: Understanding of the assembly processes. etc. | 3/10/2020 |
| 146 | Integer Plymouth, MA Associate Prototype Builder AS/AA Exp: 0-3 years |
The primary purpose of this role is to perform assembly and inspection operations over a range of new products and/or processes. Will support non-cyclical work which may include prototypes and pre-production lots in preparation for validation, clinical trials or transfers. Will also support multiple builds within the facility including lab and cleanroom environments. With guidance from Engineering on projects and using work procedures, this role provides support to the Engineering teams to meet various deadlines. May provide support to other team members or provide input to the Engineers on assembly, processes, and build/quality documentation. etc. | 3/10/2020 |
| 147 | Integer Chaska, MN Manufacturing Team Member - 4th Shift HS diploma or equivalent Exp: 0-2 years |
Key Accountabilities and Responsibilities: Adheres to Integer's Values, Behavioral Based Safety process and Integer Associate Quality Policy. Sets up equipment needed for assembly/inspection as per Manufacturing Process Instructions (MPI's) and Quality Work Instructions (QWI's). Understands own tasks and how they relate to others on their team. Works under close Supervision where duties are clearly defined. Will follow Standard Work where applicable. Assembles component parts as per print. Utilizes both manual and automatic machine operation. etc. | 3/10/2020 |
| 148 | Integer Plymouth, MA Manufacturing Team Member 1-1 HS diploma or equivalent Exp: 0-2 years |
The primary purpose of this position is to develop competency in and performance basic assembly and/or inspection operations at Integer. The incumbent is expected to follow written procedures to meet production and quality requirements. Adheres to Integer's Values and all safety, environmental, security and quality requirements including, but not limited to: Quality Management Systems (QMS), Safety, Environmental and Security Management Systems, U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements. etc. | 3/10/2020 |
| 149 | Integra Hicksville, NY Associate Sales Representative, Extremity Orthopedics Reconstruction BS/BA Exp: 0-2 years |
The Associate Sales Representative will be a responsible for Integra’s Extremity Orthopedic Reconstruction product line and solely responsible for sales of these products within a defined territory. Your primary responsibility will be to support and grow business in order to achieve or exceed sales revenue targets. You will provide case coverage, transport trays, and develop select accounts by building relationships, demonstrating extensive product knowledge and providing exceptional customer service. Your primary call points will be plastic surgeons, podiatric surgeons and orthopedic surgeons. 50% of your time will be spent in the Operating Room. You will work side by side with an experienced Account Manager for approximately 18 months. If performance qualifications are met, then you may be offered a Account Manager for a full territory anywhere in the U.S. etc. | 3/10/2020 |
| 150 | Integra Cordova, TN Warehouse Tech HS diploma or equivalent Exp: 1-5 year(s) |
Responsibilities: Load and unload incoming and outgoing materials and products. Move materials to and from loading docks, delivery trucks, storage areas, and manufacturing areas. Identify and label materials, and record their locations in the warehouse and on the shelves to maintain inventory. Prepare prep kits for production and make necessary work orders associated with each prep kit. Move these kits to assigned location. Operate trucks, forklifts, cranes, and other equipment to move freight. Perform and report cycle counts weekly. etc. | 3/10/2020 |
| 151 | Intellia Therapeutics Cambridge, MA Senior Research Associate MS in cell or molecular biology Exp: 0-3 years |
Intellia Therapeutics is developing the CRISPR/Cas9 gene editing technology for therapeutic application both in vivo and ex vivo. This work requires the generation of numerous human lentiviral or mouse retroviral tools for target discovery and target validation. The role of Senior Research Associate/Associate Scientist – Lentivirus Production is primarily responsible for the generation, concentration, titration, and curation of viral particle preparations that are needed to support numerous research efforts. etc. | 3/10/2020 |
| 152 | ThermoFisher Lexington, MA Associate I, Upstream Manufacturing BS/BA Exp: 1-3 years in cGMP manufacturing |
Responsible for cGMP Upstream manufacturing operations at the Viral Vector Services Thermo Fisher Scientific Lexington, MA. Executing aseptic operations within a biosafety cabinet and cleanroom environment. Performing operations in an aseptic seed lab, operating Wave bioreactors, operating adherent / stir tank bioreactors. | 3/7/2020 |
| 153 | ThermoFisher Millersburg, PA Material Handler I - Weekend Shift / Nights HS Diploma/GED Exp: 0-2 years related experience |
Pick, pack, sort, arrange, count, store, and correctly process items for storage and/or shipment in accordance with established procedures and customer requirements while sustaining a high level of quality to ensure customers receive correct product and in the time requested. Receive materials and/or finished goods on a daily basis. Verify the quality, type and amount of materials received are correct and that the appropriate documentation is present (e.g. packing list). | 3/7/2020 |
| 154 | ThermoFisher St. Louis, MO Biopharmaceutical Technician II- Nights HS Diploma/GED, BS/BA preferred Exp: 1-2 years in GMP preferred |
The candidate will be responsible for the performance of operations in support of the manufacture of Commercial and Clinical Biologics. He/She will be responsible for following Current Good Manufacturing Practices (cGMPs) and carrying out a variety of functions related to Upstream (cell culture) and Downstream (purification) biopharmaceutical manufacturing. These functions may include but are not limited to activities such as propagation of mammalian cell culture, conducting aseptic cell culture operations, execution of large scare production bioreactors (50L - 2000L), conducting large scale chromatography, viral inactivation, viral filtration, ultrafiltration and diafiltration, as well as aseptic filling of bulk drug substance. | 3/7/2020 |
| 155 | ThermoFisher Carlsbad, CA Biostatistician MS in statistics/biostatistics Exp: 1-3 years |
As an integral part of the Research and Development Team, you will design and execute research and development activities relating to Thermo Fisher Scientific’s next generation sequencing assays and platform development for both the research use only and in vitro diagnostic markets. | 3/7/2020 |
| 156 | ThermoFisher Fairport, NY Set-Up Technician - Days, Fairport HS Diploma/GED, Technical degree preferred Exp: 1-3 years setup experience |
Under the direction of the Engineering Manager, with a dotted line to the Shift Supervisor, this position is responsible for installing and removing molds and related auxiliary equipment and components from the molding press as well as preparation of setup for appropriate machines as defined. This individual is also responsible to make necessary adjustments to equipment to ensure quality and quantity of production for the assigned area. | 3/7/2020 |
| 157 | ThermoFisher Miami, FL Manufacturing Technician I HS Diploma/GED Exp: 0-1 years |
Commitment to Safety, by following site safety procedures and utilizing safety equipment as required for daily tasks. Ability to document Near Miss reports, safety opportunities, accident reports, etc. Uses batch record instructions, job aids, standard operating procedures, and product specifications to execute production activities. Maintains accurate documentation, records and logs in accordance with FDA (Food and Drug Administration), GMPs (Good Manufacturing Practices) and ISO9000 (International Organization for Standardization). | 3/7/2020 |
| 158 | Ultragenyx Woburn, MA Temporary Research Associate, Analytical Testing BS in biological sciences Exp: 0-2 years in industry |
Working in close collaboration with other Analytical Development team members, the Research Associate will perform analytical methods for AAV samples to support the development of our AAV gene therapy programs. Working with the senior research staff, devise improvements in AAV analytical methods, technology, and documentation. Perform basic AAV analytical methods and documentation for sample management and analysis | 3/8/2020 |
| 159 | UPM Pharmacueticals Bristol, TN Microbiologist BS/BA in microbiology or related Exp: 0-2 years |
Performs routine microbiological testing of raw material, in process, finished product and stability following approved specifications and Standard Operating Procedures (SOPs). This may include but is not limited to antibiotic testing, bioburden/microbial limit testing, antimicrobial effectiveness testing, water testing, environmental monitoring, microbial isolation and identification technique. | 3/8/2020 |
| 160 | Upsher Smith Maple Grove, MN Associate Chemist I - CAS BS/BA in chemistry Exp: 12 college credits in chemistry |
The Associate Chemist I provides analytical and technical support to new product development and completes analytical testing and various laboratory support functions in a timely manner according to cGMP's. Reads, understands and follows the current USP/NF, laboratory SOPs, analytical methods and study protocols. Documents equipment usages and analytical results in a manner that can be readily followed by reviewers and is consistent with cGMP and in-house SOPs. Performs analytical testing according to established or preliminary methods such as cleaning validation samples, dissolutions, assay, impurities/degradation products, content/blend uniformity, pH, viscosity, titrations, general USP testing, residual solvents and other analytical methods. | 3/8/2020 |
| 161 | Upsher Smith Maple Grove, MN Corporate Sales Representative I BS/BA in business, science, or communications Exp: 1-3 years |
The Corporate Sales Representative is responsible for the development and management of a designated territory with the goal of maximizing sales while improving patient lives. Patients are central to all USL strategies, and the CSR will be responsible for developing business relationships with targeted neurologists, epileptologists, seizure specialists and other healthcare practitioners and members of the health care community. | 3/8/2020 |
| 162 | Fluke Glenwood, IL Field Support Technician II unspecified Exp: 1-2 year(s) |
Performs calibration and repairs of assigned test and measurement products and equipment: Basic calibrations. Analyzes, troubleshoots, makes repairs, resolves technical problems and performs maintenance service on equipment returned to the service center by customers. Achieves a timely turn-around on all equipment and service. Enters data into Oracle and/or an asset tracking database. etc. | 3/4/2020 |
| 163 | Fluke Glenwood, IL Laboratory Technician II BS in a life science or comparable Exp: 1-2 year(s) |
We are seeking an individual to join our growing Laboratory operations team. Please read on if you are looking for a start to a long term career. Calibrates radiation detection equipment using ionizing radiation sources/techniques. Assures customer satisfaction and on time delivery of calibrated devices. Able to meet production rates. Reviews generated analytical data before assignment of official calibration certificate. etc. | 3/4/2020 |
| 164 | Fluke Everett, WA Production Assembler/Operator HS diploma or equivalent Exp: 1-2 year(s) |
Product Assembler/Operators perform wet, dry, mechanical and/or electromechanical processes to produce quality saleable product (components, instruments and/or systems). Position may require extended periods of stationary work in assembly and/or light fabrication. Primary Responsibilities: Prepare, process, wind, clean, install, assemble, rework, calibrate, test, solder and/or inspect product at various stages of assembly from component to final. etc. | 3/4/2020 |
| 165 | Gritstone Oncology Pleasanton, CA Manufacturing Associate I/II, Upstream BS in biological sciences or related Exp: 1+ year(s) |
The Manufacturing Associate will execute activities associated with cell culture manufacturing in a clean room environment. Processes will be focused on viral vector based cancer vaccine products. This role will also need to assist with aseptic filling and buffer prep processes as well as maintain material inventory in labs. etc. | 3/4/2020 |
| 166 | Gritstone Oncology Cambridge, MA Research Associate GMP/NGS BS in a scientific or health-related field Exp: 1+ year(s) |
The primary role of the Research Associate is to be responsible for the execution of established nucleic acid extraction and next-generation sequencing (NGS)-based cancer genomics workflows including exome and transcriptome sequencing in a cGMP environment. The ideal candidate will have experience in a regulated environment (CLIA/CAP, cGMP) and will be expected to maintain batch record reports, consumable inventory, equipment maintenance and calibration to maintain quality control and compliance. Individuals with experience as a Clinical Lab Technologist or Molecular Technologist are encouraged to apply. etc. | 3/4/2020 |
| 167 | Takeda Greenwood, IN Entry Level Medical Screener / Phlebotomist (Full Time) HS Diploma/GED Exp: Entry Level |
You’ll use your attention to detail to screen new and repeat donors and take and record donor vital signs and finger stick results. You will use our Donor Information System, prepare donor charts, maintain accurate records, and coordinate donor compensation. You’ll work in our fast-paced, team environment; ensure a clean and professional work environment; attend team meetings; work closely with your management team; and problem-solve together. The high-quality plasma you collect will become life-changing medicines. Here, a commitment to customer service and quality is expected. | 2/29/2020 |
| 168 | Takeda Lexington, MA Manufacturing Technician I HS Diploma/GED minimum Exp: 0-2 years in industry |
With direct supervision this individual will perform routine manufacturing operations for the production of clinical and/or commercial products. Operates production equipment according to SOPs in their assigned areas. The individual will carry out cGMP manufacturing cleaning and disinfection operations utilizing Standard Operating Procedures (SOPs). Primary responsibilities. | 2/29/2020 |
| 169 | Takeda Round Lake, IL Production Associate AS/AA or HS Diploma/GED Exp: 0-2 years in manufacturing |
The Production Associate (PA) is responsible for executing all processes in production at Takeda’s manufacturing facility in Round Lake, Illinois, while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply; fully participates in both departmental projects and any quality working teams which may be applicable; under the general direction of the lead technician and the overall direction of the supervisor, responsible for the hands-on execution of all activities in the production area | 2/29/2020 |
| 170 | Takeda Social Circle, GA Manufacturing Technician I AA or equivalent, or BS/BA Exp: BS/BA: 0 years, AS/AA: 1 year |
Executing processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Clean, Set up, operate, and teardown of equipment such as tanks, filtration systems, and production lines. Operate general production equipment (such as pH and conductivity meters, autoclave, portable mixers, etc.). | 2/29/2020 |
| 171 | TCR Therapeutics Cambridge, MA Research Associate/Senior Research Associate, Analytical Process Development BS in biological/chemical sciences Exp: 1-2 years |
This position will require execution of cell culture experiments, assisting the team in analysis of in-process samples, and support of the technology transfer to CMOs. The position represents an excellent opportunity for career development, working closely with experienced scientists, in a fast-paced and highly collaborative environment. Learn and execute on all assays used by the analytical team (qPCR, ELISA, T-cell based assays). Assist in the analysis and characterization of lentiviral vectors for use by multiple internal research groups. | 2/29/2020 |
| 172 | Teligent Buena, NJ Clean Room Services Operator – 3rd Shift HS Diploma/GED Exp: 1 year in topical/steril filling/manufacturing |
Cleaning and sanitization of controlled cleanroom environments such as Equipment Preparation rooms, , and all ancillary areas. Additional responsibilities may include cleaning and sanitization of process tanks, mixers, compounding and filling equipment, product formulation processes, terminal product sterilization, finished product inspection, etc. Proactively identify equipment issues and perform root cause analysis, make recommendations and aid in implementation for more complex and non-reoccurring issues. | 3/1/2020 |
| 173 | Tempus Chicago, IL Reagent Quality Control Technologist BS in med tech, clinical lab sciences, or related sciences Exp: 1 year in molecular lab |
Work within a cutting-edge genomics workflow to provide quality control support in a high-volume next-generation sequencing clinical laboratory. Report significant reagent findings/deviations and system deficiencies to lab management, as appropriate. Document all results and findings in order to satisfy CLIA/CAP/NYS-DOH requirements. | 3/1/2020 |
| 174 | Tempus Chicago, IL Extraction Technologist BS in med tech, clinical lab sciences, or related sciences Exp: 1 year in molecular lab |
Work in a cutting-edge clinical laboratory to support next-generation sequencing workflow with rapid turnaround times. Utilize state-of-the-art automation and robotics to extract nucleic acids. Track sample progress through the next generation sequencing workflow. Perform basic molecular biology protocols | 3/1/2020 |
| 175 | Tenaya Therapuetics South San Francisco, CA RA II/SRA I - Quality Control and Analytical Development BS/MS in chemical engineering, biological/chemical sciences Exp: 1-2 years in analytical method development |
We are seeking a motivated Research Associate with experience in viral vector analytical methods for our newly formed Technical Operations Analytical Development/Quality Control Group. In this role, you will perform key molecular biology and cell based assays to support Process Development activities; troubleshoot and optimize particular assays as needed; develop new analytical methods to determine the strength, purity and/or potency of viral vector preparations; perform other tasks such as SOP writing, lab maintenance, supply ordering and write-ups of experiments for potential regulatory submissions. | 3/1/2020 |
| 176 | Tenaya Therapuetics South San Francisco, CA Research Associate - Analytical Development BS/MS in biological sciences, chemistry, physics Exp: 1 year academic/industrial lab experience |
In this role, you will perform key potency, purity and strength assays to support Process Development activities; troubleshoot and optimize particular assays as needed; assist in the development of new analytical methods to determine the strength, purity and/or potency of viral vector preparations; and perform other tasks such as lab equipment maintenance and supply ordering. | 3/1/2020 |
| 177 | TeraRecon Fremont, CA Technical Support Specialist BS in computer engineering or related Exp: 12 months in MCSE, CCNA or equivalent |
Provide technical support to customers via phone, email or chat utilizing remote access tools provided by TeraRecon. Actively Monitor customer systems for failures/issues and follow-up on those remotely. Analyze and resolve customer service issues associated with TeraRecon products running on Windows Workstations and Windows Server Operating Systems. | 3/1/2020 |
| 178 | STAAR Surgical Monrovia , CA Quality Control Inspector II HS Diploma/GED Exp: 1 year with computers |
Perform force and functional testing and data calculations for injector cartridges. Perform QA review of Device History Records. Maintain Device History Records. Inspect, sort, disposition and transfer of returned product from receiving dept., mail, customer service or other. | 2/22/2020 |
| 179 | STAAR Surgical Monrovia , CA Production Technician (CNC) HS Diploma/GED Exp: 1-2 years in IOL, contact lense, or medical devices |
Thorough knowledge of all applicable SOP's: makes proper decisions in line with applicable SOPs and standards under normal conditions. Perform highly technical tasks in support of manufacturing including equipment set-up and manufacturing of product, tool changes, sterilization processes, and filtration of material and calibration activities as assigned. Troubleshoot issues on equipment and assist with preventative maintenance. | 2/22/2020 |
| 180 | STAAR Surgical Monrovia , CA Production Operator I HS Diploma/GED Exp: 1-2 years in medical devices |
Thorough knowledge and appropriate implementation of basic production functions. Completes required production documentation accurately. Consistently meets quality and productivity targets. Appropriately follows company policies, rules, and regulation | 2/22/2020 |
| 181 | Starkey Hear Technologies Eden Prairie, MN Microelectronic Mfg Engineer I BS/BA in engineering or physical sciences with emphasis in metrology/engineering Exp: 1-3 years in process/manufacturing engineering |
We are seeking to add a Microelectronic Manufacturing Engineer that will investigate and develop new microelectronic technologies and processes. In addition to new development work, this position is also responsible for improvements of existing assembly processes. This involves developing, prototyping, implementing and improving new thick film ceramic substrate, hybrid assemblies and PCB/flexible circuit surface mount assembly manufacturing processes required for both new product introductions and existing products. | 2/22/2020 |
| 182 | Starkey Hear Technologies Eden Prairie, MN Test Engineer I - New Products BS/BA in engineering/physical sciences Exp: 0-3 years with electronic hardware/software |
Design, develop, and implement automated systems to test product in a manufacturing environment, at component, subassembly and systems levels. Perform product requirements analysis, test requirements definition, test system hardware and software design, systems integration, and validation. Generate design, validation, and maintenance documentation to comply with corporate quality system and department policies | 2/22/2020 |
| 183 | Starkey Hear Technologies Eden Prairie, MN Firmware Engineer I MS in electrical engineering Exp: 1+ years |
Starkey Hearing Technologies is seeking a talented Firmware Verification Engineer to join the Firmware Engineering Department. The Firmware Engineering Department at Starkey Hearing Technologies is responsible for architecting, developing, and verifying firmware for DSPs and microcontrollers that define the core functionality of millions of hearing products shipped worldwide. | 2/22/2020 |
| 184 | Starkey Hear Technologies Eden Prairie, MN Electrical Engineer I - EA Engineering BS/BA in electrical engineering Exp: 1 year in product development |
Generate component requirements and review and contribute to system performance requirements. Lead the Electro-Acoustic Engineering team in documenting specific requirements in the SyRS’s and the SDR’s using the Hardware Development Hearing Aid Design Guide as a high-level reference. Work with the Project Manager to manage work efforts to ensure project schedules are met and areas of high risk are identified and mitigated with appropriate risk mitigation plans. Follow the Electroacoustic Engineering Product Development Process. Perform electrical and electro-acoustic design tasks and provide input into project timelines and schedules. | 2/22/2020 |
| 185 | Starkey Hear Technologies Eden Prairie, MN Software Tester I BS/BA Exp: 1-2 years in software test/quality assurance |
Conduct Software Testing on software applications. Follow standard Configuration Management practices and utilize a defect tracking tool. Tracking quality assurance metrics such as defect densities and open defect counts. Perform system level testing on Starkey’s Software and Hardware systems working either in a team or independently. | 2/22/2020 |
| 186 | Starkey Hear Technologies Eden Prairie, MN Test Engineer I - New Products BS/BA in electrical/mechanical/computer engineering Exp: 0-3 years with electronic hardware/software |
Design, develop, and implement automated systems to test product in a manufacturing environment, at component, subassembly and systems levels.Perform product requirements analysis, test requirements definition, test system hardware and software design, systems integration, and validation. Generate design, validation, and maintenance documentation to comply with corporate quality system and department policies | 2/22/2020 |
| 187 | SDC Tempe, AZ Biostatistician MS in biostatistics/statistics Exp: 1-3 years |
Supports lead biostatistician on clinical studies; may serve as lead biostatistician with oversight from a more senior biostatistician. Maintains the statistical integrity of clinical trials analyzed by SDC. Assists in preparing statistical analysis plans, preparing data deliverables for clinical study reports, interpreting analysis results, and writing statistical sections of clinical study reports. | 2/22/2020 |
| 188 | Stereotaxis Saint Louis, MO Field Service Engineer - (FSE.6) AS/AA in electronics Exp: 1-5 years in field service |
Provide on site and remote service and support of Stereotaxis magnetic navigation systems including permanent magnets, and servo control systems. Interface with customers and vendors to ensure a quality service experience and that all expectations are met. | 2/22/2020 |
| 189 | Steripharma Syracuse, NY New! Warehouse Technician - 1st Shift HS Diploma/GED Exp: 1+ years in warehousing |
This position is responsible for performing/controlling a combination of manual or automated tasks necessary for the receipt, storage, and shipment of product. This may include functions of receiving, picking, packing, shipping, staging, transporting, storage, delivery, etc. | 2/22/2020 |
| 190 | Steripharma Syracuse, NY Production, Clean Room Pharmaceutical Technician - 2nd Shift AS/AA or BS/BA Exp: 1+ years in hospital or manufacturing |
This position operates production equipment, to include non-sterile filling machines, and packaging and labeling machines. Position is responsible to supply assigned positions with materials/items to complete work and according to standard operating procedures. Position is also responsible to clean equipment, production areas, and inspect parts/items following prescribed procedures. Provides troubleshooting on basic issues and may assist in providing training. | 2/22/2020 |
| 191 | Steripharma Syracuse, NY Sanitation and Custodial Services Technician, 3rd Shift HS Diploma/GED Exp: 1-2 years in production environment |
This position is responsible for performing a variety of duties in support of the maintenance of buildings, facilities, and grounds. Also, this position is responsible for a variety of cleaning duties, a variety of other building maintenance work, and related duties as assigned. Sweep and mop floors, clean windows; clean restrooms and fixtures; clean and maintains lunch and break rooms. Strip and wax tiled floors as required; vacuum, buff and wax floors. | 2/22/2020 |
| 192 | Steris Coon Rapids, MN Validation Technician BS/BA Exp: 1 year in sterilization for medical devices |
The Validation Technician assists in the processing of Customer products, and coordinates production scheduling, validations and qualifications. Monitors, studies and controls the sterilization of medical devices and other items to ensure effective sterilization. Coordinates with Customers and Sales to provide quotations for validations. Works with Customers to complete validation timelines and Customer validation forms | 2/22/2020 |
| 193 | Steris Keller , TX Quality Technician I HS Diploma/GED Exp: 1 year in medical devices |
Performs medical device evaluations and monitors the quality of outgoing medical devices. Evaluates incoming medical devices in accordance with procedure guidelines to accurately prepare service/repair estimates. Performs routine testing for product release. Validates accuracy of outgoing repair documentation. Provides feedback to QA and production departments concerning technician and product performance. | 2/22/2020 |
| 194 | Steris Chicago, IL Sterile Processing Technician I HS Diploma/GED Exp: 1+ years in SPD |
Provides on-site support for the reprocessing of surgical instruments and trays to contracted facilities in compliance with the Department of Health, TJC, OSHA, CDC, AAMI and AORN standards and facilities goals and policies. Position level will be determined by previous job related experience, performance and certification requirements. | 2/22/2020 |
| 195 | Steris Palo Alto, CA Field Service Representative I AS/AA or BS/BA in electronics or mechanical engineering Exp: 1-2 years related |
Position acts as Trusted Advisor to STERIS Customers in maintenance and procurement of medical devices and consumable products as part of a high performing team. Drive an exceptional Customer experience by providing on-site preventative maintenance, troubleshooting, repair, equipment modification and installation support on complex mechanical, electro-mechanical and electronic units in a high stress healthcare environment. Provide superior Customer service by pro-actively interacting and communicating with Customers. | 2/22/2020 |
| 196 | Steris Birmingham, AL CNC Machinist I HS Diploma/GED Exp: 1+ years at CNC machine |
Operates both manual and CNC equipment for the efficient production of quality components. Responsible for the production of high-tolerance precision parts. Interpret technical prints. Setup, operate and adjust machining equipment for production efficiency with supervision. Monitors quality of parts produced to ensure customer requirements are met. | 2/22/2020 |
| 197 | Steris Charleston, SC Technician HS Diploma/GED Exp: 1-3 months training/experience |
The primary role of the Repair Technician is to perform repairs on medical instrumentation. Technicians will be trained to become familiar with various types of surgical instruments and understand how to best maintain and repair them. Repairs are completed on a repair truck onsite at a hospital or surgery center. In addition to repair work, Technicians may work with a team including Sales Representatives and RCs (Repair Consultants/Managers) to identify and capitalize on revenue opportunities. | 2/22/2020 |
| 198 | Steris Brooklyn Park, MN Quality Assurance Technician I Associates degree Exp: 1 year related role |
The Laboratory Quality Assurance Technician I position is applicable to contract laboratory, manufacturing (if applicable) and steam processing (if applicable). The position is responsible for day to day execution of the quality system including but not limited to record review and verification including laboratory reports and manufacturing and sterilization processing run records as applicable, maintenance of quality documents related to calibration, validation, software, logsheets, and training records as applicable. | 2/22/2020 |
| 199 | Strand Therapeutics Cambridge, MA Associate Scientist I, Synthetic Biology BS or MS in biological engineering/science/chemistry Exp: 1-3 years research experience |
We are looking for people who have the enthusiasm andmotivation to be a highly contributing member of a small team. This opportunity will offer the employee the ability to work closely with the founding team, as well as to form closepartnerships with team members during the development and formation of the company. Executing molecular biology experiments including molecular cloning, bacterial transformation and mammalian cell culture. | 2/22/2020 |
| 200 | Stratos Genomics Seattle, WA Research Associate/Scientist, Molecular Engineering MS or BS/BA in chemistry/chemical engineering or related Exp: 1-2 years lab experience |
Candidates will be involved in synthesizing the unique building blocks for our novel DNA sequencing technology, developing and optimizing synthesis protocols, as well as proposing and executing innovative experiments to push our technology forward. The position is salaried with hours dependent on lab needs and project deadlines. | 2/22/2020 |
| 201 | Structure Medical Naples, FL Swiss CNC Machinist I HS Diploma/GED Exp: 1 or more years in programing/operating CNC machines |
Performs entry level specialized computer numerical control (CNC) machinist work for Structure Medical, LLC. Operates CNC machines to run production per approved schedule provided. Work is performed under close supervision with minimal latitude for the use of initiative and independent judgment. | 2/22/2020 |
| 202 | Stryker Portage, MI Design Engineer - Mechanical BS/BA in mechanical engineering Exp: 0-3 years |
As a Design Engineer- Mechanical, you will work to develop innovative new products for the Surgical technologies group. A passion for innovation and creativity is desired for this role. Plan and conduct engineering research, design, development projects as assigned. Monitor and control progress of projects to ensure sound application of engineering principles are used and design intent is being followed/achieved | 2/22/2020 |
| 203 | Stryker San Jose, CA Quality Engineer BS/BA in engineering Exp: 0+ years in regulated manufacturing environment |
As a Quality Engineer you will provide support in quality assurance, control, and preventative activities with a focus on continuous improvement of internal products and processes. You will own identified internal and supplier driven non-conformances and manage the timely closure of NC's within Trackwise. You will communicate with suppliers regarding non-conformances, escalating supplier corrective action, changes and process qualifications requests as required. You will engage in the development, improvement and sustaining of the internal manufacturing processes for existing and new products. | 2/22/2020 |
| 204 | Stryker Plainfield, IN Quality Control Technician - 1st shift HS Diploma/GED Exp: 1-2 years in tolerance QC |
Will perform incoming inspection on components and Electro/mechanical products per company/regulatory specifications. Will work from engineering schematics or blueprints to perform accurate checks and tests. Will be required to comply with documentation and regulatory procedures and policies. Will work across multiple, different IT platforms and Quality Management Systems. Will interact with internal and external customers to resolve, inspection and/or components issues, across multiple divisions. | 2/22/2020 |
| 205 | Stryker Davie, FL Assembly Technician I HS Diploma/GED Exp: 1 year experience |
"Responsible for providing assembly, testing and facility support for all our production efforts. Assembly of fabricated parts and assemblies at work stations along with testing of final assemblis to meet tolerances and product specifications. Uses hand tools and power tools to assemble units according to assembly / work instructions. | 2/22/2020 |
| 206 | Stryker Leesburg, VA Entry Level Fulfillment Clerk HS Diploma/GED Exp: 1 year related experience/training |
Ensures complete fulfillment of all replenishment orders. Unloads daily shipment of incoming surgical sets and does the precautionary cleaning of incoming sets. Verifies kind and count of replenishments prior to shipping. Processes and stages outgoing replenishments. Performs the last check of replenishments and surgical sets prior to final boxing for shipment | 2/22/2020 |
| 207 | Stryker Leesburg, VA Entry Level Fulfillment Clerk HS Diploma/GED Exp: 1 year related experience/training |
Ensures complete fulfillment of all replenishment orders. Unloads daily shipment of incoming surgical sets and does the precautionary cleaning of incoming sets. Verifies kind and count of replenishments prior to shipping. Processes and stages outgoing replenishments. Performs the last check of replenishments and surgical sets prior to final boxing for shipment | 2/22/2020 |
| 208 | Sun Pharma Billerica, MA Microbiology Technician I HS Diploma/GED Exp: 1+ years related experience |
Performs routine microbiological sampling and quality control testing supporting manufacturing of commercial pharmaceutical products in accordance with current Good Manufacturing Practices (cGMP), ISO and Pharmalucence policies and procedures | 2/23/2020 |
| 209 | Sun Pharma Billerica, MA Formulation and Fill Technician I HS Diploma/GED Exp: 0-2 years related experience |
Performs the formulation and dispensing of pharmaceutical products according to current Good Manufacturing Practices (cGMPs) and utilizing Standard Operating Procedures (SOPs) in a clean room environment. Formulate and dispense product in a clean room environment for Radio-pharm as well as dermatological products. Wash and sterilize all equipment, tubing, filters, stoppers, vessels, vials, ampoules etc. | 2/23/2020 |
| 210 | Sunrise Pharma Rahway, NJ Manufacturing Operator HS Diploma/GED Exp: 0-2 years related experience |
Candidate should have knowledge of manufacturing procedures, good manufacturing systems and familiarity with regulatory and Standard Operating Procedures. Experience in granulation, milling, compression, and encapsulation. Conformance to GMP and SOP requirements by following batch records accurately in granulation, encapsulation, and compression. Perform setup, cleaning and troubleshooting of encapsulation machines and tablet presses. Demonstrated ability to read and interpret documents such as operating and maintenance instructions and procedure. Experience in a pharmaceutical or bio pharmaceutical environment. | 2/23/2020 |
| 211 | Scanlan St. Paul, MN Surgical Instrument Spec. Order Fulfilment HS Diploma/GED Exp: 0-2 years related experience |
The Surgical Instrumentation Specialist/Order Fulfillment position is responsible for preparing instruments for etching, building wet labs, maintaining demonstration cases, filling orders for repairs and reconditions, repairing and modifying surgical instruments, operating and maintaining equipment, continuous work space cleaning and upkeep, any other duties as requested by supervisor. | 2/23/2020 |
| 212 | Surrozen South San Francisco, CA Research Associate, Protein Sciences -Protein Expression/Purification BS or MS in protein biochemistry or related Exp: 1-4 years lab experience (class, internship, academic) |
The Research Associate position for Protein Expression/Purification within the Protein Sciences Group is a great opportunity for experienced associates as well as recent graduates to expand their skills in state-of-the-art biochemical techniques while accelerating therapeutic discovery and development in regenerative medicine. Characterize and purify protein samples using SDS-PAGE, chromatography, and related techniques. Perform mammalian cell transfections for recombinant protein expression | 2/23/2020 |
| 213 | Surrozen South San Francisco, CA Research Associate, Protein Sciences - Molecular Biology/Protein Expression BS or MS in protein biochemistry or related Exp: 1-4 years lab experience (class, internship, academic) |
Produce recombinant DNA clones and plasmids using standard molecular biology protocols. Perform small scale transfection in mammalian cells for recombinant protein expression. Characterize purified protein samples by SDS-PAGE and related techniquques. Preparation of presentations, technical reports, summaries and detailed protocols, and contribute to company reports as requested | 2/23/2020 |
| 214 | Surrozen South San Francisco, CA Research Associate - Senior Research Associate, In vivo Pharmacology BS or MS in molecular/cell biology, biochemistry, genomics, etc. Exp: 1+ years research experience |
Help develop and implement disease and injury models for characterization of lead molecules. Conduct independent in vivo studies and contribute to collaborative activities. Perform tissue necropsy. Perform tissue sample analysis, such as clinical biochemistry, ELISA, qPCR and immunohistochemistry. Maintain mammalian cell culture, perform gene expression studies and in vitro functional assays (e.g., RT-qPCR, reporter assays, FACS analysis). | 2/23/2020 |
| 215 | Surrozen South San Francisco, CA Research Associate-Senior Research Associate, Biochemistry/Biophysics BS or MS in biochemistry, biophysics or related Exp: 1+ years research experience |
Perform high-throughput biophysical and biochemical assays to evaluate developability properties of antibody-based molecules. Perform routine cell-culture maintenance, protein expression in mammalian cells and purification in milligram-scale protein production and characterize antigen:antibody (Fab) complexes for crystallization screens. | 2/23/2020 |
| 216 | Surrozen South San Francisco, CA Research Associate, Discovery Biology BS or MS in molecular/cell biology, biochemistry, genomics, etc. Exp: 1-4 years lab experience (class, internship, academic) |
Establish relevant mammalian cell or organoid cultures, study gene expression and perform in vitro functional assays (e.g., RT-qPCR, reporter assays, FACS analysis). Study cell fate in organoids and tissue explants. Investigate gene expression in tissue samples by RT-qPCR, RNA in situ hybridization (RNAscope@), Western blots, ELISA and immunohistochemistry. | 2/23/2020 |
| 217 | Sutro Biopharma San Carlos, CA Manufacturing Associate BS in biological sciences Exp: 1-6 years in cGMP manufacturing |
Perform various manufacturing tasks such as operating, troubleshooting, sterilizing, maintaining, preparing, and cleaning of various process equipment such as stirred-tank bioreactors, media/buffer solutions, disc stack centrifuges, homogenizer, pelletizer, dryer, TFF skid, chromatography systems, parts washers, and CIP systems, under the guidelines of established SOPs and cGMP regulations. Reliably and consistently execute well defined SOPs and batch records. Accurately document data and complete batch records. | 2/23/2020 |
| 218 | Sutro Biopharma San Carlos, CA Quality Control Associate MS in chemistry, biochemistry, bioanalytical chemistry or scientific related Exp: 1-3 years |
Perform analytical assays on daily basis. The assays include wet-lab chemistry, HPLC, CE, icIEF, ELISA, Electrophoresis, UV spectroscopic based methods, and compendial methods required for the release and stability testing of water, raw material, in-process, and final products. Perform data review and analysis. Support method transfer and validation activities | 2/23/2020 |
| 219 | Suvoda Conshohocken, PA Associate Project Manager - Entry Level BS/BA in life or computer sciences Exp: Entry Level |
Work as part of a cross-functional project team responsible for the delivery of Interactive Response Technology (IRT) for randomization and drug supply management in clinical trials. Support the Services Delivery project team in:Liaising with the client to discuss requirements, handle issues, provide status updates, and answer questions. Designing the IRT solution to meet the study requirements based on the clinical protocol, Suvoda proposal and discussions with the client | 2/23/2020 |
| 220 | Suvoda Portland, OR Associate Project Manager - Entry Level BS/BA in life or computer sciences Exp: Entry Level |
Work as part of a cross-functional project team responsible for the delivery of Interactive Response Technology (IRT) for randomization and drug supply management in clinical trials. Support the Services Delivery project team in:Liaising with the client to discuss requirements, handle issues, provide status updates, and answer questions. Designing the IRT solution to meet the study requirements based on the clinical protocol, Suvoda proposal and discussions with the client | 2/23/2020 |
| 221 | Suvoda Portland, OR Quality Control Analyst BS/BA Exp: 1-3 years |
Ensure activities and deliverables are performed during the software development process as required by Suvoda procedures. Identify issues during the development of a product (or delivery of a service) before it is released. Release Suvoda products and systems through the various phases of development. Review and approve SDLC and validation deliverables | 2/23/2020 |
| 222 | Suvoda Conshohocken, PA Quality Assurance Analyst BS/BA Exp: 1-3 years |
Manage and monitor quality assurance activities, such as the review and approval of QMS documents, investigation of issues and execution of CAPAs, preparation and conduct of audits, training management and the qualification of 3rd party vendors. Perform issue trending and work with the organization to improve processes to prevent issues from occurring during the development of products and delivery of services | 2/23/2020 |
| 223 | SVA Brookfield, WI Client Relations Specialist (CRS) HS Diploma/GED Exp: 1-2 years in financial institution preferred |
The CRS provides operational, administrative, and clerical support to the financial advisors in our Brookfield office. This role requires the ability to work at a fast pace and be able to multitask while differentiating tasks on level of importance, urgency, and estimated time of completion. Assist with client onboarding which includes preparing new account paperwork, opening accounts, and transitioning new assets. | 2/23/2020 |
| 224 | Sword Bio Carmel, IN Research Associate I BS/BA in biology, biochemistry or related Exp: 1-3 years lab experience |
Plan experiments with guidance from supervisor. Perform complex and critical laboratory experiments (primarily ELISA) with accuracy and precision. Analyze experiment results and recommend potential follow-on experiments. | 2/23/2020 |
| 225 | Synexus Anderson, SC Research Associate BS or Certified Medical Assistant Exp: 1 year in clinical research |
Assists the Clinical Research Coordinators in their responsibilities by doing the following: Assists with the basic screening of patients for study enrollment; Assists with patient follow-up visits; Assists the Clinical Research Coordinators with updating and maintaining logs and filing in charts;Perform basic lab procedures, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up, | 2/23/2020 |
| 226 | Synexus Chicago, IL Clinical Research Coordinator BS/BA in health sciences Exp: 6+ months clinical research experience |
Maintain a high level of knowledge and understanding of assigned protocols, including all protocol requirements for patient visits, obtaining informed consent, patient visit schedules, test procedures, laboratory information, and drug accountability requirements. Responsible for completion of all study documentation forms, including case report forms and other study specific documents. | 2/23/2020 |
| 227 | Synexus St. Louis, MO Research Associate BS or Certified Medical Assistant Exp: 1 year in clinical research |
Assists the Clinical Research Coordinators in their responsibilities by doing the following: Assists with the basic screening of patients for study enrollment; Assists with patient follow-up visits; Assists the Clinical Research Coordinators with updating and maintaining logs and filing in charts;Perform basic lab procedures, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up, | 2/23/2020 |
| 228 | Cytek Biosciences Fremont, CA Research Assistant - Flow Cytometry - Reagent Development BS in chemistry, biology, or other life sciences Exp: None required |
We are currently seeking a Research Associate for our Reagent Development Group. This individual will work with other scientists in the group to identify and evaluate antibodies and fluorescent dyes for developing flow cytometry reagents. Conduct immunological conjugation with different antibodies and fluorophores. Perform routine analysis of reagent using chromatographic spectrophotometer, HPLC and flow cytometry technique. Follow SOPs, policies and regulations and performing routine lab equipment maintenance. etc. | 2/24/2020 |
| 229 | Cytel Waltham, MA Financial Analyst BS/BA in finance or accounting Exp: 1-3 year(s) |
We are experiencing exponential growth on a global scale and hiring Financial Analyst to join our Finance division. Summary of Job Responsibilities: As the Finance Analyst supporting Project Leadership Team, you acquire an understanding of the project economics and profitability drivers. Under supervision, you will assist in translating them into operational actions, and proactively advising the PL on how to influence critical operational levers in order to positively impact project financials. Key Responsibilities include: Create accurate, transparent, and timely financial analysis to support project leadership in project decision making process; etc. | 2/24/2020 |
| 230 | CytomX Therapeutics South San Francisco, CA Senior Research Associate, Upstream Process Development MS in biochemistry, molecular biology, or cell biology Exp: 0-3 year(s) |
Professional Responsibilities: Operation and harvest of stirred-tank bioreactors (2-50 L, fed-batch). Performance of fed-batch cell culture studies in shake flasks or micro-bioreactors. Titer analysis using ForteBio Octet, occasional performance of other assays as-needed. Experimental design and analysis, commensurate with experience. Authorship or contribution to SOPs and development reports. Support of GMP mfg; may include BPR review and PIP duties. etc. | 2/24/2020 |
| 231 | Cytovance Oklahoma City, OK Facilities Technician I HS diploma or equivalent Exp: Entry level |
The Facilities Technician is integral to successful biologics manufacturing and to product safety. The Facilities technician maintains, calibrates, and operates equipment and utilities in an FDA-regulated environment. This is an entry level position, On the Job training will be provided. ESSENTIAL DUTIES AND RESPONSIBILITIES: Completes all scheduled maintenance and calibration activities on time. Each month, evaluates assigned workload and manages time to complete the work (ex. ordering/gathering supplies, coordinating with other departments for equipment availability, etc.). Ensures documentation of all activities is completed in compliance with company procedures. etc. | 2/24/2020 |
| 232 | Cytovance Oklahoma City, OK Upstream Manufacturing Associate AS in science or biotech Exp: 1-2 year(s) |
Executes upstream manufacturing of clinical and commercial products. Executes pre and post processing activities such as: clean of production equipment, including the operation of automated bioreactor, harvest and media prep skids. This position is accountable for executing the manufacturing processes in Contract Manufacturing Facility and/or Master Cell Banking Facility. The hours for this role will be the swing/night shift. Shift differential pay is available. ESSENTIAL DUTIES AND RESPONSIBILITIES: Ability to work with bioreactor operation and cell culture including aseptic technique. Execute and monitor critical processes supporting mammalian, microbial, and fill finish production facilities. Solid experience with the following: large-scale centrifuges, washers, autoclaves. etc. | 2/24/2020 |
| 233 | Cytovance Oklahoma City, OK Solution Prep Associate I HS diploma/AS Exp: 1-2 year(s) |
This position is accountable for producing and delivering large and small-scale media and buffers to support Upstream and Downstream Manufacturing Operations. ESSENTIAL DUTIES AND RESPONSIBILITIES: Batching and delivering both large and small-scale media and buffer batches. Assisting in the review & creation of operation documents by providing input to technical composition of documents. Effectively demonstrate understanding of GMPs & how it applies to specific responsibilities. Following accurate oral & written procedures in operating production equipment & performing processing steps. Maintain orderliness of process area. etc. | 2/24/2020 |
| 234 | Day Zero Diagnostics Boston, MA Research Lab Associate BS in molecular biology, biochemistry, or microbiology Exp: 1 year |
Day Zero Diagnostics is an infectious disease genomics start-up in Boston that is seeking a highly motivated full-time Laboratory Research Associate. The employee will become an integral member of our dynamic team as we develop a novel rapid diagnostic to provide the species ID and antibiotic resistance profile. We value intellectual curiosity and a strong work ethic. Job Duties: Perform and assist with molecular biology and microbiology experiments to support diagnostic development. Work closely with other Research Scientists and Associates to design and execute experiments. etc. | 2/24/2020 |
| 235 | Demetrix Berkeley, CA Associate Scientist/ Sr. Associate Scientist, Strain Engineering BS Exp: 1-4 year(s) |
Demetrix is a start up in the San Francisco Bay area that is making nature’s medicines in a smart and responsible way. We are seeking an Associate Scientist/Senior Associate Scientist to assist the Strain Engineering team. The individual in this role will be part of an interdisciplinary team of molecular biologists, fermentation scientists and engineers, automation engineers, software engineers, and analytical chemists working to rapidly develop microbial strains to produce natural product medicines. etc. | 2/24/2020 |
| 236 | Denison Lincoln, RI Compounder, Lincoln HS diploma or equivalent Exp: 1 year |
The successful candidate for the position of Manufacturing Operator shall be fully capable of performing all job functions listed: Job Tasks: Submitting a requisition for raw materials. Verifying the clean status of all equipment and utensils prior to use. Batch pre-staging operations. Weighing and blending raw materials. Following manufacturing instructions. Documents production by completing forms, reports, logs, and records of equipment and batches. etc. | 2/24/2020 |
| 237 | Dermtech San Diego, CA Clinical Laboratory Scientist BS in biochemistry, biology, genetics, or related Exp: 1-2 year(s) |
The successful candidate will ensure that complex molecular diagnostic assays and systems are performed under appropriate CLIA compliance and regulatory requirements. The Clinical Laboratory Scientist independently performs clinical lab testing and other scientific examinations, record appropriate test documentations, and evaluates test results. Essential Duties and Responsibilities: Perform extraction techniques involving DNA/RNA, PCR and RT-PCR reactions, qPCR and RNA/DNA sequencing. Identify problems that may affect test performance or results and, following established protocols, correct problems or escalate to Clinical Laboratory Manager, technical supervisor, clinical consultant or lab director. etc. | 2/25/2020 |
| 238 | Dicerna Lexington, MA Research Associate - RNAi Discovery BS/MS Exp: 0-5 years |
Dicerna Pharmaceuticals is looking for a BS/MS Research Associate to help in its drug discovery efforts. This is a hands-on research position that requires strong expertise in molecular and cellular methodologies. This is a full-time position. Dicerna offers an exciting work environment and strong team culture. Our company has a competitive benefits package and bonus incentive program. etc. | 2/25/2020 |
| 239 | Digirad Bismarck, ND PET/CT Technologist AS/AA Exp: 6-12 months |
The PET CT technologist operates diagnostic imaging equipment to produce images that assist physicians in the treatment and diagnosis of our patients. Essential Functions: 1. The technologist demonstrates the knowledge, skills and abilities to perform imaging procedures that meet the quality expectations of the patient, referring physician, and radiologist. 2. Following orders of the referring physician and protocols specified by Radiologist. 3. Administers medications such as contrast media, FDG, radiopharmaceuticals as prescribed by the physician order. etc.The PET CT technologist operates diagnostic imaging equipment to produce images that assist physicians in the treatment and diagnosis of our patients. Essential Functions: 1. The technologist demonstrates the knowledge, skills and abilities to perform imaging procedures that meet the quality expectations of the patient, referring physician, and radiologist. 2. Following orders of the referring physician and protocols specified by Radiologist. 3. Administers medications such as contrast media, FDG, radiopharmaceuticals as prescribed by the physician order. etc.The PET CT technologist operates diagnostic imaging equipment to produce images that assist physicians in the treatment and diagnosis of our patients. Essential Functions: 1. The technologist demonstrates the knowledge, skills and abilities to perform imaging procedures that meet the quality expectations of the patient, referring physician, and radiologist. 2. Following orders of the referring physician and protocols specified by Radiologist. 3. Administers medications such as contrast media, FDG, radiopharmaceuticals as prescribed by the physician order. etc. | 2/25/2020 |
| 240 | Digirad El Paso, TX PET/CT Technologist AS/AA Exp: 6-12 months |
The PET CT technologist operates diagnostic imaging equipment to produce images that assist physicians in the treatment and diagnosis of our patients. Essential Functions: 1. The technologist demonstrates the knowledge, skills and abilities to perform imaging procedures that meet the quality expectations of the patient, referring physician, and radiologist. 2. Following orders of the referring physician and protocols specified by Radiologist. 3. Administers medications such as contrast media, FDG, radiopharmaceuticals as prescribed by the physician order. etc.The PET CT technologist operates diagnostic imaging equipment to produce images that assist physicians in the treatment and diagnosis of our patients. Essential Functions: 1. The technologist demonstrates the knowledge, skills and abilities to perform imaging procedures that meet the quality expectations of the patient, referring physician, and radiologist. 2. Following orders of the referring physician and protocols specified by Radiologist. 3. Administers medications such as contrast media, FDG, radiopharmaceuticals as prescribed by the physician order. etc.The PET CT technologist operates diagnostic imaging equipment to produce images that assist physicians in the treatment and diagnosis of our patients. Essential Functions: 1. The technologist demonstrates the knowledge, skills and abilities to perform imaging procedures that meet the quality expectations of the patient, referring physician, and radiologist. 2. Following orders of the referring physician and protocols specified by Radiologist. 3. Administers medications such as contrast media, FDG, radiopharmaceuticals as prescribed by the physician order. etc. | 2/25/2020 |
| 241 | Digirad Ft. Harrison, MT Tech Assistant HS diploma or equivalent Exp: 1 month |
The Technologist Assistant supports the technologist with various duties including transporting patients between the facility and scanner and completing paperwork. Essential Functions: 1. Assisting the technologist with patient care by transporting patients between the facility and scanner; sanitizing and cleaning patient care and staff areas; changing table linens; entering exam and patient information electronically or on paper; and answering the telephone. 2. Demonstrates the knowledge and skills necessary to provide care appropriate to the age of the patients served. 3. Demonstrates knowledge and skills necessary to provide care appropriate to the age of the patients served. etc. | 2/25/2020 |
| 242 | DiscGenics Salt Lake City, UT Purchasing Assistant / Receptionist AS/AA in business administration or similar Exp: 1+ year(s) |
DiscGenics is a clinical stage biotechnology company performing studies to support the continued development of our cell therapy products to treat diseases of the spine. We are seeking a full time Purchasing Assistant who will fulfill a dual role as a Receptionist. The qualified candidate must be friendly, professional and detail oriented with the ability to prioritize purchasing tasks as requested by our laboratory and office personnel. Responsibilities: Create purchase orders as directed. Communicate with vendors, including placing orders and some price negotiation. Work with quality department to track qualification requirements and status of vendors and raw materials. etc. | 2/25/2020 |
| 243 | DiscGenics Salt Lake City, UT Quality Engineer BS in a relevant field Exp: 1+ year(s) |
DiscGenics is seeking an independently-driven quality engineer capable of implementing Quality Management System (QMS) processes in accordance with applicable country regulations and standards for biologics, pharmaceuticals, and medical devices. The quality engineer will also support new product development efforts including design control and risk management. Responsibilities: Serves as the voice of quality during the product design and development process. Facilitates risk assessment activities. Defines and implements the Quality Management System processes in accordance with 21 CFR 210/211, 21 CFR 820, 21 CFR 1271, including CAPA, training, internal audits, supplier controls, etc. etc. | 2/25/2020 |
| 244 | DiscGenics Salt Lake City, UT Manufacturing Operator I HS diploma Exp: Entry level |
Discgenics is a clinical stage biotechnology company that is developing a patented disc cell therapy product to help patients suffering from degenerative diseases of the spine. DiscGenics is seeking a Manufacturing Operator l. The Manufacturing Operator l is an entry level position; as a Manufacturing Operator l, your duties will include maintaining cleanroom standards along with controlled environments. The position will require supporting the DiscGenics internal manufacturing team to ensure the clinical production of cell therapies and routine maintenance and cleaning of rooms and equipment. In addition, maintains records and cleanroom environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). etc. | 2/25/2020 |
| 245 | DiscGenics Salt Lake City, UT AM Lab Associate BS in a biological or chemical field Exp: 1+ year(s) |
DiscGenics is a clinical stage biotechnology company performing studies to support the continued development of our cell therapy products to treat diseases of the spine. We are seeking a laboratory associate who can support the analytical team in developing, qualifying and performing a variety of cellular and chemical test methods. This is an entry level laboratory position that will provide experience with cell culture and cell characterization methods. The ideal candidate will be hard working and enthusiastic about our mission to aid patients with disc degeneration and have some experience with cell culture, cell based assays and/or laboratory automation. etc. | 2/25/2020 |
| 246 | DNA Diagnostics Center Irving, TX Sales Associate (Direct to Consumer) unspecified Exp: 1-2 year(s) |
DDC is growing rapidly, and our customers need fast and accurate solutions for their life-changing challenges and questions related to paternity or other family relationships. The role of the Sales Representative (Direct to Consumer) is DDC’s premier sales position. From 8am to 8pm Monday through Friday, our global customers call us for answers about relationships that they use for immigration, surrogacy, or simply confirming the father of a child. The successful candidate for this role determines the services our clients require, charts their course through the testing process, and closes the sale. Income is not capped, and six-figure upside is achievable—it is determined by your own skills and motivation. etc. | 2/25/2020 |
| 247 | DNA Diagnostics Center Gardena, CA Sales Associate (Direct to Consumer) unspecified Exp: 1-2 year(s) |
DDC is growing rapidly, and our customers need fast and accurate solutions for their life-changing challenges and questions related to paternity or other family relationships. The role of the Sales Representative (Direct to Consumer) is DDC’s premier sales position. From 8am to 8pm Monday through Friday, our global customers call us for answers about relationships that they use for immigration, surrogacy, or simply confirming the father of a child. The successful candidate for this role determines the services our clients require, charts their course through the testing process, and closes the sale. Income is not capped, and six-figure upside is achievable—it is determined by your own skills and motivation. etc. | 2/25/2020 |
| 248 | DNA Diagnostics Center Fairfield, OH Sales Associate (Direct to Consumer) unspecified Exp: 1-2 year(s) |
DDC is growing rapidly, and our customers need fast and accurate solutions for their life-changing challenges and questions related to paternity or other family relationships. The role of the Sales Representative (Direct to Consumer) is DDC’s premier sales position. From 8am to 8pm Monday through Friday, our global customers call us for answers about relationships that they use for immigration, surrogacy, or simply confirming the father of a child. The successful candidate for this role determines the services our clients require, charts their course through the testing process, and closes the sale. Income is not capped, and six-figure upside is achievable—it is determined by your own skills and motivation. etc. | 2/25/2020 |
| 249 | Mylan Pharmaceuticals Greensboro, NC Quality Technician, Inspections- 1st Shift BS/BA Exp: 0-2 years |
At Mylan, each person has the ability to make a difference. From the providers who sell and market our products, to the producers who develop and manufacture them and finally to our business partners who support the providers and producers, we all have a mission critical role. Here's how this role will help: Coordinate release documents, perform product releases in SAP, and perform product inspections. Write specifications and SOP’s, perform warehouse investigations, review rejections, place products on quality hold, process sample requests, returned goods and donations, ship studies, and review temperature data. Deliver and create training and help maintain training records. etc. | 2/25/2020 |
| 250 | Durect Birmingham, AL Manufacturing Associate I HS diploma/BS/BA Exp: 0-2 years |
To conduct manufacturing and polymer development tasks. MAIN DUTIES AND RESPONSIBILITIES: Perform manufacturing/synthesis under GMP. Clean GMP equipment. Assist in polymer manufacturing equipment calibration and maintenance. Assist in equipment qualification studies, including documentation of studies. Assist in performance of R&D development programs. etc. | 2/25/2020 |
| 251 | Editas Medicine Boulder, CO Research Associate II/Senior Research Associate, Analytical Chemistry MS in a life science Exp: 1-2 year(s) |
This new role on the Analytical Chemistry team in Boulder provides a unique opportunity to contribute to Editas’ efforts through the development of the analytical characterization of guide RNAs (identity, purity, stability), mainly in support of Process Development Team in Boulder. Key Responsibilities: Work closely with the Process Development group at the Boulder Colorado site to develop analytical methods and solve technical problems. Develop, execute, and qualify/validate methods for analytical characterization of oligonucleotides (identity, purity, impurity characterization, stability). etc. | 2/25/2020 |
| 252 | Elpis Biopharmaceuticals Lexington, MA Research Associate, Biology & Functional Assays BS/MS in a related biological field Exp: 1-3 year(s) |
We are looking for a research associate to joint the biology and functional assay group. This group will analyze and screen newly discovered therapeutic molecules for biochemical, cellular and immunological function. The candidate will be responsible for efficiently delivering high-quality research results for decision making. The candidate will also help explore and develop innovative technologies to advance biologic projects. The candidate will analyze scientific results, provide oral and written reports, and remain current to literature reports and technological developments. Specific Responsibilities: Care for and scale up cancer cell lines for experiments. | 2/25/2020 |
| 253 | Encoded South San Francisco, CA Scientist I/II, Assay Development BS/MS in a relevant science Exp: 1-2 year(s) |
This is a unique opportunity to work at the intersection of genomics and therapeutics and participate in the development of a diverse therapeutic pipeline driven by a transformative core technology. The position of Scientist I/II, Assay Development is part of the PD Analytics team and will assist the Process Development group in developing novel assays and supporting existing analytical assays used to characterize gene therapy products and processes in our pipeline. An ideal candidate will have experience in a drug development environment, analytics for viruses and viral vectors and well-versed in assay development and qualification. etc. | 2/25/2020 |
| 254 | Endologix Irvine, CA Quality Assurance Technician HS diploma or equivalent Exp: Entry level |
Performs audits, inspections, configuration checks, and functional testing of in-process materials, parts and subassemblies used in the manufacture of partially assembled or finished medical devices. Responsible for assuring that the company’s products have been manufactured, inspected and tested using company approved procedures documents and equipment. Work with R&D, Manufacturing, and Quality to implement solutions to quality related problems. Coordinates, initiates, and implements Document Change Orders. Reviews quality records to ensure completeness and compliance to applicable quality procedures. etc. | 2/25/2020 |
| 255 | Enzo Farmingdale, NY Production Associate I AS/BS in biology or related Exp: 0-2+ years |
This position is responsible for the timely and efficient scheduling and packaging of standard and custom products, and for providing support to other areas of manufacturing to ensure timely product delivery. Responsibilities: Assist in all packaging and labeling operations for Manufacturing. Assist in cGMP material inspection and receiving raw materials for Manufacturing. Maintain and organize the physical inventory of purchased and in-house materials. Assist in creating and maintaining electronic copies of all manufacturing documents. etc. | 2/25/2020 |
| 256 | Epitopix Wilmar, MN Production Technician HS diploma/AS Exp: 0-2 years |
As a key member of the fermentation department the fermentation technician is responsible for the growth of bacteria used to create vaccines based on proprietary SRP technology. This critical role will be engaged in production, process improvement, and the support functions necessary to ensure vaccine delivery to hundreds of customers throughout North America and the world. SRP technology is critical to the maintenance of the global food supply and the fermentation technician is truly in on the ground floor. etc. | 2/25/2020 |
| 257 | Eton Boston, MA Lab Technician BS in biology, biotechnology, or related life science Exp: 6 months |
Collect and analyze DNA samples to determine sample quality and concentration. Design and process DNA sequencing polymerase chain reactions (PCR) using DNA samples submitted by customers, and perform dye-terminator purification of the completed DNA sequencing reactions. Produce data files to load onto the Applied Biosystems 3730xl DNA Analyzer. Troubleshoot common problems the customers are having with their DNA sequencing. | 2/25/2020 |
| 258 | Eurofins Lancaster, PA 2nd shift - Data Review Specialist - Mycoplasma Services BS in microbiology, biology, or related Exp: 1-3 year(s) |
Employee Responsibilities: Ensures that our clients receive quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations. The Ideal Candidate would possess: Strong computer, scientific, and organizational skill. Excellent communication (oral and written) and attention to detail. Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude. Ability to learn new procedures, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies. | 2/25/2020 |
| 259 | Eurofins Lancaster, PA 2nd shift - Associate Microbiologist BS in microbiology, biology, or related Exp: Not necessary for BS candidates |
Employee Responsibilities: Perform analyses for bio/pharmaceutical microbiology (routine and non routine). Review and evaluate raw data for acceptability. Set up and validate new analytical or related processes used by the department. Perform collection of water/EM samples when required. The Ideal Candidate would possess: Strong computer, scientific, and organizational skills. Excellent communication (oral and written) and attention to detail. etc. | 2/25/2020 |
| 260 | Exactech Gainesville, FL Clinical Research Associate HS diploma/BS/BA Exp: 1 year |
Duties and Responsibilities (Key Deliverables): 1. Monitor the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), GCP, and all applicable regulatory requirements. 2. Conduct visits to assess the qualification of potential investigative sites, initiate sites, instruct site personnel on the proper conduct of studies and use of Electronic Data Capture (EDC) system, review and ensure accuracy of data collected, and terminate studies. 3. Monitor data submitted to the EDC system, perform source document verification, retrieve and/or ensure appropriate electronic submission of Case Report Forms (CRFs), and perform query resolution in a timely manner. 4. Ensure sites report adverse events according to protocol specifications. 5. Assist investigative sites with obtaining and maintaining Institutional Review Board (IRB)/Ethical Committee (EC) approval. etc. | 2/25/2020 |
| 261 | Exactech Gainesville, FL Surgical Services Technician HS diploma or equivalent Exp: 1 year |
Duties and Responsibilities (Key Deliverables): 1. Process loaner/instrument returns: sterilization, cleaning, completing required forms, updating the inventory control system, performing functional checks, and restocking. Initiate the processing of those instruments that do not satisfy the quality standards (Non-Conforming instruments). Refer complaints of service or product failure to appropriate departments. 2. Perform minor repairs on instruments and provide disposition of obsolete or worn instrumentation in accordance with established procedures. 3. Stock instrument storage bins. 4. Assist in the filling of orders. 5. Provide on call services as necessary. etc. | 2/25/2020 |
| 262 | Exonbio San Diego, CA Research Associate MS in biology Exp: 1 year |
We are looking for a RESEARCH ASSOCIATE to join our antibody development team. Requirements: Master Degree in Biology. One year experience in Cell culture and banking, PCR, Protein purification with AKTA. | 2/25/2020 |
| 263 | Exsurco Wakeman, OH Assembly Technician HS diploma Exp: 3 months |
Primary role is to perform all forms assembly activities including equipment setup and tear down where required as well as in-process verifications. In addition, this position includes several cross-functional responsibilities comprising Shipping, Receiving, Job Picking, Warehousing and Plant Cleaning and some Maintenance activities. This position also has responsibilities associated with Servicing returned products (disassembly and reassembly, diagnosis and report writing). Will be working 20 – 24 hours a week. etc. | 2/25/2020 |
| 264 | Facet Medical Technologies Atlanta, GA Quality Engineer BS in engineering, science, or related Exp: 1-3 year(s) |
The Quality Engineer plans and directs activities concerned with development, application, and maintenance of quality processes, materials, and products. Additionally, responsible for investigation manufacturing and customer nonconformance’s, determining root causes and corrective actions, reviewing and approving protocols and final reports and developing product specifications and sampling plans. etc. | 2/25/2020 |
| 265 | Fate Therapeutics San Diego, CA Associate Scientist/Senior Research Associate BS/MS in a biological science Exp: 1+ year(s) |
Fate Therapeutics is seeking a motivated professional with analytical assays experience to support Fate’s clinical and manufacturing process development programs. The successful candidate will execute and analyze experiments to assess the characteristics of hematopoietic and stem cell-based therapeutics under cGMP environment. Candidates must have experience working with mammalian cell culture, and analysis of data from flow cytometry, cell-based assays, or PCR assays. This is a full-time position located at our corporate headquarters in San Diego, California reporting to the Senior Manager, QC. etc. | 2/25/2020 |
| 266 | Finch Somerville, MA Research Associate, Process Development BS in chemical engineering, biomedical engineering, or chemistry Exp: 0-2 years |
Responsibilities: Plan, execute, and document studies related to design of novel drug products. Support scale-up and technical transfer of production processes to GMP Manufacturing. Assist with troubleshooting, root cause analysis, and identification of corrective actions to support Pharmaceutical Development or GMP Manufacturing equipment and process issues. Work cross-functionally across Quality, Research, Clinical, and Manufacturing teams to achieve company goals. etc. | 2/25/2020 |
| 267 | Flexion Therapeutics Field, Flex Sales Representative BS/BA Exp: 1-3 year(s) |
Considering a new job and company is a really big decision. Typical job descriptions don't really give you a sense of what a job is actually like. When considering a Flex Sales role at Flexion, we want you to see why this opportunity is so amazing, the impact you'll have and what the company and culture are really like. Why this role is different: First, let's talk why this role is different from other sales roles and what you'll get to do: The name says it all. Flex means it's a mix of inside sales and in person sales. This role is a fantastic way for driven, passionate and resilient individuals earlier in their career to gain experience. You'll manage daily sales call activity, with the purpose of influencing customers and increasing sales. etc. | 2/25/2020 |
| 268 | Semma Therapeutics Cambridge, MA Quality Control Associate MS in pharma/biotechnology Exp: 1 year |
This position will perform QC tests for pre-clinical and clinical material from specific manufacturing steps associated with ES derived pancreatic islet production, from cell bank thaw through fil/finish. QC testing will include stability test for cell banks and final product, in-process manufacturing tests and final product lot release tests. The candidate will be expected to assume additional QC testing responsibilities associated with specific projects | 2/16/2020 |
| 269 | Semma Therapeutics Cambridge, MA GMP Manufacturing Associate, Clinical Materials BS/BA in biological/bioengineering/chemical engineering Exp: 6 months in process development/manufacturing |
Perform product manufacturing for clinical materials according to cGMP standards. Includes assembling raw materials, following specific standard operating procedures (SOP), aseptic technique, completing batch records, reporting deviations. Participates and facilitates technology transfer and final process development from the Research to the Manufacturing group. Assists in the development of Standard Operating Procedures (SOPs) for manufacturing in collaboration with Research and Quality Systems groups | 2/16/2020 |
| 270 | LabCorp Overland Park, KS Data Entry Operator/Lab Data Entry HS Diploma/GED Exp: 1-3 years |
Operates various data entry terminals and automated data systems to record and verify billing/accounts receivable information, customer demographic data and laboratory data identification and results, for computer processing. Resolves suspend and billing problems and manually process OE batches. Follows standard sequences and coding in entering and/or keying in data in correcting, editing, and verifying all data entered into automated systems. | 2/16/2020 |
| 271 | LabCorp RTP, NC Molecular Oncology Tech Trainee/Technologist (1st Shift) BS/BA in biology/chemistry Exp: 1 year in clinical OR research lab |
Determine the acceptability of specimens for testing according to established criteria. Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. Monitor, operate and troubleshoot instrumentation. Demonstrate the ability to make technical decisions regarding testing and problem solving. | 2/16/2020 |
| 272 | LabCorp Dublin, OH Medical Technologist - Virology BS/BA in biology/chemistry/med tech/etc. Exp: 1 year in clinical lab experience |
This position will work within the Virology section of the microbiology department.Testing performed will include Virology testing, IFOBT, H.Pylori breath bag testing and cepheid testing. Determine the acceptability of specimens for testing according to established criteria. Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. | 2/16/2020 |
| 273 | LabCorp Shelton, CT Laboratory Technologist Trainee - Histology BS/BA in biology or chemistry Exp: 1 year in research lab |
Perform all technical grossing procedures required to process and submit specimens for microscopic review as per standard operating procedures under the indirect and direct supervision of pathologists. Operate and maintain automated tissue processors, perform tissue embedding, Cryostat sectioning, operate and maintain tissue embedding units. Operate and maintain H&E stainers, IHC stainers, special stains stainers and coverslipping units, perform manual coverslipping | 2/16/2020 |
| 274 | LabCorp Shelton, CT Cytotechnologist-First Shift BS Exp: 1 year of training in cryotechnology |
Screens and evaluates gynecologic and non-gynecologic specimens sent to the laboratory for the determination of possible malignant or related abnormal conditions. Maintains absolute integrity in the accurate performance and reporting of results. Ensures proper documentation of workload recording, including screening and non-screening activities as required by CLIA and laboratory guidelines | 2/16/2020 |
| 275 | LabCorp McHenry, IL Phlebotomist HS Diploma/GED Exp: Phlebotomy accredidation |
Perform blood collections by venipuncture and capillary techniques. Prepare all collected specimens for testing and analysis. Order entry of patient and specimen information . Provide superior customer service to all patients and client providers and staff | 2/16/2020 |
| 276 | LabCorp Burington, NC Specimen Processing Specialist (1st Shift) HS Diploma/GED Exp: 1-3 years in clinical lab |
This position will have first shift hours with the following schedule: 9:00am-5:30am Tuesday to Saturday. This is a multi-discipline role with 3 primary components: specimen accessioning, sample splitting/sorting and data entry. Prepares laboratory specimens for designated departments/locations prior to laboratory analysis and testing and routes specimens by type to various staging areas. Assigns specific computer generated identification numbers, checks for accuracy and records all items processed. Performs all paperwork, technical and non-technical procedures required to process and submit specimens. | 2/16/2020 |
| 277 | Sera Care Milford, MA Research Associate I BS/BA in biochemistry/molecular biology or related Exp: 1 year in a lab |
Product formulations following production batch records or written instructions. Perform general molecular techniques such as cloning, plasmid purification, gel-electrophoresis, RNA transcription, and bacterial culturing. Perform nucleic acid analyses (RNA/DNA integrity analysis, real time qPCR, digital PCR) and analyze results. Maintenance of different cell lines in Cell culture (viral or bacterial) and manufacture of cell based products as required. | 2/16/2020 |
| 278 | Seres Therapeutics Cambridge, MA Donation Operations Technician BS Exp: 1-2 years |
The Donation Operations technician is responsible for inventory receipt and management, movement and tracking in accordance with GMP guidelines and Seres policies. The technician is responsible for laboratory assays to examine and characterize donor microbiomes. This position will assist in and/or lead deviations and corrective action plans as they relate to core responsibilities as needed, and perform project based work for program improvement and growth. Some cross functional work may be required. | 2/16/2020 |
| 279 | Simbex Lebanon, NH Systems Engineer BS in mechanical/electrical engineering or related Exp: 0-3 years in testing products |
The Systems Engineer will be responsible for supporting every phase of the product development life cycle process in order to deliver high-quality products in the consumer and medical device markets. The Systems Engineer will work with the electrical, software, mechanical, product technical support, and quality teams to help develop, integrate, and test sub-assemblies into product. The ideal candidate has broad skills but deep knowledge/skills in one area, and is able to blend human-centric design with sound engineering principles across a wide range of engineering domains with a focus on quality and willingness to wear many hats. | 2/16/2020 |
| 280 | Seven Bridges Boston, MA IT Help Desk Analyst BS/BA Exp: 1+ years in helpdesk, IT, secruity, technolopgy |
The successful candidate will bring expertise in IT Laptop Support, IT Procurement, Troubleshooting Laptop and Software Issues, Networking, Facilities, IT Tooling and Implementation. The successful candidate must excel at providing excellent support to Seven Bridges employees in a fast paced environment. This role requires the right blend of technical and non-technical skills, and will be working across the Seven Bridges global organization. | 2/16/2020 |
| 281 | Shionogi Inc Florham Park, NJ Contract -- Regulatory Documentation Specialist HS Diploma required, BS/BA preferred Exp: Entry Level |
The Regulatory Documentation Specialist is responsible for supporting the Regulatory Affairs Submission Team with the preparation of regulatory documents for both eCTD (electronic common technical document), as well as traditional paper submissions. The scope of this role includes assisting in the document remediation and formatting of documentation for submissions to Health Authorities. The ideal candidate for this entry level position is enthusiastic, highly organized and flexible. | 2/16/2020 |
| 282 | Siemens Chicago, IL Power Monitoring Solution Engineer (Entry Level) BS in electrical engineering or computer informations systems Exp: Entry Level |
Siemens is looking for a Solution Engineer to join their growing team. The candidate will be responsible for the integration of hardware and software to create an overall energy monitoring system for customers. Digital Solutions & Services provides facilities with the tools which help in managing the energy costs and availability of their business. | 2/16/2020 |
| 283 | Siemens Hoffman Estates, IL Materials Support I HS Diploma/GED Exp: Entry Level |
This role will be responsible for the picking of production orders and placement of inbound materials. You will also be responsible for deliveries of materials to manufacturing. In addition, you will be required to have an active role in cycle counting inventory. You should be able to handle cross functional duties (ie Shipping, Receiving) within the area. | 2/16/2020 |
| 284 | Siemens Irving, TX Security Technician I - Service HS Diploma/GED Exp: 0-1 year in maintenance |
Coordinates with contractors in the process of servicing of systems sold by a branch office. Monitors and controls serviceability progress based on project schedules and milestones to deliverable timelines. Performs system commissioning on systems including loading software programs and implementing modifications as necessary | 2/16/2020 |
| 285 | Siemens Newkirk, OK Wind Service Technician HVAC/electrical/aviation field certification Exp: 1 year of wind technician experience |
The Field Service Technician must perform scheduled maintenance, troubleshooting, part replacement, and retrofits as necessary to maintain quality and availability for our customer. Must maintain safety and professionalism and keep accurate and detailed records of parts used and work performed | 2/16/2020 |
| 286 | Signant Health Blue Bell, PA Application Specialist BS/BA in comp sciences Exp: 1-3 years in SQL knowledge |
Perform requirements gathering and business analyst tasks for eCOA collection, reporting and data transfer. Provide guidance to the client on the most suitable solution, ensuring that all recommendations are achievable within the scope of the product. Develop eCOA solutions using proprietary TrialMax platform (Web, Slate, Touch) according to the requirements gathered and interpretation of the client clinical protocol. Present eCOA solutions at client design review and testing (UAT) meetings at customer sites (as required) | 2/16/2020 |
| 287 | Sigvaris Group Peachtree City, GA Technician 2 year degree/cert in mechanical/industrial/electrical field Exp: 1-3 years on circular knitting machines |
This position is responsible for the general repair of hosiery knitting machines to ensure first quality products are produced to company specifications. Performs required/needed maintenance knitting machines to ensure machines are operating in good working order. Addresses machine stops to keep machines operating efficiently. Performs preventative maintenance as outlined in weekly PM sheets. | 2/16/2020 |
| 288 | Sinclair Research Auxvasse, MO Report Coordinator/Technical Writer BS/BA in sciences Exp: 1 year experience |
You will be writing GLP and non-GLP reports for all research studies performed. It is your responsibility to ensure written reports meet or exceed standards for formatting, clarity, accuracy, and completeness. Reviewing data, preparing summary tables, and reviewing protocol will fill your day when you are not consulting with study personnel. Accuracy and timeliness is a must in this role. | 2/16/2020 |
| 289 | Sinclair Research Auxvasse, MO Animal Technician HS Diploma/GED Exp: 0 years |
The ideal candidate will be hard-working and ready to be hands on. In this role, you will have a chance to participate daily in our research by working closely with our study directors, senior technicians, and scientists in order to conduct studies. Animal Technicians begin by learning the basics of data collection and animal husbandry and have the chance to move up into high level Technician roles. | 2/16/2020 |
| 290 | Sinclair Research Auxvasse, MO Swine Production Technician HS Diploma/GED Exp: 1 year experience |
Sinclair Bio Resources is a unique swine production facility dedicated to producing the highest quality animal models for research facilities around the country. Your day will be spent taking care of these future heroes in medicine. Feeding, grooming, sanitation, animal health, you'll do it all! There is room for advancement and specializing in husbandry, breeding, and sample collection. Someone dedicated to animal welfare and eager to make a difference in the lives of others will excel at SBR! | 2/16/2020 |
| 291 | Sinclair Research Auxvasse, MO Animal Caretaker HS Diploma/GED Exp: 0 years |
The ideal candidate will have a passion for animal welfare and a great work ethic. Hard-working individuals looking for a great environment and a chance to make a difference will fit right in. Your primary role will be taking care of our animals and sanitizing their housing and our buildings. | 2/16/2020 |
| 292 | Sinota Solutions Bloomington, IN Singota Solutions HS Diploma/GED Exp: 0-1 years in life sciences/supply chain |
Must be very customer focused to both internal employees and external clients. Must be able to work within the FDA regulated environment per its specific requirements and those established by internal policy and standard operating procedures. Computer experience necessary or willing to take internal courses to gain such information quickly.Ability to work with Microsoft Office (Outlook, Excel, Word) a plus. Experience using ERP or inventory systems is not required, but helpful. | 2/16/2020 |
| 293 | Sinota Solutions Bloomington, IN Associate Quality Control Analyst BS in chemistry Exp: 1 year in formulations/testing/etc. |
Supportthe Quality Control function with respect to raw material, in-process, release and stability testing. Collaboratively participates in Development functionsfor the company including pre-formulation, formulation, process and analytical development activities. Operate various lab instruments and equipment including (but not limited to): Karl Fisher, pH, HPLC, FTIR, UV-VIS, DSC, TOC, Lab-ware washers, Autoclave, Laminar Flow Hoods, Bio-Hazard Hood, Microbalances, and other diverse lab equipment and various wet chemistry techniques | 2/16/2020 |
| 294 | Sinopia Biosciences San Diego, CA Computational Biologist/Data Scientist MS in bioinformatics/computational biology/comp sci, etc Exp: 0-3 years |
This individual will play a key scientific role in expanding Sinopia’s computational platform and aiding in designing the implementation of follow-up validation studies. They will leverage new computational strategies and disparate data types to discover novel interventions for unmet medical needs. | 2/16/2020 |
| 295 | Smith + Nephew Memphis , TN Distribution Associate I HS Diploma/GED Exp: 0-1 years in distribution/logistics |
The Distribution Associate I will interact with the WMS, TMS, RF scanning and/or other warehouse equipment to perform intermediate level distribution tasks in accordance with defined job processes. They will perform these tasks with a focus on safety, quality and productivity. They must comprehend and demonstrate compliance with Standard Operating Procedures and work instructions. The Distribution Associate I is responsible for providing constructive input to enhance the work process and environment. | 2/17/2020 |
| 296 | Smith + Nephew Memphis , TN Inspector Technician I HS Diploma/GED Exp: 0-2 years in product inspections |
Inspect raw materials, components, assembled product, semi-finished product & finished product per inspection procedures/drawings and to print specifications. Utilize attribute and variable measuring equipment/gauges as well as mating parts to determine as found/as left conditions of product. Review corresponding product documentation to verify acceptability per specification and QSR requirements | 2/17/2020 |
| 297 | Smith + Nephew Columbia, MD Manufacturing Technician 1 AS/AA in life sciences Exp: 1-2 years in GMP environment |
Responsible for hands-on execution of all activities in the manufacturing area including the processing and packaging of human tissue products for transplantation. All duties are performed in compliance with FDA cGMP/cGTP requirements, American Association of Tissue Banks (AATB) standards, and Osiris Therapeutics Inc. standard operating procedures (SOPs). The candidate should have a commitment to high standards of quality | 2/17/2020 |
| 298 | Smith + Nephew Memphis , TN Graduate Engineer BS in industrial/mechanical engineering Exp: Co-op experience |
Supports technology projects that add to core competencies and/or reduce costs. Supports successful new product launches as an Operations Team Member. Duties include, but are not limited to, providing input for P/DFMEA, developing robust processes, continuous improvement projects, ensuring accuracy and communication of COGS. | 2/17/2020 |
| 299 | Smiths Medical Minneapolis, MN Product Surveillance Reporting Specialist I BS/BA Exp: 1-2 year in product complaint handling |
The PSR Specialist I contributes to the strategic management of global adverse event reporting, communications with regulators, and risk management activities through the execution of timely, high quality and consistent processes. This role contributes to the on-going improvement of processes, including appropriate identification and response to risks, adverse event reporting decisions. | 2/17/2020 |
| 300 | Smiths Medical Dublin, OH Quality Engineer II MS in engineering Exp: 1-3 years |
The Quality Engineer II will support and drive continuous improvements of quality systems and manufacturing processes, including CAPA investigation and solution activities. This role will also help drive quality activities related to continued compliance to changing regulatory requirements. Conducts engineering activities of intermediate scope or degree of difficulty. This could include medium – large components/system, processes associated with a medium or large project.The Quality Engineer II will support and drive continuous improvements of quality systems and manufacturing processes, including CAPA investigation and solution activities. This role will also help drive quality activities related to continued compliance to changing regulatory requirements. Conducts engineering activities of intermediate scope or degree of difficulty. This could include medium – large components/system, processes associated with a medium or large project. | 2/17/2020 |
| 301 | Smiths Medical Denver, CO Field Support Specialist - Registered Nurse (RN) RN Degree and License Exp: 1-3 years in clinical bedside nursing |
The FSS will work closely with current customers as well as potential customers as the clinical expert on the sales team. The Vascular Access devices provide healthcare professionals access to patients’ vasculature for delivery and withdrawal of fluid and medication, as well as devices to protect health workers by helping prevent needle stick injuries.The FSS will work closely with current customers as well as potential customers as the clinical expert on the sales team. The Vascular Access devices provide healthcare professionals access to patients’ vasculature for delivery and withdrawal of fluid and medication, as well as devices to protect health workers by helping prevent needle stick injuries. | 2/17/2020 |
| 302 | SomaLogic Boulder, CO Marketing Research Associate, Diagnostic Tests BS/BA or MS Exp: 1-2 years |
The Market Research Associate will work to research and define several markets that SomaLogic might enter. This critical piece of work will include researching product-level competitors and uncovering the alignment between product opportunity and customer needs. Identify competitors for diagnostic products that are currently in the market, in development, or in the pipeline. Clarify and augment proposals for new product development. Develop detailed competitive profiles for new products. | 2/17/2020 |
| 303 | SonoSite Bothell, WA Manufacturing Associate (2nd shift Transducers, Temporary 12 months) HS Diploma/GED Exp: 0-1 years in high tech manufactruing |
Follow all required procedures such as Assembly Instruction, Personal Protective Equipment, and Device History Record while performing the job responsibilities. Weighing and mixing epoxy-based materials. Cleaning and assembling high precision molds. Light mechanical assembly of small components using hand tools and torque drivers. Work with hands under a microscope performing hand soldering of fine pitch cables and flexible circuits. | 2/17/2020 |
| 304 | Sorrento San Diego, CA Quality Control Microbiology Associate BS/BA in microbiology Exp: 1-2 years industry experience |
This individual will contribute to providing microbiological support and testing of cGMP environments, as well as contribute to in-process, drug substance, and drug release testing. Environmental monitoring of cGMP cleanrooms per FDA and USP guidelines. Input and manage environmental data. Conduct QC testing of raw materials and utility samples; QC tests include, but not limited to bioburden, endotoxin, total organic carbon, conductivity, osmolality, and pH. | 2/17/2020 |
| 305 | Sorrento San Diego, CA Research Associate BS in biological sciences Exp: 0-1 years |
The successful candidate will have a major support role for the Chemical Immunotherapy group. Responsible for execution of cell-based assays to support characterization/development of lead candidates. Aid in mechanistic and target validation studies using ELISA, SDS-PAGE, Western Blot, and flow cytometry. Partake in instruments’ maintenance and calibration, lab cleanliness and orderliness, as well as ordering and replenishing stocks | 2/17/2020 |
| 306 | Sorrento San Diego, CA Research Associate BS in bio/chemistry/nanotechnology Exp: 0 years |
We are currently seeking a Research Associate for the Nanoformulations group. This individual will play a critical role in supporting experiments to identify and evaluate molecules for nanoparticle formulation and drug delivery. They will be responsible for performing routine laboratory analysis and maintenance. We are currently seeking a Research Associate for the Nanoformulations group. This individual will play a critical role in supporting experiments to identify and evaluate molecules for nanoparticle formulation and drug delivery. They will be responsible for performing routine laboratory analysis and maintenance. | 2/17/2020 |
| 307 | Sorrento San Diego, CA Manufacturing Associate II MS or BS in biological/chemical sciences Exp: 1 year in cGMP manufacturing |
We are currently seeking a Downstream Manufacturing Associate II. This position is tasked with supporting all aspects of downstream manufacturing processes. For GMP-qualified campaigns this involves large scale buffer preparation, column chromatography using the Akta Process system and large bed volume columns, various filtration methods, ultrafiltration/diafiltration methods, and formulation. An essential component of this position will be an understanding of cGMP methodologies: SOP’s, batch record preparation and execution, deviation control and general clean room maintenance. | 2/17/2020 |
| 308 | Sorrento San Diego, CA Materials Associate HS Diploma/GED Exp: 1-2 years in inventory management |
The Materials Associate's responsibilities are divided into three primary functional areas: shipping and receiving, inventory accountability, and other duties. Create and maintain inventory records and forward to appropriate departments. Issue supplies, materials and equipment to workers and ensure that all corresponding paperwork is accurately managed. Perform physical inventory inspections to ensure 100% of inventory accuracy. | 2/17/2020 |
| 309 | Sorrento San Diego, CA Manufacturing Associate I BS/BA in biological/chemical sciences Exp: 1 year in manufacturing |
We are currently seeking a Downstream Manufacturing Associate I. This position is tasked with supporting all aspects of downstream manufacturing processes. For GMP-qualified campaigns this involves large scale buffer preparation, column chromatography using the Akta Process system and large bed volume columns, various filtration methods, ultrafiltration/diafiltration methods, and formulation. | 2/17/2020 |
| 310 | Sorrento San Diego, CA Research Associate II BS or MS in biological sciences Exp: BS: 1-2 years, MS: 0-2 years |
Sorrento Therapeutics’ is seeking an experienced Research Associate who will be responsible for the development and implementation of in vitro functional T cell assays to support pre-clinical validation of CAR-T cellular therapies against cancer. The individual must have knowledge and hands on experience in CAR-T, cell culture, Flow cytometry and T cell biology. | 2/17/2020 |
| 311 | Spark Therapeutics Philadelphia, PA Research Associate RVC (Assay) BS or MS in biological sciences, chemical sciences/engineering Exp: 1-3 years |
The successful candidate’s primary responsibilities will be to execute and improve established protocols for production, characterization and sequence verification of DNA constructs for pre-clinical grade rAAV vector production. The incumbent will also assist therapeutic area scientists in cloning and synthesis of new DNA constructs to support the translational pipeline and will be the point contact for pasmid banking. | 2/17/2020 |
| 312 | Philips Fresno, CA MR/CT Field Service Engineer 1 AS/AA in electronics Exp: 1+ years in servicing electronics |
This position will be responsible for customer relationship management through the effective use of technical knowledge to install, troubleshoot, service, and maintain equipment at customer sites; generate service revenue; adherence to state and federal regulatory requirements. This position is an entry level position for an employee with limited experience. | 2/17/2020 |
| 313 | Spherotech Lake Forest, IL Quality Control Associate BS/BA in chemistry Exp: 1 year |
Spherotech, Inc. seeks a college graduate for a Quality Control Associate opening. Duties include final product inspection, documentation, Quality Control testing etc. This position requires a Bachelor's degree in Chemistry or related field and a minimum of 1 year of experience. | 2/17/2020 |
| 314 | Sprint Cleveland, OH Sales and Customer Support Associate BS/BA Exp: 0-2 years in sales/customer support role |
Accurate, efficient and timely data management within CRM (Customer Relationship Management) Tool. Order processing and shipment. Provide phone support and coaching to patients, physicians and other internal and external resources. Assists sales team in lead creation and account management. Supports sales team by recording patient procedure and follow-up data | 2/17/2020 |
| 315 | SRI International Arlington, VA Research Analyst – Science, Technology & Innovation Policy BA or MA in public policy or related Exp: 1-5 years |
A Research Analyst will work across all these areas and will: Implement approaches to projects under the direction of senior staff. Apply a variety of methods to analyze complex issues and to generate findings and recommendations in collaboration with senior staff. Produce pieces of well-written high-quality reports and presentations for clients in collaboration with team members. Occasionally travel domestically and internationally. | 2/17/2020 |
| 316 | SRI International Princeton, NJ Project & Resource Analyst BS/BA in business/project management/related Exp: 0-2 years |
Plan and maintain detailed integrated master schedule (IMS) combining multiple projects/product lines including design and program milestones, manufacturing development, assembly, test, and into production operations. Assist in laying out and tracking major project milestones, workflow, and activities in relation to schedule and resources and identify gaps and constraints in program performance. Interface with Engineering, Finance and Business Operations, and Program Management to develop program requirements into the IMS baseline. | 2/17/2020 |
| 317 | SRI International Harrisonburg, VA Bioscience Research Associate - Macromolecular Bioscience BS/BA in biochemistry/biotechnology Exp: 1-5 years |
We are seeking an enthusiastic research associate to work in a multidisciplinary team of biochemists, chemist, and molecular biologist. Perform a variety of laboratory techniques such as peptide synthesis and purification, microscopy, flow cytometry, mammalian cell culture, PCR, mass spectrometry and routine biochemical techniques. Collaborate with scientists from other disciplines (e.g., in chemistry, molecular biology, cancer biology, and immunology) in cross-divisional teams. | 2/17/2020 |
| 318 | Charles River Mattawan, MI Research Technician - Pharmacokinetics and Acute Toxicology BS/MS Exp: No experience necessary |
We are seeking a Research Technician for our Pharmacokinetics and Acute Toxicology Team at our Safety Assessment site located Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. Please Note: we are seeking Talent for both 1st and 2nd Shift positions, as well as standard and alternate work schedules (e.g., M-F, Tu-Sat) The following are minimum qualifications related to the Research Technician position: HS/GED or Bachelor’s/Master’s with no relevant experience. etc. | 2/17/2020 |
| 319 | Charles River Mattawan, MI Research Technician - Neurobehavioral Sciences BS/MS Exp: No experience necessary |
We are seeking a Research Technician for our Neurobehavioral Sciences Team at our Safety Assessment site located Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. Please Note: we are seeking Talent for both 1st and 2nd Shift positions, as well as standard and alternate work schedules (e.g., M-F, Tu-Sat). etc. | 2/17/2020 |
| 320 | Charles River Mattawan, MI Research Technician - Developmental and Reproductive Toxicology BS/MS Exp: No experience necessary |
We are seeking a Research Technician for our Developmental and Reproductive Toxicology Team (for both In-Life and the Teratology Laboratory) at our Safety Assessment site located Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. Please Note: we are seeking Talent for both 1st and 2nd Shift positions, as well as standard and alternate work schedules (e.g., M-F, Tu-Sat). etc. | 2/17/2020 |
| 321 | Charles River Reno, NV Research Assistant 1 (Laboratory Sciences) BA/BS in a laboratory science or related Exp: 0-2 years |
We are seeking a Research Assistant I for our Safety Assessment site located in Reno, NV. This position will be responsible for handling and processing samples, and performing accurate data collection and reporting. Basic methods will be used to perform laboratory tasks with minimal supervision in the performance of studies. The following are minimum requirements related to the Research Assistant I position. Bachelor’s degree (B.A. / B.S) or equivalent in laboratory science or related discipline required. Zero to two years related experience in biology, chemistry/pharmacy, or similar lab environment GLP experience preferred. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above. etc. | 2/17/2020 |
| 322 | Charles River Shrewsbury, MA Animal Care Technician 1 HS diploma or equivalent Exp: 6+ months |
We are seeking an experienced Animal Care Technician I for our Safety Assessment site located in Shrewsbury, MA. Responsible for performing operational, administrative and technical tasks to provide comprehensive care for all species of laboratory animals at the site, including: daily health observations, feeding/watering, sanitizing primary and secondary enclosures, environmental enrichment, handling and restraint and related tasks. Assist with the movement of animals and stocking of supplies. May serve as lead/primary technician and perform technical duties with guidance. | 2/17/2020 |
| 323 | Charles River Ashland, OH Research Technician 1 HS diploma/BS Exp: 6-12 months |
We are seeking an experienced Research Technician I for our Safety Assessment site located in Ashland, OH. The Research Technician I will collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical obsercations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods. | 2/17/2020 |
| 324 | Charles River Malvern, PA Quality Assurance Auditor 1 BS/BA Exp: 1-2 year(s) |
This position is responsible for performing Quality inspections of routine processes in the Manufacturing department. These inspections may occur in aseptic production rooms. The Auditor I will also be responsible for a Quality review of basic records and reports in support of the Manufacturing department to assure compliance with applicable regulatory requirements, international standards, and corporate policies and procedures. We are seeking a Quality Assurance Auditor I for our Biologics Testing Solutions site located in Malvern, PA. The following are responsibilities related to the Quality Assurance Auditor I position. Assure Charles River’s compliance with applicable federal, state, and local regulations as well as corporate policies to avoid any business interruptions. Communicate all identified compliance and quality risk to supervisor. etc. | 2/17/2020 |
| 325 | ChemGenes Wilmington, MA Junior Chemist BS in chemistry Exp: Not necessary for BS candidates |
The job duties: Manufacture of DNA & RNA compounds. Assist Senior Chemists. Prepare test solutions, reagents and ability to carry out reactions, to produce specialized ultra pure DNA/RNA synthesis products. Operate rotary evaporators, chillers, etc. Preform column chromatography: small scale (on the bench) & large scale. Follow SOPs of standard products; report any deviations to Senior Chemists. Communicate with QC & QA department to update/create certificates of analysis. Maintain timely documentation of work. Evaluate data & prepare technical reports. General lab maintenance as necessary. etc. | 2/17/2020 |
| 326 | CheminPharma Branford, CT Associate Scientist, Medicinal/Synthetic chemistry BS/MS in synthetic chemistry Exp: 0-5 years |
The successful candidate will be an experienced chemist with state of the art knowledge of synthetic organic chemistry and will be a motivated, creative, hands-on laboratory scientist with the ability to interact effectively with team members and external customers. Major responsibilities will involve design, synthesis, purification, and characterization of novel chemical entities and the management of general chemistry lab operations under the direction of senior scientific staff. The qualified individual is expected to contribute to process development and scale-up of key intermediates. | 2/17/2020 |
| 327 | Clinlogix Chicago, IL Clinical Research Associate BS in a life science Exp: 1-3 year(s) |
The Clinical Research Associate reports to and works under the direction of the Manager, Global Clinical Monitoring. Responsible to monitor clinical trials, study sites and clinical data while ensuring compliance with protocol and overall clinical objectives and Good Clinical Practice (GCP). Provides administrative and project support to clinical programs with minimum supervision. Interfaces with all project/clinical team members and off-site personnel as needed in support of project and departmental goals and responsibilities. etc. | 2/17/2020 |
| 328 | Codexis Redwood City, CA Research Associate, Process Development-Downstream MS Exp: 1-2 year(s) |
The Process Development Associate will be responsible for the development, optimization, and scale-up of protein purification processes. The ideal candidate will have experience with the optimization of enzyme recovery/purification processes. Responsibilities Include: Perform protein recovery experiments using unit operations such as homogenization, centrifugation, depth filtration, microfiltration, and ultrafiltration. Perform resin screening, column chromatography (IEX, HIC, MMC, CHT etc.). Analyze processing samples, using biological, biochemical, and other relevant analytical methods. Communicate results of experiments to the Project team. Participate in daily operation and routine maintenance/housekeeping of process and analytical equipment. etc. | 2/17/2020 |
| 329 | Colopast Coral Springs, FL Inside Sales Representative (Physician Relationship Manager) HS diploma or equivalent Exp: 1+ year(s) |
Comfort Medical, a wholly owned subsidiary of Coloplast, is seeking an Inside Sales Representative to join our team in our Coral Springs office. You will build your own sales relationships/accounts, resolve customer questions, and offer solutions to drive company revenue. Your primary call points will include Physicians' and healthcare providers' offices. Comfort Medical preferred manufacturers, and customers. This role is heavily phone-based. Responsibilities: Present and sell company services to new and existing customers. Prospect and contact potential customers. Achieve agreed upon sales targets by the deadline. etc. | 2/17/2020 |
| 330 | Concerto King of Prussia, PA Pharmaceutical Data Analyst – Analytics BA/BS in a laboratory science or related Exp: 1-4 year(s) |
ProMetrics, a Concerto HealthAI company, is seeking a highly proficient Data Analyst who will thrive in our agile, fast-paced, and delivery-focused environment. As an integral part of the analytics team, the data you analyze will provide valuable insight to our clients, who happen to be some of the most influential brands in the pharmaceutical industry. You’ll be responsible for understanding system requirements, documentation, verifying, and testing data integrity and quality being displayed on ProMetrics’ proprietary systems. Most importantly, you’ll be accountable for delivering client data in an accurate and timely fashion. etc. | 2/17/2020 |
| 331 | Conformis Wilmington, MA CAD Engineer I BS in engineering or equivalent Exp: 1-2 year(s) |
The CAD Engineer I will be responsible for designing and reviewing patient-specific implants and surgical instruments using various software packages while ensuring Conformis quality standards. Essential Duties and Responsibilities: Develop and maintain strong internal working relationships across Conformis. Understand the objectives, responsibilities, and mission of the CAD department and works towards those goals. Prioritize and plan work activities; adapt for changing conditions. Generate 3D models from diagnostic CT images and use commercial and research software to design patient specific implants and surgical instruments. Work independently to achieve departmental and personal goals. Plan and manage workload effectively and efficiently. etc. | 2/17/2020 |
| 332 | Conformis Billerica, MA Finishing Technician I, 2nd Shift HS diploma or equivalent Exp: 1-3 year(s) |
This position is responsible for operation of post-machining finishing of medical implants in a high-volume manufacturing environment. 2nd Shift – Mon – Fri, 3:00pm – 11:30pm. Essential Duties and Responsibilities: Develop and maintain strong internal working relationships across Conformis. Understand the objectives, responsibilities, and mission of the Production Department and work towards those goals. Understand assigned quality and delivery targets, and consistently meet or exceed expectations. Prioritize and plan work activities; adapt for changing conditions. Perform blasting, hand-finishing, and polishing of metal medical implants post CNC machining. etc. | 2/17/2020 |
| 333 | Contract Pharmacal Corp Hauppage, NY Scientist I; AR&D BS/MS in chemistry or analytical chemistry Exp: 1-2 year(s) |
Design and conduct routine laboratory analysis using various analytical instruments and software such as HPLC, UPLC, ICP, and UV-Vis. Responsibilities: Responsibilities include, but are not limited to: Knowledge of USP and FDA requirements. Design and conduct full analysis of Dietary Supplements and Active Pharmaceutical Ingredients (API) products and their impurities. Conduct assay, content uniformity, dissolution, in-process blend, and blend uniformity of newly developed and stability samples in support of formulation and process development. Prepare result documentation for department and general review. etc. | 2/17/2020 |
| 334 | Contract Pharmacal Corp Hauppage, NY QA Manufacturing, Specialist AAS/BA/BS Exp: 1 year |
The QA Manufacturing Specialist has primary responsibility for handling all front office operations as outlined below. Responsibilities: Including but not limited to: Ensure that the daily batch request list, provided by Materials Management, conveys to accurate and on-time issuance of production and non-commercial batches. Request issuance of batches with related labels (bulk and IP). Updating production board accordingly. Consolidate information regarding batches on production data roster spreadsheet used by Manufacturing Operations, Account Services, and Materials Management. Maintain weekly & quarterly reporting of current production of materials processing and finished production. etc. | 2/17/2020 |
| 335 | Contract Pharmacal Corp Hauppage, NY Chemist I; QC Finished Product & Validation BS in chemistry Exp: 1+ year(s) |
A Chemist Level I is responsible for performing chemical testing and completion of real-time documentation per cGMPs and current SOPs. Essential Job Functions: Perform UPLC, HPLC, GC, UV-vis, FTIR, ICP, TOC and wet chemistry testing. Proficient in various UPLC and HPLC software programs, such as Empower and EZ-Chrom. Assist in writing SOPs and Test Procedures following good documentation practice per company's SOP and cGMP regulations. Assist in OOS investigations. etc. | 2/17/2020 |
| 336 | Corvus Pharmaceuticals Bulingame, CA Animal Technician/Lab Assistant AS/BS in biology or related Exp: 0-2 years |
Role and Responsibilities: Performs the general husbandry of research animals for experimental purposes. Performs animal welfare checks. Performs cell inoculations via multiple routes (SC, tail vein, RO). Performs dosing via multiple routes (IV, PO, SC, IM). Performs necropsy/tissue sample collection for evaluating PD endpoints. Performs bleeding via multiple techniques (RO, cardiac punch, cheek) for evaluating drug PK. Performs various vivarium cleaning duties. etc. | 2/17/2020 |
| 337 | Covance San Carlos, CA Study Technician Animal Operations-Metabolic Studies BS in the life sciences Exp: Entry level |
In this position your work will have a real life positive impact of improving health around the world. Upcoming or recent graduates in Animal Science, Biology and related life sciences field encourage to apply. Veterinary Technicians looking to to work in research setting are encouraged to apply. In this role you'll be working with Scientist performing study task with small animal models. Extensive training is provided for this entry level Study Tech position. Duties include but not limited to: Monitoring of animal health and welfare in compliance with the Animal Welfare Act, determines and documents clinical observations, body weight data, and food consumption data. Prepares Dose Formulations, buffer solutions and control substances. etc. | 2/17/2020 |
| 338 | Covance Madison, WI Research Assistant (I) - Immunotoxicology BS/BA in a related scientific field Exp: 1-2 year(s) |
We have a great opportunity for a Research Assistant (I) - Immunotoxicology in our Immunology and Immunotoxicology (InI) Group in Madison, WI. Covance’s work in developing new pharmaceutical solutions has an incredible impact on millions of lives worldwide. Be a part of this life-saving work and help improve patients' lives while growing your career. In this role, you will set up and prepare equipment for sample processing, data acquisition/analysis according to study protocol, Policies/SOPs, Methods, and regulatory guidelines. You will also be responsible for performing assays, maintenance, and general laboratory support duties. Organizes and conducts routine and non-routine processing in compliance with applicable methods, protocols, SOPs and regulatory agency guidelines. Documents work and maintains study documentation and laboratory records. etc. | 2/17/2020 |
| 339 | Covance Greenfield, IN Sampling Handling I Assistant HS diploma or equivalent Exp: Entry level |
In this role it’s a unique combination of sample management and archive tasks, including labeling, receipt, transferring, tracking, inventory, archival, shipping, and disposal of samples and/or materials. Samples include paper data, wet tissues, slides, blocks and frozen biological samples. Excellent keyboarding skills required as this position will have a high degree of data input into tracking and archive database, may involve repeated lifting of up to 50 lbs. Excellent customer service skills are required as position interfaces with internal and external customers in retrieving and storage of samples all while maintaining strict business confidentially. etc. | 2/17/2020 |
| 340 | Covance Salt Lake City, UT Sample Handling Assistant HS diploma or equivalent Exp: Not required |
Job Overview: Performs any combination of sample management and/or archive tasks, including labeling, receipt, transferring, tracking, inventory, archival, shipping, and disposal of samples and/or materials. Sample accession core tasks, including box opening, inventory/labeling, receipt/store, and pulls/returns. Uses tracking systems as appropriate to maintain sample and study integrity. Accurate protocol and relevant documentation interpretation (i.e., Sample Analysis Outline, client paperwork). Document and communicate discrepancies to appropriate personnel, and assists with problem solving. etc. | 2/17/2020 |
| 341 | Covance Princeton, NJ Associate I Regulatory Submissions BS in a life science Exp: 0-1 year(s) |
Covance is seeking candidates for an Associate I Regulatory Submissions. The Associate I Regulatory Submissions is an office based role in Princeton, NJ. Assist in the preparation of submissions filed to Regulatory Authorities (e.g.: INDs, CTAs, NDAs, NDSs, MAAs or CTDs). Contribute to the preparation of submissions to Regulatory Authorities by reviewing/summarizing scientific/research documents. Assist in the coordination, collection and organization of information required by Regulatory Authorities. Interact with the Publishing group, Copy Center or equivalent as necessary for the production of submissions. etc. | 2/17/2020 |
| 342 | Covance Denver, PA Animal Tech I (3rd Shift) HS diploma or equivalent Exp: Not required |
As an Animal Care Technician in our Immunology Services you'll have a connection to the life improving changes we make at Covance. In this position you’ll work closely with a variety of laboratory animals in barrier housing Extensive training provided! Responsibilities include but not limited to; Responsible for monitoring and maintaining the physical environment conditions of the animals in research setting. Comply with appropriate safety and health practices including personal protective equipment and barrier requirements, as applicable. Perform animal husbandry (clean, feed, sanitation, enrichment, etc.) on a regular basis. Perform and document daily observations of animal health status. etc. | 2/17/2020 |
| 343 | Covance Greenfield, IN Material Controller Tech I HS diploma Exp: 0-3 years |
Purchasing: Process purchase and material requisitions for the Facility Management Department. Coordinate and expedite stock and non-stock material requisitions for maintenance repair. Work closely with Facilities planners/schedulers, maintenance supervisors, and crafts persons to coordinate delivery schedules, provide purchase order information and resolve invoice discrepancies. Perform RCP duties as delegated. etc. | 2/17/2020 |
| 344 | Myriad Bioscience South San Francisco, CA Client Services Associate BA/BS Exp: 1-3+ year(s) |
The Client Services Associate will be on the front lines and will act as the face of the organization for our customers including physicians, clinics, medical staff, and patients. We handle a variety of complex inbound and outbound inquiries to assist and empathize with our customers, some who may be experiencing stress. We work to resolve and preempt customer issues to ensure a positive customer experience. Myriad Women’s Health Client Services team provides a differentiated customer experience because we hire amazing people to join this team. Our Client Services Associates are highly skilled, motivated people who are driven by human interactions and solving problems. etc. | 2/17/2020 |
| 345 | Crinetics San Diego, CA Research Associate, Drug Metabolism and Pharmacokinetics BA/BS/MS in a relevant scientific field Exp: 1-2 year(s) |
Crinetics Pharmaceuticals is seeking a Research Associate (RA) or Senior Research Associate (SRA) to join its growing and dynamic development team. This individual will be responsible for performing a variety of DMPK and bioanalytical assays. The work will support projects at various stages drug discovery and development thereby allowing the selected candidate to play an active role in our drug discovery and development efforts to advance small molecule therapeutics for rare endocrine disorders and endocrine-related cancers. This is a unique opportunity to work with a proven and well-funded drug discovery and development team in a small company environment in the heart of San Diego’s biotechnology community. (Position will be filled at level commensurate with experience) etc. | 2/17/2020 |
| 346 | CRISPR Therapeutics Cambridge, MA Research Assistant -II: QC Data Review MS Exp: 1-2 year(s) |
Job Summary: Support CMC Analytical activities for Crispr clinical programs by reviewing batch records, assay results. Perform Data Review for integrity and accuracy and collate data in a highly organized manner. Use statistical software to analyze the data for shelf life trending and control chart trending. Monitor stability program for time pulling of the samples, scheduling and following the results with the testing labs. This is a Cross-functional and highly visible position within Technical Operations group. The position requires active collaboration with research, process development and quality teams and CDMOs. etc. | 2/17/2020 |
| 347 | CSBio Menlo Park, CA Chemist, Quality Control MA/MS in chemistry, biochemistry, or biology Exp: Recent graduates |
We are seeking a qualified individuals to join us as Quality Control Chemists at our Menlo Park facility. This position will be responsible for conducting QC testing for release, stability, and raw materials, as well as executing experiments in support of routine QC testing utilizing various analytical techniques. Core duties and responsibilities include the following: Conduct sample analysis using various analytical techniques, including HPLC, UPLC, GC, KF, FT-IR, TLC, and LC-MS, GC-MS. Preparation of laboratory reagents and samples; operation of instruments; data analysis; preparation of analytical reports; notebook documentation. etc. | 2/17/2020 |
| 348 | CSL Behring Gresham, OR Plasma Processing Technician HS diploma or equivalent Exp: 3+ months |
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors. 1 In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. 2 Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. 3 May ensure accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. 4 Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. etc. | 2/17/2020 |
| 349 | CSL Behring Cheektowaga, NY Plasma Processing Technician HS diploma or equivalent Exp: 3+ months |
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors. 1 In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. 2 Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. 3 May ensure accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. 4 Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. etc. | 2/17/2020 |
| 350 | CTI Chicago, IL Clinical Safety Scientist I BS Exp: 1-2 year(s) |
What You'll Do: Assist with Interfacing between sponsors, vendors, and other departments in the area of safety and pharmacovigilance. Includes assisting with development of project-specific process documents such as Safety Management Plans, Project-Specific Operating Procedures (PSOPS), and/or guidelines as agreed to by CTI and sponsors. Process serious adverse events (SAEs) according to Standard Operating Procedures (SOPs) and project specific safety plans. Triage SAEs, evaluates SAE data for completeness, and regulatory reportability. Enter relevant safety data into safety database. Perform coding of SAEs, medical history, concomitant medications and diagnostic tests. etc. | 2/17/2020 |
| 351 | CTI Dallas, TX Clinical Safety Scientist I BS Exp: 1-2 year(s) |
What You'll Do: Assist with Interfacing between sponsors, vendors, and other departments in the area of safety and pharmacovigilance. Includes assisting with development of project-specific process documents such as Safety Management Plans, Project-Specific Operating Procedures (PSOPS), and/or guidelines as agreed to by CTI and sponsors. Process serious adverse events (SAEs) according to Standard Operating Procedures (SOPs) and project specific safety plans. Triage SAEs, evaluates SAE data for completeness, and regulatory reportability. Enter relevant safety data into safety database. Perform coding of SAEs, medical history, concomitant medications and diagnostic tests. etc. | 2/17/2020 |
| 352 | CTI Cincinnati, KY Clinical Safety Scientist I BS Exp: 1-2 year(s) |
What You'll Do: Assist with Interfacing between sponsors, vendors, and other departments in the area of safety and pharmacovigilance. Includes assisting with development of project-specific process documents such as Safety Management Plans, Project-Specific Operating Procedures (PSOPS), and/or guidelines as agreed to by CTI and sponsors. Process serious adverse events (SAEs) according to Standard Operating Procedures (SOPs) and project specific safety plans. Triage SAEs, evaluates SAE data for completeness, and regulatory reportability. Enter relevant safety data into safety database. Perform coding of SAEs, medical history, concomitant medications and diagnostic tests. etc. | 2/17/2020 |
| 353 | CTI Philadelphia, PA Clinical Safety Scientist I BS Exp: 1-2 year(s) |
What You'll Do: Assist with Interfacing between sponsors, vendors, and other departments in the area of safety and pharmacovigilance. Includes assisting with development of project-specific process documents such as Safety Management Plans, Project-Specific Operating Procedures (PSOPS), and/or guidelines as agreed to by CTI and sponsors. Process serious adverse events (SAEs) according to Standard Operating Procedures (SOPs) and project specific safety plans. Triage SAEs, evaluates SAE data for completeness, and regulatory reportability. Enter relevant safety data into safety database. Perform coding of SAEs, medical history, concomitant medications and diagnostic tests. etc. | 2/17/2020 |
| 354 | CTI Raleigh, NC Clinical Safety Scientist I BS Exp: 1-2 year(s) |
What You'll Do: Assist with Interfacing between sponsors, vendors, and other departments in the area of safety and pharmacovigilance. Includes assisting with development of project-specific process documents such as Safety Management Plans, Project-Specific Operating Procedures (PSOPS), and/or guidelines as agreed to by CTI and sponsors. Process serious adverse events (SAEs) according to Standard Operating Procedures (SOPs) and project specific safety plans. Triage SAEs, evaluates SAE data for completeness, and regulatory reportability. Enter relevant safety data into safety database. Perform coding of SAEs, medical history, concomitant medications and diagnostic tests. etc. | 2/17/2020 |
| 355 | CTI San Francisco, CA Clinical Safety Scientist I BS Exp: 1-2 year(s) |
What You'll Do: Assist with Interfacing between sponsors, vendors, and other departments in the area of safety and pharmacovigilance. Includes assisting with development of project-specific process documents such as Safety Management Plans, Project-Specific Operating Procedures (PSOPS), and/or guidelines as agreed to by CTI and sponsors. Process serious adverse events (SAEs) according to Standard Operating Procedures (SOPs) and project specific safety plans. Triage SAEs, evaluates SAE data for completeness, and regulatory reportability. Enter relevant safety data into safety database. Perform coding of SAEs, medical history, concomitant medications and diagnostic tests. etc. | 2/17/2020 |
| 356 | CTK Biotech Poway, CA Production Assistant AS/BS Exp: 0-3 years |
The Production Assistant is mainly responsible for manufacturing biological products following SOP and maintaining production related records. Essential Duties and Responsibilities: Production of Recombinant proteins, monoclonal antibodies, and other biologics per work instruction. Conducting general lab maintenance, including glass washing, buffer/reagent preparation, proper disposal of waste, and inventory organization. etc. | 2/17/2020 |
| 357 | CTK Biotech Poway, CA Production Associate MS Exp: 1+ year(s) |
The Production Associate is mainly responsible for manufacturing biological products following SOP, maintaining production records and generating production document. Essential Duties and Responsibilities: Produce qualified antigens, antibodies, and other biologics per work instruction. Conducting general lab maintenance, including glass washing, buffer/reagent preparation, proper disposal of waste, and inventory organization. Communicating constantly with team members and related departments. etc. | 2/17/2020 |
| 358 | Biotronik Lake Oswego, OR Master Data Analyst BS/BA Exp: 1-3 year(s) |
BIOTRONIK is looking to add a Master Data Analyst to our Finance and Sales Operations team. The Master Data Analyst will be the gatekeeper to all master data and is critical to the overall success of the organization. This position is responsible for overseeing key processes and projects associated with the accuracy, integrity and timeliness of critical master data domains. The analyst will take an active role in fulfilling the additional demand generated by the organization changing into to a data-driven company and help develop the tools to educate and empower stakeholders. Analysts in this position are also responsible for analyzing large amounts of data to develop data management recommendations, effectively communicating related results and implications of the various options across multiple integrated teams. etc. | 2/11/2020 |
| 359 | Bioventus Union County, NJ Associate Sales Representative - New Brunswick, New Jersey BS/BA Exp: 0-2 year(s) |
The Associate Sales Representative (ASR) plays a critical role in helping to improve people’s lives every day, interacting directly with healthcare providers and their patients to introduce our products. ASRs also educate patients on the proper use of our products and provide invaluable support to the entire sales team. Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. They strive for excellent performance, driven by the willingness to both teach and learn. etc. | 2/11/2020 |
| 360 | Bioventus Brooklyn, NY Associate Sales Representative - Brooklyn, NY BS/BA Exp: 0-2 year(s) |
The Associate Sales Representative (ASR) plays a critical role in helping to improve people’s lives every day, interacting directly with healthcare providers and their patients to introduce our products. ASRs also educate patients on the proper use of our products and provide invaluable support to the entire sales team. Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. They strive for excellent performance, driven by the willingness to both teach and learn. etc. | 2/11/2020 |
| 361 | Bioventus Peoria, IL Associate Sales Representative - Brooklyn, NY BS/BA Exp: 0-2 year(s) |
The Associate Sales Representative (ASR) plays a critical role in helping to improve people’s lives every day, interacting directly with healthcare providers and their patients to introduce our products. ASRs also educate patients on the proper use of our products and provide invaluable support to the entire sales team. Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. They strive for excellent performance, driven by the willingness to both teach and learn. etc. | 2/11/2020 |
| 362 | Bioventus Rockford, IL Associate Sales Representative - Rockford, IL BS/BA Exp: 0-2 year(s) |
The Associate Sales Representative (ASR) plays a critical role in helping to improve people’s lives every day, interacting directly with healthcare providers and their patients to introduce our products. ASRs also educate patients on the proper use of our products and provide invaluable support to the entire sales team. Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. They strive for excellent performance, driven by the willingness to both teach and learn. etc. | 2/11/2020 |
| 363 | Bioventus Worcester, MA Associate Sales Representative - Worcester, MA BS/BA Exp: 0-2 year(s) |
The Associate Sales Representative (ASR) plays a critical role in helping to improve people’s lives every day, interacting directly with healthcare providers and their patients to introduce our products. ASRs also educate patients on the proper use of our products and provide invaluable support to the entire sales team. Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. They strive for excellent performance, driven by the willingness to both teach and learn. etc. | 2/11/2020 |
| 364 | Bioventus Honolulu, HI Sales Rep - Hawaii BS/BA in sports medicine or life sciences Exp: 1-3 year(s) |
The Sales Representative plays a critical role in helping to improve people’s lives every day, interacting directly with healthcare providers and their patients to introduce our products. They also educate patients on the proper use of our products. The Sales Representative is fully responsible for managing their own territory – a role that’s perfectly suited to highly motivated self-starters with an entrepreneurial spirit! Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. They strive for excellent performance, driven by the willingness to both teach and learn. They are good team players, dynamic, optimistic, accurate, well-organized, and ambitious about developing as a sales professional. etc. | 2/11/2020 |
| 365 | Bioventus Bozeman, MT Sales Rep - Montana BS/BA in sports medicine or life sciences Exp: 1-3 year(s) |
The Sales Representative plays a critical role in helping to improve people’s lives every day, interacting directly with healthcare providers and their patients to introduce our products. They also educate patients on the proper use of our products. The Sales Representative is fully responsible for managing their own territory – a role that’s perfectly suited to highly motivated self-starters with an entrepreneurial spirit! Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. They strive for excellent performance, driven by the willingness to both teach and learn. They are good team players, dynamic, optimistic, accurate, well-organized, and ambitious about developing as a sales professional. etc. | 2/11/2020 |
| 366 | BioVision Milpitas, CA Sales Representative BS/MS in biochemistry, cell biology, or molecular biology Exp: 1-2 year(s) |
BioVision, Inc., a privately held Life Science company, develops and offers world-wide, a variety of products including assay kits, antibodies, recombinant proteins & enzymes, and other innovative research tools for studying Apoptosis, Metabolism, Cell Proliferation, Cellular Stress, Cell Damage and Repair, Diabetes, Obesity and Metabolic Syndrome, Stem Cell Biology, Gene Regulation, Signal Transduction, etc. We are looking for a highly motivated individual to work in our Sales & Marketing Department. etc. | 2/11/2020 |
| 367 | Blade Therapeutics San Francisco, CA Clinical Trial Associate, Clinical Operations BS/BA in the life sciences or related Exp: 1-2 year(s) |
The Clinical Trial Associate (CTA) will work within the Clinical Operations Team to implement and maintain clinical trials in phases I-IV, as applicable. The CTA will be responsible for adhering to all Blade and/or vendor Standard Operating Procedures (SOPs), in addition to ICH GCP and any applicable, regional/global regulatory authority procedures. This is an in-house role, based out of South San Francisco, CA. The CTA will have the benefit of working with a tight-knit team to drive projects and meet deliverables. In addition to working within the Clinical Operations team, the CTA will also be responsible for some cross-functional interaction. etc. | 2/11/2020 |
| 368 | BlueRock Therapeutics Toronto, ON Research Associate, Immunology MS in immunology, cell biology, or molecular biology Exp: 1 year |
We are seeking a Research Associate for our Translational Immunology Team. This position will report to the Scientist of Translational Immunology and will have various responsibilities for hands-on lab work, developing T cell, NK cell and myeloid cell assays. This is an outstanding opportunity for a talented associate to contribute to bringing a new class of cellular therapies to patients and gain valuable career experience in Translational Immunology in the life sciences industry. We are seeking a Research Associate for our Translational Immunology Team. This position will report to the Scientist of Translational Immunology and will have various responsibilities for hands-on lab work, developing T cell, NK cell and myeloid cell assays. etc. | 2/11/2020 |
| 369 | Boston Analytical Cambridge, NH Analytical Chemist *All-Levels* BS in chemistry or related Exp: 0-5 years |
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. Primary Duties and Responsibilities: Prepares and analyzes products to determine chemical and physical properties. Documents work in a clear and organized manner. Follows all safety rules and regulations and conducts periodic safety audits. etc. | 2/11/2020 |
| 370 | Boston Analytical Cambridge, NH Microbiologist BS/BA in microbiology or related Exp: 0-2 year(s) |
The QC Microbiologist I conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. Primary Duties and Responsibilities: Prepares and analyzes samples to determine microbiological quality through the following analyses: Microbial enumeration methods, absence of specified microorganisms, endotoxin, and water quality analysis (bioburden, TOC, Conductivity). Performs genetic analysis of microbial growth to determine Genus/Species of unknown isolates. Collects Environmental Monitoring Samples onsite and offsite at client manufacturing sites. Documents work in a clear and organized manner. etc. | 2/11/2020 |
| 371 | Bristol-Myers Squibb Redwood City, CA Associate Research Scientist 1 / 2 - Immuno-Oncology Translational Discovery Biology MS Exp: Not required for MS candidates |
The Associate Research Scientist will join the Translational Discovery Biology team within the Oncology Discovery organization at Bristol-Myers Squibb in Redwood City, CA to deliver potential biomarker and mechanism of action data for targets in the I-O space. Responsibilities: The qualified candidate is a highly motivated, interactive, and creative individual that possesses the ability to work across a highly matrixed environment to support progression of I-O therapeutic targets. This position will specifically support the identification of potential biomarkers, receptor occupancy, target engagement and pharmacodynamic assays for these targets. Additionally, the position will support mechanism of action studies using primary human tumors and mouse models. etc. | 2/11/2020 |
| 372 | Brooks South Plainfield, NJ Bioinformatics Scientist MS in bioinformatics Exp: 1-3 year(s) |
Responsibilities: Work collaboratively with bench scientists, comprehend project objectives, evaluate and provide informatics solutions. Develop and implement bioinformatics analyses, applications, and workflows. Integrate statistical analysis to project design and data interpretations. Work closely with IT specialists to build robust infrastructure. Support company intellectual property management. Support NGS with data analysis and delivery, pipeline development and automation. Provide customer support for NGS data analysis results. Support Sales and Marketing departments and related business development efforts. | 2/11/2020 |
| 373 | Brooks South Plainfield, NJ Laboratory Technician I HS diploma/AS/AA Exp: 1+ year(s) |
Our Lab Techs are: Quality driven processers. When our customers send us samples for sequencing, they help to prepare and process these samples as quickly and as awesomely as possible, while maintaining the highest quality standards in the industry. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. etc. | 2/11/2020 |
| 374 | Brooks South Plainfield, NJ Associate Scientist, Clinical Development BS in a biological science Exp: 1+ year(s) |
The Associate Scientist position in our Clinical Services department is a great entry-level role with room for growth and advancement. If you have the desire to work in a casual yet results-driven environment that embraces innovation- then you’re just what we’re looking for! Responsibilities: Prepare amplified template libraries for high-throughput sequencing. Carry out DNA sequencing on next-generation DNA analyzers. Perform routine maintenance of DNA analyzers and related equipment. Check inventory and replenish consumable sequencing supplies. etc. | 2/11/2020 |
| 375 | Brooks South Plainfield, NJ Sales Associate I BS in a life science Exp: 1+ year(s) |
Responsibilities (maximum 8 key tasks and responsibilities of this position): Conduct marketing and sales independently in academic and small biotech accounts including hall walking, planned meetings, vendor shows, lunch and learns, and cart shows. Conduct sales strategy, account management, partnership negotiations, and phone/email prospecting under the direction of the manager/team lead. Achieve defined metrics for sales activity revenue growth in assigned accounts. Update price lists, create new price lists, and write quotes. Execute CDA's, service agreements, and other documents. etc. | 2/11/2020 |
| 376 | Brooks South Plainfield, NJ Inside Sales Associate BS in a life science Exp: 1+ year(s) |
The Sales Associate is expected to grow the revenue and expand the GENEWIZ brand in the assigned territory/accounts with strong support, direction and mentoring by the Assistant Manager, Inside Sales Team. Key work interactions (main interfaces with who the jobholder will have regular contact): Co-workers, Managers, Customers. Responsibilities (maximum 8 key tasks and responsibilities of this position): Achieve annual sales goals within defined territory/ accounts. Develop and implement an effective territory business growth plan. Conduct sales and marketing activities independently in academic and biotech accounts. Conduct sales strategy, account management, partnership negotiations, and phone/email prospecting under the direction of the manager. etc. | 2/11/2020 |
| 377 | Brooks South Plainfield, NJ Associate Scientist I BS in a biological science Exp: 1+ year(s) |
The Associate Scientist position in our Next Generation Sequencing department is a great entry-level role with room for growth and advancement. If you have the desire to work in a casual yet results-driven environment that embraces innovation- then you’re just what we’re looking for! Responsibilities: Prepare amplified template libraries for high-throughput sequencing. Carry out DNA sequencing on next-generation DNA analyzers. Perform routine maintenance of DNA analyzers and related equipment. Check inventory and replenish consumable sequencing supplies. Communicate with customers by phone and e-mail in a friendly and professional manner. etc. | 2/11/2020 |
| 378 | Brooks Cambridge, MA Laboratory Technician I HS diploma/AS/AA Exp: 1+ year(s) |
Our Lab Techs are: Quality driven processers. When our customers send us samples for sequencing, they help to prepare and process these samples as quickly and as awesomely as possible, while maintaining the highest quality standards in the industry. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. Customer focused. Our Lab Techs strictly adhere to laboratory SOPs to ensure quality and safety and often communicate with our customers via email. They understand our customer needs with empathy and know that everything they do is making a difference. etc.Our Lab Techs are: Quality driven processers. When our customers send us samples for sequencing, they help to prepare and process these samples as quickly and as awesomely as possible, while maintaining the highest quality standards in the industry. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. Customer focused. Our Lab Techs strictly adhere to laboratory SOPs to ensure quality and safety and often communicate with our customers via email. They understand our customer needs with empathy and know that everything they do is making a difference. etc. | 2/11/2020 |
| 379 | Bruker Kennewick, WA Shipping and Receiving Associate HS diploma Exp: 1-2 year(s) |
Responsibilities: Verifies and keeps records on incoming and outgoing shipments and prepares items for shipment. Provide Quality Assurance checks prior to packaging instruments: configuration confirmation and labeling. Cleans, labels, and packages instruments into customer facing final package. Confirms packaged items to ‘pick list’. Determines method of shipment, utilizing knowledge of shipping procedures, routes and rates under direction of Shipping Department lead. Affix shipping labels on packed cartons. Assembles cardboard containers. Inserts items into containers, using spacers, fillers and protective padding. etc. | 2/12/2020 |
| 380 | C4 Therapeutics Watertown, MA Research Associate, Target Biology BS in biology or related Exp: 1-5 year(s) |
C4 Therapeutics is seeking an enthusiastic, scientifically motivated Research Associate to join our Target Biology team. This candidate will play a significant role in the implementation of in vitro studies to characterize and differentiate the biological consequences of our small molecule therapeutics to advance drug discovery programs. The ideal candidate will possess a background in biology and experience in a research laboratory setting. In addition, the successful candidate will have a strong commitment to team success, ability work effectively as part of a team, and the ability to work on multiple projects simultaneously. This position seeks individuals who are comfortable in a fast-paced environment and interested/committed to laboratory-based research. etc. | 2/12/2020 |
| 381 | Cardiovascular Systems Pearland, TX Assembly Technician HS diploma or equivalent Exp: 1 year |
The Assembly Technician I will be expected to perform basic functions to complete day-to-day production activity. The position requires a highly motivated, positive individual that can work both independently and in a “team” environment. Assembly Technician I level employees will be expected to perform all job duties in the areas they are assigned under basic supervision. They will stay on task and complete quality work with accurate documentation. He/she will be a valuable and trustworthy asset to their work area through quality work of trained processes. This individual must be dedicated to the success of CSI and its quest to continually improve its operations, as well as perform duties to manufacture CSI products, meeting FDA, OSHA, GMP/MDD and ISO compliance requirements. etc. | 2/12/2020 |
| 382 | Cardiovascular Systems St. Paul, MN Assembly Technician HS diploma or equivalent Exp: 1 year |
The Assembly Technician I will be expected to perform basic functions to complete day-to-day production activity. The position requires a highly motivated, positive individual that can work both independently and in a “team” environment. Assembly Technician I level employees will be expected to perform all job duties in the areas they are assigned under basic supervision. They will stay on task and complete quality work with accurate documentation. He/she will be a valuable and trustworthy asset to their work area through quality work of trained processes. This individual must be dedicated to the success of CSI and its quest to continually improve its operations, as well as perform duties to manufacture CSI products, meeting FDA, OSHA, GMP/MDD and ISO compliance requirements. etc. | 2/12/2020 |
| 383 | CRISPR Therapeutics Cambridge, MA Research Associate, Analytical Development BS/MS in life sciences Exp: 1+ year(s) |
We are seeking a Research Associate to join an exciting, fast-growing and well-financed company to develop novel gene editing therapies for serious diseases. The successful candidate will join the Technical Operations (Tech Ops) group at CRISPR Therapeutics, focusing on development of analytical methods for ex vivo genetically modified cells to support the development of gene editing programs. The individual will develop quantitative assays measuring gene editing in target and non-target cells, cell-based assays measuring the expression and the biological functions of specific genes. The successful candidate will independently design, perform, and analyze experiments for multiple preclinical and clinical programs, and will work independently to support process development, product characterization, and technical transfer to CMOs and GMP test labs. etc. | 2/12/2020 |
| 384 | Celgene Seattle, WA Associate Scientist, Process Analytical Technologies Development MS in biology, immunology, biological engineering or related Exp: 1-3 year(s) |
We are seeking a highly capable and enthusiastic Associate Scientist to work with a multidisciplinary group of engineers and scientists to support the development of novel Process Analytical Technologies (PAT). The Associate Scientist will be responsible for independently executing microscopy-based and cell selection experimentation. The candidate will additionally be expected to execute T cell culture experiments using a combination of scale-down models and manufacturing scale bioreactors. The successful candidate will: Work within a multi-disciplinary environment towards novel applications of Process Analytical Technologies. Independently design experiments, analyze data and draft technical reports to communicate key conclusions. Independently execute multi-parametric cell sorting and flow cytometry experiments. etc. | 2/12/2020 |
| 385 | Celgene Warren, MI Associate Bioengineer II BS in chemical or biomedical engineering or biology Exp: 0-2 year(s) |
Conducts core MSAT activities in technical transfer, lifecycle management, or validation to support cellular product commercialization. Responsible for technical deliverables, including authoring protocols and reports, with moderate supervision and feedback. Organizes, reviews, and maintains data while developing subject matter expertise. Responsibilities will include, but are not limited to, the following: With supervision, design and execute studies in one of the following areas: technical transfer, lifecycle management, or validation. Perform data analysis, and summarize empirical results, with moderate technical/scientific supervision and feedback. Present results within project team and departmental technical reviews. Conduct Facility Fit studies and work with partner organizations to implement risk mitigations. etc. | 2/12/2020 |
| 386 | Cell Signaling Technology Danvers, MA Research Associate I BS in a relevant science Exp: 1 year |
We are seeking a highly organized and enthusiastic Research Associate to join our Conjugation team. The successful candiate will assist the team with releasing new products, supporting existing products and providing technical support for all conjugated antibody product lines. Responsibilities: Performs experiments focused on conjugation including dye conjugation, bead conjugation, HRP conjugation, biotin conjugation, PE conjugation and PE tandem dyes for the purpose of enabling the release of direct conjugated antibody products and maintain existing product lines. Performs protein purification and determination. etc. | 2/12/2020 |
| 387 | Cell Signaling Technology Beverly, MA Product Supply Specialist BS/BA in business, supply chain operations, or a related field Exp: 1-2 year(s) |
We are seeking a Product Supply Specialist to join our Product Supply Team. The role of the Product Supply team is to link the suppliers of our products with our broader Global Supply Chain team, and ensure finished goods inventory is ready and available for customers. Responsibilities: Serve as Supply Chain stakeholder on diverse cross-functional new product introduction (NPI) teams. Serve as key point of contact with vendors for sourced (OEM) products and product packaging materials. etc. | 2/12/2020 |
| 388 | Cellular Technology Limited Cleveland, OH Laboratory Assistant (Contract Research Laboratory) BS Exp: 1 year |
We are seeking a Laboratory Assistant for our Contract Research Laboratory who will perform immunology testing of client specimens collected from both pre-clinical and clinical studies using the following test methods: ELISPOT, ELISA, flow cytometry, etc. You will help support our quality improvement projects in conjunction with QA, support our quality system by data quality control, communicate with fellow laboratory personnel, maintain laboratory equipment, write reports, etc. All work is performed according to general laboratory safety standards, internal standard operating procedures (SOPs), client protocols, and applicable international, federal and state regulations. | 2/12/2020 |
| 389 | CEL-SCI Elkridge, MD Assistant Immunologist I BS/BA Exp: 0-2 year(s) |
The Assistant/Associate Immunologist will assist in the day-to-day activities related to the QC testing of Leukocyte Interleukin, Injection (LI) under current Good Manufacturing Practices (cGMP) for clinical application, and QC equipment/facilities operations and maintenance. Specific experience should include: ELISA testing, ELISA assay development, aseptic technique, GMP, analytical chemistry experience, laboratory record-keeping. Skills / Abilities: Quality Control testing of all GMP Manufacturing samples (ELISA, pH, visual inspection). Adhere to written procedures and proper documentation, etc. | 2/12/2020 |
| 390 | CEL-SCI Elkridge, MD Manufacturing Support Technician AA/AS Exp: 1+ year(s) |
The Support Technician contributes to the manufacturing team effort by accomplishing related tasks and assignments. The Manufacturing Support Technician reports directly to Supervisor of Manufacturing. Responsibilities include, but are not limited to: Use of the autoclave, depyrogenation oven and sonicator. Clean Formulation and Fill Vessels. Gowning for classified areas. Stock and stage processing areas. Other duties as assigned. etc. | 2/12/2020 |
| 391 | Celsee Ann Arbor, MI Laboratory Research Technician BS in biology or biochemistry Exp: 1-2 year(s) |
The Laboratory Research Technician will work under the guided supervision of an interdisciplinary team of biologists and engineers to validate molecular assays on single-cells. The job responsibilities include: Performing various standard laboratory assays including NGS, Library Prep, PCR, Cell capture and analysis on Celsee’s proprietary devices. Working in sterile conditions to conduct cell culture experiments and maintain the growth of cell lines. Collecting and analyzing generated data. Assisting in organization and upkeep of laboratory supplies, workspace, and equipment. etc. | 2/12/2020 |
| 392 | Centrillion Hillsboro, OR Laboratory Technician BS/MS in molecular biology, chemistry, data science or other relevant field. Exp: 1-2 year(s) |
MVL is seeking Laboratory Technician for their research and development teams. These positions are in a fast-paced, start-up environment, interacting with R&D scientists from a variety of backgrounds, with a heavy focus on molecular biology and biochemistry. Lab technician will divide their time between hands-on laboratory work, data analysis, and lab organization and maintenance. The selected individuals will be working in a support role toward the development of new genomics technologies. The candidate will work with multiple scientists to assist with a broad range of duties including making buffers, following protocols, developing or adapting new protocols for new needs. etc. | 2/12/2020 |
| 393 | Centrillion Palo Alto, CA Laboratory Technician BA/BS in molecular biology, chemistry, genetics, or microbiology Exp: 1-2 year(s) |
Centrillion is seeking Laboratory Technicians for their research and development teams. These positions are in a fast-paced, start-up environment, interacting with R&D scientists from a variety of backgrounds, with a heavy focus on molecular biology and biochemistry. Lab technicians will divide their time between hands-on laboratory work, data analysis, and lab organization and maintenance. The selected individuals will be working in a support role toward the development of new genomics technologies. The candidate will work with multiple scientists to assist with a broad range of duties including making buffers, following protocols, developing or adapting new protocols for new needs. etc. | 2/12/2020 |
| 394 | Ceva Lenexa, KS Environmental Monitoring Technician I BS in microbiology, veterinary science, or equivalent Exp: Entry level |
The Environmental Monitoring Technician I will perform microbiological testing involving environmental monitoring, water, and other production utilities to help ensure quality production. The technician will ensure products are tested in a manner consistent with Standard Operating Procedures and in compliance with regulations according to 9CFR. Responsibilities and Key Duties: Perform routine daily, weekly and monthly environmental monitoring testing on processes, utilities, and personnel. Sample purified water system, clean steam, and other utilities for subsequent analysis. Perform assigned sampling tasks carefully and on schedule according to standard operating procedure and supervisor instruction. etc. | 2/12/2020 |
| 395 | Ceva Lenexa, KS Industrial Development Technician I BA/BS in biology, chemistry, pharmacology, or equivalent Exp: 0-2 year(s) |
Assist in the industrial development, process, and product improvement of viral, bacterial, parasitic and/or recombinant vaccines of licensed and unlicensed vaccines. Responsibilities and Key Duties: GID main responsibilities (including poultry, swine, bovine vaccine viruses and bacteria). Within the assigned internal site, is in charge of the manufacturing and/or analytical testing of development and first commercial batches with a yearly vision. Executes the manufacturing & testing according to the industrial development and process transfer rational (including technical, financial, and regulatory aspects) to anticipate industrial needs - may propose process validation strategy. etc. | 2/12/2020 |
| 396 | Champions Oncology Rockville, MD Veterinary Technician, Veterinary Services BS in biology, pharmacology, or related Exp: 1+ year(s) |
PRIMARY OBJECTIVES: Support in vivo oncology studies in mice as a member of the Veterinary Services Team. DUTIES AND RESPONSIBILITIES: Conduct daily and weekly assessments and treatments of animals identified with abnormalities. Support the training program by conducting didactic and hands on training courses. Administer the health surveillance program as described, including animal and sample submission and tracking of results. Proficiently perform survival animal surgeries and provide perioperative care. etc. | 2/12/2020 |
| 397 | Champions Oncology Rockville, MD Research Technician I, Study Services BS/MS in biology, pharmacology, or related Exp: 1+ year(s) |
PRIMARY OBJECTIVES: Support in vivo oncology studies in mice as a member of the Study Services Team. DUTIES AND RESPONSIBILITIES: Perform in-life technical procedures, handle, restrain, and provide care for all animals. Observe animals for general health and overall well-being. Administer therapeutic agents by various routes. Provide animal welfare assessments, including body weight and tumor volume measurement. Allocate animals to study and non-study groups. Provide preoperative animal care. Euthanize animals as directed in study protocols and directives. Under supervision, may act as lead/primary technician on studies. etc. | 2/12/2020 |
| 398 | Renaissance Lakewood, NJ Associate Microbiologist I BS/BA in natural sciences Exp: 0 years |
The Associate Microbiologist performs various types of microbiological testing under supervision. Evaluates, and records data. Assists lab management and microbiologists as directed. Schedule flexibility is required. This is a salaried position and exempt from overtime pay. | 2/8/2020 |
| 399 | Renaissance Lakewood, NJ Gown Qualified Operator, 3rd shift BS/BA in natural sciences Exp: 0 years |
The Gown Qualified Operator is responsible for the full spectrum of duties in assigned filing room. This may include but is not limited to: set-up of room and equipment for production, operate equipment to meet product specifications and batch record requirements, ensures correct components and product according to production schedule and batch record, equipment and room cleaning and sanitization, etc This is a 3rd shift position. | 2/8/2020 |
| 400 | Renaissance Lakewood, NJ Gown Qualified Technical Operator, 1st shift BS/BA in natural sciences Exp: 0 years |
The Gown Qualified Operator is responsible for the full spectrum of duties in assigned filing room. This may include but is not limited to: set-up of room and equipment for production, operate equipment to meet product specifications and batch record requirements, ensures correct components and product according to production schedule and batch record, equipment and room cleaning and sanitization, etc This is a 3rd shift position. | 2/8/2020 |
| 401 | Repligen Marlborough, MA Manufacturing Associate II - TFF AS in technical discipline Exp: 0-5 years |
Mechanical assembly and testing of custom TFF systems per assembly drawings, SOP’s, and batch records. Point to point wiring, installation of cables, installation of software, and packaging of final product. Operates and maintains production equipment as it relates to manufacturing operations. Maintains records to comply with regulatory requirements. Documents all work on batch records according to Good Manufacturing practices. Performs batch record review as required by Production management | 2/8/2020 |
| 402 | Repligen Rancho Dominguez, CA Assembler I HS Diploma/GED Exp: 0-1 years in production/manufactruing |
This assembly position performs a wide variety of fiber assembly, filtration product assembly or sub-assemblies. Determines and/or follows methods and sequence of operations in performing fiber bundling, filter potting, filter welding, fitting on assembly units and packaging. The employee also works as a team member in whatever capacity and job function is required to deliver a quality product to our customer in a timely fashion. | 2/8/2020 |
| 403 | Repligen Waltham, MA Manufacturing Associate II- Biomanufacturing 2nd Shift BS in biological sciences or related Exp: 0-2 years in biotech manufacturing |
This position is for the 2nd shift in the Biomanufacture group, however; cross training into other departments may be required. The successful candidate will play a key role in ensuring that the department’s production and quality goals are met. Applicants must have strong technical knowledge and problem-solving skills. Must be able to follow oral and written instructions accurately, learn complex tasks quickly, and complete tasks in a timely manner. Experience working in a GMP/document-controlled environment would be beneficial. Attention to detail, and the ability to work in a team environment are essential. | 2/8/2020 |
| 404 | Repligen Waltham, MA Manufacturing Associate II- Biomanufacturing 2nd Shift BS in biological sciences or related Exp: 0-2 years in biotech manufacturing |
This position is for the 2nd shift in the Biomanufacture group, however; cross training into other departments may be required. The successful candidate will play a key role in ensuring that the department’s production and quality goals are met. Applicants must have strong technical knowledge and problem-solving skills. Must be able to follow oral and written instructions accurately, learn complex tasks quickly, and complete tasks in a timely manner. Experience working in a GMP/document-controlled environment would be beneficial. Attention to detail, and the ability to work in a team environment are essential. | 2/8/2020 |
| 405 | Repligen Marlborough, MA Manufacturing Technician HS Diploma/GED Exp: 1+ years in membrane related processes |
. The successful candidate will play a key role in ensuring that the department's safety, Quality, and Production goals are met. Experience working in a classified cleanroom, and knowledge of GMP/ISO/document controlled processes and GDP would be beneficial. Attention to detail, and the ability to work in a team environment are essential. Ability to read and understand standard operating procedures is required. | 2/8/2020 |
| 406 | ReShape Life Sciences San Clement, CA Administrative Assistant HS Diploma/GED Exp: 1+ years in administrative support |
The Administrative Assistant will assist management and all visitors to the company by handling office tasks, providing polite and professional assistance via phone, mail and e-mail, making reservations or travel arrangements and generally being a helpful and positive presence in the workplace. The Administrative Assistant should be professional, polite and attentive while also maintaining accuracy and willing to meet challenges directly. | 2/8/2020 |
| 407 | Philips Monroeville, PA Usability Validation Engineer BS/BA in engineering Exp: 1+ years in engineering on med devices |
The selected candidate will work under direct supervision of the Engineering Lead to produce clear and concise validation documents for medical devices. Focus will be designing and conducting usability test programs in accordance with IEC 62366-1 and FDA Guidance “Applying Human Factors and Usability Engineering to Medical Devices” in conjunction with ISO14971. | 2/8/2020 |
| 408 | Philips Gainesville, FL Assembly Technician 1, Second Shift HS Diploma/GED Exp: 1 year in manufacturing |
Set and operate production equipment for the purpose of assembling our MRI coils during our second shift, 3:30pm to 12:00am. Performing various repetitive electronic assembly operations on components or subassemblies (under supervision). Using schematics or blueprints, wiring lists, and verbal and written instructions to assemble, modify, rework, or reassemble units. Properly executing the established process and the process parameters | 2/8/2020 |
| 409 | Philips Bothell, WA Clinical Test Engineer-Ultrasound Sonographer AS/AA or BS/BA Exp: 1+ years in clinical ultrasound |
As a member of an Agile SCRUM team, execute systems/software tests and test procedures in support of product development testing on ultrasound systems. Test Procedure execution. Test data generation/review/approval. Operating ultrasound products in a black box and white box fashion to identify defects | 2/8/2020 |
| 410 | Rho Durham, NC Research Associate BS/BA in sciences Exp: Entry Level |
The Research Associate will assist project managers in day-to-day operations of either federally-funded or commercial studies. This is an entry-level position. This is not a laboratory research position. The position will offer the opportunity to participate in all aspects of clinical research support, including document preparation, maintenance, and filing; meeting coordination and support; and data management activities including data entry and review. | 2/8/2020 |
| 411 | Rockland Limerick, PA Associate Scientist (Quality Control) BS/BA in biological/chemical sciences Exp: Entry Level |
We are seeking a talented and highly motivated team player as an addition to our Quality Control (QC) Department. The applicant should be highly motivated, demonstrate broad scientific knowledge, problem solving and troubleshooting skills, show attention to details, high level of independence and display a fundamental understanding of immunoassays. | 2/8/2020 |
| 412 | Roviant Sciences New York , NY Associate Data Engineer BS/BA Exp: 1-3 years with coding |
We are seeking a thoughtful, hands-on Data Engineer to join Roivant's Data Architecture team. Data Architecture is a broad team that develops and operates the data platform used by developers throughout the Roivant family. You will join a small team partnering with product owners and developers at Roivant and Vants to provide end-to-end data solutions for technology tools and products.You will automate and maintain data processing pipelines, implement modern ETL infrastructure, and continuously improve the efficiency of our platform. | 2/8/2020 |
| 413 | RS Medical Shreveport, LA Field Support Representative HS Diploma/GED Exp: 6 months in clinical/hospital/med office setting |
The Field Support Representative works with a Sales Account Manager within a defined sales account base to assist and support in clinical and administrative duties. Support the daily order flow within established sales accounts. Schedule patient education sessions in a timely manner. Control and account for all product inventory. Conduct patient education sessions within a clinical setting on the use of the prescribed RS Medical product. | 2/8/2020 |
| 414 | Rubius Therapuetics Cambridge, MA TEMP - Associate Engineer BS in biochem/biomedical engineering/pharma sciences Exp: 0-2 years |
We are seeking an Associate Engineer (contract) to support solution preparation and process support activities within the upstream and downstream process development of Red Cell Therapeutics at our Cambridge, MA location. This associate will perform tasks including preparation and characterization of raw material stock solutions, upstream media formulations, and downstream process buffers while also contributing significantly to the buildout of infrastructure, workflows, and procedures needed to ensure consistent delivery of solution requests and traceable documentation of all source materials. | 2/8/2020 |
| 415 | Virscio New Haven, CT Laboratory Technician BS in biological sciences or related Exp: 1 year in lab |
The position will additionally involvemanaging the receipt, storage and processing of biological specimens and thepackaging and shipment of samples. These activities will involve accurate tracking of samples, adherence to internal standard operating procedures (SOPs), preparing required sample and reagent dilutions, maintaining logbooks and complying with GLP laboratory standards. | 2/8/2020 |
| 416 | Sagent Pharmaceuticals Schaumburg, IL Contracts Analyst BS/BA Exp: 1 year in contract/finance/data entry |
General support in the processing of daily paperwork and maintenance of the contracts database. Ability to accurately complete tasks in a timely fashion in a busy environment and often with changing priorities. Data Entry into the Contract Database: product, pricing and customer updates | 2/8/2020 |
| 417 | Salubris Bio Gaithersburg, MD Associate Scientist/Scientist-Downstream Process Development MS in bio/chemical engineering Exp: 1+ years |
Develop robust and scalable downstream processes in laboratory scales for the purification of antibodies or antibody-based therapeutic proteins with chromatography (affinity, IEX and/or HIC, etc.). Support scale-up of downstream processes and technology transfer to cGMP manufacturing facilities for clinical material production, work with cGMP manufacturing team to generate and review SOPs and batch record for traceability. | 2/8/2020 |
| 418 | Samumed San Diego, CA Clinical Trials Assistant (CTA) BS/BA in life sciences or healthcare Exp: 0-2 years |
Samumed is looking for an intelligent and enthusiastic individual to join its Clinical Development team as a Clinical Trials Assistant. The Clinical Trials Assistant will provide administrative support to the Clinical Operations team across the company's ongoing clinical studies. Manage the set-up of studies and sites in the electronic Trial Master File (eTMF). Manage the set-up of studies and sites in the Samumed Grant Payments Application | 2/8/2020 |
| 419 | Sanofi Ridgefield, NJ Aseptic Technician Associate HS Diploma/GED Exp: 1-3 years in cGMP environment |
Aseptic Technician Associate will Independently perform the tasks of the production operation specific to aseptic manufacturing, filling, and packaging. Maintains batch record documentation and logs as required by corporation and regulatory agencies. Performs cleaning and sanitizing of production equipment and classified production space. Prepares, according to procedures, various stock solutions and buffers as required by the production process. | 2/8/2020 |
| 420 | Sanofi Swiftwater, PA Maintenance Technician 2 year trade certificate in HVAC or general mecahnics Exp: 0-1 years |
The Maintenance Technician is responsible for supporting the design, installation, maintenance, troubleshooting and repair of all site-wide equipment in order to maintain a Quality Class A environment in GMP facilities. This position will have interactions with HSE, Engineering, Outside Contractors/Consultants, Industrial Operations and Research & Development departments. | 2/8/2020 |
| 421 | Sanofi Swiftwater, PA Maintenance Technician 2 year trade certificate in HVAC or general mecahnics Exp: 0-1 years |
The Maintenance Technician is responsible for supporting the design, installation, maintenance, troubleshooting and repair of all site-wide equipment in order to maintain a Quality Class A environment in GMP facilities. This position will have interactions with HSE, Engineering, Outside Contractors/Consultants, Industrial Operations and Research & Development departments. | 2/8/2020 |
| 422 | SCBT Dallas, TX Warehouse Associate/Coordinator AS/AA or BS/BA Exp: 1-2 years |
This position assists in the daily processing, picking, packaging and shipping of domestic and international orders. SCBT maintains a climate controlled warehouse (heated/cooled) making for a comfortable work environment year round. SCBT’s products are generally small and lightweight commodities that are easily handled and processed for shipment. This is a full time position with career advancement opportunities within the company. | 2/8/2020 |
| 423 | SCBT Santa Cruz, CA Laboratory Assistant BS/BA in biological sciences Exp: 0-2 years |
This is an opportunity to get a jumpstart in the biotechnology industry and gain practical work experience while attending school at the same time. This position will perform routine tasks in support of analytical and preparative procedures required for the purification, analysis of antibodies and associated reagents used in the scientific community. | 2/8/2020 |
| 424 | SCBT Sun Valley, ID Research Assistant BS/BA in biological sciences Exp: 0 years |
Santa Cruz Biotechnology has an immediate opening for an entry level Research Assistant at our Ketchum, ID campus. Ability to perform standard analytical and preparative procedures required for the development and analysis of monoclonal antibodies. Ability to characterize antibodies by designing and optimizing experiments, interpreting data, and selecting the best possible products to develop. Capacity to utilize established, routine procedures and follows instructions from lab supervisor. | 2/8/2020 |
| 425 | SCBT Santa Cruz, CA Research Assistant BS/BA in biological sciences Exp: 0 years |
Santa Cruz Biotechnology has an immediate opening for an entry level Research Assistant at our Ketchum, ID campus. Ability to perform standard analytical and preparative procedures required for the development and analysis of monoclonal antibodies. Ability to characterize antibodies by designing and optimizing experiments, interpreting data, and selecting the best possible products to develop. Capacity to utilize established, routine procedures and follows instructions from lab supervisor. | 2/8/2020 |
| 426 | SCBT Paso Robles, CA Research Assistant BS/BA in biological sciences Exp: 0 years |
Santa Cruz Biotechnology has an immediate opening for an entry level Research Assistant at our Ketchum, ID campus. Ability to perform standard analytical and preparative procedures required for the development and analysis of monoclonal antibodies. Ability to characterize antibodies by designing and optimizing experiments, interpreting data, and selecting the best possible products to develop. Capacity to utilize established, routine procedures and follows instructions from lab supervisor. | 2/8/2020 |
| 427 | Sarepta Therapeutics Andover, MA Associate I, Oligonucleotide Chemistry BS in chemical engineering/organic chem, etc. Exp: 1 year in organic chem lab |
The Associate I, Oligonucleotide Chemistry will work on a rapidly growing team focused on supporting internal Research and Discovery, Analytical Development, Pre-clinical, and Toxicology groups. This role will perform high throughput synthesis, purification, and isolation of Sarepta’s phosphorodiamidate morpholino oligomers (PMOs). The Research Manufacturing Oligonucleotide Chemistry group synthesizes PMOs for lead-candidate screening, Analytical standards, and commercialization support. | 2/9/2020 |
| 428 | Sarepta Therapeutics Cambridge, MA IT Support Specialist I HS Diploma/GED Exp: 1-3 years in technical support |
Level I Specialist primary duties include Tier 1 technical support, including software/hardware installation, troubleshooting, hardware break/fix, VoIP phone support and asset management. Provide Tier 1 technical assistance for computer hardware, software systems, and printers/copiers. Analyze, troubleshoot and resolve reported issues (software, hardware, and processes) in a logical and systematic method | 2/9/2020 |
| 429 | Sarepta Therapeutics Andover, MA Research Associate I, Translational Development BS in biological/chemical sciences Exp: 1-3 years lab experience |
The qualified candidate will provide laboratory support, perform experiments to develop and validate bioanalytical assays and perform analysis of tissue in support of Sarepta’s clinical trials. This person will be expected to work within the framework of a GCLP-compliant laboratory, maintain good documentation practices, and adhere to standard chemical and biohazard safety guidelines while working in the laboratory. | 2/9/2020 |
| 430 | SCA Pharma Little Rock, AR IV Compounding Technician (1st Shift) HS Diploma/GED Exp: 1 year in pharma environment |
This Team Member will undergo stringent training program to become qualified to work in aseptic environment inside ISO 7 rooms and ISO 5 workspaces ensuring admixtures are completed properly per FDA and cGMP requirements. Undergo thorough training curriculum on gowning, compounding, aseptic manipulations, USP 797 regulations, FDA cGMP-503B regulations, media fills, internal SOP's. | 2/9/2020 |
| 431 | SCA Pharma Little Rock, AR Aseptic Sanitization Specialist (3) HS Diploma/GED Exp: 1 year in pharma |
The Aseptic Sanitization Specialist will be responsible for sanitizing products prior to them entering the cleanroom. The position will also ensure that the detail, scheduling, and methods of cleaning are sufficient according to the standard operating procedures to protect the raw materials, products, clean room (material transfer, formulation, bag fabrication and fill rooms) and non-clean room (cart loading, sterilization and pack-out areas) environments from the introduction of microbial contamination or infestation. | 2/9/2020 |
| 432 | Scantibodies Lab Santee, CA Chemist I BS/BA in life sciences Exp: 0-1 years in labs |
A Chemist I isresponsible for manufacturing products to meet or exceed customers' specifications according to manufacturing procedures by adherence to the Scantibodies Quality System and in compliance to the FDA/ISO 9001 and GMP guidelines, with moderate supervision. This employee is required to assist the supervisor and manager with production improvement, process trouble shooting, and new product development. In addition to regular production activities, this employee also is required to participate in production improvement and research related projects. | 2/9/2020 |
| 433 | Sciecure Monmouth Junction, NJ QC Document Review BS/BA in chemistry Exp: 1-2 years in GMP lab |
The QC Data Review Specialist will be responsible for GMP review and comment on laboratory raw data, procedures and reports to ensure methods, protocols and other procedures were properly followed, results are analytically accurate and correct, and that all documentation meets GMP standards. | 2/9/2020 |
| 434 | SCIEX Framingham, MA Regulatory Affairs Specialist BS in sciences Exp: 1-4 years in regulatory affairs |
Support the regulatory submission activities to obtain and maintain approvals for commercially distributing in vitro diagnostics products worldwide. Participate in activities to ensure compliance with worldwide regulatory requirements. Key Responsibilities:- Supports Design History File development, reviewing documentation for regulatory requirements and current standards. | 2/9/2020 |
| 435 | SciQuus San Diego, CA Clinical Trial Associate BS/BA Exp: 1 year in clinical research |
Establish, organize, track, and maintain essential regulatory and clinical trial files. Work with the clinical team to achieve study deliverables by assisting in the review and QC of clinical documents (e.g. protocol, informed consent templates, study manuals, forms, etc.). Interact with clinical trial sites from start-up through study close-out | 2/9/2020 |
| 436 | Seattle Genetics Bothell, WA Anatomical Pathology Lab BS/BA Exp: 1-5 years in histology |
We are seeking an individual to provide standard services in core histology (tissue trimming, processing, embedding, cutting, and histochemical stains). Organizes a large and varied daily workload, accommodating priority requests, focusing on immediate tasks despite interruptions. Assists with rodent necropsies and grossing of samples. Processes tissue specimen for microscopic examination by using appropriate methods for fixing, embedding, sectioning, staining and mounting | 2/9/2020 |
| 437 | Seattle Genetics Bothell, WA Quality Control Analyst I/II BS/BA in sciences Exp: 0-4 years in pharma/biopharma |
https://www.seattlegenetics.com/careers/job-opportunities?p=job/orMybfwG&nl=1 | 2/9/2020 |
| 438 | Seattle Genetics Bothell, WA Research Associate I/II Analytical Sciences BS or MS in biologica/chemical sciences Exp: 0-3 years |
Seattle Genetics is seeking a Research Associate to participate in the development of drug programs. Responsibilities: Conduct experiments, process/analyze data and report results to relevant parties to support manufacturing process development. | 2/9/2020 |
| 439 | SDIX Newark , DE Biotechnician I / II (Instrumentation) BS/BA in med tech, biological/chemical sciences Exp: 0-7 years |
Maintain laboratory in proper working order through organization and procurement of supplies, routine maintenance of laboratory equipment, organization and maintenance of reagents, and general laboratory hygiene. Verify and ensure that proper processes and procedures are followed in accordance with SOPs. | 2/9/2020 |
| 440 | SDIX Newark , DE Technician I / II AS/AA in animal sciences Exp: 0-2 years |
This position participates in a team of technicians responsible for animal husbandry and antibody production activities. All job responsibilities to be conducted within standard operating procedures and regulatory compliance. 1. Clean and disinfect cages, rooms and support areas. 2. Feed animals; maintain water systems, ventilation settings, pest control, and related tasks. 3. Conduct animal identification, animal breeding programs and related tasks. | 2/9/2020 |
| 441 | Sebela Holbrook, MA QC Chemist BS/BA in chemistry Exp: 0-2 years in cGMP |
Laboratory Bench Position that performs routine release testing for raw materials, intermediates, and final products within a cGMP environment. Perform testing of raw materials and products. Perform instrument qualification and maintenance. Perform test method validation/verification. Review analytical data for completeness, accuracy, and compliance. | 2/9/2020 |
| 442 | Sedia Biosciences Portland, OR MANUFACTURING TECHNICIAN AS/AA in lab discipline Exp: 0-1 years in labs |
The position will hold responsibility for assisting in the manufacturing of Sedia’s immunoassay product lines encompassing lateral flow and ELISA test. The holder of this position is expected to follow the guidance of their direct supervisor to assist in delivering company products in a timely and cost effective manner. The position will contribute in building product subassemblies or final assemblies. | 2/9/2020 |
| 443 | Sedia Biosciences Portland, OR QC Technician AS/AA in technical field Exp: 1 year in med devices |
A Quality Control Technician works independently to provide quality control support of any area assigned where Sedia Biosciences is responsible for adhering to current Good Manufacturing Practices (cGMPs) for adherence to FDA regulations and applicable ISO standards including warehouse, manufacturing processes, inspection, labeling and packaging, batch record review/disposition, and new product design review and transfer activities. | 2/9/2020 |
| 444 | Sedia Biosciences Portland, OR SCIENTIST/ASSOCIATE SCIENTIST (R&D-Product Development) MS in biological/chemical sciences Exp: 1-3 years lab experience |
The successful candidate will be responsible for running laboratory tests, recording data, performing some degree of data analysis, drafting protocols, and communicating with managers from R&D and other departments. They will also be asked to participate in production of prototype products, and assist in transition of those procedures (through training and/or record-keeping) to our manufacturing department. | 2/9/2020 |
| 445 | Seer Redwood City, CA Mass Spectrometry Research Associate BS or MS in sciences Exp: 1-3 years in lab setting |
The Mass Spectrometry group is focused on using the latest MS and associated instrumentation for proteomics molecular profiling. Areas of specific responsibility and attention will include: Carefully perform procedures on experimental samples derived from blood and blood products, urine, saliva, and other biological fluids or tissues. Perform routine calculations, data entry, and lab notebook maintenance, including electronic notebooks and other data annotation, curation, and storage formats. | 2/9/2020 |
| 446 | Seer Redwood City, CA Assay Development Research Associate BS or MS in biological sciences Exp: 1 year in molecular biology techniques |
Participate in the design, development, and implementation of biochemical experiments to support assay projects and development of the core protein assay platform, with specific emphasis on proteomic assays such as, ELISA, HPLC and mass spectrometry. Assay development with ELISA and immunoassay multiplexing technology. Duties including assay optimization, sample analyzing, assay troubleshooting, automation support, assay characterization and validation, development of protein based assays, immunoassays, protein arrays, product development of IVD and generating SOPs. | 2/9/2020 |
| 447 | Sekisui San Diego, CA Mechanical Engineer BS in mechanical/biomedical/materials engineering Exp: 1+ years in class II/III med devices |
The R&D Mechanical Engineer is responsible for assisting in the design and development of innovative instruments and consumables for IVD medical devices. The candidate should be familiar with designing mechanisms, device enclosures, machined or injection molded components, and complex assembly methods. An understanding of material selection to optimize mechanical performance, sterilization effectiveness, and biocompatibility is required. The engineer will contribute to the R&D Engineering Department by owning instrument design solutions, test method development & design for manufacturing. | 2/9/2020 |
| 448 | PSC Biotech Orange County, CA Entry Level CSV Engineer BS/BA in chemical/biomedical engineering Exp: Entry Level |
Provide CSV authoring, review and approval of validation documents developed by functional validation teams, ensuring the documentation meets regulatory requirements and quality standards. Initiate/update GxP and Risk Assessments on system.Author, Initiate, and/or review and approve IT SOPs related to compliance | 2/1/2020 |
| 449 | PSC Biotech Pomona, CA Entry Level CSV Engineer BS/BA in chemical/biomedical engineering Exp: Entry Level |
Provide CSV authoring, review and approval of validation documents developed by functional validation teams, ensuring the documentation meets regulatory requirements and quality standards. Initiate/update GxP and Risk Assessments on system.Author, Initiate, and/or review and approve IT SOPs related to compliance | 2/1/2020 |
| 450 | PsychoGenics Paramus, NJ Research Associate 1 - Behavioral Pharmacology BS/BA in life sciences, neurosciences, psychology Exp: 1+ years lab experience |
We are looking for a highly motivated Research Associate in behavioral neuroscience. The successful candidate will work in a team of scientists and researchers supporting the preclinical studies using rodent models and tests. The primary responsibilities of the candidate will include but are not limited to conducting preclinical research of drug abuse liability, pain, cognition, and other assays as needed. The candidate must be capable of working across teams and independently. | 2/1/2020 |
| 451 | PsychoGenics Paramus, NJ Animal Care Technician HS Diploma/GED Exp: ALAT cert after 1 year employment |
Review, comprehend, and comply with all SOPs, IACUC policies, safety, and quality assurance standards related to assigned work area. Daily husbandry of the rodents in the vivarium to include the provision of feed, water, clean cages, and enrichment. Basic sanitation and maintenance of colony rooms to include sweeping and mopping of animal quarters, rotating animal cages, racks and room supplies for cleaning according to schedule, disinfecting all areas in room. Monitor the health of the animals and report any sick or dead to the PVC and room lab contact staff. | 2/1/2020 |
| 452 | PTC Therapeutics South Plainfield, NJ Research Associate II, Molecular Biology/Cell Culture MS in biology Exp: 1 year experience |
The Molecular Biologist is responsible for performing scientific experiments that contribute to research and drug discovery activities at PTC. This position assists in the conduct of early stage research, the goal of which is applying new state-of-the-art technologies to research projects as well as the advancement of research programs. The Molecular Biologist is also responsible for communicating experimental results to his/her supervisor and the project team. | 2/1/2020 |
| 453 | PTC Therapeutics Bridgewater, NJ BS/MS Research Associate, Analytical Development - Gene Therapy MS in biological sciences Exp: 0-2 years |
The BS/MS Research Associate, Analytical Development - Gene Therapy is responsible for assay development and/or routine testing including, but not limited to, AUC, qPCR, cell-based assays and immunoassays. S/He is responsible for hands-on lab work, documentation and communicating results to his/her supervisor. | 2/1/2020 |
| 454 | PTC Therapeutics Bridgewater, NJ BS/MS research Associate, Analytical Development - Gene Therapy MS in biological sciences Exp: 0-2 years |
The BS/MS Research Associate, Analytical Development - Gene Therapy is responsible for assay development and/or routine testing including, but not limited to, AUC, qPCR, cell-based assays and immunoassays. S/He is responsible for hands-on lab work, documentation and communicating results to his/her supervisor. | 2/1/2020 |
| 455 | PTC Therapeutics South Plainfield, NJ BS/MS Biologist- Gene Therapy MS in biological sciences Exp: 1 year experience |
The successful candidate will be working on cloning, cell expansion, vector production and purification as well as vector characterization. The Gene Therapy Group at PTC is looking for a motivated BS-MS Biologist to join our team. The group provides a stimulating intellectual environment in a supportive atmosphere. The successful candidate will contribute to research efforts focused on applying PTC’s gene therapy platform in the field of rare genetic disorders. | 2/1/2020 |
| 456 | Pulse Bioscience Hayward, CA Clinical Research Associate BS/BA Exp: 1+ years in supporting clinical research |
The Clinical Research Associates (CRA) is responsible for assigned aspects of clinical monitoring and site management in accordance with the Code of Federal Regulations (CFR) of the Food and Drug Administration (FDA) and the International Conference on Harmonization - Good Clinical Practice (ICH-GCP). Site visits are conducted to assess protocol and regulatory compliance, data reliability, and the proper care and treatment of study subjects. Please note: This is not a remote position. | 2/1/2020 |
| 457 | Purdue Wilson, NC Pharmaceutical Technician, Rx/Granulation/Blending HS Diploma/GED Exp: 1-5 years |
The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the manufacturing and/or packaging area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines. Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging. | 2/1/2020 |
| 458 | Purdue Wilson, NC Pharmaceutical Technician, Rx/Granulation/Blending 1st Shift HS Diploma/GED Exp: 1-5 years |
The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the manufacturing and/or packaging area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines. Follow Master Batch Records for the manufacturing and packaging of controlled, oral solid dose (OSD) and other dosage forms when required. Prepare raw materials, blends, and bulk accountability throughout manufacturing processes. Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging. | 2/1/2020 |
| 459 | Purdue Wilson, NC Pharmaceutical Technician, Rx/Granulation/Blending 2nd Shift HS Diploma/GED Exp: 1-5 years |
The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the manufacturing and/or packaging area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines. Follow Master Batch Records for the manufacturing and packaging of controlled, oral solid dose (OSD) and other dosage forms when required. Prepare raw materials, blends, and bulk accountability throughout manufacturing processes. Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging. | 2/1/2020 |
| 460 | Purigen Biosystems Pleasanton, CA Research Associate I/II BS in biological/life sciences Exp: 1-3 years in biotech |
The Research Associate will be responsible for growing and maintaining various cell lines for quality control and product validation testing and performing a variety of tests on our unique Sample Preparation Instrument. Execute new and standard protocols for performance testing of Purigen’s custom Sample Preparation platform, including instrumentation and microfluidic chip prototypes. Set-up and execute bioanalytical QC assays, including qPCR, RT-qPCR, fragment sizing (e.g. Bioanalyzer assays) and nucleic acid quantitation assays (e.g. Nanodrop, Qubit) | 2/1/2020 |
| 461 | Pyramid Labs Costa Mesa, CA Manufacturing Technician HS Diploma/GED Exp: 1 year in GMP |
Under general supervision, perform various manufacturing related activities for a GMP compliant Fill/Finish operation applying standard practices, techniques and procedures. Able to assist in the preparation of reports, records, etc., for assigned tasks. | 2/1/2020 |
| 462 | Qiagen Germantown, MD Technical Associate Automated Assembly Ops HS Diploma/GED Exp: 1-3 years in biotech |
The Technical Associate Automated Assembly operations must comprehend and perform assigned automated and manual production tasks according to established Standard Operating Procedures (SOP’s). Responsible for Automated and/or Manual production and assembly procedures in compliance with relevant regulations and SOP’s. Adhere to and accurately complete all production-related documentation. | 2/1/2020 |
| 463 | Qiagen Germantown, MD Technical Associate - Kit Assembly Operations HS Diploma/GED Exp: 1-3 years |
The Technical Associate in Kit Assembly comprehends and performs assigned manual production tasks according to established standard operating procedures. Responsible for Manual production and assembly procedures in compliance with relevant regulations and Standard Operation Procedures. Adhere to and accurately complete all production-related documentation. Responsible for set up, trouble shooting and operation of production related equipment within the assembly area. | 2/1/2020 |
| 464 | Qiagen Beverly, MA Quality Control Technician I BS/BA in biology or biochemistry Exp: 0-2 years |
The Quality Control Technologist I perform assays on products to ensure product quality standards are met. Independently perform assays and evaluate results for product qualification. Adhere to quality control work instructions. Maintain complete, contemporaneous and accurate records of all work performed. | 2/1/2020 |
| 465 | QPS Newark, DE Associate Scientist I BS/Ba Exp: 0-2 years |
Perform routine lab operations, such as preparing reagents, pipetting, weighing, monitoring, recording, and replenishing supplies. Assist supervisor in performing analysis of drug or other targets in complex biologic matrices. Set-up, use and maintain complex instrumentation. Document experiment details, calculations, results and observations in accordance with GLPs and SOPs | 2/1/2020 |
| 466 | QPS Newark, DE Associate Scientist I - Bioanalysis BS/Ba Exp: 0-2 years |
Perform routine lab operations, such as sample extraction, preparing reagents, operating automatic liquid handling equipment, pipetting, weighing, monitoring, and recording, in a neat/clean manner. Assist Principal Investigator in performing quantitative analysis of drug and metabolites in biological samples utilizing validated liquid chromatography-tandem mass spectrometry (LC-MS/MS) methods under GLP regulations. | 2/1/2020 |
| 467 | Qualicaps Whitsett, NC MR Technician AS/AA in mechanics/electromechanics Exp: 6 months in QA process |
This position is responsible for managing the quality of the capsule product on their assigned machines by monitoring and evaluating the process, observing trends, adjusting/replacing minor equipment and performing general improvements on the capsule manufacturing machines. Maintain all documentation of production batches while on the production floor. | 2/1/2020 |
| 468 | Quanterix Billerica, MA Kitting Technician (Contract) HS Diploma/GED Exp: 0-1 years |
In the role, process responsibilities include kitting, labeling and inventory activities to support a diverse assay menu. Responsible for meeting kitting schedule requirements within a fast-paced environment with primary activities being: labeling, kitting and inventory accuracy; Support process development and continuous improvement; Maintain integrity of work areas; | 2/1/2020 |
| 469 | Quanterix Billerica, MA Quality Control Analyst BS/BA in chemistry/biology Exp: 1+ years in med devices/pharma |
Perform sampling, inspection and testing of incoming consumables and raw materials per compendial and non-compendial methods for GMP use in manufacturing. Perform physical inspection of Bulk Reagents and Assay Kits to support Kit release. Monitor, analyze and trend inspection/testing results and quality data | 2/1/2020 |
| 470 | Quanterix Billerica, MA Manufacturing Associate BS in biological/life sciences Exp: 1+ year in reagent manufacturing |
This role spans a broad range of activities within the manufacturing operations team at Quanterix. In the role, process responsibilities range from complex protein conjugations to diluent formulation and filling and kitting activities to support a diverse assay menu. Responsible for meeting manufacturing schedule requirements within a fast-paced manufacturing operation with primary activities being: bottle/vial filling, buffer diluent formulation and protein conjugation. | 2/1/2020 |
| 471 | Quidel Beverly, MA Development Associate BS/BA in life sciences Exp: |
Quidel is searching for an Development Associate to join our team in the Beverly, MA location. The Development Associate will participate in Research and Development activities toward development, enhancement, validation, and transfer of molecular diagnostic assays or associated technologies to manufacturing. The responsibilities include activities to support research and new molecular product development and also include activities to support manufacturing reagents for molecular diagnostics products. | 2/1/2020 |
| 472 | Quidel San Diego, CA Associate Quality Engineer BS in engineering/life sciences/tehnical discipline Exp: 1-2 years in med devices |
The Associate Quality Engineer is responsible for owning and coordinating Quality Engineering functions and activities for the defined processes. This position is also responsible for supporting the Production, Quality Control, Engineering and Quality Assurance departments and the associated activities, which include receiving inspection, in-process inspection, and finished goods inspection in achieving and exceeding company goals and objectives. In addition, this role is responsible for supporting the administration, implementation, and continuous improvement of the quality systems associated with non-conforming materials, inspection control plans, and corrective/preventive action. | 2/2/2020 |
| 473 | Quintara Biosciences South San Francisco, CA Entry Level Technician BS with lab work Exp: Entry Level |
Located at South San Francisco and Boston, we are expanding and have several entry level technician positions available. We offer competitive wages and growth opportunities within the company. Handle customer samples and perform DNA sequencing and Molecular Biology experiments . Prepare and set up customer sequencing samples. Set up molecular biology experiments as requested or needed | 2/2/2020 |
| 474 | Quintara Biosciences Boston, MA Sales Representative BS or higher Exp: 0-2 years |
Located at South San Francisco and Boston, we are expanding and have several entry level technician positions available. We offer competitive wages and growth opportunities within the company. Ability to identify qualifying leads. Ability to sell and present company services to customers. Develop and manage relationships with customers. Contribute information to market strategy by monitoring competitive services and reactions from customers; identifying needs to be filled. | 2/2/2020 |
| 475 | Quotient Sciences Boothwyn, PA Analytical Scientist I BS in chemistry or realted Exp: 0-3 years in pharma lab |
The position may reside in any one of the functional areas and carry out the responsibility under some supervision: Analytical method development, validation, and transfer activities. Formulation development work including Material characterization and physical testing. API/raw material sampling and testing, In-process and finished product testing, cleaning verification swabbing and testing. | 2/2/2020 |
| 476 | Quotient Sciences Boothwyn, PA Lab Assistant BS/BA preferred, HS Diploma Exp: 0-3 years with chemicals |
The position supports any one of the functional areas and carries out the responsibility under full supervision. Clean and organize laboratory glassware. Dispose solvent waste as per the laboratory procedures. Monitor and maintain lab cleanliness. Make buffers, mobile phases, etc. as directed by the supervisor | 2/2/2020 |
| 477 | Quotient Sciences Boothwyn, PA Analytical Scientist II MS in chemistry Exp: 0-2 years in pharma lab |
The position may reside in any one of the functional areas and carry out the responsibility under some supervision: Operate and troubleshoot the following instruments/equipment to test pharmaceutical samples. Follow analytical test methods, compendial methods, experimental procedures and SOP’s. Document test results in laboratory notebook, in real-time, and communicate status of test results to supervisor | 2/2/2020 |
| 478 | QuVa Sugar Land, TX Production Technician - Post Compounding HS Diploma/GED Exp: 1 year in pharma manufacturing preferred |
This position supports daily manufacturing activities for non-sterile and sterile bulk/CSP operations. Perform line clearances, assure equipment is operating correctly, and assure Post Compounding checks are performed according to current SOPs and Batch Record Instructions. Maintains records of every movement of Controlled and Non-Controlled Substances from the point they are received from compounding. Monitors the daily use of Controlled and Non-Controlled Substances throughout the process to assure people and processes are in a continuous state of compliance with DEA regulations, company policies and procedures and safety requirements | 2/2/2020 |
| 479 | QuVa Sugar Land, TX Quality Assurance Technician HS Diploma/GED Exp: 1-2 years in FDA regulated operations |
The Quality Assurance Technician performs basic QA functions related to verification of incoming and/or outgoing materials. Quality review / verification of critical information related to the receipt of incoming goods or the distribution of finished goods for customer orders. Ensures compliance of incoming materials prior to use in Manufacturing Operations. Supports packaging of finished goods for customer shipments and verifies accuracy of the order | 2/2/2020 |
| 480 | QuVa Sugar Land, TX Supply Chain Technician HS Diploma/GED Exp: 1-2 years in distribution/warehousing/shipping/etc |
QuVa Pharma is seeking a motivated and organized Supply Chain Technician to complete inventory replenishment process utilizing manual or automated technology. You will be integral in ensuring that inventory is correctly stocked and labeled, protecting the integrity of sterile supplies. Our ideal candidate is highly organized, a master of prioritization and able to shift gears at a moments notice. | 2/2/2020 |
| 481 | QuVa Sugar Land, TX Compounding Pharmacy Technician HS Diploma/GED Exp: Pharmacy Technician liscensed |
Compounds sterile preparations as per work instructions under pharmacist supervision. Assists in cleaning and maintenance of the work environment. Complies with all state and federal laws, rules, and regulations governing the practice of pharmacy. Ensures cleansing and garbing policy is performed exactly per sterile preparations. | 2/2/2020 |
| 482 | QuVa Bloomsbury, NJ Quality Systems Specialist HS Diploma/GED Exp: 1-2 years in QA, GMP production |
To maintain and coordinate Quality Systems related documents for compliance with cGMP and company procedures with minimal supervision. To review and write cGMP procedures under supervision. To process changes in controlled batch records via Change Control process. To issue effective documents including procedures, forms and batch records. To process changes to the procedures. | 2/2/2020 |
| 483 | RefleXion Medical Hayward, CA Software Quality Engineer BS/BA in engineering Exp: 0-7 years in medical product development |
The Quality Engineer for software process supports compliance to IEC 62304, ISO 13485, and ISO 14971 to ensure full adherence to these standards, in addition to the FDA’s Quality System Regulation and software-related guidance. This position represents the Quality Assurance function on product development teams from early design stages through product implementation to manufacturing, ensuring that all products comply with internal, customer, and regulatory requirements. | 2/2/2020 |
| 484 | Regeneron Tarrytown , NY R&D Associate - Neurodegenerative Diseases MS in neuro/biological sciences Exp: 1+ years |
The successful candidate will be responsible for the design and execution of experiments to understand the mechanisms of neurodegenerative diseases, discover new therapeutic targets and validate novel therapeutic strategies. We are looking to recruit a candidate with in vitro experience and strong in vivo expertise in neuroscience and models of neurodegenerative disease. Perform cell culture and cell-based assays with immortalized cell lines and primary neurons. | 2/2/2020 |
| 485 | Regeneron Tarrytown , NY Process Development Associate II - Purification Development BS or MS in chemical/biochem engineering or biochemistry Exp: 0-5 years |
The qualified individual will be responsible for purification process development and support purification of various pre-clinical and clinical biological molecules at pilot scale. Development of technology and automation to increase process throughput and efficiency of preclinical manufacturing. Documents experiments, results, and findings in electronic laboratory notebook; presents work at group and department meetings. Maintain instruments and troubleshoot instrumental/experimental problems. | 2/2/2020 |
| 486 | Regeneron Rensselaer, NY Associate Process Engineer (Filling) BS or MS in engineering Exp: 0 years |
Provides engineering support for the design and development of robust drug product processes that enable the delivery of life transforming medications to patients globally. The individual will support drug product unit operations from primary container development through drug product filling and inspection, with specialization in the development, industrialization, and technical oversight of primary container components. | 2/2/2020 |
| 487 | Regeneron Rensselaer, NY QA Validation Specialist (Filling Equipment) BS/BA in engineering, chemistry, or life sciences Exp: 0-2 years |
Summary: Validate/qualify equipment, systems, and processes in accordance with regulatory requirements and support, follow and implement company manufacturing standards policies and procedures. Generates, executes and/or reviews master and completed qualification and validation protocols, summary reports and associated data for conformance to regulations, SOPs, specifications and other applicable acceptance criteria | 2/2/2020 |
| 488 | Regeneron Rensselaer, NY Associate Biotech Production Specialist BS/BA in life sciences Exp: 0-2 years |
Please note that this would be a 1st shift position, 6:00 a.m.-4:30 p.m., with potential for double weekends. Performs all tasks necessary for the manufacturing operations of both clinical and commercial manufacturing programs. Reviews, edits, completes, and revises completed batch records, Logbooks, and SOPs in accordance with cGMP standards and compliant with written procedure. Includes all aspects of biotech production activities related to cell culture | 2/2/2020 |
| 489 | Regeneron Rensselaer, NY Process Engineer (Filling) BS or MS in engineering Exp: 0 years |
Provides technical support for the development of robust drug product processes that enable the delivery of life transforming medications to patients globally. The individual will characterize and support drug product unit operations from freeze/thaw through filling and inspection and will be part of a team responsible for development, industrialization, troubleshooting, and validation of drug product processes at our new fill/finish manufacturing site. | 2/2/2020 |
| 490 | Regeneron Rensselaer, NY QC Stability Technician BS/BA in life sciences Exp: 0-2 years |
Performs a variety of activities to maintain stability chambers and stability inventory in support of the company’s quality program. Ensures that equipment operates in a compliant state; qualified, calibrated and properly maintained. Monitors Environmental Chamber conditions, ensuring continuous documentation. Collaborates with Stability Coordinators and other departments to receive material to be put on stability. | 2/2/2020 |
| 491 | RegenxBio Rockville, MD Associate Scientist, Formulation and Drug Product Development BS/BA in chemical/biological sciences Exp: 1-3 years |
Execute scientifically rigorous formulation screening, development, stability, and characterization studies to select stable formulations for our proprietary recombinant AAV gene delivery products. Perform laboratory studies to develop and characterize formulations and processes, using a variety of analytical techniques. Generate protocols and reports on the experimental work and deliver progress presentations at the team and department level | 2/3/2020 |
| 492 | RegenxBio Rockville, MD R&ED Project Coordinator BS in life sciences Exp: 1-2 years in admin/project support |
Develop agendas, draft document meeting minutes, track action items, maintain project decisions and perform all other project management-related activities. Building and maintenance of R&ED Integrated Master Schedules (IMS); identify appropriate task relationships, display critical path and project baseline to track progress. Serve as formatting lead for presentations, abstracts, papers, reports; coordinates the insertion of draft changes from all team members for final text and graphics. | 2/3/2020 |
| 493 | AMETEK Middleboro, MD Associate Engineer BS/BA in mechanical/electrical engienering Exp: 0-1 years |
Assist in the design and development of SEPs and engineering projects for new and existing products. Identify new designs, methods or processes to reduce cost and improve quality. Associate Engineers will be given a lead role on projects and SEPs with appropriate scope. Provide technical support to vendors, and manufacturing and assembly departments, and assist with the resolution of problems and questions as required. | 2/3/2020 |
| 494 | AMETEK Wallingford, CT Industrial Maintenance Technician I HS Diploma/GED Exp: 1-3 years |
Maintenance Technician is a multi-disciplined technician responsible for the repair and maintenance of production, support and facility equipment to ensure safe, reliable operation. They also contribute to support activities, continuous improvement efforts and special equipment projects as directed. | 2/3/2020 |
| 495 | AMETEK Waukegan, IL Production Operator I HS Diploma/GED Exp: 0-1 years |
Performs processing duties as trained in the laser cutting, preparation, cleaning and inspection of production parts while maintaining all necessary production goals and accurate documentation. Maintains a clean work area and good documentation practices at all times. Complies with all relevant safety policies in area and company. | 2/3/2020 |
| 496 | AMETEK San Diego, CA Technician, Test - PCB HS Diploma/GED Exp: 1-3 years |
To test a variety of assemblies and sub-assemblies of printed circuit boards using various test measurement equipment and automated test systems. Perform basic to intermediate level troubleshooting on digital and analog circuitry to component level. Read schematics and engineering drawing. | 2/3/2020 |
| 497 | Renaissance Lakewood, NJ Associate Microbiologist I BS/BA in natural sciences Exp: 0 years |
The Associate Microbiologist performs various types of microbiological testing under supervision. Evaluates, and records data. Assists lab management and microbiologists as directed. Schedule flexibility is required. This is a salaried position and exempt from overtime pay. | 2/3/2020 |
| 498 | Beigene San Mateo, CA Associate, Regulatory Information Management, Regulatory Operations BS/BA in library science, life sciences, computer science, or related Exp: 1-3 year(s) |
The Regulatory Operations Associate supports the regulatory submission process by managing archiving of submission documents both in paper and electronic format, correspondence and communications, data management, and process evaluation and control. All in compliance with applicable regulations, standards, and internal policies and procedures. This position responsible for maintaining the regulatory archive. Essential Functions of the job: Archiving: Manage and maintain submissions and correspondence in the regulatory archive system. Coordinate exchange of records using document sharing platforms. Generate metrics, reports, and dashboards. Reconcile data o Archives/retrieves regulatory documents (both paper and electronic) as necessary. etc. | 2/3/2020 |
| 499 | Bicycle Therapeutics Lexington, MA Research Associate - Immuno-oncology/Oncology BS/MS in immunology, immuno-oncology, or translation oncology Exp: 1-5 year(s) |
The Research Associate located in Lexington, MA USA will be primarily responsible for developing and executing immune-oncology in vitro and ex vivo assays of Bicycle® T-cell modulators to enhance progress of Bicycle’s oncology pipeline towards the clinic. In this lab-based role, he or she will be a key player in implementing in vitro characterization of lead T-cell modulator series. Key Responsibilities: The successful applicant will have a strong scientific background and hands-on laboratory skills in immunology, immuno-oncology and/or translational oncology with experience in immunological assay development and in vitro pharmacology. etc. | 2/3/2020 |
| 500 | BillionToOne West Menlo Park, CA Laboratory Technician BS in biology or a clinical science Exp: 6+ months |
BillionToOne (Y Combinator S17) is looking for a Laboratory Technician - Clinical Laboratory Associate (CLA) I to perform UNITY, the only non-invasive prenatal test that can detect inherited disorders such as sickle cell disease, spinal muscular atrophy, and cystic fibrosis in the baby directly from maternal blood. You will join our growing CLIA team responsible for processing of pregnancy blood samples in a high complexity CLIA setting. This is a full-time 12-month contract position with an hourly rate of $25/hr. Hours and days may vary depending upon operational needs. The CLA I is responsible for assisting with the day-to-day operations and equipment maintenance in the Clinical Laboratory. etc. | 2/3/2020 |
| 501 | Biocare Medical Pacheco, CA Quality Assurance Associate AA/AS/HS diploma Exp: 0-2 years |
Responsible for coordinating various activities related to product design, development, manufacture, and release in compliance with Company’s Quality Management System. Essential Duties and Responsibilities: Ensures the accuracy and completeness of the QA document system, performs daily filing and organizes contents. Coordinates the review and revision of procedures, specifications and forms as well as maintaining and updating the document control and tracking databases. Reviews batch records, QC records, labels and other documentation. Identifies quality improvement opportunities, compliance concerns, identify, prevent and resolve deviations. Coordinates Periodic Procedure Reviews to ensure documents are reviewed as required. Etc. | 2/3/2020 |
| 502 | Bioclinica Franklin, TN Medical Imaging Services Technician I BS/BA in a science or health related field Exp: 0-1 year |
Primary Responsibilities: Communicates with Clinical Project Managers, Clinical Operations Associates and/or Specialists regarding image quality, deliverables, and data discrepancies. Communicates with Image Analysis Lead, Clinical Operations Manager, and/or Scientific Director regarding troubleshooting of reading systems, image quality concerns, and deliverables. Maintains study-specific reading tracking tools. Attends all central analysis and quality control training sessions. Completes validation of relevant central analysis types by meeting pre-defined validation requirements. Performs quality control of site qualification- scans using phantom or patient, and on-going patient data within study-specific turnaround times to Clinical Project Manager, Clinical Operations Associate, and/or Specialist responsible for the study. etc. | 2/3/2020 |
| 503 | Bioclinica Princeton, NJ Inside Sales Associate BS/BA Exp: 1-3 year(s) |
The Inside Sales Associate is an in-house sales position supporting the business development efforts across the United States, working closely with the eHealth Business Development team. The Inside Sales Associate will contact clients directly at an early stage of the sales lifecycle to initiate meetings and support the development of the RFP pipeline for the Sales Directors. This position will also be responsible for developing relationships with clients to expand the Bioclinica portfolio with new and existing clients in partnership with the Sales Directors. etc. | 2/3/2020 |
| 504 | Biodesix Boulder, CO Billing Specialist I HS diploma/BS/BA Exp: 1+ year(s) |
Billing Specialist I will be responsible for obtaining necessary patient information to submit on medical claims sent to insurance plans. They will make phone calls to insurance plans and facilities, accurately record information obtained in patient files, and submit claims and appeals to insurance on behalf of patients. Billing Specialist I will work closely with Customer Support Patient Advocates and Billing Team to ensure accurate information is recorded and billing concerns are addressed. etc. | 2/4/2020 |
| 505 | BioFire Diagnostics Salt Lake City, UT Cost Accountant I BS/BA in accounting or related Exp: 1 year |
BioFire Diagnostics, LLC. is looking to add a Cost Accountant to our growing Finance and Accounting team! This Cost Accountant is responsible for assisting with the planning, implementation and maintenance of the cost accounting system. Major responsibilities include accurate and timely analysis, as well as contributing to reporting and compliance activities. Essential Job Duties and Responsibilities: Perform all work in compliance with company policy and within the guidelines of BioFire Diagnostics’ Quality System. Monitor inventory activities from purchase of raw material through the production process to finished goods. Assist with tracking and reporting scrap and supply expense. Support cost system development and associated internal controls. Assist with preparing the monthly, quarterly and year-end close, prepares related reports and presentations and meets reporting deadlines. etc. | 2/4/2020 |
| 506 | BioFire Diagnostics Salt Lake City, UT ETL Developer I BS/MS in computer science or related Exp: 1+ year(s) |
BioFire Diagnostics, LLC. is looking for an ETL Developer I to join our growing team! The ETL Developer will analyze, design, develop, test and maintain the data pipeline component of BioFire’s Data Warehouse. This includes refinement of stored procedures to improve daily and real-time data loads in effort to make them more efficient and scalable. ETL Developer will work closely with BI Analysts and Engineers to build a Data Warehouse that provides quality, accurate, accessible and governed data capable to deliver business insight to various BioFire business domains through reporting, dashboards and visualizations. ETL Developer will promote Kimball methodology and utilize current technology stack to find innovative solutions to complex data problems. Ability to work as a team player alongside a talented group of individuals for the same cause is essential to success in the role. etc. | 2/4/2020 |
| 507 | BioFire Diagnostics Salt Lake City, UT Manufacturing Engineering Stock Room Attendant I - Night Shift HS diploma or equivalent Exp: None required |
BioFire Diagnostics, LLC. is looking to add a Manufacturing Engineering Stock Room Attendant to join our growing night shift Manufacturing Engineering team! The Manufacturing Engineering Stock Room Attendant I works within a Manufacturing Engineering Team – generally under the leadership of a more experienced individual (e.g. Engineers and/or Managers). The attendant I uses experience and knowledge to perform the types of activities which are generally considered within Spare Parts Inventory. The Manufacturing Engineering Stock Room Attendant I is expected to work and communicate well with other team members and leadership as assigned in order to meet the goals of the department, the project, and the company. etc. | 2/4/2020 |
| 508 | BioFire Diagnostics Salt Lake City, UT Manufacturing Engineering Technician Trainee HS diploma/AS/AA Exp: None required |
BioFire Diagnostics, LLC. is looking for a Manufacturing Engineering Technician Trainee to join our growing team! This engineering technician works within a manufacturing engineering team under the leadership of a more experienced individual. This engineering technician uses experience and education to perform the types of technician activities which are within the realm of manufacturing engineering technician and This engineering technician is expected to work and communicate well with other team members and leadership as assigned in order to meet the goals of the project, the department, and the company. etc. | 2/4/2020 |
| 509 | BioFire Diagnostics Salt Lake City, UT Manufacturing Technician I - Swing Shift HS diploma or equivalent Exp: 6+ months |
BioFire Diagnostics, LLC. is currently in need of Manufacturing Technician I's to work our swing shift schedule of 3:00 PM - 11:30 PM Monday - Friday. This position is responsible for manufacturing products efficiently, accurately, safely, and on time. Operates manufacturing equipment and in-process instrumentation to manufacture regulated products in accordance to QSRs, company policy, and safety regulations. Works on assignments that are routine in nature where ability to recognize deviation from accepted practice is required. This position requires attention to detail and relies on instructions and pre-established guidelines to perform the functions of the job. Requires direct supervision or oversight by a senior employee. etc. | 2/4/2020 |
| 510 | BioFire Diagnostics Salt Lake City, UT BioReagents Formulator - Day Shift AS Exp: 1+ year(s) |
This is a full-time non-exempt position. Responsible for manufacturing and formulation of all BioReagents products and sub-assemblies including Film Array. Operates production equipment and performs duties under compliance of cGMP manufacturing. Weighs, measures, and checks raw materials to assure that manufactured batches, lots, buffers and sub-assemblies contain the proper reagents and qualities. Has knowledge of commonly used concepts, practices, and procedures including PCR, RT-PCR real-time PCR, and use of fluorescence based nucleic acid detection techniques. Assists in complex functional testing and troubleshooting product, process material or formulation processes. Applicant must be mathematically competent, detail orientated, and able to follow written directions well. etc. | 2/4/2020 |
| 511 | BioFire Diagnostics Salt Lake City, UT BioReagents Formulator - Swing Shift AS Exp: 1+ year(s) |
This is a full-time non-exempt position. Responsible for manufacturing and formulation of all BioReagents products and sub-assemblies including Film Array. Operates production equipment and performs duties under compliance of cGMP manufacturing. Weighs, measures, and checks raw materials to assure that manufactured batches, lots, buffers and sub-assemblies contain the proper reagents and qualities. Has knowledge of commonly used concepts, practices, and procedures including PCR, RT-PCR real-time PCR, and use of fluorescence based nucleic acid detection techniques. Assists in complex functional testing and troubleshooting product, process material or formulation processes. Applicant must be mathematically competent, detail orientated, and able to follow written directions well. etc. | 2/4/2020 |
| 512 | Biogen Cambridge, MA Operations Associate I, In-Vivo Resource Center AS/BS in animal science or related Exp: 0+ years |
Job Description: Perform daily health observations and effectively record and communicate abnormalities to the scientists. Perform husbandry duties for rats and mice. Perform daily census, handle related documentation and follow reporting procedures. Perform animal receipt and housing of animals. Utilize internal databases to perform the receipt of animals and processing of supplies. etc. | 2/4/2020 |
| 513 | Biogen Research Triangle Park, NC Senior Instrumentation and Calibration Technician I (Metrology) AS in electronics or instrumentation Exp: Not necessary for AS candidates |
Due to continued growth and the introduction of new technologies across the site, we are looking for a qualified candidate to support the Instrumentation and Controls (I&C) Dept. in a GMP and Non-GMP environment. In this role you will be responsible for performing corrective and preventative calibrations on manufacturing and laboratory analytical instrumentation as well as supporting manufacturing and laboratory personnel in the use, maintenance and repair of on-site instrumentation and test equipment. Applicants will become trained and skilled in all unit operations in their area and performs most functions with minimal supervision. etc. | 2/4/2020 |
| 514 | Biogen Cambridge, MA Engineer I, Pilot Cell Culture, Gene Therapy BS/MS in bioengineering, chemical engineering, biochemistry, or related Exp: 0-2 years |
Engineer I position within the Gene Therapy BioProcess Development Pilot Facility. Candidate must be motivated and innovative with exceptional analytical and communication skills. Essential Responsibilities: 1) Assist with scale up design and execute laboratory experiments with minimal guidance. 2) Perform independent data recording, analysis, and troubleshooting. 3) Establish manufacturable large-scale cell culture operations. 4) Document development work in concise reports and provide project updates in written and oral presentations. etc. | 2/4/2020 |
| 515 | Biogen Research Triangle Park, NC Engineer I, Validation BS in a relevant discipline Exp: 1-2 year(s) |
The Validation Engineer I designs and develops validation protocols in addition to provides expertise to associated equipment and automation design / modifications. Additional responsibilities include but are not limited to: Coordinates Equipment & Cleaning Validation Protocols (development & management) for specific equipment areas – including presentation of technical training & support to personnel, with on-floor guidance. Leads validation innovation project efforts requiring cross-functional & contract resources. etc. | 2/4/2020 |
| 516 | Biogen Cambridge, MA Associate Scientist II/Engineer I, Technical Development BS/MS in bio/chemical engineering or a life science Exp: 0-3 years |
This position will focus on development of high productivity and robust cell culture processes through classically and statistically designed experiments. The candidate’s goals will be to increase process robustness and productivity through comprehensive understanding of levers important to mammalian cell culture. A major component of the role will involve conducting and documenting laboratory bioreactor experiments with a focus on process definition and understanding, experimental design and troubleshooting, and data analysis. etc. | 2/4/2020 |
| 517 | BioLegend San Diego, CA Manufacturing Technician- Recombinant Antibody & Protein AS/BS in a life science or related Exp: 1+ year(s) |
This position is responsible for manufacturing cutting edge recombinant protein research products in Molecular Cellular Immunology (MCI) group. The successful candidate will be involved in routine task of cell culture, plasmid DNA isolation, buffer preparation, equipment maintenance and support inventory management. Another part of the job responsibility includes transferring the products to other groups for testing, preparing product/project related documentation, and maintaining the inventory and record for recombinant protein products. etc. | 2/4/2020 |
| 518 | BioLegend San Diego, CA Manufacturing Support Technician - Brilliant Violet Conjugation HS diploma/AS in a life science Exp: 1+ year(s) |
BioLegend develops world-class, cutting-edge antibodies and reagents for biomedical research, manufactured in our state-of-the-art facility in San Diego, CA. Our mission is to accelerate research and discovery by providing the highest quality products at an outstanding value, along with superior customer service and technical support. Our product expertise covers a diverse set of research areas including Immunology, Neuroscience, Cancer, Stem cells, and Cell Biology. The Manufacturing Support Technician position will be a key member of our Manufacturing team and will work closely with the BV Conjugation group to assist with the smooth operation of the BV Conjugation laboratory. etc. | 2/4/2020 |
| 519 | BioLegend San Diego, CA Development Associate - Conjugation BS in biology, biochemistry, or chemistry Exp: 1-3 year(s) |
BioLegend’s Process Development Associate will be responsible for performing all essential functions related to antibody-fluorescence and oligo conjugation, including following Standard Operating Procedures (SOPs) and batch records and maintaining and analyzing lot histories. The Process Development Associate will be an integral member of a team that ensures the highest quality of our finalized antibody products. This position offers the opportunity to gain experience with different types of conjugation chemistries and different chromatography methods to purify conjugated antibodies and offers the opportunity to work in small scale to large scale product projects and to learn to utilize the (Enterprise Resource Planning) ERP database to track production schedules and deadlines and to enter production results. etc. | 2/4/2020 |
| 520 | BioLegend San Diego, CA Bottling Technician - Formulation Group (2nd shift 3:30pm - 12:00am) HS diploma or equivalent Exp: 6+ months |
BioLegend is looking for a Bottling Process Technician for our Formulation Group. This role will be responsible for processing product formulations, filling, capping, labeling, and completing batch records, and putting away Finished Good Inventory (FGI). This is a highly team oriented group which involves working closely with other core teams within the Bottling Department as well as other departments such as Planning, Receiving, Inventory Control, Custom Solution Team (CST), Packaging and Quality Control groups. etc. | 2/4/2020 |
| 521 | BioLegend San Diego, CA Research Associate (Cell Analysis) BS in a life science or related Exp: 1 year |
We are seeking a self-motivated Research Associate to join our Product Development team in San Diego. The incumbent will actively participate in all the stages of the development, optimization, and validation of new products. The work requires routinely handling small animals and biological samples from animals and human donors. Prior experience in tissue culture, flow cytometry, immunoassays (eg ELISA, Western Blotting), molecular biology techniques (eg PCR, cloning, etc.), data analysis, and project management are preferred. etc. | 2/4/2020 |
| 522 | BioLegend San Diego, CA Manufacturing Associate - Chemistry BS in chemistry, biochemistry, material science, or related Exp: 1 year |
BioLegend has an opening for a Manufacturing Associate in our Chemistry group for our MojoSort Product Development team. The main responsibility for this position will be to assist in the large-scale manufacturing of magnetic nanoparticles conjugated with proteins such as streptavidin and antibodies according to established Standard Operating Procedures (SOPs). Other duties will include completion of appropriate batch record forms and updating relevant databases. etc. | 2/4/2020 |
| 523 | BioLegend San Diego, CA Quality Control Associate (2nd Shift) BS in a science Exp: 1 year |
BioLegend has an immediate opening for a 2nd Shift Quality Control Associate that will be responsible for testing products such as antibodies and proteins in the following application(s): flow cytometry, immunohistochemistry, western blotting, ELISA, multiplex immunoassays and/or functional bioassays. This position will also perform all aspects of the assays following SOPs and ISO requirements. Additional responsibilities include culturing mammalian cell lines, isolating primary cells, and maintaining laboratory equipment and supplies. The selected individual will be required to train during 1st Shift hours prior to switching to a 2nd Shift schedule. etc. | 2/4/2020 |
| 524 | Biolife Solutions Albuquerque, NM QC Technician - evo Platform BS in a related field Exp: 1-2 year(s) |
Albuquerque based advanced thermal shipping solution manufacturer is looking to hire a full-time Quality Control Technician with starting pay depending on experience. SAVSU Technologies builds integrated, innovative hardware and software solutions designed to protect live cell therapies during transport and storage. Our customers include cell and gene therapy companies, specialty couriers, biotech/biopharma, research institutions, governments, and NGOs. Quality Control Technician at SAVSU Technologies is responsible for maintaining and improving the existing quality management system alongside the Quality Assurance team. etc. | 2/4/2020 |
| 525 | Biomarin Novato, CA Specialist, QC I (Temporary) BS/BA in the life sciences Exp: 0-3 years |
Coordinate the calibration, maintenance and repair of analytical laboratory instruments and support equipment using the BioMarin’s Enterprise Computerized Maintenance Management System (CMMS). Responsible for the completion of QC equipment related documentations. Perform change request using the BioMarin’s Enterprise Quality Management System (Trackwise). Maintain vendor service contracts using BioMarin’s SpringCM system. Maintain good working relationships with vendors to ensure vendor meets BioMarin’s current and future needs. Work with vendors to troubleshoot equipment. Maintain the laboratory equipment inventory for tracking equipment assets and vendor contacts. etc. | 2/4/2020 |
| 526 | Biomarin Novato, CA Material Handler I (Temporary) High school diploma/AA/AS/BA/BS Exp: 1-2 year(s) |
Material Handler I will be responsible for sampling, weighing, and dispensing raw materials to produce buffer, solution, and media kits for manufacturing facilities. Material Handler I is also responsible for receiving and verifying materials and ensuring that material storage locations are properly stocked and maintained. Responsibilities include, but are not limited to the following: Receives, verifies and coordinates raw material receipts and returns from warehouses to manufacturing facilities and vice versa. Contact for raw material issues and reconciliation. Coordinates and reconciles raw materials that are in Quarantine. etc. | 2/4/2020 |
| 527 | Biomarin San Rafael, CA Research Associate I (Temporary) MS Exp: 0-2 years |
Duties: Performing Immunohisotchemical and In Situ Hybridization Assays. Performing basic histologic techniques (including but not limited to): Fixation, Embedding, Sectioning, and Staining. Epifluorescence and Confocal Microscopy. Image Analysis. Assay development and trouble-shooting. Performing mammalian cell line maintenance and cell based assays. Execute and document laboratory procedures and experiments with great attention to detail. | 2/4/2020 |
| 528 | Biomarin Novato, CA Associate , Manufacturing (Temporary) BS in a related science or engineering Exp: Not necessary for BS candidates |
PROCESS KNOWLEDGE: Understanding of process theory and equipment operation. Ability to learn biopharmaceutical manufacturing processes including mammalian cell culture, depth filtration, tangential flow filtration, column chromatography, protein purification and formulation of bulk drug substance. Support initiatives for process optimization. Identify and elevate processing issues and support solutions. Demonstrated proficiency Gain experience with automation systems (LIMS, MES, PI, etc.). etc. | 2/4/2020 |
| 529 | Biomarin Novato, CA Analyst, QC I (Temporary) BS/BA in a biological or biochemical science Exp: 0-2 years |
The Quality Control Microbiology, Environmental Monitoring, Analyst I under direct supervision, is responsible for performing microbiological, biochemical, and chemical evaluations of the manufacturing facilities, utilities, and equipment. With experience they would perform as a back-up for QC In-process and QC Microbial ID testing. Under direct supervision, the incumbent will be primarily responsible for performing environmental monitoring sampling and testing of the facilities, equipment, and utilities under cGMP guidelines. In addition they will be responsible for performing biochemical and microbiological assays of samples under cGMP and GLP guidelines. Work assignments will encompass activities from routine to semi-routine in nature with the ability to recognize deviations from accepted limits and practices. etc. | 2/4/2020 |
| 530 | Biomerics Athens, TX Engineering Technician HS diploma/BS/BA Exp: 1 year |
Engineering Technician will provide technical support in the design and development of processes needed to manufacture products that are safe and cost effective. RESPONSIBILITIES: Assist Engineering in the design of product and processes that have the capability to be robust and produce parts and assemblies so that the normal distribution is well within specification and yet cost effective. etc. | 2/4/2020 |
| 531 | Bio-Rad Hercules, CA Field Service Engineer I AS/AA in electronics Exp: 0-1 year(s) |
Bio-Rad is seeking a Field Service Engineer. This position requires up to 75% travel throughout the San Francisco Bay Area. Responsibilities: Provide customer site service on all CDG/LSG products including emergency service. Maximizes system uptime through proactive preventive maintenance. Act as customer advocate to ensure satisfaction and repeat business. Maintains company assets including parts inventory and leased vehicle. | 2/4/2020 |
| 532 | Bio-Rad Seattle, WA Field Service Engineer BS/BA Exp: 1 year |
Bio-Rad is seeking a Field Service Engineer who will perform repairs, upgrades, and preventive maintenance on our instruments for clinical diagnostics, life science, and biopharma customers in the Greater Seattle Area. Responsibilities: Provide customer site service on all CDG/LSG products including emergency service. Maximizes system uptime through proactive preventive maintenance. Act as customer advocate to ensure satisfaction and repeat business. Maintains company assets including parts inventory and leased vehicle. etc. | 2/4/2020 |
| 533 | Bio-Rad Cincinnati, OH Field Service Engineer BS/BA Exp: 1 year |
Bio-Rad is seeking a Field Service Engineer who will perform repairs, upgrades, and preventive maintenance on our instruments for clinical diagnostics, life science, and biopharma customers based in Cincinnati, OH traveling 50 – 75%. Responsibilities: Provide customer site service on all CDG/LSG products including emergency service. Maximizes system uptime through proactive preventive maintenance. etc. | 2/4/2020 |
| 534 | Bio-Rad Pleasanton, CA Research Associate II MS in molecular biology, biochemistry, cell biology, or a related life science Exp: 0-2 years |
Bio-Rad’s Digital Biology Center is a multidisciplinary team developing products using our Droplet DigitalTM technology that are having a large impact in both research and healthcare. Every day, scientists and clinicians around the world use our ddPCRTM and ddSEQTM NGS sample prep systems to make new discoveries, and are revolutionizing clinical decision making with break-through liquid biopsy applications. We’re looking for an energetic and talented Research Associate II (IVD Development) to join our team. Responsibilities: You will work in an assay research and development team on new in vitro diagnostic (IVD) oncology tests using state-of-the-art droplet digital PCR (ddPCR) technology, in a multi-disciplinary department that includes assay research and development scientists, hardware engineers and software engineers. etc. | 2/4/2020 |
| 535 | Bio-Rad Nashville, TN Field Service Engineer BS/BA Exp: 1 year |
Bio-Rad is seeking a Field Service Engineer who will perform repairs, upgrades, and preventive maintenance on our instruments for clinical diagnostics, life science, and biopharma customers based in Nashville, TN traveling 50 – 75%. Responsibilities: Provide customer site service on all CDG/LSG products including emergency service. Maximizes system uptime through proactive preventive maintenance. etc. | 2/4/2020 |
| 536 | Bioserv San Diego, CA Manufacturing Technician I/II HS diploma or equivalent Exp: 1-2 year(s) |
The Manufacturing Technician is responsible for supporting and performing routine procedures associated with the manufacture of the customer’s product with minimal direction from Supervisor. Manufacturing Technicians responsibilities include performing environmental monitoring, cleaning and sterilizing of glassware, cleaning of clean-room suites, manufacturing preparatory activities and clean-up, assist in formulation, visual inspections, labeling and packaging. They may be aseptically qualified to perform aseptic manufacturing set-up, filtration, filling and closure of product. etc. | 2/4/2020 |
| 537 | Biotherapeutics Inc. Blacksburg, VA Chemistry Technician BS/BA Exp: 1+ year(s) |
Biotherapeutics Inc. is looking for a highly motivated Chemistry Technician passionate about science and teamwork. The ideal candidate will be well-versed in analytical chemistry skills. Responsibilities: Chemistry Work: Set up a recrystallization pipeline at BioTherapeutics for abscisic acid (ABA) and punicic acid (PUA), with the intention of recrystallizing additional compounds. Conduct recrystallization optimization analytics. Interface with chemistry department with the ABA and PUA development. Setup chemistry work space and keep detailed records of all activities, record these activities in ASANA, the Google Drive, and in a laboratory notebook. etc. | 2/4/2020 |
| 538 | Arthrex Santa Barbara, CA Product Manager - Associate Bachelor's or Master's in business, marketing, or engineering Exp: 0-1 year(s) |
Essential Duties and Responsibilities: Participates in overall marketing, product strategy, research and development requirements, development, and manufacturing coordination for new and emerging products. Works on technical product development, estimates of potential profits, and release to production. Assists in the management of day-to-day progress and maintenance of products. Provides technical expertise and training to other departments in support of product development. Works with Product Team to develop marketing analysis to determine product definitions. Collaborates with a wide variety of functional areas such as sales, engineering, marketing, manufacturing, and operations to develop and provide product definitions responsive to customer needs and market opportunities. etc. | 1/28/2020 |
| 539 | Arthrex Santa Barbara, CA Technician I HS diploma or equivalent Exp: 1+ year(s) |
Main Objective: Performs production assembly work of light electro-mechanical assembly operations of moderately high complexity with close attention to detail following manufacturing assembly procedures. Essential Duties and Responsibilities: Manufacture electro-mechanical medical products to specified work orders. Follows engineering drawings, manufacturing assembly instructions and standard operating procedures. Inspects own work as well as the work of others. Operate a variety of hand tools and light manufacturing equipment. Perform tasks such as but not limited to installing circuit boards, power supplies, face plates, product labels, cables and wire harness using screws and adhesives. etc. | 1/28/2020 |
| 540 | Arthrex Sandy Springs, SC Engineer Tech - Manufacturing AS in engineering technology Exp: Not necessary for AS candidates |
Main Objective: Support the development, implementation and improvements of manufacturing processes to produce cost effective quality products. Essential Duties and Responsibilities: Load part number, product structure and router steps in SAP or any equivalent ERP system. Understand correct revision levels of components to upper level and coordinate with planning regarding CR inventory and WIP run-out including effectivity dates. Handle multiple project management at a pre-determined lead-time and prioritize and respond to special assigned projects. Follow thru newly set-up projects to assure smooth production. Use CAD skills to make drawing revisions. etc. | 1/28/2020 |
| 541 | Arthrex Naples, FL Product Manager Associate - Imaging & Resection Bi-Polar/ RF BS/BA/MBA Exp: 1+ year(s) |
Arthrex is actively searching for a Product Manager Associate, to actively participate in our fast paced and dynamic bipolar RF product line. The candidate will lead our product management initiatives with regards to cross functional product development, product launches, training and sales support. The successful candidate will build relationships with cross functional team members, sales management, sales representatives and surgeons and add value beyond transactional tasks by pursuing creative and innovative opportunities to provide timely, meaningful, market research, product collateral and training materials. Excellent interpersonal and leadership skills along with one year or more of related experience and a Bachelor's degree or Master’s degree are essential for this position. etc. | 1/28/2020 |
| 542 | Arthrex Chicago, IL Vet Sales Associate BS/BA Exp: 1+ year(s) |
The Arthrex Veterinary Sales Associate is responsible for generating sales of products and equipment to both existing veterinarians and new customers within an assigned sales territory. The Arthrex Veterinary Sales Associate plans and makes sales calls, and selects products and programs that motivate customers to buy products. ESSENTIAL DUTIES AND RESPONSIBILITIES: Call on target, current and prospective customers in order to generate sales, improve market share, and increase income for AVS. Utilize the computer as a sales aid and be competent in the use of Outlook, and the Arthrex Veterinary website. Seek to understand the needs of the veterinarian and clinic and, in turn, select products and services to satisfy those needs. Establish appropriate relationships with veterinarians and clinics. etc. | 1/28/2020 |
| 543 | Arthrex Naples, FL International Exhibit Coordinator BS/BA Exp: 1-2 year(s) |
To provide administrative and on-site support to the exhibits department, focusing on international logistics and execution. Assist with all pre-planning, onsite and post events tasks. Serve as a liaison to internal and external clients, including employees, vendors and associations. Essential Duties and Responsibilities: Correspond with exhibitor appointed contractors and association meeting organizers on international exhibit requests as needed. Work with marketing project manager on project requests related to international exhibits activities, and assist & update marketing on changes and deadlines. Work with the AXIS project team and Exhibit Data Specialist on details required for of the leads app and list management. Post show download leads generated, run through the Denied Parties List for GTO and distribute to global team members. Coordinate with global partners to collect user data, conference details and focus products to update the AXIS lead system. etc. | 1/28/2020 |
| 544 | Arthrex Cleveland, OH Vet Sales Associate BS/BA Exp: 1+ year(s) |
The Arthrex Veterinary Sales Associate is responsible for generating sales of products and equipment to both existing veterinarians and new customers within an assigned sales territory. The Arthrex Veterinary Sales Associate plans and makes sales calls, and selects products and programs that motivate customers to buy products. ESSENTIAL DUTIES AND RESPONSIBILITIES: Call on target, current and prospective customers in order to generate sales, improve market share, and increase income for AVS. Utilize the computer as a sales aid and be competent in the use of Outlook, and the Arthrex Veterinary website. Seek to understand the needs of the veterinarian and clinic and, in turn, select products and services to satisfy those needs. Establish appropriate relationships with veterinarians and clinics. etc. | 1/28/2020 |
| 545 | Astellas Marlborough, MA Research Associate I BS/BA Exp: 0-3 years |
We are seeking a highly motivated Research Associate, who will work on multiple stem cell and exosome related projects at AIRM. The research associate will be supporting cell culture and differentiation needs for the ocular team. They will also provide technical support for cell characterization through qPCR, ICC etc. They will also be supporting the extracellular vesicle (EV) team for multiple projects for EV isolation, characterization, in vivo studies etc. | 1/28/2020 |
| 546 | AstraZeneca Gaithersburg, MD R&D Associate I/II - Upstream & Downstream - BPD BS/MS in a scientific or engineering discipline Exp: 0-2 years |
As a Research Associate, you would enter a 2-year program that would give you experience creating our new next generation manufacturing process in three areas: upstream process development, downstream process development, and either pilot-scale equipment design, debugging, and automation, or analytical sciences. You would join a team developing AstraZeneca’s Next Generation Manufacturing Platform. You and the team would develop the continuous and integrated purification platform for biological therapeutics, including antibodies, bispecific antibodies, and Fc-fusions. You would apply the Next Generation Manufacturing methods to drug candidates in Phase I, II, and those entering Phase III. etc. | 1/28/2020 |
| 547 | AstraZeneca Gaithersburg, MD Research Associate II - Lab Support MS in a biological or chemical science Exp: 0-2 years |
As a Research Associate II, you will function as the point person for the procurement and management of laboratory reagents and supplies. Coordinate maintenance of non-computer-based equipment and prepare associated documentation in accordance with GXP; supporting operations of a regulated laboratory that performs PK and ADA bioanalyses in compliance with GLP / GCP guidelines. Specific Responsibilities include: Responsible for the ordering and stocking of laboratory reagents and supplies to meet development, validation and sample testing needs of regulated bioanalytical lab (HBS and GXP compliance). Coordinates across departments, vendors and systems to schedule preventative maintenance, calibration and validation activities of laboratory non-computer-based equipment to ensure GLP compliance. etc. | 1/28/2020 |
| 548 | AstraZeneca West Chester, OH Aseptic Control Technician - Operations HS diploma or equivalent Exp: 1-2 year(s) |
The Aseptic Control Technician Autonomously performs tasks related to environmental monitoring to support regulatory requirements of a sterile manufacturing site. The position requires operating equipment in various classified/non-classified areas up to a Class 100 aseptic environment and in a laboratory setting. Essential Job Functions: Prepare documentation of activities, actions, and results. Ensure proper documentation practices during job activities. Read SOPs (Standard Operating Procedures) and excerpts from technical documentation. Maintain accurate and complete records (for example: laboratory notebooks, quality records, sample receipts). Complete required training. etc. | 1/28/2020 |
| 549 | Athenex Clarence, NY Manufacturing Process Operator I (2nd Shift - 2pm to 10:30pm) HS diploma or equivalent Exp: 1-3 year(s) |
Our Manufacturing Process Operator I is responsible for ensuring the accurate production and documentation of pharmaceutical products and maintain a safe manufacturing environment. Essential Job Functions/Responsibilities: Participate in the manufacturing process by performing visual inspection of compounded drug product per procedure. Participate in the manufacturing process by performing labeling and final packaging of drug product. etc. | 1/28/2020 |
| 550 | Athenex Clarence, NY Manufacturing Process Operator I (1st Shift 7am to 3:30pm) HS diploma or equivalent Exp: 1-3 year(s) |
Our Manufacturing Process Operator I is responsible for ensuring the accurate production and documentation of pharmaceutical products and maintain a safe manufacturing environment. Essential Job Functions/Responsibilities: Participate in the manufacturing process by performing visual inspection of compounded drug product per procedure. Participate in the manufacturing process by performing labeling and final packaging of drug product. etc. | 1/28/2020 |
| 551 | Athenex Clarence, NY Quality Control Laboratory Technician BS in chemistry Exp: Not necessary for BS candidates |
Support the laboratory workflow in an efficient and effective manner. Support Analytical group in maintaining the laboratory to make work flow more efficient. Essential Job Functions/Responsibilities: Responsible for promoting and maintaining safe and healthy working conditions in his / her assigned work area; instructs and enforces compliance with established safe work practices and procedures; ensures assigned trainees receive appropriate training and information necessary to conduct their activities in a safe and healthy manner. Properly disposes of solvent waste in appropriate containers and disposes of empty bottles in the recycling bins according to health, safety and environmental practices. Performs laboratory, office and maintenance on a routine basis. etc. | 1/28/2020 |
| 552 | Atreca South San Francisco, CA Research Associate, Antibody Inventory BS/MS Exp: 0-3 years |
In this position, the successful candidate will help manage and maintain Atreca’s antibody inventory by using automated liquid handling technology, database-driven inventory management systems, and equipment used for quality control. The position reports in the Protein Engineering group, and the work will involve interacting with multiple research groups. Furthermore, he/she will perform quality control on received antibodies as well as process them to be used in downstream assays. This very central position will be in a very dynamic and motivated team dedicated to the discovery of novel, antibody-based cancer therapies. etc. | 1/28/2020 |
| 553 | Atreca South San Francisco, CA Senior Research Associate, Protein Biochemistry (Temporary) BS/MS in molecular biology, biochemistry, cell biology, or related Exp: 1-10 year(s) |
Atreca's IRC technology identifies anti-tumor human antibodies in a highly accurate and precise fashion. Our goal is to apply this technology to elucidate and characterize novel tumor targets and associated biologic processes that were selected for attack by the patient's immune system. In this position, the successful candidate will apply their skills and expertise in protein biochemistry to further understand the unique biology associated with our targets and contribute to the clinical application of our antibodies using protein biochemistry and molecular biology techniques. The candidate will have extensive experience in molecular biology and protein biochemistry as related to the identification and characterization of proteins driving tumorigenesis. etc. | 1/28/2020 |
| 554 | Atreca South San Francisco, CA Senior Research Associate, Protein Engineering MS in cell biology, immunology, bioengineering or related Exp: Not necessary for MS candidates |
We are seeking a motivated and enthusiastic Research Associate or Sr Research Associate to join our Protein Engineering group. The successful candidate will play a key role in further developing our yeast display platform and applying it to optimize and generate differentiated antibody and bispecific therapeutics. Primary Duties & Responsibilities: Establish yeast cultures and perform flow cytometry assays. Sort libraries of antibody variants by FACS and help with NGS sample preparations. Develop methods for selecting yeast-displayed antibodies bound to cancer cells. Follow laboratory safety guidelines and practices. | 1/28/2020 |
| 555 | Avion Pharmaceuticals Boston, MA Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 1/28/2020 |
| 556 | Avion Pharmaceuticals Brooklyn, NY Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 1/28/2020 |
| 557 | Avion Pharmaceuticals Charleston, SC Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 1/28/2020 |
| 558 | Avion Pharmaceuticals Charlotte, NC Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 1/28/2020 |
| 559 | Avion Pharmaceuticals Chicago, IL Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 1/28/2020 |
| 560 | Avion Pharmaceuticals Fayetteville, NC Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 1/28/2020 |
| 561 | Avion Pharmaceuticals Flint, MI Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 1/28/2020 |
| 562 | Avrobio Cambridge, MA Research Associate (Process Development Group) BS/MS in biology, biochemistry or related discipline Exp: 1+ year(s) |
We are seeking a Research Associate to join an exciting and fast-growing company to develop gene therapies for rare diseases. The successful candidate will join the process development group at Avrobio, focusing on development of analytical methods for ex vivo genetically modified cells to support the development of gene therapy programs. The individual will develop quantitative assays measuring gene modification in target cells, cell-based assays measuring the expression and the biological functions of specific genes. The successful candidate will, perform, and analyze experiments for multiple preclinical and clinical programs and will work independently to support process development, product characterization, and technical transfer to CMOs and GMP test labs. etc. | 1/28/2020 |
| 563 | Axsome New York, NY Clinical Trials Assistant BS in a biological or physical science Exp: 1 year |
The Clinical Trials Assistant is responsible for supporting the organization to successfully develop and implement clinical trials across its product portfolio and development pipeline. The Clinical Trial Assistant provides a key support function to the clinical operations team. Under general guidance from Clinical Operations, you will support the Clinical team responsible for management of multiple clinical trials (all phases), and assure compliance with SOPs, FDA regulations, GCP and ICH guidelines. etc. | 1/28/2020 |
| 564 | Bachem Torrance, CA Quality Assurance Specialist I BS in a related field Exp: 1-2 year(s) |
The Quality Assurance Specialist I fulfills a critical role for Quality Assurance. This individual will conduct real time batch record review, perform internal audits, contribute to GMP system improvements, write technical documents, and review GMP documentation and reports. This individual must also provide GMP and related training. Your Tasks: Review validation protocols, data and reports, as assigned. Coordinate assigned quality systems, such as GMP training program, deviations, CAPAs, or change controls. etc. | 1/28/2020 |
| 565 | Bachem Torrance, CA Building Services Technician HS diploma or equivalent Exp: 1-3 year(s) |
The Building Services Technician supports the Facilities, Maintenance, and other teams as needed to ensure manufacturing is performed according to schedule and quality demands. Job responsibilities include, but are not limited to, basic maintenance tasks for facilities and equipment, etc. Your Tasks: Follow Standard Operating Procedures (SOPs) and approved directions to perform basic maintenance tasks on facilities and equipment. Follow SOPs and approved directions to clean glassware and equipment used in GMP processes. Maintain cleaning logs and maintenance logs. Maintain stock of parts, supplies, materials, and tools within areas of responsibility. etc. | 1/28/2020 |
| 566 | Bachem Vista, CA QA Specialist I QA BSD BS in a related field Exp: 1-2 year(s) |
The Quality Assurance Specialist I fulfills a critical role for Quality Assurance. This individual will conduct real time batch record review, perform internal audits, contribute to GMP system improvements, write technical documents, and review GMP documentation and reports. This individual must also provide GMP and related training. Your Tasks: Review validation protocols, data and reports, as assigned. Coordinate assigned quality systems, such as GMP training program, deviations, CAPAs, or change controls. Perform annual product quality reviews and system reviews as assigned. etc. | 1/28/2020 |
| 567 | BardyDx Houston, TX Holter Analysis Technician HS diploma/AS Exp: 1-3 year(s) |
Currently, we are looking for Holter Analysis Technicians to join our Clinical Services Team who are passionate about cardiac rhythms and helping cardiac patients through our innovative remote patient monitoring body sensor technologies. The right individuals will join a dynamic and fast-paced start-up environment. Ideal candidates will have CCT or CRAT certification or specialize in cardiac rhythm recognition and interpretation skills. Experience with cardiology or electrophysiology can be advantageous. This position requires PC proficiency, excellent written and verbal communication skills, and meticulous attention to detail. This exciting role also provides excellent growth and advancement opportunities along with a bonus incentive program. etc. | 1/28/2020 |
| 568 | unspecified, NJ Holter Analysis Technician HS diploma/AS Exp: 1-3 year(s) |
Currently, we are looking for Holter Analysis Technicians to join our Clinical Services Team who are passionate about cardiac rhythms and helping cardiac patients through our innovative remote patient monitoring body sensor technologies. The right individuals will join a dynamic and fast-paced start-up environment. Ideal candidates will have CCT or CRAT certification or specialize in cardiac rhythm recognition and interpretation skills. Experience with cardiology or electrophysiology can be advantageous. This position requires PC proficiency, excellent written and verbal communication skills, and meticulous attention to detail. This exciting role also provides excellent growth and advancement opportunities along with a bonus incentive program. etc. | 1/28/2020 |
| 569 | Bausch Health Clearwater , FL Manufacturing Associate II HS diploma or equivalent Exp: 1+ year(s) |
Perform various operations in the fabrication of intraocular lenses according to production specifications and standards. Responsibilities: Performs various lens fabrication and inspections duties to include operating lathe and milling machines, lens polishing, finished production inspections and primary packaging. Ensure product meets all acceptable criteria per SOP's. Follow all regulatory guidelines and regulations regarding traceability, and safety procedures. Support, encourage and participate in team related activities; report ideas or suggestions to supervisor. Assist in training manufacturing associates using prescribed training methods and tools as assigned by supervisor/management. Report unusual conditions and problems to supervisor and manufacturing lead; practice good housekeeping. etc. | 1/28/2020 |
| 570 | Baxter Cleveland, MS Quality Lab Assoc I BS in chemistry, chemical engineering, or biology Exp: 0-3 years |
Perform chemical and physical analysis on medical products through all stages of the manufacturing process from incoming raw materials through to product release. Areas include raw materials, initial, in-process and finished products, Stability Program, protocol support, instrumental analysis and instrument calibration/qualifications. Responsibilities also include adherence to regulatory and procedural requirements that govern the operations and products (e.g., Specifications and Cleveland standard operating procedures). etc. | 1/28/2020 |
| 571 | Baxter Mountain Home, AR Production Technician I (3rd Shift) HS diploma/AS/AA Exp: 0-1+ year(s) |
Cleans, sanitizes and monitors equipment related to assembly, machinery, processing and/or packaging for all local manufacturing operations. Sets up and operates automatic or semiautomatic machines and related equipment in a continuous production/processing operation. Monitors meters, gauges, valves, flow ratios, temperatures, pressures, and/or related controls and guidelines to ensure adherence to production/process specifications. Responsible for executing all processes in production while strictly adhering to cGMP, SOPs, environmental health and safety guidelines and any other related regulations which could apply. Reports any malfunctions or abnormalities and performs all work in accordance with established safety procedures. etc. | 1/28/2020 |
| 572 | Bayer Indianola, IA Assembler I - 2nd Shift 2:00pm - 10:20pm HS diploma or equivalent Exp: 0-1 year(s) |
The primary responsibilities of this role, Assembler I 2nd Shift 2:00pm - 10:20pm, are to: Assemble various products; Package various products; Performing rework and inspection on the product; Backing up higher-level positions; Awareness of quality standards and ability to identify defects in Products; Recording data related to product quality and traceability; etc. | 1/28/2020 |
| 573 | Bayer Kansas City, KS Bayer Crop Science OIT Chemical Operator Rotating Shift HS diploma or equivalent Exp: 1 year |
The primary responsibilities of this role, Bayer Crop Science OIT Chemical Operator are: Prepares packaging materials; Read and understand SOP's; Stages raw and finished materials; Takes required samples during production process; contaminates equipment and piping for maintenance or disposal; Utilizes Personal Protective Equipment Matrix; Maintains inventories of disposable, production, and safety related materials; Recognizes material compatibilities; etc. | 1/28/2020 |
| 574 | Bayer New Orleans, LA Lab Tech AS/BS in chemistry or related Exp: 1-3 year(s) |
The primary responsibilities of this role, Laboratory Technician, are to: Determine conformance to accepted specifications for a particular chemical or physical property; Monitor and verify quality in accordance with statistical process or other control procedures; Perform troubleshooting and calibration of instruments; Prepare reagents, solutions, and standards; Maintain instruments and apparatus according to established procedures to support testing activities of the unit; etc. | 1/28/2020 |
| 575 | Bayer Myerstown, PA Associate Technician-3rd Shift HS diploma or equivalent Exp: 6+ months |
The primary responsibilities of this role, Associate Technician, are to: Comply with all workplace standards and safety procedures, including lockout tagout, current good manufacturing practices (CGMPS), occupational safety and health administration requirements (OSHA), standard operating procedures (SOPS), and company guidelines; Take ownership of training and learning to develop high performance competencies such as technical skills, communication skills, and skills to build a team-oriented culture; Demonstrate willingness to learn, maintaining qualifications/skills, training team members, motivating and supporting team members, sharing knowledge to continuously improve the process, etc.; etc. | 1/28/2020 |
| 576 | Bayer St. Louis, MO Agronomic Research Specialist MS in agronomy, engineering, life sciences, or computer sciences Exp: 0+ years |
The primary responsibilities of this role, Agronomic Research Specialist, are to: Collaborate with project team members to deliver detailed experimental protocols that enable advancement decisions by our scientists and placement decisions to our customers; Handle the operation of research equipment, note taking, data management with internal IT systems, comply with regulated seed stewardship standards, complete and/or participate in safety inspections/training and comply with all policies and standard operating procedures; etc. | 1/28/2020 |
| 577 | Bayer Lubbock, TX Agronomic Research Specialist MS in agronomy, engineering, life sciences, or computer sciences Exp: 1 year |
The primary responsibilities of this role, Agronomic Research Specialist, are to: Responsible for Delivering the highest quality field data as part of North America’s Plant Breeding R&D pipeline by providing optimal trial management, at times working on an internal R&D effort that spans across crops, sites, and a region; Independently Responsible for the implementation of unique and innovative technology solutions designed to improve research design and operations success through the use of new tools and methodologies to improve overall plant breeding phenotyping such as the pilot and use of geospatial systems, agronomic planting and harvesting tools, harvesting shelling systems, and data capture applications; etc. | 1/28/2020 |
| 578 | PCI Pharma Services Rockford, IL Entry Level Packaging Validation Analyst HS Diploma/GED Exp: 1-3 years experience or training |
The Validation Analyst I is responsible for overall validation project ownership of limited risk project(s) under heavy supervision. Responsible for generation and execution of validation protocols, assistance in audits, and determination of validation needs. This job has no supervisory responsibilities. | 1/25/2020 |
| 579 | PCI Pharma Services Philadelphia, PA IT Helpdesk Technician AS/AA in related Exp: 1-3 years experience or training |
The role of the Helpdesk Technician is to assist customers with IT applications, products or services. Complex and/or high priority problems are elevated to specialized support groups for resolution however the HelpDesk Technician is responsible to ensure that an effective solution is provided to the user. Provides support for all Information Technology products and services. Support may include answering questions, troubleshooting problems, teaching or instructing customers regarding software or hardware functionality, and communicating policy. | 1/25/2020 |
| 580 | PCI Pharma Services Rockford, IL Operations Process Engineer BS/BA in related Exp: 1-5 years |
This position will work to continuously improve processes and systems that ultimately lead to improved profitability to the company. Using all available Engineering, Lean and Six Sigma tools, this position will work independently and cross functionally to drive out waste and reduce process variability. Gather and analyze data using the operations data collection systems, including but not limited to: Overall Equipment Efficiency (OEE), uptime, scrap, margin, staffing, quality, capacity, safety and direct labor cost per unit to facilitate decision-making as well as identify and prioritize initiatives. This will require ownership of the data collection systems to insure the purity and consistency of the source. | 1/25/2020 |
| 581 | PCI Synthesis Newburyport, MA Quality Control Analyst: 3rd shift Overnight BS in chemistry or related Exp: 1+ years |
The analyst is responsible for providing accurate and timely results for the samples submitted for analysis to support our manufacturing and research and development departments. Use liquid chromatography, gas chromatography, ultra violet spectroscopy, infrared spectroscopy, titrimetry, and other techniques to assess the quality of samples. The resulting data is interpreted by the analyst and submitted for review. The analyst is also responsible for ensuring that the instruments used for analysis are calibrated to industry standards. | 1/25/2020 |
| 582 | PCI Synthesis Newburyport, MA Kilo Lab Chemist AS/AA in related Exp: 0-2 years, experience preferred |
PCI Synthesis is a leading manufacturer of Active Pharmaceutical Ingredients (APIs) and clinical drug substances. We are seeking a highly motivated, experienced Kilo Lab Research Scientist who would like to join our growing company. Proactive participation on project teams to guide R&D work prior to manufacturing runs • Preparation of Master Production Records (MPRs) based on lab procedures from R&D • Preparation of other regulatory documents • Active involvement in troubleshooting + investigations when problems are encountered. | 1/25/2020 |
| 583 | PCI Synthesis Devens, MA Process Chemist R&D BS or MS in chemistry Exp: 0-5 years |
Highly productive, results-oriented individual, who will generate and implement original ideas and solutions that contribute to improvements in processes used to synthesize valuable compounds. Support drug substance process development via laboratory development, kilo lab scale-up. Prepare and characterize molecules using appropriate analytical tools including IR, NMR, MS, GC, and HPLC. | 1/25/2020 |
| 584 | Pevalon na, FL Patient Sales Advocate BS/BA in related Exp: 1-3 years in medical field |
This is a Florida based Patient Sales Advocate position. Your position will be a blended position where you will work by phone calling patients and presenting The Eclipse solution as well as meeting with patients and medical practitioners in the field to educate and present the product. The ultimate goal of your phone calls is to convince the patient to schedule an appointment with a doctor to seek further information. The goal of your field work is to educate patients and practitioners on the benefits and use of the Eclipse solution. | 1/25/2020 |
| 585 | Penumbra Alameda, CA Game QA Tester and Generalist HS Diploma/GED Exp: 1 year in gaming/software QA |
MVI Health is developing a revolutionary new product that uses state-of-the-art virtual reality technology to transform physical rehabilitation. As our QA Tester and Generalist, you will play a key role in ensuring quality in our product in order to deliver a great experience to our customers. If you are a fire-and-forget tester who can solve problems independently, and who wants to make a positive difference in people's lives, this position may be for you. | 1/25/2020 |
| 586 | Penumbra Alameda, CA Quality Control Inspector HS Diploma/GED Exp: 1 year in QC inspection in med devices or similar |
As a Quality Control Inspector, you will test and inspect components and products in the laboratory. By ensuring that Penumbra's products meet the highest standards of quality and safety, you will play a key role in saving lives every day. Perform routine inspection at incoming Quality Control and finished device level. Inspect components, products, labels, boxes, pouches, and coatings visually and mechanically. Take measurements using micrometers, calipers, snap gages, gage pins and other measuring instruments. | 1/25/2020 |
| 587 | Penumbra Alameda, CA R&D Engineer BS/BA or higher in mechanical/biomedical engineering Exp: 1-10 years |
As an R&D Engineer at Penumbra, you will be charged with designing game-changing medical devices to address some of the world’s toughest disease states. Design, prototype, and optimize meaningful medical devices that revolutionize treatment paradigms for a variety of challenging disease states. Create test protocols and conduct testing to mitigate clinical risk for a wide range of medical device concepts. Coordinate with suppliers and other external resources to source components and refine component specifications. | 1/25/2020 |
| 588 | Penumbra Roseville, CA Quality Engineer BS/BA in engineering or sceicnes Exp: 1-5 years in biomedical/chemical/material engineering |
As a Quality Engineer at Penumbra, you will participate in all aspects of product manufacturing in order to ensure the highest level of quality in new and existing products, and their compliance to applicable regulations and standards. You will apply your passion for detailed analysis to identifying problems and determining the appropriate course of action. You will be looked to for ensuring compliance and building a culture of quality within your project teams. Represent Quality Engineering on process improvement projects, interfacing among multiple departments and teams such as Manufacturing, QC, R&D, Regulatory Affairs, Operations/Planning, and Marketing. | 1/25/2020 |
| 589 | Performance Validation Multiple Locations, IN Level 1 Staff Validation Engineer / Specialist BS/BA in engineering or sceicnes Exp: Entry Level |
The Level 1 Validation Engineer/Specialist works within a small team environment to provide technical services to pharmaceutical or medical device manufacturers. Technical services may include interpreting drawings, manuals, or other technical information to develop requirement documents, developing testing documents that verify installation, and/or operation of the equipment, and execution /documentation of these testing documents. These documents are used by our life science customers to demonstrate compliance with USFDA regulations (or other regulatory bodies) for current Good Manufacturing Practices. | 1/25/2020 |
| 590 | Perkin Elmber Waltham, MA Entry Level Consolidations Accountant BS/BA accounting or finance Exp: 0-2 years |
The Entry Level Consolidations Accountant will be an integral part of the Corporate Accounting team. The key areas of focus will be supporting the monthly close process, reviewing worldwide results and working with sites to make corrections, resolving accounting issues, and preparing global internal financial statements and financial data to support the consolidated external financials. This position also supports cross-functional finance teams across the organization through maintaining reliable financial reporting which requires an understanding of finance and accounting concepts as well as an aptitude for working with financial systems. | 1/25/2020 |
| 591 | Perrigo Allegan, MI Associate Scientist / Scientist - Analytical R&D MS in chemistry or pharma sciences Exp: 1-2 years in cGMP/cGLP |
The Allegan Michigan based Analytical Research and Development department, specializing in solid and liquid Over-the-Counter (OTC) product development, is looking to add a talented colleague to our New Product Development team. Our focus is on the development of analytical methods for small molecules in support of research and characterization of new and reformulated drug products. Chief techniques include HPLC/UPLC-UV stability-indicating methods with various separation chemistries. Perform physical and chemical testing on raw materials, in-process and finished product samples with superior attention to detail and a focus on operational excellence. | 1/25/2020 |
| 592 | Personalis Menlo Park, CA Laboratory Assistant (Temp to Perm) BS in molecular biology or related Exp: 0-2 years |
Within a dynamic startup environment, the successful candidate, under direction of the Laboratory management, will help grow the sequencing services laboratory. You will participate in the daily activities of the laboratory in order to effectively maximize turnaround time, equipment, and material utilization while adhering to quality technical standards. Adhere to the laboratory's quality control policies. Participate in laboratory support work as required by the team needs and at the direction of laboratory management. Lead the general upkeep, orderliness and cleanliness of the laboratory | 1/25/2020 |
| 593 | Fc Performance Romeoville, IL Inside Sales Representative BS/BA Exp: 1-3 years in customer service |
Sell company products and services to customers by processing orders, price and delivery inquiries, providing technical and application information, soliciting customer orders and suggesting additional products in a fast paced multi-tasking environment. Processes and expedites orders, customer returns and returns to vendors in an accurate and timely manner. Locates product and creates purchase orders. Follows-up with vendors to ensure timely delivery. Works closely with Outside Salesman in soliciting business, executing order transactions and maintaining superior customer service levels. | 1/25/2020 |
| 594 | Fc Performance Cleveland, OH Valve Technician HS Diploma/GED Exp: 1-3 years |
Mechanically and electrically troubleshoot, inspect, and test valves at specified job worksites. Primary worksites include FCX valve repair centers with occasional customer in-field work sites. Perform pre-testing, disassembly, cleaning, in process inspection, machining, lapping, painting, assembly, testing, and final inspection on various types of valves and actuation. Repair relief valves, control valves, on/off valves and pneumatic actuators in FCX actuation facility or customer plant locations. | 1/25/2020 |
| 595 | Pii Pharmaceuticals Hunt Valley, MD QA Associate HS Diploma/GED, BS/BA preferred Exp: 1 year in QA |
To ensure the timely and accurate inspection of raw materials, in-process blends, and finished drug products while adhering to the cGMP and ICH guidelines as well as USP/NF/EP/JP/Health Canada, and other regulatory statues as written. To ensure that the day-to-day tasks of the Quality Assurance Unit supports the overall business plan while maintaining the highest quality drug products, ensuring the safety, identity, strength, purity, and quality that the drug is purported to possess. | 1/25/2020 |
| 596 | Pii Pharmaceuticals Hunt Valley, MD Manufacturing Tech HS Diploma/GED Exp: 1-2 years in manufacturing |
Responsible for the mechanical setup, operation, control, monitoring and cleaning of various manufacturing equipment to produce solid dosage, semi-solid and liquid dosage forms following Standard Operating Procedures (SOPs). Performs assigned duties as outlined in the SOPs for manufacture of pharmaceutical products according to written instructions from Product Batch Records whilst following all safety requirements. To ensure that OPS services are compliant with the site’s quality standards, practices, procedures and documentation requirements and with site, local and federal safety requirements. | 1/25/2020 |
| 597 | PharmaIN Bothell, WA Research Associate – Biology BS in biology Exp: 1+ years |
We are seeking a highly motivated Research Associate to support our growing Biology team. The successful candidate will enjoy working in a fast-paced environment, and have hands-on experience with laboratory maintenance, cell culture, ELISA, and laboratory rodent handling. | 1/25/2020 |
| 598 | Pharm-Olam Houston, TX Clinical Trial Associate BS/BA Exp: 1 year as CTA II |
Acts as the primary administrative support to local Pharm-Olam clinical study teams, as required by Project Managers and Sponsors, thus ensuring that the clinical trial is conducted in accordance with international and local regulatory and ethic laws, ICH Guidelines for Good Clinical Practice and Standard Operating Procedures. Assists the local study team with the day-to-day conduct of international clinical studies. | 1/25/2020 |
| 599 | Physical Science Inc Lanham, MD Contamination Control Engineer MS in chemistry, material science, physics or related Exp: 0-3 years |
Research Support Instruments is looking for a scientist/engineer with a broad range of experience for the development of optical space flight instrumentation. Contamination in the form of particulates, films, or scattered light can significantly degrade instrument performance and/or lifetime. Management of the cleanliness of optical and nearby surfaces throughout the lifecycle of assembly, integration, test, launch and operations requires a system approach. A successful contamination control engineer must work with designers and engineers throughout the entire process: design, process control, monitoring, cleaning, training, performance modeling, integration, and testing. | 1/25/2020 |
| 600 | PhysIQ Chicago, IL Software Development Engineer in Test BS/BA or MS in technical field Exp: 1-3 years |
PhysIQ is looking for someone to join our growing team as a full-time employee in Test Engineering. This will involve testing new features, verifying bug fixes, and contributing to test automation across our front-end, back-end, mobile app, or api teams. This could involve Python, Java, Groovy, Kotlin, JS/TypeScript, WebDriver, Cucumber, or other technologies. | 1/25/2020 |
| 601 | Platelet Biogenesis Watertown, MA Research Associate, Stem Cell Team BS or MS in biological sciences Exp: 0-2 years in lab/research setting with cell culture |
We are looking for a driven independent thinker with a monster work ethic who shares our long‐term vision for developing a source of donor-independent human platelets, and leveraging Mother Nature’s drug delivery system to cure diseases. Perform maintenance and differentiation cultures of human induced pluripotent stem cells, hematopoietic progenitors and megakaryocytes. Perform routine cellular and molecular biology procedures including but not limited to flow cytometry and microscopy | 1/25/2020 |
| 602 | PMI BioPharma Solutions Nashville, TN Engineering Maintenance Technician I HS Diploma/GED Exp: 1-2 years maintenance |
Reporting to the Supervisor of Engineering, the Facilities Technician will be responsible for PMI’s maintenance and equipment support activities. The Facilities Technician performs with minimal supervision preventive maintenance, demand maintenance and calibration tasks on critical equipment, utilities, and facilities. | 1/26/2020 |
| 603 | PMI BioPharma Solutions Nashville, TN Chemist I, Analytical Development BS/BA in chemistry, biology or related Exp: 1-2 years in pharmacueticals |
The Chemist I position, reporting to the Director, Analytical Development, will operate under moderate supervision to perform chemical analyses of samples according to standardized procedures to determine the identity, content, purity, stability, and other characteristics of the samples analyzed. He/she may perform method development activities related to the development of methods for testing of raw materials and clinical drug product as well as formulation development. | 1/26/2020 |
| 604 | PolarityTE Salt Lake City, UT Research Specialist I, II, or III BS in biological sciences/technology, or engineering Exp: 0-2 years as research associate or similar |
Under the general supervision of the Director of BME, the Research Specialist I, II or III will support R&D in conducting research projects by contributing to the following: develop protocols for and maintain laboratory equipment; troubleshoot and resolve problems; ensure compliance with lab protocols and safety standards, policies and procedures; performing complex data gathering and analysis. This role serves to assist with conducting pre-clinical research aimed at validating, testing products and discovering, developing innovative medical technologies | 1/26/2020 |
| 605 | Poly Peptide Group San Diego, CA Quality Control Chemist BS/BA in chemistry or biochemistry Exp: 0-2 years |
Prepare samples for analysis, analyze, and report results. Prepare controlled documentation in support of the sampling, analysis, and reporting of results. Analyze data with respect to standards or to previously determined parameters. Perform sampling and testing of raw materials according to PPL-SD procedures. | 1/26/2020 |
| 606 | Poly Peptide Group San Diego, CA GC Specialists- Quality Control BS/BA in chemistry or biochemistry Exp: 0-2 years |
Prepare samples for analysis, analyze, and report results. Prepare controlled documentation in support of the sampling, analysis, and reporting of results. Analyze data with respect to standards or to previously determined parameters. Perform sampling and testing of raw materials according to PPL-SD procedures. | 1/26/2020 |
| 607 | Poseida Therapeutics San Diego, CA Research Technician or Associate Nanoparticle Formulation BS or MS in pharma sciences, bioengineering, chemistry Exp: 1+ years in industry |
his position offers an exciting opportunity to develop non-viral delivery tools for gene editing and gene therapy applications. This person will be engaged in execution of formulation discovery experiments directed toward discovering and developing novel nanoparticle systems for delivering nucleic acids and proteins. Work at the direction of senior Formulation scientists to formulate multi-component nanoparticles encapsulating nucleic acids | 1/26/2020 |
| 608 | Poseida Therapeutics San Diego, CA Research Associate, In Vivo Gene Therapy MS in immunology or biological sciences Exp: 0+ years |
The Research Associate will play a key role in advancing exploratory gene therapy programs that leverage our cutting-edge piggyBac® DNA Modification technology. Actively participate in our proprietary gene therapy platform technologies to create new human therapeutic candidates. Develop and perform research involving various in vitro and animal laboratory techniques including PCR, ELISA, cell/tissue isolations, microscopy, in vivo procedures and animal imaging | 1/26/2020 |
| 609 | Poseida Therapeutics San Diego, CA Research Associate, In Vivo MS in biological sciences or pharmacology Exp: 1+ years in biopharmacueticals |
This position offers an excellent opportunity to develop CAR-T in an exciting and dynamic environment focused on cutting-edge technology. This person will be engaged in in vivo activities directed toward discovery and characterization of novel CAR-T for oncology. Execute studies in mice in support of in vivo pharmacology projects, including tumor cell inoculation, tumor measurement by caliper or imaging, i.v. injections, and blood draws | 1/26/2020 |
| 610 | Poseida Therapeutics San Diego, CA Research Technician, Gene Editing and Gene Delivery BS in biological sciences/technology, or engineering Exp: 0-2 years |
The Research Technician will play a key role in advancing exploratory gene therapy programs that leverage our cutting-edge piggyBac® DNA Modification technology. Actively participate in our proprietary gene therapy platform technologies to create new human therapeutic candidates. Develop and perform research involving various molecular and cell biology techniques including nucleic acid development, transfection, cell culture and transgene expression. | 1/26/2020 |
| 611 | PPD Richmond, VA Scientist - Cell Culture - Vaccine Sciences MS in biological sciences or pharmacology Exp: 0-2 years |
As a Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and sample analysis serves as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. Performs a variety of complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and /or biological matrices for stability and analytical testing. | 1/26/2020 |
| 612 | PPD Middleton, WI Associate Business Systems Analyst II BS/BA Exp: 1-2 years in software environment |
Assists in formulating and defining systems scope and objectives through research and fact-finding combined with a basic understanding of business systems and industry requirements. Analyzes business and user needs and documents requirements. Gathers and writes requirements and design specification for basic to moderately complex systems. Verifies requirements and design comply with industry regulations and SOPs/WPDs. | 1/26/2020 |
| 613 | PPD Middleton, WI QA Auditor I - Labs BS/BA or AS/AA Exp: 1-2 years in QA or lab experience |
As a QA Auditor I, you will assure the quality of lab data and reports. Conduct internal and/or external audits to ensure compliance with established quality assurance processes, standards, global regulatory guidelines and/or client contractual obligations. Identify and address non-conformance issues. Assist in the delivery of quality services for contracted quality assurance audits, internal site audits, laboratory audits and file audits for clients and projects. Apply company policies and procedures to resolve routine issues. | 1/26/2020 |
| 614 | PPD Middleton, WI Assistant Scientist BS/BA Exp: 0-2 years previous experience |
As an Assistant Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and sample analysis serves as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. | 1/26/2020 |
| 615 | PPD Richmond, VA Assoc QC Reviewer BS/BA or equivalent vocational qualification Exp: 0-2 years |
The Associate QC Reviewer ensures the quality of laboratory data and reports and reviews chromatographic data and related notebooks as specified by Standard Operating Procedures (SOPs). This position also evaluates data to ensure compliance with analytical methods, client criteria, Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). | 1/26/2020 |
| 616 | PPD Middleton, WI QA Auditor I - Labs BS/BA or AS/AA Exp: 1-2 years |
As a QA Auditor I, you will assure the quality of lab data and reports. Conduct internal and/or external audits to ensure compliance with established quality assurance processes, standards, global regulatory guidelines and/or client contractual obligations. Identify and address non-conformance issues. Assist in the delivery of quality services for contracted quality assurance audits, internal site audits, laboratory audits and file audits for clients and projects. Apply company policies and procedures to resolve routine issues. | 1/26/2020 |
| 617 | PPD Middleton, WI Cell Biologist - 1yr Experience BS/BA or equivalent vocational qualification Exp: 1+ years |
As an Associate Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Problem solving with assistance pertaining to extraction and/or instrumentation problems. Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP). Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers | 1/26/2020 |
| 618 | PRA Health Sciences Salt Lake City, UT Medical Research Associate HS Diploma/GED Exp: 1+ year in medical/clinical field |
Performs basic medical procedures according to protocol for specified study participants, including but not limited to informed consent, vital signs, Height,/Weight/BMI measurements, meals, water fast, phlebotomy (straight stick/draw from IV catheters), finger stick blood sugar, ECGs, UA, UDS, urine collection, fecal collection, pulse oximetry, AE/ConMed assessment , obtain medical history and assists with Investigational Product accountability | 1/26/2020 |
| 619 | Precision Redwood City, CA Research Assistant - Fresh Biological Samples BS chemical or life sciences Exp: 1-2 years lab experience |
In this role you will: You will process fresh patient specimens and nonclinical samples. You will perform PMBC or cell subset isolations, plasma fractionations, serum separations, cell thawing, cell counting and generating whole blood aliquots. You will receive and process nonclinical samples such as whole blood units and/or leukopaks. | 1/26/2020 |
| 620 | Prevail New York, NY Clinical Trial Assistant BS in sciences Exp: 1 year in clinical research |
The Clinical Trial Assistant will assist in the delivery of clinical development objectives by providing administrative support to the clinical team and will report to the Director of Clinical Operations. We are looking for an organized, detail-oriented, enthusiastic, self-motivated, hands-on collaborative person with excellent interpersonal skills. | 1/26/2020 |
| 621 | Principia Biopharma South San Francisco, CA Clinical Trial Associate BS/BA in biological/chemical sciences Exp: 1 year in clinical trial setting |
Responsible for assisting with site feasibility and recruitment, including drafting of Site Information Questionnaires. Review assigned clinical documents for clarity and accuracy. Participate in the design and implementation of case report forms (CFRs), CRF and completion guidelines. Responsible for creation and update of Investigator Site Files from template supplied, including printing of required study documents. Review of data fields within the electronic data capture (EDC) systems, including performing and collating and downloading reports to support study management and data review | 1/26/2020 |
| 622 | Principia Biopharma Emeryville, CA Software Quality Assurance Engineer BS/BA in technical field Exp: 1 year in customer hardware devices |
As a Medical Device Software Quality Assurance Engineer at Profusa you’ll work with small teams of hardware engineers, software engineers and scientists to make products that will truly improve human health. Develop test procedures to verify software and hardware according to subsystem requirements and execution sprints. Work with Hardware and Software Engineering, Design, and Product Management teams to identify high-impact issues | 1/26/2020 |
| 623 | Progenity Ann Arbor, MI Quality Associate BS/BA Exp: 0-2 year in clinical molecular diagnostics lab |
The Quality Associate serves as a member of Progenity’s Quality Management team, whose focus is on supporting quality processes required by CLIA, CAP, NYS and other state and local requirements to ensure quality of patient test results in collaboration with the laboratory medicine and operations teams. | 1/26/2020 |
| 624 | Progenity Ann Arbor, MI Research Associate BS or MS in life sciences Exp: 0-2 years |
The Research Associate is responsible for conducting experiments aimed at developing human genomics-based products for the NIPT, carrier screening, women’s health and human disease molecular diagnostics industries. Activities include developing experimental designs with supervisory input and carrying out well planned and controlled experiments. Data analysis activities are also practiced according to approved organizational standards followed by determination of future experimental and assay development activities resulting from such analyses. Experimentation will be aimed at implementation and optimization of technologies and completing the development and verification/validation of new Laboratory Developed Tests (LDTs). | 1/26/2020 |
| 625 | Promega Madison, WI Custom Product Finishing Technician 1 HS Diploma/GED Exp: 2 year in product environment |
Work in a team environment to finish products to quality standards in order to meet custom production goals and productivity guidelines set by Promega. Fulfill customer requirements, meet and exceed customer expectations, to produce high quality, safe and effective products. This position will have a basic understanding of product finishing including process order execution, labeling, dispensing, and kitting. | 1/26/2020 |
| 626 | Bio-Techne Woburn, MA Research Associate, Flow Cytometry BS/BA in biological sciences Exp: 0-2 years |
We are looking for an outstanding Research Associate to work in our Immunology Cell & Gene Therapy R&D group. This position will provide technical and logistical support for our R&D team with an emphasis on performing immunoassays to support our QuickGelTM related products. Use flow cytometry to perform experimental and quality control assays for characterization of products. Perform product development-related experiments under general supervision. | 1/26/2020 |
| 627 | Bio-Techne San Jose, CA Manufacturing Laboratory Technician (Consumable--WES) AA Exp: 1+ year lab experience |
As a part of our San Jose team, the successful applicant will work with other members of Consumables Production, as well as a multidisciplinary team of engineers and scientists, to support the assembly of microfluidic cartridges for biotech products. Operate and maintain robotic and manufacturing equipment. Ability to use hand tools such as small wrenches, pliers, tweezers, etc. | 1/26/2020 |
| 628 | AMRI Grafton, WI Quality Assurance Associate BS in chemistry or related Exp: 1-3 year(s) |
The Quality Assurance Associate is an integral part of the AMRI team, contributing to our success by assuring that all documentation, procedures and protocols comply with GMP and FDA guidelines. In this role, you will: Conduct batch record and test data reviews, and approve batches for release. Assist in maintaining compliance of Environmental Monitoring, Equipment Calibration, and the Equipment Maintenance Program. Issue Deviation, CAPA, and OOS investigations. Track investigations and outcome. Review and recommend approval of indicated actions to senior associates or quality management. etc. | 1/20/2020 |
| 629 | ARL Bio Pharma Oklahoma City, OK Sample Administrator I / Receiving HS diploma or some college experience Exp: 0-2 years |
Occupations that fit well with this position are pharmacy technician and medical office administrative assistant. The job is performed in an office environment. This position is to perform all data entry processes needed or required to facilitate the accurate reporting of all samples submitted for testing. The Accessioner maintains sample integrity to ensure accurate and timely testing and reporting by the appropriate lab. Additionally, the Accessioner may perform additional duties requested by the Accessioning Supervisor. Minimal to moderate supervision is required. This is a safety sensitive position as defined by state and federal laws that will require working with hazardous materials and/or handling medicine. As a "safety sensitive" classification, you will be subject to drug and alcohol testing, including random testing. Marijuana is one of the substances included in the drug panel screening. etc. | 1/20/2020 |
| 630 | ARL Bio Pharma Oklahoma City, OK Data Review Chemist I BS in chemistry or related Exp: 0-2 years |
With moderate guidance, the Data Review Chemist I is responsible for utilizing the Quality Management System (QMS) standard operating procedures (SOP) and work instructions (WI) to perform quality review and approval of test results and data for compliance. The Data Review Chemist I will independently apply technical aptitude and experience to troubleshoot non-compliant data and work supportively with other Chemists to ensure generation of compliant data. This is a safety sensitive position as defined by state and federal laws that will require working with hazardous materials and/or handling medicine. As a "safety sensitive" classification, you will be subject to drug and alcohol testing, including random testing. etc. | 1/20/2020 |
| 631 | ARL Bio Pharma Oklahoma City, OK Research & Development Scientist I BS in chemistry or related Exp: 0-2 years |
The position requires the performance of variety of task including development and validation of analytical methods and qualitatively/quantitatively testing routine and non-routine client samples. This position requires knowledge of commonly used concepts, practices, procedures, and instrumentation (HPLC/IC) used in a chemistry laboratory. Research Scientist I work with direct supervision and reports to the lab supervisor. The Research Scientist I must be able to think and work independently, yet share ideas and work toward team goals. Ability to express thoughts in a clear concise manner both orally and written is also expected. Works to establish the ability to effectively prioritize and plan multiple work activities with varying deadlines and complexities. etc. | 1/20/2020 |
| 632 | ARL Bio Pharma Oklahoma City, OK Laboratory Technician - Microbiology Lab AS/BS in chemistry or related Exp: Not necessary for AS/BS candidates |
Under the supervision of the laboratory supervisor the Microbiology Lab Technician provides support tasks in a fast-paced laboratory setting. This is a safety sensitive position as defined by state and federal laws that will require working with hazardous materials and/or handling medicine. As a "safety sensitive" classification, you will be subject to drug and alcohol testing, including random testing. Marijuana is one of the substances included in the drug panel screening. Possession of a medical marijuana license will not excuse you from the testing process, or the consequences of testing positive for marijuana. etc. | 1/20/2020 |
| 633 | ARL Bio Pharma Oklahoma City, OK Laboratory Technician - Chemistry Lab AS/BS in microbiology or related Exp: Not necessary for AS/BS candidates |
This position is responsible for maintaining the cleanliness of the laboratory, the organization of supplies, reagents and standards. Additionally, this position is responsible for the daily calibration and/or verification of the balances and pH meter. The employee will have basic knowledge of commonly used laboratory concepts, practices, procedures and instrumentation and will perform limited tests under supervision. This is a safety sensitive position as defined by state and federal laws that will require working with hazardous materials and/or handling medicine. As a "safety sensitive" classification, you will be subject to drug and alcohol testing, including random testing. etc. | 1/20/2020 |
| 634 | ARL Bio Pharma Oklahoma City, OK Laboratory Technician - Analytical Lab AS/BS in microbiology or related Exp: Not necessary for AS/BS candidates |
Under general supervision, the Laboratory Technician is responsible for working collaboratively with Chemists and performing integral support tasks to ensure overall efficient testing of samples. Essential Functions: Adhere to Quality Management System (QMS). Follow prescribed safety rules and regulations in performing all assigned duties. Follow written and oral instruction. Prepare reagents, solutions, and mobile phases required for testing. Perform timely peer review of laboratory notebooks. Sample management including retrieval, storage, and disposal. Work and think independently, yet share ideas and work towards team goals. etc. | 1/20/2020 |
| 635 | Angiodynamics Queensbury, NY Engineer I, Quality BS in engineering or related Exp: 0-5 years |
The Quality Engineer is responsible for assuring product quality through participation in cross-functional product development teams and by supporting manufacturing operations. Provide QE support for existing products and assist with the transfer of new products to production to drive continual improvement. Utilize quality tools to implement quality improvements, process mapping, process validations, software validations, production efficiency improvements, and process controls. Support product complaint failure investigations. Create and/or approve process validation protocols and reports. Initial corrective action reports as appropriate and investigates and implements corrective and preventive action plans. Participate with the material review board in determining the disposition of nonconforming materials. Design verification and validation strategy development and review and approval of validation and verification protocols and testing activities. etc. | 1/20/2020 |
| 636 | ANGLE Toronto, ON Laboratory Manufacturing Associate HS diploma or equivalent Exp: 1-2 years |
The Manufacturing Associate works in a laboratory and clean room environment maintaining and operating standard laboratory equipment and executing routine manufacturing procedures following prescribed SOPs. Essential Duties and Responsibilities: Assembly of consumables in a clean room environment. Maintenance and operation of standard laboratory equipment such as centrifuges, pipettes, balances and pH meters. Receipt of incoming materials. Labelling and packaging manufactured products. Recording all data and results with accuracy and responsibility. etc. | 1/20/2020 |
| 637 | ANI Pharmaceuticals Baudette, MN Contracts and Government Pricing Associate AS in finance, accounting, or related Exp: 1-2 years |
The Contracts and Government Pricing Associate assists in managing pricing for commercial contracts and assists in managing medicaid. Position Responsibilities: Pricing for Commercial Contracts: Direct support/backup for Contract Support Department. Contract Manufacturing; Wholesalers/Distributors; Retailers and Mass Merchandisers; Group Purchasing Organizations; and Buying Cooperatives. etc. | 1/20/2020 |
| 638 | ANI Pharmaceuticals Baudette, MN Environmental, Health & Safety (EHS) Technician AS/BS in EHS, engineering, or a technical field Exp: 0-3 years |
The EHS Technician will support ANI’s Environmental, Health and Safety (EHS) program that provides for the occupational health and safety of ANI personnel, as well as compliance with environmental regulations at our facilities in Baudette, MN and Oakville, Ontario, Canada. Position Responsibilities: - Complete EHS program compliance support activities and procedure writing, as necessary. Maintain files and records pertaining to environmental, safety and industrial hygiene programs. Assist with the ANI Safety Committee activities. Coordinate and/or conduct site specific EHS trainings and activities (e.g. Lock Out/ Tag Out (LOTO) annual compliance tasks, incident investigation, ergonomics, respirator user clearance coordination, respirator fit testing, audiometric testing coordination, emergency action planning, hazard communication, lab safety inspections, etc.) and ensure these are documented appropriately. etc. | 1/20/2020 |
| 639 | ANI Pharmaceuticals Baudette, MN Microbiologist BS in microbiology, biochemistry, or related Exp: Entry level |
This position is responsible for independently performing microbiological testing, as defined by governing standard operating procedures. This is an entry level professional position in the Quality Control Microbiology Laboratory. Position Responsibilities: - Perform microbiological testing on raw materials and finished product samples. Prepare standards, stock cultures, microbiological media and samples in accordance with approved methods. Identify microorganisms. Set-up and confirm suitable operation of equipment and instrumentation. Collect data and generate/report results in accordance with governing test methods and SOPs. Perform review of data collected under approved methods. Provide accurate assessments of data integrity, and document findings. Perform calibration, preventative maintenance and repairs as needed on instrumentation. Perform cGMP tasks such as laboratory housekeeping, auditing documentation, and maintenance of microbiology laboratory supplies. | 1/20/2020 |
| 640 | ANI Pharmaceuticals Baudette, MN Operator I - Production HS diploma or equivalent Exp: 1-2 year(s) |
This position is responsible for operating pharmaceutical packaging machines/equipment. Position Responsibilities: Assists in material handling, equipment set-up and breakdowns, documents process according to Master Production Records, and works with trained operators at assigned work centers to learn all aspects of the position, including batch record documentation, equipment set-up, operation and clean up. | 1/20/2020 |
| 641 | ANI Pharmaceuticals Baudette, MN QA Validation Technician HS diploma or equivalent Exp: 0-2 years |
This position is responsible for providing support to the Validation Department in execution of validation activities necessary to support department objectives and procedures. Position Responsibilities: Performance validation protocols to include but not limited to: Installation and Operation Qualification of Equipment, Process Validation and Qualification, Environmental Monitoring, Cleaning Validation swabbing. Coordination of required documentation in support of the validation packages: routing document for review and approval, coping / scanning / filing of documents. Preparation of sampling to include generation of sample labels and coordination of physical resources required to perform sampling. Audit of Validation protocol documentation to ensure that the information contained in the validation package is consistent with the supporting raw data. etc. | 1/20/2020 |
| 642 | ANI Pharmaceuticals Baudette, MN QC Analyst BS in chemistry, pharmacy, or related Exp: Entry level |
This position is responsible for independently performing laboratory testing, as defined by governing test methods and standard operating procedures. This is an entry level professional position in the Quality Control Laboratory. Position Responsibilities: Perform testing on raw material, in-process, and finished product samples. Prepare standards and samples in accordance with approved methods. Set up and confirm suitable operation of equipment and instrumentation. Collect data and generate/report results in accordance with governing test methods and SOPs. Perform review of data collected under approved test methods. Provide accurate assessments of data integrity, and document findings. etc. | 1/20/2020 |
| 643 | ANI Pharmaceuticals Baudette, MN QC Technician HS diploma/AS/AA Exp: 0-5 years |
This position is responsible for support of QC testing activities. These responsibilities include: Position Responsibilities: Washing Laboratory Glassware. Sampling of Raw Materials. Inspection of Packaging Components. Minor Raw Material Testing. Filing of Laboratory Records and Documents. Special Project Assignments. Auditing Samples, Logbooks and Data Records. | 1/20/2020 |
| 644 | Applied Medical Rancho Santa Margarita, CA Software Engineer - Web Developer (Full Stack) BS in computer science, computer engineering, or related Exp: 0-2 years |
The Applied Medical Simulation team was developed by Applied Medical as a result of the company’s founding purpose to improve patient outcomes through the delivery of affordable, accessible and high quality healthcare solutions. We maintain that surgical education, developed in close collaboration with the surgical community, is critical to advancing skills and improving clinical outcomes. As an Engineer I you will be responsible for working within the framework of a team and performing the following activities: Communicate with product experts, UI designers, and engineers to fully understand business requirements. Break down business requirements into clear and actionable tasks. Turn business requirements into clean, testable, and maintainable code. etc. | 1/20/2020 |
| 645 | Applied Medical Rancho Santa Margarita, CA Production Associate - Assembly/Packaging (2nd shift) unspecified Exp: 1-2 year(s) |
As a Production Associate on 2nd shift, you will be responsible for working within the framework of a team in a cleanroom or manufacturing environment, and performing the following activities: Perform all manufacturing operations in a cleanroom or non-cleanroom environment such as assembly, inspection, and machine operations. Comply with Applied Medical Quality Systems (QS) including SOPs, MIs, QIs and TMs. Comply with safety and company policies. Comply with engineering drawings, shop order operations and sequence. Follow production schedules and meet production and quality goals. Perform manufacturing operations efficiently with or without tools and/or equipment. etc. | 1/20/2020 |
| 646 | Applied Medical Rancho Santa Margarita, CA Production Associate - Assembly/Packaging (3rd shift) unspecified Exp: 1-2 year(s) |
As a Production Associate on 2nd shift, you will be responsible for working within the framework of a team in a cleanroom or manufacturing environment, and performing the following activities: Perform all manufacturing operations in a cleanroom or non-cleanroom environment such as assembly, inspection, and machine operations. Comply with Applied Medical Quality Systems (QS) including SOPs, MIs, QIs and TMs. Comply with safety and company policies. Comply with engineering drawings, shop order operations and sequence. Follow production schedules and meet production and quality goals. Perform manufacturing operations efficiently with or without tools and/or equipment. etc. | 1/20/2020 |
| 647 | Aprecia Pharmaceuticals East Windsor, NJ Process Development Engineer BS in a technological field Exp: 1-2 year(s) |
This position typically works days, but responsibilities for this role may be covered across multiple shifts. Knowledge, Skills and Abilities: Solid knowledge of material characterization and process experience with pharmaceutical powder based solid oral formulations. Practical understanding of statistical control and software for data management and evaluation. Experience working with technical projects that span multi-functional teams. Excellent problem solving skills using team-based approach and known techniques for root cause analysis. Good writing skills for clear communication and accurate reporting. etc. | 1/21/2020 |
| 648 | Aprecia Pharmaceuticals East Windsor, NJ Analytical Development Scientist MS in chemistry or related Exp: Not necessary for MS candidates |
This position is responsible for performing routine testing of raw materials, intermediates, and finished product to support product development. Works with minimal supervision to assist in analytical method development and pre-validation. Interacts extensively with Product Development and Quality functions to proactively deliver Analytical Development supports and to leverage analytical sciences to characterize and understand formulations and novel 3DP (three-dimensional printing) manufacturing processes. In addition, this position is also responsible for writing protocols, development reports, and SOPs (standard operating procedures); training others on analytical techniques; being familiar with USP/NF (United States Pharmacopeia/National Formulary) analytical procedures; and maintaining an understanding of cGMPs (current Good Manufacturing Practices) and ICH (International Conference on Harmonization) guidelines. etc. | 1/21/2020 |
| 649 | Aptar Pharma Congers, NY Injection Molding Technician unspecified Exp: 1-3 year(s) |
Aptar Pharma is growing rapidly and has an exciting opportunity for a skilled Injection Molding Technician within in our Production team at our facility in Congers, New York. Aptar Pharma is part of Aptar Group, a global leader in the development and production of dispenser systems for the packaging industry. Aptar Pharma has been setting the standard for the drug delivery industry for decades and continue to break new ground providing innovative drug delivery devices, components and services, enabling the success of our clients. If you are eager for new challenges in Production in a fast-paced growing Company, we are the next step in your career! etc. | 1/21/2020 |
| 650 | Aptar Pharma Congers, NY Quality Control Technician HS diploma or equivalent Exp: 1+ year(s) |
The Quality Control Technician performs dimensional and functional testing on Aptar Congers product to ensure compliance with established quality standards and customer specifications. The Quality Control Technician is responsible for documenting and communicating nonconformities to supervision. All Quality specifications, work instructions, as well as actions that support team work, safety, efficiency and cGMP adherence are to be followed. Primary Duties and Responsibilities: Perform incoming inspection and disposition of components. Perform analytical testing such as Spray Pattern testing, measurements, in-process and release testing as per the Quality specification. Initiate Discrepant Material Report for non -conformities. etc. | 1/21/2020 |
| 651 | Evotec Watertown, MA Associate Scientist - ADME BS/MS in biology, chemistry, or pharmaceutical science Exp: BS: 1+ year(s), MS: 0-3 years |
The team seeks a scientist that is a highly motivated individual to performing a range of in vitro ADME assays (ex: solubility, microsomal stability, PPB, Cyp inhibition, Permeability) and PK studies to support the discovery and development of small molecule and peptide therapeutics. In this lab-based position, the qualified candidate will work closely with our established team to develop and conduct ADME assays to address ADME questions and support projects. The successful candidate would have the opportunity to interact with multidisciplinary project teams. | 1/21/2020 |
| 652 | Evotec Rahway, NJ Lab Technician AS/BS Exp: BS: entry level, AS: 1-2 year(s) |
Evotec (US) Inc. has a Lab Technician position available, located at a compound management department at a Merck facility. The position entails following a specific set of guidelines to weigh, transfer and record chemical compounds. More specifically, the individual will prepare vials and tubes, place them in a chemical hood on an analytical balance, and transfer the vials or tubes using spatulas and pipettes and record the results. The balance will be connected to a computer that will collect the weights as they are measured. Responsible for services including but not limited to the day to day tasks of Screen File Build, as well as general compound management services including, but not limited to: robotics, validation, and overall laboratory maintenance. etc. | 1/21/2020 |
| 653 | Evotec Princeton, NJ Research Associate MS in biological engineering or a biological science Exp: 1 year |
The candidate will join a cross-functional team responsible for profiling and production of recombinant proteins and assay ready cells for assays and biophysics. The applicant will be part of a team of up to 25 people in cell sciences, recombinant protein expression and purification from eukaryotic and prokaryotic hosts. Candidates will be responsible for the production, purification and/or characterization of a range of protein targets within the pharmaceutical arena. etc. | 1/21/2020 |
| 654 | Archer Boulder, CO Software Engineer in Test I/II/III BS/BA Exp: 0-6+ years |
Software Engineers in Test build tools and test cases to verify software used in next-generation sequencing. They apply software engineering and computer science techniques to the unique problems of software testing. You will be working on a day to day basis with a team of software engineers and technical product managers defining and updating software requirements and design and translating them into automated tests. You will be responsible for writing, reviewing, updating regulated documents. As required, you will build test harnesses and other testing tools to accelerate testing. etc. | 1/21/2020 |
| 655 | Archer Boulder, CO Regulatory Affairs Associate BS/BA Exp: 3-12 months |
The Regulatory Affairs Associate, reporting to the Regulatory Affairs Director, will help develop, implement and maintain the Regulatory Processes within the Quality Management System (QMS), including creation and maintenance of the documentation associated with filing for high risk medical device for the US and OUS submissions. RESPONSIBILITIES: Assist with the development and implementation of regulatory procedures. Assist in the communication with regulatory agencies. Support creation and manage filings for IDE, 510(k), PMA and EU Technical Files. etc. | 1/21/2020 |
| 656 | Arcus Biosciences Hayward, CA Bioanalysis Research Associate BS/MS in chemistry, biochemistry, or related Exp: 1-4 year(s) |
Arcus Biosciences is seeking a highly motivated and team-oriented candidate for the position of Research Associate in the Drug Metabolism and Pharmocokinetics (DMPK) Department. The successful applicant will be responsible for performing bioanalysis of in vitro and in vivo samples to support discovery and development programs. Core responsibilities: Develop, troubleshoot, and validate LC-MS/MS based bioanalytical methods. Analyze, summarize and report preclinical pharmacokinetic and toxicokinetic results. Conduct in vitro ADME experiments such as metabolic stability, plasma protein binding, CYP inhibition and induction assay as necessary. etc. | 1/21/2020 |
| 657 | Arcus Biosciences Hayward, CA Research Associate BS/MS in immunology, cell biology, biochemistry or related Exp: 1-2 year(s) |
Our Pharmacodynamics (PD) group is focused on the development and execution of assays to evaluate engagement of our drugs and their biological effects in patient samples. Our role within the Quantitative Biology (QB) department is a central, critical element of our translational research engine. We are looking to expand the size and scope of this team, with positions available immediately. The ideal candidate will have a working knowledge of immune-based in vitro assays, flow cytometry, ELISA, common molecular biology techniques, and data analysis/visualization software. Direct experience with isolation and culture of primary cells is strongly preferred. etc. | 1/21/2020 |
| 658 | Argonaut Manufacturing Services Carlsbad, CA Drug Product Manufacturing Assistant HS diploma or equivalent Exp: 0-2 years |
The purpose of this position is to perform tasks and operations relevant to the bulk formulation and/or filling operations required for sterile production of liquid injectable pharmaceutical products under cGMP regulations in Drug Product Manufacturing. General Responsibilities: Performs various routine manufacturing tasks under the direction of internal SOP’s and cGMP guidelines. Prepares material components for manufacturing operations. Documents steps clearly and completely in production batch records, log books and other controlled forms. Participates in inspection readiness activities. Performs basic arithmetic and algebraic computation. Maintain cleanliness of areas and equipment. etc. | 1/21/2020 |
| 659 | Argonaut Manufacturing Services Carlsbad, CA Quality Control Assistant BS/BA in a life science Exp: 1-2 year(s) |
The purpose of this position is to provide support services by means of executing the analysis of in-process, finished product, and stability test samples. Further support services include Environmental Monitoring and Raw Material receipt activities. QC personnel are responsible for compliance with QC policies and procedures within the QC laboratory, company policies, and cGMP guidelines. This position will report to the Director, Quality Control. General Responsibilities: Directly contributes to daily laboratory operations for QC Chemistry and Microbiology, in full compliance with applicable SOPs and safety guidelines. Analyzes on a routine basis in-process, release, and stability test samples in accordance with established QC test methods and specifications. etc. | 1/21/2020 |
| 660 | Arrakis Therapeutics Waltham, MA Research Associate, Target Biology and Translational Medicine BS in biology or related Exp: 1+ year(s) |
The mission of Arrakis Therapeutics is to extend small molecule medicines into new realms of biology by discovering and developing compounds that selectively target RNA (“rSM”). By targeting distinct RNA structure/function relationships, Arrakis is generating drug candidates with novel mechanisms of action for molecular targets that are challenging to drug in disease areas with high unmet medical need. As cell-based assay development and in-cell evaluation of high priority targets are critical to our mission, the Research Associate will make a major impact by assisting in the development and validation of new cell-based assays for high throughput screening. The Research Associate will also provide tissue culture support to aid critical projects, leveraging a broad array of tissue culture techniques, including cutting-edge techniques such as CRISPR editing. etc. | 1/21/2020 |
| 661 | Arrakis Therapeutics Waltham, MA Research Associate, Molecular Biology BS in molecular biology, biochemistry, or biology Exp: 1+ year(s) |
The mission of Arrakis Therapeutics is to extend small molecule medicines into new realms of biology by discovering and developing compounds that selectively target RNA (“rSM”). By targeting distinct RNA structure/function relationships, Arrakis is generating drug candidates with novel mechanisms of action for molecular targets that are challenging to drug in disease areas with high unmet medical need. As Arrakis uses next generation sequencing (NGS) to enable the RNA structure and function assays that are central to our mission, the Research Associate will have an opportunity to make a large impact on our effort to establish world-class NGS methods and perform sequencing-based assays. etc. | 1/21/2020 |
| 662 | Arraystar Rockville, MD Lab Assistant - Molecular Biology BS in a biological field Exp: 1-2 year(s) |
Responsibilities: Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. Assist with the generation and updating of laboratory SOPs. Perform basic lab maintenance tasks such as ordering lab supplies, and keeping detailed lab records. Communicate with clients to obtain/verify information of their projects, orders or requests. | 1/21/2020 |
| 663 | Arrowhead Pharmaceuticals Madison, WI Research Technician BS in cell biology, molecular biology, biochemistry or related Exp: Entry level |
Arrowhead Research seeks a full time Research Technician to join its drug targeting team at its research and development facility in Madison, WI. The candidate should be highly motivated, and enjoy working with a team of scientists in a fast-paced and highly cross-disciplinary environment. The individual will be primarily responsible for providing technical assistance in RNA and DNA isolations, cell culture, and general laboratory maintenance. | 1/21/2020 |
| 664 | Arrowhead Pharmaceuticals Madison, WI Scientist, Biology BS/MS in cell biology, molecular biology, or biochemistry Exp: 0-3 years |
Arrowhead is seeking a senior biologist to join our Research Department. The candidate will be a key member of drug discovery and development teams. S/He will be expected to: Design and execute/conduct in vitro or in vivo studies to facilitate drug discovery and development. Participate in new mechanistic studies. Present research findings to project teams and governance bodies and prepare technical reports. Maintain a high level of productivity in the lab and perform critical experiments. May mentor/supervise a team of one or more and guide and evaluate the performance of those individuals; is accountable for the effective performance of the team/individuals. | 1/21/2020 |
| 665 | Arrowhead Pharmaceuticals Madison, WI Associate Chemist, Bioconjugation BS/MS in chemistry or biochemistry Exp: Entry level |
Arrowhead Pharmaceuticals is seeking an Associate Scientist to join the Chemistry Department. The successful candidate will primarily focus on bioconjugation, analytical chemistry, formulation, and some small molecule organic synthesis. S/He will be joining a team of highly motivated and experienced scientists, and will contribute to the success of Arrowhead programs. S/He will be expected to: Perform bioconjugation, purification, and characterization of oligonucleotide conjugates. Identify critical issues/steps in a conjugation and solve the problems in a timely fashion. Maintain a well-documented laboratory notebook. Track progress against project timelines, generate regular status updates, and communicate progress and issues to management. etc. | 1/21/2020 |
| 666 | Arrowhead Pharmaceuticals Madison, WI Associate Scientist, Discovery Analytical Chemistry BS/BA in chemistry or biology Exp: 1+ year(s) |
Arrowhead is seeking a highly motivated associate analytical chemist to join our growing Discovery Chemistry team. The successful candidate will be tasked with biological sample preparation and running HPLC to support ongoing discovery activities. S/He will be expected to: Follow the instructions to prepare samples from various biological matrix such as plasma, urine, tissues etc. Perform sample analysis using HPLC. Communicate on a timely basis with other functional groups. Generate regular status updates, and communicate progress and issues to management. Keep good documentation. Detail oriented and flexible for changes. Self-motivated team player with the ability to thrive in a fast paced, multi-disciplinary, matrixed environment. Maintain a high level of productivity in the lab and perform critical experiments. etc. | 1/21/2020 |
| 667 | Arrowhead Pharmaceuticals Madison, WI Associate Chemist, CMC MS in chemistry or biochemistry Exp: Entry level |
Arrowhead Pharmaceuticals is seeking a highly motivated individual to become a part of its scientific team. We have an immediate opening for an Associate Scientist to work as a Chemist in the Chemistry, Manufacturing, and Controls Group focusing on oligonucleotide synthesis development. This is an ideal position for an individual with an organic or biological chemistry background who has an interest in projects related to novel technology in synthesis and purification of oligonucleotides and bioconjugates. The successful candidate will be expected to: Work closely with senior chemists on development of new synthetic approaches to desired compounds with an eye toward large-scale synthesis. Cooperate with other chemists in the group in preparation of complex organic constructs. Perform solid-phase synthesis and purification of oligonucleotide drug candidates. Analyze small-molecule and macromolecular targets using standard methods. etc. | 1/21/2020 |
| 668 | OriGene Rockville, MD Research Associate - Molecular Biology BS in life sciences Exp: 1+ year in DNA cloning/cell culture |
The qualified candidate will support company’smolecular biology operations,principally performing DNA cloning and molecular biology experiments following protocols. Perform experimentsfollowing protocols for plasmid DNA purification, DNA digestion, gel electrophoresis,DNA fragment purification, ligation, transformation, DNA quantitation,DNA sequencing,PCRand cell culture. | 1/18/2020 |
| 669 | OriGene Rockville, MD ResearchAssociate, Protein Purification BS or MS in biological sciences Exp: 1+ year in DNA cloning/cell culture |
Research Associate in Protein Department: TheOriGene ProteinDepartmenthas been developing genome-wide purified recombinant proteinfrom human HEK293 cells, over-expressed lysates,Knockout (KO) cell lysates,cancer cell lines lysatesandheavy-labeled full-length protein.We are looking for individuals who would like to be a part of our Protein Department. Willingness to learn relevant molecular biology, transfection and hands on skills of various biochemical assays such as SDS-PAGE electrophoresis, BCA, ELISA. Western blot, recombinant protein purification | 1/18/2020 |
| 670 | OriGene Rockville, MD Research Associate –Immunology BS in biology/biochemistry or life sciences Exp: 1-2 years in industry |
Involves multiple de novo R/D projects for antibodyand assay products development.Performsvalidation tests on variant sera or antibody samples. Participates other duties such as antibody production, purification and conjugation. Strong organizational skills and possess strong ability to identify, analyze and solve the problems independently. Records experiment procedure and results in notebooks and computer accurately. | 1/18/2020 |
| 671 | Johnson & Johnson Eugene, OR Junior Sales Consultant (Trauma) – Eugene, OR BS/BA Exp: 0-3 years relevant experience |
Assist team in retaining and supporting further penetration with existing customers, while supporting product conversions with new customers. Assist in the attainment of established sales goals including market share objectives in prescribed territory. Apply knowledge of sales process, product portfolio and customer knowledge to improve sales outcomes. | 1/18/2020 |
| 672 | Johnson & Johnson Malvern, PA Associate Scientist, Drug Product Development Engineer MS in related sciences Exp: 1 year lab experience |
The Associate Scientist, Drug Product Development Engineer in the Parenterals and Liquids (P & L) group will be responsible for performing experimental studies related to process improvement and quality compliance efforts as it relates to formulation/process development and testing of therapeutic proteins or other biologics including monoclonal antibodies (mAbs). This includes the mathematical modelling; and development and optimization of the technical operations associated with liquid and lyophilized biologics formulations/processes, as well as execution of pharmacy manual and stability studies. | 1/18/2020 |
| 673 | Johnson & Johnson Malvern, PA Assistant Scientist BS or MS in biological sciences Exp: BS: 1-2 years, MS: 0 year |
The Assistant Scientist in the Parenterals and Liquids (P & L) group in Drug Product Development will be responsible for performing experimental studies as it relates to process development and testing of therapeutic proteins or other biologics including monoclonal antibodies (mAbs), virus like substances, cell-based therapeutics (CAR-T) and gene therapy related molecules. This includes the development and optimization of the technical operations associated with liquid and lyophilized biologics processes, as well as execution of stability studies. Additional responsibilities include but are not limited to development and optimization of liquid and lyophilized biologics formulations, as well as execution of characterization plans and stability studies | 1/18/2020 |
| 674 | Bausch Health Lynchburg, VA Distribution Associate I (579) HS Diploma/GED Exp: 6 months distribution/warehouse experience |
As directed by the supervisor and/or group leader perform functions to fulfill orders for shipment to customers. This may include but is not limited to customer service support, returns processing, replenishment, cycle counting, picking, packing, and manifesting. Employee may be trained in any or all of the required disciplines depending on business needs. Employee must work all assigned hours and may also be required to perform other duties as directed by the supervisor and or group leader. | 1/18/2020 |
| 675 | Bausch Health Greenville, SC Distribution Associate (306) HS Diploma/GED Exp: 1 year distribution/warehouse experience |
Receiving operation is responsible for accurately receiving product from the B&L Manufacturing Operation along with other third party vendors, putting product into assigned storage locations, and retrieving product and delivering it to the pick area and/or shipping lanes. Also, perform shipping duties including preparing orders for shipment consisting of pallet stacking, labeling and wrapping. All order transaction controlled via RF computer. Shipping operation is responsible for accurately retrieving product from the pick area. Also, perform shipping duties including pallet stacking, labeling and wrapping. Other responsibilities include truck loading and general warehouse housekeeping. All order transaction controlled via RF computer. | 1/18/2020 |
| 676 | Orthofix Remote, na Associate Territory Manager, PhysioStim - Philadelphia HS Diploma/GED Exp: 1 year sales experience (business to business) |
To assist Territory Manager in achieving sales results at or above established quotas for total and individual product segments. To provide direct, personal and timely service, via a consultative approach, to physicians, podiatrists, patients, managed care or other payors, representing Orthofix in a professional and straight forward manner. Additional responsibilities will include managing, directing, and assisting any authorized Orthofix distributor. Some shift in emphasis from calling on doctors to calling on payors is dictated by changes in the health care environment. | 1/18/2020 |
| 677 | Orthofix Lewisville, KY Assembler I - BioStim HS Diploma/GED Exp: 1-2 years electrical assembly |
Perform basic electrical and mechanical assembly functions as defined by the Manufacturing Procedure. Must have the ability to meet or exceed all minimum departmental performance levels in the areas of Quality, Attendance and Productivity. Perform a wide range of electrical and mechanical assembly functions utilizing soldering and hand-eye coordination skills. Receive and comprehend formal documentation, safety, GMP, Workmanship and Hazardous Chemical Training. | 1/18/2020 |
| 678 | Miltenyi Biotec Sunnyvale, CA Manufacturing Science and Technology Associate BS/BA in biological sciences Exp: 1-3 years in cell culture/clinical processing |
The unique duties of this position will consist of supporting the development of scalable cell culture processes as well as the manufacturing of primary human cells including activities that involve graft engineering for cellular therapies. Furthermore, you will be responsible for completing successful qualifications and material flow procedures for clean room operations and assisting in the development, writing, and review of SOPs, material specifications, standard manufacturing procedures, batch records and other GMP documentation. This position will primarily involve routine GMP cell processing and facility/equipment support with research and development work on an as needed basis. | 1/18/2020 |
| 679 | Miltenyi Biotec Gaithersburg, MD PD Associate I BS/BA Exp: 1+ year experience will cell culture/filtration/chromotography |
As a member of the Lentigen Technology Process Development team, you will have the exciting opportunity to support the development and tech transfer of processes to manufacture purified Lentiviral vectors used for pre-clinical and clinical products. You will apply your knowledge and prior laboratory experience to support the pre-clinical and clinical manufacturing of Lentiviral vector products. Familiarity with cell culture and/or purification technologies and analytical methods will enable you to assist in the development and tech transfer of processes compliant with GMP manufacturing requirements. | 1/18/2020 |
| 680 | Miltenyi Biotec Sunnyvale, CA Manufacturing Associate BS/BA in biological sciences Exp: 1-3 years in cell culture/clinical processing |
As a member of the Miltenyi Biotec Manufacturing team, you will have the exciting opportunity to participate in both the manufacture and process development of T-cells and multiple other cell therapy products within a GMP environment. The unique duties of this position will primarily consist of manufacturing primary human cells including activities that involve graft engineering for cellular therapies as well as supporting the development of scalable cell culture processes. Furthermore, you will be responsible for completing successful qualifications and ongoing support procedures for clean room operations and assisting in the development, writing, and review of SOPs, material specifications, standard manufacturing procedures, batch records and other GMP documentation. | 1/18/2020 |
| 681 | Miltenyi Biotec Gaithersburg, MD R&D Scientist, Purification & Characterization MS in molecular biology/immunology/virology Exp: 0-2 years |
As a member of the Lentigen Technology team, you will have the opportunity to develop methods for the separation of different particle types and their characterization. Also, you will develop, evaluate and implement novel analytical methods for the fine characterization of viral vectors and exosomes, in view of the distinction of viral vectors from exosomes. You will design specific experiments to test LV function, perform statistical analysis of results, and communicate results internally, for use in publications, and in scientific meetings. Your responsibility will also include the development of chromatography-based separation steps in-view of the optimization of an existing purification protocol and their standard characterization. | 1/18/2020 |
| 682 | Miltenyi Biotec Sunnyvale, CA Process Development Associate BS/BA in life sciences Exp: 0-2 years |
As a member of Miltenyi Biotec’s Process Development team, you will have the exciting opportunity to support the development of new processes that will generate cellular therapeutic products. You will apply your GLP/GMP experience to perform and maintain cell cultures using aseptic techniques. Ideally, you will be able to order materials and maintain inventory with the goal in mind that every effort is aimed at developing and qualifying processes required for clinical cell and gene therapy products. In addition to your primary responsibilities, you will document activities for reproducibility, clean and maintain laboratory equipment and support team members as needed | 1/18/2020 |
| 683 | Miltenyi Biotec Auburn, CA Accounting Associate AS/AA Exp: 1-3 years in corporate business/accounting |
As a key member of the Miltenyi Biotec Accounting team, you will provide accounts payable and accounts receivable support including collecting and posting payments, assisting in debits and credits when needed, reconciling back-up documents to invoices, processing invoices through receipt and account verification, maintaining vendor and accounting files, and preparing and verifying bank deposits. Within this role, you will perform month end duties as required inclusive of GL review and journal entries, as well as providing general administrative support. | 1/18/2020 |
| 684 | Pace Analytical Golden Valley, MN Food Sample Handling HS Diploma/GED Exp: 0-3 years relevant experience |
The Sample Handling Lab Technician will work as part of a fast-paced sample prep team that organizes and processes materials for further analytical testing. Responsibilities include knowledge or use of various grinding mills and procedures for the preparation of samples for Analytical testing. Other responsibilities include filing, data entry, customer service and general lab upkeep (e.g. ordering and stocking supplies, cleaning, equipment maintenance) | 1/18/2020 |
| 685 | Pace Analytical Maplewood, MN Complaint Analyst - Health Care BS/BA in biomedical sciences or pre-med Exp: 1+ years |
This candidate will manage and support complaint handling workflow for one or more client products. Assure appropriate prioritization and timely closure of complaints. Assure compliance with all FDA regulations and internal procedures related to complaint handling. Manage complaint handling workflow. Meet daily team and individual complaint handling output goals. Perform complaint investigation to either close the complaint or determine need for more in-depth analysis | 1/18/2020 |
| 686 | Pace Analytical Maplewood, MN Lab Analyst - Mechanical Engineer BS in sciences/engineering Exp: 0-1 years in mechanical engineering |
This Lab Analyst will work in a product development lab to design and build hardware related to food safety equipment. Perform reliability testing and analysis related to hardware usage. Design and develop high level prototypes. Analyze data and create summary reports . | 1/18/2020 |
| 687 | Pace Analytical Naperville, IL Lab Analyst - Chemical and Physical Testing AS/AA in applied sciences, BS in chemistry/biology preferred Exp: 0-2 years |
The main function of a laboratory technician is to conduct chemical and physical laboratory tests to assist scientists in making qualitative and quantitative analyses of solids, liquids, and gaseous materials. Set up and conduct chemical experiments, tests, and analyses using techniques such as chromatography, spectroscopy, physical and chemical separation techniques, and microscopy. Conduct chemical and physical laboratory tests to assist scientists in making qualitative and quantitative analyses of solids, liquids, and gaseous materials | 1/18/2020 |
| 688 | Pace Analytical Minneapolis, MN Quality Engineer Assistant BS in chemistry or related Exp: 1+ years in QA |
Candidate will work with Quality Assurance as a Quality Engineer Assistant to ensure compliance of manufacturing processes in a GMP environment. This person will serve as reviewer and/or approver for required documentation in a pilot plant/manufacturing setting. This position is very project orientated, so the QE Assistant can expect every day to be different with changing responsibilities and priorities. | 1/18/2020 |
| 689 | Pacific BioLabs Hercules, CA CLIENT SPECIALIST BS/BA Exp: 1 year in client facing role |
The Client Specialist (CS) is a full-time, on-site position to support testing department client account operations. This position will work closely with Pacific BioLabs Testing Department Heads and Business Development in ensuring that Client/Sponsor testing needs are met. The duties of the CS include 1) supporting the Client Account Manager in quote creation and quote follow-up and 2) department log-in and study file preparation. | 1/19/2020 |
| 690 | Pact Pharma South San Francisco, CA Research Associate - Tumor Immunology MS in biological sciences Exp: 1+ year in immunology/immuno-oncology |
The person in this role will be responsible for performing immunological assays to functionally characterize the patient private NeoE-specific T cells, as part of product selection for the manufacture of the adoptive cell therapy product (neoTCR-P1). This process is performed in a GMP-like laboratory setting. The candidate should enjoy operating in an exceptionally dynamic and cooperative environment and will communicate results to and coordinate efforts with a larger cross-disciplinary team of immunologists, biologists, engineers and bio-informaticians. | 1/19/2020 |
| 691 | Pact Pharma South San Francisco, CA Lab Automation Engineer BS or MS in engineering or sciences Exp: 1 year in lab |
he primary role is to interface with scientists to understand their workflows, and then develop automated solutions based on in house equipment or by identifying and bringing in the proper equipment/software solutions. More specifically the role requires scripting, testing and validating method and process development on Hamilton Vantage and Star liquid handling platforms, as well integrations with Agilent, Thermo, and other automation equipment. | 1/19/2020 |
| 692 | Pact Pharma South San Francisco, CA Research Associate II - Gene Editing MS in molecular biology/immunology/virology Exp: 1+ year |
Responsibilities will include the generation of “next generation” DNA constructs utilizing various molecular cloning techniques. The incumbent will also be involved in the use of the DNA constructs and other genome editing tools to generate modified T cells for proof-of-concept experiments. This position will also be responsible for the proper analysis and documentation of studies, the presentation of findings, and assistance generating new SOPs. The incumbent will work closely with the Tumor Immunology group for the cellular analysis of product candidates, and may also assist with novel genetic analyses. | 1/19/2020 |
| 693 | Pact Pharma South San Francisco, CA Research Associate - Clinical Immunology MS in cellbiology/immunology or related Exp: 1+ year in research |
Perform flow cytometry staining, sample acquisition, and analysis on clinical patient samples according to established standard operating procedures. Thoroughly document all work according to good documentation practices. Communicate clearly and concisely, both verbally and in the form of written reports. | 1/19/2020 |
| 694 | Pact Pharma South San Francisco, CA Research Associate I or RA II - Tumor Immunology MS in biological sciences Exp: 1+ year in immunology/immuno-oncology |
We are currently recruiting for a Research Associate I or an RA II who will report to Scientist in Tumor Immunology and continue advancing PACT’s cutting edge engineered cell product. The candidate will perform and thoroughly document ex vivo T cell functional assays according to established procedures. She/he must have excellent organizational skills and should be able to communicate clearly and concisely, both verbally and in the form of written reports. She/he will aid in drafting new protocols, improving existing workflows, and provide data for regulatory filings to support clinical development. | 1/19/2020 |
| 695 | Pall Syracuse, NY Engineer I BS in mechanical/material science engineering Exp: 0-5 years |
Looking for an enthusiastic team member to join Pall’s Inorganic Additive Manufacturing Team. Associate should be ready for hands-on engineering work in addition to working in a team environment. Duties: test stand set-up and evaluation; becoming subject matter expert on related processes; critical thinking and data analysis; creating 3D drawings; general lab duties | 1/19/2020 |
| 696 | Pall Houston, TX Material Handler I HS Diploma/GED Exp: 1 year in distribution/warehouse |
Incumbents must possess basic material handling skills and must be willing to learn and continuously expand knowledge, skills and abilities required to support this large distribution center. Collaboration and assisting/training others in completing daily work is an expectation and is critical for the role. Read and understand Standard Operating Procedures. Learn and follow standard work for all areas within a Value Stream. | 1/19/2020 |
| 697 | Pall Cortland, NY RDLP Associate MS in science or engineering Exp: 0 years |
During the two-year program, you will work alongside some of the brightest minds in the industry and will participate in four, six-month assignments engaging your technical and leadership skills. In these assignments you will experience at first hand many facets of R&D – project management and project team direction; process application studies, product design using tools like CAD or our proprietary in house filter design modules; prototype manufacture and testing; and product transfer to manufacturing. | 1/19/2020 |
| 698 | Par Pharmaceutical Rochester, MI Chemist I BS in chemistry/chemical engineering Exp: 0-1 years |
The Chemist I, under direct supervision, learns and performs QC laboratory chemical analyses of raw materials, in-process materials, stability and finished products, and testing to support process validation. May participate in investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. | 1/19/2020 |
| 699 | Par Pharmaceutical Chestnut Ridge, NY Manufacturing Operator l HS Diploma/GED Exp: 0-2 years |
The Manufacturing Operator I performs functions relating to the processing of drug products, ensuring product compliance to established current Good Manufacturing Practices (cGMPs), customer requirements and in conjunction with all Standard Operating Procedures (SOPs). Follows standard procedures to complete tasks, some of which may vary in scope, sequence, complexity and timing. Learns to apply skills and knowledge to recognize issues and to increase efficiency, throughput and quality. Learns, understands and runs processes to meet the assigned standards/routers and fulfills the assigned schedule; when these are not achieved, may participate in the debrief to understand the reasons why and what needs to be corrected moving forward. | 1/19/2020 |
| 700 | Catalent Bloomington, IN Associate Scientist - Product Development MS in sciences Exp: 0-2 years |
This role will also work to develop a thorough understanding of the techniques, processes, and applications of technical knowledge to implement a process suitable for manufacturing of both drug substance (DS) and drug product (DP). A scientist in analytical development will be responsible for developing and executing analytical methods (ELISA, HPLC, Mass Spectrometry, Spectroscopic, Biophysical, etc.) for supporting process development activities. | 1/19/2020 |
| 701 | Catalent Madison, WI Biomanufacturing Operations, Senior Associate MS/MA in biotechnology Exp: 0 years |
The Biomanufacturing Operations, Senior Associate position will independently perform batch record/date review, drafting technical documents protocols and reports. The Biomanufacturing Operations, Senior Associate will also be responsible for training/mentorship of junior staff and driving process improvement initiatives. You will work Wednesday through Saturday (4/10) on second shift and enjoy a shift premium. | 1/19/2020 |
| 702 | Catalent Harmans, MD Quality Assurance Associate I BS in life sciences Exp: 1+ years |
Quality Associate I (QA Operations) is responsible to provide Quality Assurance support real-time for GMP Manufacturing of master/working cell banks, biological bulk drug substance and finished drug product to be used for human consumption. Responsibilities include providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. Continuously monitor systems and procedures to ensure compliance with applicable regulatory and industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products. Quality Associate I (QA Operations) is responsible to provide Quality Assurance support real-time for GMP Manufacturing of master/working cell banks, biological bulk drug substance and finished drug product to be used for human consumption. Responsibilities include providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. Continuously monitor systems and procedures to ensure compliance with applicable regulatory and industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products. | 1/19/2020 |
| 703 | Catalent Madison, WI Associate, Quality Control BS/BA in biotechnololgy Exp: 0 years |
The Associate, Quality Control position requires a variety of skills necessary for biotech company operations. The position is an entry level laboratory role with the expectation that the candidate is able to be trained on technical procedures and once trained, execute them consistently and reliably. Additionally, this position will support Preventative Maintenance and basic Laboratory maintenance activities while maintaining a GMP quality system. Other duties may include data review/archiving, database entry and contributions to process improvement initiatives. | 1/19/2020 |
| 704 | Catalent Kansas City, MO Associate Scientist - Biologics BS/BA Exp: 0-3 years relevant experience |
In support of large molecule therapeutics, execute laboratory work plan / schedule developed with input from supervisor or senior team member. Sample types include in-process, release or stability. Analytical techniques may include any or all of the following: HPLC/UPLC techniques/methods (e.g. SEC, IEX, RP-HPLC, HIC, peptide map, glycan analysis, etc.). Karl Fischer, Compendia assays, (i.e. appearance pH, etc.). UV-Vis, Solo-VPE, Nano Drop | 1/19/2020 |
| 705 | Catalent Harmans, MD Quality Control Analyst - Cell Culture AS in life sciences Exp: 1-4 years in GMP clean rooms |
Perform adherent and cell culture testing in a Phase III/Commercial GMP Manufacturing facility. Includes but is not limited to: thawing, enumeration, passaging and cryopreservation of various cell line types required for QC assays. Provide support to analytical/process development to onboard new client assays or enhancement to the testing capabilities of the cell culture laboratories. Provides input on SOP revisions and may assist in the creation and editing of protocols. Works closely with manufacturing and QA to coordinate cell culture activities required to support manufacturing operations and product release activities. | 1/19/2020 |
| 706 | Catalent Harmans, MD Manufacturing Associate I AS/AA or BS/BA in engineering or biotechnology Exp: AA/AS: 0-2 years, BS/BA: 0-1 years |
The Manufacturing Associate I performs and documents cGMP activities to support upstream or downstream production areas and operations. This involves operation of process equipment, execution of validation protocols, completion of cGMP documents, creating/ revising cGMP documents and other assignments as directed. The Manufacturing Associate I performs and documents cGMP activities to support upstream or downstream production areas and operations. This involves operation of process equipment, execution of validation protocols, completion of cGMP documents, creating/ revising cGMP documents and other assignments as directed. | 1/19/2020 |
| 707 | Paragon Genomics Hayward, CA Research Associate, Operations BS/BA in life sciences Exp: 1+ years in NGS lab, or entry level |
This is a laboratory-based position with great career potential for a junior scientist or technically oriented entry level candidates who already have or wishes to gain hands-on molecular biology experience in the next-generation sequencing space. This position offers a rare opportunity to build a strong multidisciplinary foundation in an exciting space. The ideal candidate must have good interpersonal and problem-solving skills. He/she should be driven to learn and motivated to develop great products and maintain the highest quality standards. | 1/19/2020 |
| 708 | Paramit Morgan Hill, CA Functional Test Development Engineer I BS in EE, ME, or CS Exp: 0-2 years |
The effort involves following a test fixture development process that includes understanding the theory of operation of the UUT, architect/design fixtures, developing automation software GUI with a clear Pass/Fail indication and parametric record retention. Each project is unique and requires project management understanding like scheduling, working with customer as well as cross-functional team members to achieve the outcome at estimated cost, within lead time. | 1/20/2020 |
| 709 | Parexel Billerica, MA Software Engineer BS in computer science, information systems, or related Exp: 0-3 years relevant experience |
Provide programming skills and expertise in the design and development of Enterprise Architecture projects: System Integrations, Analytical and Metrics Clinical Data Warehouse, Management of Production Release processes. Independently implement solutions following provided design blueprints, using established frameworks and design patterns, adhering to requirements, standards, and functional specifications. Responsible for unit testing of all code produced using preferred unit test frameworks and technologies | 1/20/2020 |
| 710 | Parexel Billerica, MA Software Engineer BS in computer science, information systems, or related Exp: 0-3 years relevant experience |
Provide programming skills and expertise in the design and development of Enterprise Architecture projects: System Integrations, Analytical and Metrics Clinical Data Warehouse, Management of Production Release processes. Independently implement solutions following provided design blueprints, using established frameworks and design patterns, adhering to requirements, standards, and functional specifications. Responsible for unit testing of all code produced using preferred unit test frameworks and technologies | 1/20/2020 |
| 711 | PBL Assay Sciences Piscataway , NJ Assay Services Scientist I/II BS/BA in life sciences Exp: 1+ year lab experience |
The Assay Services Scientist I / II works primarily with cell culture-based bioassays, executing antiviral bioassays, ELISAs and other highly sensitive immunoassays for characterizing proteins and reagents; analyzing data and drafting client reports; and developing new and custom assays to support the growth of the Assay Services Group. Execute immunoassays on ELISA, and other highly sensitive platforms like Electrochemiluminescence (MSD), Single Molecule Array (Simoa), and Single Molecule Counting (Erenna) | 1/20/2020 |
| 712 | PBL Assay Sciences Piscataway , NJ Laboratory Technician BS/BA in biological sciences Exp: 0-3 years |
The Laboratory Technician is responsible for product manufacturing and ELISA kit optimization and stability testing following established guidelines and procedures and completing required documentation. The individual will routinely analyze raw data and generate summaries of work performed in compliance with Standard Operating Procedures (SOPs). | 1/20/2020 |
| 713 | PBL Assay Sciences Piscataway , NJ Quality Control Scientist I BS/BA in biological sciences Exp: 1-2 years lab experience |
To ensure the quality of PBL reagents the Quality Control (QC) Scientist I will perform release and stability testing of interferons, antibodies, and manufactured ELISA kits. In addition, the QC Scientist I will perform bioassays or immunoassays to troubleshoot relevant customer issues and design and initiate experiments and projects to improve the quality of PBL products. The QC Scientist I may also serve as back up to the Product Development, Assay Services, or Manufacturing departments as needed: such additional duties may include designing and performing ELISA testing protocols, custom bioassays, and solution preparation. This individual will be involved with document control, SOP writing, and recordkeeping. | 1/20/2020 |
| 714 | PBL Assay Sciences Piscataway , NJ R&D Scientist I/II/III MS in life sciences Exp: 0-2 years |
The R&D Scientist is responsible for the hands-on development of immunoassays, such as ELISAs and cell-based assays, for commercial production. This individual plans and executes design, development, and Manufacturing transfer of bioanalytical assays for product commercialization. The R&D Scientist is also responsible for development of custom assays and reagents for clients. | 1/20/2020 |
| 715 | PBS Biotech Camarillo, CA Research Associate, BioprocessR&D (full-time) MS in chemical/biochemical engineering, or life sciences Exp: 0-2 years |
Participate in research efforts for various cell culture processes based on client needs. Perform experiments for bioprocess development, optimization, and characterization. Prepare scientific data for external publications, abstracts, and presentations, including those at international conferences and trade shows. Support root-cause analysis for unexpected results and provide new approaches or experimental strategies for problem solving. Characterize quality attributes of cells during process development, either independently or collaboratively with a customer’s analytical team or an external service provider. Support internal product improvement efforts by providing biological performance data using PBS products | 1/20/2020 |
| 716 | PCI Pharma Services Rockford, IL Entry Level Packaging Validation Analyst HS Diploma/GED Exp: 1-3 years |
The Validation Analyst I is responsible for overall validation project ownership of limited risk project(s) under heavy supervision. Responsible for generation and execution of validation protocols, assistance in audits, and determination of validation needs. This job has no supervisory responsibilities. Prepares validation protocols, validation statements, reports, summaries, and master validation plans for new customer / product / system project launch and maintains existing validated processes / programs at multiple sites as well as organizing and coordinating internal and customer approvals, as needed | 1/20/2020 |
| 717 | PCI Pharma Services Philadelphia, PA IT Helpdesk Technician AS/AA in related field Exp: 1-3 years |
The role of the Helpdesk Technician is to assist customers with IT applications, products or services. Complex and/or high priority problems are elevated to specialized support groups for resolution however the HelpDesk Technician is responsible to ensure that an effective solution is provided to the user. Provides support for all Information Technology products and services. Support may include answering questions, troubleshooting problems, teaching or instructing customers regarding software or hardware functionality, and communicating policy. | 1/20/2020 |
| 718 | Novo Nordisk Clayton, NC Manufacturing Process Technician I HS Diploma/GED Exp: 1 year in manufacturing or BioWork Certification |
Operate manufacturing equipment to achieve production goals. Work in a safe and environmentally responsible manner. Assist during equipment maintenance including restoration of lost function, predictive and preventative maintenance. Reviewing and authoring standard operating procedures (SOP’s) and other documents as required | 1/11/2020 |
| 719 | Novo Nordisk Clayton, NC API Manufacturing Associate BS/BA or higher Exp: 0-2 years in FDA regulated manufactruing industry |
Operate Active Pharmaceutical Ingredients (API) manufacturing equipment to achieve production goals. Work in a safe & environmentally responsible manner. Real time review of electronic batch records ensuring compliance to Standard Operating Procedures (SOPs) & current Good Manufacturing Practices (cGMP) standards. Utilize investigation skills during troubleshooting & assist during equipment maintenance, including restoration of lost function, predictive & preventative maintenance | 1/11/2020 |
| 720 | Novum Las Vegas , NV Phlebotomist Phelbotomy certified Exp: 1-2 years |
The Phlebotomist will perform highly skilled, rapid-draw venipuncture and process collected biological samples according to Standard Operating Procedures (“SOPs”), sample collection and processing instructions; verify, pack and ship samples to appropriate facility. | 1/11/2020 |
| 721 | Novum Las Vegas , NV Respiratory Therapist Respiratory therapy license Exp: 1 year in medical/research field |
The Respiratory Therapist will be responsible for performing all duties associated with respiratory function testing in accordance with Study Protocol and Standard Operating Procedures (SOPs). Responsible for performing and documenting respiratory function testing; observes dosing of study subjects to ensure appropriate respiratory function and compliance. Performs and documents drug devise training. Observes participant behavior during the study and will communicate pertinent observations and adverse events to the Study Manager or Investigator. | 1/11/2020 |
| 722 | Novum Las Vegas , NV Screening Technician HS Diploma, training/experience in phlebotomy required Exp: 0-6 months |
The Technician in our Screening Department will be responsible for performing and assisting with screening activities according to study protocol and Standard Operating Procedures. Responsibilities include performing vital signs/measurements, EKGs, drug/pregnancy tests and other laboratory tests. Observes, obtains and processes all laboratory specimens required by the protocol. The Technician will perform quality control of lab results and charts prior to inclusion/exclusion to study. Performs service oriented duties in relation to participant needs, and provides general support to all phases of the screening process. | 1/11/2020 |
| 723 | Novum Las Vegas , NV Research Technician (FT) HS Diploma/GED or 1-year cert from college/tech school Exp: 0-3 months |
The entry level Research Technician will be responsible for supporting study progression according to study protocol and Standard Operating Procedures. Responsible for obtaining vital signs, performing EKGs, and drug/pregnancy testing from study participants as required by the protocol. Observes, obtains and processes all laboratory specimens. Performs service oriented duties along with stocking supplies and general support to all phases of screening process. | 1/11/2020 |
| 724 | Novum Las Vegas , NV Research Technician (PT) HS Diploma/GED or 1-year cert from college/tech school Exp: 0-3 months |
The entry level Research Technician will be responsible for supporting study progression according to study protocol and Standard Operating Procedures. Responsible for obtaining vital signs, performing EKGs, and drug/pregnancy testing from study participants as required by the protocol. Observes, obtains and processes all laboratory specimens. Performs service oriented duties along with stocking supplies and general support to all phases of screening process. | 1/11/2020 |
| 725 | Novum Fargo, ND Entery Level Technician (PT) HS Diploma/GED or 1-year cert from college/tech school Exp: 0-3 months |
The entry level Research Technician will be responsible for supporting study progression according to study protocol and Standard Operating Procedures. Responsible for obtaining vital signs, performing EKGs, and drug/pregnancy testing from study participants as required by the protocol. Observes, obtains and processes all laboratory specimens. Performs service oriented duties along with stocking supplies and general support to all phases of screening process. | 1/11/2020 |
| 726 | Nortech Bemidji, MN Assembler 1 - Bemidji (Day Shift HS Diploma/GED Exp: 0-1 month experience/training |
Duties include: Preforming basic assmebly tasts at a proficiency and quality standard rate set by the plant. Read/follow written build instructions (process sheets) to perform assigned operations. | 1/11/2020 |
| 727 | Nortech Blue Earth, MN Quality Technician 1 year certificate from college/technical school Exp: 3-6 months related experience |
Coordinate the development/implementation of the quality systems, researching, developing and implementing the process improvements necessary to eliminate waste and reduce inventory. Responsible for development of the performance metric system used to report on continuous process improvements | 1/11/2020 |
| 728 | Nortech Merrifield, MN Inspector 1 HS Diploma/GED Exp: 1-3 months related |
Newly hired and/or fully trained in one or more areas of quality. Works under close supervision on assignments that are routine in nature where limited judgement is required and typically detailed instructions on work are given. Examines compnay records to secure such information as size and weight of the product and results of quality test. Inspects produc to determine compliance with order specifications. | 1/11/2020 |
| 729 | Nortech Blue Earth, MN Manufacturing Engineer BS in mechanical/manufacturing engineering Exp: 0-4 years |
Develops manufacturing methods, systems and processes; provides product support to engineering and manufacturing teams; resolves engineering problems; evaluates manufacturing system applications and equipment; confirms systems and components capabilities; develops manufacturing processes and stardards... | 1/11/2020 |
| 730 | Nortech Maple Grove, MN Staff Accountant BS/BA Exp: 1 year experience |
Works independently with general supervision and works on assignments of moderate scope where judgement is required in resolving problems and making recommendations. Will exercise judgement within defined procedures and practices to determine appropriate action, and normally recieves general instructions on routine work and detailed instructions on new assignments. | 1/11/2020 |
| 731 | Nortech Blue Earth, MN Assembler 1 - Blue Earth HS Diploma/GED Exp: 0-1 month experience/training |
Duties include: Preforming basic assmebly tasts at a proficiency and quality standard rate set by the plant. Read/follow written build instructions (process sheets) to perform assigned operations. | 1/11/2020 |
| 732 | Nortech Blue Earth, MN Quality Technician 2 AA or 2 year degree Exp: 6-12 months related experience/training |
Works under general supervision on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required. Normally recieves general instructions on routine work and detailed instructions on new assignments. Performs internal audits for processes and products to assure compliance to the documented quality system. | 1/11/2020 |
| 733 | NuVasive West Carrolton, OH Production Associate - 2nd shift HS Diploma/GED Exp: 0-1 years |
The Associate Post Processing Technician is responsible for the finishing/assembly operations to ensure quality products are produced. The Post Processing Technician helps in driving best practices and creates open communication across all teams to foster a collaborative, high functioning culture. Follow standard applications in order to achieve dimensional integrity and required finish characteristics. Follow the router protocol to ensure the product moves through channels efficiently and GDP is correct prior to moving the product to the next area. | 1/11/2020 |
| 734 | NuVasive West Carrolton, OH Associate Quality Engineer BS in engineering Exp: 0-2 years in regulated quality environment/engineering |
This role is responsible for the, implementation, and improvement of overall quality systems. The Associate Quality Engineer will participate in Design Control activities and provide guidance to engineering on successful creation and maintenance of design history files during new product introductions. The Associate Quality Engineer may work closely with suppliers or contractors, including auditing, developing inspection/testing plans, performing risk analysis. | 1/11/2020 |
| 735 | nView Medical Salt Lake City, UT Software Developer BS or MS in computer science/engineering Exp: 1+ years in design |
High throughput data processing and management. Algorithm development and optimization. Algorithm parallelization via General Purpose GPU computing. Computer vision, image creation, and image processing. Eliminating defects in our code and refactoring it to reduce its length, complexity and time required to test or add functionality | 1/11/2020 |
| 736 | NxStage Medical Lawrence, MA Quality Analyst - NxStage BS/BA Exp: 0-3 years in related |
The incumbent will be responsible for receiving and processing customer product complaints in Fresenius/NxStage’s postmarket surveillance department with a primary focus on performing functions in support of the quality engineering and clinical teams. Process incoming customer complaints and adverse events as assigned for device and drug-related incidents. Interface with distributor contacts and customer clinical staff to obtain detailed information regarding reported incidents as required, ensuring patient confidentiality throughout | 1/11/2020 |
| 737 | Ofni Systems Raleigh, NC Computer Systems Validation Engineer BS in math/science/engineering Exp: 1 year in software testing |
We are hiring a Validation Engineer to be on the cutting edge of automated validation techniques. You will be responsible for implementing our validation solutions while working with industry-leading companies. Ideal candidates are experts on the requirements of 21 CFR 11, have excellent critical thinking and interpersonal skills, and are motivated to meet client needs for compliance. If you are an A-level engineer who enjoys the challenge of solving real-world compliance problems then we would like to talk with you. | 1/11/2020 |
| 738 | Ology Bioservices Alachua, FL QC Support Tech II AAS/AS in sciences Exp: 1 year experience |
Support of QC Laboratories including, but not limited to: Work with the procurement department to order reagents, materials, services and equipment for QC. Maintain inventories of materials for the QC departments. Perform equipment/laboratory cleaning and routine maintenance tasks. Responsible for washing and maintaining glassware. | 1/11/2020 |
| 739 | Ology Bioservices Alachua, FL Assistant Scientist, Cell Assay BS in biological sciences or related Exp: 1-2 years performing tests in cGMP envi |
The Assistant Scientist, Cell Assay, reports to the Cell Assay Manager and performs QC laboratory tests on in-process, intermediate and finished products performing a range of additional varied work activities including: Assist in routine organization and upkeep of the laboratory, including maintenance of inventory, cleaning, and waste disposal. Writing and updating laboratory documentation including equipment SOPs and test methods. Performing routine immunoassays, cell-based assays, molecular biology assays and virology testing in support of product release, in-process testing as appropriate. | 1/11/2020 |
| 740 | Ology Bioservices Alachua, FL Supplier QA Technician AA/AS Exp: 0-2 years in FDA-regulated industry |
Write standard operating procedures, work instructions, forms, material specifications, deviations, CAPA's, change controls and other relevant GMP records. Perform sampling, inspection and release of incoming material. Perform sampling and inspection intermediate and final product. Assess supplier quality performance | 1/11/2020 |
| 741 | Ology Bioservices Alachua, FL QA Associate HS Diploma/GED Exp: 1 year in biologics/pharma industry |
The QA Associate is responsible for providing clerical and administrative support related to documentation. The QA Associate reports to the Kimberley Planter and will be responsible for activities related to generation and maintenance of documentation, including but not limited to: Converting the format of documents to match the template format. Assisting employees with document preparation including formatting and pagination. Assisting with progression of documents through Document Control Lifecycle in MasterControl | 1/11/2020 |
| 742 | Olympus San Jose, CA Regulatory Affairs Analyst II BS in sciences Exp: 0-3 years in related |
The Regulatory Affairs Analyst II maintains responsibility for the review and investigation of medical device complaints. He/ she coordinates the resolution of complaints and ensures that timely investigations are performed. The incumbent prepares and files Medical Device Report (MDR) for Medical Systems Group(MSG) products. The incumbent maintains quality documents to ensure compliance with FDA regulations and guidance documents relating to these areas of responsibility. He/ she functions as part of MSGs Regulatory Affairs team in fulfilment of corporate objectives for FDA regulatory compliance. The Regulatory Affairs Analyst II performs routine assignments with occasional direction from supervisor;requires general instruction for new or special assignments from Supervisor and/or more experienced staff. | 1/11/2020 |
| 743 | Olympus Southborough, MA R&D Engineer II MS in engineering, biomedical preferred Exp: 0 years |
As an Engineer II working on the R&D team, you will be empowered and inspired to do your best work. You will contribute to our mission by developing Surgical Platforms used primarily in Ear Nose and Throat surgery. In a typical day, you will develop hand held surgical instruments both and instrument consoles on your own and in conjunction with outside and inside design partners. The designs will require creative design solutions and component designs that are innovative and effective in meeting the needs of our customers | 1/11/2020 |
| 744 | Olympus Richmond Hill, On Endoscope Technician I HS Diploma/GED Exp: 0-1 years in technical repairs |
The Endoscope Technician must understand and accept the responsibility to ensure the safety of all Olympus products that are repaired by strictly following established processes and procedures. Under the direction of the Manager, the incumbent shall evaluate, troubleshoot, disassemble, assemble, repair and inspect Endoscopes, Electronics, or Microscopy products to meet company product standards and ensure full and proper functioning of the repaired product. Level I Technician: Assignments are semi-routine difficulty level. Requires daily supervision, detailed instruction on new assignments. | 1/11/2020 |
| 745 | Olympus State College, PA Assembler I HS Diploma/GED Exp: 0-1 years |
Electronic Assembler I is an entry-level assembler position performing a wide variety of mechanical assembly operations. Follows methods and sequence of operations in assembling cables, soldering, bonding, limited testing and manufacturing of transducers. Ability to follow procedures and drawings. | 1/11/2020 |
| 746 | Olympus New Brunswick, NJ Field Service Engineer I AS/AA in electronics, computer science, or related Exp: 1 year as field service engineer or equivalent |
As a Field Service Engineer, the incumbent will engage with some of the country’s most influential hospitals and work closely with our world-class sales teams. He/ She will use your in-depth knowledge of our products to provide expert technical support to our existing and new customers. Perform new equipment installations, upgrades, post installation testing, troubleshooting and all other aspects of technical support for all assigned products. Build and maintain relationships of trust with customers by responding to inquiries and complying with all regulatory and quality requirements. | 1/11/2020 |
| 747 | Olympus Center Valley, PA Technical Support Engineer I AS/AA in related field Exp: 1 year |
As a Technical Support Engineer I working on the Technical Assistance Center team, you will be empowered and inspired to do your best work. You will contribute to our mission by assisting customers with technical issues, researching complex problems, and striving for customer satisfaction. In a typical day, you will: Answer inbound customer calls make outbound calls as necessary. Investigate and resolve issues problems concerning all Medical products and update incident tickets and enter information in department database to permit generation of accurate reports regarding frequency of incidents and costs of repairs. | 1/11/2020 |
| 748 | ThermoFisher Scientific West Hills, CA Scientist I, Manufacturing Sciences BS in biological sciences or related Exp: 1-2 years biological lab experience |
The Scientist I, Manufacturing Sciences is responsible for understanding, performing daily testing, and analysis for development and, improvement of DNA-based diagnostic reagents. Simultaneously manage and prioritize multiple projects and products across multiple functional groups while meeting target due dates with guidance of supervisor/lead. Design, create experimental task, run tests and be able to look at data and complete analysis using Fusion, Orchid, or equivalent software. Can provide experimental task(s) to designated Scientist with Supervisor approval. | 1/11/2020 |
| 749 | ThermoFisher Scientific St. Louis, MO Formulation Technician II HS Diploma/GED or Associates Exp: 1-2 years in related |
The candidate will be responsible for the performance of operations in support of the manufacture of Commercial and Clinical Biologics. He/She will be responsible for following Current Good Manufacturing Practices (cGMPs) and carrying out a variety of functions related to Upstream (cell culture) biopharmaceutical manufacturing, with a primary focus on Harvest and Media Preparation. | 1/11/2020 |
| 750 | ThermoFisher Scientific Cambridge, MA Specialist I, Quality Assurance BS/BA in sciences Exp: 0-2 years in quality |
The Quality Assurance Specialist will be the primary point of contact for the customer on all matters related Quality Assurance Operations. Perform activities in support of dispositioning product and/or raw materials while ensuring compliance with directives and procedures, customer requirements, and regulatory standards. | 1/11/2020 |
| 751 | ThermoFisher Scientific Suwanee, GA Lab Tech II BS/BA Exp: 1-3 years |
The Lab Technician II performs sample handling, receipt, storage, and shipment for a biorepository as well as entering inventory information into a laboratory information management system. Additionally, he/she performs specialized services including sample manipulation, aliquoting, and other sample handling functions that may require aseptic technique. | 1/11/2020 |
| 752 | ThermoFisher Scientific Alachua, FL QA Specialist, GMP Plant Quality BS/BA in life or chemical sciences Exp: 1+ years in GMP environment |
Ensures the quality of all GMP manufacturing activities, executing manufacturing record reviews in accordance with specified timelines. Performs robust master and executed batch review and disposition activities to meet specified timelines. Performs robust document review and approval activities to meet specified timelines and ensure the adherence to Quality Agreements. Documentation may include batch records, SOPs, investigations, corrective actions, change controls, technical documents, | 1/11/2020 |
| 753 | ThermoFisher Scientific Allentown, PA Associate Project Engineer BS in mechanical/industrial engineering Exp: 0-3 years in related |
The individual will establish a solid focus on long-term continuous improvement activities through interaction with the entire Engineering and Operations Staff.Recommend methods for improving worker efficiency, reducing waste, and utilities such as restructuring job duties, reorganizing workflow, relocating workstations, equipment, and justify and oversee purchase of new equipment / technology.Recommend and lead cost saving initiatives as it relates to business objectives, current projects, future investments in technology and Production / Manufacturing processes.Will lead and manage multiple project engineering driven assignments from start to finish with sound project management methodologies | 1/11/2020 |
| 754 | ThermoFisher Scientific Lenexa, KS Customer Service Representative I HS Diploma/GED Exp: 1+ years in call center/customer service |
Employee is responsible for entering order into the MBD-Lenexa ERP system and assisting our internal and external customers with resolution of customer service issues and complaints. Enter orders as they are received via fax, email and/or phone as assigned by management; perform quality verification of customer shipping information, order details, and pricing. | 1/11/2020 |
| 755 | ORA Andover, MA Clinical Trial Associate - Medical Devices BS in nursing or life sciences Exp: 1 or more years in clinical trials |
Assists project managers in clinical study conduct for ophthalmic clinical projects across all investigator sites and ensures compliance with protocol and overall clinical objectives. As a member of the clinical team, relies on instructions and pre-established SOP’s to perform the functions of the job while working under immediate supervision of a supervisor or manager. Performs day-to-day activities under the guidance of the project managers. | 1/11/2020 |
| 756 | Organogenesis Norwood, MA QC Analyst I/II - Microbiology BS/BA Exp: 6-12 months in GMP/Medical devices/Pharma |
The QC Analyst I/II performs quality activities in support of product production and releases. The position has interaction with other internal departments, including Quality Assurance, Validation, Calibration, Materials, and Logistics. The position also has interactions with external entities including contractors and suppliers. The QC Analyst I/II performs a wide variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, and reporting results. | 1/11/2020 |
| 757 | Organogenesis Norwood, MA Production Associate I - Human Tissue Processing Certificate in biotechnology preferred but not required Exp: 1-3 years |
The Human Tissue Processing (HTP) Production Associate I is an entry level position. The HTP Production Associate I will perform the production activities associated with HTP Products, produced at Organogenesis Norwood, with supervision. The associate will adhere to the appropriate SOPs, MBRs, and cGMP procedures in the general lab area as well as the Class 10,000 clean room. The HTP Production Associate I will report to the HTP Supervisor. | 1/11/2020 |
| 758 | AGC Biologics Bothell, WA Manufacturing Associate, Downstream BS in chemistry, biology, or related Exp: 1-8 year(s) |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. PRINCIPAL RESPONSIBILTIES: Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. Clean, assemble/disassemble, sterilize and operate primary process equipment. Complete required processing documentation including deviation reports, change control, product change over, etc. Ensure compliance with company quality systems, safety procedures, and other company policies. etc. | 1/12/2020 |
| 759 | AGC Biologics Bothell, WA Manufacturing Associate I-IV BS in chemistry, biology, or related Exp: 1-8 year(s) |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. PRINCIPAL RESPONSIBILTIES: Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. Clean, assemble/disassemble, sterilize and operate primary process equipment. Complete required processing documentation including deviation reports, change control, product change over, etc. Ensure compliance with company quality systems, safety procedures, and other company policies. etc. | 1/12/2020 |
| 760 | AGC Biologics Bothell, WA Manufacturing Associate I-IV, Team 2 BS in chemistry, biology, or related Exp: 1-8 year(s) |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. PRINCIPAL RESPONSIBILTIES: Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. Clean, assemble/disassemble, sterilize and operate primary process equipment. Complete required processing documentation including deviation reports, change control, product change over, etc. Ensure compliance with company quality systems, safety procedures, and other company policies. etc. | 1/12/2020 |
| 761 | AGC Biologics Bothell, WA Manufacturing Support Technician I-IV BS in engineering or science Exp: 0-2 years |
The Manufacturing Support Technician is an entry level position for an individual to support the Technical Operations group. Primary responsibilities include generating and editing documentation in support of Process Transfer activities, helping manage equipment procurement and implementation, reviewing technical documentation, and providing general support to Manufacturing improvement initiatives. PRINCIPAL RESPONSIBILITIES: Work with the Technical Operations team to support the transfer of new processes into the Manufacturing operation. Key responsibilities include managing the creation of Manufacturing Batch Records, supporting development of Raw Material estimates, and helping to manage the closure of key equipment gaps. Support the implementation of new technology into the manufacturing operation. etc. | 1/12/2020 |
| 762 | AGC Biologics Bothell, WA QC Associate I BS/BA Exp: 1-3 year(s) |
The Quality Control Associate I will perform QC analysis and document activities according to SOPs following good manufacturing processes (GMP). This individual will also demonstrate the ability to learn QC methods, procedures and systems. PRINICIPAL RESPONSIBILITIES: Supports projects / initiatives / team goals by delivering on all assigned tasks. Analyzes issues and makes decisions based on standardized processes and procedures under direct supervision. Seeks opportunities for continual learning. Receives close and regular instruction, guidance and direction from others in the form of steps and tasks. Perform general QC testing such as pH, Osmolality, Protein Concentration. etc. | 1/12/2020 |
| 763 | AGC Biologics Bothell, WA QC Associate I/II BS/BA Exp: 1-3 year(s) |
The Quality Control Associate I will perform QC analysis and document activities according to SOPs following good manufacturing processes (GMP). This individual will also demonstrate the ability to learn QC methods, procedures and systems. PRINICIPAL RESPONSIBILITIES: Supports projects / initiatives / team goals by delivering on all assigned tasks. Analyzes issues and makes decisions based on standardized processes and procedures under direct supervision. Seeks opportunities for continual learning. Receives close and regular instruction, guidance and direction from others in the form of steps and tasks. Perform general QC testing such as pH, Osmolality, Protein Concentration. etc. | 1/12/2020 |
| 764 | AGC Biologics Bothell, WA Development Associate I (Upstream) AA/BS in a life science or engineering field Exp: 0-3 years |
This is a Development Associates position in the Upstream Process Development group. Primary responsibility will be to support mammalian cell culture processes used for the manufacture of therapeutic recombinant proteins. The successful candidate will be responsible for supporting shake flask and bioreactor experiments, sampling, inoculating, feeding & harvesting bioreactors. Under general supervision, this person carries out routine to moderately complex experiments or procedures. PRINCIPAL RESPONSIBILITIES: Maintain lab including cleaning, autoclaving reactors, stocking laboratory supplies and performing maintenance on laboratory equipment. Prepare and filter media. etc. | 1/12/2020 |
| 765 | Agilent Boulder, CO Manufacturing Quality Engineer - Entry BS/BA Exp: 1+ year(s) |
Ensures that high-quality products are designed, engineered and manufactured by Agilent, in conformance with required standards and regulations. This is a Quality position with direct support of manufacturing floor responsibilities. Provides guidance, expertise and services to ensure process, data and product quality. Participates in process improvement opportunities and provides quality-related services to quality control, R&D, manufacturing engineering, production, procurement, and others. etc. | 1/12/2020 |
| 766 | Agilent Boulder, CO Manufacturing Tech (2nd Shift) unspecified Exp: None required |
Responsible for performing a variety of technical support duties in one or more manufacturing areas. Duties may be related to installation, maintenance, repair and support of manufacturing equipment, technical support of one or more production processes, product test and troubleshooting, and technical analyses and problem-solving. Conducts tests, experiments and/or problem resolution associated with components, parts, products or processes/systems. May design and/or build tools. etc. | 1/12/2020 |
| 767 | Agilent Wilmington, DE Analytical Instruments Technical Support BS in chemistry, biology, or related Exp: None required |
As an Analytical Instruments Technical Support person, you will sit at our Agilent site in WIlmington, DE and join Agilent Technologies CrossLab Group's Online Technical Support Team. We support U.S. external customers. As an active team member, you will support customers requesting hardware, software and applications assistance with Analytical Products and Solutions and route those customers whom you can't help to the appropriate groups. Our group's organizational goal is that as part of a world-class technical support group, we provide insights to customers at their very first contact. In order to be successful, our response needs to be quick and well-informed. etc. | 1/12/2020 |
| 768 | Agilent Wilmington, DE R&D Electrical Engineer BS/MS in electrical engineering Exp: None required |
As an Electrical Engineer in our R&D group, you'll be part of a team that analyze, design, prototype and test new products for Agilent's Gas Chromatograph, Automated Sample Handling and Automated Sample Preparation products. Most projects require mechanical, electrical and firmware engineers, as well as chemists and software engineers, to create a complete system. As part of those projects, you will also work with our marketing, manufacturing, purchasing and service organizations to transform your designs into shipping products. etc. | 1/12/2020 |
| 769 | AGTC Gainesville, FL Research Assistant - Assay Development Preclinical Research & Development MS in a biological science Exp: Not required for MS candidates |
The Research Associate Assay Development Preclinical Research and Development is responsible for support of the Assay Development team by developing,qualifying and troubleshooting quantitative, semi-quantitative, and qualitative assays in support of research, nonclinical, and clinical programs. The Research Associate will report directly to the Supervisor, Assay Development Preclinical Research & Development. Develop and qualify new assay methods in support of IND enabling non-clinical animal studies, including in vitro cell-based assays, immunoassays, and molecular assays. Plan strategies for and participate in the development, qualification, and transfer of quantitative and semi-quantitative bioanalytical methods to support product release. May assist in preparing technology transfer, assay validation and clinical sample testing at CROs. etc. | 1/12/2020 |
| 770 | AGTC Gainesville, FL QA Specialist I BS in a scientific background Exp: None required |
Essential Duties and Responsibilities: Support the development, implementation, and improvement of corporate quality systems that support early, mid and late phase gene therapy clinical programs. Increase compliance awareness and promote a culture of quality throughout the company, with a focus on laboratory and manufacturing operations. Collaborate with multiple functions to perform QA oversight and ensure quality-related activities are executed efficiently. Write, review and revise standard operating procedures. Provide training to laboratory and manufacturing staff on GLP/GMP regulations, best practices and internal requirements. Review and approve product-related documentation, including raw material release, batch records, quality control test results and resolve discrepancies, as needed. etc. | 1/12/2020 |
| 771 | Ajinomoto Bio-Pharma Services San Diego, CA Aseptic Cleaning Technician HS diploma or equivalent Exp: 0-2 years |
Ajinomoto Bio-Pharma Services is currently seeking a Part Time Aseptic Cleaning Technician (3rd shift) responsible for formulating cleaning solutions and sanitizing manufacturing core, operation equipment, and monitoring production processes and operations as necessary. The Aseptic Cleaning Technician will record information in documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), and review documentation as appropriate. This role frequently works in a professional manufacturing environment with computer equipment, machinery, tools, and loud noise and activity. etc. | 1/12/2020 |
| 772 | Ajinomoto Bio-Pharma Services San Diego, CA Document Control Assistant HS diploma or equivalent Exp: 0-2 years |
Ajinomoto Bio-Pharma Services is currently seeking a Document Control Assistant responsible for coordinating the review and approval of GMP documents using an electronic document management system. Responsibilities: Coordinates document changes within an electronic document management system. Issues batch records, laboratory notebooks, and logbooks for use in GMP production and testing activities. Collaborates with document authors and reviewers to process document changes within project timelines and in accordance with established procedures. Facilitates client review and approval of documents. Esures proper maintenance of document master copies and original production records. | 1/12/2020 |
| 773 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Inspection Technician - 1st and 2nd Shift HS diploma or equivalent Exp: 0-2 years |
We are looking for multiple Drug Product Inspection Technicians for 1st and 2nd shifts. In this role you will be responsible for performing a wide variety of product inspection and packaging tasks. You will complete training and pass qualification testing for visual inspection of various product forms, perform accurate visual inspection and handling of products following SOPs while working under cGMP regulations. Please Note: 1st shift hours are 6:30 - 3:00 pm and 2nd shift hours are 3:00 - 11:30 pm. Responsibilities: Performs various manufacturing tasks under the guidelines of established SOP and cGMP regulations. Performs visual inspection. Labels and boxes filled goods. etc. | 1/12/2020 |
| 774 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Manufacturing Assistant HS diploma or equivalent Exp: 0-2 years |
We are looking for multiple Drug Product Manufacturing Assistants for 1st Shift! The Drug Product Manufacturing Assistant is responsible for implementation of routine production and manufacturing procedures to optimize processes and regulatory requirements. Responsibilities: Performs various routine manufacturing tasks under the guidelines of established SOP’s and cGMP regulations. Implements production and manufacturing procedures. Performs visual inspection. Prepares components, media, buffers, and other solutions as needed. Accurately documents data and completes batch records as needed. May cross train and/or focus in various manufacturing tasks including fill/finish, formulation, fermentation, preparation. etc. | 1/12/2020 |
| 775 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Packaging Assistant HS diploma or equivalent Exp: 1-2 year(s) |
Ajinomoto Bio-Pharma Services is currently seeking a Drug Product Packaging Assistant. This position is responsible for performing a wide variety of packaging and labeling tasks in a GMP environment. In this role you will utilize automated equipment as well as perform manual packaging activities to support commercial drug product operations. Typical hours for this role are 7:00 to 3:30 pm Monday through Friday. Responsibilities: Performs various routine manufacturing tasks under the guidelines of established SOP and cGMP regulations. Performs final product assembly, packaging, and labeling and has completed required qualifications where applicable. Accurately documents data under cGMP guidelines. etc. | 1/12/2020 |
| 776 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Substance Manufacturing Assistant - Support Services HS diploma or equivalent Exp: 0-2 years |
Ajinomoto Bio-Pharma Services is currently seeking a Drug Substance Manufacturing Assistant - Support Services responsible for performing solution formulation and/or sterilization of in-process manufacturing materials in support of cGMP manufacturing under the guidelines of established SOP's and cGMP regulations. Responsibilities: Transfers raw materials from warehouse staging area to production suite, labels materials for applicable client use. Conducts inventory and storage of raw materials in production area. Prepares components, buffers and other solutions and/or operates autoclave, washer, or depyrogenation oven. Completes in-process analytical testing as needed to confirm suitability of solutions and submits samples to QC for release testing via LIMS system. etc. | 1/12/2020 |
| 777 | Ajinomoto Bio-Pharma Services San Diego, CA Environmental Monitoring Assistant HS diploma/BS in a life science Exp: 0-2 years |
We are looking for an Environmental Monitoring Assistant to support Ajinomoto Bio-Pharma Services’ manufacturing. This is a vital role within our Quality Control group and is responsible for supporting manufacturing through collection and testing of water, surface and utility samples during various manufacturing and lab processes. As an Environmental Monitoring Assistant you will acquire an understanding of aseptic technique, continuously exhibit proper clean room behavior, and adhere to cGMPs. Responsibilities: Performs environmental monitoring within the microbiology laboratory, manufacturing suites, clean rooms, and drug product operations. Performs enumeration and gram staining of bacterial colonies. Sampling and analysis of the utilities including water, steam, and compressed gasses. etc. | 1/12/2020 |
| 778 | Akorn Cranbury, NJ Analytical Scientist I BS in a chemical or life science Exp: 1-4 year(s) |
We seek talented Analytical Scientists at various levels to join our expanding R&D team. You will be responsible for methods and process development for ANDA topical, suspensions and solutions, nasal sprays, inhalations, sterile injectable and ophthalmic products. You will develop and validate new analytical methods, conduct stability studies and perform sample testing to support regulatory submissions. ESSENTIAL FUNCTIONS: Independently develop analytical methods for drug substances, drug product, preservatives and degradation/impurities in the new drug products. Perform validation experiments as per approved method validation protocols, Company SOP and ICH guidelines. Perform in-process, finished product/release and stability testing of dosage forms as per the approved methods. Perform Extractable/leachable studies for container closure systems of drug products. etc. | 1/12/2020 |
| 779 | Alcami Durham, NC Assistant Scientist II BS in pharmaceutical science, chemistry, or related Exp: 1-2 year(s) |
The Assistant Scientist II is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Analytical Assistant Scientist II may also assist with method development/method validation projects. Typical types of testing: assays (potencies, related substances, residual solvents, metals etc.), rate of release (dissolution), moisture content, identification, and various other wet chemistry based measurements. HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company). The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. etc. | 1/13/2020 |
| 780 | Alcon Huntington, WV Production Technician HS diploma or equivalent Exp: None required |
The role of the Production Technician is to perform a number of different tasks and operations typically within a full-scale environment production manufacturing operation while maintaining compliance with Standard Operating Procedures, Good Documentation Practices and regulatory requirements. | 1/13/2020 |
| 781 | Alcon Fort Worth, TX Scientist I BS/BA Exp: None required |
Job Description: Assist with in-vivo testing of raw materials, finished goods, products, investigations per schedule and per standards/SOPs. Collect, calculate, and interpret test results. Enter and report test results. Take ownership and execute revisions for SOPs related to testing programs, laboratory operations and/or equipment operation. Assist with investigative testing to support laboratory investigations. Conduct peer review of data collected by co-workers. Coordinate equipment calibration & maintenance. etc. | 1/13/2020 |
| 782 | Alcon Fort Worth, TX Associate Scientist, Pre-Clinical Development BS in chemistry or related Exp: 0-1 year(s) |
Responsibilities: Follows established procedures, protocols, or best practices to analyze stability and development samples. Perform assigned tasks under minimal supervision in support of approved projects and documents work properly. Executes a well-designed study, conducts testing and analyzes data without deviation following established procedures under general supervision. Applies general technical skills to complete assigned work, and solves routine problems of limited scope. etc. | 1/13/2020 |
| 783 | AliveCor Mountain View, CA Hardware Test Engineer BS in electrical engineering Exp: 1-5 year(s) |
AliveCor, the creator of the Kardia Mobile ECG app, seeks a Hardware Test Engineer to join an exciting start-up that is changing the face of mobile health. As the Hardware Test Engineer, you will be a crucial member of hardware R&D team responsible for ensuring that AliveCor products perform as intended and meet/exceed customer expectations. You will work closely with our Quality, Regulatory, Software Engineering, Product Management, and Creative teams to ensure new products perform as intended while fully documenting the verification process. You will also work with our manufacturing team to implement and support manufacturing test fixtures. If you have what it takes to drive change in the medical marketplace, then this is the opportunity for you. etc. | 1/13/2020 |
| 784 | Alturas Analytics Moscow, ID Laboratory Assistant HS diploma Exp: 1-3 year(s) |
The Laboratory Assistant provides support to other laboratory personnel through a variety of duties and tasks. Essential Duties and Tasks: Maintains all lab supplies (including purchase, receipt, stock, inventory, and disposal). Prepares various reagents and solutions for laboratory use. Assists laboratory personnel to enable efficient laboratory operations. Performs routine facility maintenance and inspections. Cleans laboratory glassware. Additional Duties and Tasks: May perform QC review of data if needed. Performs other duties as needed or assigned. | 1/13/2020 |
| 785 | APi North Augusta, SC MFG - Laboratory Technician HS diploma or equivalent Exp: Entry level |
The Laboratory Technician position is an entry level position. The person in this position will be trained and responsible for following instructions and procedures in support of manufacturing processes in a controlled GMP environment, as well as performing related activities. SPECIFIC DUTIES AND RESPONSIBILITIES: Must manage and organize the glass cleaning operation according to approved standard operating procedures. Works closely with Warehouse technician and Quality Assurance to perform and complete all Final Product packaging’s. Must manage time well. Must be able to perform daily tasks in a timely manner – improving productivity while minimizing idle time. Follow approved GMP manufacturing directions such as standard operating procedures and other instructions in support of production. etc. | 1/13/2020 |
| 786 | APi North Augusta, SC Purification Chemist BS in chemistry or related Exp: Entry level |
The Purification Chemist I position is an entry level chemist position. The person in this position will be trained and responsible for following the peptide manufacturing process in a controlled cGMP environment, as well as performing related activities. PRIMARY RESPONSIBILITIES: Work in a cGMP environment to perform the peptide purification processes through chromatography as well as other various purification techniques. Use analytical skills to prevent and solve possible process complications and problems. Work as part of a team to complete specific projects in a timely manner. Follow approved cGMP manufacturing directions such as production batch records, standard operation procedures and standard test procedures. Help the team to install, test, operate and maintain equipment for manufacturing and in-process testing. etc. | 1/13/2020 |
| 787 | APi North Augusta, SC MFG - Laboratory Technician II HS diploma or equivalent Exp: 1-2 year(s) |
The Laboratory Technician II position is an experienced lab position. The person in this position will be trained and responsible for following instructions and procedures in support of manufacturing processes in a controlled GMP environment, as well as performing related activities. SPECIFIC DUTIES AND RESPONSIBILITIES: 1) Must manage and organize the glass cleaning operation according to approved standard operating procedures. 2) Works closely with Warehouse technician and Quality Assurance to perform and complete all Final Product packaging’s. 3) Must manage time well. Must be able to perform daily tasks in a timely manner – improving productivity while minimizing idle time. etc. | 1/13/2020 |
| 788 | APi North Augusta, SC Quality Control Chemist I BS in chemistry or related Exp: 1-2 year(s) |
Primary Responsibilities: Use basic understanding and knowledge of techniques, instrumentation and lab functions to identify problems and support the completion of work assignments. Perform and review QC release testing. Support routine analytical testing using GC, KF, and HPLC. Assist the QC/QA group with writing and editing of SOPs and STPs. Support analytical method development. Perform method transfer and validation activities. Perform OQ/PQ for the Quality Control Equipment. Other duties as assigned. | 1/13/2020 |
| 789 | American Regent New Albany, OH Maintenance Technician - 2nd Shift HS diploma or equivalent Exp: 1+ year(s) |
American Regent, Inc., a Daiichi Sankyo Group Company, develops, manufactures, and supplies high quality sterile injectables for healthcare providers, clinics, hospitals and veterinary practices across the United States and Canada. We have locations in New York, Ohio, and Pennsylvania and sales territories nationwide. Nature and Scope: A technical position involving equipment repairs and maintenance activities intended to keep the facility equipment (i.e. process, utility, and general equipment) within compliance of cGMPs. etc. | 1/13/2020 |
| 790 | American Regent New Albany, OH Metrology Technician I - 2nd Shift HS diploma/AS in electronics Exp: 1-5 year(s) |
NATURE AND SCOPE: A technical position involving instrument calibrations and operation intended to keep the facility instrumentation and equipment (i.e. process, utility, and general equipment) within compliance of cGMPs. ESSENTIAL DUTIES AND RESPONSIBILITIES: Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time. Perform Calibrations. Follow written calibration procedures. etc. | 1/13/2020 |
| 791 | American Regent New Albany, OH Equipment & Process Technician I - 1st Shift HS diploma or equivalent Exp: 1+ year(s) |
The Equipment and Process Technician I works with the Inspection and Packaging Supervisor in the activities associated with the inspection and packaging of sterile pharmaceuticals in accordance with company procedures and cGMPs. The incumbent meets inspection and packaging schedules while maintaining accurate records and professional behavior within the inspection/packaging areas. The Technician will perform manual inspection and train in the automatic inspection/packaging area for setup, of automated equipment and manual inspection processes, labeling and packaging equipment duties, line clearances and assist with inspection/packaging schedule. In conjunction with the Supervisor, the Technician plays a critical role in assuring safe, effective and compliant activities are performed in the manual inspection process while maintaining production schedules. The Equipment and Process Technician I will be proficient in all activities associated with the inspection process and be able to work with minimal supervision. etc. | 1/13/2020 |
| 792 | American Regent Hilliard, OH Component Prep Operator I - 2nd Shift HS diploma or equivalent Exp: 1 year |
This entry level position is a member of the Manufacturing Team. The Manufacturing Team is responsible for activities associated with the manufacture of safe, effective, and sterile pharmaceuticals in accordance with company SOPs, policies and cGMPs. The Manufacturing Team ensures aseptic and sanitary conditions are maintained where required, that appropriate manufacturing area and equipment records are neat and accurate and that safe, effective and professional behavior is displayed at all times. In conjunction with Production Management the Manufacturing Team provides input and assistance to other Departments as needed, playing a critical role in maintaining production schedules and meeting Company Goals. The Team Member will be able to participate in all aspects of the Component Prep Process. The Component Prep Process includes dispensing components (Caps and Seals), vial washing and component sterilization in accordance with established production records in a concentrated effort to manufacture sterile liquid pharmaceuticals. etc. | 1/13/2020 |
| 793 | Amneal Pharmaceuticals Piscataway, NJ Regulatory Affairs Associate BA/BS in a scientific field Exp: 0-2 years |
The Regulatory Affairs Associate supports the business and Regulatory Affairs team in day-to-day activities associated with the compilation and submission of regulatory submissions such as ANDAs to the FDA within company timelines and in accordance with regulatory guidelines and applicable federal laws. Essential Functions: With some guidance compile and complete the ANDAs with high-quality, following the regulatory guidelines and internal processes within time lines. Coordinates with external vendors for project support activities. This may include but not limited to RS statements, TSE/BSE statements, Melamine free certificates, cGMP certificates, Debarment certificates, US agent letters, DMF LoAs, Technical data sheets, and technical drawings, Quantitative compositions of colors, flavors e.t.c. etc. | 1/13/2020 |
| 794 | Amneal Pharmaceuticals Branchburg, NJ QA Inspector I - 2nd Shift HS diploma or equivalent Exp: 1+ year(s) |
The Quality Assurance Inspector I monitors and ensures all incoming raw materials, packaging components and returned goods are sampled, inspected and tested (where applicable) for the purpose of determining compliance with established specifications. The QA Inspector I must monitor and ensure all phases of drug manufacturing are in compliance with established specifications; receive, inspect, release and control of labels and outserts, to ensure quality compliance before, during and after each packaging run. Essential Functions: Perform Inspection, sampling and testing where applicable on all incoming raw materials, packaging components and returned goods following detailed written procedures. etc. | 1/13/2020 |
| 795 | Amneal Pharmaceuticals Brookhaven, NY Scientist I, Quality Control BA/BS in chemistry or related Exp: 0-1+ year(s) |
The Scientist I - QC is an entry-level role responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents. Essential Functions: Performs physical and chemical analysis of raw materials, in-process and finished pharmaceutical products, including products on stability, according to written methods or compendial methods as applicable, material specifications, using analytical techniques such as IR spectroscopy, UV-Vis spectroscopy, and chromatographic techniques adhering to company policies as identified in standard operating procedures (SOPs). etc. | 1/13/2020 |
| 796 | Amneal Pharmaceuticals Brookhaven, NY Lab Technician I - 2nd Shift AS Exp: 0-1 year(s) |
The Lab Technician will be responsible for performing daily calibration of lab equipment, reports and maintain results. Essential Functions: Conduct daily calibration of instruments by utilizing small equipment like Balances, pH meters, Desiccators and Refrigerators. Login and maintain incoming samples for analysis in APR web. Prepare laboratory supply, chemical purchase request and maintain chemical inventory in APR web. Maintain column log books for HPL, GC and UPLC analysis. Dissolution media preparation and keep dissolution apparatus clean after each use by Scientist. Document reference standards and impurities in incoming material log book and update as needed. etc. | 1/13/2020 |
| 797 | AMRI Grafton, WI Quality Control Analyst I BS in chemistry or other natural science Exp: 1-3 year(s) |
The Quality Control Analyst is an integral part of the AMRI team, contributing to our success by ensuring that our products meet all specifications before being released to the customer through raw material testing, method development, validation, equipment calibrations, environmental monitoring, stability testing and final product testing. Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients’ lives with the pharmaceuticals we develop and manufacture. etc. | 1/13/2020 |
| 798 | Xeris Pharmaceuticals Chicago, IL Legal & HR Associate BS/BA Exp: 0-2 years |
The Legal & HR Associate is a key role responsible for supporting the Legal and Human Resources teams in an administrative capacity, working with employees across multiple states in the USA. The Legal & HR Associate is the face of Legal and Human Resources, interacting with and supporting all employees. The ideal candidate is ambitious, high energy and excited to get their foot in the door of an innovative company. This is a fantastic opportunity for someone interested in the legal or human resources functions within a company. etc. | 1/6/2020 |
| 799 | ZeteoTech Sykesville, MD Chemist BS in chemistry or related Exp: 1-5 years |
Zeteo Tech, Inc, a venture backed company developing solution for Medical and Biodefense applications, is seeking a motivated chemist to join our team. The ideal candidate should be interested in working in an entrepreneurial environment developing game changing solutions to healthcare and national security challenges. You will use your expertise to conduct chemical and physical laboratory tests to assist scientists in development of tools to detect and identify biological organisms and materials. etc. | 1/6/2020 |
| 800 | ZeteoTech Sykesville, MD Microbiologist BS in microbiology, biology, biochemistry, or related Exp: 1-5 years |
Zeteo Tech, Inc, a venture backed company developing solution for Medical and Biodefense applications, is seeking a motivated microbiologist to join our team. The ideal candidate should be interested in working in an entrepreneurial environment developing game changing solutions to healthcare and national security challenges. You will use your expertise to conduct biological laboratory tests to assist scientists in development of tools to detect and decontaminate biological organisms and materials. This is an entry-level position with room for growth. | 1/6/2020 |
| 801 | Zoetis Durham, NC Associate, Research & Diagnostic Services BS in microbiology or other life sciences Exp: 1-2 years |
The U.S. Poultry Research & Diagnostics Services team provides diagnostics, research and development, outcomes research, and biodevice support through theoretical and applied scientific evaluations. The Associate is primarily responsible for assay testing; ARC (Avian Research Center) study implementation and reporting; meta analysis to inform health decisions and process interventions; day-to-day operations of the diagnostics laboratory (e.g., supplies, budget management, etc.); and assisting the Sr. Associate with duties as needed. In addition, the Associate is the primary commercial leads for the Laboratory Information Management Software (LIMS) system, providing superior service to internal colleagues and customers. etc. | 1/6/2020 |
| 802 | Zoetis Parsippany, NJ Associate/Sr. Associate, Business Integration BS/BA in business, computer science, or related Exp: 1-5 years |
The Associate/Sr. Associate, Business Integration is responsible for helping to implement and execute the organization’s business integration objectives. The Associate/Sr. Associate will partner cross-functionally to build and execute the Zoetis integration strategy by assisting the Director, Business Integration in project management, change management, and process improvement initiatives. etc. | 1/6/2020 |
| 803 | 10X Genomics Pleasanton, CA Production Associate 1 BS/MS in molecular biology, chemical engineering, analytical chemistry or related Exp: 1+ years |
10x Genomics is looking for an outstanding individual to join its consumable manufacturing team. This individual will be responsible for production consumable products associated with Next Generation Sequencing chemistries. This role requires excellent laboratory skills in performing production operations consistently. The ideal candidate will have an education background in one or more of the following disciplines: Molecular Biology, Analytical Chemistry, Chemical Engineering, or equivalent. Experience in production and QC of similar products in a manufacturing environment a plus. etc. | 1/6/2020 |
| 804 | 10X Genomics Pleasanton, CA QC Associate 1 BS in chemical or biological engineering, molecular biology, or analytical chemistry Exp: 0-2 years |
10x Genomics is looking for an outstanding individual to join its Quality Control team. This person will be responsible for the qualification of consumable products associated with Next Generation Sequencing chemistries. As well as ensuring a reliable supply of quality consumables, this person will be a key contributor to the development of manufacturing infrastructure required to support a commercial product in the life science field. etc. | 1/6/2020 |
| 805 | 10X Genomics Pleasanton, CA Computational Biologist – Microscopy MS in computer science, electrical engineering, mathematics or related Exp: 1-5 years |
10x is looking for an outstanding individual to join its Computational Biology group to work on its next generation spatial genomics assays. The ideal candidate has experience implementing robust algorithms for detecting and modeling features in microscopy images and drawing inferences from them. Candidate should have deep knowledge of optical image analysis and will be well served by the ability to combine published algorithms with original ideas and quickly turning it into efficient code. Candidate will be expected to be highly independent, relied on for their expert technical opinion and thrive in a quickly changing environment. etc. | 1/6/2020 |
| 806 | 3M Charlotte, NC Manufacturing Associate HS diploma or equivalent Exp: 1+ year(s) |
Primary Responsibilities include but are not limited to the following: Follow standard operating procedures to assemble, test and package products. Follow all job safety recommendations. Enter data into ERP systems. Experienced in the use of hand tools, powered tools including routers, sanders, dremmel tools and measuring devices. Must be able to work with minimal supervision but also to take direction from team members in a small but highly motivated manufacturing team. Must have excellent housekeeping skills and be able to work with a very sticky Epoxy adhesive and 2-propanl without causing contamination of product, tools and equipment. etc. | 1/6/2020 |
| 807 | AbbVie South San Francisco, CA Associate I/Associate II, In Vivo Pharmacology BS/MS Exp: 0-3 years |
We are looking for an Associate Scientist I/II with experience in in vivo pharmacology study execution, start to finish including tumor implantation, data collection, and data analyses. Additional opportunities to learn new skills and to work on ex vivo lab experiments will be provided based on project need and candidate’s interest. The ideal candidate will have experience working with various mouse models of cancer. Above all, we are looking for a highly motivated and collaborative individual with a passion for oncology research, who enjoys working in a fast-paced and highly dynamic working environment. etc. | 1/6/2020 |
| 808 | AbbVie Lake County, IL Writer I & II, Development Document BS/BA Exp: 1-2 years |
The Development Document Writer I is accountable for authoring Development's quality documents by leveraging knowledge and expertise in writing standards and working with stakeholders to ensure the end to end processes are well-defined and articulated clearly in alignment with AbbVie's quality document system. Responsible for ensuring quality document standards are applied when authoring new and updating Development's quality documents. Responsible for understanding AbbVie's Quality System and applying the knowledge when authoring new and updated Development's quality documents. Provides internal stakeholders with the understanding of AbbVie Quality System and its practical application. etc. | 1/6/2020 |
| 809 | AbbVie Worcester, MA Manufacturing Technician 2nd Shift BS/BA Exp: 0+ years |
Responsibilities: Shipping finished materials. Maintaining inventory levels. Sampling of in process and raw materials. Running glass washer / autoclave. Buffer / media preparation. Equipment preparation (CIP / SIP). Cell culture (from vial thaw to production scale). Column chromatography. Tangential flow filtration. | 1/6/2020 |
| 810 | Abcam Branford, CT Senior Research Associate BS/MS in molecular biology or related Exp: 1-3 years |
The successful candidate will play a hands-on role in the company’s use of a variety of molecular biology, assay development, and protein purification techniques in support of various commercial and academic customer projects to deliver high-quality and on-time customized recombinant antibodies. He or she will partner closely with other team members within the group and be required to make observations, analyze data, and interpret results with supervision. etc. | 1/6/2020 |
| 811 | Abcam Eugene, OR Research Associate (temporary) BS in biology, immunology, or related Exp: 1+ year(s) |
We are seeking a Research Associate to assist in the development of novel immunoassays in our Eugene, OR facility. The core responsibility will be to provide support to the immunoassay development team through the use of antibody-based laboratory techniques such as sandwich ELISA, Western blot, immunocytochemistry, and flow cytometry as well as the generation of biological materials for analysis. etc. | 1/6/2020 |
| 812 | AbSci Vancouver, WA Research Associate - Fermentation BS in chemical or biochemical engineering, microbiology, or related Exp: 1-2 years |
The Fermentation Research Associate will play a significant role in our upstream process development. Core responsibilities include executing bench-scale fermentations with the goal of achieving high cell densities and maximizing yields of recombinantly expressed proteins. This position will be responsible for independently operating bioreactors at small scale (1L or less), preparing media, processing samples, and analyzing results. Candidate is enthusiastic about laboratory bench work, exhibits meticulous attention to detail, and an eagerness to learn new techniques. etc. | 1/6/2020 |
| 813 | Absorption Systems Exton, PA Associate Scientist – Cell & Molecular Biologist BS/MS in biochemistry, molecular biology or related Exp: 0-2 years |
Absorption Systems provides analytical support for gene and cell therapy products through every stage of development and non-clinical testing services to pharmaceutical and biotech companies to support research and development of drugs, biologics, and medical devices. Absorption Systems is headquartered in Exton, PA. Currently we are seeking a talented and highly motivated Associate Scientist – cell and molecular biologist in Exton, PA to contribute to multiple bioassay development projects. etc. | 1/6/2020 |
| 814 | Absorption Systems Exton, PA Associate Scientist / Scientist – GMP Molecular Biology & Gene Expression BS/MS Exp: 1-3 years |
Primary Responsibilities: Conduct GMP study projects: Preparation for protocol of assay, planning and conducting experiments under the direction of a senior scientist. Conduct studies on molecular biology assays, such as qPCR assays. Prepare and maintain cell cultures and reagents. Document all results in GMP laboratory notebooks and present research data in group and other meetings. Write report for the study project under the direction of management. | 1/6/2020 |
| 815 | Absorption Systems Exton, PA Associate Scientist / Scientist – Drug Transport & Metabolism BS/MS Exp: 1-3 years |
Absorption Systems provides analytical support for gene and cell therapy products through every stage of development. Absorption Systems also provides non-clinical testing services to pharmaceutical and biotech companies to support research and development of drugs, biologics, and medical devices. Absorption Systems is seeking a candidate for either an Associate Scientist or Scientist position with drug transport and metabolism experience at the headquarter location in Exton, Pennsylvania. etc. | 1/6/2020 |
| 816 | Accelerate Diagnostics Tucson, AZ Research Associate, Quality Control BS in chemistry, molecular biology, or related Exp: 1+ year(s) |
The Research Associate for Quality Control (QC) is a key member of the Operations Team under the direction of the Team Lead for Consumable Quality Control. This individual will be responsible for testing of incoming product both analytically and biologically in support of manufacturing. This will include, but not limited to, operation of pH/conductivity meter, HPLC-MS, refractometer and in-house biotechnology systems. This person will be part of a team that executes these tasks on a daily basis. The ideal candidate will be a team player, demonstrate excellent communication skills, be flexible, and excel in a fast-paced environment. etc. | 1/6/2020 |
| 817 | Accelerate Diagnostics Tucson, AZ Research Associate BS in microbiology or related Exp: 1+ year(s) |
The Research Associate is a member of the Core Lab Team and help bring the company's innovative clinical microbiology technology to market. The ideal candidate will be a motivated self-starter with experience in the following areas: microbiology, biochemistry, and/or molecular biology. The successful candidate will be responsible for the day-to-day execution of experiments supporting assay development. etc. | 1/6/2020 |
| 818 | Acceleron Pharma Cambridge, MA Facilities Technician AS/AA Exp: Not necessary for Associate degree candidates |
The Facilities Technician will handle multiple duties and daily activities as well as drive Facilities operations to meet deadlines in support of activities including, but not limited to, operation and maintenance of building systems, inventory management, conducting routine inspections, safety compliance, vendor management, and basic manual labor. etc. | 1/6/2020 |
| 819 | Acella Pharmaceuticals Indianapolis, IN Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. etc. | 1/7/2020 |
| 820 | Acella Pharmaceuticals Portland, OR Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. etc. | 1/7/2020 |
| 821 | Acella Pharmaceuticals Seattle, WA Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. etc. | 1/7/2020 |
| 822 | ACIST Medical Systems Eden Prairie, MN Quality Engineer BS in engineering or related Exp: 0-5 years |
Provide hands-on quality engineering technical support for to the development of new medical devices, as well as changes to existing commercialized devices. This will include development of quality requirements/plans for new products, design/process validation requirements, test method validation and ongoing change management for finished device manufacturing. The Product Quality Engineer plays an active role in the processes to ensure product changes meet quality standards consistent with ACIST Medical Systems policies, while meeting all applicable regulatory requirements. The role works upstream and downstream ensuring the total product lifecycle is maintained and that our products continue to perform as designed. etc. | 1/7/2020 |
| 823 | Acumed Nashville, TN Associate Sales Representative BS/BA in a business or medical discipline Exp: 0-2 years |
The Associate Sales Representative (ASR) exceeds sales quota within an assigned territory by delivering Acumed product on time and providing high quality technical assistance in the OR. The ASR assists in the assessment of the customer base to identify new business opportunities and executes a targeted sales strategy for each identified opportunity proactively ensuring all leads are followed up on appropriately. etc. | 1/7/2020 |
| 824 | Acumed Hillsboro, OR Regulatory Associate BS in a science, health, or technical discipline Exp: 0-2 years |
The Regulatory Associate supports the overall regulatory function by helping to maintain regulatory processes and systems. S/he utilizes computer and software proficiencies to create, coordinate, procure and/or maintain data and documentation to support US and OUS medical device registration. The Regulatory Associate also employs an attention to detail and developing familiarity with products and processes to ensure databases, dashboards and documents are current and correct. etc. | 1/7/2020 |
| 825 | Acumed Danville, PA Sales Associate BS/BA in a business or medical discipline Exp: 0-3 years |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. etc. | 1/7/2020 |
| 826 | Acumed New York, NY Sales Associate BS/BA in a business or medical discipline Exp: 0-3 years |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. etc. | 1/7/2020 |
| 827 | Acumed Boston, MA Sales Associate BS/BA in a business or medical discipline Exp: 0-3 years |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. etc. | 1/7/2020 |
| 828 | Acumed Wichita, KS Sales Representative BS/BA in a business or medical discipline Exp: 0-2 years |
The Sales Representative (SR) exceeds sales quota within an assigned territory by delivering Acumed product on time providing high quality technical assistance in the OR and assists in driving market acceptance and adoption of Acumed Products utilizing technical and surgical knowledge. The SR assists continuously assesses the customer base to identify new business opportunities and develops a targeted sales strategy for each identified opportunity proactively ensuring all leads are followed up on appropriately. etc. | 1/7/2020 |
| 829 | Acumed Nashville, TN Sales Representative BS/BA in a business or medical discipline Exp: 0-2 years |
The Sales Representative (SR) exceeds sales quota within an assigned territory by delivering Acumed product on time providing high quality technical assistance in the OR and assists in driving market acceptance and adoption of Acumed Products utilizing technical and surgical knowledge. The SR assists continuously assesses the customer base to identify new business opportunities and develops a targeted sales strategy for each identified opportunity proactively ensuring all leads are followed up on appropriately. etc. | 1/7/2020 |
| 830 | Adaptimmune Philadelphia, PA Manufacturing Cell Therapy Specialist (2nd Shift) BS in cell biology, bioengineering, or medical technology Exp: 1+ year(s) |
RESPONSIBILITIES: Performs cell manufacturing related activities while wearing clean room attire in an aseptic cGMP manner. Documents production operations in corresponding batch records and log books per established procedures ensuring accuracy and timely completion. Identifies real time manufacturing issues (deviations and atypical results) and communicates them to the Manufacturing Manager and the Quality team in a timely manner. Responsible for drafting or modifying manufacturing documents with the Manager and Quality Team oversight. etc. | 1/7/2020 |
| 831 | Adaptive Biotechnologies Seattle, WA Clinical Laboratory Technologist I-IV BS in medical technology or a physical or biological science Exp: 1-2 years |
The Production Associate position will be responsible for processing client samples using high throughput DNA sequencing technology. This role will work within a team of other Laboratory Technicians in a fast-paced, high production setting to process research and clinical diagnostic samples. The shift for this job is 7am-4pm, Sunday's through Thursday's. Responsibilities: Perform DNA/RNA extractions, PCR amplification and high-throughput sequencing assays on DNA libraries. Perform QC and carry out routine tasks accurately and following strict methodologies. Completes assignments of complex nature requiring a basic knowledge of techniques and practices related to the research area. Supports business goals, knowledge and skills, and cross-functional teamwork. Keep accurate and detailed records for all workflows. Ability to work independently and carry out optimization and validation experiments. etc. | 1/7/2020 |
| 832 | Adaptive Biotechnologies Seattle, WA Study Management Specialist III BS/BA in biology or related Exp: 1+ year(s) |
The Study Management Specialist II is responsible for ensuring that incoming clinical trial and research projects are appropriately entered into laboratory information systems (LIMS) to ensure data integrity and conformance to project requirements prior to release of samples to the production laboratory operation. Job Responsibilities: Work cross functionally with computational biology and business development teams to generate data definitions and maps for incoming samples as defined in data transfer agreements. Ensure data definitions can be mapped to corresponding laboratory information management system (LIMS) fields, and hence ensure that data can be entered in a systematic manner. Prepare manifests that ensure consistency of data entry, and hence data integrity. etc. | 1/7/2020 |
| 833 | Adare Pharmaceuticals Vandalia, OH Operator I HS diploma or equivalent Exp: 1+ year(s) |
Scope: Learning to disassemble, clean and reassemble production equipment to prepare for processing. Learning to conduct pre-processing staging to assure that required raw materials are assembled, weighed, and meets specified consistency as outlined in written procedures. Learning to operate the process equipment to create product that meets predetermined specifications. Learning to monitor and record critical process parameters. Learning to make necessary adjustments to assure finished product meets customer specifications. Learning to transfer processed materials through production equipment to include dryers, filtration systems, blenders, and sieving equipment. Learning to package finished product and transfer to warehouse. Learning to operate solvent recovery system to assure cyclohexane ingredient is of the purest form. etc. | 1/7/2020 |
| 834 | Admera Health South Plainfield, NJ Associate Bioinformatics Scientist, Clinical Services MS in bioinformatics Exp: 0-2 years |
Responsibilities: Work collaboratively with bench scientists, comprehend project objectives, provide informatics solutions. Develop and implement bioinformatics analyses, applications, and workflows to expand our genomics and bioinformatics capabilities. Integrate computational analysis to project design and data interpretations. Maintain and improve back end of cloud-based genomic interpretation system. etc. | 1/7/2020 |
| 835 | Admera Health South Plainfield, NJ Senior Clinical Technician BS in medical technology or life sciences Exp: 1+ years |
Responsibilities: Perform high complexity laboratory tests in accordance with SOPs and CLIA/CAP regulations. Evaluate and interpret results. Maintain accurate documentation and records (accessioning through result reporting). Proper handling of clinical samples. Maintain and operate lab equipment and instruments. Order supplies and reagents. Additional tasks may be assigned. etc. | 1/7/2020 |
| 836 | Aesculap Allentown, PA General Manufacturing Associate (Detailed Assembler) 3rd Shift - Pain Control HS diploma or equivalent Exp: 0-1 years |
This position is to assemble, package and inspect medical devices in accordance with the quality and production standards established by our organization. This includes working with chemicals, machines and measurement equipment. This position must follow procedures, policies and applicable regulatory policies to meet the requirements of our Quality Policy. Responsibilities: Essential Duties: Follows established procedures and guidelines to manufacture the organizations products according to specifications and schedules; volume, cost and waste targets; quality standards. etc. | 1/7/2020 |
| 837 | Aesculap Allentown, PA General Manufacturing Associate (Detailed Assembler) 2nd Shift - Pain Control HS diploma or equivalent Exp: 0-1 years |
This position is to assemble, package and inspect medical devices in accordance with the quality and production standards established by our organization. This includes working with chemicals, machines and measurement equipment. This position must follow procedures, policies and applicable regulatory policies to meet the requirements of our Quality Policy. Responsibilities: Essential Duties: Follows established procedures and guidelines to manufacture the organizations products according to specifications and schedules; volume, cost and waste targets; quality standards. etc. | 1/7/2020 |
| 838 | NantKwest La Jolla, CA Research Associate BS Exp: 1 year in lab |
The individual will be responsible for laboratory maintenance, group-support activities to further our NK & T cell initiative from primary tissue sources. This is a great opportunity for a recent college graduate or individual willing to diligently take care of laboratory maintenance and pick up cutting edge scientific skills at the same time to support different projects. Laboratory maintenance that includes ordering, stocking of laboratory and accessory facilities with necessary reagents and supplies. | 12/30/2019 |
| 839 | NantKwest La Jolla, CA Research Associate BS or MS in biochemistry, biological sciences Exp: 1-3 years as research technician |
Daily tasks associated with the construction and purification of vaccine vectors. Demonstrated proficiency and understanding of concepts of chromatography: HPLC and/or FPLC. Operation and maintenance of laboratory instruments such as centrifuges, incubators, electrophoresis instruments, TFF, imagers, and other measuring instruments and devices. Preparation of laboratory reagents, stocks, cultures, and cell lines | 12/30/2019 |
| 840 | Natera Austin, TX Production Engineer - Statistics/Data Analysis BS/BA in engineering, bioinformatics, math or related Exp: 0-2 years |
Production Engineer - Statistics performs basic data analysis to manage daily operations for the product and its algorithms. Manage daily operations for the product algorithms. Track ongoing product performance metrics and investigate any variations, in cooperation with lab operations. Investigate data quality concerns using Python/R. Drive informed and timely solutions for unexpected scenarios. Track issues, coordinate new feature releases, and provide data analysis support to laboratory operations. | 12/30/2019 |
| 841 | Natera San Carlos, CA Quality Assurance Specialist BS/BA in life sciences, engineering or software Exp: 1+ years in biotech |
This is an entry-level position to assist the Quality Department in continuous compliance and improvement. Assist with collecting and trending quality metrics. Assist with assigning IDs for CAPAs, Deviations, SCAR, Complaints, and NCRs and filing completed records. Stays current on applicable regulation and guidance from FDA, ISO13485, CLIA, CAP, etc. Assist with review and approval of qualification records | 12/30/2019 |
| 842 | Natera San Carlos, CA IQC Associate HS Diploma/GED Exp: 1-2 years in medical device manufacturing |
The IQC Associate conducts incoming material inspections required to assure product safety and compliance to specifications, GMP’s, and ISO requirements. Works with other Quality Inspectors and Laboratory personnel to complete testing, special projects and other projects as required. Ensures compliance with quality systems, policies, procedures and practices and all local, state, federal and safety regulations, policies and procedures. | 12/30/2019 |
| 843 | Natera Austin, TX QC Equipment Specialist 1 BS/BA in biological sciences Exp: 0-2 years |
The Quality Control Equipment Specialist 1 is responsible to ensure superior performance of all equipment and instrumentation utilized in the Operations laboratory. The QC Equipment Specialist will be the primary point of contact for production lab personnel when equipment and instruments are not operating or not meeting operational specifications | 12/30/2019 |
| 844 | Natera Austin, TX Clinical Laboratory Operator I BS/BA in biological sciences Exp: 0-2 years |
Assists in analyzing specimens and maintains equipment in good operating condition. Assist in testing of patient samples according to standard operating procedure. Responsible for maintaining updated understanding and knowledge of methods performed in the lab. Recognizes, escalates, and troubleshoot equipment malfunctions and common processing errors according to the laboratory’s standard operating procedures. Follows GLP (good laboratory practice): maintain clean and organized workspace | 12/30/2019 |
| 845 | Natera San Carlos, CA Clinical Lab Scientist II BS/BA in med tech/biological sciences, or related Exp: 1-2 years as medical technologist |
Analyzes specimens and maintains equipment in good operating condition. Verify the proper specimen being analyzed and perform tests that need to be completed. Analyze clinical laboratory specimens following the standard methods and procedures in an efficient manner with little to no errors. Responsible for maintaining updated understanding and knowledge of methods performed in the lab | 12/30/2019 |
| 846 | Natera Austin, TX Clinical Data Operator 1 HS Diploma/GED Exp: 0-1 years |
Clinical Data Operator 1 accessions patient samples according to standard operating procedures (SOP) with high efficiency and accuracy. Create new orders on Laboratory Inventory Management System (LIMS) and perform necessary checks to ensure proper accessioning. Accession samples with high accuracy and efficiency. Accurately enter patient data into the Laboratory Inventory Management System (LIMS). Ensure that the information in LIMS is up-to-date. | 12/30/2019 |
| 847 | Natus Medical Madison, WI Repair Technician (I or II) AA in relevant field Exp: 0-6 months |
Test and calibrate assemblies to meet quality standards as well as perform electronic calibration and verify fixtures. Trouble shoot assemblies independently with exceptional computer skills. Maintain a strong commitment to high quality work with less than 2% failure rate on repairs. Maintain a 10 business day repair turnaround time on customer owned properties. Maintain minimum stock with refurbished parts to assure same day order fulfillment to assure best in class customer satisfaction | 12/30/2019 |
| 848 | Natus Medical Boston, MA Field Service Technician AA or equivalent Exp: 6-12 months experience/training |
The Field Service Technician provides industry-best technical support on computer-based medical instrumentation and establishes strong relationships with customers, managers and the national service team. This position will be based remotely and responsible for multi-state service coverage (Region:CT, ME,MA, NH, RI and VT). | 12/30/2019 |
| 849 | Navitas Life Sciences Rockville, MD Research Specialist - KAI Research BS/BA in biological/health sciences Exp: 0-1 years |
Demonstrate a thorough understanding of the application of basic clinical research methodologies to meet protocol and regulatory requirements. Develop client materials according to project requirements, including but not limited to, project-specific documentation, operating procedures, standards, and work flows. Monitor project changes to ensure documentation and systems/software conforms to new requirements. Process incoming and outgoing project materials to monitor, verify, and track receipt of documentation and ensures appropriate distribution of materials to internal and external research personnel and sites. | 12/30/2019 |
| 850 | Navitas Life Sciences Rockville, MD Research Assistant - KAI Research BS/BA in biological/health sciences Exp: 0-1 years |
Apply basic clinical research methodologies to meet protocol and regulatory requirements. Assist in the development of client deliverables according to project requirements, including but not limited to, project-specific documentation, operating procedures, and work flows with direction of more experienced staff. Process incoming and outgoing project materials to monitor, verify, and track receipt of documentation and ensure appropriate distribution of materials to internal and external research personnel and sites. | 12/30/2019 |
| 851 | Nelson Lab Itasca, IL Lab Analyst - Chemistry - M-F, Days HS Diploma/GED to BS Exp: 0-1 years |
The Laboratory Analyst conducts testing in accordance with established procedures using Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and under the supervision of the Study Director. Additionally, Laboratory Analysts record data concurrently, maintain traceability of samples throughout testing and notify the Study Director of any unforeseen circumstances that occur during testing. | 12/30/2019 |
| 852 | Nelson Lab Salt Lake City, UT Lab Analyst HS Diploma/GED to BS Exp: 0-1 years |
The Laboratory Analyst conducts testing in accordance with established procedures using Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and under the supervision of the Study Director. Additionally, Laboratory Analysts record data concurrently, maintain traceability of samples throughout testing and notify the Study Director of any unforeseen circumstances that occur during testing. | 12/30/2019 |
| 853 | Nelson Lab Salt Lake City, UT Development Chemist BS/BA in chemistry or related Exp: 1-3 years |
This position involves decision making in the areas of analytical chemistry, equipment maintenance, data quality, and workflow. Duties include analysis of a wide variety of samples following establish methods or standards, and supporting the development and implementation of laboratory policies and procedures. Experience with instrumentation/equipment and software, such as gas chromatography/mass spectroscopy (GC/MS), high performance liquid chromatography/mass spectroscopy (HPLC/MS), and Inductively coupled plasma/mass spectrometry (ICP/MS). (Ideal candidate needs to have experience with least one of these instruments.) | 12/30/2019 |
| 854 | Neocis Miami, FL Control Software Engineer BS in computer science/electrical engineering Exp: 0-2 years |
Neocis is looking for a robot control software engineer to contribute significantly to the core design. You will be responsible for software design and development of a real-time robot controller, verification and validation testing for safety and reliability and support and contribute to intellectual property development. You will work with cross-functional teams including software and electrical engineers and marketing as well as clinicians and clinical staff. | 12/30/2019 |
| 855 | Nephron Pharma West Columbia, SC Quality Assurance OnlineEvening 12 hour Shift ONLY HS Diploma/GED Exp: 1-2 years in QA/Production |
Performs Weight Check and Quality Attributes Inspection of the product through the filling and packaging process in compliance with company policies / procedures, FDA and cGMP regulations. Ensures the accuracy and completeness of batch records. Assists with additional work duties or responsibilities as evident or required. Performs other duties as assigned or apparent. | 12/30/2019 |
| 856 | Nephron Pharma West Columbia, SC Microbiology Analyst I BS in biological/life sciences Exp: 1 year in pharma preferred |
Perform microbiology department related tests according to USP methods and established procedures that follow cGMP guidelines and demonstrate outstanding aseptic techniques. Demonstrate high proficiency level on tests performed. Apply quality scientific techniques in the microbiological analysis of raw materials; in-process & finished product samples to include: sterility, bioburden, identification, environmental monitoring, growth promotion, microbial recovery and media fill tests following approved procedures. | 12/30/2019 |
| 857 | NeuMoDx Ann Arbor , MI Manufacturing Specialist, Reagent BS/BA in science or chemistry Exp: 1+ year in lab/reagent production |
Manufacturing Specialists are required to have a strong knowledge of manufacturing methods and techniques, process development experience, work flow understanding, ability to understand formulations and follow recipes and testing protocols for any in-process Quality checks | 12/31/2019 |
| 858 | Neurocrine Bioscience San Diego, CA Associate Scientist, In Vivo BS/BA in biology or related Exp: 1 year or more related experience |
The primary tasks for this position will include transgenic animal colony maintenance and breeding, compound formulation and dosing, behavioral assessments, stereotaxic surgery and tissue collection. This position requires a high level of organization and attention to detail as well as the willingness and ability to work both independently and as part of a team. Previous experience with stereotaxic surgery, AAV administration and mouse colony maintenance preferred. | 12/31/2019 |
| 859 | Nevro Redwood City, CA Quality Engineer I - Temp BS in technical sciences Exp: 0-2 years in quality/regulatory |
The Quality Engineer I is responsible for Quality Assurance activities related to the life cycle of the product. Trave to and manage manufacturing assembly process at Suppliers. Perform data analysis for root cause investigations | 12/31/2019 |
| 860 | Nevro Redwood City, CA Firmware Engineer BS in computer engineering or related Exp: 1-2 years, familiarity with C, C++, C# or other |
The Firmware Engineer shall participate in research and product development activities ranging from product concept through transfer to manufacturing. This position will apply knowledge of engineering principles and practices for software development of implantable medical devices and accessories. | 12/31/2019 |
| 861 | Nevro Redwood City, CA Technial Support Specialist - Temp BS in scientific, technical, or medical field Exp: 1+ year in customer service |
Great Customer Experience is one of the keys to Nevro’s success. The Quality Compliance Specialist is one of the few roles in Nevro that has a direct customer touchpoint to resolve product and therapy questions or issues. This role is critical to ensure that the customer is served as best as we can to ensure that our product and therapy continues to deliver much needed relief to our customers. | 12/31/2019 |
| 862 | New England Biolabs Bethesda, MD Associate Field Representative - Mid-Atlantic BS in core life sdciences Exp: 1 year in lab preferred |
New England Biolabs (NEB) is seeking a Part-Time Sales Associate to assist the Mid-Atlantic Field Account Manager with prospecting, generating and closing sales leads in the territory. With guidance from the Account Manager, a goal for the Part-Time Sales Associate will be to eventually work independently on assigned accounts. This is a 20 hour a week position. The ideal candidate will live in the Bethesda, MD area. | 12/31/2019 |
| 863 | New England Biolabs New York, NY Associate Field Representative - Tri-State BS in core life sdciences Exp: 1 year in lab preferred |
New England Biolabs (NEB) is seeking a Part-Time Sales Associate to assist the Tri-State Field Account Manager with prospecting, generating and closing sales leads in the territory. With guidance from the Account Manager, a goal for the Part-Time Sales Associate will be to eventually work independently on assigned accounts. This is a 20 hour a week position. The ideal candidate will live in the Manhattan, NY area. | 12/31/2019 |
| 864 | New England Peptide Gardner, MA Lab Technician BS/BA in biology or chemistry Exp: 1 year preferred |
Duties include: Operations and maintenance of peptide synthesis instrumentation, liquid chromatography instrumentation, etc. Peptide cleavage data analysis and characterization of peptides using HPLC and Mass Spec. | 12/31/2019 |
| 865 | New England Peptide Gardner, MA Facility Maintenance AS/AA in industrial/electrical/mechanical engineering Exp: 1-2 years in related |
This role will be responsible for assisting in the completion of the day-to-day activities involving the maintenance of the facility, equipment and machinery and the overall facility appearance. Participate and assist in the maintenance of all company property, including but not limited to, manufacturing equipment, buildings, grounds, HVAC, electrical, plumbing, safety and others as necessary. | 12/31/2019 |
| 866 | New England Peptide Gardner, MA Lab Assistant HS Diploma or higher Exp: 1 year preferred |
NEP is seeking a highly motivated individual interested in a career in the Biotech/Pharmaceutical industry. Local candidates only. No experience necessary, we will train! Working alongside other Peptide Scientists and Technicians, the Lab Assistant will help support the production process. | 12/31/2019 |
| 867 | New England Peptide Gardner, MA Lab Technician BS/BA in biology or chemistry Exp: 1 year preferred |
Duties include: Operations and maintenance of peptide synthesis instrumentation, liquid chromatography instrumentation, etc. Peptide cleavage data analysis and characterization of peptides using HPLC and Mass Spec. | 12/31/2019 |
| 868 | Avecia Pharma Services Irvine, CA Chemist I - QC BS/BA in chemistry or related Exp: 1-2 years in pharma |
Perform routine laboratory analysis of raw material and container closure system samples according to established specifications and procedures using basic analytical chemistry techniques in accordance with Customer, Company and cGMP requirements. | 1/5/2020 |
| 869 | Nkarta Therapeutics South San Francisco, CA Research Associate MS in molecular/cell biology, immunology Exp: MS: 0-3 years |
The ideal candidate will interact closely with group leaders, scientists and research associate to drive discovery and development of new therapeutics in pre-clinical development. Duties include: Mammalian tissue culture, including isolation and culture of primary human cells from whole blood. Perform studies utilizing cellular immunology to develop and analyze in vitro cell-based assay to support early discovery efforts and pipeline. Perform studies utilizing cellular immunology to develop and analyze in vitro cell-based assay to support early discovery efforts and pipeline. | 1/5/2020 |
| 870 | Nkarta Therapeutics South San Francisco, CA Research Associate (in vivo) MS in biological sciences Exp: 1 year in pharma/biotech |
Conducts pharmacological evaluation of test agents (cell products or small molecule) in subcutaneous, systemic and orthotopic in vivo oncology models. Assists in sample processing, homogenization, or generation of single cell suspensions for ex vivo flow cytometry analysis or PCR analysis | 1/5/2020 |
| 871 | Nkarta Therapeutics South San Francisco, CA Research Associate/Senior Research Associate MS in biological sciences Exp: 0-3 years in lab |
Execute a broad range of cell based functional and phenotypic assays for characterization of engineered NK and T-cells to accelerate projects in pre-clinical development. Conduct in vitro mechanism of action studies using primary human or mouse immune cells and cell lines to evaluate activity of candidate therapies. | 1/5/2020 |
| 872 | Nkarta Therapeutics South San Francisco, CA Research Associate/Senior Research Associate MS in cell biology or related Exp: 0-3 years in lab |
Generate stable cell lines and master cell banks for both in vitro assays and in vivo pharmacology studies. Oversee and perform daily activities related to the maintenance and scale up of in-house cell lines and primary human immune cells | 1/5/2020 |
| 873 | Nkarta Therapeutics South San Francisco, CA Research Associate/Senior/Process Engineer MS in biological sciences Exp: 1-6 years |
Support process development of phase appropriate cell therapy production processes. Evaluate raw materials and culture systems for use in cell therapy manufacturing processes. Support process optimization efforts to increase process robustness, reduce costs and improve yield | 1/5/2020 |
| 874 | Nobel Life Sciences Woodbine , MD Study Coordinator BS/BA in sciences Exp: 1 year related work |
Assist Study Director in determining staffing requirements, scheduling and documenting all critical events. Assist Study Director with protocols and reports preparation. | 1/6/2020 |
| 875 | Nobel Life Sciences Woodbine , MD Quality Control Associate BS/BA in sciences Exp: 1 year in QC position |
Responsibilities include: Supervise day to day quality control operations and documentation. Assist in writing and reviewing SOPs, study protocols and reports. Coordinate in-house and external routine maintenance including calibration and certification and maintenance of lab equipment. etc. | 1/6/2020 |
| 876 | Nobel Life Sciences Woodbine , MD Animal Lab Tech BS/BA in sciences Exp: 1 year in GLP, preferred |
Follow and perform standard operating procedures (SOP) & Protocols on study and stock animals, including, but not limited to: clinical observations, food consumptions, body weights, urine collection, administering anesthesia, mating procedures, blood draws dose administration, restraint, euthanasia, catheter placement, feeding, food removal, on laboratory animals. | 1/6/2020 |
| 877 | Nobel Life Sciences Woodbine , MD Animal Care Tech BS/BA in sciences Exp: 1 year in GLP, preferred |
Read, understand and follow all SOP’s, Quality Assurance Standards and perform duties in accordance with the study protocol. Monitor daily animal health and wellness checks and report any abnormal animal conditions to the supervisor and/or the Study Director and record observations in appropriate log. | 1/6/2020 |
| 878 | Nordson Minneapolis, MN NPI Engineer I BS in mechanical/biomedical/manufacturing engineering Exp: 0-3 years in medical device product development |
The desired individual will possess a broad range of medical device design and development skills and experience, as well as depth of knowledge of process development, process validation, lean manufacturing methodology, and statistical process control. Develop and document manufacturing processes for medical devices (disposable and reusable), catheters, implants, and/or packaging, from concept through market introduction. | 1/6/2020 |
| 879 | Nordson Elk Grove Village, IL Field Service Technician AS/AA Exp: 0-2 year |
Responsible for performing on-site installation, servicing and repair of complex equipment and systems. Works on problems of moderate scope where analysis of situations or data requires a review of identifiable factors. Exercises judgment within defined procedures and practices to determine appropriate action. | 1/6/2020 |
| 880 | Nordson Salem, NH Production Associate 1 (Balloons) Third Shift Temp to Hire HS Diploma/GED Exp: 0 years required |
Position consists of manufacturing of medical components in a clean room environment while under general supervision in accordance with specifications and written procedures. This position may include machine operation, manual production using hand tools, visual inspection, physical measurements, and packaging of finished product. This position requires the ability to work with small and delicate components using a high degree of dexterity and accuracy. | 1/6/2020 |
| 881 | Norwich Pharma Norwich, NY Validation Engineer I BS/BA or work experience Exp: 0-4 years |
The Validation Engineer I - Cleaning conducts validation assessments of equipment, facilities and process systems. Compile and analyze validation data, prepare protocols, reports and make recommendations for changes and/or improvements and maintains appropriate validation documentation and files. | 1/6/2020 |
| 882 | Norwich Pharma Norwich, NY Technician I Pilot Manufacturing HS Diploma/GED Exp: 1-3 years in manufacturing enviornment |
Primary Responsibilities include: support pilot plant functions. Accurately execute all GMP documentation including batch records, cleaning records, logbooks, etc. Escalates documentation and process errors, events, and deviations immediately to PDTS Manager/Group Leader and PDTS QA. | 1/6/2020 |
| 883 | Nostrum Laboratories Kansas City, MO Packaging Technician HS Diploma/GED Exp: 1 year in pharma/food/manufacturing |
The Packaging Technician performs routine packaging operations for the production of pharmaceutical products; operates packaging line equipment according to established SOPs and department procedures. Prepares and cleans room, equipment, facility and documents for manufacturing and packaging process | 1/6/2020 |
| 884 | Notable Foster City, CA Research Associate - High Throughput Screening BS/MS in biological sciences/engineering Exp: 6 months in lab experience |
You will be supporting our numerous projects and be an integral part in scaling up for future upcoming projects. Will be responsible for processing primary samples and preparing them for our automated high-throughput screens. | 1/6/2020 |
| 885 | Nova Biomedical Waltham, MA Repenishment Associate HS Diploma Exp: 1+ year in distribution/ordering |
Essential Responsibilities are to ensure the accurate movement (stocking, replenishing, consolidating, blocking, fulfilling) of materials and products within the Distribution Department and report any /all batch number or quantity discrepancies related to Distribution materials. Perform cycle counting of assigned materials / products, assist in reconciling variances, identify materials/ products with assigned placards (short-dated, Quality holds, etc.) | 1/6/2020 |
| 886 | Nova Biomedical Waltham, MA Reagent Packager I - First Shift HS Diploma/GED Exp: 1+ year in related |
The Packager, under general supervision, will follow established procedures in packaging reagent kits. This individual is responsible for working on an assembly line to assemble the various kits within the established quality and time standards. The individual will work with various packaging equipment such as: automated/manual tape machines, manual pallet trucks, conveyors, flow racks and other packaging devices | 1/6/2020 |
| 887 | Nova Biomedical Waltham, MA Jr Electornic Technician HS Diploma/GED Exp: 1+ year as test technician |
The Jr. Electronic Technician at Nova Biomedical is responsible for operating test and measurement equipment, such as Oscilloscopes and multimeters, to test instruments and assemblies. Essential Responsibilities include: ability to troubleshoot with limited supervision to the component level on low complex boards (thru-hole). Ability to use small hand tools for soldering. Basic knowledge of computers and electronic components. Basic understanding of menu driven computer programs. | 1/6/2020 |
| 888 | Vicarious Surgical Charlestown, MA Artificial Intelligence Engineer MS in computer science Exp: 1-3 years |
Joining the Research & Development team as an Artificial Intelligence engineer, you will lay the groundwork for a brand new team at Vicarious Surgical giving intelligence to the next generation of surgical robotics. We are looking for dynamic, collaborative individuals with a passion for AI who thrive in a fast-paced, creative, and strategic environment. You will enjoy working with a highly talented and diverse team of engineers to develop Artificial Intelligence, Perception, Computer Vision, and Robotic Controls features for our robots. This job entails: Research and develop technologies for conventional AI, Computer Vision, Machine Learning, multi-sensory perception, sensor fusion, scene understanding etc. for robotics applications. etc. | 12/17/2019 |
| 889 | Viracor Lee's Summit, MO Clinical Laboratory Scientist I BS/BA in a laboratory science Exp: 1 year |
This is a Full Time position. Schedule is Tuesday - Saturday, 1:00 AM to 9:30 AM (opportunity for 10-hour shift with rotating day off following training), with overtime as needed. Candidates currently living within a commutable distance of Lee’s Summit, Missouri are encouraged to apply. The Clinical Laboratory Scientist (CLS) performs laboratory testing, preventive maintenance, troubleshooting, calibration of equipment, quality control procedures and is responsible for the validity of test results. Employee Responsibilities: Perform laboratory assays in accordance with Viracor-IBT’s standard operating procedures. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Maintain adequate inventory of supplies, reagents and materials. etc. | 12/17/2019 |
| 890 | Viracor Lee's Summit, MO Clinical Laboratory Scientist I BS/BA in a laboratory science Exp: 1 year |
This is a Full Time position. Schedule is Tuesday - Saturday, 8:00 AM to 4:30 PM (opportunity for 10-hour shift with rotating day off following training), with overtime as needed. Candidates currently living within a commutable distance of Lee’s Summit, Missouri are encouraged to apply. The Clinical Laboratory Scientist (CLS) performs laboratory testing, preventive maintenance, troubleshooting, calibration of equipment, quality control procedures and is responsible for the validity of test results. Employee Responsibilities: Perform laboratory assays in accordance with Viracor-IBT’s standard operating procedures. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Maintain adequate inventory of supplies, reagents and materials. etc. | 12/17/2019 |
| 891 | Viracor Lee's Summit, MO Clinical Laboratory Scientist I BS/BA in a laboratory science Exp: 1 year |
This is a Full Time position. Schedule is Monday - Friday, 8:00 AM to 4:30 PM (opportunity for 10-hour shift with rotating day off following training), with overtime as needed. Candidates currently living within a commutable distance of Lee’s Summit, Missouri are encouraged to apply. The Clinical Laboratory Scientist (CLS) performs laboratory testing, preventive maintenance, troubleshooting, calibration of equipment, quality control procedures and is responsible for the validity of test results. Employee Responsibilities: Perform laboratory assays in accordance with Viracor-IBT’s standard operating procedures. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Maintain adequate inventory of supplies, reagents and materials. etc. | 12/17/2019 |
| 892 | Viracor Lee's Summit, MO Clinical Laboratory Scientist I BS/BA in a laboratory science Exp: 1 year |
This is a Full Time position. Schedule is Tuesday - Saturday, 12:00 PM to 8:30 PM (opportunity for 10-hour shift with rotating day off following training), with overtime as needed. Candidates currently living within a commutable distance of Lee’s Summit, Missouri are encouraged to apply. The Clinical Laboratory Scientist (CLS) performs laboratory testing, preventive maintenance, troubleshooting, calibration of equipment, quality control procedures and is responsible for the validity of test results. Employee Responsibilities: Perform laboratory assays in accordance with Viracor-IBT’s standard operating procedures. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Maintain adequate inventory of supplies, reagents and materials. etc. | 12/17/2019 |
| 893 | Viracor Lee's Summit, MO IT Business Analyst I AS/BS in laboratory science Exp: 1-2 years |
This is a Full Time position. Schedule is Monday - Friday, 8:00AM – 5:00PM, with overtime as needed. Candidates currently living within a commutable distance of Lee’s Summit, Missouri are encouraged to apply. The IT Business Analyst supports the organization by assessing the impact of requested changes, capturing and documenting requirements, and ensuring that those requirements are delivered by IT. In addition, the Business Analyst is responsible for the documentation and execution of test plans for the delivered functionality while supporting the business through the implementation process. Business Analysis is part of the Software Development Life Cycle (SDLC) and the Business Analyst will be involved from initial concept through final implementation, including requirements gathering, design, testing and implementation. Employee Responsibilities: Consult with different areas of the organization to identify and document the requirements for new systems and enhancements to existing systems. Document business functions and processes using a best practice standard developed by the Business Analysis team. etc. | 12/17/2019 |
| 894 | Viracor Lee's Summit, MO Research Scientist I BS/BA in a laboratory science Exp: 0-3 years |
This is a Full Time position. Schedule is Monday – Friday, 1:00pm- 9:30pm with overtime as needed. Candidates currently living within a commutable distance of Lee’s Summit, Missouri are encouraged to apply. The Research Scientist is primarily responsible for conducting research, development, validation and execution of assays to meet the development requirements within corporate/client timelines and cost objectives. Employee Responsibilities: Learn new techniques and instrumentation. Implement research plans, designs and testing protocols. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Keep accurate documentation of all research project steps according to Viracor Eurofins regulatory guidelines. etc. | 12/17/2019 |
| 895 | Viracor Lee's Summit, MO Research Scientist I BS/BA in a laboratory science Exp: 0-3 years |
This is a Full Time position. Schedule is Monday – Friday, 8:30pm- 5:00pm with overtime as needed. Candidates currently living within a commutable distance of Lee’s Summit, Missouri are encouraged to apply. The Research Scientist is primarily responsible for conducting research, development, validation and execution of assays to meet the development requirements within corporate/client timelines and cost objectives. Employee Responsibilities: Learn new techniques and instrumentation. Implement research plans, designs and testing protocols. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Keep accurate documentation of all research project steps according to Viracor Eurofins regulatory guidelines. etc. | 12/17/2019 |
| 896 | Visterra Waltham, MA Research Associate BS in biochemistry or related Exp: 1 year |
Visterra, Inc., is looking to hire a highly motivated Research Associate with research experience in biochemistry, protein sciences and/or molecular biology applied in the context of antibody-based therapeutic drug discovery. This individual will play a key technical role in advancing Visterra’s early research programs in autoimmunity, immunology and other related areas of therapeutic interest through the design and implementation of library-based screening methods, recombinant protein production, protein engineering, and biochemical, biophysical, and biological characterization of early and late stage leads to support the discovery andvalidation of therapeutic antibody candidates. etc. | 12/17/2019 |
| 897 | Voyager Therapeutics Cambridge, MA Clinical Trial Associate (Contract) BS in a life science Exp: 0-2 years |
The Clinical Trial Associate (CTA) will support the clinical trial team, ensuring that all essential documentation is collected, maintained and filed during the study. The CTA will also assist the CTM for assigned studies in the operational and logistical aspects of clinical trials according to ICH-GCP and Voyager standard operating procedures. This position reports in directly to the Associate Director of Clinical Operations. Responsibilities: Support project meeting logistics such as: calendar management, room & equipment set up, attendance tracking, agenda preparation, drafting of meeting minutes, and collation of materials. Set up, maintain and periodically audit Trial Master Files and ensure all relevant study documents are filed and archived based on the appropriate guidelines/processes. Execute assigned study tasks, awareness of priorities and timelines, assist in tracking study metrics, maintenance and distribution of trackers, support preparation of study newsletters, communicate with and oversee CRO for assigned start-up activities. etc. | 12/17/2019 |
| 898 | Voyager Therapeutics Cambridge, MA Research Associate/Senior Research Associate, Molecular Biology BA/BS Exp: 1-3 years |
Voyager Therapeutics seeks a highly motivated and experienced molecular biologist to contribute to its research team at its facility in Cambridge, Massachusetts. The candidate will be involved in novel AAV capsid discovery, screening AAV variant libraries in small and large animals and engineering capsids for desired properties. This is an ideal position for an individual with extensive hands-on cellular and molecular expertise, who has a can-do attitude and strong work ethic, and thrives in a team-oriented, fast-paced, and cross-disciplinary start-up biotech environment. Requirements: Molecular cloning and prepare rAAV constructs or AAV capsid libraries. Perform plasmid purification by miniprep and maxiprep. Maintain and culture mammalian cell lines, perform transient transfection for gene expression or AAV vector production at a small or medium scale. etc. | 12/17/2019 |
| 899 | WAVE Life Sciences Cambridge, MA Research Associate – Biology BS/MS in biology or related Exp: 0-3 years |
WAVE Life Sciences USA seeks a highly motivated biologist to join its research team in Boston, Massachusetts. This is an ideal position for an individual who is interested in learning cutting edge technologies and who thrives in a team-oriented, fast-paced, and crossdisciplinary biotech environment. The candidate will be responsible for designing, executing and analyzing experiments as a member of teams focused on advancing therapeutic programs and discovery research platforms. This candidate will contribute to all levels of in vitro and in vivo discovery research to support development of optimized nucleic acid therapies in multiple disease areas. Prior experience in animal handling and tissue processing are preferred, but not required. Position Responsibilities: Experience in cell and molecular biology, including primary cell culture, transfections, mRNA quantitation by qPCR, and protein quantification by ELISA or western blot. etc. | 12/17/2019 |
| 900 | WCCT Global Cypress, CA Laboratory Accessioner HS diploma or equivalent Exp: 3-6 months |
The Laboratory Accessioner is responsible for entering all patient information, demographics, and ordered tests in the laboratory information system. The Accessioner will QC daily data entry and work under the direct supervision of the Research Laboratory Supervisor. Daily tasks include organizing requisition forms, data entry, filling out send out requisitions for outside testing, cleaning up work area, and performing waived testing. Essential Job Functions: Enter all pertinent information from the requisition into the computer correctly. Enters "special handling" and/or frozen requisitions. When handling frozen samples, will set up work areas by retrieving dry ice, ice chests, racks, and stickers. Accessioners will also be responsible for signing for the integrity of frozen specimens, received from the couriers. At the end of each night, the accessioners will deliver the specimens to the appropriate departments. Take complete inventory of contents of envelope. etc. | 12/17/2019 |
| 901 | WCCT Global Cypress, CA Laboratory Assistant HS diploma or equivalent Exp: 3-6 months |
The Laboratory Assistant is responsible for conducting the biological sampling activities related to each clinical trial. This position assists with the preparation, collection, documentation, processing, inventory and shipment of biological specimens for each study and reports to the Laboratory Supervisor. ESSENTIAL JOB FUNCTIONS: Conducts all operational activities within the laboratory related to the preparation of sample collection containers, processing biological specimens, performing testing, documenting procedures, and preparing specimen shipments. Ensures that all lab procedures are done correctly with minimal error. Follows the policies and procedures for laboratory facilities and equipment maintenance. etc. | 12/17/2019 |
| 902 | WCCT Global Cypress, CA Phlebotomist/Medical Assistant - On Call HS diploma or equivalent Exp: 3-6 months |
The On Call Research Assistant is an entry level position assisting in a variety of duties involved in the collection, compilation, and documentation of clinical research data in various departments as assigned. All data collected is quality control reviewed and is compliant with study and non-study regulations including, but not limited to the study protocol, HIPAA, OSHA, GCP, GDP, CFR, ICH Guidelines and site SOPs and Work Instructions. ESSENTIAL JOB FUNCTIONS: Follow all study and non-study regulations including, but not limited to: Patient/Volunteer Privacy (HIPAA), OSHA, Good Clinical Practice (GCP), Good Documentation Practice (GDP), Standard Operating Procedures (SOP), and department specific Work Instructions (WI). Follow proper safety and emergency policies and procedures as set forth by WCCTG. etc. | 12/17/2019 |
| 903 | Westat Rockville, MD Research Assistant BA/BS in social sciences or education Exp: 1 year |
Westat has an immediate opening for a research assistant who will work with a project team to train and support staff in state education agencies to implement a national assessment of students and to develop data analyses and reports. Provide analytical and operational support to the project and to staff in state education agencies; Develop and manage training materials; conduct web-based and in-person trainings; Provide secondary support to project Support Desk and project intranet website on an as-needed basis; Develop and maintain project schedule of web-based trainings; Review and manage data for quality control purposes and project evaluation, maintain and enhance databases of project information; Monitor the productivity and quality of the data collection effort; Work with IT and project staff on system requirements. | 12/17/2019 |
| 904 | Westat Rockville, MD Research Assistant MS/MA in a quantitative social science Exp: Not necessary for MS/MA candidates |
Westat is seeking a research assistant to work on survey research projects, assisting expert data managers in defining and processing survey data and metadata from collection through delivery to Westat’s clients. Data review and documentation writing are both part of the role. Write technical specifications for programming survey instruments and analytic variables. Define data dictionaries for complex files, test survey instruments to ensure accurate data capture, and review collected data at the detailed level. Create data descriptions and harmonize data from multiple sources; the data are collected in a variety of technologies and formats with a wide breadth of subject areas. etc. | 12/17/2019 |
| 905 | Westat Rockville, MD Research Assistant BS/BA Exp: 1 year |
We have an immediate opening for a research assistant with experience in data collection procedures and materials along with a background in quantitative research and data analysis. The successful candidate will work closely with a multidisciplinary research team working on an innovative longitudinal health and aging study and a caregiving study. Job Responsibilities: Develop specifications for computer-assisted survey data collection instruments. Draft instrument testing scripts and related materials. Working with project and IT staff on technical specifications for survey management systems. Assist in developing data collection procedures, respondent materials, and field memos. etc. | 12/17/2019 |
| 906 | Wolfe Laboratories Woburn, MA Research Associate BS/MS in chemistry, biochemistry, or related Exp: Recent graduates |
We are seeking a talented and passionate scientist who is eager to be part of our success, and who embraces our core values: Integrity, Excellence, and Teamwork. This role requires a highly driven and proactive scientist with a passion for drug development, the curiosity and flexibility to work on diverse projects, and the tenacity to tackle complex questions by developing/applying new methods to solve previously intractable problems in drug development in a dynamic, fast-paced, team-oriented and collaborative environment. etc. | 12/17/2019 |
| 907 | Worldwide Clinical Trials Austin , TX Bioanalysis Support BS Exp: 0-2 years |
The Scientific Associate, Bioanalysis Support works under the guidance of the Senior Manager, Leader of Bioanalysis and is responsible for providing support and performing analyses ranging from routine to complex using accurate and efficient analytical techniques. Understand and apply GLP guidelines in all aspects of work. Perform chemical assays ranging from routine to complex with consistent accuracy and precision. Accurately prepare stocks, reagents, standards and quality controls as needed. Work with a variety of scientists/technicians. Perform basic mathematical calculations. Document promptly and clearly all procedural processes. etc. | 12/17/2019 |
| 908 | WuXi AppTec San Diego, CA Research Associate I AS/BS in biology or related Exp: 0-1 years |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology Division. We’re seeking a highly motivated Research Associate I to join the team. Responsibilities: Assist with in vivo pharmacology experiments for preclinical contract research. Perform in vivo studies to evaluate anti-cancer efficacy of test agents in tumor mouse models with supervision. Monitor mouse groups enrolled in drug efficacy, mechanism of action, PKPD and proof-of-concept studies. Perform drug dosing by various routes of administration. Perform in-life blood sampling through various routes. Perform necropsy and tumor/organ sampling and processing. Monitor in-life study measurements: tumor volume, body weight, tracking overall health condition and survival of mice. etc. | 12/17/2019 |
| 909 | WuXi AppTec Cranbury, NJ Associate Scientist I BS in animal science, biology, or related Exp: 0-3 years |
Plans and carries out in vivo experiments and associated research assignments in rodents. Maintains the vivarium, labs, and program to AAALAC standards. Operates lab equipment including oxidizers, centrifuges, LS counters, and cage/tunnel washers. Essential Job Functions: Under regular close supervision, performs routine in vivo experimental functions in rodents, which may include: in life observations, dose administrations, sample collections, sample analysis, necropsy, and euthanasia procedures. Trains on various techniques to become proficient in in vivo. Performs husbandry tasks including observations, cage change outs, daily cleaning, and operating the cage washer. Assists with routine vivarium facility environmental monitoring (RODAC, pest control, lighting checks, etc.). etc. | 12/17/2019 |
| 910 | WuXi AppTec King of Prussia, PA Scientist Downstream Process Development BS/MS Exp: 0-5 years |
The successful candidate will be responsible for conducting experiments to support client based processes with a focus on vaccine Downstream cell culture processes. Responsibilities: Work independently on defined biopharmaceutical projects for development and/or characterization of vaccine downstream manufacturing processes. Design and execute lab-scale experiment in supporting downstream process development, verification, characterization. Perform purification experiments in BSL-2 labs and document experiments in lab notebooks. Support maintenance tasks and new technology evaluations for laboratory instrumentation; interact with outside clients/vendors/suppliers. | 12/17/2019 |
| 911 | WuXi AppTec King of Prussia, PA Scientist Upstream Process Development BS/MS Exp: 1-2 years |
The successful candidate will be responsible for conducting experiments to support client based processes with a focus on vaccine upstream cell culture processes. Responsibilities: Work on defined biopharmaceutical projects for development and/or characterization of vaccine upstream manufacturing cell culture processes. Perform bench scale and pilot scale bioreactor operations in supporting upstream process development, verification, characterization, and tech transfer. Perform data analysis and interpretation, and develop strategies for optimization and troubleshooting. Support technical transfer of processes into the non-GMP pilot plant or GMP production facility. etc. | 12/17/2019 |
| 912 | WuXi AppTec Austin , TX Clinical Project Associate HS diploma/AA/AS Exp: 1 year |
The Clinical Project Associate I provides administrative support to clinical research projects by assisting project teams in the completion of assigned project activities. This is an in-office position with that does not require travel. Provides operational support for Clinical Operations. Under direct supervision prepares, reviews and distributes the regulatory documentation according to Essential Regulatory Document Guidelines and Trial Master File (TMF) Plan. Under direct supervision prepares the investigator regulatory binders and other study start-up materials, following established procedures. Under direct supervision designated Clinical Trial Management System (CTMS) to track and process clinical trial information, (e.g., site lists/personnel, regulatory documents, Institutional Review Board re-approvals) in order to provide analysis of information to PM. Prepares and provides status reports to customers with oversight from assigned PM. Under direct supervision assures the maintenance of the TMF. etc. | 12/17/2019 |
| 913 | WuXi AppTec Philadelphia, PA Research Associate, Analytical Development - Virology BS in a biological science Exp: 1+ year(s) |
Performs research & development activities and assay validations as required under direct supervision. Drafts test methods and clearly documents all experiments according to SOPs and cGMP guidelines. Performs laboratory maintenance duties. Works closely with Testing Operations during assay transfer and validation activities. Responsibilities: Executes R&D studies planned by supervisor or technical lead. Works under close supervision from supervisor or senior personnel. Executes QP and VPs, and other GMP methods under supervision by supervisor or technical lead. Drafts test methods/RPs/SOPs under guidance of supervisor or technical lead. etc. | 12/17/2019 |
| 914 | Micr Indianapolis, IN Medical Research Coordinator Associate: BS/BA Exp: 1-3 years clinical research experience preferred |
We are seeking an experienced individual who has been involved in clinical research. 1-3 years of clinical research experience is preferred for this full-time position. | 12/8/2019 |
| 915 | MRIGlobal Kansas City, MO Electrical Engineer MS in eletrical/electronics engineering Exp: 0-3 years |
MRIGlobal has an exciting full-time opportunity for an Associate Electrical Engineer in our Intelligence, Surveillance, and Reconnaissance Division located in Kansas City, MO. In this unique opportunity, the selected candidate will work with other engineering and technical disciplines in the design, prototyping, and testing of custom systems to meet customer requirements. Furthermore, the selected candidate will: Design a broad range of analog and digital circuits, Design and layout custom circuit boards to meet challenging packaging and performance requirements, etc. | 12/9/2019 |
| 916 | Merck KGaA Verona, WI Associate Production Scientist BS in Chemistry, Biochemistry, Chemical Engineering, or equivalent Exp: <1 year |
Position primarily involves the safe and efficient manufacturing of API’s according to cGMP requirements. Kilo Lab and Pilot Plant manufacturing of APIs and intermediates. Demonstrate proper lab safety practices, and work in accordance with FDA, OSHA, EPA, DNR, DOT, and other regulatory agency guidelines. Maintain the safety and cleanliness of production areas and all related equipment during each shift, specifically potent compound handling techniques | 12/9/2019 |
| 917 | Merck KGaA Billerica, MA Research Associate - Protein Expression Bachelor’s degree in Biology, Microbiology or other related Science Exp: <1 year |
We are seeking a motivated researcher to join our recombinant protein expression team at EMD Serono. The Operations group, as part of the Protein and Cell Sciences (PCS) department, generates micrograms to grams of purified protein. The successful candidate will primarily be responsible for small and large scale expression of therapeutic and reagent proteins primarily by transient transfection of mammalian cells lines or from stable cell lines to support preclinical research. The incumbent would also be responsible for maintaining expression cell lines, cell passaging, generating stable mammalian cell lines, selection of high expressing cell lines, creation of research cell banks, optimizing cell growth and protein expression. | 12/9/2019 |
| 918 | Merck KGaA Oakland, CA Field Service Engineer - Northern CA HS Diploma/GED Exp: 1+ year in field service/mechanics |
In the role of Field Service Engineer (FSE), you will be responsible for the installation, repair, preventative maintenance and qualification of water purification systems throughout Northern CA (Oakland/North Bay/Richmond/Walnut Creek) area. You will also be responsible to provide backup support to nieghboring territoriess as required. | 12/9/2019 |
| 919 | Merck KGaA St. Louis, MO Packaging Operator I HS Diploma/GED Exp: 3+ months in ISO/GMP environment |
To stage, fill (manually or semi-automatically), cap, label, and over pack liquid, powder, and lyophilized products per approved packaging specifications. Clean laboratory glassware and batch tanks. Complete appropriate packaging documentation per FDA, ISO, and GMP procedures and deliver products to inventory. Assemble and package chemical kits. Fill, cap, and label chemical products. Manually fill liquids or powders. Utilize semi-automated equipment to fill liquids or powders. Fill products utilizing aseptic techniques. Perform fills in environmentally controlled areas. Fill hazardous products. Transfer bulk utilizing peristaltic pumps. Filter bulk materials using pumps and in-line filters or vacuum filters. Operator automated and semi-automated cappers. Manually torque caps with wrenches | 12/9/2019 |
| 920 | Merck KGaA Rockville, MD Flexible Resource Associate Scientist BS or MS in sciences Exp: BS: 1+ years, MS: 0 years |
The Flexible Resource Associate Scientist is a dynamic contributor with an opportunity to work in many different laboratories. You will conduct important assays by making scientific observations, maintaining detailed workbooks, and documenting to GLP/GMP standards. Deployment duration and the specific laboratory and will be coordinated via the Sales and Operations Planning (S&OP) process. | 12/9/2019 |
| 921 | Merck KGaA Springfield, MA Research Engineer, Life Sciences BS or MS in Mechanical, Electrical, Bioprocessing, Biochemical or Biomedical engineering Exp: <1 year |
You will be working in the life sciences group focusing on the development of the acoustic affinity cell selection platform. You will work on all aspects of the early stages of new product development, i.e., brainstorming, concept selection, engineering design and analysis, prototype assembly, testing and documentation. You will perform acousto-fluidic affinity cell selection experiments participate in design of experiments. You will take on SOP writing and lab management duties as needed to enable the team to maintain a fast and steady flow of experiments. You will develop into an independent thinker, innovator and contributor to the development of the cell selection platform. | 12/9/2019 |
| 922 | Merck KGaA St. Louis, MO cGMP Associate Production Scientist BS/BA in chemistry, biochemistry, biology, chemical engineering or related Exp: <1 year |
The cGMP Associate Production Scientist is responsible for the manufacturing of active pharmaceutical ingredients (APIs) Chemicals and bulk pharmaceuticals regulated by the Food and Drug Administration (FDA). They are responsible for following manufacturing protocols, consistent with and established according to current Good Manufacturing Practices (cGMP), and ensuring the accuracy of documentation. | 12/9/2019 |
| 923 | Miltenyi Biotec Gaithersburg, MD Manufacturing Associate - Upstream and Downstream BS/BA Exp: 0-2 years in GMP setting |
The qualified candidate will be responsible for adhering to GMP’s by following Standard Operating Procedures and executing Batch Production records using good documentation practices. Your exceptional ability to perform aseptic processes in a GMP cleanroom environment will contribute to the manufacture of lentiviral vectors used in human clinical trials, and propel Lentigen Technology’s continued growth and success. | 12/9/2019 |
| 924 | Miltenyi Biotec Auburn, CA Accounting Associate AS/AA Exp: 1-3 years in business/accounting |
As a key member of the Miltenyi Biotec Accounting team, you will provide accounts payable and accounts receivable support including collecting and posting payments, assisting in debits and credits when needed, reconciling back-up documents to invoices, processing invoices through receipt and account verification, maintaining vendor and accounting files, and preparing and verifying bank deposits. Within this role, you will perform month end duties as required inclusive of GL review and journal entries, as well as providing general administrative support. You will use your collaborative nature to effectively coordinate intercompany communications and transactions with various departments, with management, and the parent company to enable the continuous success of Miltenyi Biotec as a whole. | 12/15/2019 |
| 925 | Miltenyi Biotec Sunnyvale, CA Manufacturing Associate BS/BA in biological sciences Exp: 1-3 years in clinical processing/cell culture |
As a member of the Miltenyi Biotec Manufacturing team, you will have the exciting opportunity to participate in both the manufacture and process development of T-cells and multiple other cell therapy products within a GMP environment. The unique duties of this position will primarily consist of manufacturing primary human cells including activities that involve graft engineering for cellular therapies as well as supporting the development of scalable cell culture processes. Furthermore, you will be responsible for completing successful qualifications and ongoing support procedures for clean room operations and assisting in the development, writing, and review of SOPs, material specifications, standard manufacturing procedures, batch records and other GMP documentation. Overall, your keen ability to carry out key cell processing and manufacturing procedures will champion the continued development of Miltenyi Biotec products and growing success. | 12/15/2019 |
| 926 | Miltenyi Biotec Sunnyvale, CA Process Development Associate BS/BA in life sciences Exp: 0-2 years |
As a member of Miltenyi Biotec’s Process Development team, you will have the exciting opportunity to support the development of new processes that will generate cellular therapeutic products. You will apply your GLP/GMP experience to perform and maintain cell cultures using aseptic techniques. Ideally, you will be able to order materials and maintain inventory with the goal in mind that every effort is aimed at developing and qualifying processes required for clinical cell and gene therapy products. In addition to your primary responsibilities, you will document activities for reproducibility, clean and maintain laboratory equipment and support team members as needed. Your superb organizational and documentation skills will be instrumental in the tracking and communication of data and will ensure efficient progress towards achieving team objectives. Overall, your attention to detail and keen ability to reliably produce cell cultures in a cross-functional team will champion the continued development of Miltenyi Biotec’s new products and growing success. | 12/15/2019 |
| 927 | Miltenyi Biotec Gaithersburg, MD Research and Development Scientist, RCL/HIV MS in molecular biology, immunology, or virology Exp: 0-2 years |
As a member of the Lentigen Technology team, you will have the opportunity to perform duties within the area of development of new tests, including the development of a standard RCL test and in a second instance of an automatized RCL test. This includes the set-up of a standard test based on the use of C8166 cells, the characterization of the C8166 cells with respect to susceptibility and propagation of HIV over many cell passages, etc. A very issue related to this development is that the test has to comply with FDA requirements with at the end the transfer of the test to the QC department for routine use. Furthermore, you will be involved in the automatization of this specific test and eventually of other tests in the future. In this context, you will be directly involved in the conceptualization of such a test, responsible for designing specific experiments and analyzing the data using appropriate statistical methods. The particular duties of this position will allow you to work as part of a collaborative team environment | 12/15/2019 |
| 928 | Miltenyi Biotec Gaithersburg, MD PD Associate I BS/BA Exp: 0-2 years |
As a member of the Lentigen Technology Process Development team, you will have the exciting opportunity to support the development and tech transfer of processes to manufacture purified Lentiviral vectors used for pre-clinical and clinical products. You will apply your knowledge and prior laboratory experience to support the pre-clinical and clinical manufacturing of Lentiviral vector products. Familiarity with cell culture and/or purification technologies and analytical methods will enable you to assist in the development and tech transfer of processes compliant with GMP manufacturing requirements. | 12/15/2019 |
| 929 | Miltenyi Biotec Sunnyvale, CA Manufacturing Associate BS/BA in biological sciences Exp: 1-3 years in clinical processing/cell culture |
As a member of the Miltenyi Biotec Manufacturing team, you will have the exciting opportunity to participate in both the manufacture and process development of T-cells and multiple other cell therapy products within a GMP environment. The unique duties of this position will primarily consist of manufacturing primary human cells including activities that involve graft engineering for cellular therapies as well as supporting the development of scalable cell culture processes. | 12/15/2019 |
| 930 | Miltenyi Biotec San Diego, CA Executive Assistant AS/AA in business or related Exp: 0-2 years |
As a key member of the Miltenyi Biotec team, you will have the opportunity to provide administrative support to the President as well as other department heads in assigned activities. The unique duties of this position will allow you to oversee schedules, track activities, and serve as key contact between executives and internal/external clients. Additionally, you will assist in preparing agendas and presentation materials for associated events, meetings, and seminars. Overall, your particular skillset and efforts will drive Miltenyi Biotec’s continuing business success. | 12/15/2019 |
| 931 | Miltenyi Biotec Gaithersburg, MD R&D Scientist, Purification & Characterization MS in molecular biology, immunology, or virology Exp: 0-2 years |
As a member of the Lentigen Technology team, you will have the opportunity to develop methods for the separation of different particle types and their characterization. Also, you will develop, evaluate and implement novel analytical methods for the fine characterization of viral vectors and exosomes, in view of the distinction of viral vectors from exosomes. You will design specific experiments to test LV function, perform statistical analysis of results, and communicate results internally, for use in publications, and in scientific meetings. Your responsibility will also include the development of chromatography-based separation steps in-view of the optimization of an existing purification protocol and their standard characterization. | 12/15/2019 |
| 932 | Mirus Madison , WI Shipping and Product Finishing Assistant HS Diploma/GED Exp: 1-2 years |
This position is required to provide department coverage 11am-3pm Monday-Friday. The position is offered at 32-40 hours per week. Prepare and execute domestic and international shipping of Mirus products using FedEx, UPS, DHL and freight forwarders. Receipt of incoming deliveries (e.g. supply orders, freight and parcel deliveries) | 12/15/2019 |
| 933 | Mission Pharma Boerne, TX Particle Technician HS Diploma/GED Exp: 1 year related experience |
Produces bulk pharmaceuticals, operates machinery and equipment, handles raw materials with and without handling equipment, completes documentation, and cleans and sanitizes equipment and rooms per SOP’s. Performs duties such as weighing, labeling, storing, moving, raw materials. Operates a mixer, forklift, powered pallet jacks, scales, dust collectors, hand tools, Fitzmill and sifter, NOL-TEC system and moisture removal controller. Weighs out and sample finished product. Processes the finished product for transport. Performs mixing duties such as introducing materials into the mixer, watching for overflow, dumping materials, scraping the inside of mixers and transfer s materials to drying racks and/or bins. | 12/15/2019 |
| 934 | Qiagen Frederick, MD QC Associate Scientist II MS in biological sciences Exp: 0-2 years |
Perform routine testing on manufactured products including incoming raw materials, in-process products, and finished goods. Testing covers reagents of multiple product groups with a focus on NGS-related panels, chemistry, and indices using NGS platforms and various PCR platforms. Support tech transfer and QC workflow implementation during new product transfer and launch. These include performing validation tests, help to writing of instruction and protocol/SOP. Support continuous quality improvement by conducting tests for root cause analysis, or for revised QC process validation, or for new QC instrument verification and validation. | 12/15/2019 |
| 935 | Qiagen Beverly, MA QA Associate BS/BA Exp: 1-3 years in QA |
The QA Associate role assists with all QA compliance activities; including reviews of CAPAs, deviations, NCMRs, customer complaints and recalls. Position responsibilities also include participation at internal and external regulatory audits, document reviews and support of companywide QA initiatives. | 12/15/2019 |
| 936 | Qiagen Germantown, MD Technical Associate - Kit Assembly Operations HS Diploma/GED Exp: 1-3 years |
The Technical Associate in Kit Assembly comprehends and performs assigned manual production tasks according to established standard operating procedures. Responsible for Manual production and assembly procedures in compliance with relevant regulations and Standard Operation Procedures. Adhere to and accurately complete all production-related documentation. Responsible for set up, trouble shooting and operation of production related equipment within the assembly area. Assist in the setup and preparation of required production related materials. | 12/15/2019 |
| 937 | Qiagen Germantown, MD Technical Associate - Automated Assembly Operations HS Diploma/GED Exp: 1-3 years |
The 2nd shift Technical Associate in Production and Assembly comprehends and performs assigned automated and manual production tasks according to established standard operating procedures. Responsible for Automated and/or Manual production and assembly procedures in compliance with relevant regulations and Standard Operation Procedures. Adhere to and accurately complete all production-related documentation. Responsible for set up, trouble shooting and operation of automated assembly equipment, as well as other production related equipment within the assembly area. | 12/15/2019 |
| 938 | Qiagen Mobile, AL Field Service Specialist (Mobile, AL area) BS/BA in sciences, med technology, or engineering Exp: 0-3 years |
On site Field support of QIAGEN, Peak Service and Excalibur supported instrumentation. Position based in Mobile, AL area. Install, maintain, troubleshoot, repair, and support instruments on all levels (Hardware and Software). Maintain and develop positive relationships with customers and references. Assist in meeting/exceeding sales targets and related KPI's in relation to maintaining high customer satisfaction. Ensure all paperwork is completed accurately, in a timely fashion and in lines with any regulatory requirements. Utilize relevant databases to input and provide information to the organization. | 12/15/2019 |
| 939 | Moderna Cambridge, MA Candidate Experience Associate HS Diploma/GED Exp: 1 year in HR environment |
This role is the steward of Moderna’s candidate experience at every step of our recruitment process. The ideal hire for this role is curious about people, is completely ‘customer focused’ and has a desire to grow their career in Talent Acquisition or Human Resources. Partner with our Talent Acquisition Team and Hiring Leaders to provide a streamlined and efficient interview scheduling process. Create and communicate interview schedules, travel and hotel details to talent and third party executive search partners. Help define and reinforce a consistent interview scheduling process at Moderna that results in a superior candidate and hiring manager experience. This includes pushing back, where needed, and educating others on SLA’s (service level agreements). | 12/15/2019 |
| 940 | Moderna Cambridge, MA (Contract) Sr. / Research Associate, Cell-based Assay Development MS in biological sciences Exp: 0-2 years |
The individual will participate in the development and performance of cellular and biochemical assays to support advancement of Moderna’s mRNA clinical development candidates. Standard mammalian cell culture support including maintaining and plating of cell lines. Development of in vitro assays (e.g. immunoassay, ELISA, PCR, Western blot, luminescence, bDNA, functional activity) using cultured mammalian cells to support product development. Optimize assay performance (precision, accuracy, robustness) and implement high throughput sample testing to support product development The individual will participate in the development and performance of cellular and biochemical assays to support advancement of Moderna’s mRNA clinical development candidates. Standard mammalian cell culture support including maintaining and plating of cell lines. Development of in vitro assays (e.g. immunoassay, ELISA, PCR, Western blot, luminescence, bDNA, functional activity) using cultured mammalian cells to support product development. Optimize assay performance (precision, accuracy, robustness) and implement high throughput sample testing to support product development The individual will participate in the development and performance of cellular and biochemical assays to support advancement of Moderna’s mRNA clinical development candidates. Standard mammalian cell culture support including maintaining and plating of cell lines. Development of in vitro assays (e.g. immunoassay, ELISA, PCR, Western blot, luminescence, bDNA, functional activity) using cultured mammalian cells to support product development. Optimize assay performance (precision, accuracy, robustness) and implement high throughput sample testing to support product development | 12/15/2019 |
| 941 | Moderna Cambridge, MA (Contract) Research Associate, Analytical Operations BS or MS Exp: BS: 1-3 years, MS: 0-2 years |
The primary responsibilities of this role will be to support development and performance of analytical methods for messenger RNA therapeutic drug substance and drug products. The incumbent will be expected to undertake laboratory work to support testing and data collation. Additional responsibilities include developing high throughput methods using liquid handling and end-to-end sample tracking for drug substance/product components and impurities. This position will support cross-functional teams in Research and Development, Production and Quality. Additionally it is expected that the role will require the individual to generate technology transfer documents and enable the physical transfer of methods to receiving groups as part of a broader functional responsibility. The anticipated time frame for this assignment is six months. | 12/15/2019 |
| 942 | Moderna Cambridge, MA (Contract) Document Associate BS in related Exp: 1-2 years in regulatory operations |
This role is an exciting opportunity to be an integral part of the talent engine fueling a high growth organization that is radically changing the biotech industry. Reporting to the Senior Director, Regulatory Operations, the Document Associate, Regulatory Operations will be responsible for assisting with document formatting, publishing, quality control, and interactions with third party vendor(s) to ensure compilation of high-quality electronic submissions. | 12/15/2019 |
| 943 | Danaher Fremont, CA Customer Success Representative HS Diploma/GED Exp: 1-3 years in customer service |
In this role you will have an impact on the customer experience, helping to create and sustain customer loyalty through enablement of their success. A successful candidate will have a positive attitude with the ability to readily adapt to change and solve problems. Additionally, the candidate should be able to demonstrate empathy for both internal and external customers, and will be expected to work closely with sales, product support, repair teams, and customer support to create value and enable an exceptional customer experience. | 12/15/2019 |
| 944 | Molecular Templates Austin, TX Research Associate BS/BA in life sciences Exp: 1 year in lab setting |
This position will perform functions related to production of pre-clinical drug product and early-stage process development for protein sciences, including routine protein purification, equipment maintenance checks and calibration, data management, and assist in review and development methods and procedures to control or modify the process. This position will also aid in identifying continuous process improvement areas. This will require excellent technical, analytical and organizational skills, along with adherence to written and verbal instructions and accurate and timely completion of manufacturing batch records. | 12/15/2019 |
| 945 | Molecular Templates Austin, TX downstream process development AS/AA in biotechnology preferred Exp: 1-2 years previous experience preferred |
This position will be responsible for working with fellow team members to develop robust, efficient and scalable methods for protein purification/manufacture. This position will perform functions related to downstream process development of recombinant biologics, including experimentation involving protein purification, cell lysis, clarification, chromatography, ultrafiltration, diafiltration and filling. Additional activities will include solution preparation, equipment maintenance and calibration, data management, report authoring, and review of manufacturing processes. | 12/15/2019 |
| 946 | Molecular Templates Austin, TX Associate Scientist BS/BA in life sciences Exp: 1 year in lab setting |
The Associate Scientist will be responsible for working with fellow team members to develop robust, efficient and scalable methods for protein purification/manufacture. This position will perform functions related to downstream process development of recombinant biologics, including experimentation involving protein purification, cell lysis, clarification, chromatography, ultrafiltration, diafiltration and filling. Additional activities will include solution preparation, equipment maintenance and calibration, data management, report authoring, and review of manufacturing processes. | 12/15/2019 |
| 947 | Molecular Templates Austin, TX Manufacturing Associate AS/AA in life sciences, engineering or related Exp: 1 year or more in GMP manufacturing |
This position will perform functions related to production and GMP manufacturing operations, including execution of protein fermentation steps. Equipment, facility, process and people will be prepared to deliver quality ETBs, the next generation of immunotoxins, to patients in clinical trials. The Manufacturing Associate will provide on-the-floor execution to bioprocessing unit operations requiring attention to detail, working in a team environment and interest in learning about bioprocessing operations. The Manufacturing Associate will be responsible for adhering to Standard Operating Procedure (SOP) guidelines, Good Manufacturing Practices and all safety requirements in a state-of-the-art biologics manufacturing facility. | 12/15/2019 |
| 948 | Molecular Templates Austin, TX Manufacturing Associate AS/AA in life sciences, engineering or related Exp: 1 year or more in GMP manufacturing |
This position will perform functions related to production and GMP manufacturing operations, including execution of protein purification steps. Equipment, facility, process and people will be prepared to deliver quality ETBs, the next generation of immunotoxins, to patients in clinical trials. The Manufacturing Associate will provide on-the-floor execution to bioprocessing unit operations requiring attention to detail, working in a team environment and interest in learning about bioprocessing operations. The Manufacturing Associate will be responsible for adhering to Standard Operating Procedure (SOP) guidelines, Good Manufacturing Practices and all safety requirements in a state-of-the-art biologics manufacturing facility. | 12/15/2019 |
| 949 | Mylan Sugar Land, TX Quality Assurance Specialist MS in pharma/med devices Exp: 0-2 years |
Perform quality assurance documentation record review and batch disposition. Determines the disposition (i.e. release or rejection statuses) for packaging components (container/closures), raw materials, bulk products and finished packaged products. Assists in compiling data for Annual Product Reviews. Assists in QA product complaint activities which include: Daily electronic reviews - Logging – Investigating- Trending. | 12/15/2019 |
| 950 | Mylan Greensboro, NC Quality Technician, Inspections- 2nd Shift BS/BA Exp: 0-2 years |
Coordinate release documents, perform product releases in SAP, and perform product inspections. Write specifications and SOP’s, perform warehouse investigations, review rejections, place products on quality hold, process sample requests, returned goods and donations, ship studies, and review temperature data. Process sample requests as requested. Process and/or review returned goods and assign disposition. Process shipping studies when received. | 12/15/2019 |
| 951 | Myriad Genetics Salt Lake City, UT Laboratory Technician BS or MS in sciences Exp: 0-2 years |
The Laboratory Technician is responsible for specimen processing, testing and monitoring test performance. The technician must demonstrate competency, as defined in the department’s training program, prior to performing independent testing. This position will work with department management and quality team members to ensure that laboratory activities are defined, documented and completed to support inspection readiness and that compliance is maintained through procedures, training, documentation and continuous improvement projects. | 12/15/2019 |
| 952 | Myriad Genetics South San Francisco, CA Intake Associate BS/BA Exp: 0-2 years |
At Myriad Women's Health, the Intake team is responsible for the timely and accurate data entry and management of patient orders. You will be a significant contributor to our high-throughput workflow and an integral part of our busy CLIA lab. Input and manage patient data from a variety of sources, and ensure that orders are fully processed at the highest level of accuracy. Identify issues and trends and collaborate with your team and leadership to develop best practices to ensure we are providing the best service and experience to all customers | 12/15/2019 |
| 953 | Myriad Genetics Salt Lake City, UT Laboratory Technician III MS in clinical lab science, chemical/physical/biological science Exp: 6 months |
The Laboratory Technician III is responsible for specimen processing, testing and monitoring test performance. The technician must demonstrate competency, as defined in the department’s training program, prior to performing independent testing. This position will work with department management and quality team members to ensure that laboratory activities are defined, documented and completed to support inspection readiness and that compliance is maintained through procedures, training, documentation and continuous improvement projects. | 12/15/2019 |
| 954 | Myriad Genetics Salt Lake City, UT Clinical Laboratory Assistant HS Diploma/GED Exp: 1-3 months |
Myriad Autoimmune is seeking a Clinical Laboratory Assistant to assist in the preparation of sample aliquots; retrieving samples for testing as directed by work schedule; performing inventories and orders for laboratory and office supplies; performing clerical duties that do not involve interpretation or judgment; receiving and accessioning samples into the CLIMS; and assisting CLS' with various lab duties (temperature monitoring, CLIMS sample batching, preparation of buffers), reporting issues to management. | 12/15/2019 |
| 955 | Myriad Genetics Salt Lake City, UT Laboratory Technician BS in chemical, physical, biological or clinical laboratory/medical technology science Exp: 0-2 years |
The Laboratory Technician in the LegacyX Lab is responsible for preparing high-performance liquid handling robots for specimen processing. The technician must maintain patient sample integrity through demonstrating competency and repeatability in performing specimen processing as defined by the department’s standard operating procedures. This is a production environment, not a research environment. Pay starts around $18/hour depending on experience. | 12/15/2019 |
| 956 | Myriad Genetics Austin, TX RBM Laboratory Technician - Testing BS/BA in engineering/sciences Exp: 0-3 years |
The goal of the Lab Technician I is to ensure that process’s required for a production run as it pertains to samples and reagents are done in an organized and expedient manner. The Technician is accountable for following company procedures and working to the best of their ability to ensure quality in all aspects of the job. | 12/15/2019 |
| 957 | NAMSA Irvine, CA Microbiology Technologist BS/BA Exp: 0 years |
May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. May be required to perform personal gowning environmental testing, and submit organisms from gowning, environmental and sterility test positives for identification and inclusion in monthly trending data, as required for specific testing as applicable. | 12/15/2019 |
| 958 | NAMSA Northwood, CA Lab Technologist - In Vivo BS in sciences Exp: 0-3 years |
May prepare all testing/test article and animals according to written instructions and protocols. May execute routine testing per NAMSA SOPs, with appropriate data analysis. May communicate test schedule updates to NAMSA management as needed. May prepare and maintain reagents and/or test articles as required for testing.May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. | 12/15/2019 |
| 959 | NAMSA Irvine, CA Microbiology Technologist BS/BA Exp: 0 years |
May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. May be responsible for checking laboratory equipment, being on-call and respond to continuous monitor. May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. May be required to perform personal gowning environmental testing, and submit organisms from gowning, environmental and sterility test positives for identification and inclusion in monthly trending data, as required for specific testing as applicable. | 12/15/2019 |
| 960 | Nanostring Seattle, WA Manufacturing Research Associate I/II BS/BA in sciences Exp: 0-2 years in lab |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to use equipment, perform SOPs, use Document Control systems, ERP systems, etc. | 12/15/2019 |
| 961 | Nanostring Bothell, WA Manufacturing Research Associate I BS/BA in sciences Exp: 0-2 years |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to use equipment, perform SOPs, use Document Control systems, ERP systems, etc. | 12/15/2019 |
| 962 | Nanosyn Santa Clara, CA Research Associate / Screening and Compound Profiling BS in biology/chemistry Exp: 0-2 years in biotech/pharma |
The candidate will play a key role in the organization by being responsible for the planning and timely execution of in vitro biochemical and cell-based assays for Nanosyn’s screening and profiling services. He/She will be responsible for consistently generating high quality data and meeting agreed upon timelines. Applicants must have a strong focus on quality and attention to detail, have the ability to work on multiple projects simultaneously, and be productive both independently and as part of a team. | 12/15/2019 |
| 963 | Upsher-Smith Maple Grove, MN Network Systems Analyst I BS in computer science or related Exp: 0-2 years |
The Network Systems Analyst will be primarily responsible for managing and configuring security information and event monitoring (SIEM) tool. Research security enhancements and identifies solutions to enhance IT security. Evaluates and recommends security products, services, and/or procedures to enhance productivity and effectiveness. Provides technical support of IT infrastructure at all Upsher-Smith locations. Support will include assisting with installation, configuration, recovery, administration and security of infrastructure components. Incumbent will work on implementation projects as well as have responsibility for daily monitoring and support activities. etc. | 12/10/2019 |
| 964 | Upsher-Smith Maple Grove, MN Corporate Sales Representative BS/BA in business, science, communication or related Exp: 1-3 years |
The Corporate Sales Representative is responsible for the development and management of a designated territory with the goal of maximizing sales while improving patient lives. Patients are central to all USL strategies, and the CSR will be responsible for developing business relationships with targeted neurologists, epileptologists, seizure specialists and other healthcare practitioners and members of the health care community. The CSR may work in a team with a Corporate Sales Specialist (CSS), Regional Trainer, Managed Care - Regional and National Account Manager to increase sales, market share and profitability of USL products. Time allocation of 75% inside sales and 25% field sales is expected; however, this may vary as business needs arise. | 12/10/2019 |
| 965 | United States Biological Salem, MA Information Technology and Marketing Associate BS/BA in computer science Exp: 1+ year(s) |
United States Biological is a local, growing manufacturing company seeking enthusiastic individuals to be part of our team. We specialize in thousands of antibodies, ultra pure molecular biology reagents, cell culture media and enzymes. Troubleshoot and provide hands-on support to all personnel. Work with company president on all areas of website, graphics and IT. Set up and format new workstations as needed. Design and create newsletters. Maintain systems, databases and website, as needed. | 12/10/2019 |
| 966 | Veeva Toronto, ON Associate Software Engineer BS in computer science, engineering, mathematics, or related Exp: Recent graduates |
As part of our Network development team, working on our master data management product (MDM), or as part of our Vault team, working on our Enterprise Content Management (ECM) product, you will be part of a team building scalable solutions that complement our existing solutions. In these exciting roles, you would have the opportunity to work with technologies like Java, Spring, Hibernate, Mule, Maven, Git, Tomcat, Solr, MySQL, and more. We work in a fast-paced, agile environment that releases features every four weeks. What You'll Do: Responsibility for all aspects of the software cycle: design, implementation, tuning, testing, and monitoring of the functional areas that you will own. etc. | 12/10/2019 |
| 967 | Veeva Toronto, ON Associate Performance Engineer BS in computer science or related Exp: Recent graduates |
The Vault Performance Engineering Team works within the Vault Development Team and participates in all phases of the software development life cycle. What You'll Do: Test new features pre-production to make sure they will scale and perform. Collaborate with Vault team members in Product Management, Engineering Management and Quality Assurance to help design and develop performance tests. Implement and execute load tests in JMeter. Use and update Python scripts for managing test systems. Work with Senior Performance Engineers to profile code and identify bottlenecks. | 12/10/2019 |
| 968 | Veeva Philadelphia, PA Associate Consultant (Remote) BA/BS in a business, computer, engineering, or life science field Exp: Recent graduates |
You will work on project teams implementing Veeva’s cloud software applications. Participate in business process discovery workshops, gather requirements, configure the solution, help with testing and final deployment. Explain solutions to a variety of audiences and provide subject matter expertise on Veeva applications and technical design. What You'll Do: Collaborate with experienced Senior Consultants and Solution Architects. Learn technical consulting, application design, industry knowledge and project management skills. Conduct solution design, application configuration, and documentation of system requirements to help deliver successful implementations. Passion to use technology to make business processes more efficient. etc. | 12/10/2019 |
| 969 | Veeva Pleasanton, CA QA Engineer BS in mathematics or computer science Exp: 0-5 years |
Veeva Systems is looking for an energetic and enthusiastic Engineer to join our rapidly growing team. This is a hands-on position for delivering a quality SaaS product. As part of Veeva CRM Multi Channel software QA team, you will be given an opportunity to test a high quality product that was built from scratch. We are a fast-paced team who takes pride in building great software and making customers happy. What You'll Do: Design and implement test strategies. Develop deep expertise in the product. Build effective test cases that are used for manual and automation testing. etc. | 12/10/2019 |
| 970 | Veracyte South San Francisco, CA Clinical Lab Scientist BS/MS in a biological science or medical technology Exp: 1 year |
The Veracyte Clinical Laboratory continues to grow! We are seeking a new Clinical Laboratory Scientist (CLS) to perform cutting-edge diagnostic testing on patient specimens in our collaborative, high-energy work environment. S/he will accurately perform molecular genetic testing, using a variety of molecular biological techniques including expression microarray analysis. Other key aspects of the role include: Conduct daily quantitative and qualitative assessment of molecular data generated during the course of testing. Carry out QC/QA activities as part of the company’s Quality program and commitment to patient safety. etc. | 12/10/2019 |
| 971 | Vericel Cambridge, MA Engineer, Validation I MS Exp: 1+ year(s) |
Responsible for performing validation in a GMP biotech manufacturing facility. Core Responsibilities: Perform validation activities in the media preparation, cell culture, utilities and QC areas of a cGMP biotech manufacturing facility. Perform hands on execution of Installation, Operational and Performance Qualifications for equipment, facilities, utilities, as well as cleaning, sterilization, and manufacturing processes in accordance with predefined test protocols. Analyze validation results and compile data into reports for initial qualifications and re-qualifications. Coordinate testing schedule with impacted area managers and quality control based on project needs. Provide input to technical composition of standard operating procedures. etc. | 12/10/2019 |
| 972 | Vericel Cambridge, MA Sales Operations Associate BS/BA in business administration, marketing, or related Exp: 1+ years |
Essential Functions: Coordinate on-boarding of all new sales personnel with internal departments. Administer all sales training content through company’s Learning Management System. Primary administrative resource for two sales teams (first point of contact). Provide logistical support for all sales training meetings and events. Work with marketing to provide regular updates to brand websites. Work with marketing to provide logistical support for tradeshows, surgeon training programs and other commercial programs/events. etc. | 12/10/2019 |
| 973 | Verge Genomics South San Francisco, CA Molecular Biology Research Associate / Senior Research Associate MS in molecular biology, neuroscience, or equivalent Exp: 0+ years |
What you'll do: Perform and enable high-throughput sample processing and RNA extraction for transcriptomic analysis, which impacts all drug discovery and development efforts. Successfully conduct library prep of samples for RNAseq. Have the opportunity to learn across function and discipline, by contributing to ongoing studies and by utilizing techniques such as cell culture, high-throughput screening, plasmid preparation, virus preparation, IF, qPCR, or WB. Be responsible for evaluating and presenting your work at team and company level meetings. | 12/10/2019 |
| 974 | Vero Biotech Atlanta, GA Manufacturing Technician Technical degree Exp: Not needed |
Routine Manufacturing operations for the production of clinical and/or commercial products, operation of production equipment according to SOPs and other daily activities on the manufacturing floor. Essential Duties and Responsibilities: Performs manufacturing activities including but not limited to work functions in electromechanical assembly and disposable assemblies (cassettes, cartridges) in a correct and timely manner. Maintains records and controlled-room environment to comply with regulatory requirements, GMPs, and SOPs. Provide in process testing to assure batches meet specifications. Will train personnel in new and revised procedures. etc. | 12/10/2019 |
| 975 | Verve Therapeutics Cambridge, MA Associate Scientist, In Vivo Pharmacology MS in biology, biochemistry, pharmacy, or related Exp: 1-2 years |
Verve is seeking an Associate Scientist with experience in in vivo pharmacology to execute pivotal studies in rodents. You will be responsible for planning gene editing studies in mice and rats, dosing of animals (IV or IP), collecting blood samples (serial and terminal bleeds), necropsy and tissue harvesting. In addition, you will be analyzing the collected samples using a series of ex vivo and in vitro assays. The role requires hands-on experience in rodent handling, dosing and sampling as well as the ability to develop and run assays such as ELISA, qPCR or FACS. The scientist in this position will be part of an integrated R&D project team. | 12/10/2019 |
| 976 | LabCorp Monrovia, CA Histotechnician - (3rd Shift) AS/AA in related Exp: 1-3 years in Histology |
The Monrovia lab is seeking a 3rd shift Histotechnician for the Histology department. This position will perform all technical duties related to the production of histo-pathological slides including but not limited to the following: Examines and prepares histologic slides from tissue sections for microscopic examination and patient diagnosis. Uses rapid tissue processing and frozen section technique to freeze, cut, mount, and stain tissue specimen received from surgery, biopsy, and anatomical tissues upon preparation of sections of human or animal tissue for immediate examination. Operates computerized laboratory equipment to fix, dehydrate, and infiltrate with wax, tissue specimens to be preserved for study by Pathologist. | 12/8/2019 |
| 977 | LabCorp Utica, NY Specimen Processing Specialist (Laboratory Associate) HS Diploma/GED Exp: 1 year in lab |
Prepare laboratory specimens for analysis and testing, Spin samples, pour urine tubes, and create frozen samples, Pick up and deliver samples to, clients/hospitals, Unpack and route specimen to their respective staging areas, Accurately identify and label specimens, Pack and ship specimen to proper testing facilities, Properly prepare and store excess specimen samples | 12/8/2019 |
| 978 | LabCorp Raritan, NJ Lab Assistant - 3rd Shift HS Diploma/GED Exp: 1 year in health-related work or college level courses in lab sciences |
The Forensic Accessioning (Processing) Lab Assistant works in fast paced, production type environment performing a vital component of medical laboratory science. Receive on the job training for the pre-analytical processing of medical samples. Complete all documents accurately and neatly. Monitor chain of custody, and custody and control forms for completeness and acceptability. Perform all duties accordingly to standard operating procedures and/or supervisory instructions | 12/8/2019 |
| 979 | LabCorp Richmond, VA Specimen Accessioner HS Diploma/GED Exp: 0-2 years related experience |
Prepare laboratory specimens for analysis and testing, Spin samples, pour urine tubes, and create frozen samples, Pick up and deliver samples to, clients/hospitals, Unpack and route specimen to their respective staging areas, Accurately identify and label specimens, Pack and ship specimen to proper testing facilities, Properly prepare and store excess specimen samples | 12/8/2019 |
| 980 | LabCorp Huntsville, AL Technologist BS/BA in biology, chemistry, med tech, or related Exp: 1 year clinical lab experience |
Determine the acceptability of specimens for testing according to established criteria. Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. Monitor, operate and troubleshoot instrumentation. Demonstrate the ability to make technical decisions regarding testing and problem solving. | 12/8/2019 |
| 981 | LabCorp Oklahoma City, OK Laboratory Data Entry/Specimen Accessioner HS Diploma/GED Exp: 1-2 years in data entry |
Our LabCorp office in Oklahoma is expanding its team and looking for dynamic individuals to be Specimen Accessioner (s) who will perform specimen preparation duties. Their work involves receiving and unpacking specimens, preparing them for lab tests and ensuring that they are correctly preserved before they are sent off. | 12/8/2019 |
| 982 | LabCorp McLeansville, NC Customer Service HS Diploma/GED Exp: 1-3 years in call center/customer service |
Customer Service- FT 10-7pm OR 11-8pm- Work from Home Opp-Onsite needed first! Answer 70+ inbound calls per day from patients, doctor's office and/or private insurance carriers. Initiate payment plans for patients for outstanding balances. Maintain telephone statistics and quality goals | 12/8/2019 |
| 983 | Medtronic Danvers, MA Associate Regulatory Affairs Specialist - Coronary and Structural Heart BS/BA in biology, chemistry, med tech, or related Exp: 0 years in medical device |
The Associate Regulatory Affairs Specialist (ARAS) is responsible for planning and executing global regulatory activities necessary to obtain and maintain regulatory approvals within the US and International Regions. The Regulatory Affairs Specialist will provide support for regulatory activities including: technical writing to support regulatory submissions, product labeling and instructions for use creation. | 12/8/2019 |
| 984 | Medtronic North Haven, CT Manufacturing Engineer I BS/BA Exp: 0 years |
The Associate Manufacturing Engineer is a key operations representative within the Advanced Stapling Technology Manufacturing Engineering team. The Associate ME will be responsible for completing tasks which support the completion of operations deliverables for AST Focused Factory. General responsibilities include manufacturing process evaluation, mechanical product troubleshooting and support of in-house manufacturing processes. They will assist with engineering studies to support process validation and contribute to maximizing production performance. The Associate ME will work under the direction of Principal/Senior level Engineer in a fast paced collaborative environment supportive of program initiatives and compliant with company best practices. | 12/8/2019 |
| 985 | Medtronic Memphis, TN R&D Engineer II MS in engineering Exp: 0 years |
This position has the responsibility and authority to apply education and learned knowledge toward developing world class medical products for Spinal surgery. Designs, develops, analyzes, troubleshoots and provides technical skills during research and/or product development. Uses multidisciplinary engineering knowledge to design and develop medical devices or components / subsystems in support of strategic plans. | 12/8/2019 |
| 986 | Medtronic Tempe, AZ IC Test Engineer I BS/BA in electrical/computer engineering Exp: 1-2 years in circuit testing/design/verification |
As a member of this Test Engineering Team, you will be involved in all phases of product development, including definition, design for testability, test hardware and software design, hands-on debug, characterization, manufacturing release under a heavily regulated quality and regulatory standard operating procedures. You will be an important part of an experienced test development team whose goal is to deliver the highest quality test application to test ICs for use in live saving medical devices | 12/8/2019 |
| 987 | Medtronic Memphis, TN Assoc Supplier Qual Engineer BS in engineering/sciences Exp: 0 year of work |
Develops and prioritizes an auditing schedule to ensure that designated suppliers are audited on a regular basis to ensure good manufacturing practices (GMP) and quality standards are met. Ensures that suppliers deliver quality parts, materials, and services. Qualifies suppliers according to company standards and may administer a Certified Supplier Program in receiving inspection to ensure cost effectiveness. Monitors parts from acquisition through the manufacturing cycle and communicates and resolves supplier-related problems as they occur. | 12/8/2019 |
| 988 | Medtronic Irvine, CA Design Quality Engineer I BS in engineering/sciences Exp: 0 years in quality/engineering |
Applies knowledge of Design Control principles and quality engineering techniques positively influence new product development efforts, including those for design verification, validation, specification development, and risk management. Hands on participant in early stages of product development including but not limited to physician interaction, product engineering, competitive product testing, and prototype testing. Identifies and manages risk throughout the development process with the use of FMECA and/or other risk management tools. | 12/8/2019 |
| 989 | Medtronic Jacksonville, FL Supplier Qual Engineer I BS/BA Exp: 0 years |
The Restorative Therapies Group (RTG) develops life-restoring therapies and healthcare solutions that span the care continuum; integrating technologies and applying clinical and economic evidence to increase patient access, improve efficiency of procedures and deliver successful patient outcomes. Within RTG the Supplier Quality department focuses on developing Supplier Owned Quality (SOQ). This is a process allowing suppliers to use portal system in which supplier data is electronically transmitted to Medtronic via an Internet or secure FTP port. The portal system provides real-time material acceptance confirmation, shipment authorization and feedback to supplier prior to release of the product and identifies opportunities to reduce variation in the process. It also reduces the burden on Incoming Quality Assurance. | 12/8/2019 |
| 990 | Merck West Point, PA Associate Scientist, Vaccine Process Development BS in engineering or biological sciences Exp: 2020 graduate |
The successful candidate will perform lab-scale process development/scale-up studies, develop robust, efficient, scalable cell culture processes for vaccine production, participate in the manufacture of Current Good Manufacturing Practices (CGMP) clinical bulks, and transfer processes to clinical or commercial manufacturing facilities for vaccine candidates. Duties may include: lab scale fermentation, cell culture, and/or bioconjugation process development, in-process assay support, process scale-up and engineering, CGMP document preparation and modifications, maintaining/coordinating raw material, and equipment inventories, technology transfer to manufacturing, and functioning as a key member of a process development team. | 12/8/2019 |
| 991 | Merck West Point, PA Associate Shift Engineer BS in engineering or sciences Exp: 1 year |
The function of this position is to provide technical support for ourfacility while actively supporting, participating in, and embracing an empowered culture. This role is for Off-Shift Engineering Support (3rd shift Monday through Friday). Specifically, the position will be required to: Provide on-the-floor support of operational and technical issues; collaborating with the shop floor to provide immediate responses to deviations and potential deviations. Performing deviation investigations aimed to prevent deviation re-occurrence, including determining the root cause, identifying corrective/preventative actions, identifying event scope, and conducting a product impact assessment. Where applicable, complete investigational test protocols to determine root cause, product impact, event scope, etc | 12/8/2019 |
| 992 | Merck Elkhorn, NB Technician, Operations HS Diploma/GED Exp: 1-2 years in production lab |
The Operations Technician is responsible for critical laboratory procedures and duties in the production of veterinary products. Technicians work with a variety of technical equipment while completing duties involved in blending, filling vials or packaging finished products for distribution. At all times technicians must follow Good Manufacturing Practices and Standard Operating Procedures (SOP) and adhere to all safety and company policies while performing assigned duties. | 12/8/2019 |
| 993 | Merck West Point, PA Shift Engineer BS in engineering Exp: 1 year |
The function of this position is to provide technical support for our facility while actively supporting, participating in, and embracing an empowered culture. This role is for Off-Shift Engineering Support (2nd Shift Monday through Friday). Specifically, the position will be required to: Provide on-the-floor support of operational and technical issues; collaborating with the shop floor to provide immediate responses to deviations and potential deviations.Performing deviation investigations aimed to prevent deviation re-occurrence, including determining the root cause, identifying corrective/preventative actions, identifying event scope, and conducting a product impact assessment. Where applicable, complete investigational test protocols to determine root cause, product impact, event scope, etc | 12/8/2019 |
| 994 | Merck Ames, IA Technician, Operations AS/AA in biology, microbiology, or related Exp: |
The primary purpose of this position is to perform entry-level laboratory procedures and assist others in more advanced procedures for the production of veterinary biologicals according to strict government and company imposed guidelines. Assist in all areas of the production of RNA (RP) Particle Vaccine products manufactured in a USDA licensed facility. | 12/8/2019 |
| 995 | Merck North Wales, PA Entry Level Field Sales - Chronic Care - (Forest Hills, NY) BS/BA Exp: Entry level, some sales experience |
The entry level Chronic Care Representative (CCR) is the primary point of contact for a variety of customers within their assigned geography. The Chronic Care Representative is a key member of the local Customer Team that works collaboratively with other Company field-based employees such as the Account Executives, Integration Delivery Systems leaders as well as other members of the extended team. Professionals to align customer needs and Company products in accordance with product labeling. | 12/8/2019 |
| 996 | Merck West Point, PA Entry Level Field Sales - Vaccines -Chico, CA BS/BA Exp: Entry level, some sales experience |
He/she is responsible for engaging with customers in a way that supports the local market focus on population health and centers on the highest potential business opportunities that will improve our impact on public health. He/she will work with the local market team to understand and identify customer needs, proactively align products and services, support pull-through activities relative to integrated strategies, and ensure that MV is viewed as demonstrating value and better health outcomes to healthcare professionals and their patients. Responsible for ensuring all activities adhere to the spirit and letter of all Company Policies and US Laws and Regulations. | 12/8/2019 |
| 997 | Meridian North Billerica, MA Clinical Research Associate - MAG BA/BS in biological/health sceinces Exp: 1 year as CRA |
The Clinical Research Associate assists in the administrative of clinical research projects including development of key study documents, over-site of the clinical trial, and ensuring the quality and integrity of the data according to GCP, ICH and SOPs. Interact with data management and study sites with generation and reconciliation of queries in order to meet business timelines. Provide answers to common protocol study related questions under the supervision of the Clinical Director or Associate Trial Manager | 12/8/2019 |
| 998 | Meridian Cincinnati, OH Quality Systems Software Engineer BS/BA in Communications, Computer Systems, or equivalent Exp: 0-2 years related experience |
The Quality Systems Software Engineer position at Meridian Bioscience within the Quality Assurance department supports the Quality System by developing and maintaining electronic document and data management systems. The Quality Systems Software Engineer works with cross functional teams to identify areas that can be streamlined or improved by implementing processes that meet regulatory requirements and standards associated with electronic data management. The Quality Systems Software engineer.is responsible for application systems administration within the scope of Quality Systems. This includes developing electronic form records, document management and workflow processes, and authoring supporting documentation including but not limited to validation protocols and reports and verification test methods and procedures. | 12/8/2019 |
| 999 | Merieux NutriSciences Madison, WI Entry-Level Laboratory Sample Receiving Technician HS Diploma/GED Exp: Entry Level |
We are looking for an Entry-Level Laboratory Sample Receiving Technician to sit in our Madison, WI location. Receive and log in sample in preparation for analysis. Review sample and any attached documentation to assign an identification number and enter information into Laboratory Information Management System (LIMS). Prepare documentation as necessary. Contact client, when necessary, to obtain and clarify missing or unclear information to ensure that identification of client code, test code, and sample contents are accurate. Store sample in appropriate manner until analysis is completed and appropriately dispose of extra sample. Ensure sample integrity is maintained. | 12/8/2019 |
| 1000 | Merieux NutriSciences Crete, IL RESEARCH MICROBIOLOGIST AS/AA or BS/BA in chemistry/biology Exp: 1-2 years |
This position is responsible for working in a cooperatively team environment where scientists collaborate on contract research designed to promote the safety, quality and nutrition of the global food supply. The incumbent is responsible for the testing of samples supporting research studies using various microbiological analyses. The incumbent provides analytical support for the lab by ensuring that laboratory procedures are being performed within specified quality guidelines. The incumbent contributes to defined contract research projects by performing lab tests, data interpretation and maintaining documentation in accordance with required specifications, established procedures, and customer service standards. | 12/8/2019 |
| 1001 | Merieux NutriSciences Crete, IL CHEMIST I BS/BA in chemistry Exp: 1-2 years |
The incumbent is responsible for performing chemical analysis on food/pharmaceutical samples. The incumbent analyzes the concentration of certain components in food samples. The incumbent must accurately prepare and process the samples to obtain the needed results. This position reports to the Supervisor of Chemistry. Ensure that proper analysis methods are conducted on the appropriate samples. Maintain chemistry quality control records and procedures for each test. Extract desired components from samples with appropriate processes such as distillation, solvent extraction and acid digestion, so that concentrations can be determined. | 12/8/2019 |
| 1002 | Merieux NutriSciences Allentown, PA Lab Assistant HS Diploma/GED minimum Exp: No experience needed |
Work as a member of a team to prepare food samples for testing. Carry out a number of procedures including reading test labels and preparing samples for analysis by recording, weighing and blending. Pipette sample solution into tubes or plates according to the analysis process being performed. Set up and sterilizing equipment needed for analysis of food samples. | 12/8/2019 |
| 1003 | Merieux NutriSciences Columbus, OH Micro Tech HS Diploma/GED minimum Exp: No experience needed |
Work as a member of a team to prepare food samples for testing. Carry out a number of procedures including reading test labels and preparing samples for analysis by recording, weighing and blending. Pipette sample solution into tubes or plates according to the analysis process being performed. Set up and sterilizing equipment needed for analysis of food samples. | 12/8/2019 |
| 1004 | Merieux NutriSciences Grand Prairie, TX Microbiology Technician BS/BA Exp: 1 year of PCR/ELISA experience |
The incumbent is responsible for the testing of samples using various microbiological analyses. The incumbent provides analytical support for the lab by ensuring that laboratory procedures are being performed within specified quality guidelines. This position serves as a technical resource and provides ongoing technical support related to method and process implementations. This position spends the majority of time or all of their time in diagnostics. | 12/8/2019 |
| 1005 | Merieux NutriSciences Salida, CO Micro Tech HS Diploma/GED minimum Exp: No experience needed |
Work as a member of a team to prepare food samples for testing. Carry out a number of procedures including reading test labels and preparing samples for analysis by recording, weighing and blending. Pipette sample solution into tubes or plates according to the analysis process being performed. Set up and sterilizing equipment needed for analysis of food samples. | 12/8/2019 |
| 1006 | MeritMedical South Jordan, UT Process Operator Wafer I HS Diploma/GED Exp: 6 months in silicon wafer fab. Preferred |
This position is for a Process Operator Wafer I at Merit Sensor Systems. Merit Sensor Systems is a manufacturer of piezoresistive pressure sensors (learn more at www.merit-sensor.com). This Process Operator Wafer I could be working in the wafer fabrication, wafer dicing, and/or electronic assembly areas. | 12/8/2019 |
| 1007 | MeritMedical South Jordan, UT Material Handler I / with a $500 Hiring Bonus HS Diploma/GED Exp: 3 months work experience |
Responsible for pulling parts from the warehouse and seeing that line production workers have the raw materials they need to perform their jobs. Obtains parts from the warehouse for use in production and verifies the part's lot number to ensure that the proper materials are used. Pulls supplies for assembly workers and ensures that supplies are stocked and readily available for assembly workers. | 12/8/2019 |
| 1008 | MeritMedical South Jordan, UT Molding Technician I - Day Shift HS Diploma/GED Exp: 6 months molding experience |
This position provides entry level mold set-up services under the direction and supervision of a Technician and/or Supervisor. Assists in mold changes and EOAT setup/verification. Assists in set up of all auxiliary equipment related to the process. Ensures that correct materials are utilized, safety checks are performed, and that room organization and cleanliness is maintained. | 12/8/2019 |
| 1009 | MeritMedical South Jordan, UT Technician II (Injection Molding) AS/AA Exp: 1 year |
Performs routine technical tasks including assembling or constructing simple or standard equipment or parts in an injection molding environment, and may service or repair simple instruments or equipment. Prepares test specimens, adjusts and operates equipment, and records test data, pointing out deviations resulting from equipment malfunction or observational errors. Extracts engineering data from various prescribed sources and processes the data following well-defined methods, then presents the data in prescribed form. | 12/8/2019 |
| 1010 | MeritMedical South Jordan, UT Accounts Payable Clerk I HS Diploma/GED Exp: 1 year |
This position provides accounting support for processing employee expense reports, maintaining the filing system, processing the daily customer checks and maintaining the Construction Work in Progress (CWIP) filing system. | 12/8/2019 |
| 1011 | MeritMedical South Jordan, UT Production Operator II - Part Time HS Diploma/GED Exp: 6 months experience preferred |
Performs a variety of medical assembly and processing tasks as a production team member. Assembles medical products on an assembly operation, performing a variety of tasks on a rotating basis. Performs on-line and in-process visual inspection of products to ensure specifications per work order and procedure are followed. Assists Team Leader and Technicians with product and/or machine change-overs | 12/8/2019 |
| 1012 | MeritMedical South Jordan, UT Material Handler I HS Diploma/GED Exp: 3 months work experience |
Responsible for pulling parts from the warehouse and seeing that line production workers have the raw materials they need to perform their jobs. Obtains parts from the warehouse for use in production and verifies the part's lot number to ensure that the proper materials are used. Pulls supplies for assembly workers and ensures that supplies are stocked and readily available for assembly workers. | 12/8/2019 |
| 1013 | Merz Franksville, WI Supply Chain Associate BS/BA Exp: 1-3 years work or intern experience in supply, manufacturing, or quality |
The individual will be involved with people and processes associated with various aspects of Supplier Management and Procurement at Merz. The successful candidate will implement the supplier selection and approval process; manage existing suppliers; place purchase orders (PO’s); evaluating supplier performance; resolve delivery issues; assess and reduce supply chain risk; save money by reducing TCO (total cost of ownership). | 12/8/2019 |
| 1014 | Merz Franksville, WI Tech Ops Development Associate BS/BA in engineering, sciences, business or communications Exp: Entry |
As a member of Merz’s Technical Operations Development Program, you will have three assignments over the course of three years. The roles are crafted to help you develop exceptional functional and leadership traits by working on a wide range of projects while providing exposure to different leaders in the company. These Operational experiences will develop you and put you on the fast track to future operations leadership opportunities at Merz. | 12/8/2019 |
| 1015 | MSD Gaithersburg, MD Research Associate I, Immunoassay Development BS in life sciences, chemical sciences, MS preferred Exp: 1 year in assay development |
A Research Associate is responsible for independently designing and executing experiments and analyzing the resulting data in support of reagent and assay development projects. This is a laboratory based position performing protein-based immunoassays on a routine basis with relatively high throughput (3-10 plates per day). The incumbent is expected to display a wide-degree of latitude, creativity and self-management. | 12/8/2019 |
| 1016 | MSD Rockville, MD Production Control Tech I BS in life sciences, chemical sciences, MS preferred Exp: 1 year in biotech lab/manufacturing |
The Production Control Technician I is responsible for assisting in the control of production, documentation and inventory maintenance for multiple groups within Consumable Operations. The position will help standardize and improve documentation, manufacturing procedures and processes to increase production efficiency and ensure best practices are followed. The position will also help implement new products, projects and processes within Manufacturing Operations. Some degree of professional latitude, creativity and self-management is expected. | 12/8/2019 |
| 1017 | MSD Rockville, MD Customer Service Rep I BS/BA Exp: 1 year in customer support |
The Customer Service Representative I will provide professional, courteous, customer-centric service to the MSD customer base. This individual will directly interact with various customers and interface with multiple internal departments to facilitate the processing of quotes, orders and customer requests to allow for timely shipping of MSD products worldwide. | 12/8/2019 |
| 1018 | MSD Rockville, MD Customer Service Rep I BS/BA Exp: 1 year in customer support |
The Customer Service Representative I will provide professional, courteous, customer-centric service to the MSD customer base. This individual will directly interact with various customers and interface with multiple internal departments to facilitate the processing of quotes, orders and customer requests to allow for timely shipping of MSD products worldwide. | 12/8/2019 |
| 1019 | MSD Gaithersburg, MD Research Associate I, Immunoassay Development BS in life sciences, chemical sciences, MS preferred Exp: 1 year in assay development |
A Research Associate is responsible for independently designing and executing experiments and analyzing the resulting data in support of reagent and assay development projects. This is a laboratory based position performing protein-based immunoassays on a routine basis with relatively high throughput (3-10 plates per day). The incumbent is expected to display a wide-degree of latitude, creativity and self-management. | 12/8/2019 |
| 1020 | MSD Gaithersburg, MD Research Associate I, Immunoassay Development BS in life sciences, chemical sciences, MS preferred Exp: 1 year in assay development |
A Research Associate is responsible for independently designing and executing experiments and analyzing the resulting data in support of reagent and assay development projects. This is a laboratory based position performing protein-based immunoassays on a routine basis with relatively high throughput (3-10 plates per day). The incumbent is expected to display a wide-degree of latitude, creativity and self-management. | 12/8/2019 |
| 1021 | Analytical Lab Group Concord, CA QA Assistant BS in sciences Exp: 0-2 years in pharma/biotech |
The main duties of the Quality Assurance (QA) Assistant are to ensure timeliness of testing, meeting client requirements and providing a safe work environment for employees. The QA Assistant must provide services that are compliant to the ALG-West Quality Manual, client requirements and regulatory requirements as applicable, including ISO/IEC 17025:2017, USP, EU, GLP, GMP, FDA and ICH guidelines. | 12/8/2019 |
| 1022 | Analytical Lab Group Concord, CA EM Technician AS/AA Exp: 0-2 years in cleanrooms |
Analytical Lab Group is looking for laboratory technicians to perform environmental monitoring at client facilities and microbiology testing in the microbiology lab. This is a full-time position at our West Coast location. The schedule will be Monday-Friday, 7 a.m. to 3:30 p.m., but you must be able to work flexible hours, including different shifts and weekends. At this time, the starting hour is 5 a.m. and will require OT. | 12/8/2019 |
| 1023 | Micropoint Santa Clara, CA Quality Control Associates MS in chemistry, biology or related Exp: 0-2 years |
We are looking for highly motivated QC Associates (two openings) to join our quality team. These positions are responsible for participating as team members in a laboratory environment for finished product/or development programs focused on the goal of testing and releasing the immunoassays found in Micropoint's in-vitro diagnostic products for point-of-care (POC) testing. | 12/8/2019 |
| 1024 | Micropoint Santa Clara, CA Manufacturing Operators HS Diploma/GED Exp: 0-2 years in pharma/food/med manufacturing |
There are two openings. These positions are responsible for basic and routine tasks involved in the manufacture and assembly of the company's disposable test cartridges. Follow written procedures for set-up, operation, and clean up of manufacturing equipments, final assembly, and packaging. Responsible for manual tasks including, pipette solution, pouch and box labeling, product inspection. Prepare materials used in the cartridge production process | 12/8/2019 |
| 1025 | Micr Indianapolis, IN Medical Research Study Coordinator: BS/BA Exp: 1-3 years clinical research experience preferred |
We are seeking an experienced individual who has coordinated the implementation of clinical research protocols. 1-3 years of clinical research experience and CCRC certification is preferred for this full-time position. | 12/8/2019 |
| 1026 | LGC Manchester, NH Junior Staff Accountant BS/BA in accounting or finance Exp: 1-3 years in accounts |
The Junior Staff Accountant will be responsible for supporting a fast growing company at two locations (Manchester, NH & Charleston, SC) by providing transactional and reconciliatory assistance to the local Finance and Accounting team which supports both sites. The candidate will contribute across multiple key accounting areas including Fixed Assets, Accounts Receivable, and Accounts Payable. The position is located in Manchester, NH. | 11/28/2019 |
| 1027 | LGC Novato, CA EH&S Technician AS/AA or BS/BA in sciences Exp: 0-2 years |
This role is responsible for all EH&S and Material Management functions at the Novato facility. This includes but is not limited to managing raw materials coming in to the facility, movement throughout the facility, waste management, and emergency equipment inspection. Responds to all EH&S requests at the Novato facility. Organizes all hazardous waste and interfaces with hazardous waste contractor for waste disposal. Performs all safety inspections throughout the Novato facility. Documents all inspection finding and informs functional manager of pertinent findings. Acts as the Facility Operations liaison when necessary. | 11/28/2019 |
| 1028 | LGC Manchester, NH Sales Representitive BS in chemistry or life sciences Exp: 1 year in sales |
The person in this position will function primarily as a sales representative and develop and profitably grow the North American (US & Canada) revenue of the Standards business, primarily in the Food, Beverage and Cannabis sectors. The successful candidate will sell into both private and public organizations associated with Food, Beverage and Cannabis Industries and will possess ability to develop strong customer relationships. | 11/28/2019 |
| 1029 | American Regent Hilliard, OH Process Equipment Technician I - 1st Shift HS Diploma/GED Exp: Entry Level |
This entry-level position is a member of the Manufacturing Team. The Manufacturing Team is responsible for activities associated with the manufacture of safe, effective and sterile pharmaceuticals in accordance with company SOPs, policies and cGMPs. The Manufacturing Team ensure aseptic and sanitary conditions are maintained where required, that appropriate manufacturing area and equipment records are neat and accurate and that safe, effective and professional behavior is displayed at all times. In conjunction with Production Management the Manufacturing Team provides input and assistance to other Departments as needed, playing a critical role in maintaining production schedules and meeting Company goals. The Team Member will be able to participate in all aspects of the Equipment Process. The Equipment Process includes cleaning, assembling, and sterilizing small and large pieces of equipment in accordance with established production records in a concerted effort to manufacture sterile liquid pharmaceuticals. | 11/28/2019 |
| 1030 | American Regent New Albany, OH R&D Technical Services Chemist I MS in chemical engineering/pharma chemistry Exp: 0-1 years |
Conduct the experiments under the supervision of Scientists for Tech Transfer, Process R&D/Scale up/Validation, and other activities needed for introduction of a new product into cGMP manufacturing site or to support process improvements of existing products. Execute laboratory experiments as per the protocols or under supervision to study material compatibility studies and/or cleaning validation activities. Ensure all work is performed and documented in accordance with existing company policies, procedures, current Good Manufacturing Practices, and health and safety requirements. | 11/28/2019 |
| 1031 | American Regent Shirley, NY Compounder I HS Diploma/GED Exp: Entry Level |
This entry level position is a member of the Formulation Team, who comprise a portion of the Manufacturing Team. This position will be expected to execute the required responsibilities and tasks necessary to perform as a Compounder I using current Good Manufacturing Practices (cGMP) according to approved SOPs in order to support the overall mission of the Manufacturing Team. | 11/28/2019 |
| 1032 | American Regent Shirley, NY QC Microbiologist I, EM Lab BS/BA in sciences Exp: 0-2 years in pharma lab |
The QC Microbiologist I will perform microbial testing according to current guidance and established procedures for analysis of samples in the Environmental Monitoring laboratory. Perform support work such as Quality control testing of in-house prepared and commercially purchased media, stock culture maintenance, data trending, etc. | 11/28/2019 |
| 1033 | Lumen Bioscience Seattle , WA Lab Technician BS/BA in biological sciences Exp: 1-2 years lab experience |
The full-time Lab Technician will join an essential team involved in our development of oral antibody-based therapeutics. The team member will be expected to execute leading edge molecular biology protocols, support the construction of novel cyanobacteria strains, and aid in the continued development of protocols that have made Lumen Bioscience the worldwide leader in Spirulina genetic engineering. The position requires strong organizational skills to meet quality and productivity goals. Effective communication skills are also crucial in coordinating with other members of the team, providing status updates, and raising quality or trouble shooting issues as they may arise. | 11/28/2019 |
| 1034 | Lumenis Salt Lake City, UT Test Technician AS in Laser/Electro Optics is highly desired Exp: 1-2 years in laser/optics preferred |
Responsible for performing the set-up, calibration, testing, troubleshooting of circuits, components, instruments, optical and mechanical assemblies. Determines and may develop test specifications, methods and procedures from blueprints, drawings and diagrams. Tests and troubleshoots assemblies and Laser systems. May complete rework on assemblies and or systems as a result of testing. As required, prepares technical reports summarizing findings and recommending solutions to technical problems. May assist in the selection and set-up of specialized test equipment. Works on assignments that are moderately complex in nature where judgment is required in resolving problems and making recommendations. | 11/28/2019 |
| 1035 | Luuminex Austin, TX LOGISTICS COORDINATOR I - Limited Assignment -SHIPPING HS Diploma/GED Exp: 1 year in logistics/supply chain |
The Logistics Coordinator I performs a variety of shipping, stockroom, and receiving tasks. This coordinator prepares items for shipment ensuring cost effective courier services and compliance to global trade, OSHA, DOT and other regulations. Must have a high regard for compliance, attention to detail, and inventory accuracy. Responsible for material transactions within ERP System. Compares information on packing slip with purchase order to verify accuracy; Also includes reverse logistics support. | 11/28/2019 |
| 1036 | Luuminex Northbrook, IL LOGISTICS COORDINATOR I - US HS Diploma/GED Exp: 1 year in logistics/supply chain |
Performing administrative and physical duties to successfully execute shipments. This position coordinates with transportation companies, handles routine questions and problems, and communicates with other departments and customers throughout the delivery cycle to ensure a high rate of customer satisfaction. Completing documentation that is in compliance with international, hazmat, or FDA standards. | 11/28/2019 |
| 1037 | Lundbeck San Diego, CA Research Associate BS or MS biological sciences Exp: 1-3 years lab/bench experience |
The Research Associate In Vitro Screening and Biochemistry will contribute to the identification and development of novel small-molecule drugs and support Lundbeck’s CNS discovery programs. The successful candidate will work in multidisciplinary teams to discover new therapeutics, collaborating with biologists and medicinal chemists to select molecules for further in vitro characterization and to identify trends in structure-activity relationships. | 11/28/2019 |
| 1038 | United Therapeutics Corporation Silver Spring, MD Clinical Trial Administrator I BS/BA Exp: 0-1 years related experience |
The Clinical Trials Administrator I provides administrative and operational support with the set-up, execution and close-out of clinical studies as well as infrastructure development projects. Supports the department’s requirements to adhere to GCP and oversight of clinical trials. Assist the Clinical Operations team in completion of all required tasks to meet departmental and project/study goals. Develop and maintain knowledge of relevant Lung Biotechnology Inc. SOPs and Lung Biotechnology internal tracking systems. | 11/28/2019 |
| 1039 | United Therapeutics Corporation RTP, NC Research Associate I/II - Tissue Engineering, Bioprocess Development BS or MS in biological sciences/engineering Exp: BS: 1-3 years, MS: 0-2 years |
Evaluate the function of native and engineered lung tissues and assist with implementation of new analytical regimes to characterize the function of the engineered lung tissues. Assist with data collection and analysis in support of these objectives. Contribute to preparation of human and non-human organs and tissues for experimentation. Prepare specific supplies and materials for designated testing, including design and construction of tubing circuits, preparation of perfusate, and maintenance of equipment used for functional assessment experiments. | 11/28/2019 |
| 1040 | United Therapeutics Corporation RTP, NC Bioprocess Technician - Cell Biology AAS/BA/BS in biological sciences Exp: 1+ year in industry/lab |
Conduct and assist in research efforts to develop novel cell and cell-based products for treating pulmonary hypertension and other lung diseases. Routinely perform large-scale primary lung cell culture in 2D and 3D to support process development activities for a tissue engineered product. Routinely perform bioanalytical assays to phenotypically and functionally characterize cells (such as flow cytometry and plate-based assays). Generate data for process development studies to improve yield, purity, and quality of primary lung cell types | 11/28/2019 |
| 1041 | Lygos Berkeley, CA Analytical Chemistry Research Associate I BS in chemistry or related Exp: 0-3 years analytical experience |
Lygos is seeking an analytical chemistry research associate candidate to set up, run, clean, and maintain HPLC instruments. The successful candidate will have experience with general lab procedures, data interpretation, and reporting in a fast-paced and dynamic work environment. Execute analytical methods including: sample, standard, and mobile phase preparation, HPLC operation, HPLC calibration, data analysis, and data entry. Collaborate with the metabolic engineering team, fermentation team, and downstream processing team to ensure that results and conclusions are communicated clearly. | 12/2/2019 |
| 1042 | Lygos Berkeley, CA Software Engineer BS or higher in computer sceinces Exp: 1+ years |
The successful applicant will serve as a software engineer developing systems for that improve and automate data handling and analysis related to R&D processes at Lygos. Investigating users’ workflows and needs, creating specification documents, writing applications, and supporting both deployment and end users of applications will be necessary elements of the successful applicant’s duties. The successful applicant will be expected to advance critical aspects of Lygos’ software development efforts through both effective individual and team efforts. | 12/2/2019 |
| 1043 | LSNE Bedford, NH QC Microbiology Technician (A shift - Sun - Wed 6:00 - 4:30 pm) BS Exp: 0-1 years in cGMP environment |
Conducts sampling of incoming raw materials, product environments, and/or facility clean utilities, as per approved procedures and submits these samples to the appropriate testing facility for documented and controlled results. Applies material / system status labels, as indicative of testing status and/or results obtained. Assists with lab maintenance and inventory. | 12/2/2019 |
| 1044 | LSNE Bedford, NH QC Chemist I (Mon - Fri 1st shift) BS in analytical chemistry or related chemistry Exp: 0-3 years in analytical chemistry/QC |
This position will have responsibility for supporting all activities in the Quality Control Laboratory. This includes the testing of in-process samples, finished product and stability samples and raw materials. This may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management. | 12/2/2019 |
| 1045 | LSNE Bedford, NH QA Associate I - Ops (Wed - Sat 3:30 pm - 2:00 am) BS in sciences Exp: 0-2 years |
This position provides QA support in the manufacturing of clinical and commercial drug products/medical devices to ensure compliance with the principles and guidelines of cGMP. QA Associates maintain the quality systems, such as laboratory control, investigation management, materials management, document control and training to ensure control of the manufacturing process. This position will actively partner with Manufacturing Operations, Facilities, Materials Management, and other supporting departments to provide compliance and technical guidance to ensure quality issues are identified and resolved in a timely manner. | 12/2/2019 |
| 1046 | LSNE Bedford, NH QA Associate I - Ops (Sun - Wed 6:30 am - 5:00 pm) BS in sciences Exp: 0-2 years |
This position provides QA support in the manufacturing of clinical and commercial drug products/medical devices to ensure compliance with the principles and guidelines of cGMP. QA Associates maintain the quality systems, such as laboratory control, investigation management, materials management, document control and training to ensure control of the manufacturing process. This position will actively partner with Manufacturing Operations, Facilities, Materials Management, and other supporting departments to provide compliance and technical guidance to ensure quality issues are identified and resolved in a timely manner. | 12/2/2019 |
| 1047 | LSNE Bedford, NH Manufacturing Technician I/III (Wed - Sat 3:30 pm - 2:00 am) HS Diploma/GED Exp: 0-2 years in GMP manufacturing, pharma/medical devices preferred |
This position is responsible for performing a variety of tasks in support of all manufacturing activities in accordance with current GMPs. Executes basic manufacturing procedures (cleaning, solution prep, equipment prep) under direct supervision. Accurately follows and completes required documentation (batch records, forms, Quality system documentation) under direct supervision. Expected to adhere to all procedures, including gowning and safety requirements, at all times. Supports manufacturing activities outside of core hours under direct supervision. | 12/2/2019 |
| 1048 | Mallinckrodt Pharmaceuticals St. Louis , MO Quality Tech II AAS/AA or BS/BA in chemistry/biology Exp: 1-3 years in cGMP |
Depending on the laboratory area, will perform analysis on Raw Materials, Intermediates, In-Process, Finished Product, or Stability samples using established analytical methods. Follow good documentation practices for the accurate and timely documentation of all activities. Perform wet chemistry testing using GMP documentation in notebooks and also ELN. Assist with establishing and maintaining safe work standards in the lab | 12/2/2019 |
| 1049 | Mallinckrodt Pharmaceuticals Hobart, NY Maintenance Tech I HS Diploma/GED Exp: 1-2 years in mechanical/electrical trades |
Performs basic preventative maintenance activities and repairs to buildings and facilities including; office areas, pharmaceutical manufacturing and processing areas, laboratories, warehouse areas, loading docks, and parking lots and driveways. May perform maintenance or simple repairs to selected types of plant equipment or systems for which mechanic has received training on. Works with various types of construction materials used for construction and finishing of walls, ceilings, and floors. Works under the supervision of the Facilities Maintenance Supervisor or, a more highly-skilled mechanic. | 12/2/2019 |
| 1050 | Mallinckrodt Pharmaceuticals Hobart, NY Blending Technician I - A Shift 4on/4off 6am-6pm HS Diploma/GED Exp: 3-12 months |
Blend defined quantities of designated raw materials (per specific manufacturing instructions) into final dosage blend stage. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Blending Technician is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. Maintains accurate and compliant documentation on all activities. | 12/2/2019 |
| 1051 | Mallinckrodt Pharmaceuticals St. Louis , MO Quality Assurance Technician II HS Diploma, AS/AA or BS/BA preferred Exp: 1-3 years in document review in cGMP environment |
The Quality Assurance Technician II performs a variety of review processes with the intent to correct record errors in manufacturing process documentation that includes batch record review and documentation issue resolution. This role is also responsible for return good inspections, cGMP area inspections and product inspections. This role ensures QA compliance and that cGMP principles are adhered to. | 12/2/2019 |
| 1052 | Mallinckrodt Pharmaceuticals St. Louis , MO Chemical Process Engineer BS in chemical engineering Exp: 1-3 years related experience |
The Chemical Process Engineer is the recognized technical leader for chemical manufacturing processes and for the improvement of existing chemical processes. Consistently seeks for and evaluates methods to improve overall customer satisfaction through improved manufacturing efficiencies. Serve as main point of contact for chemical manufacturing processes in their area in regards to safety, quality, and continuous improvement activities. | 12/2/2019 |
| 1053 | Mallinckrodt Pharmaceuticals Hobart, NY Packaging Maintenance Technician - 2nd Shift HS Diploma/GED Exp: 1-2 years in mechanical/electrical trades |
Performs preventative maintenance activities on specific pharmaceutical manufacturing and/or packaging equipment and systems. Provides maintenance support to manufacturing personnel during the operation of manufacturing and packaging equipment and systems. Diagnoses problems and performs repairs on manufacturing and packaging equipment. | 12/2/2019 |
| 1054 | Mallinckrodt Pharmaceuticals Hobart, NY Project Engineer BS in engineeering Exp: 1-3 years |
Works as a key technical resource in supporting company objectives with respect to engineering design and project management in the implementation of capital projects and non-capital process improvements. Responsibilities include working with and/or leading the team to help identify, develop and execute projects to meet or exceed all company goals with respect to quality, schedule and spending. This could include: developing design concepts with the users; providing detailed design documents for some projects (e.g. P&IDs, construction drawings) ; equipment and instrument specification and installation; engineering calculations, developing request for proposals to bid projects; coordination with customers, contractors and consultants; reviewing documents, preparing capital appropriation requests, creating purchase orders, reviewing and paying invoices;; monitoring progress; assisting with training; executing commissioning activities; and ensuring proper project closure. | 12/2/2019 |
| 1055 | Mammoth Biosciences San Francisco, CA Research Associate BS/BA or MS in biology or chemistry Exp: 1-3 years in molecular biology/genetics |
Mammoth is seeking a Research Associate experienced in nucleic acid and protein biochemistry techniques to support our product development team. The ideal candidate will have experience with assay development and product commercialization related to molecular tests and reagent kits. The candidate will be comfortable working as part of a team, be highly motivated, and display excellent time management skills. The Research Associate will report directly to Director of Assay Development. | 12/2/2019 |
| 1056 | Masimo Irvine, CA [CLINICAL] Clinical Research Associate BS/BA in sciences Exp: 0-4 years |
The Clinical Research Associate is responsible for clinical studies, site management and compliance monitoring of assigned clinical projects undertaken in support of a given product line or marketing initiative. This position must ensure that all activities will be conducted in accordance with Government Regulations (FDA, MDD and International), Good Clinical Practices (GCP) and Department Operating Procedures (DOP). Plan, implement and conclude clinical studies in support of project timelines/market release goals with minimal supervision; An advanced individual may conduct more complicated studies, as well as contribute to study proposals and protocols, applying principles of clinical study design and research methodology to assigned research projects; | 12/2/2019 |
| 1057 | Master Control Salt Lake City, UT Enterprise Support Engineer II 4-year technical degree Exp: 0-4 years |
The Enterprise Support Engineer (TSE) provides in depth, high-level technical support to MasterControl customers. The ESE II maintains systems-level expertise and root cause-level troubleshooting while resolving advanced technical issues for customers. ESE II's work with fellow team members, service consultants, sales operations and other company resources to increase customer satisfaction and loyalty. TSE's are responsible for special projects, and will maintain one or more team projects that track team analytics and team success. TSE's will be subject matter experts (SME) in one or more subjects pertaining to the support of MasterControl Customers. | 12/2/2019 |
| 1058 | Masy Bioservices Pepperell, MA Quality Associate I HS Diploma/GED Exp: 1+ year in related |
This position provides day to day support assisting in areas such as GMP, ISO 9001 and ISO 17025 compliance and the company’s quality system. Duties include quality assurance and control activities in technical, systems, operations and service areas. This position may require frequent interaction with multiple departments. Works under general supervision of management or team lead. | 12/2/2019 |
| 1059 | MDxHealth Irvine, CA Specimen Accessioner I HS Diploma, degree preferred Exp: 1-2 years |
The Specimen Accessioner I performs all paperwork and non-technical procedures required to prepare, process, and submit specimens to the laboratory for testing. Responsibilities will include but not limited to: receiving, triaging and accessioning patient samples, distribution of patient reports and specimens to clients, performing quality control of accessions and labeling. | 12/2/2019 |
| 1060 | MED Institute West Lafayette, IN Mechanical/Biomedical Engineer BS or MS in biomed/mechanical engineer Exp: 1-3 years |
This position requires a technically sound engineer capable of driving a project to completion with minimal supervision. A qualified candidate should be able to demonstrate a solid understanding of first principles, build a design from the ground up, perform independent research utilizing all available tools and resources, communicate well with customers, maintain good documentation practices, and develop and validate new test methods. Examples of commonly performed tests include accelerated fatigue, corrosion, electrosurgical, simulative use, and others that are used to evaluate material properties and/or functionality of a finished medical device. In addition, this person will be responsible for the maintenance of well-controlled documentation, including written protocols and reports, data forms, and laboratory notebooks. | 12/2/2019 |
| 1061 | Medicomp Melborne, FL Amazing Cardiac Monitoring Technician HS Diploma Exp: Certified Cardiovascular Technician |
Review data from Cardiac monitors to provide physicians with results to help determine treatment for patients. This position requires a strong ability to read and interpret EKG strips as well as communicate with Doctors, patients, and other departments throughout the organization. This is a 24/7 facility and shifts are scheduled with differential available for 2nd, 3rd and weekend shifts. | 12/2/2019 |
| 1062 | Medicomp Melborne, FL Technical Services Associate AS/AA degree Exp: 0-1 year |
We are seeking a Technical Services Associate that under minimal supervision and using average manual dexterity, performs varied skilled assembly tasks and soldering tasks necessary to produce a product by performing the following duties. In addition, this position requires basic computer skills to make transactions, transfer yield rates and data into Excel. | 12/2/2019 |
| 1063 | Medidata Metropark, NJ B2B Marketing Associate BS/BA Exp: 1-3 years in marketing/sales |
This marketer will drive direct targeted marketing for our platform and solutions by developing programs that leverage outbound marketing efforts - across online/digital and tele-prospecting tactics - to drive overall preference, satisfaction, technology adoption of our platform/portfolio and amplify market impact of our technology innovation stories. Assist and lead in the development of outbound marketing programs across a variety of product offerings, industries, segments, and personas (e.g., Clinical Ops, Data Management, Finance, IT). | 12/2/2019 |
| 1064 | Medidata New York, NY Software Engineer (C# / .Net) BS/BA Exp: 1-3 years in various coding languages |
Coder is a mature, single-instance, multi-tenant web service supporting hundreds of clinical trials. Our application is built with C#, leverages Microsoft’s SQL server database and is hosted in AWS. Our front end uses Asp.NET, HTML/CSS, Bootstrap and AngularJS. As an engineer on Coder, you'll be challenged both to develop new features in response to market demand and improve the performance and scalability of the application to meet the rapidly growing user base. | 12/2/2019 |
| 1065 | AstraZeneca Wilmington, DE Contract Operations Analyst BS/BA Exp: 0-4 years |
The Sr. Contract Operations Analyst is responsible for working with internal/external customers on all aspects of Market Access; Master Data, Contracting, Membership, Chargebacks and Rebates. They are responsible for the receipt, analysis, impact, resolution and posting/reporting of all contractual payments across multiple customer segments including Health Plans, GPOs, Specialty Pharmacies, Physicians and Wholesalers as well as maintaining all related documentation for those payments. The Sr. Contract Operations Analyst is responsible for developing Market Access contracts including: template development, strategy interpretation, language negotiation, approval, and execution In this role, they will manage and meet deliverables of business operations to monitor, evaluate and administer claims to be paid and ensure payments are accurate, timely, formulary compliant and entered in contract systems consistent with agreement terms, following corporate controls/approved guidelines and SOX regulations. | 12/2/2019 |
| 1066 | AstraZeneca Frederik, MD Quality Control Analyst BS in sciences/biotech/pharma Exp: 0-5 years |
Performs selected quality control testing activities, dependent upon assigned area, including the following: Responsible for conducting raw materials, in process, finished product and stability testing according to standard operating procedures. Completes appropriate documentation supporting testing procedures, including data capture forms, equipment logbooks, and inventory forms. Identifies and troubleshoots equipment problems. Enters data evaluated for compliance to specifications and reports abnormalities. Reads, understands, and follows SOP’s and complies with cGMP’s | 12/2/2019 |
| 1067 | AstraZeneca Gaithersburg, MD Research Animal Technician I BS/BA in biological sciences Exp: 0-1 years |
At AstraZeneca as the Research Animal Technician I, you will support oncology using basic technical skills such as performing daily health/mortality checks, evaluating health status of animals and performing basic technical procedures such as SC, and IP injections, cardiac blood collection, and oral gavage. Observe appropriate safety and study requirements by reading, understanding and following Standard Operating Procedures (LAR Guidelines), applicable regulations and study protocols. Observe appropriate safety and health practices including personal protective equipment and barrier requirements. | 12/2/2019 |
| 1068 | AstraZeneca Wilmington, DE Patient Safety Associate (Quality Excellence) BS/BA in biosciences, healthcare, IS/IT Exp: 1 year in pharma |
The BioPharmaceuticals Business Unit (BBU) creates and executes meaningful therapeutic area and product strategies that are focused on addressing the unmet needs of patients around the world. Conducts activities and interactions consistent with company values and in compliance with the Code of Conduct and supporting policies and standards relevant to the role. Completes all required training on AstraZeneca’s Code of Conduct and supporting policies and standards on time. Reports potential issues of non-compliance. Demonstrates a working knowledge and compliance with organizational global and local procedural documents and local implementation of objectives, policies, processes and procedures and regulatory requirements, guidelines and obligations relevant to pharmacovigilance activities and adverse event reporting, including periodic safety reporting. | 12/2/2019 |
| 1069 | AstraZeneca Frederik, MD Quality Control Technician - Laboratory Management Services (LMS) - Operations HS Diploma/GED Exp: 0-2 years work experience |
Sampling of the Utilities Systems (for example WFI, Specialty Gases, Compressed Air, Steam). Sample management activities including receipt, visual inspection for integrity, storage, distribution and disposal. Parts and glassware washing and autoclaving, including proper documentation of these activities. Detailed supervision and detailed instructions given for routine work as well as any new activities or special assignments. | 12/2/2019 |
| 1070 | Kimball Electronics Jasper, TX Manufacturing Engineer BS/BA in eletrical/mechanical engineering Exp: 0-3 years |
Leads manufacturing efforts with respect to direct customer product launches and sustaining activities. Guides, mentors and manages engineering support teams. Development of processes and DFx activities to meet customer requirements. Selection, specification and implementation of manufacturing equipment. Work directly with program management and quality engineering to ensure profitability. | 12/2/2019 |
| 1071 | Cantel Medical Pomezia, IT R&D Microbiology Associate MS in biology or related Exp: 1 year in R&D projects |
The junior microbiologist will assure to support the “in vitro” test according to EN/ISO Standards requirements. Respecting the deadlines; Check the expiration date of the reagents and the microbial strains; Fill laboratory notebooks and record the results. Ability of preparation of culture media and microbial strains suspension. They will report to local manager. | 12/2/2019 |
| 1072 | MedPace Home based, na Home-Based Clinical Research Associate - Clinical Research Coordinator Experience BS/BA in health/sciences Exp: 1 year minimum |
This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Perform qualification, initiation, monitoring, and closeout visits; Establish an open line of communication with site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Evaluate the quality and integrity of site practices – escalating quality issues as appropriate; | 12/2/2019 |
| 1073 | MedPace Cincinnati, OH Clinical Research Associate-Cincinnati Entry Level BS/BA in health/sciences Exp: 1 year work experience preferred |
Our successful Clinical Research Associates possess various backgrounds in medical and other science-related healthcare fields. This role takes you on a journey through travel and excitement which will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices. No research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. Through our PACE Training Program, you will join other Professionals Achieving CRA Excellence: PACE provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA. | 12/2/2019 |
| 1074 | Viant Collegeville, PA Process Engineer - Metals BS/BA in material science/metallurgy or mechanical engineering Exp: 1 year |
The Process Engineer must be able to recognize, communicate, and measure technical risk for a variety of metals for use in medical, aerospace, and industrial products along with the processes and equipment used to manufacture these products. The process engineer is a central leader for addressing concerns of a technical nature. Provide diversified range of technical services to both internal and external customers supporting the attainment of company goals. Areas of support include mechanical testing, cold drawing, heat treating, nondestructive testing, and failure analysis of metal tubes | 12/2/2019 |
| 1075 | MedSpark San Luis Obispo, CA Product Development Engineer BS/BA in mechanical engineering Exp: 1 year |
You will be part of a small and nimble team that conceptualizes, develops, and proves-out designs that make an impact on the world of medicine. Your primary role is driving conceptualization, development, and prototyping of new product concepts, focused on inventive uses of new and existing technologies that open up entirely new product concepts. Work hours and days are extremely flexible, based on need and your availability. | 12/2/2019 |
| 1076 | T2Biosystems Lexington, MA Research Associate, Molecular Assay Development BS in biology, biochemistry, or related Exp: 0-2 years |
As a motivated, curious and goal-oriented research associate, you will join a dynamic R&D team and contribute towards the development of novel molecular methodologies and assays for diagnostic applications. You will execute studies, conduct data analysis, and document results. As a contributor you will interact with other individuals and groups across our research and product development teams. You must have strong communication, analytical and quantitative skills and thrive working with highly skilled teams on multiple, simultaneous projects in a fast-paced technical setting. etc. | 12/4/2019 |
| 1077 | T2Biosystems Lexington, MA Research Associate - Process Development BS/MS in biology, biochemistry, biotechnology, or related Exp: 1-2 years |
We are seeking a talented and highly motivated individual to join our multi-disciplinary team as a Research Associate. This individual will be a key contributor to executing reagent formulation activities including technology transfer, process development, analytical method development, verification and validation. The position will be located in Lexington, MA. Responsibilities: Development, optimization, scale up, and validation of reagent processes and measurement systems; including DOE and capability analysis. Experimental planning, execution, and data analysis. etc. | 12/4/2019 |
| 1078 | T2Biosystems Lexington, MA Research Associate /Research Associate II - Microbiology (Contract to Perm) BS/MS in molecular biology or related Exp: 0-3 years |
This position is to fill a need within our Microbiology group working in our Lexington, MA location. The RA will provide aid in the development of laboratory protocols for the cultivation and characterization of pathogenic organisms. The individual will work with the T2 Microbiology staff to expand on our established protocols and methods to enable the accurate production of test samples for development of novel assays in conjunction with the Assay Development group. This role consists of hands-on execution in the laboratory and data analysis within the Microbiology group. etc. | 12/4/2019 |
| 1079 | Talis Biomedical Menlo Park, CA Research Associate MS in biology, microbiology, molecular biology, biochemistry or related Exp: 0-3 years |
The candidate will join the Assay Development group in the R&D division where focus is on molecular assays development such as nucleic acid isolation, purification, amplification and labeling technologies. We are seeking talented, motivated individuals to join a collaborative effort to enable development of rapid diagnostic tests of several pathogens from various clinical specimens. Position Responsibilities: Work with senior scientists and run hands-on experiments for microbiology, sample preparation, nucleic acid extraction and amplification. Participate in design of molecular assays. etc. | 12/4/2019 |
| 1080 | Talis Biomedical Menlo Park, CA Test Engineer - Embedded Software & Firmware BS in an engineering field Exp: 0-4 years |
Position: Learn and develop expertise on our firmware and embedded software requirements, in order to create automatable test scripts. Author basic functionality, stress, and reliability tests using state-of-the art tools, and novel in-house test fixtures. Document and perform root cause analysis on testing failures. Collaborate closely and clearly communicate test plans and results to cross-functional team members. Other duties as assigned. | 12/4/2019 |
| 1081 | Tango Therapeutics Cambridge, MA Associate Scientist, Immunology BS/MS in immunology or related Exp: 0-8 years |
We are seeking an innovative, collaborative and enthusiastic immunologist to work on building our immunology and Immuno-Oncology Programs. This individual will work primarily at the bench to help drive target identification, validation, and patient selection strategies. Job Responsibilities: Culture and engineer primary human T cells and murine T cells using genetic tools. Culture and engineer primary human tumor cell lines and murine cell lines using genetic tools. etc. | 12/4/2019 |
| 1082 | TCR2 Therapeutics Cambridge, MA Research Associate/Senior Research Associate, Analytical Process Development BS in biochemistry, cell biology, immunology or related Exp: 1-2 years |
Responsibilities: Learn and execute on all assays used by the analytical team (qPCR, ELISA, T-cell based assays). Assist in the analysis and characterization of lentiviral vectors for use by multiple internal research groups. Work with process development teams to investigate, improve, and implement advanced vector production processes. Analyze results, solve problems, and troubleshoot assays. Participate in assay development of established analytical tools and help develop new assays. Develop and maintain various cell lines used in cell-based analytical assays. etc. | 12/4/2019 |
| 1083 | TCR2 Therapeutics Cambridge, MA Research Associate, Vector Production BS/MS in molecular biology, biochemistry, protein chemistry, or related Exp: 1-2 years |
Responsibilities: Generation and maintenance of various cell lines and used by internal research groups. Production of retroviral vector stocks using various transfection methodologies. Assist analytics team in evaluation of in-process and endpoint samples. Thorough documentation of procedures and experiments. Coordinate with various internal groups for the generation and evaluation of emerging vector products. Assist in drafting of SOPs, technical documents, batch records, etc, for transfer to external CMOs. Participation in internal and external meetings detailing ongoing work. etc. | 12/4/2019 |
| 1084 | TE Connectivity Manfield, OH Electrical Engineer BS in physics or electrical or mechanical engineering Exp: 0-1 years |
TE Connectivity’s R&D/Product Development Engineering Teams conceive original ideas for new products, introduce them into practice. They are responsible for product development, and qualification from market definition through production and release; assist in the qualification of suppliers for new products to ensure suppliers deliver quality parts, materials, and services for new or improved manufacturing processes; conduct feasibility studies, testing on new and modified designs; direct and support detailed design, testing, prototype fabrication and manufacturing ramp. The R&D/Product Development Engineering Teams provide all required product documentation including, but not limited to, Solid Model, 2D/3D production drawings, product specifications, and testing requirements. They create and modify detailed drawings and drafting or conceptual models from layouts, rough sketches or notes and contribute to design modifications to facilitate manufacturing operation or quality of product. etc. | 12/4/2019 |
| 1085 | TechLab Blacksburg, VA Research Technician BS in a life science Exp: 1 year |
TechLab, Inc. develops, manufactures and distributes medical diagnostic tests. Our company places emphasis on science and collaboration with Universities. We are hiringa Research TechnicianforourScientific Affairs teams.The Research Technicianwill aidthe team with experiments and research. The Research Technician can be expected to perform protein purification using chromatography, write Standard Operating Procedures and Master Batch Records, and assist with assay development and optimization. etc. | 12/4/2019 |
| 1086 | Tecomet Warsaw, IN Material Associate HS diploma or equivalent Exp: 1-3 months |
The Material Associate will receive, unpack, verify, and store raw materials. Issue raw material to job routers and deliver to appropriate work areas. Maintain movement of subcontract production parts returning from vendors. This is accomplished by maintaining Tecomet principles of Safety, Quality, Customer Satisfaction and Innovation. Essential Duties and Responsibilities: Receive raw material and out-vend production parts and enter receipt into computer. Receive delivery of UPS, Fed-Ex and other transportation carriers and document receipt in computer. Issue raw material to specific job routers and deliver to specific production unit.Document receipt in computer. Perform weekly cycle-counting to ensure material counts are correct. etc. | 12/4/2019 |
| 1087 | Tempus , MI Account Associate BS in a life science, business, or marketing Exp: 0-2 years |
Responsibilities: Building and maintaining relationships with physicians and office staff to drive clinical orders in the community. Building and maintaining relationships with pathology departments to ensure smooth specimen sendouts - tissue procurement. Maintain a regular cadence of touch points (in person, emailing value adds) with certain targeted accounts (ie 3 x month per physician). Coordinating Medical Affairs report review with physicians after clinical orders. Order Kit and literature replenishment at accounts. Identifying and attending approved local conferences. Working with accounts to obtain necessary clinical data / progress notes for Tempus-tested patients. etc. | 12/4/2019 |
| 1088 | Tempus Chicago, IL Clinical Molecular Technologist MS in medical technology, clinical laboratory science, or related science Exp: Not necessary for MS candidates |
What you’ll do: Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Utilize automation and robotics to standardize the discovery pipeline from sample acquisition to sequencing output. Maintain quality metrics and data generation for next-generation sequencing platforms. Work to maintain CLIA/CAP compliance in a novel field. Work our daytime shift Monday - Friday. | 12/4/2019 |
| 1089 | Tempus Chicago, IL Clinical Molecular Technologist (Shift Diff - Tuesday to Saturday) MS in medical technology, clinical laboratory science, or related science Exp: Not necessary for MS candidates |
What you’ll do: Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Utilize automation and robotics to standardize the discovery pipeline from sample acquisition to sequencing output. Maintain quality metrics and data generation for next-generation sequencing platforms. Work to maintain CLIA/CAP compliance in a novel field. Work our daytime shift Monday - Friday. | 12/4/2019 |
| 1090 | Tempus Chicago, IL Clinical Molecular Technologist (Sunday-Wednesday with Shift Diff.) MS in medical technology, clinical laboratory science, or related science Exp: Not necessary for MS candidates |
What you’ll do: Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Utilize automation and robotics to standardize the discovery pipeline from sample acquisition to sequencing output. Maintain quality metrics and data generation for next-generation sequencing platforms. Work to maintain CLIA/CAP compliance in a novel field. Work our daytime shift Monday - Friday. | 12/4/2019 |
| 1091 | TeVido BioDevices Austin, TX Biotech Manufacturing Technician AS/BS in biological sciences or engineering Exp: 0-1 years |
TeVido BioDevices is seeking a highly motivated individual to join our team as a Biotech Manufacturing Technician. We are a small Austin, TX-based biotech company that is addressing unmet needs in reconstructive and cosmetic surgery. The company has launched the manufacturing of our first product, cellular grafts, to treat patients with skin pigmentation disorders such as vitiligo. The person in this role will be responsible for performing daily production operations, including processing, quality control tests, and production facility cleaning; documenting work; and aiding improvement projects. This individual should be detail-oriented and self-motivated. An Associate’s degree in biological sciences or bioengineering and experience with aseptic technique in a laboratory or cleanroom is required. This is a challenging and exciting opportunity to contribute to an innovative, fast-paced startup in Austin, TX whose mission is to enhance patients’ quality of life using their own tissue. etc. | 12/4/2019 |
| 1092 | Thermalin Cleveland, OH Research Associate-Protein Formulation MS in biochemistry or related Exp: 1 year |
Thermalin is looking for a Research Associate – Protein Formulation to join our team. In this role, you will formulate insulin analogs for preclinical development. Research Associate Responsibilities: Formulate novel insulin analogs using established protocols. Quantify insulin analogs using reverse-phase (RP) analytical chromatography. Characterize insulin formulations with novel excipients using various biochemical methods. Develop new formulation schemes for insulin analogs. Optimize procedures and protocols to improve throughput. Perform laboratory tasks safely, rapidly, and efficiently. Report results in written and verbal format. Record results accurately and meticulously. | 12/4/2019 |
| 1093 | ThermoFisher Scientific Greenville, NC Formulation Technician II HS diploma/AS Exp: 1 year |
How will you make an impact? Sets-up, operates, and maintains the classified environments and manufacturing equipment for pharmaceutical products. Ensures operations are performed in a safe and responsible manner striving to create an injury-free and incident free workplace. What will you do? Operation of aseptic filling, freeze drying and capping equipment. Ensures pharmaceutical products in manufacturing are in accordance to SOPs and current GMP and other batch related activities. Verifies and documents production activities in batch records, logbooks, etc. Assists in troubleshooting operational and production problems in order to identify appropriate corrective actions. Performs the disassembly, assembly, cleaning, and operation of area manufacturing equipment. etc. | 12/4/2019 |
| 1094 | ThermoFisher Scientific , IL Field Service Technician BS in engineering, biology, chemistry, or related Exp: 1+ years |
The Field Service Technician (FST) performs planned maintenance, repairs and other verification/qualification services on a variety of laboratory instruments in assigned territory. The FST engages with customers and provides basic instrument services in a professional and timely manner. Essential Functions: Provides planned maintenance (PM), basic repair services and temperature verifications. Displays professionalism, understanding, tact, fairness and technical knowledge in all customer interactions. Follows all reporting responsibilities of Remote Service Dispatch (RSD), Escalation, Field Problem Report (FPR) and Field Service Report (FSR) submissions. etc. | 12/4/2019 |
| 1095 | ThermoFisher Scientific Gainesville, FL Associate, Quality Assurance HS diploma Exp: 1 year |
The QA Associate will participate in the day to day operations related to release functions in the Quality Assurance Department. The incumbent is responsible for the timely review and disposition of controlled materials needed to support manufacturing. These materials include, but are not limited to, sterile supplies, cell banks, viral banks, and reagents used by manufacturing or for testing processes. The associate identifies areas for improvement and ensures materials, products, and equipment within the warehouse remain in a state of control. etc. | 12/4/2019 |
| 1096 | ThermoFisher Scientific Los Angeles, CA Sales Representative BS Exp: 0+ years |
Our Sales Representative is responsible for the sales of research products and services within a defined territory, serving customers engaged in pharmaceutical, biomedical, chemical, and other fields of research and development, as well as quality assurance labs such as in food and environmental testing. The Sales Representative maintains effective customer relations, develops opportunities for growth within an existing customer base, and assures market penetration and profitability while achieving sales and profit forecasts. etc. | 12/4/2019 |
| 1097 | ThermoFisher Scientific Cincinnati, OH QC Lab Technician AS in chemistry or related Exp: 1-2 years |
Responsibilities: Testing of raw materials, finished product, and stability samples while meeting deadlines and following an assigned schedule. Accurately documenting all tests/test materials/equipment used and all results obtained. Work in accordance with approved methods, SOPs, and cGMPs/GLPs, while performing tests. Responsible for safety and to protect themselves and fellow employees from harm. | 12/4/2019 |
| 1098 | ThermoFisher Scientific High Point, NC Continuous Process Verification (CPV) Engineer BS in pharmaceutical science, chemistry, statistics, or related Exp: 1+ years |
The CPV Engineer will apply Project Management and technical expertise within the pharmaceutical industry to successfully deliver CPV program goals and outcomes while interacting with customers and meeting their expectations. CPV is a global regulatory compliance requirement which focuses on ensuring product and process stability, control, and operation within the intended design space. What will you do? Demonstrate highly effective oral and written communication skills and possess project management skills including the ability to engage the organization at multiple levels and organize CPV efforts. Work with Business Managers and the business team with Technical Transfers, new business, or other situations as related to CPV. etc. | 12/4/2019 |
| 1099 | ThermoFisher Scientific Lenexa, KS Quality Control Technologist I BS in a biological science Exp: 1-2 years |
Responsible for all quality control aspects of finished product testing. Ensure that performance of finished product is in compliance with testing standards per IFU and SOP's in addition to customer requirements and regulating agencies' guidelines. Documentation control duties per Quality assurance compliance requirements. Key Responsibilities: Review and maintain product compliance specifications, documentation control. Gain proficiency on all performance benches. Documentation of testing results and determining disposition. Maintain consistency in training in Master Control. Establish and maintain SOP criteria for inspection/testing. Responsible for maintaining department equipment and requesting consumables as needed. etc. | 12/4/2019 |
| 1100 | Invenra Madison, WI Research Associate - Antibody Display BS in biological sciences Exp: 1 or more year in research |
This individual will support the development of the Invenra antibody discovery platform. Aspects of the job entail cloning, antibody library panning and protein target preparation. The successful candidate will work with other scientists within the team and will become proficient in antibody display technologies. The position requires excellent scientific and problem-solving skills, with a strong focus on creative solutions to technical problems. | 11/20/2019 |
| 1101 | Invenra Madison, WI Laboratory Support Technician HS Diploma/GED and enrolled in college Exp: 0 years |
Invenra is seeking a highly motivated laboratory support technician. This individual will maintain the laboratory and laboratory supplies in a clean, ready and working order. The position will work collaboratively with others to implement process improvements that increase efficiency and quality in the laboratory. This is a part-time position. | 11/20/2019 |
| 1102 | Invicro Boston, MA Associate Scientist, Chemistry MS Exp: 1-3 years in academic/pharma labs |
We seek individual who is an accomplished scientist with some experience in radiochemistry of small and large molecule imaging tracers for preclinical nuclear medicine imaging studies, including both PET and SPECT. Though the radiochemistry experience is not mandatory, the ideal candidate needs to have experience in organic synthesis and analytical chemistry. The candidate should have strong desire to learn radiochemistry and be able to operate and troubleshoot automated synthesis systems and analytical equipment. Most of the radiochemistry training will be provided but hands-on experience with handling radioactive materials, labeling with radioactive isotopes, purification, and formulation for in vivo imaging and biodistribution studies will be an advantage. | 11/20/2019 |
| 1103 | Invicro Boston, MA Histology Technician BS or histotech certification Exp: 0-2 years in histology/autoradiography |
The Histology Technician works in the laboratory to perform and support ex vivo studies including, but not limited to, histology, autoradiography, 3D fluorescence imaging, and cell culture. The ideal candidate will have hands-on experience in a pharmaceutical histology laboratory performing standard histology studies – embedding, sectioning and chromagen/fluorescent antibody staining. In addition, the ideal candidate will have a proven track record and competence in histology or autoradiography method development. The individual in this role will be expected to understand and carry out analysis to inform his/her own development efforts and assist in-house analysts. | 11/20/2019 |
| 1104 | Invitae San Francisco, CA Lab Accessioning BS in sciences/clinical lab studies Exp: 0-2 years |
Our Laboratory Accessioning Associates are responsible for preparing laboratory specimens prior to laboratory analysis and testing. This individual should have excellent attention to detail, effective communication skills and the ability to work independently and in a team environment. This role requires being on-site at our SF office location, with either a Monday - Friday or Tuesday - Saturday schedule. | 11/20/2019 |
| 1105 | Thermo Fisher Scientific Fair Lawn, NJ Distillation Tech. - Liquids HS Diploma/GED or AA/AS Exp: 1-2 years in admin |
The Distillation technician supports the Operations Manager and Production Supervisor in achieving daily production targets prioritized by Safety, Quality, Delivery and Cost. Following the priorities set by the Manager and Supervisor ensures that distillation columns are operating safely per procedures and to meet daily production goals laid out by supply chain. | 11/20/2019 |
| 1106 | Thermo Fisher Scientific Cambridge, MA Lab Technician BS in life sciences Exp: 1-3 years industry experience |
The Sr. Associate is an associate with a moderate level of technical expertise and experience. May perform complex activities outside of routine manufacturing operations commensurate with their experience and training. Will participate in the day to day operation of a cGMP compliant Manufacturing facility. Responsibilities include performing basic to complex activities related to operating bioprocess manufacturing equipment, completing the associated documentation of those activities, monitoring assigned processes using automated production systems and controls under limited supervision. Other activities include keeping the GMP manufacturing facility in a state of inspection readiness, using performance tools (Human Performance), and routine housekeeping activities. | 11/20/2019 |
| 1107 | Thermo Fisher Scientific Foster City, CA Labware Technician I HS Diploma/GED Exp: 0-2 years in cGMP environment |
This position is focused on service delivery excellence for UnityTM Lab Services. Specific activities relative to the job function could include: laboratory glassware and inventory management. This position will utilize the basic functionality of systems and equipment relevant to the job function, such as: industrial glasswasher, sterilizers, and ovens. Strong communication skills are also required | 11/20/2019 |
| 1108 | Thermo Fisher Scientific Foster City, CA Labware Technician II HS Diploma/GED Exp: 0-2 years in cGMP environment |
This position is focused on service delivery excellence for UnityTM Lab Services. Specific activities relative to the job function could include laboratory glassware and inventory management. This position will utilize the basic functionality of systems and equipment relevant to the job function, such as: industrial glasswasher, sterilizers, and ovens, Microsoft Office suite. Strong communication skills are also required. | 11/20/2019 |
| 1109 | Thermo Fisher Scientific Cincinnati, OH QC Scientist I BS/BA in physical sciences, chemistry or biology preferred Exp: 0 years required |
Conducts routine chemical and physical testing of pharmaceutical raw materials, packaging components, finished products, microbiological, and stability samples by internally developed and compendial test methods. Executes validated test methods for pharmaceutical raw materials and finished products for strength, impurities, identity, and dissolution by HPLC, GC, dissolution, spectroscopy, and traditional quantitative analysis, utilizing HPLC, GC, LC/MS, dissolution, spectroscopy, and/or traditional wet chemical testing. Recognizes and reports out-of-specification or unexpected results and non-routine analytical and product problems. Performs daily instrument calibrations / verifications as required. | 11/20/2019 |
| 1110 | Thermo Fisher Scientific Eugene, OR Manufacturing Operator I HS Diploma/GED or AS/AA preferred Exp: 0 years required, lab experience a plus |
Operate processing and packaging equipment. Equipment includes: balances, labelers, band sealers, pumps, filtration systems, and other packaging equipment. Weigh, measure and check raw materials with assistance of computer interface to assure batches manufactured contain proper materials and quantities. Calibrate/operate semi-automated and automated manufacturing equipment. Complete and maintain Quality Records in compliance with regulatory requirements, GMP’s and standard operating procedures. | 11/20/2019 |
| 1111 | Thermo Fisher Scientific Eugene, OR Manufacturing Operator I HS Diploma/GED or AS/AA preferred Exp: 0 years required, lab experience a plus |
Operate processing and packaging equipment. Equipment includes: balances, labelers, band sealers, pumps, filtration systems, and other packaging equipment. Weigh, measure and check raw materials with assistance of computer interface to assure batches manufactured contain proper materials and quantities. Calibrate/operate semi-automated and automated manufacturing equipment. Complete and maintain Quality Records in compliance with regulatory requirements, GMP’s and standard operating procedures. | 11/20/2019 |
| 1112 | Invivoscribe San Diego, CA Manufacturing Associate I/II BS in sciences Exp: 1+ years in GMP lab |
As a Manufacturing Associate I/II for Invivoscribe you will assist with all aspects of production, including the production of master mixes, controls and assay kits. You will contribute to the drafting and review of new documents, including SOPs, Batch Records and Purchasing Specifications. Details include: Oversee, perform, plan and schedule production. Work with suppliers of core raw materials to ensure quality, quantity, price and availability. Create, review and revise production documents. Implement and train on the use of those documents. Participate in the production of master mixes and ASR, reconstitution of oligonucleotides, controls, reference standards and general purpose reagents by following manufacturing batch records, work instructions, standard operating procedures, forms and validated Excel spreadsheets. | 11/20/2019 |
| 1113 | Invivoscribe San Diego, CA Research & Development Associate I/II BS in technical/science field Exp: 1+ years in lab |
As a Development Associate I/II at Invivoscribe you are responsible for generating and documenting laboratory data with direct supervision. Your performance will contribute to a quality data generation in a regulated environment following good laboratory practices. More specifically: Support development projects that can include generating analytical data for an FDA submission. Use laboratory techniques such as PCR, gel and capillary electrophoresis, aseptic technique for mammalian cell culture, magnetic beads purification, DNA quantification and NGS. Execute and document experiments that support the development of diagnostic reagents and assays. Experimental design will include all of the appropriate controls. | 11/20/2019 |
| 1114 | Invivoscribe San Diego, CA Quality Control Laboratory Associate I/II BS in sciences Exp: 1+ years in GMP lab |
As a for a Quality Control Laboratory Associate I/II at Invivoscribe you will be responsible for receiving samples and performing data entry for specimens received as well as performing all aspects of clinical laboratory patient testing. More specifically: Test raw materials in process and final product and generate testing data. Releases products to QA for final approval. Ensure that all customer complaints and inquiries are resolved. Conduct and maintain the real time stability study testing. | 11/20/2019 |
| 1115 | Medical Diagnostic Laboratories, LLC Broken Arrow, OK Entry Level Sales Executive BS/BA Exp: 0-2 years |
As a Entry Level Sales Executive, you will be responsible for maintaining and growing a client base of both hospital and physician customers for MDL. Responsible for achieving annual sales and profit objectives for a defined territory. Obtain new business and exceed annual territory sales budget each year by presenting new test information, up selling and seeking out new sources of revenues from clients. Develop and present personalized sales presentations to professional audiences (physicians, laboratory staff, clinics and group practices); demonstrate how MDL's technical features and services could benefit the practice and help medical personnel provide quality patient care. | 11/20/2019 |
| 1116 | Medical Diagnostic Laboratories, LLC Multiple Locations, na Entry Level Sales Executive BS/BA Exp: 0-2 years |
As a Entry Level Sales Executive, you will be responsible for maintaining and growing a client base of both hospital and physician customers for MDL. Responsible for achieving annual sales and profit objectives for a defined territory. Obtain new business and exceed annual territory sales budget each year by presenting new test information, up selling and seeking out new sources of revenues from clients. Develop and present personalized sales presentations to professional audiences (physicians, laboratory staff, clinics and group practices); demonstrate how MDL's technical features and services could benefit the practice and help medical personnel provide quality patient care. | 11/20/2019 |
| 1117 | Invivotek Hamilton, NJ Research Associate - Animal Science/In-vivo BS in life sciences Exp: 1-2 years with rat/mouse handling |
We are seeking a motivated and talented Research Associate to develop and perform in vivo and in vitro bioassays on mice and rats. The Research Associate should have excellent skills in basic rodent procedures. Rodent surgery skills are a plus. Experience with biochemical and tissue culture techniques is a plus. Excellent communication and computer skills and motivation to learn new assays are essential. Ability to work in a highly interactive and multidisciplinary team environment. | 11/20/2019 |
| 1118 | Invivotek Hamilton, NJ Vivarium Technician HS Diploma/GED Exp: 0-2 years |
We are seeking a motivated and talented Research Associate to perform laboratory assays for validation of potential drug development targets and characterization of pharmacological compounds. The Research Associate should have excellent laboratory skills to conduct in vitro bioassays on murine tissues and primary cells. Experience with tissue culture techniques and primary cell-based assays are required with a variety of readout technologies including flow cytometry, RT-PCR and ELISA. Excellent communication skills and motivation to learn are essential. Ability to work in a highly interactive and multidisciplinary team environment. | 11/20/2019 |
| 1119 | Iovance San Carlos, CA Contract Drug Safety Associate Healthcare professional degree w/BS or AA Exp: 0-2 years |
The Drug Safety Associate candidate works in a team-oriented, dynamic, and collaborative environment. This person would manage the drug safety mailbox, track case workflow, support the drug safety team, review serious/adverse event information, and review case narratives. | 11/24/2019 |
| 1120 | Iqvia Atlanta, GA Vaccine Sales Representative BS/BA Exp: 1 year in healthcare/sciences |
Vaccine Sales RepresentativeThe Vaccine Sales Representative will be responsible for achieving stated business goals of product sales within assigned portfolio and geography through strategic territory and account management and building solid working relationships. Responsible for providing healthcare providers with all relevant information that promotes quality healthcare decisions. Maintains an expert product knowledge base including patient education, consumer education, and factors influencing the market environment. Understands and uses approved promotional materials to support marketing message. | 11/24/2019 |
| 1121 | Iqvia San Juan Capistrano, CA Vaccine Study Specialist BS/BA in sciences Exp: 1 year in GCLP lab |
Provides internal oversight and conducts the day to day running of a project throughout its life at Q2 Solutions, including method development, method validation, and sample analysis while adhering to timelines, SOPs and performance metric standards. Serves as internal liaison between the production lab scientists and project management team. Provides daily direction and feedback to laboratory staff regarding Vaccines studies. Effectively and efficiently coordinates and communicates with relevant internal support groups as needed for the study. | 11/24/2019 |
| 1122 | Iqvia New Brunwick, NJ QA Engineer 1 BS/BA in related field Exp: 1-2 years in software testing |
Work closely with Development, Functional/Business and QA teams in all the phases of SDLC. Review the requirements and provide the QA estimations and raise any concerns or issues as needed . Involved right from the requirements grooming and will prepare the logical test scenarios & test cases as needed. Prepare test scenarios & test cases and requirements traceability matrix (RTM) to ensure the complete coverage | 11/24/2019 |
| 1123 | Ironwood Albany, NY Clinical Sales Specialist BS/BA Exp: 1 year in pharma sales |
Develop superior product and disease state knowledge and effectively educate and engage healthcare professionals in dialogue about clinical evidence, approved indications, and product efficacy/safety profiles to support on-label prescribing for appropriate patients. Representative must demonstrate a strong understanding of relevant disease states and possess a solid ability to communicate necessary technical, scientific, and product and disease management information to customers. Drive sales performance in a compliant manner and work to meet or exceed territory sales goals through execution of regional and national marketing strategies | 11/24/2019 |
| 1124 | Ironwood Tyler, TX Clinical Sales Specialist BS/BA Exp: 1 year in pharma sales |
Develop superior product and disease state knowledge and effectively educate and engage healthcare professionals in dialogue about clinical evidence, approved indications, and product efficacy/safety profiles to support on-label prescribing for appropriate patients. Representative must demonstrate a strong understanding of relevant disease states and possess a solid ability to communicate necessary technical, scientific, and product and disease management information to customers. Drive sales performance in a compliant manner and work to meet or exceed territory sales goals through execution of regional and national marketing strategies | 11/24/2019 |
| 1125 | FujiFilm Santa Ana, CA Powder Formulation Tech HS Diploma/GED Exp: 1-2 years hands on experience |
We are hiring for a Powder Formulation Tech. The Powder Formulation Tech is responsible for the formulation of our company’s powder cell culture media products. NOTE: The current opening is on our second shift (1:00 PM – 9:30 PM). Formulates Powder media formulas per manufacturing protocols utilizing various weighing equipment such as scales and balance. Uses Mettler-Toledo IND780 terminal system to ensure correct raw materials assigned in the batch record are used and at the specified quantity. Reviews lot folders for accuracy, completeness and availability of components necessary to complete job prior to the scheduled date of production | 11/24/2019 |
| 1126 | Genetech San Francisco, CA QC Analyst BS/BA in sciences Exp: 0-5 years |
The Senior QC Analyst will perform analytical, biochemical, and/or biological testing; data review; and/or related activities that support QC operations. Perform a broad variety of basic and moderately complex tests with documentation according to GMP. Maintain accountability for deliverables affecting department and organizational objectives. Accountable for exhibiting behaviors as described by Genentech/Roche Core Competencies. | 11/24/2019 |
| 1127 | Jubilant Spokane, WA Technician IV, Environmental Monitoring HS Diploma/GED Exp: 1 year in pharma/lab |
The Environmental Monitoring (EM) Technician IV is required to perform the basic functions associated with environmental monitoring. Incumbents are required to learn the laboratory functions, sanitization procedures, and donning scrubs for ISO 8 sampling requirements. Sampling, initiating tests and collecting test results related to defined quality parameters for surface, air, product and utility systems such as compressed gases and WFI. | 11/24/2019 |
| 1128 | Just-Evotec Biologics Seattle, WA Associate Scientist, Drug Product BS in Chemistry, Biochemistry, Molecular and Cellular Biology, Chemical Engineering, Bioengineering or related Exp: 0-3 years |
Support scientific staff with various protein characterization methods including SE-HPLC, sub-visible particle analysis (HIAC and Flowcam), protein concentration (UV-Vis), pH, osmo, buffer exchange and viscosity. Execution of established high throughput biophysical methods. Perform lab maintenance tasks will include buffer preparation, tracking/ordering consumables, and shipping/receiving samples. | 11/24/2019 |
| 1129 | Just-Evotec Biologics Seattle, WA Associate Scientist, Process Development BS in Chemistry, Biochemistry, Molecular and Cellular Biology, Chemical Engineering, Bioengineering or related Exp: 0-3 years |
The successful candidates will have some experience in one or more of the following areas including chromatography, filtration, electrophoresis, analytical chemistry, cell culture and/or bioreactor operations. Experience with high throughput, robotic techniques for analytical testing, chromatography, and/or protein expression, as well as statistical design of experiments and/or process modeling, is a plus. The ideal candidate has strong written and verbal communications skills and works well independently and in teams. This position may include the opportunity to rotate through different functional areas to gain experience in different techniques and disciplines. | 11/24/2019 |
| 1130 | Just-Evotec Biologics Seattle, WA Process Engineer I/II – Purification BS in biological sciences/engineering Exp: 1-3 years |
This team member will be responsible for the manufacture of mammalian cell-based biotherapeutics for clinical use under cGMP conditions. Under direct/moderate supervision, job responsibilities include set-up, operation, and maintenance of disposable-based manufacturing equipment; execution of manufacturing process operations; and assist in general lab operations. The staff member is expected to comply and follow written procedures for safety requirements, cGMP Practices, Standard Operating Procedures, and manufacturing documentation. | 11/24/2019 |
| 1131 | Navitas Rockville, MD Research Assistant - KAI Research BS/BA Exp: Entry Level |
Assist in the development of client deliverables according to project requirements, including but not limited to, project-specific documentation, operating procedures, and work flows with direction of more experienced staff. Process incoming and outgoing project materials to monitor, verify, and track receipt of documentation and ensure appropriate distribution of materials to internal and external research personnel and sites. Prepare general correspondence, agendas and meeting minutes, reports, and other project-specific documentation. Ensure review, approval, and distribution to internal staff and external project participants. | 11/24/2019 |
| 1132 | KBI Biopharma Durham, NC Research Associate I-Analytical Development (6 month temp to hire) BS Exp: 0-2 years |
Perform contract development services, including analytical development programs for monoclonal antibodies, recombinant proteins and peptides. Capable of performing bio-analytical techniques such as HPLC/UPLC, IEF, CE, Plate-based assays (ELISA, etc), qPCR, SDS- PAGE, Western Blot, with minimum training and under supervision. Prior hands-on experience or knowledge with chromatography, CE, IEF and plate-based assay is a plus. | 11/24/2019 |
| 1133 | KBI Biopharma Durham, NC Manufacturing Associate I-Upstream (temp to hire) BS/BA or AA Exp: 0-1 years |
Responsible for a wide variety of cell-related functions, including producing cells, intermediate product, and manufacturing final product for commercial distribution. Follow SOPs, perform daily tasks in a clean-room, retain records and write reports. May also be responsible for troubleshooting. Assist in execution of procedures for cell culture manufacturing, purification, or support area of manufacturing using SOP’s and batch records. Responsible for various duties that are required to produce product including but not limited to cell expansion; cell feeding, harvesting, counting and freezing; product seeding; growth system maintenance; labeling, packaging and freezing of product; and culture media preparation. Follow specific techniques and operations while demonstrating an understanding of cGMPs and how they apply to specific responsibilities. | 11/24/2019 |
| 1134 | KBI Biopharma Durham, NC Quality Systems Software Architect I/II BS/BA in pharma/biological sciences/ or chemistry Exp: 1-2 years in quality or validation |
Responsible for quality computer system administration, providing technical/end user support for quality computer system, and maintaining close communication with management to keep stakeholders apprised of quality computer system incidents/ resolutions, project validation status, and other relevant issues. The role requires leading and/or assisting in quality computer system validation efforts and ensuring all work is carried out in compliance with cGMPs, company policies and procedures, 21 CFR Part 11, EU Annex 11, ICH guidelines, and other applicable industry regulations. | 11/24/2019 |
| 1135 | KBI Biopharma Boulder, CO Engineer I/II - Manufacturing Science and Technology BS/BA or MS in sciences or engineering Exp: BS/BA: 1-5 years, MS: 0-3 years |
The successful candidate will apply scientific and engineering principles to support new biopharmaceutical process enrollments into the cGMP manufacturing facility. The candidate will: Perform all aspects of facility fit activities to support program enrollment including generating process flow diagrams, bill of materials (BOM), new specifications, and Äkta chromatography methods. Collaborate with process development and manufacturing teams to perform technical transfer and facility fit activities for downstream processes. | 11/24/2019 |
| 1136 | KBI Biopharma Durham, NC Research Associate/Sr. Research Associate BS or MS in chemistry/biochemistry Exp: 0 years |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals. Makes detailed observations and carries out elementary data analysis. Assures proper labeling, handling, and storage of all chemicals used in the area; assures proper labeling and disposition of hazardous waste in satellite areas; adheres to all safety requirements and follows safe procedures, and attends all required safety and health training, including handling hazardous waste. | 11/24/2019 |
| 1137 | KBI Biopharma Boulder, CO Manufacturing Associate I/II HS/GED, or BS/BA Exp: HS: 0-3 years, BS: 0 years |
This position is for a 2-week cycle, day shift with every other weekend off. Coordinate and perform cGMP manufacturing operations for biopharmaceutical products. Ensure the effective use of material, equipment and personnel while making products with the highest quality.Assist in execution of procedures for microbial manufacturing, purification, or support area of manufacturing using SOP's and batch record. Responsible for completing paperwork for each task, cleaning procedures, aseptic processing techniques, Good Manufacturing Practices (GMP) and laboratory safety practices and procedures. | 11/24/2019 |
| 1138 | KBI Biopharma Boulder, CO Microbiology Environmental Services Associate BS in sciences Exp: 0 years |
Performs microbiological in-process and release testing in support of GMP manufacturing. Tests include, but are not limited to, bioburden, microbial purity and endotoxin. Execute environmental monitoring within all classified manufacturing areas according to approved SOP’s and cGMP’s. Review EM data for completeness and accurate, and assist with data trending. Provide EM support for manufacturing during specified dynamic conditions. | 11/24/2019 |
| 1139 | Keystone Nano State College, PA Research Chemist MS in biological sciences/chemistry/engineering Exp: 0-2 years lab experience |
Keystone Nano is looking for a Research Chemist able to play an important role in developing novel drug products for cancer applications. The successful candidate will join our laboratory in State College, PA to conduct chemical and physical experiments using our proprietary manufacturing techniques to develop and scale this technology for a variety of markets. Set up and conduct chemical experiments, tests, and analyses using techniques such as spectroscopy, chromatography, physical and chemical extractions, dynamic and quasi-electric light scattering and microscopy, Compile and interpret results of tests and analyses Prepare graphs and charts to document experimental results for presentation to management. | 11/24/2019 |
| 1140 | KSQ Therapeutics Cambridge, MA Associate Scientist, ImmunoBiology Target Discovery/Validation BS or MS in biology/immunology Exp: 1-2 years research experience |
KSQ Therapeutics, Inc. is seeking an exceptional and highly motivated Associate Scientist, Target Discovery/Validation in the Immunobiology group to apply their experience in immunology towards the development of the next generation of impactful immunotherapies. This person will contribute to both target discovery and target validation efforts as well as in supporting our pre-clinical Immuno-Oncology small and large molecule portfolio. | 11/24/2019 |
| 1141 | KVK Tech Newtown, PA Microbiologist MS in biological sciences Exp: 0-5 years |
Validate Bacterial Endotoxin test method and test of finished products with gel clot and kinetic method; Perform and validate anti-microbial effectiveness Testing; Perform Sterility testing and validation using Steritest equinox System for finished products, Aseptic process stimulation; Identify genus level microorganisms using Vitek-2 ID; Perform Environmental Monitoring in aseptic and other controlled areas in ISO-5/6/7/8; Recover Bio burden by Various Microbial enumeration methods; Endotoxin recovery studies, Qualification of Microbiological equipments like Steritest Equniox | 11/24/2019 |
| 1142 | KVK Tech Newtown, PA Topical Formulation Associate MS in bio/chemistry/pharma sciences Exp: 1-3 years |
Person exhibits aptitude in assisting in the development of topical product pharmaceutical formulations, as well as meeting timelines for the department. Assist in the development of broad range of topical product pharmaceutical formulations including gels, creams, solutions and ointments. Develop pharmaceutical formulations utilizing Quality by Design (QbD) and risk assessment concepts. Contribute and support the analytical efforts and interpretation of data generated from experimental batches. | 11/24/2019 |
| 1143 | KVK Tech Newtown, PA Quality Control Microbiologist BS in microbiology Exp: 0-1 years |
Executes the activities of QC Microbiology Laboratory by following approved microbiological and chemical test procedures and ensure their delivery in an accurate and timely manner following proper safety precautions. Also provide QC microbiology support to the Aseptic Manufacturing and validation process. | 11/24/2019 |
| 1144 | LabCorp Lakewood, CO Specialty Lab Assistant HS Diploma/GED Exp: 1-2 years |
This position will work both in the processing of cytology samples for testing, as well as working in the accessioning department to receive samples. Processing of samples by loading them into instrumentation to make slides. Handling/Processing/Centrifugation of laboratory specimens, primarily blood and urine specimens. Running image guided slides through imager to prepare for testing | 11/24/2019 |
| 1145 | LabCorp Houston, TX Medical Technologist/Medical Technician AA/AS or BS/BA in med lab technology Exp: 1-3 years |
Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. * Monitor, operate and troubleshoot instrumentation (can include specific dept instrumentation) * Demonstrate the ability to make technical decisions regarding testing and problem solving. * Able to resolve technical, computer, and customer service problems within the specified department. * Deliver quality patient care while maintaining efficiency. * Perform preventive maintenance and quality control with appropriate documentation and communication. * Assist in processing of specimens when needed. | 11/24/2019 |
| 1146 | LabCorp Humble, TX Medical Technologist/Medical Technician AA/AS or BS/BA in med lab technology Exp: 1-3 years |
Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. * Monitor, operate and troubleshoot instrumentation (can include specific dept instrumentation) * Demonstrate the ability to make technical decisions regarding testing and problem solving. * Able to resolve technical, computer, and customer service problems within the specified department. * Deliver quality patient care while maintaining efficiency. * Perform preventive maintenance and quality control with appropriate documentation and communication. * Assist in processing of specimens when needed. | 11/24/2019 |
| 1147 | LabCorp South Bend, IN Lab Assistant HS Diploma/GED Exp: 1-2 years |
The position will receive samples and prepare them for analysis via plating, centrifugation, gram stain preparation and maintenance of instrumentation.This position will include repetitive motion and extended time on feet, and also includes handling of biological samples (Urine, stool, bacterial swabs, sputum, body fluids). Prior experience handling samples preferred. | 11/24/2019 |
| 1148 | Lake Pharma Worcester, MA Associate Scientist I, Cell Culture BS Exp: 0-5 years |
The successful candidate will be able to execute hands-on laboratory work in cell culture including planning and executing shake flask, bench scale bioreactor, bench scale purifications and large-scale bioreactor experiments. The position requires a drive to provide outstanding customer service by maintaining regular communications with clients, meeting or exceeding quality and timeline expectations. | 11/24/2019 |
| 1149 | Lake Pharma Worcester, MA Associate Scientist I, Molecular Biology AS or BS in biology Exp: 0-3 years |
The employee will be responsible for executing projects within the laboratory, writing study/research plans, and summarizing data to clients and colleagues via technical reports. The position requires a drive to provide outstanding customer service by maintaining regular communications with clients, meeting or exceeding quality and timeline expectations. | 11/24/2019 |
| 1150 | LifeMine Cambridge, MA RA, Microbiology BS or BA in biology Exp: 1 year of lab experience |
We are seeking a Research Associate level candidate to support media production and to handle and clean glassware and perform the appropriate cleaning services required for each piece of glassware. This individual will perform machine washing, handwashing, dry sterilizing, autoclaving, plugging and oven and air-drying of glassware. Plus prepare diverse media to support the discovery and scale-up fermentation teams. The incumbent will be enthusiastic about working in an exciting start up. | 11/24/2019 |
| 1151 | LifeSensors Malvern, PA Entry Level Scientist BS or MS in biological sciences or related Exp: 0-2 years lab experience |
We are seeking individuals who arepassionate about research, bringout of the box thinking and take bold steps todevelopinnovativetechnologies with applications in the ubiquitin research field.Successful candidates will have basic knowledge of biochemistry and molecular biology techniques, in particular experience with, protein expression andpurification and cloning. Knowledge of the ubiquitin proteasome pathwayis desired. | 11/24/2019 |
| 1152 | Lipocine Salt Lake City, UT Associate Scientist BS or MS in life sciences, chemical engineering or related Exp: 1-3 years in pharma/chemical lab |
Associate scientist needed in the area of pharmaceutical drug delivery research. Responsibilities include conducting laboratory experiments in support of formulation and process development. Qualified candidates will possess a BS/MS in life Science, chemical engineering or related field or 1-3 years experience in a pharmaceutical or chemistry laboratory. Knowledge of laboratory practices and demonstrated skills in analytical instrumental techniques (e.g. HPLC) are preferred. Excellent communication skills needed for preparing and following standard test methods and reporting experimental results. | 11/24/2019 |
| 1153 | LoXo Oncology South San Francisco, CA Clinical Research Asscoiate BS in relevant Exp: 1-3 years in clinical trials |
The Clinical Research Associate in collaboration with the Clinical Trial Manager, contributes to the operational execution of clinical studies to ensure delivery on time, within budget, and of high quality in compliance with ICH/GCP, Regulatory Authorities’ regulations/guidelines, and applicable SOPs/WPs. Responsibilities may include participation on one or more cross-functional study team(s) and/or performance and quality oversight of one or more Contract Research Organization (CRO) teams and vendors. | 11/24/2019 |
| 1154 | Starkey Hearing Technologies Eden Prairie, MN Software Tester I BS/BA Exp: 1-2 years |
Software Tester: Conduct Software Testing on software applications. Perform system level testing on Starkey’s Software and Hardware systems working either in a team or independently. Follow standard Configuration Management practices and utilize a defect tracking tool. Tracking quality assurance metrics such as defect densities and open defect counts. Resolve and provide solutions to internal and external customer related issues. Participate in the development and implementation of structured testing concepts, methodologies and automated testing tools where applicable. etc. | 11/26/2019 |
| 1155 | Starkey Hearing Technologies Eden Prairie, MN Mechanical Designer I - F&T AS/AA Exp: Not necessary for Associate candidates |
This position is responsible for designing new assembly tooling and assembly fixtures for product assembly. The position also requires designing tooling and solutions for specific tests and departments as requested. All tools/solutions must meet quality and manufacturing specifications provided by standards and the customer. Approach and Deployment: Design tools for production and specialty use. Utilize CREO to create accurate component, assembly and system models and drawings. Ensure designs meet performance, manufacturing, quality, cost and design requirements. Coordinate and lead design reviews as required. etc. | 11/26/2019 |
| 1156 | Starkey Hearing Technologies Eden Prairie, MN Financial Analyst BS/BA in accounting, finance, or economics Exp: 1-2 years |
Starkey Hearing Technologies, a well-respected, mission focused and high-impact organization, is currently seeking a Financial Analyst. This position is responsible for analyzing and communicating the financial performance for assigned product lines and cost centers. The Financial Analyst will identify and implement lean work-processes and key reporting measurements. The Financial Analyst is responsible for the preparation and completion of annual operation and capital budgets – for assigned cost centers and product lines. etc. | 11/26/2019 |
| 1157 | SDC Tempe, AZ Biostatistician MS in biostatistics, statistics, or related Exp: 1-3 years |
Supports lead biostatistician on clinical studies; may serve as lead biostatistician with oversight from a more senior biostatistician. Maintains the statistical integrity of clinical trials analyzed by SDC. Assists in preparing statistical analysis plans, preparing data deliverables for clinical study reports, interpreting analysis results, and writing statistical sections of clinical study reports. etc. | 11/26/2019 |
| 1158 | Stealth Biotherapeutics Newton, MA Supply Chain Associate BS Exp: 1 year |
This position will report to our Director, Clinical & Commercial Supply Chain. This role is responsible for supporting continuous material supply in support of clinical and commercial demands. The individual will work with internal/external customers and suppliers in order to assist in developing processes for shipment of material and inventory reporting. Responsible for monitoring inventory levels and providing feedback regarding expiry and resupply. etc. | 11/26/2019 |
| 1159 | Stellartech Milpitas, CA Quality Engineer I/II BS Exp: 0-2 years |
Stellartech is looking for a Quality Engineer to join our Team. Responsibilities: Perform quality engineering development activities for new product designs by assisting Engineering in the preparation of design and development plans, Design History File documentation, and Design History File preparation. Review and approve Device Master Record documentation for new product design and maintenance, including: bills of material, assembly procedures, manufacturing operations, assembly diagrams, test procedures, component specifications, labeling, and operator’s manuals. etc. | 11/26/2019 |
| 1160 | Stellartech Milpitas, CA Electrical Engineer BS in hardware or electrical engineering Exp: 0-2 years |
Stellartech is looking for a Electrical Engineer to join our Team. Responsibilities: Design, develop, and document electronic hardware for medical devices. Specify procedures and fixtures to test electronic medical devices. Assist manufacturing in prototype and pilot builds of electronic medical devices. Assist manufacturing in hardware problem analysis and solutions. Assist in training of technicians and manufacturing staff on new products and procedures. etc. | 11/26/2019 |
| 1161 | Stereotaxis Saint Louis, MO Field Service Engineer AS/AA in electronics or equivalent Exp: 1-5 years |
Provide on site and remote service and support of Stereotaxis magnetic navigation systems including permanent magnets, and servo control systems. Interface with customers and vendors to ensure a quality service experience and that all expectations are met. ESSENTIAL JOB RESPONSIBILITIES: Interface with customers to obtain accurate details of the equipment service needs and provide updates regarding the progress of the service/installation. Diagnose and repair control servo control systems. etc. | 11/26/2019 |
| 1162 | Stereotaxis New York City, NY Clinical Specialist BS in biomedical engineering, life sciences or related Exp: 1-3 years |
The Clinical Specialist (CS) provides customers and end users with product, clinical/ technical, educational, and sales support to maximize recurring revenue, utilization of company products, and customer service objectives. Must meet customer expectations by striving without reserve for the greatest possible reliability and quality in our products, processes, and systems by being accountable, having a voice, and taking action. Clinical Specialist will spend a high percentage of their time in procedures which requires a person to develop clinical knowledge within electrophysiology (EP), develop in-depth expertise of the Niobe remote navigation system, along with displaying outstanding sales abilities and the assertiveness needed to drive the Stereotaxis business. etc. | 11/26/2019 |
| 1163 | Steripharma Syracuse, NY Production, Clean Room Pharmaceutical Technician - 3rd Shift AS/BS Exp: 1+ year(s) |
This position operates production equipment, to include non-sterile filling machines, and packaging and labeling machines. Position is responsible to supply assigned positions with materials/items to complete work and according to standard operating procedures. Position is also responsible to clean equipment, production areas, and inspect parts/items following prescribed procedures. Provides troubleshooting on basic issues and may assist in providing training. etc. | 11/26/2019 |
| 1164 | Steripharma Syracuse, NY Production Maintenance Technician, 2nd Shift, Pharma HS diploma or equivalent Exp: 0-2 years |
This position is responsible for the maintenance and efficient operation of production/manufacturing equipment for pharmaceutical operations. Position also responsible to perform both maintenance and preventative maintenance, and repair work to production equipment as needed. Provides troubleshooting on rudimentary issues and seeks guidance as part of an escalation process. How you make a difference . . . you will . . . Performs maintenance work, to include equipment repair and preventative maintenance work as required or assigned. Performs the repair and maintenance of APA area floors and walls. Completes work orders and projects as assigned, supporting each team member as directed. etc. | 11/26/2019 |
| 1165 | Steripharma Syracuse, NY Production, Clean Room Pharmaceutical Technician - 2nd Shift AS/BS Exp: 1+ year(s) |
This position operates production equipment, to include non-sterile filling machines, and packaging and labeling machines. Position is responsible to supply assigned positions with materials/items to complete work and according to standard operating procedures. Position is also responsible to clean equipment, production areas, and inspect parts/items following prescribed procedures. Provides troubleshooting on basic issues and may assist in providing training. etc. | 11/26/2019 |
| 1166 | Steripharma Syracuse, NY Production, Pharmaceutical Production - 2nd Shift HS diploma or equivalent Exp: 1+ year(s) |
This position operates vial wash/packaging production equipment. Position is responsible to supply assigned positions with materials/items to complete work and according to standard operating procedures. Position is also responsible to clean equipment, production areas, and inspect parts/items following prescribed procedures. Provides troubleshooting on basic issues and may assist in providing training. etc. | 11/26/2019 |
| 1167 | Steripharma Syracuse, NY Production Maintenance Technician, 3rd Shift, Pharma HS diploma or equivalent Exp: 0-2 years |
This position is responsible for the maintenance and efficient operation of production/manufacturing equipment for pharmaceutical operations. Position also responsible to perform both maintenance and preventative maintenance, and repair work to production equipment as needed. Provides troubleshooting on rudimentary issues and seeks guidance as part of an escalation process. How you make a difference . . . you will . . . Performs maintenance work, to include equipment repair and preventative maintenance work as required or assigned. Performs the repair and maintenance of APA area floors and walls. Completes work orders and projects as assigned, supporting each team member as directed. etc. | 11/26/2019 |
| 1168 | Steris Scranton, PA Installation Technician AS/AA in electronics, mechanical, or similar Exp: 1+ year(s) |
STERIS’ Installation Technicians act as the face of STERIS by achieving One of a Kind Service for our Customers. The Installation Technician is a field-based, Customer-facing role that primarily travels to Customer sites (medical facilities) to install Operating Room and Sterile Processing Department equipment. They provide complete equipment installation in accordance with plans and specifications including scheduling, delivery, installation, check-out, and final inspection of equipment. Installation Technicians are also responsible for building positive relationships with Customers and peers, as well as completing necessary administrative tasks. | 11/26/2019 |
| 1169 | Steris Sacramento, CA Field Service Representative I AS/BS in electronics, mechanical, or similar Exp: 1-2 years |
Position acts as Trusted Advisor to STERIS Customers in maintenance and procurement of medical devices and consumable products as part of a high performing team. Drive an exceptional Customer experience by providing on-site preventative maintenance, troubleshooting, repair, equipment modification and installation support on complex mechanical, electro-mechanical and electronic units in a high stress healthcare environment. Provide superior Customer service by pro-actively interacting and communicating with Customers. Utilize advanced technology to complete administrative requirements, aid in troubleshooting issues and improve the overall Customer experience. Promote STERIS growth through identifying and recommending products and services to Customers. etc. | 11/26/2019 |
| 1170 | Steris Martinez, CA Field Service Representative I AS/BS in electronics, mechanical, or similar Exp: 1-2 years |
Position acts as Trusted Advisor to STERIS Customers in maintenance and procurement of medical devices and consumable products as part of a high performing team. Drive an exceptional Customer experience by providing on-site preventative maintenance, troubleshooting, repair, equipment modification and installation support on complex mechanical, electro-mechanical and electronic units in a high stress healthcare environment. Provide superior Customer service by pro-actively interacting and communicating with Customers. Utilize advanced technology to complete administrative requirements, aid in troubleshooting issues and improve the overall Customer experience. Promote STERIS growth through identifying and recommending products and services to Customers. etc. | 11/26/2019 |
| 1171 | Steris Chicago, IL Sterile Processing Technician HS diploma or equivalent Exp: 1+ year(s) |
Provides on-site support for the reprocessing of surgical instruments and trays to contracted facilities in compliance with the Department of Health, TJC, OSHA, CDC, AAMI and AORN standards and facilities goals and policies. Position level will be determined by previous job related experience, performance and certification requirements. Duties: Operates all mechanical machinery; cart washers, instrument washers, steam sterilizers, low temp sterilizers, ultrasonic and drying cabinets, within sterile processing. Uses established policies and procedures to complete work assignments. Learns and trains in all areas of sterile processing including decontamination, cleaning, assembly, wrapping, sterilization, and storage processes within all set professional standards and regulations. etc. | 11/26/2019 |
| 1172 | Steris Birmingham, AL Customer Care Representative I BS/BA Exp: 0-2 years |
The primary focus of this position is to provide an outstanding Customer experience. Individuals in this role will be assigned to a manageable level of sales representatives and will serve as a liaison between the sales representative and the Customer. In this role, the Customer Care Specialist must have a thorough knowledge of all the Company’s products and services. Duties: Creates a personalized relationship with each assigned Account Mangers. Owns the service support experience for assigned Sales Representatives. Must be knowledgeable on where to send what repairs including responding to inquiries about IMS capabilities. Creates critical paperwork for the Customer and develops knowledge on how to make corrections, split orders and work multiple orders. etc. | 11/26/2019 |
| 1173 | Steris Denver, CO Integration Technician AS/AA Exp: 1 year |
Install operating room integration equipment as directed by Integration Specialist (I and/or II) and/or Integration Project Manager. Perform preventative maintenance, troubleshooting, repair, equipment modifications, and installation on all integration equipment serviced by STERIS. Help drive STERIS initiatives for growth and development of business. Interact with customers in a professional and knowledgeable basis. Complete administrative requirements as required. Duties: Help install operating room integration systems. This includes physical placement of equipment, installation, termination and interconnection of all cables, downloading and configuration of software; and testing of all functions per test documentation as required. etc. | 11/26/2019 |
| 1174 | Steris Bellevue, WA Field Service Technician AS/AA in electronics, mechanical, or similar Exp: 1 year |
The Field Service Technician provides preventive maintenance, troubleshooting, repair, calibration and installation support on various mechanical, electro-mechanical, and electronic units. The Technician Interacts with customers on a daily basis and completes associated administrative tasks as required. Think of this as an electrical-mechanical-plumber-Customer Service Technician all rolled into one! Every day, something special happens at STERIS. What will YOU help us do next? Duties: Perform preventive and corrective maintenance required on STERIS and related product lines. This includes: disassembling, replacing, or repairing defective parts; reassembling as required; troubleshooting, adjusting/calibrating ready for use by using standard and specialized tools by using technical manuals etc. etc. | 11/26/2019 |
| 1175 | Surgical Specialties Tampa/Orlando, FL Sales Representative, Ophthalmic BS/BA in business or a medical field Exp: 1-3 years |
Caliber Ophthalmics is currently seeking a Surgical Sales Representative to be based in Florida. As a valued employee at Caliber, you will enjoy a total benefits package including competitive salary, medical/dental/vision/life insurance, short-and long-termdisability, 401k, and more. The Surgical Sales Representative is responsible for managing the Floridasales territory, working directly with surgeons for the sale and promotion of our Caliber Ophthalmic portfolio of surgical device products to include our disposable knives, suture, and other microsurgical products. Target call points are hospitals and ambulatory surgery centers. In this surgical sales role, you will be responsible for maintaining and growing annual sales volume in Florida. | 11/26/2019 |
| 1176 | Saptalis Pharmaceuticals Hauppage, NY Analytical Scientist/Chemist BS in pharmacy, analytical chemistry, or related Exp: 0-3 years |
Develop analytical methods for actives, degradation and impurities, preservatives, and residual solvents in the new drug products.Perform analytical validation experiments per approved method validation protocols. Perform method verification and supplemental validation studies for active pharmaceutical ingredients and excipients. Perform release testing on actives, excipients, and packaging components to be used in GMP batch manufacturing. etc. | 11/19/2019 |
| 1177 | Sciecure Pharma Monmouth Junction, NJ QC Data Review Specialist BS in chemistry or related Exp: 1-2 years |
The QC Data Review Specialist will be responsible for GMP review and comment on laboratory raw data, procedures and reports to ensure methods, protocols and other procedures were properly followed, results are analytically accurate and correct, and that all documentation meets GMP standards. Responsibilities: Review of documentation generated during method validation, method verification, stability testing, routine testing and other analyses. Review documentation, results and reports from raw material and finished product analysis for accuracy and completeness. etc. | 11/19/2019 |
| 1178 | Seattle Genetics Bothell, WA Research Associate I BioProcess Development BS in biology, chemical engineering, or related Exp: 1+ year(s) |
The BioProcess Development Department at Seattle Genetics is seeking a Research Associate to participate in the cell culture and purification efforts to support process development for our antibody and antibody-drug conjugate programs. Responsibilities: Generate monoclonal antibody (mAb) in support of Research and Process Sciences Program development. Responsible for all stages of mAb generation, from thaw of cryogenically stored vials through filling final formulated intermediate. etc. | 11/19/2019 |
| 1179 | Seattle Genetics Bothell, WA Research Associate II/III Pharmaceutical Sciences MS in pharmaceutical sciences, chemistry, biology, or related Exp: 0-2 years |
The Pharmaceutical Sciences group at Seattle Genetics is seeking a highly motivated research associate to support development of therapeutic antibody-drug conjugates. This person will play a critical role in the formulation and drug product process development of a novel pre-clinical ADC. The ideal candidate will have working knowledge of biologics formulation development and experience in common analytical techniques, as well as strong critical thinking skills and the ability to design, execute, and draw conclusions from experimental studies with managerial guidance. The ideal candidate should have a background in formulation development or analytical biochemistry or a related discipline, good interpersonal skills, and an ability to work effectively in intra-departmental teams to achieve program goals. | 11/19/2019 |
| 1180 | Sedia Biosciences Portland, OR QC Technician AS Exp: 1 year |
A Quality Control Technician works independently to provide quality control support of any area assigned where Sedia Biosciences is responsible for adhering to current Good Manufacturing Practices (cGMPs) for adherence to FDA regulations and applicable ISO standards including warehouse, manufacturing processes, inspection, labeling and packaging, batch record review/disposition, and new product design review and transfer activities. Demonstrates a high level of independent judgment and discretion in the timely identification, investigation and resolution of events impacting the Quality of products and processes. etc. | 11/19/2019 |
| 1181 | Sedia Biosciences Portland, OR Manufacturing Technican AS in biology, chemistry, or related Exp: 1 year |
The position will hold responsibility for assisting in the manufacturing of Sedia’s immunoassay product lines encompassing lateral flow and ELISA test. The holder of this position is expected to follow the guidance of their direct supervisor to assist in delivering company products in a timely and cost effective manner. The position will contribute in building product subassemblies or final assemblies. The Manufacturing Technician will adhere to all applicable regulations, policies, and procedures for health, safety, and environmental compliance. etc. | 11/19/2019 |
| 1182 | Sekisui Xenotech Kansas City, KS Research Assistant BS in a biological or chemical science Exp: 1+ year(s) |
Sekisui XenoTech, LLC is currently hiring for a Research Assistant for our Enzyme Incubations Team within the Program Execution department. The Research Assistant assists with routine laboratory functions including diluting, labeling and dispensing of biological samples, reagent solution preparation, equipment repair, laboratory upkeep, maintains inventory of supplies, and various other responsibilities. Essential duties and responsibilities include, but are not limited, to the following: Design and conduct routine and atypical experiments. Maintains laboratories and equipment and performs minor repairs on equipment, with supervision. etc. | 11/19/2019 |
| 1183 | Seven Bridges San Francisco, CA Bioinformatics Support Engineer BS/MS in bioinformatics or related Exp: 1 year |
As a Bioinformatics Support Engineer you will be exposed to a wide range of translational applications and will work and learn from experts spanning numerous disciplines from informatics through cloud optimization and clinical data. You will work back to back with various members of our support and bioinformatics teams, helping our clients overcome obstacles they encounter. You will diagnose, resolve and explain issues and questions raised by our clients. Main responsibilities: Understand each client’s use case and their bioinformatics data processing pipelines. Debug, troubleshoot and resolve client issues associated with bioinformatics tools on the Seven Bridges platform. etc. | 11/19/2019 |
| 1184 | Silicon Therapeutics Boston, MA Research Associate, Software Engineering BS in engineering or computer science Exp: 1-2 years |
Silicon Therapeutics is seeking a highly motivated Software Engineering Research Associate who wants to work in a multi-disciplinary organization with the aim of treating challenging diseases. Job Responsibilities: Build software infrastructure to support platform development. Implement and maintain software engineering best practices. Ensure scalability, extensibility, and portability of platform code. Integrate and maintain databases for storage and access of results. Scripting and workflow development for scientific applications. | 11/19/2019 |
| 1185 | Silicon Therapeutics Boston, MA Research Associate, Machine Learning BS/MS in computer science, mathematics, engineering or related Exp: 1-6 years |
Silicon Therapeutics is seeking a highly motivated Research Associate, Machine Learning who wants to work in a multi-disciplinary organization with the aim of treating challenging diseases. Job Responsibilities: Work with a multi-disciplinary team (e.g. chemists, biologists, biophysicists) to discover novel medicines for challenging disease targets. Apply machine learning techniques to real-world drug discovery problems. Develop methods to improve the robustness of predictions from molecular dynamics simulations and quantify uncertainties associated with free energy simulations. Build state of the art machine learning infrastructure and workflows for molecular design. Work closely with bench scientists to understand critical project bottlenecks and how machine learning can help. | 11/19/2019 |
| 1186 | Simbex Lebanon, NH Test Engineer AS/BS in engineering Exp: 1-3 years |
The Test Engineer will be responsible for component and system testing throughout the product life cycle from development through release for products in the consumer health and medical device markets. The Test Engineer will work closely with project and cross-functional teams to help develop and execute test plans. The ideal candidate is self-motivated, detail oriented, and quick learner who can work in a fast-paced environment and values quality and accountability. etc. | 11/19/2019 |
| 1187 | Simbex Lebanon, NH Systems Engineer BS in mechanical or electrical engineering or related Exp: 0-3 years |
The Systems Engineer will be responsible for supporting every phase of the product development life cycle process in order to deliver high-quality products in the consumer and medical device markets. The Systems Engineer will work with the electrical, software, mechanical, product technical support, and quality teams to help develop, integrate, and test sub-assemblies into product. The ideal candidate has broad skills but deep knowledge/skills in one area, and is able to blend human-centric design with sound engineering principles across a wide range of engineering domains with a focus on quality and willingness to wear many hats. etc. | 11/19/2019 |
| 1188 | Smith & Nephew Oklahoma City, OK Quality Engineer BS Engineering/Science Exp: Entry level |
This position will be responsible for ensuring the effective investigation of devices and information supplied through the complaint management process, as well as the facilitation of actions identified to improve device quality, reliability, customer experience and patient safety. This position will participate in the identification and implementation of complaint management system improvements, including updates to procedures and forms used in the investigative process. The role may support multiple business sites both remotely and through on-site visits as needed. etc. | 11/19/2019 |
| 1189 | Smith & Nephew Memphis, TN Quality Assurance Inspector I HS diploma or related Exp: 0-2 years |
The Quality Assurance Inspector 1 shall be responsible for performing basic visual/dimensional/functional inspections of incoming purchased product as well as product manufactured/assembled in-house, determining whether or not product meets specifications and documenting these decisions. Essential Responsibilities: Inspect raw materials, components, assembled product, semi-finished product & finished product per inspection procedures/drawings and to print specifications. Utilize attribute and variable measuring equipment/gauges as well as mating parts to determine as found/as left conditions of product. Support the qualification/validation processes for company product. etc. | 11/19/2019 |
| 1190 | Smith & Nephew Oklahoma City, OK Bench Technician I HS diploma or related Exp: 0-3 years |
Performs routine assembly and/or rebuilding of electromechanical medical instruments and assemblies using released procedures, drawings, blueprints, etc.. to meet established quality and performance metrics. Performs functional testing of assemblies/instruments. etc. | 11/19/2019 |
| 1191 | Smith & Nephew Andover, MA Quality Assurance Engineer I BS in engineering Exp: 1-3 years |
Support, and sustain elements of Smith & Nephew’s quality system through procedure generation, training, auditing, and technical support. Leading and supporting quality project initiatives. This position provides support and services in CAPA, complaints, validations, audits, quality holds, calibration and various other requirements of the medical device (US & International) regulations for R&D, Process Engineering, Manufacturing, Quality, and Regulatory plus any quality system support required. etc. | 11/19/2019 |
| 1192 | Smiths Medical Southington, CT Team Technician 3rd Shift HS diploma/AS Exp: 1-2 years |
The Team Technician is responsible for ensuring the correct operation of automatic and semi-automatic assembly production equipment in accordance with governing documentation. This person will also initiate action to prevent the occurrence of nonconformances related to the product and equipment. Additionally, this role will identify and record problems relating to the product, process and or quality system. The Team Technician will also initiate recommendations, provide solutions, and verify the affectivity of continuous operational improvements. | 11/19/2019 |
| 1193 | Solid Biosciences Cambridge, MA Contract QC Associate AS/BS Exp: 1-2 years |
Reporting to the Solid Quality Control (QC) Unit, the QC Associate is responsible for day to day operations related to sample submission and data management in support of QC GMP and cross-functional development. The candidate will maintain documentation in accordance with internal data entry, analysis and trending SOPs. In addition, coordinate domestic and international biologic sample shipments (at room temperature, on dry ice, or in liquid nitrogen) according to applicable guidelines. etc. | 11/19/2019 |
| 1194 | Sorrento Therapeutics San Diego, CA Research Associate II BS/MS in immunology, molecular biology or related Exp: 0-2 years |
Sorrento Therapeutics’ is seeking an experienced Research Associate who will be responsible for the development and implementation of in vitro functional T cell assays to support pre-clinical validation of CAR-T cellular therapies against cancer. The individual must have knowledge and hands on experience in CAR-T, cell culture, Flow cytometry and T cell biology. WHAT YOU’LL DO: Design and execute experiments for development of preclinical CAR-T therapies. Isolate, expand, and manipulate T cells. Perform in vitro functional assays measing cellular activation, cytokine release, proliferation and killing. etc. | 11/19/2019 |
| 1195 | Sorrento Therapeutics San Diego, CA Manufacturing Associate I BS/BA in a biological or chemica science. Exp: 0-1+ year(s) |
We are currently seeking a Downstream Manufacturing Associate I. This position is tasked with supporting all aspects of downstream manufacturing processes. For GMP-qualified campaigns this involves large scale buffer preparation, column chromatography using the Akta Process system and large bed volume columns, various filtration methods, ultrafiltration/diafiltration methods, and formulation. This position will also be responsible for supporting the inventory control for the downstream group. etc. | 11/19/2019 |
| 1196 | Sorrento Therapeutics San Diego, CA Manufacturing Associate II BS/MS in a biological or chemical science Exp: 1+ year(s) |
We are currently seeking a Downstream Manufacturing Associate II. This position is tasked with supporting all aspects of downstream manufacturing processes. For GMP-qualified campaigns this involves large scale buffer preparation, column chromatography using the Akta Process system and large bed volume columns, various filtration methods, ultrafiltration/diafiltration methods, and formulation. An essential component of this position will be an understanding of cGMP methodologies: SOP’s, batch record preparation and execution, deviation control and general clean room maintenance. This position will also responsible for supporting the inventory control for the downstream group. etc. | 11/19/2019 |
| 1197 | Spectrum Pharmaceuticals Irvine, CA Clinical Trials Assistant BS in a life science Exp: 1-2 year |
Responsibilities: Provide support to the Clinical Trial Managers and Clinical Research Associates in clinical trial conduct via preparation, distribution, and tracking of study supplies, mass mailings, copying, data entry, etc. Demonstrate superior communication and organizational skills in addition to the technical skills required for overseeing clinical studies. Recognize the urgency of meeting established schedules and be able to prioritize tasks and time to meet those schedules. Help manage and report on the conduct of clinical studies, as directed. Help identify and select trial sites. Conduct qualification, initiation, interim monitoring close-out visits, and perform drug accountability (approximately 25% travel required). etc. | 11/19/2019 |
| 1198 | SQZ Biotech Watertown, MA Engineer/ Sr. Engineer BS/MS in bio, biomedical, or chemical engineering or related Exp: 0-2 years |
We are seeking a highly motivated Engineer/ Sr. Engineer to join our Process Development and Manufacturing team. The candidate will support process development efforts for novel cell therapy products. The candidate will perform hands-on laboratory work, data analysis, develop and maintain technical documentation, and collaborate with internal and external terms such as vendors to ensure successful execution of key development studies. The incumbent will also support manufacturing for technology transfers at CMOs and on-going cGMP production of clinical products. etc. | 11/19/2019 |
| 1199 | Icon PLC North Wales, PA CTA BS/BA in life sciences Exp: Entry Level |
This unique opportunity is designed for individuals with a Bachelor's Degree in Life Sciences, strong organizational skills, excellent written and verbal communication, and working knowledge of computer systems including Microsoft Word, Excel, Outlook, and PowerPoint. ICON, a leading Clinical Research Organization, is seeking passionate, resilient and inspiring Graduates to join our team as a Clinical Trial Assistant. This opportunity offers an entry-level permanent position to highly skilled individuals interested in a career in clinical research. | 11/11/2019 |
| 1200 | Icon PLC Portland, OR Laboratory Assistant (Maintenance Tech) BS/BA Exp: 1 year in operations/sciences/equipment |
The Lab Assistant (Maintenance Technician) supports the activities of Production, Development, and the Clinical Laboratories. The Maintenance Technician performs equipment maintenance and cleaning, qualification, assists in the development of equipment specifications and other equipment or facility related activities to ensure proper qualification, function and reliability. | 11/11/2019 |
| 1201 | ICON Boston, MA Laboratory Assistant - Full Time Days HS Diploma/GED Exp: 1 year lab experience |
As a Laboratory Assistant will assist and aid the technical staff with handling and accounting for biological lab specimens, reagent inventory, and any other relevant tasks. Assists with retrieval and set up of samples for analysis. Receives samples from Sample Management and segregate and distribute to the lab as per standard operating procedure. Monitor Sample Logistic Scan/pending list and search for lost samples. Troubleshoot issues with Sample Management when required. Member of the Lost sample Team. | 11/16/2019 |
| 1202 | ICON North Wales, PA Clinical Research Associate HS Diploma/GED Exp: 18+ months as CRA |
As a Clinical Research Associate at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results. | 11/16/2019 |
| 1203 | ICON Farmingdale, NY Laboratory Study Start-Up Specialist BS Exp: 1 year in clinical trails, lab, etc. |
Our Configuration & QC Specialist plays a key role within ICON Laboratory Services (ILS). Support the Project Management Team (PM) in configuring and QC'ing new studies in all ILS systems according to the specifications of the Client Laboratory Worksheet (CLW) and create all supporting documents and site instructions to facilitate proper specimen collection, packaging and shipping, including visit requisitions, reference range tables and study specific Lab Manuals. | 11/16/2019 |
| 1204 | ICON Lexington, KY DPC Assistant HS Diploma/GED Exp: 1 year in medical office/admin |
The DPC Assistant will provide support services (logistical, technical and administrative) to the Direct to Patient Contact (DPC) project team all along the project, while complying with the deadlines, budgets, quality and regulatory requirements defined for each project. For each project, the Direct to Patient Contact Manager (DPCA) works under the technical and functional supervision of the dedicated Direct to Patient Contact Manager (DPCM). | 11/16/2019 |
| 1205 | ICON North Wales, PA Configuration & QC Spec I BS Exp: 1 year in clinical trails, lab, etc. |
Our Configuration & QC Specialist plays a key role within ICON Laboratory Services (ILS). Support the Project Management Team (PM) in configuring and QC'ing new studies in all ILS systems according to the specifications of the Client Laboratory Worksheet (CLW) and create all supporting documents and site instructions to facilitate proper specimen collection, packaging and shipping, including visit requisitions, reference range tables and study specific Lab Manuals. | 11/16/2019 |
| 1206 | ICON Portland, OR Laboratory Assistant (Maintenance Tech) HS Diploma/GED Exp: 1 year in operations/scientific equipment |
The Lab Assistant (Maintenance Technician) supports the activities of Production, Development, and the Clinical Laboratories. The Maintenance Technician performs equipment maintenance and cleaning, qualification, assists in the development of equipment specifications and other equipment or facility related activities to ensure proper qualification, function and reliability. | 11/16/2019 |
| 1207 | ICU Medical Austin, TX Technician I, Biological Quality/Environmental Quality BS/BA in microbiology/biological sciences Exp: 1 year general micro course with lab, or 1 year working experience |
The BQ/EQ Scientific Technician I is responsible for performing routine and non-routine testing in support of all aspects of the manufacturing operations including but not limited to the utility systems, sterilizer systems, incoming raw materials, in-process product solutions and final product solutions while adhering to safety, standard operating procedures (SOPs), standard test methods (STMs) and specifications, current good manufacturing practices (cGMP), standard laboratory practices (SLP), current good documentation practices (cGDP) and plant policies/guidelines. | 11/16/2019 |
| 1208 | IDEXX Memphis, TN Histology Laboratory Technician HS Diploma/GED, higher degree preferred Exp: 1-5 years |
You will be using microtomes, processors, embedding centers, automatic slide stainers and other diagnostic tools to perform tissue analyses that diagnose animal illnesses and diseases in support of veterinarian animal treatment. You will be responsible for transforming a tissue sample into a slide that will be read by a board-certified veterinary anatomic pathologist. It is expected you will follow SOPs (Standard Operating Procedures) and maintain a safe working environment. | 11/16/2019 |
| 1209 | IDEXX Westminster, CO Sample Management Technician HS Diploma/GED, higher degree preferred Exp: 0-1 years |
The Sample Management Technician receives and prepares samples for laboratory analyses and tests. Prepares samples on slides or other testing format, records required information and sends to appropriate specialty lab area. May be cross-trained to perform basic Laboratory Technician duties, such as performing less complex tests. May be responsible for various support activities, including maintaining supply inventory, record-keeping, cleaning, clerical tasks, supply shipping and receiving, mail distribution and other related duties. Collects and prepares samples as requested/ required for R&D project teams. | 11/16/2019 |
| 1210 | IDEXX Westminster, CO Medical Laboratory Technician - Parasitology HS Diploma/GED, higher degree preferred Exp: 0-1 years |
The Medical Laboratory Technician performs laboratory analyses and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. May perform variety of customer service activities for internal and external customers. Testing cell-related components of blood samples to enumerate and identify their cellular components, including the microscopic evaluation of blood smears and the use of automated and manual counting techniques. Processing blood and body fluids for microscopic examination by pathologists. Includes slide preparation and staining, utilizing manual and automated counting techniques. | 11/16/2019 |
| 1211 | IDEXX West Sacramento, CA PCR Laboratory Technician Certified Vet Tech or Medical Lab Tech Exp: 0-1 years |
You will be using automated analyzers, microscopes, and other laboratory diagnostic tools to perform analyses and tests that diagnose animal illnesses, injuries, and diseases in support of veterinarian animal treatment. You will be responsible for setting up and running lab tests, and reading and releasing results according to SOPs (Standard Operating Procedures). You can expect to specialize in one or more of the following areas: | 11/16/2019 |
| 1212 | Imbed Biosciences Madison, WI Production Technician, Medical Device Manufacturing BS in sciences Exp: 1-4 years in chemistry/biological lab |
Work with Medical Device Production team in a moderate-volume commercial laboratory to fabricate polymeric films, perform and assist in daily laboratory tasks and work flow, maintain and edit standard operating procedures and work instructions, record data, write reports and communicate results. Ensure quality control of materials and end products of the company in a consistent manner. | 11/16/2019 |
| 1213 | Immucor Norcross, GA Medical Laboratory Technologist I AS/AA or BS/BA Exp: 6-12 months related experience |
Immucor is seeking a Medical Laboratory Technologist to join our Quality Laboratory team. The Medical Laboratory Technologist is responsible for performing laboratory testing (including potency, specificity, reactivity and hemagglutination assays) and chemical evaluations (including protein, absorbance, chloride, osmolality, and pH) of Immucor products according to approved Standard Operating Procedures (SOP’s) within defined timeframes. | 11/16/2019 |
| 1214 | Immucor Warren, NJ Manufacturing Associate AS/AA Exp: 1 year in cGMP manufacturing |
As the Manufacturing Associate, you will perform setup, operation, re-supply, documentation, cleaning, minor equipment adjustments and minor preventative maintenance tasks to meet standards for safety, quality and efficiency. Performing the following activities in a quality focused cGMP manufacturing environment: Formulating custom bulk reagents - involves working with pipettes and balances. Support BeadChip carrier assembly - involves both manual and automated equipment processes. Following detailed work instructions, forms, and SOPs | 11/16/2019 |
| 1215 | Immucor Norcross, GA Medical Laboratory Technologist I AS/AA or BS/BA Exp: 6-12 months related experience |
Immucor is seeking a Medical Laboratory Technologist to join our Quality Laboratory team. The Medical Laboratory Technologist is responsible for performing laboratory testing (including potency, specificity, reactivity and hemagglutination assays) and chemical evaluations (including protein, absorbance, chloride, osmolality, and pH) of Immucor products according to approved Standard Operating Procedures (SOP’s) within defined timeframes. | 11/16/2019 |
| 1216 | Immune Technology Corp New York , NY Sales Associate BS/BA in life sciences Exp: 1 year of sales/marketing experience |
Full/part time position, responsible for ensuring customer retention through account management and increasing revenue through marketing activities and generation of sales leads. Establishing and retaining customer relationships primarily through phone, e-mail and personal visit . Delivering requested documents, literature, and information to customers. Organizing and maintaining a database of customers and sales leads | 11/16/2019 |
| 1217 | Immunomedics Morris Plains, NJ QC Sample Coordination Technician - (2nd shift) BS/BA in sciences Exp: 0-2 years |
The primary purpose of this second shift position is to provide support to the sample management group in a QC laboratory setting in support of commercial manufacturing. Responsibilities of the QC Sample Coordination Technician include collating receipt of samples and coordination of testing, preparation of samples using aseptic technique, organizing and tracking lot release data, submission of samples to contract testing laboratories and tracking sample custody. Activities include equipment maintenance, coordinating with Shipping and Receiving, and receipt of test results from contract laboratories. | 11/16/2019 |
| 1218 | Immunomedics Morris Plains, NJ Manufacturing Specialist I AS/AA or BS/BA in engineering or sciences Exp: 0-2 years |
Responsible for pharmaceutical manufacturing in compliance with current Good Manufacturing Practice (cGMP). Ensures consistent completion of all the planned manufacturing activities assigned to him/herself. Organize workplace to maximize the throughput and minimize risks of errors. Follow well defined procedures closely, with attention to detail. Operate manufacturing equipment according to well defined procedures. Daily monitoring of the process. | 11/16/2019 |
| 1219 | Imprimis RX Ledgewood, NJ Production Support Associate HS Diploma/GED Exp: 1 year in pharma, med devices or related |
The Production Support Associate is part of our production team. The Production Support Associate supports our production team by assisting in the main production area. Performs various routine production tasks under the guidelines of established SOP’s and CGMP regulations. Prepares components needed for production, such as washing vials, wiping of supplies needed for the clean room. Performs cleaning and disinfecting of manufacturing and clean rooms per established procedures. | 11/16/2019 |
| 1220 | Indigo Biosciences State College, PA Associate Scientist MS in biological sciences Exp: 0-5 years |
The successful candidates will have formal training and demonstrated technical proficiencies / expertise in one or more of the following areas: mammalian cell biology, mammalian toxicology, receptor biology, assay development, molecular biology, and/or biochemistry methods. | 11/16/2019 |
| 1221 | Indivior Austin, TX Specialty Pharmaceutical Sales Rep/Clinical Specialist (Austin) BS/BA Exp: 1+ year in pharma/medical/healthcare |
The Clinical Specialist is responsible for calling on practicing physicians, hospitals, clinics and other health-related organizations within an assigned territory. The Clinical Specialist must provide the healthcare professional with the most current information pertaining to Indivior products and their approved indications in a manner which will ensure the appropriate use of these products and achieve the business potential of the territory. Accomplishments of these goals must comply with the terms and conditions outlined in the Company Policy and Procedure Manual. | 11/16/2019 |
| 1222 | Inova Diagnostics San Diego , CA Chemist I- Elisa Controls BS/BA in biological sciences Exp: 0-2 years in ELISA lab |
Participates in the activities associated with the manufacturing of ELISA reagents such as control, calibrator and HRP conjugate components in accordance with established procedures and schedules. Ensures supplies, testing components, raw materials and equipment required to meet manufacturing schedules are available. Alerts the supervisor of any material shortages, potential expiration date problems, equipment requirements and/or other circumstances, which may cause delays in the planned, manufacturing schedule. Maintains detailed Device History Records and/or any associated documentation for all manufacturing activities in accordance with current Quality Systems Regulations (QSRs). | 11/16/2019 |
| 1223 | Inova Diagnostics San Diego , CA Lab Assistant I HS Diploma/GED Exp: 0-4 years lab work experience |
Assists with the activities required to manufacture autoimmune diagnostic products by following established procedures. Major duties include the manufacturing of tissue sections and their placement onto glass microscope slides for use in Immunofluorescent Assay products. Participates in all activities associated with the manufacturing of the tissue sections and their placement onto glass microscope slides in accordance with written documentation and established procedures. Manufactures 8.5 eight-well ANA Plus Slides per hour after three months of training. 10 eight-well ANA Plus slides per hour within one year of employment. Thereafter, manufactures 10.5 slides per hour for eight-well slides and 21 slides per hour for four-well slides (all tissue types). Assists with the activities required to manufacture autoimmune diagnostic products by following established procedures. Major duties include the manufacturing of tissue sections and their placement onto glass microscope slides for use in Immunofluorescent Assay products. Participates in all activities associated with the manufacturing of the tissue sections and their placement onto glass microscope slides in accordance with written documentation and established procedures. Manufactures 8.5 eight-well ANA Plus Slides per hour after three months of training. 10 eight-well ANA Plus slides per hour within one year of employment. Thereafter, manufactures 10.5 slides per hour for eight-well slides and 21 slides per hour for four-well slides (all tissue types). Assists with the activities required to manufacture autoimmune diagnostic products by following established procedures. Major duties include the manufacturing of tissue sections and their placement onto glass microscope slides for use in Immunofluorescent Assay products. Participates in all activities associated with the manufacturing of the tissue sections and their placement onto glass microscope slides in accordance with written documentation and established procedures. Manufactures 8.5 eight-well ANA Plus Slides per hour after three months of training. 10 eight-well ANA Plus slides per hour within one year of employment. Thereafter, manufactures 10.5 slides per hour for eight-well slides and 21 slides per hour for four-well slides (all tissue types). | 11/16/2019 |
| 1224 | Inovio San Diego , CA Research Associate I, Preclinical (2 positions available) BS in biological sciences Exp: 0-1 years research experience |
The Research Associate I (RA) is responsible for performing in vitro and in vivo experiments as part of a team to support development of DNA-based vaccines and therapeutics prior to clinical development. The RA performs a variety of techniques, including treatment and sample collection, immunoassays, cell-based assays, flow cytometry, and cell line maintenance. The RA troubleshoots problems, reviews and documents results, and presents findings at departmental or company meetings. The RA performs general lab duties as needed. | 11/16/2019 |
| 1225 | Inovio Plymouth Meeting, PA Clinical Trial Associate BS in biological sciences Exp: 0-2 years in clinical trails monitoring/management |
The Assistant, Clinical Trials (CTA) is responsible for supporting, under the direct supervision of the supervisor/Clinical Project Lead (CPL), clinical trial execution, investigator sponsored research and program level activities as assigned within Clinical Operations at Inovio. This position assists in various tasks and projects related to clinical trials as well as basic, administrative duties. | 11/16/2019 |
| 1226 | Omnipod Salt Lake City, UT Intake Associate AS/AA Exp: 0-1 years working experience |
The primary responsibility of this role is to review and process clinical documentation promptly and accurately to ensure proper reimbursement from contracted payors. The Intake Associate will utilize this clinical documentation to perform benefit investigations as well as prior authorizations with our contracted payors. This role will work with all department functions and must have a thorough understanding of the reimbursement process, clinical guidelines and medical policies. | 11/16/2019 |
| 1227 | Omnipod Salt Lake City, UT Inside Sales OmniPod Associate AS/AA or BS/BA Exp: 0-1 years in medical devices/pharma/healthcare |
The Inside Sales - OmniPod Associate role is responsible for all patient communication during the sales process of starting patients on the OmniPod system. This role works closely and collaborates with the field sales and internal team members to provide the best patient experience possible. This role is responsible for communicating insurance benefit guidelines and cost share information with patients and assists them with their decisions regarding insulin pump therapy. | 11/16/2019 |
| 1228 | Omnipod Billerica, MA Associate SQA Engineer BS in software engineering/computer sciences Exp: 0-2 years in software QA |
This position assists in the software quality assurance efforts related to new product development and product modifications for the Research and Development group. The position is responsible for ensuring that new products have been effectively and efficiently verified and validated prior to their release for shipment and that these designs effectively meet documented and implied user needs and requirements. Software quality assurance efforts are lifecycle oriented beginning during product requirements development and continuing throughout its lifetime. | 11/16/2019 |
| 1229 | Omnipod Atlanta, GA Clinical Services Specialist BS/BA Exp: 0-2 years in clinical setting |
The Clinical Services Specialist (CSS) is primarily responsible for meeting all clinical initiative expectations. This responsibility will require extensive travel and extended stays in a field based territory to support open territory needs. The CSS will provide product sales, training, downloading and technical support in accordance with company policy. They will also in-service physicians, mid-level staff, CDE’s, and ancillary staff on the OmniPod Insulin Management System, build relationships with our customers, and skilled at selling and using the OmniPod Insulin Management System. | 11/16/2019 |
| 1230 | Omnipod Dallas, TX Clinical Services Specialist BS/BA Exp: 0-2 years in clinical setting |
The Clinical Services Specialist (CSS) is primarily responsible for meeting all clinical initiative expectations. This responsibility will require extensive travel and extended stays in a field based territory to support open territory needs. The CSS will provide product sales, training, downloading and technical support in accordance with company policy. They will also in-service physicians, mid-level staff, CDE’s, and ancillary staff on the OmniPod Insulin Management System, build relationships with our customers, and skilled at selling and using the OmniPod Insulin Management System. | 11/16/2019 |
| 1231 | Omnipod Acton, MA Business Analyst, Post Market Surveillance BS in sciences/engineering Exp: 1-3 years in data management/Quality systems |
This position is integral to supporting the department through complaint software enhancements, upgrades, report creation, data structure, and validation activities/documentation. The BA will be the primary connection to IT resources supporting the business unit. The BA will have a strong understanding of the business unit’s processes, context surrounding why the processes are in place, and what happens if processes are not functioning/followed. The BA will be an expert in the systems utilized by the business unit and understand the implications of system structure, how changes may impact systems, and how system data is utilized for reporting. | 11/16/2019 |
| 1232 | Integer Trenton, GA Manufacturing Engineer I -1st shift BS Exp: 0-3 years related |
Manufacturing Engineer providing basic engineering support for existing or new products. Learning to use professional concepts. This position will provide hands-on engineering support for existing products and products transitioning from New Production Introduction (NPI) to manufacturing. | 11/17/2019 |
| 1233 | Integer Plymouth, MN Design Engineer BS/BA in related field Exp: 0-3 years related |
Initiates, directs and manages the design, development, constructing and modification of products and processes from conception to implementation. Works closely with other departments to coordinate design engineering activities. Reviews, initiates or approves engineering drawings, layouts, changes orders and specifications. | 11/17/2019 |
| 1234 | Integra LifeSciences Mansfiled, MA Associate Product Development Engineer BS in engineering (electrical/computer) Exp: 0-3 years in product design/new product development |
The Engineer will participate in projects of varying scope and complexity across Integra with a focus on the Neuro Critical Care and will be responsible for the software and electrical design aspects of a project, interacting with external design and development partners, participating on cross-functional project team through all phases of the product development process, and assisting the technical team with planning, executing, documenting and communicating testing activities. The engineer will develop tools that will assist marketing and sales demonstrate Integra’s devices in an effective manner, and will develop test setups to automatize verification testing of different products. | 11/17/2019 |
| 1235 | Integra LifeSciences Cincinnati, OH Finishing Technician HS Diploma/GED Exp: 0-2 years in manufacturing |
Performs deburr, finishing, and cleaning in a job shop or high volume applications. Processes components to meet print and or geometric tolerance requirements. Responsible for the setup, operation and maintenance of production equipment needed for deburr, finishing, and cleaning operations, maintenance of proper documentation, and support of the manufacturing engineering function. Under close supervision, completes tasks as directed by SOPs, routers, prints, work instructions, and manufacturing schedules. | 11/17/2019 |
| 1236 | Integra LifeSciences Plainsboro, NJ Accoutant- Entry Level BA in accounting Exp: 0-3 years |
The accountant position is responsible for performing a combination of cost and general ledger accounting and financial close tasks, as assigned. Perform the monthly financial close process for the local ledger, including preparation of the monthly journal entries and balance sheet (cash, inventory, payables) and P&L account reconciliations, as assigned. Run various reports used to reconcile or analyze general ledger account balances. Assist in the preparation of the standard monthly management reports. Perform detailed monthly variance analysis on items in the P+L and balance sheet. | 11/17/2019 |
| 1237 | Integra LifeSciences Plainsboro, NJ Accoutant- Entry Level BA in accounting Exp: 0-3 years |
The accountant position is responsible for performing a combination of cost and general ledger accounting and financial close tasks, as assigned. Perform the monthly financial close process for the local ledger, including preparation of the monthly journal entries and balance sheet (cash, inventory, payables) and P&L account reconciliations, as assigned. Run various reports used to reconcile or analyze general ledger account balances. Assist in the preparation of the standard monthly management reports. Perform detailed monthly variance analysis on items in the P+L and balance sheet. | 11/17/2019 |
| 1238 | Integral Philadelphia, PA Biotechnology Marketing Associate BS/BA in sciences or marketing Exp: 1-2 years |
Plan and implement the creation of scientific and promotional materials in close collaboration with marketing, sales and scientific teams. Generate email blasts, website content, brochures, Google Adwords campaigns and slides. Create and update content to the company website using WordPress. Coordinate and organize team for appearances at industry conferences. Monitor and analyze effectiveness of marketing campaigns and website design | 11/17/2019 |
| 1239 | Integral Philadelphia, PA Business Development Associate MS or MBA Exp: 0-2 years in tech transfer, consulting or product commercialization |
Our company is in an exciting growth phase where we are launching new products and reaching new markets. To support our growth, we seek a Business Development Associate to help launch new partnerships, businesses, and growth strategies. Successful candidates will also be involved with our marketing and sales teams to assist with strategic growth plans. | 11/17/2019 |
| 1240 | Integral Philadelphia, PA Laboratory Instrumentation Engineer BS/BA Exp: 0-2 years in lab support/equipment |
We seek an associate to join us as our Laboratory Instrumentation Engineer. This is a specialized position that will be responsible for maintaining and using flow cytometers, robotic liquid handlers, and other equipment. You will be part of the team that supports lab operations, with opportunities for conducting experiments and leadership of the team. | 11/17/2019 |
| 1241 | Integral Philadelphia, PA Research Associate I BS/BA in biology or bioengineering Exp: 1-2 years in lab/cell culture experience |
We seek a Research Associate I, who will work with a dedicated group of scientists on the development and commercialization of biomedical technologies. Conduct laboratory research and support general R&D efforts for customer-based biomedical research. Projects may involve cell culture, virology, DNA preparation, and liquid-handling automation. Perform cell-based assays (Western blot, ELISA, immunofluorescence, flow cytometry) | 11/17/2019 |
| 1242 | IDT Morrisville, NC Future Lab Technician Roles Early 2020 BS/BA in sciences Exp: 0 years |
Synthesizes oligos on various synthesizer platforms. Cleaves and deprotects oligos utilizing appropriate methods. Quantifies and samples oligos for quality control tests. Attaches modifications utilizing various techniques. Adheres to safety regulations, lab SOPs, and contamination controls. | 11/17/2019 |
| 1243 | IntegrityBio Camarillo, CA Research Associate BS in biochemistry, chemistry, or biological sciences Exp: 1-5 years |
To meet the growing demand on the part of our clientele regarding the outsourcing of projects and technologies, we are seeking candidates for the position of Research Associate I or II in Research and Development (R&D). Assemble study designs, perform laboratory experiments, organize data, and analyze results under minimal supervision. Analyzes, records, and reports the results and conclusions for laboratory experiments. Summarizes and interprets data. The candidate should also be open to learn new laboratory techniques and work under the guidance of experienced researchers. | 11/17/2019 |
| 1244 | Intrexon Davis, CA Research Associate, Plant Traits BS or MS Exp: 1-3 years in molecular biology/plant biology |
Intrexon Corporation is seeking a highly motivated Research Associate, Plant Traits with molecular biology skills for our growing Agricultural Biotechnology Division (ABD) at Davis, California. The candidate will join a team to work on innovative technology to develop various traits in crops. The successful candidate will have hands-on experience with molecular techniques as well as supporting the senior scientist to develop other methodology to enable high-through-put, low-cost genotyping in multiple crops. Strong technical, organizational, and communication skills, as well as the ability to develop creative solutions to challenging problems in a fast-paced, milestone driven company, are essential. | 11/17/2019 |
| 1245 | Intrexon South San Francisco, CA Research Associate I or II, Pilot Plant Ops BS in sciences, engineering or related Exp: 0-3 years industry experience |
We are seeking a talented Research Associate (level determined by candidate experience), Pilot Plant Operations for our Industrial Products Division (IPD) located in South San Francisco. The Research Associate will be responsible for operating pilot plant equipment, performing maintenance tasks, and have the skill set to thrive in a dynamic team environment. | 11/17/2019 |
| 1246 | Intuitive Sunnyvale, CA Manufacturing Trainer 1 HS Diploma/GED Exp: 12 months in ISI product manufacturing |
Partner with Manufacturing to develop and sustain a well-trained and flexible workforce through hands-on training, mentoring, and formal certification. Maintain accurate manufacturing and training documentation to ensure the effectiveness of the training process. Develops and prioritizes quarterly training plans based on input from Production and Training Supervision. Conducts training, mentoring and formal certification of production technicians in accordance with S & V Training DOP’s and Manufacturing Process Instructions. | 11/17/2019 |
| 1247 | Intuitive Sunnyvale, CA MRMA Repair Technician AA/AS Exp: 1-3 years related experience |
A Mechanical RMA Repair Technician II works under general direction, follows oral and/or written instructions, and performs repair and testing processes to produce tested electro-mechanical assemblies or associated sub-assemblies. Performs some-what complex tasks in preparation for repair and testing. Is able to verify assembly documentation accuracy, read engineering drawings etc. Sets up and operates machines/equipment /fixtures needed to perform repair and testing processes. | 11/17/2019 |
| 1248 | Intuitive Los Angeles, CA da Vinci Clinical Territory Associate- North Los Angeles BS/BA in sales or related Exp: 1 year of sales or leadership experience |
The Clinical Territory Associate (CTA) will work closely with the Clinical Sales Manager to gain knowledge in all aspects of our business to include technical, clinical, and sales. He or She will train to be a da Vinci® Surgery technical and sales expert across all primary surgical specialties to develop surgical robotics programs in the assigned territory. During the first year of the job, the CTA will focus on the technical and clinical aspect of the job, and during the second year of the job, the CTA will progress and begin to focus on the sales aspect of the job. The CTA will have the opportunity to support a specific region by maximizing the utilization of installed da Vinci® Surgical Systems by leading product demonstrations/in-services and sales activities. | 11/17/2019 |
| 1249 | Precision Biosciences Durham, NC Data Scientist - BioAnalytical Development MS in computer science, statistics, computional biology or related Exp: 0-2 years |
The Associate Scientist, Data Science works within the BioAnalytical Team at Precision Biosciences focused on the development of genome-edited allogeneic CAR-T therapeutics. The incumbent will play a lead role in the identification and implementation of existing and/or novel algorithms, analytical techniques and computational procedures to mine, clean, and interpret a wide variety of data derived from genomic, proteomic, metabolomic, and cellular phenotypic methods. This team member will be a part of our broader CMC organization which aims to drive technical excellence for the successful development of Precision Biosciences’ Cell and Gene Therapy Products, including allogeneic CAR-T cells, AAV viral vectors, and Lipid Nanoparticle-Encapsulated mRNA spanning a broad range of indications in immuno-oncology, infectious disease, and rare genetic disease. etc. | 11/12/2019 |
| 1250 | Precision Medicine Group Frederick, MD Biorepository Technician - Entry Level BS in related field Exp: Entry level |
Play a critical role in helping patients gain access to the treatment they need. This position is responsible for specimens in our state of the art Specialty Labs facility that have been collected by our clients who are managing clinical trials to secure the required approval for potentially life-saving patient treatments. Clinical trials depend on biological specimen samples being withdrawn and deposited on a continual basis. etc. | 11/12/2019 |
| 1251 | Precision Medicine Group Carlsbad, CA Biostatistician I – Clinical Trial Services MS in biostatistics/statistics Exp: Entry level |
What to expect day-to-day: Generating randomization schedules and providing sample size calculations. Providing input into development of case report forms (CRFs). Authoring and reviewing statistical analysis plans, including development of table and listing shells. Generating analysis datasets, tables, figures, and listings to support the analysis of clinical trials data using SAS. Providing programming support and quality control for SAS Programs and other study documents. etc. | 11/12/2019 |
| 1252 | Precision Medicine Group Norton, MA Clinical Data Associate BS/MS Exp: Entry level |
How you will make a difference: Review, analyze, validate and maintain clinical trial data to ensure consistency, integrity and accuracy. Query data inconsistencies and update the databases by understanding standard operating procedures, client guidelines and regulatory agency guidelines. Perform User Acceptance Testing. Prepare Patient and Study Level Status/Metric reporting. Utilize dictionary coding such as MedDRA and WhoDrug. Generate data retrievals and summaries. | 11/12/2019 |
| 1253 | Precision Medicine Group Oakland, CA Associate Research Statistician - HEOR MS in economics, health services, biostatistics or related Exp: 1+ year(s) |
As Research Statistician, you will perform a wide range of activities including: literature reviews; analysis; preparing reports, slide decks and meeting notes; and quality assurance/review. You will independently complete, evidence synthesis projects, including: client management; systematic literature review (SLR); (network) meta-analysis; economic modeling; and dissemination of results. etc. | 11/12/2019 |
| 1254 | Precision Medicine Group Houston, TX Technologist – PBMC / IHC BS in medical technology, biology, or related Exp: 0-1 years |
As a Technologist, you will participate in simple and complex processing of tissue, PBMCs, blood and body fluids, both routine and non-routine procedures. You will work with scientists to carry out qualification of assays for new projects and be engaged in IF / IHC / Opal staining tasks. This position requires flexibility to work on different shifts as needed. etc. | 11/12/2019 |
| 1255 | Promega Madison, WI Quality Technician HS diploma or equivalent Exp: 1-3 year(s) |
JOB OBJECTIVE: Perform Quality inspection and analysis activities including: Receiving inspection of purchased components and materials in accordance with written procedures, statistical sampling plans, inspection standards and engineering drawings and specifications, using measuring equipment. In-process and finished device inspection and release activities in accordance with the Device Master Record. etc. | 11/12/2019 |
| 1256 | ProSciento San Diego, CA Clinical Data Associate BS in the life sciences Exp: Not necessary for BS candidates |
Under the supervision of the Associate Director, CRA Services, conducts site monitoring for clinical research studies according to ProSciento Standard Operating Procedures (SOPs) and ICH/GCP/GLP guidelines. Prepares monitoring reports and assists with query resolution. Performs duties in accordance with the company’s values, policies, and procedures. Essential Duties and Responsibilities include the following. Other duties may be assigned at the Company’s sole discretion. Responsible for all aspects of study site monitoring including site qualification visits, pre-study visits, site initiation visits, routine monitoring visits, and close-out visits of clinical sites. etc. | 11/12/2019 |
| 1257 | PTC Therapeutics South Plainfield, NJ Research Associate - Neuroscience BA/BS Exp: 1-2 year(s) |
Reporting to a PhD Scientist in the Neuroscience Group at PTC, the Research Associate is involved in performing experiments using a variety of techniques, including analysis of RNA, protein, electrophysiology on brain tissue and imaging of cells and tissue sections. The successful candidate will: Work collaboratively with other PTC researchers to execute experiments in a highly matrixed environment. Analyze and interpret data generated. Assure that timelines are adhered to through efficient time management. Communicate effectively within the research team and across functional areas. Present data at internal meetings. etc. | 11/12/2019 |
| 1258 | PTC Therapeutics Mountainview, CA Laboratory Technician/Research Assistant, Compound Management AS/BS in chemistry, biochemistry, or biology Exp: 0-2 years |
We are seeking a highly organized technician/research assistant to manage the proprietary compound collection at the PTC Mountain View Research Site. This individual will be a key member of the research group, providing samples to internal and external collaborators. Additionally, the compound management technician will perform routine chemical and biological assays to support various programs. The successful candidate will be almost pathologically detail-oriented and thrive performing high precision work. etc. | 11/12/2019 |
| 1259 | Pyramid Laboratories Costa Mesa, CA Manufacturing Technician No degree required Exp: 1 year |
Under general supervision, perform various manufacturing related activities for a GMP compliant Fill/Finish operation applying standard practices, techniques and procedures. Able to assist in the preparation of reports, records, etc., for assigned tasks. PRINCIPAL DUTIES: Familiar with related GMP procedures and requirements, as directly related to the position. Ensure that appropriate procedures and processes are utilized without unauthorized modifications. Ability to set-up, maintain and perform various manufacturing related activities as required for a GMP compliant Fill/Finish operation. etc. | 11/12/2019 |
| 1260 | Quick Biology Pasadena, CA Research Associate MS in biochemistry, molecular, or biological science Exp: 1-4 year(s) |
We are seeking a Research Associate I to perform sample preparation, RNA/DNA extraction, QC/QA, sequencing library construction and Illumina Hiseq sequencer operation in our sequencing team. The successful candidate should have knowledge of next-generation sequencing using the Illumina platform. The successful candidate should work somewhat independently to conduct laboratory experiments on NGS projects within well-defined guidelines; Ability to independently design and execute SOPs to meet project goals is essential. | 11/12/2019 |
| 1261 | Regeneron Tarrytown, NY R&D Associate - Neurodegenerative Diseases MS in neuroscience, biochemistry, biology or related Exp: 1+ year(s) |
We are seeking a talented and motivated R&D Associate / Specialist to join our highly dynamic neuroscience team. The successful candidate will be responsible for the design and execution of experiments to understand the mechanisms of neurodegenerative diseases, discover new therapeutic targets and validate novel therapeutic strategies. We are looking to recruit a candidate with in vitro experience and strong in vivo expertise in neuroscience and models of neurodegenerative disease. etc. | 11/12/2019 |
| 1262 | Repligen Waltham, MA Manufacturing Associate - ELISA AS/BS Exp: 1-2 year(s) |
This position is in Repligen’s ELISA group. The successful candidate will be responsible for the manufacture of ELISA kits and its components as well as in-process testing. The individual must be able to follow oral and written instructions accurately and complete tasks in a timely manner. Experience working in a GMP/ISO/document-controlled environment would be beneficial. Attention to detail and the ability to work in a team environment are essential. Candidates must be willing and able to learn new manufacturing processes as the company grows. | 11/12/2019 |
| 1263 | RTI Surgical Alachua, FL Materials Tech 1 HS diploma or equivalent Exp: Entry level |
The Materials Tech 1 position at RTI represents an entry level function. Employees will develop technical skills in their assigned areas, an understanding of the rules and regulations that RTI administers, and the basic operating approach at RTI including: reading, understanding, and following work instructions; working in a team environment; and learning to work with minimal supervision. POSITION SUMMARY: Performs daily activities in accordance with applicable Standard Operating Procedures (SOPs) and Work Instructions (WIs). Unpacks, segregates, organizes, wraps, and packages various supplies and equipment. etc. | 11/12/2019 |
| 1264 | RTI Surgical Alachua, FL BMS Technician HS diploma or equivalent Exp: 1 year |
POSITION SUMMARY: Maintains accurate records of all specimens received or sent out of the laboratory. Completes test request forms and enters the information into the Laboratory Information System. Performs specimen preparation for testing and archiving. Makes determinations as to acceptability of specimens, and files appropriate specimen rejection forms and revision request forms when necessary. Performs non-licensed testing, interprets non-licensed testing results, and prepares reports. Performs quality control and quality assurance in areas of the laboratory. etc. | 11/12/2019 |
| 1265 | Samdi Tech Chicago, IL Research Assistant (Full-time) BS in biology, biochemistry, chemistry or related Exp: 0-3 years |
The Research Team leads target/enzyme-based projects for biotech and pharma clients to develop assays for high-throughput screening, and characterization of drug candidates and reaction mechanisms. The successful candidate will be organized and able to work under strict timelines in a fast paced environment. Primary responsibilities may include supporting the preparation of reagents and materials for running biochemical assays, assisting in executing biochemical assays utilizing state of the art MALDI TOF mass spectrometry, integrating automated liquid handling, and supporting fundamental laboratory functions. | 11/12/2019 |
| 1266 | Samdi Tech Chicago, IL Research Associate- Biochemical Assay Specialist (Full-time) MS in biology, biochemistry, chemistry or related Exp: 1+ year(s) |
The Research Team leads target/enzyme-based projects for biotech and pharma clients to develop assays for high-throughput screening, and characterization of drug candidates and reaction mechanisms. The successful candidate will be organized and able to work under strict timelines in a fast paced environment. Primary responsibilities may include handling and processing of reagents and materials for running biochemical assays, designing and performing biochemical assays utilizing state of the art MALDI TOF mass spectrometry, take a project leadership role on multiple targets/enzymes, integrating automated liquid handling, and writing and maintaining Standard Operating Protocols (SOPs). | 11/12/2019 |
| 1267 | GBT South San Francisco, CA CONTRACT - CLINICAL TRIALS ASSISTANT BS/BA or equivalent Exp: Experience preferred but not required |
The Clinical Trials Assistant (CTA) is responsible for providing support to the lead Clinical Trial Manager and the study execution team, clinical tracking and document maintenance as applicable to study vendors and clinical trial sites. The CTA will work closely with a cross-functional team to ensure that clinical trials are conducted in a timely fashion and in compliance with GBT SOPs, ICH/GCP/regulatory guidelines, company goals, and budgets. | 11/9/2019 |
| 1268 | Global Pharma Tek Edison , NJ Clinical Project Assitant BS in pharmacy, health care, or related Exp: 1-2 years |
Responsible for strategic and operational activities of clinical research studies in blood cancer metabolism to ensure adherence to intended timelines and achievements of study goals, while ensuring quality by FDA, EMEA, ICH and GCP guidelines. Facilitating interdisciplinary activities, participating in the clinical trial working group (CTWG), Site Management Team (SMT), and internal team meetings to meet the goals and established timelines | 11/9/2019 |
| 1269 | Global Pharma Tek Edison , NJ Equipment Validation Engineer BS in mechanical/industrial engineering Exp: 1-2 years |
Develop, Implement and Install filter integrity testing methods to available automated Filter Integrity Testers (FITs) available on site to verify the integral of the vent filters that will used in the process for WFI Tanks, Autoclaves, supply clean compressed air and as required. Prepare protocols and reports for Validation Project Plan, Validation Master Plan, IQ, OQ, OQ, Traceability Matrix, Engineering test Plans, and Commissioning test strategies following the site Good Data and Documentation Practices (GDP) during protocol execution for qualifying the system or facility | 11/9/2019 |
| 1270 | Global Pharma Tek Edison , NJ Regulatory Affairs II BS in pharma sciences or related Exp: 1-2 years |
Managing and delivering regulatory submissions to global health authorities required to support the maintenance, development and registration of products and performing the following required activities depending on the particular project and assigned submission(s). Establishing Dossier Plans for the assigned Global submission types as needed to support the lifecycle of one or more products in generating dossier plans that will reflect inputs from functional area representatives and key stakeholders; | 11/9/2019 |
| 1271 | Global Pharma Tek Edison , NJ Lab Equipment Qualification Engineer BS/BA in pharmacy or chemistry Exp: 1-2 years |
Execute Validation and Qualification protocols which include installing, operating and maintaining of GMP Lab Equipment and Instruments (HPLC, UV-Vis Spectrometers, FTIR, GC, pH meters, Conductivity meters, Analyzers etc.) and manufacturing equipment like sterilizers and autoclaves to confirm if the instrument is compatible and compliant with Manufacturing, analysis, Company and FDA regulations. Perform validation and qualification documents include User requirement specifications, functional requirement specifications, Installation Qualifications (IQ), Operational Qualifications (OQ), Performance Qualifications (PQ), Validation summary reports, Change Control etc. for various lab instruments utilized by Quality control and Quality assurance teams; | 11/9/2019 |
| 1272 | Global Pharma Tek Edison , NJ Associate Operations Specialist BS/BA in pharmacy or pharmacology Exp: 1-2 years |
Review, assess and process Lifecycle Safety data and information, across all service lines received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members. Perform data entry for tracking and safety database, coding relevant medical terminology, writing, descript narratives, generating queries pertinent to the case, performing quality control, assisting with reconciliation, driving case closure, coordinating translations and ensuring reports are sent to the customer within assigned deadlines. | 11/9/2019 |
| 1273 | Global Pharma Tek Edison , NJ Submission Specialist - Regulatory Affairs BS in regulatory affiars/health admin Exp: 1-2 years |
Performing hands-on daily submission compilation and publishing activities associated with preparation of various dossier types and safety reports, for both new product marketing applications and/or marketed product maintenance packages. Performing overall quality of the assigned documents and dossiers which must comply with all internal Bayer best practices, meet global regulatory requirements, and facilitate the review and timely approval by appropriate regulatory authorities. Supporting the compilation of global dossiers and to deliver technically compliant submission documents/reports, which contribute to the development of submissions that meet the technical requirements and standards set by relevant health authorities. | 11/9/2019 |
| 1274 | Global Pharma Tek Edison , NJ Specialist Study Management BS in regulatory affiars/health admin Exp: 1-2 years |
Review and process start up documents, including Sub Investigator’s documents in compliance with ICH-GCP, and client’s Procedural Documents; Assist SATS with obtaining and maintaining essential documents in compliance with ICH-GCP, and client’s Procedural Documents; Attend weekly study team meetings and be prepared to provide a report on vendor spreadsheet status and sub I document status; Create and/or import clinical-regulatory documents into the A New Global Electronic Library (ANGEL) according to the Global Document List (GDL) ensuring compliance with the client’s Authoring Guide for Regulatory Documents to support publishing in ANGEL; | 11/9/2019 |
| 1275 | Goodwin Biotechnology Plantation, FL Upstream Manufacturing Technician HS Diploma or AS in biological/physical sciences Exp: Entry Level |
Assists Upstream Manufacturing and Cell Culture Operations with Manufacturing in accordance with Master Batch Records and in compliance with GMP regulations and guidelines. Monitors Manufacturing Processes, Operates Analytical Laboratory Equipment and provides Operational Support for USP-MFG activities. Compiles electronic /laboratory notebooks, maintains laboratory equipment, and equipment logs and monitors supplies. | 11/9/2019 |
| 1276 | Goodwin Biotechnology Plantation, FL Upstream Manufacturing Technician BS in biological/physical sciences Exp: 1-2 years in cell culture |
Responsible for the execution of a Manufacturing Batch Records (MBR) for specific projects to manufacture cell derived biopharmaceuticals in compliance with cGMP guidelines and regulations. Activities include cell culture in various cell culture vessels including preparation of inocula for bioreactor production, and operation of various bioreactors. Assists in all Upstream Development/Manufacturing activities including; cell culture, cell banking, media optimization, seed train design, feed strategy, bioreactor parameter optimization, harvest clarification, and technology transfer to manufacturing. | 11/9/2019 |
| 1277 | Gore Elkton, MD R&D Technician BS in chemical/sciences/engineering Exp: 1-3 years |
W.L. Gore & Associates Inc. is seeking an associate to join the R&D Technician Lab Team at one of the Fabrics Division’s facilities in Elkton, Maryland. The primary focus of this commitment is to support projects and hands on testing needs for our Durable Water Repellent coating on laminates. Performing lab functions accurately and efficiently, including but not be limited to: Hands on testing, sample preparation, and test method development. Writing and implementing procedures.Operating and maintaining analytical equipment | 11/9/2019 |
| 1278 | Gore Flagstaff, AZ Electrical Automation Design Engineer BS in engineering Exp: 1 or more year (can be coop/internships) |
In this role, you will be involved in software design, electrical design, specification, installation, startup, validation, project management, and support for new and existing equipment and systems. Performing electrical design and hands-on support for process equipment (e.g., drives, programmable logic controller [PLC] logic programming, human-machine interfaces [HMIs], wiring schematics, power systems, instrumentation, and motor control systems). Being an integral member of a project team that specifies, constructs, commissions and validates new manufacturing equipment | 11/9/2019 |
| 1279 | Gradalis Carrollton, TX Clinical Research Assistant BS in life/health sciences Exp: 1 or more years |
The Clinical Research Assistant coordinates the research and administrative activities of clinical trials for Gradalis. The Clinical Research Assistant works for the Clinical Operations Manager to provide support in compliance with the FDA Code of Federal Regulations (CFR), the ICH Good Clinical Practice (GCP) Guidelines, OHRP/DHHS guidelines and Gradalis Standard Operating Procedures. | 11/9/2019 |
| 1280 | Grail Menlo Park, CA Research Associate 2 - R&D Technology Development MS in molecular biology, biochemistry, or related Exp: 1 year or more |
GRAIL is seeking a Research Associate for the R&D technology development team to contribute to the development and optimization of assays for early cancer detection. The successful candidate will be responsible for planning and execution of experiments and data analysis with the guidance of senior scientists. Develop experiment plans to support study objectives. Ensure laboratory activities are performed in compliance with best practices for assay and instrument operation, safety, and result documentation | 11/9/2019 |
| 1281 | Grail Menlo Park, CA Equipment Engineering Technician BS/BA in engineering or sciences Exp: 0-2 years in lab |
As an Equipment Engineering Technician, you are responsible for supporting laboratory equipment management procedures, in alignment to our internal Quality Management System, to ensure better performance within Laboratory Operations. This will include global laboratory equipment support, sustainment, and operations activities across Production/Clinical, Product Development, Research and Development laboratories, in accordance with CLIA/CAP, FDA, cGMP and/or GLP guidelines. | 11/9/2019 |
| 1282 | Grail Menlo Park, CA Clinical Lab Associate I BS/BA in Biomedical Laboratory Science, Clinical Science or related field preferred. Exp: 1-2 years |
The Clinical Laboratory Associate (CLA) is responsible for assisting the Clinical Laboratory Scientist and supporting the daily operations of the Clinical Laboratory. CLA may serve as a team lead to the CLA team to coordinate tasks, divide workload, manage projects and review documents as assigned. The work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask, be flexible with tasks and schedules and ability to work independently in a team environment. | 11/9/2019 |
| 1283 | Grand River Grand Rapids, MI ASEPTIC MANUFACTURING ASSOCIATE - 3RD SHIFT HS Diploma/GED Exp: 0-1 years in manufacturing or lab work |
Responsible for performing various routine manufacturing tasks following established procedures and cGMP regulations under guidance of a production supervisor and/or senior management. Follow production and manufacturing procedures. Perform equipment preparation, bulk drug formulation, and aseptic filling duties as needed. Train in various manufacturing tasks including, but not limited to: fill/finish, formulation, lyophilization, sanitization, component and equipment preparation, and finished product inspection and packaging activities. | 11/9/2019 |
| 1284 | GreenLight Biosciences RTP, NC Research Technician Formulations BS in pharma sciences, or chemistry Exp: 0-2 years in lab |
GreenLight Biosciences is seeking for a Formulation Laboratory Technician to be part of the Formulation team to work on the design of new formulations under the guidance of a formulation scientist as well as the improvement of existing formulations and provide support to the manufacturing operations. The technician will be responsible for evaluating formulations, troubleshooting production when necessary and sample preparation. Strong technical, organizational and communication skills are essential. Applicant must be a team player able to function in a highly collaborative and fast-paced environment. | 11/9/2019 |
| 1285 | Grifols San Diego, CA Research Associate 2 BS/BA or MS Exp: 1-3 years |
Research Associate 2 is responsible for designing and performing experiments while collaborating and communicating effectively. Performs moderately complex experiments with input from supervisor. Able to summarize related groups of experiments. Provides input to the experimental design. Is able to analyze experimental data with minimal input from supervisor. Interprets experimental results in context of overall experimental goal. | 11/9/2019 |
| 1286 | Grifols Clayton, NC Associate Chemist-QC AS/AA or BS/BA Exp: 0-2 years with chemistry courses for degrees |
Performs chemical testing of moderate to advanced complexity within a Quality Operations Laboratory in a safe, accurate, and efficient manner following established written procedures while maintaining complete and accurate records of the work and results. This testing is required for the release of raw materials, in-process materials, and final containers. Conducts various routine and non-routine chemical testing (assays) according to procedure. Learns and follows the methods and the techniques of the chemical tests to be performed. This learning is a continuation of learning that occurred as Assistant Chemist. | 11/9/2019 |
| 1287 | Grifols Savannah, GA Phlebotomist HS Diploma/GED Exp: 0-1 years |
You assist in determining the suitability of donors to undergo plasmapheresis prior to venipuncture. You establish rapport with donors to ensure overall customer happiness with the center to support long-term donation, all while ensuring donor confidentiality. Sets up, disconnects, and operates the automated plasmapheresis machines including response and evaluation of all autopheresis troubleshooting displays, documentation of exceptions, etc. Ensures the proper calibration and maintenance of autopheresis machines and associated equipment. May be trained to repair plasma equipment. Disconnects and disposes of all contaminated disposable equipment. Ensures proper cleaning of equipment and work area between donors. Maintains accurate and thorough documentation of production records. | 11/9/2019 |
| 1288 | Grifols Ocala, FL Biomedical Technician HS Diploma/GED Exp: 6-12 months as medical assistant or phlebotomy training |
Identify and screen donors by reviewing medical records and logs and evaluate the donor as to suitability. Screening includes asking health related questions and referring to medical staff when necessary; taking vital signs (blood pressure, pulse and temperature), performing fingerstick (HCT & Total Protein), and reviewing results using the applicable donor management system Maintain donor confidentiality at all times in all areas. Responsible for preparing donors for plasmapheresis procedure. Review donor record files for accuracy and completeness. Collect plasma by setting up the autopheresis instrument, performing the venipuncture and utilizing an Automated Plasmapharesis machine. Evaluate vein performance by checking data with known norms to identify possible problems; make corrections in order to expedite donation time and ensure product quality. Conducts all phlebotomies in compliance with all federal, state, and Biotest regulations. | 11/9/2019 |
| 1289 | Grifols Rock Hill, SC Biomedical Technician HS Diploma/GED Exp: 6-12 months as medical assistant or phlebotomy training |
Identify and screen donors by reviewing medical records and logs and evaluate the donor as to suitability. Screening includes asking health related questions and referring to medical staff when necessary; taking vital signs (blood pressure, pulse and temperature), performing fingerstick (HCT & Total Protein), and reviewing results using the applicable donor management system Maintain donor confidentiality at all times in all areas. Responsible for preparing donors for plasmapheresis procedure. Review donor record files for accuracy and completeness. Collect plasma by setting up the autopheresis instrument, performing the venipuncture and utilizing an Automated Plasmapharesis machine. Evaluate vein performance by checking data with known norms to identify possible problems; make corrections in order to expedite donation time and ensure product quality. Conducts all phlebotomies in compliance with all federal, state, and Biotest regulations. | 11/9/2019 |
| 1290 | Grifols Clarkville, TN Quality Associate HS Diploma/GED Exp: 0 years |
Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual. Participate in the Quality Assurance meetings and be part of the Quality Assurance team. Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product. Perform weekly review of equipment incident logs. | 11/9/2019 |
| 1291 | Grifols Moorhead, MN Phlebotomist HS Diploma/GED Exp: 0-1 years |
You assist in determining the suitability of donors to undergo plasmapheresis prior to venipuncture. You establish rapport with donors to ensure overall customer happiness with the center to support long-term donation, all while ensuring donor confidentiality. Sets up, disconnects, and operates the automated plasmapheresis machines including response and evaluation of all autopheresis troubleshooting displays, documentation of exceptions, etc. Ensures the proper calibration and maintenance of autopheresis machines and associated equipment. May be trained to repair plasma equipment. Disconnects and disposes of all contaminated disposable equipment. Ensures proper cleaning of equipment and work area between donors. Maintains accurate and thorough documentation of production records. | 11/9/2019 |
| 1292 | Gritsone Pleasanton, CA MANUFACTURING ASSOCIATE I/II, DOWNSTREAM BS in biological/physical sciences Exp: 0-2 years in cGMP manufacturing |
The Manufacturing Associate will execute activities associated with purification manufacturing in a clean room environment. This role will also need to assist with cell culture, aseptic fill, and buffer prep processes as well as maintain material inventory in labs. Possess experience in purification activities including but not limited to tangential flow filtration, anion exchange chromatography, and diafiltration. Responsible for day to day manufacturing activities including stocking of materials, preparation of documentation, cleaning and sanitization of rooms and equipment, operation of process equipment. | 11/9/2019 |
| 1293 | Guardant Redwood City, CA Clinical Trials Assistant BS/BA in biological sciences Exp: 1 year in clinical research |
The Clinical Trial Assistant (CTA) is primarily responsible for the coordination of activities associated with the setup and management of clinical studies under the direction of, or as delegated by a member of the Clinical Trial team. Responsibilities will range from clinical study coordination to data entry projects and general office work. | 11/9/2019 |
| 1294 | Guardant Redwood City, CA Reporting Assistant II AS/AA or BS/BA in lab/clinical sciences Exp: 1 year of lab experience |
The Reporting Assistant (RA)II is responsible for assisting the reporting Clinical Laboratory Scientists (CLS) and supporting the daily operations of the post-analytical reporting process.The RA IIis responsible for preparing all preliminary reports, labeling folders, documenting controls for CLS review and assisting sample status in the Clinical Laboratory. | 11/9/2019 |
| 1295 | Guardant Redwood City, CA Client Services Associate BS/BA Exp: 1 year in client services |
We are looking for a full-time Client Services Associate (CSA). The CSA is responsible for providing exceptional support to Guardant Health customers, the Guardant Health Clinical Laboratory, Sales Representatives, and our billing partners. CSA is responsible for receiving and responding to all types of communication: phone, email and web inquiries from customers (physician offices, laboratories, and hospitals), sales representatives and patients. | 11/9/2019 |
| 1296 | Harpoon Therapeutics South San Francisco, CA Clinical Research Associate BS/BA in science/health care Exp: 1-2 years in drug development |
The Clinical Research Associate is a key member of the team responsible for planning, successful implementation and management of one or multiple clinical trial(s). Responsibilities include assisting in the development of study protocols, case report forms, clinical reports, performing site monitoring visits, and interfacing with site coordinators, field clinical staff, CROs and other company representatives. High level relationships across all functional areas that interact with Clinical Operations (including Product Development, Research, Translational Medicine, etc.) will also be required. | 11/9/2019 |
| 1297 | HealPros Atlanta, GA IT Support Technician HS Diploma or higher Exp: 6-24 months of electornics work |
We have an immediate opening for an IT Support Technician to be based out of our corporate office in Buckhead, GA. This is a full-time position and will be responsible for managing HealPros's equipment in our facility or at the location of our technologists. Under the supervision of the IT Administrator, the IT Support Technician will perform troubleshooting techniques to resolve equipment issues and maintain it in good working order. | 11/9/2019 |
| 1298 | Health Decisions Durham, NC Business Development Associate (Inside Sales) BS/BA Exp: 1 year in sales |
We are seeking a Business Development Associate who will be responsible for lead generation by proactively prospecting and qualifying targeted leads by telephone and email. The ideal candidate will be highly skilled in fostering relationships with the goal of converting leads to new sales opportunities. Initate initial client engagement, including ensuring client-readiness of materials for client meetings including briefing documents and call presentation development; develops call agenda and hosts prep sessions with internal teams in advance of client engagement . | 11/9/2019 |
| 1299 | Helmer Scientific Noblesville, IN Manufacturing Trainee HS Diploma/GED Exp: None |
Performs repetitive assembly/fabrication/materials tasks using basic hand tools to build either parts for or actual temperature-controlled storage units, refrigerators/freezers and thawing systems, Cleans and packs units, handles material for distribution. Regular and reliable attendance, which includes punctuality and working scheduled overtime, is necessary to meet our commitment to provide quality products and service to our customer. Ensure that device history records are completed according to FDA GMP requirements. Complete nonconformance records according to established procedures and GMP requirements. | 11/10/2019 |
| 1300 | Helmer Scientific Noblesville, IN Assembler I* HS Diploma/GED Exp: 1-3 years in general assembly |
The Assembler I: Performs repetitive assembly tasks using basic hand tools to build temperature controlled storage units, refrigerators/freezers and thawing systems or under counter temperature controlled storage units. May clean and pack units. Regular and reliable attendance, which includes punctuality and working scheduled overtime, is necessary to meet our commitment to provide quality products and service to our customer. Performs repetitive assembly task using basic hand tools to build temperature controlled storage units, refrigerators/freezers and thawing systems. May be assigned to clean and pack units. | 11/10/2019 |
| 1301 | Helmer Scientific Noblesville, IN Assembler I - Clean & Pack* HS Diploma/GED Exp: 1-3 years in general assembly |
Performs repetitive assembly tasks using basic hand tools to build temperature controlled storage units, refrigerators/freezers and thawing systems or under counter temperature controlled storage units. May clean and pack units. | 11/10/2019 |
| 1302 | High Point Clinical Trials Center High Point, NC Lab Supervisor CLS/MT Associates, BS, BA Exp: 1 year lab experience |
This position ensures the full reconciliation of all specimens submitted to outside client and vendors in a manner fully compliant to Good Clinical Practice under FDA guidelines. Completes all study procedures as per FDA regulations, GCP guidelines and protocol requirements. Assists with and performs laboratory procedures including sample check-in, preparation, centrifugation, storage and shipment. Applicants should have demonstrated team management skills as well as working knowledge of IATA sample shipment processes, CLIA-waivered laboratory processes, and ability to fully manage external vendors for our clinical trial testing needs. | 11/10/2019 |
| 1303 | High Point Clinical Trials Center High Point, NC Research Nurse NC nursing license Exp: 1 year practical nursing experience |
Assist in conduct of clinical studies. Provides licensed nursing coverage for studies and performs procedures as allowed by training and delegation. Assist in the conduct of clinical studies while providing licensed coverage. Performs all job responsibilities in accordance with standards of Good Clinical Practice (GCP), clinic standard operating procedures (SOP’s), and OSHA guidelines. Perform tasks such as EKG’s, vital signs, phlebotomy, insertion and maintenance of IV catheters. | 11/10/2019 |
| 1304 | Hikma Cherry Hill, NJ Quality Lab Associate I, Env. Monitoring BS/BA Degree in Microbiology or Biology Exp: 0-2 years |
Perform functions within the Microbiology Laboratory related to Environmental Monitoring of controlled production areas. The duties also include equipment maintenance and LIMS management. Document EM testing into the EM database prior to incubation, ensure samples are correctly incubated, and record sample results in the EM database following incubation. Audit personnel aseptic technique in controlled areas including during process simulations (media fills). Document test data clearly and accurately. Maintain data integrity and ensure compliance with company policies, procedures, cGMPs, and regulatory requirements. | 11/10/2019 |
| 1305 | Hikma Columbus , OH Technician II, Chemstore 2nd Shift HS Diploma/GED Exp: Entry LEvel |
Performs the set of tasks referred to as “window work” within the Chemstore while collecting, washing, and redistributing laboratory glassware. Escalates any washer issues discovered to the GMP department and communicates shortages/inventory needs to their Manager. | 11/10/2019 |
| 1306 | Hillrom Alexandria, LA Field Service Technician I HS Diploma/GED Exp: 0-2 years in FDA related industry/customer service |
The primary duties of a Medical Equipment Service Representative involve client facing customer service and minor medical equipment repairs. Responsible for the pick-up and delivery of medical equipment, using a company provided vehicle to customer facilities. Periodically work on an on-call rotation that involves a 24/7/365 operation. Responsible for direct customer contact | 11/10/2019 |
| 1307 | Hillrom Albuquerque, NM Field Service Technician I HS Diploma/GED Exp: 0-2 years in FDA related industry/customer service |
The primary duties of a Medical Equipment Service Representative involve client facing customer service and minor medical equipment repairs. Responsible for the pick-up and delivery of medical equipment, using a company provided vehicle to customer facilities. Periodically work on an on-call rotation that involves a 24/7/365 operation. Responsible for direct customer contact | 11/10/2019 |
| 1308 | Hillrom Batesville, IN Engineer I R&D - Embedded Software BS/BA in computer science/engineering Exp: 0-2 years in engineering/technical role |
As an Embedded Software Engineer, you will develop innovative medical software in a fast-paced environment. The ideal candidate will have a passion for bringing cool ideas to life and maximizing hardware and software performance. You will be responsible for writing firmware for device drivers, task manager, device manger, control algorithms, and various communication protocols which make our products exceptional. You develop tools which automate the software build process, system design and production testing. | 11/10/2019 |
| 1309 | Homology Bedford, MA Research Associate, Analytical Development (6 Month Contract) BS/BA in biological sciences Exp: 0-2 years in biochemical/biological analyses |
The role of Analytical Development Research Associate is to aid in developing and refining analytical methods to characterize AAV vector products. The individual in this role will be a highly-skilled, talented and motivated researcher who will focus on the analysis of research/development-grade vector samples using multiple AAV-specific analytical methods. The candidate will participate in the comparison of AAV vector products produced internally with those produced externally as well as the optimization and qualification of molecular and bioanalytical assays such as HPLC and capillary electrophoresis. | 11/10/2019 |
| 1310 | Hovione East Windsor, NJ Process Technician - Drug Product Continuous Manufacturing BS in engineering Exp: 1-2 years in chemical/pharma operations |
The Process Technician will support the installation and qualification of a GMP continuous tablet manufacturing line, highly automated, with Process Analytical Technology enabled control. This position will also support the development and manufacturing activities for drug product and formulation development projects. | 11/10/2019 |
| 1311 | Hovione East Windsor, NJ Process Engineer BS in chemistry/chemical engineering Exp: 1-3 years in chemical/pharma operations |
The Process Engineer will ensure that the use of the best process engineering knowledge will be applied in scaling up chemical and spray drying projects to maximize customer satisfaction and Hovione’s interests and in compliance with all Federal, State, Local and internal policies. Plan and design manufacturing processes based on chemical procedures to run safely and effectively in a pilot plant/kilo lab in accordance with the best known practices ensuring cGMP compliance. Contributes to the Process Hazard Analysis (PHA) of all processes under his/her responsibility and assures that all identified hazards are addressed prior to performing any activities within operations. | 11/10/2019 |
| 1312 | iCAD San Jose, CA Mechanical Engineer - R&D BS in Mechanical Engineering, or closely related Exp: 1- 5 years |
Fundamental understanding of Mechanical Design and Engineering. Product design experience in plastics, ceramics and/or metals. Fixture design for assembly and inspection. Lead experimental builds related to the development of the product. Run validation protocols related to design and production. | 11/10/2019 |
| 1313 | Icon PLC Farmingdale, NY Laboratory Study Start-Up Specialist BS Exp: 1 year in clinical trials |
This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Our Configuration & QC Specialist plays a key role within ICON Laboratory Services (ILS). Support the Project Management Team (PM) in configuring and QC'ing new studies in all ILS systems according to the specifications of the Client Laboratory Worksheet (CLW) and create all supporting documents and site instructions to facilitate proper specimen collection, packaging and shipping, including visit requisitions, reference range tables and study specific Lab Manuals. | 11/10/2019 |
| 1314 | Icon PLC Lexington, KY DPC Assistant HS Diploma/GED Exp: 1 year in medical office/admin |
The DPC Assistant will provide support services (logistical, technical and administrative) to the Direct to Patient Contact (DPC) project team all along the project, while complying with the deadlines, budgets, quality and regulatory requirements defined for each project. For each project, the Direct to Patient Contact Manager (DPCA) works under the technical and functional supervision of the dedicated Direct to Patient Contact Manager (DPCM). | 11/10/2019 |
| 1315 | Icon PLC Brentwood, TN CTA BS/BA in life sciences Exp: Entry Level |
This unique opportunity is designed for individuals with a Bachelor's Degree in Life Sciences, strong organizational skills, excellent written and verbal communication, and working knowledge of computer systems including Microsoft Word, Excel, Outlook, and PowerPoint. ICON, a leading Clinical Research Organization, is seeking passionate, resilient and inspiring Graduates to join our team as a Clinical Trial Assistant. This opportunity offers an entry-level permanent position to highly skilled individuals interested in a career in clinical research. | 11/10/2019 |
| 1316 | Icon PLC Raleigh, NC Client Services Assoc II, PCS BS/BA Exp: 1-2 years in clinical research |
As a Client Services Associate II, you will be responsible for supporting efforts to maintain and expand upon client relationships for the assigned PCS service area(s) through costing and proposal development, single service project planning and support, and client communication management. Support clinical research projects in the areas of scale management, translations, printing and distribution, and technology implementation. | 11/10/2019 |
| 1317 | Icon PLC North Wales, PA Configuration & QC Spec I BS Exp: 1 year in clinical research |
Our Configuration & QC Specialist plays a key role within ICON Laboratory Services (ILS). Support the Project Management Team (PM) in configuring and QC'ing new studies in all ILS systems according to the specifications of the Client Laboratory Worksheet (CLW) and create all supporting documents and site instructions to facilitate proper specimen collection, packaging and shipping, including visit requisitions, reference range tables and study specific Lab Manuals. | 11/10/2019 |
| 1318 | Freudenberg Jerffersonville, IN Medical Device Assembly / Manufacturing Associate- 1st Shift HS Diploma/GED Exp: 0-2 years |
Hand assemble manufactured components. Complete required documentation for work performed. Quality inspect work performed. Follow defined work procedures. Provide suggestions of continuous line/process improvementsHand assemble manufactured components. Complete required documentation for work performed. Quality inspect work performed. Follow defined work procedures. Provide suggestions of continuous line/process improvementsHand assemble manufactured components. Complete required documentation for work performed. Quality inspect work performed. Follow defined work procedures. Provide suggestions of continuous line/process improvements | 11/2/2019 |
| 1319 | Freudenberg Carpinteria, CA Tool Room Associate HS Diploma/GED Exp: 0-3 years |
Secondary operations and simple machining, including manual machining, grinding, honing, deburring, squaring of stock, and precision material removal to complex specifications with minimal instructions to the requirements of supplied Engineering Documentation. Maintenance of tool room equipment, and of production line molding, extrusion, and assembly equipment are vital functions of the role. Purchasing and stocking of hand tools, metalworking tools, and machining tools. Organization, cleaning, and maintenance of a 5S systematic program for workplace organization in the tool room. | 11/2/2019 |
| 1320 | Frontage Exton, PA Associate Scientist, Bioanalytical Services BS or MS in sciences Exp: Entry level |
Associate Scientist / Bioanalytical Services Essential Functions Provide support for running sensitive, reliable and efficient LC-MS/MS bioanalytical assays for TK/PK assessment. Coordinate study activities with Responsible Scientist to ensure efficiency and quality. Maintain the proper level of regulatory compliance for each study, helping to address QA audit findings | 11/2/2019 |
| 1321 | Frontage Secaucus, NJ Lab Technician Associates or bachelors in biomedical discipline Exp: 1-3 years in clinical research |
Develop a high level of familiarity and knowledge of the study protocol and flow chart of study procedures. Develop a strategy for implementing study procedures in compliance with study protocols. Performs laboratory procedures (g., preparation for admission testing, safety labs, and processing of biological specimen samples, shipment of samples and documentation of sample processing steps, etc.) as required by study protocol under the supervision of the Clinical Research Coordinator, Principal Investigator, and Sub-Investigators. | 11/2/2019 |
| 1322 | Frontage Exton, PA Associate Scientist-Product Development- CMC MS in pharma sciences, chemistry or biology Exp: 0-4 years |
Perform assigned tasks per procedures compliant with cGMPs and participate in the clinical manufacturing of parenteral, ophthalmic, and other sterile dosage forms. Assist with manufacturing area maintenance such as area monitoring and qualification, purchase of gowning supplies, purchase of equipment and room cleaning supplies, microbiological monitoring supplies. Assist in the equipment set up, operation, maintenance, cleaning as required for the project | 11/2/2019 |
| 1323 | FujiFilm College Station, TX Information Technology – Technical Support I HS Diploma/GED or BS in computer sciences Exp: 1 year in technical support |
Deployment and relocation of desktop systems. Maintenance and repair of desktops, printers and associated peripherals. Supports other IT staff in installing, configuring, testing, maintaining and troubleshooting network, systems hardware and software. Administration of FDBT’s Building Information Management System (BIMS). | 11/2/2019 |
| 1324 | FujiFilm RTP, NC Downstream Production Technician HS Diploma/GED or BS in computer sciences Exp: 1+ year in cGMP production |
Executing Development and Production processes as well as process documentation. Understanding processing principles and scientific theory behind operations steps. Demonstrating proficiency at the advanced skill level. Troubleshooting of equipment/processes. Authoring and routing SOP’s for approval. Assisting in the execution of validation protocols. | 11/2/2019 |
| 1325 | FujiFilm College Station, TX Downstream Manufacturing Technician I AS/AA in biological sciences/engineering, or HS Diploma/GED Exp: HS: 1 year, AA: 0 years |
The Downstream Manufacturing Technician I will work directly with viral purification (either whole particle or split particle), continuous flow centrifuge operation, and sucrose gradient separation, techniques for filtration and chromatographic separation (i.e. column chromatography and HPLC) and viral inactivation. | 11/2/2019 |
| 1326 | FujiFilm College Station, TX Cell Biology Technician BS/BA in biological sciences Exp: 0-2 years |
Writes and revises Standard Operating Procedures (SOPs) and other related Good Laboratory Practices (GLP)/Good Manufacturing Practices (GMP) documentation. Manages test samples, reagents and reference standards. Provides QC support for the Sample receipt for Manufacturing. Perform other duties as assigned. | 11/2/2019 |
| 1327 | FujiFilm College Station, TX Calibration Technician II BS or MS in sciences/engineering Exp: 1-2 years in cGMP operations |
Perform calibrations of complex instrumentation on production, laboratory and facility systems ensuring all systems and devices are calibrated in accordance with manufacturer’s specifications and FBDT SOP’s. Assist in the development of investigations resulting from ‘out of tolerance’ conditions with respect to instrumentation. Assist in interfacing with calibration contractors ensuring work is compliant with FBDT SOP’s and cGMP’s to maintain state of the art technology within the facility. Assist in maintaining all calibration records, work orders, and investigations in an orderly and accurate manner in compliance with cGMP’s by the utilization of the site CMMS and Document Management Systems. | 11/2/2019 |
| 1328 | FujiFilm RTP, NC Associate Scientist, Microbial MS or BS Exp: BS: 1+ years, MS: 0 years |
The Upstream Process Development group is seeking an Associate Scientist with experience in microbial technologies. An Associate Scientist assists in conducting experiments for programs. The individual monitors on going experiments and can identify unusual occurrences. An Associate Scientist understands and applies knowledge within area of expertise and can take an active role in non-routine process development activities. | 11/2/2019 |
| 1329 | FujiFilm College Station, TX Associate Scientist – Downstream Process Development MS in chemistry, biology, or life sciences Exp: 1 year experience |
Assist in the development, optimization, and scale-up of chromatography processes (including affinity, IEX, HIC, etc.) and filtration processes (including UF/DF, depth filtration, and sterile filtration, etc.). Operation of chromatographic systems (GE AKTA, and other Unicorn based equipment). Maintaining detailed laboratory notebooks following FDBT procedures. Participate in developing and carrying out experimental protocols. | 11/2/2019 |
| 1330 | Cosette South Plainfield, NJ ASSOCIATE SCIENTIST PRODUCT DEVELOPMENT MS in engineering, or life/pharma sciences Exp: 1-2 years |
he Product Development Scientist will assist the Manager of Product Development in all aspects of new drug product and process development including but limited to – prototype development, lab stability, document creation, process design and optimization, pilot scale-up, assist the process development group in supervising clinical trial manufacturing material, Registration/exhibit batch manufacturing, and process optimization to full scale commercial batch size. Collaborate with all of the Scientific Affair Department (including Process Development, Analytical R&D, Regulatory Affairs, Clinical and Project Management), commercial manufacturing and quality group. | 11/2/2019 |
| 1331 | Cosette South Plainfield, NJ MANUFACTURING OPERATOR 1 - 3rd Shift HS Diploma/GED Exp: 1 or more year as machine operator |
Operate a number of machines used in the manufacturing of pharmaceutical products and have a good working knowledge of elements used in association with batch production, such as equipment cleaning, running filling machines, etc. The operator is responsible for producing acceptable product that meets G&W internal standards, and is also in conformance with GMP and safety standards. 3rd Shift Hours are 11:00 p.m. to 7:00 a.m. | 11/2/2019 |
| 1332 | GenapSys Redwood City, CA Signal Processing Engineer/Data Analyst MS in electrical engineering, physics, math, stats, etc. Exp: 1-4 years in signal processing |
As a Signal Processing Engineer, you would be working in a cross functional R&D team to improve the performance of the core technology through close collaboration with lab scientists, genomic application scientists, and data scientists. You will develop DOE (design of experiments) for troubleshooting and failure mode analysis, extract information from biomedical sensors, develop DNA sequencing base calling algorithms, present written and oral reports and proposals to peers and management, and play an important role in shaping and productionizing new products and cutting-edge applications. | 11/2/2019 |
| 1333 | GeneDx Gaithersburg, MD Microarray Lab Technician BS in medical tech/life sciences Exp: Entry Level |
The Laboratory Technician performs an entry level role in the testing of clinical DNA specimens for the purpose of diagnosing genetic disease, using manual and automated methods in a team environment, and following established policies and procedures in a professional manner. | 11/2/2019 |
| 1334 | GeneDx Gaithersburg, MD Quality Systems Specialis BS in related field Exp: 1-3 years in life science lab |
Implements Quality Systems programs that are consistent with company policies and regulatory standards. Audits and reviews quality data according to established procedures. Maintains tools for monitoring compliance training, corrective actions, audits, and document control. Supports corrective action task force initiatives | 11/2/2019 |
| 1335 | GeneDx Gaithersburg, MD NGS Lab Tech BS in medical technology Exp: 0-1 years |
A GeneDx NGS Lab Technician performs a higher than entry level role in the testing of clinical DNA specimens for the purpose of diagnosing genetic disease using manual and automated methods in a team environment, and following established policies and procedures in a professional manner. | 11/2/2019 |
| 1336 | GeneDx Gaithersburg, MD DNA Extraction Technician BS in biology Exp: 0-1 years |
The Lab Technician performs all lab procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. Prepares DNA dilutions and aliquots for use by downstream testing teams. Conducts diligent record-keeping and reporting. Prepares solutions. Performs equipment maintenance | 11/2/2019 |
| 1337 | GenerationBio Cambrige, MA Associate Scientist, (Molecular Biology, Analytical Development) BS in biological sciences Exp: 0-2 years |
Generation Bio seeks a highly motivated Research Associate to support analytical molecular biology activities in a cross-platform function. The successful candidate will work part of an analytics team responsible for the development and testing of research drug substance, as well as performing experiments to better characterize and understand the composition of our drug. Perform bioanalytical assays, including purity, copy number, expression, and activity assays to support the Production, Pre-clinical, and Process Development groups | 11/2/2019 |
| 1338 | Genewiz Cambridge, MA Laboratory Technician I, Genetic Analysis HS Diploma/GED or AA/AS Exp: 1+ years in lab preferred |
Quality driven processers. When our customers send us samples for sequencing, they help to prepare and process these samples as quickly and as awesomely as possible, while maintaining the highest quality standards in the industry. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. | 11/2/2019 |
| 1339 | Genewiz South San Francisco, CA Laboratory Technician I HS Diploma/GED or AA/AS Exp: 1+ years in lab preferred |
Our Lab Techs strictly adhere to laboratory SOPs to ensure quality and safety and often communicate with our customers via email. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. | 11/2/2019 |
| 1340 | Genewiz South Plainfield, NJ Laboratory Technician I, Molecular Biology Prep HS Diploma/GED or AA/AS Exp: 1+ years in lab preferred |
When our customers send us samples for sequencing, they help to prepare and process these samples as quickly and as awesomely as possible, while maintaining the highest quality standards in the industry. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. | 11/2/2019 |
| 1341 | Genewiz South Plainfield, NJ Laboratory Technician I, Molecular Biology Prep HS Diploma/GED or AA/AS Exp: 1+ years in lab preferred |
Our Lab Techs strictly adhere to laboratory SOPs to ensure quality and safety and often communicate with our customers via email. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. | 11/2/2019 |
| 1342 | Genewiz South Plainfield, NJ Sales Executive Continuous Recruitment- NY/NJ BS/BA in life sciences/biological sciences Exp: 1 year |
GENEWIZ is seeking technical sales professionals to join our New Jersey/New York based Sales team. Achieve annual sales goals within defined territory/accounts through the development, maintenance, and enhancement of customer accounts. Develop and implement an effective territory business growth plan. Retain current business baseline revenue by managing relationships with customers and other account contacts by collaborating with business leaders and the customer interface teams | 11/2/2019 |
| 1343 | Genewiz South Plainfield, NJ Bioinformatics Scientist MS in bioinformatics Exp: 1-3 years |
Work collaboratively with bench scientists, comprehend project objectives, evaluate and provide informatics solutions. Develop and implement bioinformatics analyses, applications, and workflows. Integrate statistical analysis to project design and data interpretations. Work closely with IT specialists to build robust infrastructure. | 11/2/2019 |
| 1344 | Genewiz South Plainfield, NJ Associate Scientist I, NGS BS/BA in biological sciences Exp: 1+ year in lab |
Prepare amplified template libraries for high-throughput sequencing. Carry out DNA sequencing on next-generation DNA analyzers. Perform routine maintenance of DNA analyzers and related equipment. Check inventory and replenish consumable sequencing supplies . Communicate with customers by phone and e-mail in a friendly and professional manner | 11/2/2019 |
| 1345 | GenMark Carlsbad, CA Research Associate II MS in biochemistry, molecular biology, or chemistry Exp: 0+ years |
Conducts general molecular biology tasks, including nucleic acid purification, quantification, amplification and analysis on multiple platforms. Prepares reagents and solutions as needed, using appropriate procedural and documentation methods, including industry standard good laboratory practices. Identifies and solves problems in experiments or protocol designs, suggests improvements. Prepares documents meeting company standards, including data summaries, reports, SOPs and procedures | 11/2/2019 |
| 1346 | GenMark Carlsbad, CA Quality Control Specialist I BS in life science or engineering Exp: 0-3 years in QC |
This position conducts incoming, in-process and final release QC testing in a controlled manufacturing environment. This position may also execute validation studies, execute test protocols, analyze data, generate analytical reports, investigate Non-Conformance's, evaluate processes & procedures, utilize statistical techniques, review specifications, and inspect & test equipment. May conduct training on quality related tools, methods, and procedures. Interfaces with R&D, Manufacturing, Quality, and Supply Chain within the company and when appropriate with customers and suppliers on quality related issues. | 11/2/2019 |
| 1347 | GenMark Carlsbad, CA Research Associate II, Technology Development MS in biochemistry, molecular biology, or chemistry Exp: 0 years in bio lab |
The Research Associate II will execute a range of molecular biology and bioanalytical procedures, reagent preparation, and laboratory duties under supervision for our technology development team. Conducts general molecular biology tasks, including nucleic acid purification, quantification, amplification and analysis on multiple platforms. Prepares reagents and solutions as needed, using appropriate procedural and documentation methods, including industry standard good laboratory practices | 11/2/2019 |
| 1348 | Genomatica San Diego, CA Research Associate I/II MS Exp: 0-2 years |
Genomatica is seeking a highly motivated Research Associate I/II, Microbiology/Molecular Biology to join the Strain Engineering team. This team is responsible for construction, characterization, evolution and characterization of host strains. The successful candidate will utilize her/his knowledge of Microbiology/Molecular Biology for cloning genes, genetically engineering chromosomal DNA, sequencing and analyzing the genome, characterizing product titers, growth and by-products when grown with various feedstocks. | 11/2/2019 |
| 1349 | Genomatica San Diego, CA Fermentation Associate I BS in Chemical/Biochemical Engineering, Bioengineering, Molecular Biology, Microbiology, or Biochemistry Exp: 1-4 years bio lab experience |
This position delivers high-quality fermentation data by applying optimal fermentor operating procedures, communicating observations clearly to Fermentation Science personnel, and works collaboratively to maximize experimental precision. This position will interface closely with the Fermentation engineers and scientists in the Fermentation Science Group to produce conclusive fermentation results that will guide process optimization and scale-up efforts | 11/2/2019 |
| 1350 | NeoGenomics Aliso Viejo, CA Project Data Administrator I AS/AA or higher Exp: 1 or more years in data entry |
The Project Data Administrator I works under general supervision to support Pharma Services projects with a focus on study data entry, QC, and associated documentation. You will support internal teams, data entry and QC activities for many projects at a time. This is the Early role in the Project Data Administrator job category. In this position, you will handle data and perform related tasks from a full range of projects including Molecular, IHC, Flow Cytometry, MultiOmyx, FISH, and Cytogenetics. | 11/2/2019 |
| 1351 | NeoGenomics Carlsbad, CA Clinical Laboratory Technologist I BS/BA in med technology, or chemical/biological/physical sciences Exp: 1+ year in clinical reference lab |
As a Clinical Laboratory Technologist I or II or III you will work under general supervision and you will be responsible for accurately performing highly complex laboratory testing procedures. You will determine acceptability of specimens for testing, prepare clinical specimens and identify specimen related problems. You will also analyze specimens, review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. | 11/2/2019 |
| 1352 | NeoGenomics Carlsbad, CA Client Advocate I HS Diploma/GED Exp: 1-3 years in customer service |
The Client Advocate I provides support and communications with NeoGenomics customers (physicians & medical staff) and couriers (FedEx and contracted couriers); as well as serves as the point of contact for internal customers such as territory business managers (sales), internal doctors, operational teams and senior leadership in relation to specialized diagnostic oncology testing via excellent telephone, written, and chat communication. This is the entry level in the Client Service organization and employees perform the full range of customer service activities; including inside sales functionality. | 11/2/2019 |
| 1353 | NeoGenomics Ft. Myers, FL Order Entry Specialist I - Data Integrity AS/AA Exp: 1+ year in healthcare/med billing |
As an Order Entry Specialist I, you will enter patient demographic characteristics and insurance information into a proprietary database using company specific software and internal documents. Additionally, you will input diagnosis codes, charges and verify insurance in accordance with company policies. | 11/2/2019 |
| 1354 | NeoGenomics Houston, TX Histotechnologist I AS/AA in histotechnology Exp: 1+ years related |
As a Histotechnologist I, II, III, you will work under general direction to precisely and accurately conduct a variety of routine and specialized histology procedures. You will research, troubleshoot, and resolve histology related inquiries and problems within the laboratory. This position requires you to produce the highest quality of embedding, microtomy, tissue grossing, tissue processing, and H&E staining, special staining and equipment maintenance. | 11/2/2019 |
| 1355 | NeoGenomics Aliso Viejo, CA Laboratory Assistant I HS Diploma Exp: 1-2 years |
As a Laboratory Assistant you will assist the department technologist in performing various basic laboratory procedures laboratory instrumentation to facilitate production. This in an entry level position in the clinical laboratory job category and employees in this position may not manipulate samples. | 11/2/2019 |
| 1356 | NeoGenomics Aliso Viejo, CA Accessioning Technician I AS/BS preferred, HS Diploma min Exp: 1+ year as acessioning technician |
As an Accessioning Technician I you will ensure proper handling of all specimens received and prepare specimens for laboratory testing. You will be performing functions such as matching patient information, data entry, and scanning documents. You will be responsible for reviewing all requisitions for missing information, working closely with Customer Care in order to obtain missing information in a timely fashion, and distributing new information to all departments involved. You will need to report problem holds and provide resolution in a timely fashion. | 11/2/2019 |
| 1357 | GenScript Piscataway, NJ Lab Technician - Ligation BS/BA Exp: 0-3 years |
We are looking for a Laboratory technician to assist our daily production tasks. The successful candidate should have biology or related science background, excellent time management skills, strong problem solving ability. He or she will need to work directly with production team, fit with collaborative and competitive culture in GenScript. | 11/2/2019 |
| 1358 | GenScript Piscataway, NJ Lab Technician - Plasmid Prep BS/BA Exp: 0-3 years |
We are looking for a Laboratory technician to assist our daily production tasks. The successful candidate should have biology or related science background, excellent time management skills, strong problem solving ability. He or she will need to work directly with production team, fit with collaborative and competitive culture in GenScript. | 11/2/2019 |
| 1359 | GigaGen South San Francisco, CA Research Assistant BS/BA Exp: 1-3 years lab experience |
GigaGen seeks a talented, highly motivated Research Assistant to work alongside PhD-level scientists on research funded by a $50 million co-development deal with Grifols, plus Phase II SBIR grants from the NCI and NIAID. This project involves high-throughput discovery and development of therapeutic antibody drug candidates from human and mouse immune repertoires. The work involves significant cell culture work, including a bioreactor and flow cytometry. | 11/2/2019 |
| 1360 | Gilson Middleton, WI Verification and Validation Specialist I BS/BA in sciences Exp: 0-3 years |
The job holder is introduced to and performs a wide variety of laboratory tasks and procedures related to the verification and validation of hardware and software products. Operates and maintains laboratory equipment and computers to perform product verification. Performs lab maintenance tasks. Conducts accuracy and precision analysis on liquid handling instruments. Uses lab methods (HPLC, SPE, PCR, bio-assays, etc.) to verify product function and design | 11/2/2019 |
| 1361 | Ginkgo Bioworks Boston, MA Research Associate - Protein Engineering BS/MS in biological sciences/engineering Exp: 1+ years in lab setting |
We are looking for someone who is excited about the field of synthetic biology and loves a challenge. We want a person who is eager to learn and has a desire to utilize automation to work more efficiently. Our ideal candidate will elevate our team through creative solutions while working closely with other foundry groups. Responsibilities include: Enzyme purification and characterization, Data analysis, Automation of protocols | 11/2/2019 |
| 1362 | Glaukos San Clement, CA Engineer, I BS in mechanical engineering Exp: 1-3 years |
Performs a variety of manufacturing engineering activities on ocular related products including manufacturing scale up, development, and sustaining activities. Responsibilities include developing creative solutions to manufacturing problems, development and execution of process, equipment, and product validations, ensuring the proper engineering deliverables are accurately generated, generation of 3D CAD models and 2D CAD drawings for assembly tools and fixtures, test procedures, project management and leadership, and maintaining schedule. May lead manufacturing related project teams with other engineers, technicians, and manufacturing staff with a focus on meeting manufacturing requirements with technically strong, high quality, cost effective approaches. | 11/2/2019 |
| 1363 | Glaukos San Clement, CA Regional Clinical Research Associate I BS/BA in biological sciences, nursing or related Exp: 0-2 years as CRA |
Lead/manage assigned sites through regular contact with investigators and site staff to monitor progress, answer questions, and provide guidance during the course of the clinical study. Critically review and analyze site activities through frequent visits and contacts to monitor study sites and performance. Travel to investigative sites to conduct site qualification, initiation, interim monitoring, and close-out visits | 11/2/2019 |
| 1364 | GSK Lincoln, NE Production Maintenance Technician AS/AA in lectromechanical Technology or Electronic Engineering Technology Exp: 1-3 years in industrial setting |
As Production Maintenance Technician you will be responsible for maintaining, troubleshooting, calibrating and modifying electrical and mechanical systems and equipment and document work on mechanical, electrical, hydraulic, and pneumatic equipment involved in the manufacture and packaging of pharmaceutical products. | 11/3/2019 |
| 1365 | GSK Lincoln, NE Supply Chain – Future Leaders Program BS in business, supply chain, analytics, IT systems, or any sciences/enginnering Exp: 2020 Graduate |
Over three years, our Future Leaders Graduate Program will challenge and support you to grow professionally and personally. You’ll have three stretching rotations within Pharmaceutical or Consumer Healthcare Supply, depending on your area. In both cases, you’ll take on business-critical roles that offer amazing insights into our end-to-end supply chain. You’ll learn about the synergies and challenges that come with delivering optimum value to the business and the customer. | 11/3/2019 |
| 1366 | GSK Lincoln, NE Automation Engineer BS in engineering Exp: 1-3 years |
As an Automation Engineer, you will manage and execute projects related to industrial machine automation for both new and existing equipment. Lead the design and installation of instrumentation and control systems in some of the following areas: building automation systems, data systems, process control, DCS and utility PLC’s which are harmonized with GSK-standards. Provide technical support for existing instrumentation and automation systems. Analyze repairs and maintenance requirements in order to proactively address system weaknesses. | 11/3/2019 |
| 1367 | GSK East Durham, NY Mechanical Engineering – Future Leaders Program, US – 2020 BS in mechanical/manufacturing/biomedical/etc. engineering Exp: 2020 Graduate |
Over three years, our Future Leaders Graduate Program will challenge and support you to grow professionally and personally. You’ll have three stretching rotations in business-critical roles within consumer healthcare supply. Your responsibilities will depend on your engineering discipline, but whatever your specialist area, you’ll get to meet senior leaders and network with other graduates. You’ll also improve your technical skills while gaining valuable leadership expertise. | 11/3/2019 |
| 1368 | GSK Collegeville, PA Reagent Scientist BS ro MS in sciences Exp: 0-3 years |
Development and quality of critical reagents, including characterizing external antibody’s, building isotype-specific antibody reagents, purifying proteins, conducting protein conjugations (e.g. biotin, ruthenium and fluorescent labels), assessing their purity and affinity, and generating certificates of analysis (CofA). Monitor reagents life cycle and characterization to assist with reagent trouble shooting effort. | 11/3/2019 |
| 1369 | GSK Carlisle, PA Packaging Operator- First Shift HS Diploma/GED Exp: 0-1 years in manufacturing |
As a Packaging Operator you will manually assemble, glue, tape and package boxes, cases and other material as needed. Activities also involve set-up, operation, and verification of printing, weighing and robotic equipment as well as staging packaging material, documenting, cleaning, and performing in-process quality checks. The work involves lifting up to 50 lb. containers on a regular basis and moving pallets, totes, and film using a hand truck or similar tools. A thorough understanding of each job function within the work center is essential. | 11/3/2019 |
| 1370 | GSK Rockville, MD Calibration & Instrumentation HS Diploma/GED Exp: 0-1 years cGMP experience |
As Calibration and Instrumentation Staff you will be responsible for supporting the team to ensure manufacturing systems are current on calibration requirements. You will also assist the team with the calibration process system, laboratory equipment, and facilities related utilities. | 11/3/2019 |
| 1371 | Global PharmaTek Edison, NJ Clinical Project Assitant BS in pharmascience,s pharma, health care, etc Exp: 1-2 years |
Responsible for strategic and operational activities of clinical research studies in blood cancer metabolism to ensure adherence to intended timelines and achievements of study goals, while ensuring quality by FDA, EMEA, ICH and GCP guidelines. Providing oversight in clinical research Organization (CRO), Central labs and other external vendors to ensure deliverables are met and methods of communication are developed to facilitate an efficient workflow. Facilitating interdisciplinary activities, participating in the clinical trial working group (CTWG), Site Management Team (SMT), and internal team meetings to meet the goals and established timelines | 11/3/2019 |
| 1372 | Global PharmaTek Edison, NJ Equipment Validation Engineer BS in mechanical/industrial engineering Exp: 1-2 years |
Develop, Implement and Install filter integrity testing methods to available automated Filter Integrity Testers (FITs) available on site to verify the integral of the vent filters that will used in the process for WFI Tanks, Autoclaves, supply clean compressed air and as required. Provide technical support in developing, authoring, and executing the Commissioning, Installation and Qualification protocols for the chromatography skids and other supporting equipment that are used in the production of drug | 11/3/2019 |
| 1373 | Global PharmaTek Irvine, CA Quality Engineer BS in mechanical engineering Exp: 0-2 years |
The Mechanical Engineer, Research & Development will support the Critical Care Mechanical team working on new product designs, technology development and sustaining of core product lines with an emphasis on hands on new product development. | 11/3/2019 |
| 1374 | Pfizer St. Louis, MO Associate Scientist, Cell Line Development BS in cellular/molecular biology or related Exp: 0-3 years |
A technical, lab-based position is available within Pfizer’s Cell Line Development (CLD) organization. The position will be primarily involved in mammalian CLD portfolio advancement, novel technology development and process optimization. Working with a group of scientists, the successful candidate will be responsible to perform platform cell line development activities to fulfill the need of moving Pfizer’s biotherapeutics pipeline projects towards either clinical or commercial developmental phase. This role will involve all aspects of cell line development from vector design/construction, cell culture maintenance, clone screening, and cell line characterization. The successful candidate will possess excellent aseptic technique and have experience with mammalian cell culture and recombinant protein expression. etc. | 11/5/2019 |
| 1375 | Pfizer Andover, MA Associate Scientist, Cell Line Development BS in cellular/molecular biology or related Exp: 0-3 years |
A technical, lab-based position is available within Pfizer’s Cell Line Development (CLD) organization. The position will be primarily involved in mammalian CLD portfolio advancement, novel technology development and process optimization. Working with a group of scientists, the successful candidate will be responsible to perform platform cell line development activities to fulfill the need of moving Pfizer’s biotherapeutics pipeline projects towards either clinical or commercial developmental phase. This role will involve all aspects of cell line development from vector design/construction, cell culture maintenance, clone screening, and cell line characterization. etc. | 11/5/2019 |
| 1376 | Pfizer Groton, CT Technical Associate, Comparative Medicine HS diploma to BA/BS Exp: 1 year |
The Technical Associate’s primary responsibility is to provide basic husbandry, handling, restraint and health surveillance of laboratory animals in compliance with local regulatory requirements. This individual will also provide daily record keeping of common laboratory species, their environments, and provide basic technical assistance (i.e., restraint, injections, bleeds) to other technicians and researchers. Other more specialized functions, depending on interest and aptitude may be assigned in the areas of technical and research services. etc. | 11/5/2019 |
| 1377 | Pfizer Sanford, NC Quality Control Associate Scientist BS/BA in related field Exp: No experience necessary for BS/BA candidates |
This position is an analyst role in the QC Bioanalytical laboratory. Experience with ELISA, PCR, and/or slot blot is preferred. Analyst will be responsible for ensuring the routine testing is scheduled and completed within appropriate timeframes as needed for manufacturing to maintain schedules (STAT testing) or the QA disposition group to disposition batches. Other responsibilities may include, SOP revisions, validation/qualification testing support, etc. etc. | 11/5/2019 |
| 1378 | Pfizer Groton, CT Associate Scientist, Materials Science BS in pharmaceutical science, chemistry, engineering or other related science Exp: 0-2 years |
Pfizer’s Materials Science group is seeking team members with a desire to bring new, cutting edge medicines to patients around the world. The Associate Scientist, Materials Science position is a laboratory-based position with responsibility for investigating and understanding the solid-state chemistry and particle properties of Pfizer’s drug molecules. Responsibilities include generating and interpreting data using state-of-the-art instrumentation and computer models to allow new medicines to be brought to the market. etc. | 11/5/2019 |
| 1379 | PMI Bio. Nashville, TN Chemist I, Analytical Development BS in chemistry, biology or related Exp: 1-2 years |
The Chemist I position, reporting to the Director, Analytical Development, will operate under moderate supervision to perform chemical analyses of samples according to standardized procedures to determine the identity, content, purity, stability, and other characteristics of the samples analyzed. He/she may perform method development activities related to the development of methods for testing of raw materials and clinical drug product as well as formulation development. etc. | 11/5/2019 |
| 1380 | PMI Bio. Nashville, TN Microbiologist I, Analytical Development BS in biology or related Exp: 0-1 years |
Reporting to the Microbiology Supervisor, the Microbiologist I will be responsible for performing environmental monitoring sampling of ISO class environments and assisting with preparation, characterization, and identification of environmental isolates. He/she will perform raw material and drug product method development and cGMP testing. etc. | 11/5/2019 |
| 1381 | PolarityTE Salt Lake City, UT Research Specialist I BS in biotechnology, engineering, computer science, or related science Exp: 0-2 years |
Under the general supervision of the Director of BME, the Research Specialist I, II or III will support R&D in conducting research projects by contributing to the following: develop protocols for and maintain laboratory equipment; troubleshoot and resolve problems; ensure compliance with lab protocols and safety standards, policies and procedures; performing complex data gathering and analysis. This role serves to assist with conducting pre-clinical research aimed at validating, testing products and discovering, developing innovative medical technologies. etc. | 11/5/2019 |
| 1382 | Portola South San Francisco, CA Clinical Trial Associate unspecified Exp: 1+ year(s) |
The CTA will support the operational management and oversight of aspects of a clinical program. The CTA will participate in the activities associated with the evaluation, initiation, management, and close-out of clinical trials within the Clinical Operations Department. The CTA role provides an outstanding opportunity to work in a cross-functional environment and collaborate with colleagues in Clinical Research, Biometrics, Regulatory & QA, and Program Management. This individual will report into the Sr. Director of Clinical Operations. This is an in-house position. etc. | 11/5/2019 |
| 1383 |