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5244 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 InformationDescription Date Added
1 FHC
Bowdoin, ME
Shipping & Receiving Technician
AS/BS
Exp: Not necessary for AS/BS candidates
The Shipping & Receiving Technician is responsible for all of FHC, Inc.’s incoming and outgoing shipments. The position requires a basic knowledge of FHC products and an extensive knowledge of shipping requirements. Interfacing with multiple departments to ensure the best delivery dates and methods are used to meet customers’ requirements and to assure a unique and satisfying experience for both internal and external customers. ESSENTIAL DUTIES AND RESPONSIBILITIES: Other duties may be assigned. Responsible for processing Return Material Authorizations RMAs Inbound and Outbound. etc. 9/14/2020
2 Foundation Medicine
Cambridge, MA
Histotechnician (Contract)
AS/AA
Exp: 1+ year(s)
The Histotechnician performs routine testing in FMI’s high complexity clinical diagnostic laboratory and is responsible for receipt of patient samples as well as the preparation of samples for microscopic examination and analysis by Pathology. This role focuses on cutting, mounting, staining, and batching slides. Key Responsibilities: Operate a microtome to produce slides or curls from paraffin blocks. Prepare and initiate samples for nucleic acid extraction. Manage sample movement through lab facilities. Ensure and maintain molecular safe integrity and quality of the specimens. etc. 9/14/2020
3 Foundation Medicine
Morrisville, NC
Accessioning Technician II
BS/BA
Exp: 0-1+ year(s)
The Accessioning Technician II performs critical sample receipt and data entry functions in FMI’s CLIA-certified clinical laboratory. Specifically, the Accessioning Technician II receives incoming samples and ensures that necessary information has been received to move forward with processing. The Accessioning Technician II is assigned to one of three shifts and may be assigned to work any day that the lab is operational. This is a regulated position and additional information may be available from FMI Quality Assurance regarding regulatory guidelines. etc. 9/14/2020
4 Freudenberg
Baldwin Park, CA
Quality Specialist - Process Monitoring and Material Release
BS
Exp: Not necessary for BS candidates
Your tasks: Complete all incoming/raw material and component inspections, to include verifying all documentation, and properly identify/release those materials in ERP. Perform inspection and verification of incoming materials, to include subcomponents and molded parts that have undergone off-site processing such as laser etch coatings, etc. Supports in the review and disposition of raw material, in-process and finished goods to include (NCMR/sNCMR/Material Hold Quality Notifications), departmental training/cross-training, Coordinates and monitors calibration requirements of test, measurement, and diagnostic equipment (TMDE). Administers assignment of new TMDE asset numbers, calibration requirements, calibration frequencies, and their control. Generates and investigates non-conformance reports (OOT’s – Out of Tolerance Reports) when TMDE is found to be out of calibration or missing calibration interval. etc. 9/14/2020
5 Frontage
Exton, PA
Scientist-002
MS in biology, biomedical science, or related
Exp: 1 year
Job Duties: Conduct in vitro and in vivo metabolism studies using radiolabeled and non-radiolabeled compounds. Conduct bioanalytical assays using HPLC and LC/MS/MS. Use LSC and sample oxidizers to generate data for radioactive mass balance studies. Develop sample analysis method and perform metabolites identification. Isolate and identify radioactive and non-radioactive metabolites from in vivo and in vitro. Provide routine animal care and perform technical work related to the care and use of research animals. Maintain mammalian and primary cell lines for preclinical experiments. Perform work in regulated environment. etc. 9/14/2020
6 Immy
Norman, OK
Quality Assurance Technician I
Associates in science or engineering
Exp: 0-2 years
Under moderate supervision, the Quality Assurance Technician I is responsible for performing all monthly, quarterly, and yearly calibrations of laboratory equipment, maintaining equipment lists, performing quality inspections on incoming items, and manufacturing materials needed to support the Quality Management System. 8/29/2020
7 Immy
Norman, OK
Upstream Technician
BS/BA in biological sciences
Exp: 0-2 years in lab
The Upstream Technician is responsible for the manufacture of immunoassays. This includes buffer manufacturing, testing, and manipulation for all products lines (LFA, EIA, Complement Fixation, Latex Agglutination, and Immunodiffusion). This person will perform various types of conjugations, quantifications, purifications, and antigen/antibody pairing and must have a high attention to detail. Upstream Technicians will be trained to excel in one product line before training in another. 8/29/2020
8 Cook Group
West Lafayette, IN
Research Engineer
BS in engineering
Exp: 1-5 year(s)
The Research Engineer at Cook Research Incorporated is responsible for completing project deliverables and tasks to support the evaluation of novel design concepts for new medical products and providing support to projects in development at Cook Group companies. The successful candidate will support research and development of novel medical devices supporting the MedSurg Division for Cook. This candidate will also be expected to work with a project team to identify clinical needs, formulate new concepts, produce prototypes, conduct feasibility assessments and produce documentation for designs. Familiarity with a variety of medical device materials would be advantageous. etc. 9/7/2020
9 Editas Medicine
Cambridge, MA
Clinical Trial Assistant
BA/BS
Exp: 1-3 year(s)
The Clinical Trial Assistant is an individual contributor providing clinical trial coordination support, along with implementing the clinical operational plans in accordance with regulatory guidelines and ICH/GCP standards. The Clinical Trial Assistant will be responsible for providing Clinical Operations support of study specific reports and site and vendor management activities. throughout the full lifecycle from study start-up through database archive. This includes collaboration with CROs and cross-functional teams. The position reports to the VP Clinical Science Operations and Clinical Quality. These responsibilities include: Supports the clinical team in the overall management of studies, including planning, execution and closeout of one or more clinical trials. etc. 9/8/2020
10 Envigo
Alice, TX
Animal Care Technician
Unspecified
Exp: 6-12 months
To assist with daily primate husbandry in accordance with SOPs and assist with maintenance of work area. How you will contribute to make a difference: Perform daily rounds to observe primates for signs of illness. Perform routine weighing of primates. Capture and restrain primates as needed. Maintain and sanitize animal enclosures. Assist with administration of medications. Perform blood collections. Perform documentation as required by operating procedures. Conduct general animal husbandry procedures. Assist in preparing and crating primates for incoming or outgoing shipments. Outside maintenance, grounds keeping. etc. 9/8/2020
11 Celerion
Tempe, AZ
Clinical Research Coordinator
BA/BS
Exp: 1-2 year(s)
We have an exciting opportunity for Clinical Research Coordinator to join our Tempe, AZ clinical team! As a you work closely with our clinic operations team to ensure the success of our phase one clinical trials, Research Coordinators interpret study protocols to generate needed source documents, they add time and event codes into our systems to account for the needed tasks in a trial, they coordinate needed supplies for a given study and ensure we are ready to deliver. A background in clinical research or health care is a plus, but it is not required. We are seeking someone with well honed critical thinking skills, an ability to manage multiple projects at once, and well-developed time management skills. 9/1/2020
12 Celerion
Tempe, AZ
Entry-Level Project Coordinator (Clinical Research)
BA/BS
Exp: 1-2 year(s)
We have an exciting opportunity for beginning project manager to join our Tempe, AZ clinical team! As a Clinical Project Coordinator you work closely with our clinic operations team to ensure the success of our phase one clinical trials. Project Managers interpret study protocols to generate needed source documents, they add time and event codes into our systems to account for the needed tasks in a trial, they coordinate needed supplies for a given study and ensure we are ready to deliver. A background in clinical research or health care is a plus, but it is not required. We are seeking someone with well honed critical thinking skills, an ability to manage multiple projects at once, and well-developed time management skills. 9/1/2020
13 Celerion
Tempe, AZ
Research Laboratory Assistant -- FT -- 6AM-2PM Shift
AS/BS in a laboratory life science
Exp: 1+ year(s)
Research Laboratory Assistants handle human biological samples (primary blood and urine) and prepare them for routine testing and analysis. Additionally, they record raw data, transfer prepped samples to the onsite clinical laboratory, and barcode samples. This position is not involved in sample collection (i.e. phlebotomy). We are specifically seeking candidates with laboratory sample preparation and/or biological sample processing experience. This is a full time position scheduled for 40 hours per week with weekend availability expected. This position is slated to start on September 14, 2020. 9/1/2020
14 Celerion
Tempe, AZ
Fulltime Entry-level Lab Assistant
BS in a laboratory science
Exp: 1+ year(s)
Research Lab Assistants handle human biological samples (primary blood and urine) and prepare them for routine testing and analysis. Additionally, they record raw data, transfer prepped samples to the onsite clinical laboratory, and barcode samples. This position is not involved in sample collection (i.e. phlebotomy). If you have recently graduated with a laboratory-based science degree (i.e. Biology, Microbiology, Chemistry) and are looking to begin fulltime work at a clinical site, we'd love to speak with you! 9/1/2020
15 Celerion
Tempe, AZ
Research Laboratory Assistant -- FT --2PM-10PM Shift
AS/BS in a laboratory life science
Exp: 1+ year(s)
Research Laboratory Assistants handle human biological samples (primary blood and urine) and prepare them for routine testing and analysis. Additionally, they record raw data, transfer prepped samples to the onsite clinical laboratory, and barcode samples. This position is not involved in sample collection (i.e. phlebotomy). We are specifically seeking candidates with laboratory sample preparation and/or biological sample processing experience. This is a full time position scheduled for 40 hours per week with weekend availability expected. This position is slated to start on September 14, 2020. 9/1/2020
16 Celerion
Tempe, AZ
Research Laboratory Assistant -- FT --10PM-6AM Shift
AS/BS in a laboratory life science
Exp: 1+ year(s)
Research Laboratory Assistants handle human biological samples (primary blood and urine) and prepare them for routine testing and analysis. Additionally, they record raw data, transfer prepped samples to the onsite clinical laboratory, and barcode samples. This position is not involved in sample collection (i.e. phlebotomy). We are specifically seeking candidates with laboratory sample preparation and/or biological sample processing experience. This is a full time position scheduled for 40 hours per week with weekend availability expected. This position is slated to start on September 14, 2020. 9/1/2020
17 Celerion
Tempe, AZ
Entry Level Clinical Data Assistant (FT)
AS/AA/BS/BA
Exp: 1-2 year(s)
We seek an eager data entry master to join our data management team at our Tempe, AZ Phase 1 Research Clinic. This is a great entry-level opportunity to begin a career in clinical data management. This is a fulltime position, working 40 hours per week with shifts occurring onsite between 9AM-5PM, Monday-Friday. Essential Functions: Perform accurate data entry and verification for study specific External Studies, Celerion Standard, Spondor Provided EDC, and Sponsor Provided Paper CRFs (if applicable). Work with Clinical Data Manager for External Studies to create a working copy of the completed paper CRFs to ensure accurate and consistent data entry. Collate source data and signed disposition pages into final CRFs. 9/1/2020
18 CheminPharma
Woodbridge, 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. 9/1/2020
19 Codiak
Lexington, MA
Manufacturing Associate, Internal Drug Product Manufacturing
AS/BS in biology, chemistry, mechanical engineering, or related
Exp: 1-3 year(s)
The Manufacturing Associate, Internal Drug Product Manufacturing is a production position focused on the activities associated with a closed-RABS isolator drug product filling operation. The position will be heavily manufacturing floor-based during preparation and execution of drug product filling, inspection and labeling activities. This position will report to the Supervisor of Internal Drug Product Manufacturing and is expected to interact with Quality Assurance and Control, Facilities Operations and Materials Management groups. The position is based in Codiak’s new clinical manufacturing facility “CMF” in Lexington, MA. 9/1/2020
20 Bristol Myers Squibb
New Brunswick, NJ
Associate Scientist GQAST Pharma & Forensics
BS/BA
Exp: 1-3 year(s)
The Associate Scientist will be involved in hands on laboratory testing of foreign matter samples associated with manufacturing investigations, product quality complaint samples, and suspect product samples using spectroscopic techniques (NIR, Raman and mid-IR), microscopy, and wet chemistry methods. This work will cover the entirety of the BMS commercial portfolio, including both biologics and small molecule assets. They will provide analytical support to Global Quality, Corporate Security, External Manufacturing, and Manufacturing Operations, and to both internal and external sites as required. Duties: Support manufacturing investigations through characterization and identification of extraneous/foreign matter samples using relevant analytical techniques (mid-IR, Raman, SEM/EDS, microscopy). 8/26/2020
21 Bristol Myers Squibb
Devens, MA
Associate / Assistant Scientist
BS/MS in chemical engineering, bioengineering, biology or chemistry
Exp: 0-6 years
The Associate/Assistant Scientist within the Biologics Development - Upstream group will participate in the development and optimization of upstream processes for production of biologics at different clinical stages. The successful candidate will participate in the execution of bench-scale experiments using high-throughput, shake flask, or bioreactor cell culture systems to improve cell culture processes. Under general direction, the position requires participation in the design and execution of experiments, interfacing mainly with other upstream and occasionally with downstream and analytical personnel to achieve process development objectives. A successful candidate will work effectively in a cross-functional process development team and also be able to work independently to accomplish overall project goals. 8/26/2020
22 Brooks
South Plainfield, NJ
Part-time Night Shift Laboratory Technician
HS diploma/AS
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. 8/25/2020
23 Brooks
South Plainfield, NJ
Associate Bioinformatics Scientist
BS/MS in bioinformatics
Exp: 0-3 years
Responsibilities: Perform data analysis and generate reports for customer projects. Develop novel algorithms and build customized pipelines for clinical service projects. Build LIMS workflows for operation service lines. Evaluate and identify optimal NGS data analysis solutions. Conduct literature search for various genomics research areas etc. 8/25/2020
24 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. etc. 8/25/2020
25 BD
El Paso, TX
Quality Assurance Technician I
AS/AA in quality, life sciences, or engineering
Exp: 1 year for AS/AA candidates
This position is critical to the accurate evaluation of incoming materials, component, subassembly and finished product quality. Responsibilities include inspection, analysis of results, determining final disposition of some product and detecting nonconforming conditions. The Quality Assurance Tech I is also responsible for working within an established framework of compliance and developing and/or implementing improvements to product quality and the quality system. Principal Accountabilities: Inspect incoming and in-process materials, for compliance with established quality specifications. Work with production, receiving, and materials personnel to accurately complete required testing and documentation, determine correct disposition, and apply correct status labeling. Update material disposition status in SAP. etc. 8/25/2020
26 Solique
St. Cloud, MN
Optical Lab Operator (Distribution, 3rd Shift | 20% Shift Differential)
HS diploma or equivalent
Exp: 0-2 years
Performs routine production duties associated with various aspects of lens production paying close attention to quality, quantity and efficiency. This position focuses on our Freeform Surfacing area washing lenses, inspecting and taping lenses, matching tools, polishing, running generators, inspecting and coating (backside). Qualifies and inspects product to ensure compliance with CZV specifications and standards. Complies with all safety regulations as well as maintains a clean and safe work environment. etc. 8/26/2020
27 CRISPR Therapeutics
Cambridge, MA
Research Associate II, Analytical Development
MS
Exp: 1+ year(s)
We are seeking a highly organized Research Associate II 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, with a multi-functional skill set, such as developing and managing primary cell banks, execution of assays, as well as building a sample management system. The sample management aspect will be concentrated on the use of databases, such as Microsoft Access, Excel, and SharePoint and aid in organizing and keeping track of samples and internal distributions, where there is opportunity for movement. The cell banking aspect will focus on generating cell banks by isolating and characterizing primary cells from donor samples, complete donor screening, and work independently to support process development and product characterization. etc. 8/26/2020
28 Bio-Rad
Irvine, CA
Field Service Engineer
AS/BS in electronics or related
Exp: 0-2 year(s)
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 the Washington DC area traveling 50 – 75%. 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. 8/18/2020
29 BioReference Laboratories
Elmwood Park, NJ
Medical Lab Technician or Technologist, Hepatitis
BS in medical technology, chemistry, biology or related
Exp: 1 year
The Medical Laboratory Technician will perform all necessary laboratory testing in the detection, diagnosis, and prognosis of disease. The Medical Laboratory Technician will work collaboratively with the laboratory team to provide testing services to the clients. Additional tasks can be assigned at the discretion of the Supervisor/Manager/Director. Duties may include but are not necessarily limited to the following: Follows written lab procedures for the correct handling and processing of specimens. Performs lab procedures of moderate and high complexity in accordance with standards set forth in sectional laboratory procedures. etc. 8/18/2020
30 BioReference Laboratories
Columbus, OH
TEMP Medical Lab Technician or Technologist
BS in medical technology, chemistry, biology or related
Exp: 1 year
The Medical Laboratory Technician will perform all necessary laboratory testing in the detection, diagnosis, and prognosis of disease. The Medical Laboratory Technician will work collaboratively with the laboratory team to provide testing services to the clients. Additional tasks can be assigned at the discretion of the Supervisor/Manager/Director. Duties may include but are not necessarily limited to the following: Follows written lab procedures for the correct handling and processing of specimens. Performs lab procedures of moderate and high complexity in accordance with standards set forth in sectional laboratory procedures. etc. 8/18/2020
31 BioReference Laboratories
Elmwood Park, NJ
Medical Lab Technician or Technologist, Microbiology (FT, 40 Hours)
BS in medical technology, chemistry, biology or related
Exp: 1+ year(s)
The Medical Tech performs all laboratory procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. Duties may include but are not necessarily limited to the following: Maintain standards in routine & STAT testing. Complete work in a timely manner. Write legibly when documenting QC, problems or information. etc. 8/18/2020
32 BioReference Laboratories
Elmwood Park, NJ
Medical Lab Technician or Technologist, Overnight (FT, 40hrs per week)
BS in medical technology, chemistry, biology or related
Exp: 1+ year(s)
The Medical Tech performs all laboratory procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. Duties may include but are not necessarily limited to the following: Maintain standards in routine & STAT testing. Complete work in a timely manner. Write legibly when documenting QC, problems or information. etc. 8/18/2020
33 Bioventus
Stamford, CT
Associate Sales Rep - Biomedical - Stamford, CT
BS/BA in sports medicine, life science or a commercial discipline
Exp: 0-2+ year(s)
The Associate Sales Representative (ASR) is an entry level sales role at Bioventus. The ASR is primarily responsible for consulting with and providing clinical and technical information to healthcare professionals and their staff to achieve the sales objectives. Associate Sales Representatives will operate within company policies and procedures and demonstrate a high degree of compliant and ethical behaviors. Successful candidates should be open to relocation, at least to bordering states. Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. etc. 8/18/2020
34 Bristol Myers Squibb
Phoenix, AZ
Operator I, Aseptic
HS diploma or equivalent
Exp: 1 year
The Operator I is responsible for executing production activities required to successfully manufacture sterile injectable products. This is accomplished by ensuring equipment, materials, and other resources are in place to meet production demands. The Operator I demonstrates and assures production activities within manufacturing operations are executed following all GMP’s. In addition, work will be performed in complete accordance with all SOPs, Specifications, Batch Records, regulatory expectations, and company policies. This position will require overtime, shift work, and flexibility in scheduling of “set” shift hours at times, based on production demands or extraordinary circumstances. etc. 8/18/2020
35 Bristol Myers Squibb
Syracuse, NY
Assistant Scientist
BS in a biological science
Exp: 0-3 years
Duties/Responsibilities: Perform laboratory analysis of samples, using aseptic technique, following established procedures and in full compliance with official compendial, health authority regulations, and established BMS policies. Conduct qualification of methods and/or other laboratory studies, according to scientific protocols. Maintains accurate records of work performed and documents results, according to Good Documentation Practices and established procedures as well as perform data entry into LIMS, MODA and LES. Assist with review of worksheets and laboratory data as assigned. Assists in the investigation of OOS results in areas of assigned responsibility. Operates and maintains laboratory instruments, while ensuring the reliability of instrumentation through proper maintenance, with ability to troubleshoot minor issues. Must analyze, evaluate, and interpret data, notifying clients of results, and assisting to resolve issues, if applicable. etc. 8/18/2020
36 Bristol Myers Squibb
Syracuse, NY
Dispensary Warehouse Technician I
BS/BA
Exp: 1+ year(s)
The primary role of the Dispensary Warehouse Technician is to perform functions relevant to Warehouse, Dispensary, and staging activities in the manufacturing facility. Core functions include Receiving materials, Material Transfers, SAP functions for inventory control, dispensing, material returns, and raw material sampling. Related activities include supply upkeep, cleaning, and bulk chemical transfers. All operations are to be performed in a safe and compliant manner. Duties/Responsibilities: Accurate receipt and unpacking of all process related direct inventory materials, indirect supplies, miscellaneous equipment, and material transfers. Including wipe down processes, SAP transactions, and proper storage adherence. Material transfers and movements from location to location. etc. 8/18/2020
37 Bristol Myers Squibb
Summit, NJ
Manufacturing Associate, CAR-T
BS/BA
Exp: Not necessary for bachelor's candidates
Manufactures human blood derived components per Batch Record and Standard Operating Procedures in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Duties and Responsibilities: Production of blood component lots through selection, activation, transduction, cell culture, harvest, and cryopreservation. Aseptic technique is required for most activities: tube welding, connections, and transfers, at minimum. Weighs and measures in-process materials to ensure proper quantities are added/removed. Adheres to the production schedule ensuring on-time, internal production logistics. etc. 8/18/2020
38 Icon
Raleigh, NC
Associate Project Manager Translations
BS/BA in languages/translations
Exp: 1-3 years in translation
As Translation Associate Project Manager you are responsible for the coordination, execution, control and completion of single service projects ensuring consistency with ICON SOPs, service-line best practices, project contracts and budgets. Lead the planning and implementation of single service projects. Define project tasks and resource requirements based on project plans 8/16/2020
39 Icon
Knoxville, TN
CRA I
BS/Ba
Exp: 12 months as an independent monitor
As a Clinical Research Associate I 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 - III, ensuring adherence to applicable regulations and principles of ICH-GCP. 8/16/2020
40 Icon
Raleigh, NC
Clinical Research Associate II
BS/BA in healthcare/sciences
Exp: 12-18 months as independent monitor 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. 8/16/2020
41 Immucor
Norcross, GA
Medical Laboratory Technologist
Associates or BS/BA
Exp: 6-12 months related experience
As a Medical Technologist, you will perform all assigned tasks following applicable laboratory SOPs, OSHA regulations and cGMP regulations (i.e. blood borne pathogens and chemical hazards). You will assist the department supervisor and/or manager with investigations, root cause analyses, and reports of out-of-specification results and deviations. You will also be responsible for maintaining and compiling Device History Records. 8/16/2020
42 Immucor
Warren, NJ
Manufacturing Associate
Assocites
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. Formulating custom bulk reagents - involves working with pipettes and balances 8/16/2020
43 Immucor
Norcross, GA
Production Technician
HS Diploma/GED or AS in technical discipline
Exp: 0-2 years in clean room environment
As a Production Technician, you will perform tasks and administrative aspects regarding packaging operations according to department procedures, specifications or work instructions. This includes starting up/breaking down operations, clearing operations areas, calculating component usage, verifying counts of products in and out of operations, and visual inspections of products for defects. 8/16/2020
44 Immucor
Waukesha, WI
Production Chemist
BS/BA in chemistry/life sciences
Exp: 0-2 years working with automated filling equipment a plus
As Production Chemist, you will be responsible for subassembly formulation, raw material preparation and/or processing, QC testing reagent or component formulation, and some in-process testing. You will manage the development, planning, and implementation of manufacturing methods, processes, and operations for new or existing products or technologies. 8/16/2020
45 Bayer
Jerseyville, IL
Agronomic Research Specialist
MS/MA
Exp: 0-2 years
The primary responsibilities of this role, Agronomic Research Specialist II, are to: Be 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; Collaborate with project team members to deliver detailed experimental protocols that enable advancement decisions by our scientists and placement decisions to our customers; etc. 8/11/2020
46 Bayer
Kansas City, MO
R&D Specialist II-Product Support
MS in chemistry, biology, engineering or related
Exp: Not necessary for MS candidates
The primary responsibilities of this role, R&D Specialist II, are to: Provide development expertise for new formulations by providing Pilot Scale knowledge and advise and Startup assistance for production plants; Assist Product Supply and Supply chain by performing studies related to product quality and assurance of supply; Prioritize and can coordinate work within a large team; Provide training to third party reports; Maintain detailed record keeping and required documentation; Be accountable for cross-functional work within platform and/or across process areas; etc. 8/11/2020
47 Beckman Coulter Diagnostics
Chaska, MN
Scientist I Production Operations
BS in biology, microbiology, or related
Exp: 0-2 years
Key Responsibilities: Read, comprehend and follow established work instructions and procedures with emphasis on quality. Execute the daily production plan to due date conformance and quality standards. Train to Standard Operating Procedures (SOPs). Follow engineering drawings, work order information, SOPs, and other written and verbal specifications in the manufacturing process while maintaining FDA requirements. Handle a variety of cell lines with a strict attention to detail while working aseptically. Independently execute work regarding maintenance of cell cultures, processing cellular material and releasing builds according to schedule. Apply basic analytical skills, critical thinking and scientific methods to perform daily tasks. Perform the set-up, calibration, testing and troubleshooting of instruments, such as large-scale bioreactor systems. Assure compliance with FDA Quality System Regulations (QSR), Good Manufacturing Practices (GMP), and ISO regulatory requirements. etc. 8/11/2020
48 Beckman Coulter Diagnostics
Chicago, IL
Field Service Engineer - Laboratory Instrumentation and Automation: Chicago
AS/BS
Exp: 1-3+ year(s)
Beckman Coulter Diagnostics Field Service Engineers provide excellent customer service to clients while installing and maintaining diagnostic instrumentation and systems in hospital and stand-alone laboratory environments. As a Field Service Engineer (FSE) you will be the face of Beckman Coulter to customers and support them, directly impacting patient health and overall well-being. Would you like to be part of a team providing front line support to hospital laboratories? Are you ambitious and seeking to drive healthcare forward? The Field Service Engineer in this position will: Under minimal supervision, serve as lead to assigned customers; complete troubleshooting, installation, validation, maintenance, and service repair needs on designated equipment. May assist and/or train newer Field Engineers. Provide excellent and efficient service to Beckman Coulter’s customers, along with technical training on products. Repair, maintain, and install product line(s). etc. 8/11/2020
49 Beckman Coulter Diagnostics
Louisville, KY
Field Service Engineer-Louisville, KY
AS/BS
Exp: 1-3+ year(s)
Beckman Coulter Diagnostics Field Service Engineers provide excellent customer service to clients while installing and maintaining diagnostic instrumentation and systems in hospital and stand-alone laboratory environments. As a Field Service Engineer (FSE) you will be the face of Beckman Coulter to customers and support them, directly impacting patient health and overall well-being. Would you like to be part of a team providing front line support to hospital laboratories? Are you ambitious and seeking to drive healthcare forward? The Field Service Engineer in this position will: Under minimal supervision, serve as lead to assigned customers; complete troubleshooting, installation, validation, maintenance, and service repair needs on designated equipment. May assist and/or train newer Field Engineers. Provide excellent and efficient service to Beckman Coulter’s customers, along with technical training on products. Repair, maintain, and install product line(s). etc. 8/11/2020
50 Beckman Coulter Diagnostics
Brea, CA
Systems Engineer II
MS in electrical, mechanical, biomedical, or related engineering
Exp: 0-2 years
We are looking for an engineer to be part of our Clinical Diagnostics Chemistry and Immunoassay Instrument R&D group in Brea, CA. This is an exciting product development opportunity where the primary responsibility will be to perform the following Systems Engineering functions. In this role, you will have the responsibility to: Collect appropriate data to define, identify, analyze, correct and prevent potential system failures. Develop test plans and conduct bench and system level testing that cover the expected customer use environment and operation conditions. Analyze and develop system and sub-system requirements and relationships with component specifications. Analyze, summarize, present, and interpret experimental data to formulate conclusions and make recommendations. etc. 8/11/2020
51 BioAgilytix
Durham, NC
Business Development Assistant (temporary)
BS in biological science, business administration or related
Exp: 1+ year(s)
Essential Responsibilities: Schedules initial teleconferences with relevant prospects for the Business Development team through cold calling and personalized email messaging; uses established contact lists, email templates, and call scripts to send 300+ emails and make 200+ calls per week. Tracks all activities and ensures meetings scheduled are properly inputted into CRM system (Salesforce). Performs administrative support work specific to sales and marketing departments. Other duties as needed. etc. 8/11/2020
52 BioAgilytix
Durham, NC
Analyst, Business Development
BS/BA in business administration, finance, marketing or related
Exp: 0-2 years
The Business Development Analyst will identify, analyze, and interpret trends in complex data sets and complete internal reporting on key sales metrics. He or she will present insights and recommendations in a consultative manner to internal stakeholders. Essential Responsibilities: Maintains schedules and completes routine internal reporting on key sales metrics. Prepares and provides supporting analysis for month-end, quarter-end, and year-end reporting and metrics. Generates sales performance dashboards and reports using SalesForce. etc. 8/11/2020
53 BioAgilytix
Boston, MA
Analyst
BS/MS in molecular biology, biochemistry, immunology or related
Exp: 1 year
Essential Responsibilities: Prepare worksheets with minimal supervision. Prepare plate maps. Serve as lead analyst on sample analysis projects. Troubleshoot assays. Compile/process data (make power export). Prepare summary tables. Peer review raw data. Order reagents. Participate in assay development and validation. Run assays independently. Adhere to provided method/directive. Prepare buffers. Use LIMS system. Participate in sample analysis. Pipetting. etc. 8/11/2020
54 BioAgilytix
Durham, NC
Analyst
BS/MS in molecular biology, biochemistry, immunology or related
Exp: 1 year
Essential Responsibilities: Prepare worksheets with minimal supervision. Prepare plate maps. Serve as lead analyst on sample analysis projects. Troubleshoot assays. Compile/process data (make power export). Prepare summary tables. Peer review raw data. Order reagents. Participate in assay development and validation. Run assays independently. Adhere to provided method/directive. Prepare buffers. Use LIMS system. Participate in sample analysis. Pipetting. etc. 8/11/2020
55 Biogen
Cambridge, MA
Associate Scientist II, Technical Development
MS in biology, molecular biology, biochemistry or related
Exp: 0-3 years
We are seeking a highly motivated individual with mammalian cell culture experience, a background in molecular or cellular biology, and a strong interest in automation to join our Cell Line Development Team. Our group is focused on generating industry-leading cell lines for clinical and commercial programs. The candidate’s goals will be to engineer highly productive cell lines that enable fast-tracked program timelines that rely upon plasmid construction, transfection, cloning, high-throughput cell culture platforms, and ambr bioreactors. Additionally, the individual will be empowered to explore technology improvements geared toward advancing efficiency, with special consideration given to candidates with experience or passion for working with automation for custom needs as we push to expand throughput, implement novel production cell lines, develop continuous screening and integrate multi-level omics understanding. etc. 8/11/2020
56 Biogen
Research Triangle Park, NC
Patient Services Coordinator
BS/BA
Exp: 1-2 year(s)
The primary role of the Patient Service Coordinator is to facilitate the customer lifecycle by assisting patients, healthcare providers and others with activities related to starting and staying on therapy. Patient base includes both newly diagnosed and existing Alzheimer patients. Daily interactions involve contact via phone not only with patients but also health care providers, Biogen field force representatives, business service partners, nursing services and other internal work groups. The competitive candidates will have an ability to utilize strong interpersonal skills that will allow for the support and education of patients in their disease state, understanding of medical benefits, Biogen product education and the offering of service option explanations. etc. 8/11/2020
57 Biogen
Cambridge, MA
Engineer I, Pilot Upstream, Gene Therapy
BS/MS in bioengineering, biochemical engineering, biochemistry or related
Exp: 0-2 years
The successful candidate will join a team of scientists responsible for the development of scalable cell culture and purification processes used for the clinical and commercial manufacturing of adeno-associated virus (AAV) gene therapy vectors. Success in this position will require the candidate to independently plan and execute projects and experiments across multiple viral vector and precursor production platforms to support pilot-scale material generation runs and to effectively collaborate with different groups within Gene Therapy and Process Development. Candidates must be motivated and innovative with exceptional analytical and communication skills. etc. 8/11/2020
58 Biogen
Cambridge, MA
Associate Scientist III, Gene Therapy - Formulation and Drug Product Development
MS
Exp: 0-2 years
As a member of Biogen’s Gene Therapy Drug Product development team, the candidate will be responsible for providing analytical, formulation and process development support for drug product development programs. Conducting laboratory studies, both in-house and through external contract laboratories is a requirement of the position. Candidate is expected to work collaboratively in a matrix environment with other members of the gene therapy development team. Essential Responsibilities: Execution of formulation and process development study protocols, stability and product characterization studies with adeno-associated viral vectors. Performing analytical characterization of study samples using various biochemical or biophysical methods. etc. 8/11/2020
59 Biogen
Cambridge, MA
Associate Scientist II/III – Fluid Biomarker Assay Development
MS
Exp: 1+ year(s)
The Fluid Biomarkers group (Section of Clinical Sciences) is seeking a creative and collaborative lab-based scientist engaged in targeted proteomics for the detection of proteins and metabolites in different biological matrices (including plasma, serum, CSF, urine, tissues. This role is required to develop and implement clinically robust LC-MS assays to support clinical programs across the Neurology portfolio. The successful candidate will be capable of multitasking and effective planning to consistently meet deadlines. Responsibilities: Targeted protein biomarker assay development using state of the art liquid-chromatography-mass spectrometry (LC-MS) platforms including nano-LC, orbitrap (Q-Exactive, Q-Exactive +, Q-Exactive HF/HFX, Fusion) and UPLC-QQQ MS (AB Sciex). Sample preparation (tissues and cell lysates) for protein quantification. Biotinylation and various bead-antibody conjugation techniques. etc. 8/11/2020
60 Biogen
Cambridge, MA
Associate Scientist II, Gene Therapy - Cell Line Technology
BS in biology
Exp: 1 year
The successful candidate will work efficiently with team members and independently to plan, conduct, analyze, and document experiments to drive innovation in a cutting-edge modality. Qualifications: Team player with ability to execute tasks independently. Skilled molecular biologist (cloning, PCR, plasmid generation). Experience with mammalian cell culture (aseptic technique, proficiency with suspension cell culture, and experience with high-throughput cell culture desired). Proven track record of successfully planning, executing, and troubleshooting projects and experiments. Demonstration of strong organizational skills. Excellent written and verbal communication skills. etc. 8/11/2020
61 Biogen
Research Triangle Park, NC
Mechanic II, Maintenance (Drug Product Facility)
BS/BA
Exp: 1 year
Major Responsibilities Include: Collaborate with Responsible Engineers and Manufacturing personnel to troubleshoot equipment problems. Provide customer-oriented service and support in a fast-paced manufacturing environment. Sterile Filling equipment Isolators, Cartoner, labeling, Ink Jet Printers Automatic Vial Inspection equipment. Suggest practical changes or improvements to equipment and department work practices. Complete all assigned corrective work orders and Preventative Maintenance work with attention to detail and maintaining required GMP documentation. Follow Standard Operating Procedures in performance of assigned duties. Support manufacturing operations 12/7. etc. 8/11/2020
62 Harvard Bioscience
Holliston, MA
Manufacturing Engineer
BS/BA
Exp: 0-2 years in electro-mechanical assemblies
The qualified candidate will work within a multi-disciplinary team of engineers on DFM, cost reduction, and transfer to production activities. Work closely with assemblers and production leaders to improve manufacturability. Investigate quality issues for engineering improvements. Work closely with operations on design improvement and continuous improvement initiatives. 8/9/2020
63 Heska
Loveland, CO
Accounts Receivable Clerk I
HS Diploma/GED
Exp: 6 months
Under the direct supervision of the AR Supervisor, the Accounts Receivable Clerk I will answer and responds to incoming customer calls and email requests. This position will regularly assist with making outbound calls to past due accounts as well as invoice processing, filing and sorting monthly statements, as needed. 8/9/2020
64 Homology Medicines
Bedford, MA
Research Associate - Molecular Analytical Development (6 Month Contract)
MS in biological sciences
Exp: 0-4 years
The individual in this role will be a talented and motivated technician who will focus on the analysis of research/development-grade vector samples using multiple AAV-specific analytical methods. This is a largely laboratory-based position with a focus on providing analytical support for characterizing research-grade vectors. 8/9/2020
65 Hovone
Hovione, NJ
Process Engineer
BS in chemical science or engineering
Exp: 1-3 years in industrial operations
At Hovione, a Process Engineer's job mission is to ensure the best process engineering knowledge is applied in scaling up chemical and spray drying projects to maximize customer satisfaction ad Hovione's interests and in compliance with all Federal, State, Local and internal policies. It also includes the development of process engineering technical skills to increase the knowledge and offering on the best and state of the art technologies used in the industry. 8/9/2020
66 HTG
Tucson, AZ
Helpdesk Technican
Working towards degree in comp sci or IT
Exp: 1+ years
The Helpdesk Technician’s primary responsibility is to manage all daily operations of the Helpdesk, including but not limited to troubleshooting and resolving inbound tickets, collecting additional information, documenting steps taken, and escalating to other Information Technology team members. The Helpdesk Technician will be challenged to research new issues and increase working knowledge of IT systems through on the job training and mentorship. 8/9/2020
67 Hemosconics
Durham, NC
Cartridge Automation Technician
BS/BA
Exp: 1 year in regulated manufacturing environment
Setup and Shutdown of all equipment associated with the automation line per applicable Work Instruction. Operation of automation equipment in a controlled manufacturing environment. Completion of batch-related documentation in a timely manner and in accordance with regulatory requirements. 8/9/2020
68 Harpoon Therapeutics
South San Francisco, CA
Clinical Trial Assistant
BS/BA in biological sciences
Exp: 1 year in clinical research
Maintain and/or accelerate timelines for achieving clinical operational milestones. File, track and maintain study activity. Manage and ensure the paper and electronic Trial Master File (eTMF) meets FDA/ICH/GCP requirements. Coordinate execution of Non-Disclosure and Confidentiality Agreements (NDAs and CDAs) with study sit 8/9/2020
69 Harpoon Therapeutics
South San Francisco, CA
Research Associate, Protein Expression
BS/BA or MS in biological sciences
Exp: BS: 1-5 years, MS: 1-3 years
Stable and transient transfections of mammalian cell lines. Cryopreservation of cell lines and clarification of conditioned medium. SDS-PAGE, Octet BLI, and Western blot analysis of purified proteins. Materials management and inventory database maintenance. Maintenance of electronic lab notebook and databases, preparation of reports, and regular presentations to summarize results and update management 8/9/2020
70 Baxter
Opelika, AL
Quality Lab Tech I
BS in chemistry or biological sciences
Exp: 0-2 years
Performs required tests in the performance, microbiological, and chemical labs on finished dialyzers and raw materials to support product acceptance. This includes performing analyses, calibrations and maintenance on multiple lab equipment/instruments and entering results in MES. May assist with environmental and process media monitoring by taking samples and testing as required by defined procedure. Maintains cleanliness of labs and lab instruments. Analyze issues on out of specification (OOS) conditions and unusual trends and immediately initiate NCR or deviation and notify Lab Supervisor/Quality Engineer and/or QRM Manager. Orders and maintains lab supply stock (reagents, chemicals, standards etc.) to maximize efficiency. etc. 8/5/2020
71 Baxter
Round Lake, IL
Research Associate I
BS
Exp: 1-3 year(s)
Essential Duties and Responsibilities: Perform microbiology testing in support of medical device and pharmaceutical projects. Record data and assist in the preparation of documentation using Good Documentation Practices (GDP). Support the maintenance of microbiological laboratories and equipment. Understand and apply applicable corporate and divisional Standard Operating Procedures (SOP). Under direction, conduct routine research and/or developmental activities. Plan details of assigned tasks within specific parameters. etc. 8/5/2020
72 Baxter
Alliston, ON
Associate I, Quality Operations
BS in microbiology, chemistry, biological sciences, or engineering
Exp: 1-3 year(s)
Responsible for maintaining Quality and Compliance by ensuring product and manufacturing operations conform to Specification, Standard Operating Procedures and Regulatory Standards (Health Canada & FDA). ESSENTIAL DUTIES AND RESPONSIBILITIES: Provide front line day to day support on product quality issues to ensure GMP, regulatory and procedural compliance to maintain high standards of quality. Support the day shift, with requirement to support plant overtime and planned shutdowns when applicable. Provide technical support on product quality issues. Partner with Quality and Production personnel to ensure mitigating actions are identified and implemented. Support timely follow-up on quality exceptions and their preventative/corrective actions. etc. 8/5/2020
73 Baxter
Alliston, ON
Associate I, Quality Operations - Weekend Days
BS in microbiology, chemistry, biological sciences, or engineering
Exp: 1-3 year(s)
Responsible for maintaining Quality and Compliance by ensuring product and manufacturing operations conform to Specification, Standard Operating Procedures and Regulatory Standards (Health Canada & FDA). ESSENTIAL DUTIES AND RESPONSIBILITIES: Provide front line day to day support on product quality issues to ensure GMP, regulatory and procedural compliance to maintain high standards of quality. Support the day shift, with requirement to support plant overtime and planned shutdowns when applicable. Provide technical support on product quality issues. Partner with Quality and Production personnel to ensure mitigating actions are identified and implemented. Support timely follow-up on quality exceptions and their preventative/corrective actions. etc. 8/5/2020
74 Astella
Seattle, WA
Research Associate II, Analytics
MS
Exp: 0-2 years
The primary purpose of Research Associates working in Analytics (RA II and Senior RA) for our Core Technologies Department is to support the molecular engineering of our gene edited Universal Donor Cells. They will work as a key member on a fast-paced team to develop molecular and cellular assays to characterize our proprietary Universal Donor Cells. Essential Job Responsibilities: Developing and routinely executing standard analytical assays including genotyping PCR/qPCR and flow cytometry. Performing standard molecular biology techniques including primer design, molecular cloning, and Sanger sequencing. etc. 8/4/2020
75 AstraZeneca
Gaithersburg, MD
R&D Associate I/II - Purification Process Sciences
BS/MS in biochemistry or chemical engineering or related
Exp: 0-2+ years
The successful candidate will: Develop and characterize downstream processes for the manufacture of biopharmaceuticals (monoclonal antibodies and other proteins) in late stage clinical development through commercial launch. Be responsible for a portion of a purification development project. Make observations, analyze data and interpret results. Maintain accurate records of experimental results, review, analysis, and interpretation of experimental data. Make periodic presentations in group meetings, project team meetings, and in one-on-one situations. Prepare/review development reports, tech transfer and process validation documents, regulatory submissions. etc. 8/4/2020
76 Avion Pharmaceuticals
Wichita Falls, TX
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, Rheumatology, 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. 8/4/2020
77 Avion Pharmaceuticals
Tallahassee, FL
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, Rheumatology, 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. 8/4/2020
78 Avion Pharmaceuticals
Lynchburg, VA
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, Rheumatology, 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. 8/4/2020
79 Avion Pharmaceuticals
Cherry Hill, NJ
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, Rheumatology, 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. 8/4/2020
80 Avion Pharmaceuticals
Alphretta, GA
Inside Sales Representative
AS/AA/BS/BA
Exp: 1 year
The Inside Sales Representative/ Customer Service Associate will assist the Sales & Marketing function by building a rapport and strong relationships that are necessary to increase sales and product placement for Avion's product portfolio. We are looking for a positive and motivated individual who would be passionate about our company and product portfolio. The ideal candidate will also have excellent customer service, communication, and organizational skills. ESSENTIAL DUTIES AND RESPONSIBILITIES: Initiate introductory calls with the objective of developing a long-term business relationship with customer accounts (70% doctors and 30% pharmacies). Build, sustain & maximize customer relationships through timely routine contact with new and existing customers. etc. 8/4/2020
81 Assembly Bio
Groton, CT
Contract Lab Technician I/II (Microbiome)
AS/AA
Exp: 0-2 years
The Laboratory Technician I or II, Drug Substance Process Development (Microbiome) will provide support functions in the development and qualification of robust processes for production of human commensal bacteria suitable for use as therapeutic agents. The individual will assist laboratory operations by preparing media, equipment, and executing housekeeping duties such as autoclaving, according to written procedures. Documentation of these duties in laboratory notebook systems is expected. Key Responsibilities include: Follow written procedures for consistent and reliable preparation of complex media recipes. Documentation in laboratory notebook systems. etc. 8/4/2020
82 Gritstone Oncology
Cambridge, MA
BIOREPOSITORY TECHNICIAN CONTRACTOR (Specimen Management)
AS/AA or BS/BA in sciences or healthcare
Exp: 1-2 years in lab setting
The Biorepository Technician Contractor is directly responsible for supporting the manufacturing and research labs under the direction of the Translational Medicine Operations function at Gritstone. The Contractor performs a variety of tasks associated with the tracking, receipt, storage, maintenance and retrieval of biospecimens collected as part of Gritstone’s research programs. 8/2/2020
83 GSK
St. Louis , MO
Manufacturing Material Handler
HS Diploma/GED
Exp: 1-5 years in production
Ensure quality and compliance in accordance with established procedures and standards of the Quality System. Locate finished tablets bins and correctly stage and issue bins as needed to support packaging department. Locate and transport raw materials to floors as needed. Collect, transport, and cleanout empty bins. Support the removal of trash and waste on an as needed basis. Fill blending dump stations as required. Fill preweigh intermediate bulk containers as required. 8/1/2020
84 GSK
Lincoln, NE
HVAC Technician (2nd Shift)
Associates in HVAC technology
Exp: 0-3 years
As a GMP system owner, the HVAC Technician is responsible to maintain a compliant state, troubleshoot, inspect, repair and document work on core facilities equipment or systems that support the manufacture and packaging of over the counter, dietary supplement and medical device products. 8/1/2020
85 Globus Medical
San Antonio, TX
Manufacturing Technician
HS Diploma/GED
Exp: 1 year in manufacturing
The Manufacturing Technician is responsible for performing human tissue processing activities in accordance with FDA regulations, AATB Standards and SOPs. Preparing sections of human tissue for surgical implantation. Utilizing special techniques, instrumentation, and equipment to evaluate, cut, shape, grind and package tissue to exacting specifications and protocols 8/1/2020
86 Globus Medical
San Antonio, TX
Manufacturing Technician
HS Diploma/GED
Exp: 1 year in manufacturing
The Manufacturing Technician is responsible for performing human tissue processing activities in accordance with FDA regulations, AATB Standards and SOPs. Preparing sections of human tissue for surgical implantation. Utilizing special techniques, instrumentation, and equipment to evaluate, cut, shape, grind and package tissue to exacting specifications and protocols 8/1/2020
87 Grail
Menlo Park, CA
Research Associate 1/2
BS/BA in biological or chemical sciences
Exp: 1-2 years in BSL2 labs
As a Research Associate in GRAIL’s R&D Group, you will play an integral role in the development of technology and workflows for genomics-based clinical assays. The ideal candidate should be detail-oriented and have experience with blood processing, nucleic acid extraction, and strong molecular biology skills. 8/1/2020
88 Grail
Menlo Park, CA
Process Engineer 1/2 (Equipment Qualification)
BS or MS in biological sciences or engineering
Exp: 1-4 years in process engineering/R&D in med/pharma
Design and characterize new laboratory equipment qualification processes within an NGS setting. Participate in the development of product plans, evaluation of processes and process risk, and development of project timelines. Develop and execute qualification studies for new and existing equipment in accordance with ISO standards. 8/1/2020
89 Grail
Menlo Park, CA
Core Services Research Associate 1/2
BS in relevant
Exp: 1+ years in NGS
Execute on forecasted R&D experiments ranging from reagent evaluation and qualification to general data generation activities. Execute on automated and manual sample preparation and NGS assays. Be responsible for accurately recording work performed per GLP, including results and methodology. 8/1/2020
90 Grand River
Grand Rapids, MI
QC Biochemist I
BS/BA in chemistry
Exp: 0-3 years in pharma
Responsible for supporting quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties will include, but are not limited to, providing general laboratory support for raw material, in-process, stability, and finished product testing. Perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients, excipients and finished pharmaceutical products. 8/1/2020
91 Globus Medical
Audubon, PA
Regulatory Associate
BS/BA in health or sciences, engineering is a plus
Exp: 0-2 years in med devices
The Regulatory Affairs Associate assists in drafting, submitting and gaining clearance for 510(k) submissions, and approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products. This position entails development of FDA submissions, requiring working knowledge of products under review and of relevant regulations and guidance documents. 8/1/2020
92 Abbvie
Lake County, IL
Pharmacy Technician
HS diploma/AS/AA
Exp: 1+ year(s)
The Pharmacy Technician position exists to support the pharmacist(s) in completing the duties associated with entering and managing drug therapy orders, fulfilling, and dispensing prescriptions, maintaining pharmacy records and other professional activities. This position is responsible for collaborating with and supporting Pharmacy Leads and Supervisors in day to day activities, issue resolution, and completion of project tasks. Responsibilities: Assist the pharmacist with practice of pharmacy in accordance with federal, state and local regulations, HIPAA guidelines, corporate and departmental policies and procedures. Assist pharmacists in the picking, labeling, packing and shipping of orders; by accurately interpreting healthcare provider’s prescription orders and entering it into the core pharmacy system; etc. 7/28/2020
93 APi
North Augusta, SC
QC Associate Microbiologist I or II
BS in microbiology or other life sciences
Exp: 1-5 year(s)
Primary Responsibilities: Sampling and testing of city and pharmaceutical grade water per USP guidelines, SOP and Test method for bioburden, TOC, conductivity and endotoxin. Testing of product for release and stability for bioburden and endotoxin per USP guidelines, Test Method and SOP; endotoxin testing includes gel clot, chromogenic and turbidimetic. Bioburden testing includes method verification per USP <61>. Environmental monitoring sampling (viable and non-viable) per USP guidelines and SOP, as scheduled (daily, weekly, monthly, quarterly). Support production in qualification of clean rooms and water systems. Data entry for trending reports. etc. 7/28/2020
94 APi
North Augusta, SC
MFG Cleaning Technician
HS diploma or equivalent
Exp: Entry level
Perform scheduled cleaning of all water rooms. Perform scheduled cleaning of all Lyophilizer mechanical area. Help perform daily POU Flushes and twice a week POU Sanitizations. Perform any non-GMP cleaning as assigned. Must have good time management skills. Must be able to perform daily tasks in a timely manner – improving productivity while minimizing idle time. Follow approved GMP manufacture directions such as standard operating procedures and other instructions for in support of production. Responsible for documenting all production operations and cleaning activities in logbooks and/or batch records. etc. 7/28/2020
95 ARL BioPharma
Oklahoma City, OK
Sample Administrator I - Part Time
HS diploma or equivalent
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 other duties requested by the Accessioning Supervisor. Minimal to moderate supervision is required. etc. 7/28/2020
96 Acella Pharmaceuticals
Dallas, TX
Pharmaceutical Sales Representative (NP)
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. Responsible for providing healthcare providers with all relevant information that promotes quality healthcare decisions. Employ effective selling techniques, including pre-call planning, effective opening, presentation focus, productive questions, issues identification and effective close. etc. 7/22/2020
97 Acumed
Wichita, KS
Sales Associate, Wichita, Kansas - Future Opportunities
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. 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. 7/22/2020
98 Acumed
Hillsboro, OR
Quality Engineer I
BS in engineering or a science
Exp: 1-3 year(s)
The Quality Engineer is responsible for providing Quality Assurance support to product development and manufacturing to increase product quality, reliability, and process capability. Responsible for identifying, documenting, assessing, correcting and presenting quality issues using risk and root cause analysis tools. Supports quality of new products being released to the market through participation in the product development process to ensure product and process conformance to global standards (including FDA and ISO 13485). Serves as a quality representative to design control, verification and validation, design transfer, and risk management on assigned product development teams ensuring compliance with Acumed policies and global regulations, including FDA Quality System Regulation and ISO 13485. etc. 7/22/2020
99 Acumed
Kansas City, KS
Associate Sales Representative - Kansas City, KS
BS in engineering or a science
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. Duties/Responsibilities: Execute business plans to identify and close new business. Identifies the needs of new prospects and develops/delivers appropriate responses to meet or exceed needs (written, telephone and face-to-face). etc. 7/22/2020
100 Adare Pharmaceuticals
Vandalia, OH
Document Control Specialist I
BS/BA
Exp: Not necessary for BS/BA candidates
Responsible for conducting day to day quality documentation processing for cGMP documents, and provide support to internal end users on document management processes. ESSENTIAL DUTIES AND RESPONSIBILITIES: The primary duties and responsibilities of this position include the following. Other duties may be assigned. Formats, tracks and issues controlled cGMP documents. Assist in review of cGMP controlled documents as necessary. Issuance of batch production records, tracking of master batch records, and tracking of all batch production records. Supports quality audits (internal and external), troubleshooting efforts, and other Quality System processes. Evaluates issues received from end users and makes decision on appropriate follow-up steps. Scan, image, organize and maintain documents, adhering to the company's document lifecycle procedures, and they archive inactive records in accordance with the records retention schedule. Maintains filing of all master documents. Maintains an efficient and easily retrievable documentation system for all the documents. etc. 7/22/2020
101 Ajinomoto Bio-Pharma Services
San Diego, CA
Temporary Drug Product Support Technician
HS diploma
Exp: 0-1 year(s)
We are currently seeking multiple Temporary Drug Product Support Technicians to join the team. In this role you will be responsible for packing and labeling and offload activities for our various drug products. Responsibilities: Operates filled drug product offloading equipment. Accurate receipt and counting of filled units from Fill Finish manufacturing. Responsible for product transfers to Materials Management. Responsible for assisting with pre and post Line Clearance, and Good Documentation Practices (GDP). H24Perform Bulk Packaging and Labeling of Vials or Syringes. Follow all proper gowning procedures. etc. 7/22/2020
102 Ajinomoto Bio-Pharma Services
San Diego, CA
Drug Product Manufacturing Assistant
HS diploma/BS in a life science
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. Operates production equipment and may prepare buffers and media, inspect, label, or box. etc. 7/22/2020
103 Agilent
Santa Clara, CA
Business Process Associate
BS/BA/MS/MA
Exp: 1+ year(s)
The Business Process Associate role reports into the Global Sales Enablement (GSE) team, which supports LSS Global Sales and Marketing functions. This team collaborates cross-functionally with sales, marketing, service, SUs and other supporting organizations, to effectively execute strategic LSS and Corporate programs across the world. We're looking for a talented and motivated professional to join the team. Responsibilities include: Responsible for analysis and evaluation of user business problems and development of business system or process recommendations to meet requirements, including problem definition, evaluation of requirements, and implementation of systems/processes. etc. 7/22/2020
104 Alcami
Charleston, SC
Environmental Monitoring Tech I- 3rd Shift
BS/BA
Exp: 0-2 years
The Environmental Monitoring Technician I is accountable for results in a fast-paced environment. The Level I Technician follows applicable SOPs and cGMPs to perform environmental monitoring for the facility, and may also perform simple, routine basic interpretation of environmental monitoring (EM) results, typically under supervision. This position is also responsible for hazardous waste and sanitation/cleaning of the Microbiology laboratory. The position requires strong leadership behaviors of the Alcami core competencies and non-negotiables, as well as the functional competencies of this profile. Essential Functions: Performs routine daily, weekly and monthly sampling of Water for Injection, compressed gas and the environment to detect microbial, non-viable and chemical contamination. Supports manufacturing operations by continuous environmental monitoring viable and non-viable particles. etc. 7/22/2020
105 Alcami
Germantown, WI
Regulatory Affairs Specialist I
BS/MS in science or engineering
Exp: 1+ year(s)
The Regulatory Affairs Specialist is accountable for driving results in a fast-paced environment by performing activities to ensure that regulatory submissions support active pharmaceutical ingredient (API) business needs and that the business remains compliant with regulatory filings. Activities include preparation and submission of regulatory filings, written and verbal communication with regulatory agencies and clients, and providing regulatory affairs information and counsel to other site functions. 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. Essential Functions: Remain informed about regulations and regulatory trends concerning US FDA and other countries’ regulatory agencies. etc. 7/22/2020
106 Alcami
Charleston, SC
Manufacturing Tech- 3rd Shift
HS diploma/AS/AA
Exp: 0-2 years
The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employs acceptable techniques while working in manufacturing environments, including PPE gowning. The Manufacturing Technician I works collaboratively to support other manufacturing areas as required. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies for the role. etc. 7/22/2020
107 Alcami
Morrisville, NC
Manufacturing Tech I
HS diploma/AS/AA
Exp: 0-2 years
The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employs acceptable techniques while working in manufacturing environments, including PPE gowning. The Manufacturing Technician I works collaboratively to support other manufacturing areas as required. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies for the role. etc. 7/22/2020
108 Alcami
Charleston, SC
Manufacturing Tech- Weekend Shift
HS diploma/AS/AA
Exp: 0-2 years
The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employs acceptable techniques while working in manufacturing environments, including PPE gowning. The Manufacturing Technician I works collaboratively to support other manufacturing areas as required. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies for the role. etc. 7/22/2020
109 Alcami
Charleston, SC
Material Control Tech I
HS diploma/AS/AA
Exp: 0-2 years
The Materials Control Technician I is accountable for results in a fast-paced environment by following applicable SOPs and cGMPs to perform tasks for the receipt, storage, inventory and distribution of raw materials, intermediate or finished drugs or drug products and components. The Materials Control Technician I uses the electronic inventory system to track, document and control all inventory. 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. 7/22/2020
110 Alkermes
Wilmington, OH
Training Technology Specialist I
BS in information technology
Exp: 1-3 year(s)
This position supports the Operations Training Group in use of technology software, hardware, applications, video, etc.… for training development and delivery. Supports the development of content for the departmental training materials for Good Manufacturing Practices (GMP) training. Provides basic information technology training classes and training resources to departmental areas of responsibility. Provides training information technology guidance to area trainers and maintains/updates the departmental Sharepoint site. This position supports a comprehensive operations training strategy that aligns to the departmental talent strategies and supports the overall organizational strategy. etc. 7/22/2020
111 Alkermes
Wilmington, OH
QC Analyst II - Micro
BS in biology, microbiology, biotechnology, biochemistry
Exp: 1 year
QC Analyst Il must have broad knowledge of all the techniques within the laboratory required for the routine support of the microbiology laboratory operations. In this role the Analyst will be a fully functional member of the team responsible for testing, data entry and occasional review of data for finished product, in-process samples, stability samples, clinical materials and raw material release in a cGMP regulated environment. Major Responsibilities: Execution of microbiological tests including but not limited to bioburden, LAL, growth promotion, sterility, particulate profiling and microbial identification of bulk, raw materials, in-process material, components, clinical materials and finished product. If required, must be able to perform cGMP biological testing (bioassays, flow cytometry, qPCR, and ELISA). Review and data entry for testing results following GMP regulations into the electronic data management systems. etc. 7/22/2020
112 B. Braun
Irvine, CA
Machine Attd (Titan Filling)
HS diploma or equivalent
Exp: 1-5 year(s)
Responsibilities: Essential Duties: Follows established procedures and guidelines to manufacture the organization's products according to production specifications and schedules, volume, cost, and wastage targets or quality standards. Operates machines and production equipment safely and in accordance with instructions. Monitors the quality of output to identify, discard or remanufacture faulty products. Maintains accurate daily production records so that manufacturing performance can be analyzed. Troubleshoots and resolves technical problems from the product line/process to minimize reject levels.-For more senior position, might act as a team leader to ensure that the work meets agreed targets by directly overseeing team members. etc. 7/22/2020
113 B. Braun
unspecified, US
Sales Associate
BS/BA
Exp: 0-4 years
The Sales Associate Program is a full time, entry-level development program designed to serve as an entry point to a career in Sales at B. Braun Medical Inc. We will provide rigorous, comprehensive, hands on training for up to 24 months. At the conclusion of the program, participants will have the opportunity to be placed in a Sales role in a dedicated geography. Program participants will have exposure to the many different elements of Sales, while learning B. Braun's processes to achieve success. There are endless opportunities to build networks, develop strong relationships, and gain credible work experience. This program enables growth and development across the Sales organization, with structured mentoring from senior account managers. etc. 7/22/2020
114 B. Braun
Hazelwood, MO
Technician, Endoscopic
HS diploma
Exp: 6 months
Summary: Responsible for repairing, refurbishing and cleaning of basic precision Endoscopic/Laparoscopic surgical instruments under supervision of lead. Principal Duties Responsibilities: Buffs, Polishes, grinds, and performs minor repairs on basic surgical instruments. Instruments include but are not limited to Aesculap Endoscopic/Laparoscopic instruments. Surface treatment. Red-wheeling and bead blasting as needed. Repair, replace, realign to complete full refurbishment of basic instrumentation. etc. 7/22/2020
115 FYR Diagnostics
Missoula, MT
Lab Technician
BS or MS in biological sciences
Exp: 0-2 years in lab
Learn laboratory-based skills and work with an interdisciplinary team investigating novel isothermal PCR-based technology. Work with other researchers and technicians to execute, analyze and interpret PCR-focused experiments and miscellaneous in vitro experiments. Preparation of reagents and samples for experiments 7/18/2020
116 GenapSys
Redwood City, CA
Research Associate, Systems Integration
MS in biological sciences or engineering
Exp: 0-2 years in lab
Participate in development and optimization of NGS Platform workflow steps, in order to improve the existing performance of our NGS platform. Participate in short-term and long-term exploratory studies of assay development on Genapsys platforms. Plan and execute experiments, perform in-depth data analysis and present results and conclusions for internal review, and evaluate the research of peers. 7/18/2020
117 GeneDx
Gaithersburg, MD
Medical Lab Technologist 
BS in med technology, biology, or chemistry
Exp: 1 year in CLIA lab
The Medical Lab Technologist performs all laboratory procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. Maintain standards in routine & STAT testing. Complete work in a timely manner. Write legibly when documenting QC, problems or information. 7/18/2020
118 GeneDx
Gaithersburg, MD
DNA Extraction Technician 
BS in medical technology or life sciences
Exp: 0-1 years
Learns and follows the established standard operating procedures for specimen handling and processing, test analysis, reporting of results to team leads, supervisors and test managers, and record-keeping. Adheres to quality control policies; documents all quality control activities, instrument and procedural calibrations, reagent preparation and testing, and instrument maintenance performed 7/18/2020
119 GeneDx
Gaithersburg, MD
Lab Technician, Microarray
BS in medical technology or life sciences
Exp: 1 year in technologies
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.Implements the standard operating procedures for specimen handling and processing, test analysis, reporting of results to team leads, supervisors and test managers, and record-keeping. 7/18/2020
120 Generation Bio
Cambridge, MA
Associate Scientist / Senior Associate Scientist, Drug Product Formulation-CMC
MS in pharmacuetics, chemical sciences/engineering
Exp: 0-2 years
Execute on development work for the manufacturing processes for Drug Product formulation using both DNA vectors and Lipid Nanoparticles (LNPs). Ensures all appropriate materials, equipment, protocols and documentation are available and completed for multiple Drug Product formulations targeted for research and pre-clinical programs. 7/18/2020
121 Genewiz
South Plainfield, NJ
Associate Scientist I
BS/BA in biological sciences
Exp: 1+ year in biological laab
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 7/18/2020
122 Neo Genomics
Carlsbad, CA
Logistics Technician
HS Diploma/GED
Exp: 1 year as accessioning technician
The Logistics Technician will ensure proper handling of all specimens received and prepare specimens for laboratory testing. This position includes such functions as matching patient information, data entry, and scanning documents. This is entry level in the Logistics job category, and employees perform the full range of specimen processing procedures. 7/18/2020
123 Ginkgo Bioworks
Boston, MA
Build Engineer / Research Associate
BS or MS in microbiology or genetics
Exp: 1+ year in lab
We are seeking inquisitive research associates to join our Build team to help us run and improve several high-throughput molecular biological processes. A demonstrated ability to evolve a process in response to changing technology and demands is essential. Experience in a mixed team of software developers, process engineers, and biologists is important. 7/18/2020
124 GenapSys
Redwood City, CA
Research Associate, Development
MS in molecular biology
Exp: 1+ year in industry
Help to define technical requirements for consumable products and generate data to support the specifications that are established and used for incoming QC. Participate on both short-term and long-term stability studies to establish high risk reagents, work flow and storage issues. Help to develop orthogonal analytical methods that can correlate with performance on our sequencing platform. 7/18/2020
125 Genewiz
Cambridge, MA
Laboratory Technician I
HS Diploma/GED
Exp: 1+ year in lab
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. 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. 7/18/2020
126 Genewiz
South Plainfield, NJ
Associate Scientist I
BS in biological sciences
Exp: 1+ year in biological laab
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 7/18/2020
127 Genewiz
La Jolla, CA
Laboratory Technician I
HS Diploma/GED
Exp: 1+ year in lab
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. 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. 7/18/2020
128 Neo Genomics
Carlsbad, CA
Laboratory Technician - Covid-19 Unit
BS/BA in life sciences or engineering
Exp: 0-2 years
As a Laboratory Technician you will work under the direct supervision of licensed personnel to prepair Covid-19 samples for processing. You will assist with responsibilities associated with processing specimens for clinical testing and will provide general support for the laboratory following established policies and procedures. 7/18/2020
129 Neo Genomics
Ft. Myers, FL
Clinical Laboratory Technologist I - Molecular- Tuesday -Saturday; Day Shift
BS/BA in biological/chemical sciences
Exp: 1+ year in clinical lab
In this position, you will need to analyze specimens and 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. 7/18/2020
130 Neo Genomics
Carlsbad, CA
Clinical Laboratory Technologist -Covid-19 Testing Unit
BS/BA in biological/chemical sciences
Exp: 1+ year in clinical lab
In this position, you will need to analyze specimens and 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. 7/18/2020
131 Neo Genomics
Carlsbad, CA
Clinical Laboratory Technologist - Covid-19 Unit
BS/BA in biological/chemical sciences
Exp: 1+ year in clinical lab
In this position, you will need to analyze specimens and 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. Documents all corrective actions taken when test systems deviate from the laboratory’s established performance specifications 7/18/2020
132 Ginkgo Bioworks
Boston, MA
Research Associate, Protein Engineering
BS or MS in biological sciences or engineering
Exp: 1+ years in industry working with enzymes
The protein engineering team works to address the complex challenges of enzyme discovery, characterization, and engineering. We utilize state-of-the-art computational software developed at Ginkgo to discover novel enzymes and employ cutting-edge software like Rosetta for rationally designing improvements. We want a person who is eager to learn and has a desire to utilize automation to work more efficiently 7/18/2020
133 Genentech
Hillsoboro, OR
QC Lab Technician (Contract)
AA degree in sciences
Exp: 1 year in related
Perform routine and semi-routine work that supports QC operations. Sampling and testing of utility systems (Color, Appearance, Odor, TOC, Conductivity, Bioburden, Endotoxin, Particulates and Moisture), facility monitoring (viable monitoring plates and non-viable particulate). Share maintenance responsibilities with other laboratory personnel such as reagent preparation, media growth promotion, and cleaning of incubators and biosafety cabinets. 7/18/2020
134 Genentech
Vacaville, CA
Manufacturing Technician - BioProcess
BS/BA in life sciences or engineering
Exp: 0-2 years
The Manufacturing Technician is responsible for producing innovative bio-therapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment. The individual will be required to work in and maintain a clean room environment. Area of work must remain in a high state of inspection readiness at all times. 7/18/2020
135 Genentech
South San Francisco, CA
PV Clinical Associate
Health Care degree
Exp: 0-2 years clinical experience
Completes drug safety monitoring and tracking in a timely, thorough and accurate manner in accordance with pharmacovigilance (PV) and related standards, regulations and Genentech/Roche Standard Operating Procedures (SOPs). Reviews, evaluates and verifies potential AE information during Preliminary Assessment (PA) to determine required action per internal policies and procedures and perform data entry of adverse event by timely completion of the case via Roche global safety database. Performs seriousness / validity / causality and conducts quality review of all cases (as applicable) based on their medical assessment 7/18/2020
136 Zynex Medical
Champaign, IL
Medical Device Sales - Addressing the Opioid Crisis
BS/BA
Exp: 1-3 year(s)
Zynex is seeking college graduates or individuals with 1-3 years of outside sales experience in either B2B or medical device sales. Must be a self-starter, resourceful, assertive, and organized with a proven track record of documented sales success. This is an opportunity to build your own prescription-based business. Call points include: Pain Management doctors, Orthopedic groups and Physical Therapy clinics for our NexWave and other DME devices that offer an alternative to opioid pain medication. This is an autonomous sales position that requires you to be independent and dedicated to becoming a top medical device sales representative. You must be able to build trusting relationships quickly and possess the drive to accomplish goals on a weekly basis. etc. 7/15/2020
137 Zynex Medical
Carbondale, IL
Medical Device Sales - Addressing the Opioid Crisis
BS/BA
Exp: 1-3 year(s)
Zynex is seeking college graduates or individuals with 1-3 years of outside sales experience in either B2B or medical device sales. Must be a self-starter, resourceful, assertive, and organized with a proven track record of documented sales success. This is an opportunity to build your own prescription-based business. Call points include: Pain Management doctors, Orthopedic groups and Physical Therapy clinics for our NexWave and other DME devices that offer an alternative to opioid pain medication. This is an autonomous sales position that requires you to be independent and dedicated to becoming a top medical device sales representative. You must be able to build trusting relationships quickly and possess the drive to accomplish goals on a weekly basis. etc. 7/15/2020
138 Zynex Medical
Olney, IL
Medical Device Sales - Addressing the Opioid Crisis
BS/BA
Exp: 1-3 year(s)
Zynex is seeking college graduates or individuals with 1-3 years of outside sales experience in either B2B or medical device sales. Must be a self-starter, resourceful, assertive, and organized with a proven track record of documented sales success. This is an opportunity to build your own prescription-based business. Call points include: Pain Management doctors, Orthopedic groups and Physical Therapy clinics for our NexWave and other DME devices that offer an alternative to opioid pain medication. This is an autonomous sales position that requires you to be independent and dedicated to becoming a top medical device sales representative. You must be able to build trusting relationships quickly and possess the drive to accomplish goals on a weekly basis. etc. 7/15/2020
139 Zynex Medical
Bismarck, ND
Medical Device Sales - Addressing the Opioid Crisis
BS/BA
Exp: 1-3 year(s)
Zynex is seeking college graduates or individuals with 1-3 years of outside sales experience in either B2B or medical device sales. Must be a self-starter, resourceful, assertive, and organized with a proven track record of documented sales success. This is an opportunity to build your own prescription-based business. Call points include: Pain Management doctors, Orthopedic groups and Physical Therapy clinics for our NexWave and other DME devices that offer an alternative to opioid pain medication. This is an autonomous sales position that requires you to be independent and dedicated to becoming a top medical device sales representative. You must be able to build trusting relationships quickly and possess the drive to accomplish goals on a weekly basis. etc. 7/15/2020
140 Zynex Medical
Burlington, VT
Medical Device Sales - Addressing the Opioid Crisis
BS/BA
Exp: 1-3 year(s)
Zynex is seeking college graduates or individuals with 1-3 years of outside sales experience in either B2B or medical device sales. Must be a self-starter, resourceful, assertive, and organized with a proven track record of documented sales success. This is an opportunity to build your own prescription-based business. Call points include: Pain Management doctors, Orthopedic groups and Physical Therapy clinics for our NexWave and other DME devices that offer an alternative to opioid pain medication. This is an autonomous sales position that requires you to be independent and dedicated to becoming a top medical device sales representative. You must be able to build trusting relationships quickly and possess the drive to accomplish goals on a weekly basis. etc. 7/15/2020
141 Zynex Medical
Jonesboro, AR
Medical Device Sales - Addressing the Opioid Crisis
BS/BA
Exp: 1-3 year(s)
Zynex is seeking college graduates or individuals with 1-3 years of outside sales experience in either B2B or medical device sales. Must be a self-starter, resourceful, assertive, and organized with a proven track record of documented sales success. This is an opportunity to build your own prescription-based business. Call points include: Pain Management doctors, Orthopedic groups and Physical Therapy clinics for our NexWave and other DME devices that offer an alternative to opioid pain medication. This is an autonomous sales position that requires you to be independent and dedicated to becoming a top medical device sales representative. You must be able to build trusting relationships quickly and possess the drive to accomplish goals on a weekly basis. etc. 7/15/2020
142 Zynex Medical
Dallas, TX
Medical Device Sales - Addressing the Opioid Crisis
BS/BA
Exp: 1-3 year(s)
Zynex is seeking college graduates or individuals with 1-3 years of outside sales experience in either B2B or medical device sales. Must be a self-starter, resourceful, assertive, and organized with a proven track record of documented sales success. This is an opportunity to build your own prescription-based business. Call points include: Pain Management doctors, Orthopedic groups and Physical Therapy clinics for our NexWave and other DME devices that offer an alternative to opioid pain medication. This is an autonomous sales position that requires you to be independent and dedicated to becoming a top medical device sales representative. You must be able to build trusting relationships quickly and possess the drive to accomplish goals on a weekly basis. etc. 7/15/2020
143 10x Genomics
Pleasanton, CA
Research Associate 2-Molecular Biology/Product Development
MS in molecular biology, biochemistry, genetics or related
Exp: 1+ year(s)
We are seeking an outstanding Research Associate to join the Product Development group 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. 7/15/2020
144 3T Biosciences
South San Francisco, CA
Research Associate, Protein Engineering
MS
Exp: 0-2+ year(s)
Your Typical Responsibilities: Protein engineering to support TCR-T cell programs, and identify compounds with optimal therapeutic index. TCR engineering for improved efficacy, and specificity. Performing cell-based assays to test prospective optimized leads. Discovery of TCR mimetic (mTCR) compounds that bind selectively to pMHC targets identified at 3T. Improvement of existing yeast display platforms and development of next-generation pMHC libraries. etc. 7/15/2020
145 Abbvie
Cambridge, MA
Associate Scientist II/Scientist I, In Vivo Pharmacology
MS in biology or related
Exp: 0+ years
AbbVie is seeking an experienced, hands-on in-vivo scientist to join the In Vivo Pharmacology team at the Cambridge Research Center in Cambridge, MA. This individual will be responsible for designing and executing in vivo studies to support Parkinson’s Disease drug discovery projects. Key Responsibilities: Working closely with team members to design and execute in vivo experiments to support drug discovery efforts including target identification, target validation and efficacy of novel molecules. Developing new technologies and methods to understand disease pathophysiology and target biology. Responsible for implementation of in vivo studies and data collection as well as interpretation/analysis and presentation of results as needed. etc. 7/15/2020
146 Abzena
Bristol, PA
Bioconjugation Scientist
MS in biochemistry, chemistry, protein chemistry or related
Exp: 1-5+ year(s)
Responsible for contributing to the optimization and development of bioconjugation techniques and related processes, including but not limited to the areas of Antibody Drug Conjugates (ADCs), protein drug conjugates, conjugated vaccine, Fluorescent-Probe Bioconjugation and Protein-Protein cross-linking. Typical Duties Include: Planning of synthetic routes/strategies, the execution and delivery of bioconjugation projects for Abzena’s clients. Preparation, purification and characterization of all materials including the protein and the drug molecules. Maintaining clear and current records of their work within a laboratory notebook and performing all applicable analytical work. etc. 7/15/2020
147 Absorption Systems
Exton, PA
Associate Scientist / Scientist – Molecular or Immunology
BS/MS
Exp: 1-3 year(s)
Absorption Systems, provides analytical support for gene and cell therapy products through every stage of development, is seeking a candidate for either an Associate Scientist position in molecular biology and gene expression at the headquarter location in Exton, Pennsylvania. Absorption Systems also provides non-clinical testing services to pharmaceutical and biotech companies to support research and development of drugs, biologics, and medical devices. Primary Responsibilities: Preparation for protocol of assay, planning and conducting experiments under the direction of a senior scientist. Conducting studies on molecular biology assays, such as purification of DNA/RNA/Protein from samples, qPCR, protein assays. etc. 7/15/2020
148 Xellia Pharmaceuticals
Cleveland, OH
Aseptic Operator, IV Bag Manufacturing I
HS diploma or equivalent
Exp: 0-1 year(s)
The contents contained in this job description are the minimum requirements required to be met for the aforementioned position. Under the direction of area management or designee, the Aseptic Operator I is responsible for performing all necessary tasks both in and outside of the classified manufacturing suites in support of manufacture of safe and effective sterile (injectable) pharmaceutical products at the Xellia Cleveland plant. Key Responsibilities: Perform job functions with in compliance of 21CFR part 210 and 211, FDA, OSHA and other regulatory agencies. Ensure that the current requirements for Environmental, Health, Safety (EHS) issues are met within the production operations. Ensure training compliance for assigned curriculum prior to performing any work task. Set-up, Operation, and troubleshooting of key manufacturing equipment: including (but not limited to) lyophilizer, autoclave, parts washers, filler, capper, CIP/SIP skid, etc. 7/14/2020
149 Xellia Pharmaceuticals
Cleveland, OH
Inside Sales Representative - Southwest Territory (Remote)
BS/BA
Exp: 1-3 year(s)
As a part of Xellia’s growing, energetic, and innovative pharmacy injectables sales seam, the Digital Sales Representative is responsible for driving sales to new customers while meeting established individual and organizational sales objectives. You will build and maintain valuable sales skills, cross-functionally learn about all facets of the business and help develop a pathway for growth opportunities and career advancement. Key Responsibilities: Manage, prospect, and build relationships within an assigned territory to drive new business, increase revenue growth and ensure customer satisfaction. Manage a sales pipeline, sales activity, and monthly business forecasting through customer interfacing activities and sales data analysis. Present regular updates to the Management team. etc. As a part of Xellia’s growing, energetic, and innovative pharmacy injectables sales seam, the Digital Sales Representative is responsible for driving sales to new customers while meeting established individual and organizational sales objectives. You will build and maintain valuable sales skills, cross-functionally learn about all facets of the business and help develop a pathway for growth opportunities and career advancement. Key Responsibilities: Manage, prospect, and build relationships within an assigned territory to drive new business, increase revenue growth and ensure customer satisfaction. Manage a sales pipeline, sales activity, and monthly business forecasting through customer interfacing activities and sales data analysis. Present regular updates to the Management team. etc. 7/14/2020
150 Xellia Pharmaceuticals
Cleveland, OH
Aseptic Operator II - 12 Hour Shift
HS diploma or equivalent
Exp: 1-2 year(s)
The contents contained in this job description are the minimum requirements required to be met for the aforementioned position. Under the direction of area management or designee, the Aseptic Operator II is responsible for performing all necessary tasks both in and outside of the classified manufacturing suites in support of manufacture of safe and effective sterile (injectable) pharmaceutical products at the Xellia Cleveland plant. Key Responsibilities: Perform job functions with in compliance of 21CFR part 210 and 211, FDA, OSHA and other regulatory agencies. Ensure that the current requirements for Environmental, Health, Safety (EHS) issues are met within the production operations. Ensure training compliance for assigned curriculum prior to performing any work task. Set-up, Operation, and troubleshooting of key manufacturing equipment: including (but not limited to) lyophilizer, autoclave, parts washers, filler, capper, CIP/SIP skid, etc. Documentation of perform tasks as per established Good Documentation Practices, and review of executed documentation (batch records, logbooks, etc.) in a timely manner. etc. 7/14/2020
151 Xellia Pharmaceuticals
Cleveland, OH
Inside Sales Representative - Midwest Territory (Remote)
BS/BA
Exp: 1-3 year(s)
As a part of Xellia’s growing, energetic, and innovative pharmacy injectables sales seam, the Digital Sales Representative is responsible for driving sales to new customers while meeting established individual and organizational sales objectives. You will build and maintain valuable sales skills, cross-functionally learn about all facets of the business and help develop a pathway for growth opportunities and career advancement. Key Responsibilities: Manage, prospect, and build relationships within an assigned territory to drive new business, increase revenue growth and ensure customer satisfaction. Manage a sales pipeline, sales activity, and monthly business forecasting through customer interfacing activities and sales data analysis. Present regular updates to the Management team. etc. 7/14/2020
152 Xeris Pharmaceutical
Chicago, IL
Desktop Support Technician (Temp to Hire)
AS/AA in information technology or related
Exp: 1-2 year(s)
The Desktop Support Technician is responsible for supporting the organization’s end users via phone, email, and in person, in a dynamic, fast-paced environment. Strong customer service skills are a key component of this position which requires excellent communication and interpersonal skills, as well as the ability to resolve problems. Support may include but is not limited to hardware troubleshooting, software installations and/or configuration, imaging and deploying laptops/desktops, break/fix troubleshooting and end user education. This position will also require the ability to recognize root cause issues and document, resolve or escalate the root cause problem as necessary for resolution. The position will also require various other assigned tasks and responsibilities to be carried out as new projects and changes in the infrastructure occur. etc. 7/14/2020
153 Wuxi AppTec
San Diego, CA
Research Associate I
AS/BS in biology
Exp: 0-1 year(s)
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. etc. 7/14/2020
154 Freudenberg
Baldwin Park, CA
Project Engineer I – Injection Molding
BS/BA in engineering
Exp: 1-2 years is engineering
Work closely with project managers to gather/prepare all documentation relevant to a particular project. Responsible for Drafting and issuing validation protocols and production documents using information provided by customers and project managers. Responsible for gathering customer and technical information as required to make changes to documents or procedures at the customers request. 7/12/2020
155 Freudenberg
Carpinteria, CA
Manufacturing Quality Engineer I
BS in engineering or life sciences
Exp: 1-3 years in regulated industry
Responsible to provide Customer and Engineering feedback in regards to MSA, Critical to Quality Characteristics (CTQ’s) and Acceptance Activities. Lead Measurement System Analysis activities including Gage RnR, Test Method Validations, Test Procedures, etc. as part of the Design Transfer process. Provides all planning necessary to ensure effective product acceptance. This includes, but is not limited to, inspection instructions, equipment and gage requirements, and sampling plans. 7/12/2020
156 Freudenberg
Jeffersonville, IN
Manufacturing Associate - 2nd Shift
HS Diploma/GED
Exp: 0 years
Hand assemble manufactured medical components. Complete required documentation for work performed. Quality inspect work performed. Follow defined work procedures. Provide your suggestions and ideas of continuous improvements 7/12/2020
157 FujiFilm Diosynth
College Station, TX
Downstream Manufacturing Technician I
HS Diploma or Associates in biological sciences
Exp: 0-1 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. 7/12/2020
158 Frontage
Concord, OH
Maintenance Technician
HS Diploma/GED
Exp: 1 year in facility services
Assist in keeping building systems operational by completing assigned preventive maintenance requirements; following manufacturer’s instructions; troubleshooting malfunctions with oversight from supervisor and facilities staff. Assist in the maintenance and repair of various building equipment and systems including, but not limited to plumbing and piping systems, HVAC, electrical distribution, and boilers. 7/12/2020
159 FHC
Greenville, PA
Production Technician
HS Diploma/GED or Associates
Exp: 0-2 years general experience
The Production Technician assists FHC Greenville. This position involves some production duties, a variety of ERP System activities, and other general business office activities. Assemble product following work and print instructions as specified on manufacturing job orders generated from FHC’s ERP system. Relieve inventory physically and/or electronically through FHC’s ERP system if needed and follow the procedures to account for all items. 7/11/2020
160 FHC
Greenville, PA
Manufacturing Support Specialist
HS Diploma/GED or Associates
Exp: 0-2 years general experience
The Manufacturing Support Specialist assists GNS Production. This position involves some production duties, a variety of general accounting activities, and other general business office activities. Assists in performing secretarial, data entry and/or other general administrative tasks as required. Prepare and process Job order, Sales Orders. 7/11/2020
161 Foundation Medicine
Cambridge, MA
Accessioning Technician II
BS/BA in life sciences
Exp: 0-1 years in CLIA lab
The Accessioning Technician II performs critical sample receipt and data entry functions in FMI’s CLIA-certified clinical laboratory. Specifically, the Accessioning Technician II receives incoming samples and ensures that necessary information has been received to move forward with processing. The Accessioning Technician II is assigned to one of three shifts and may be assigned to work any day that the lab is operational. 7/11/2020
162 FreeThink Technologies
Branford, CT
Laboratory Scientist, Analytical Sciences
BS or MS in chemistry or chemical engineering
Exp: 1-2 years in pharma preferred
Analyze products to determine chemical and physical properties following Company, client and Pharmacopeial methodologies with minimal supervision. Ensure all work performed is in compliance with standard operating procedures, good laboratory practices and good manufacturing practices. Document laboratory work concurrently in a clear, detailed and organized manner 7/11/2020
163 Foundation Medicine
Cambridge, MA
CAPA Coordinator
BS in related field
Exp: 1-2 years in QA or medical/pharma
The CAPA Coordinator assists with the CAPA System at FMI and supports with day to day administration of the CAPA process, documentation, and retention of the quality records. The Coordinator is responsible for expediting and coordinating a multitude of interrelated project activities pertaining to different daily tasks with changing priorities to ensure the successful completion of CAPA work stream. This position interacts with all departments within FMI. 7/11/2020
164 Fate Therapeutics
San Diego, CA
Process Development Engineer, MSAT
MS in biological or chemical sciences/engineering
Exp: 1 year in biopharma
The candidate will assist seniormembers of the MSAT teamin thedevelopment ofscaled-upculture, differentiation, purification and characterization methods foriPSC-derived cellulartherapy products. Furthermore,they will activelysupport laboratory operations by coordinating the inventory,purchaseandaliquoting of key reagents. 7/11/2020
165 Molecular Devices
San Jose, CA
New Product Introduction Engineer, BioImaging
BS in engineering
Exp: 1-4 years (interships included)
The NPI Engineer supports all aspects of the product development process, from concept definition through production transfer, training, and support with a focus on delivering manufacturability, serviceability, and reliability throughout the product lifecycle. Manage the prototype assembly process and tooling readiness. Qualify key technology suppliers and facilitate the R&D supply chain 7/11/2020
166 Wuxi AppTec
Philadelphia, PA
Laboratory Technician II
BS in biology, chemistry, or related
Exp: 1-2 year(s)
Laboratory Technician II in Molecular Biology will be responsible for performing nucleic acid based assays where proficiency in nucleic acid extraction methods and qPCR is required. Experience in a GMP and/or high throughput lab where day to day activities are heavily driven by meeting deadlines is preferred. Independent data analysis experience preferred. Experience with automation and LIMS systems a plus. Responsibilities: Performs assays and lab procedures according to and in compliance with cGMP, CFR and/or PTC guidelines, and SOPs using appropriate laboratory techniques for the lab group assigned to. Performs laboratory support functions (e.g. inventory management and equipment calibration) to help ensure lab is operational; contributes to the overall operations and to the achievement of departmental goals and objectives. etc. 7/8/2020
167 Upsher-Smith
Maple Grove, MN
CNS Field Sales Representative - Connecticut
BS/BA in business, communications, marketing or related
Exp: 1-3+ year(s)
The CNS Field Sales Representative - Connecticut 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 our strategies and the Representative will be responsible for a physician and patient centric focus. The role is responsible for developing business relationships with targeted neurologists, epileptologists, seizure specialists and other identified healthcare practitioners and members of the health care community. The time allocation for this role is 70% field based selling and 30% utilization of virtual technology and inside approach to remote customer contact, however, this may vary as business needs arise. etc. 7/8/2020
168 Upsher-Smith
Baltimore, MD
CNS FIeld Sales Representative - Maryland
BS/BA in business, communications, marketing or related
Exp: 1-3+ year(s)
The CNS Field Sales Representative - Baltimore, MD 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 our strategies and the Representative will be responsible for a physician and patient centric focus. The role is responsible for developing business relationships with targeted neurologists, epileptologists, seizure specialists and other identified healthcare practitioners and members of the health care community. The time allocation for this role is 70% field based selling and 30% utilization of virtual technology and inside approach to remote customer contact, however, this may vary as business needs arise. etc. 7/8/2020
169 Upsher-Smith
Plymouth, MN
Maintenance & Automation Technician/Mechanic - 2nd shift
AS/AA
Exp: 1 year
The Maintenance & Automation Technician/Mechanic - 2nd shift repairs, maintains and assists manufacturing & packaging operations to ensure automated packaging line and large-scale manufacturing equipment is maintained. Troubleshoots, diagnoses, repairs and maintains manufacturing pharmaceutical manufacturing and packaging equipment/machinery. Follows all required safety practices and completes required documentation to ensure compliance to cGMP's. Essential Duties: Effectively troubleshoots and resolves automated machinery/mechanical equipment issues utilizing a systematic logical approach until the root cause is identified. Completes work orders and preventative maintenance tasks using fundamental, mechanical applied knowledge and experience. etc. 7/8/2020
170 Stryker
Indianapolis, IN
Associate Sales Representative
BS/BA
Exp: 1+ year(s)
You’ll work closely with experienced Sales Representatives and Managers to build your knowledge, skill and comfort with clinical and product knowledge as well as selling styles and techniques. They will serve as your coaches and mentors to share lessons learned for how to build and grow a successful business. You’ll receive training and be expected to study and prepare independently to perform at the highest levels in the operating room, working amongst surgeons and healthcare professionals. The expectations are challenging, yet rewarding. You’ll represent Stryker as a leader in our industry and the marketplace. etc. 7/7/2020
171 Tenaya Therapeutics
South San Francisco, CA
RA I/II, Gene Therapy
BS/MS in biology, biochemistry, or related
Exp: 1+ year(s)
Tenaya has an immediate need for a Research Associate I/II to support the Gene Therapy Research team. Tenaya is seeking a creative, self-motivated individual with a passion for experimental science and teamwork. The ideal candidate is a self-starter and problem-solver who will work closely with the team to drive the company’s future success. Key Responsibilities: Execute a diverse range of cell-based and molecular assays to characterize lead gene therapy candidates. Functionally assess transduction and other gene therapy mechanisms in vitro and in vivo. etc. 7/7/2020
172 Stryker
Albany, NY
Associate Mako Product Specialist
BS/BA
Exp: 1 year
In this role, you’ll be responsible for helping surgeons use Stryker’s Mako robot– our newest product used in robotic-arm assisted surgery. Acting as a helpful source for all things related to the Mako, you’ll provide clinical support to all end-users, offer guidance and assistance during surgical procedures, and resolve technical product and service issues as needed. In addition, you’ll also provide customer education and ongoing in-services, such as assisting surgeons in pre-operative implant planning. We’ll count on your attention to detail to ensure all cases are planned and reviewed with surgeons prior to scheduled surgeries, and that all inventory is accounted for. etc. 7/7/2020
173 Stryker
Columbus, OH
Associate Sales Representative
BS/BA
Exp: 1-2 year(s)
As a Spine Enabling Technologies Associate Sales Representative, you assist in strategically promoting and selling Stryker Spine Enabling Technologies products to meet our customers’ needs. You confidently conduct product evaluations in Operating Room and office settings, persuasively demonstrating the value of our products. Systematically tracking your territory progress, you proactively communicate your findings with your Regional Manager and Sales Representative(s) you are supporting to push yourself to exceed each goal. When onsite with clients, you use your product knowledge and quick thinking to solve product problems and inform doctors, nurses and other staff as to the proper use and maintenance of our products. etc. 7/7/2020
174 Stryker
Raleigh, NC
Clinical Sales Representative - Endoscopy
BS/BA
Exp: 1-2 year(s)
RESPONSIBILITIES: Drive continuous expansion of SPY Elite, SPY PHI and PINPOINT IMAGING SYSTEMS’S imaging system’s customer base in hospitals to achieve sales goals. Partner with multiple Sales Representatives to pull through usage of installed PINPOINT devices across multiple surgeon specialties. Become a Stryker expert across all imaging platforms, procedures, industry trends and competitive issues. Develop strong relationship with the Endoscopy and Regional Capital sales representatives. Drive adoption and usage of DermACELL advanced decellularized dermis in hospitals for use in various reconstructive applications. etc. 7/7/2020
175 Stryker
Scottsbluff, NE
Joint Replacement 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. Learn or hone selling skills and processes by coaching/mentoring support from Joint Replacement Sales Representatives and Managers. etc. 7/7/2020
176 Stryker
Chicago, IL
Trauma Sales Associate
BS/BA
Exp: 1+ year(s)
What you will do: 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. You will develop well-rounded field exposure to prepare you in all aspects of the selling/ servicing process when a territory opportunity arises. etc. 7/7/2020
177 Synthego
Redwood City, CA
Factory Service Engineer, Generalist
BS in biology, biomedical engineering, or related
Exp: 1+ year(s)
Join our operations team as a Factory Service Engineer-Generalist working to fully automate genome engineering. You will be a key member of the Service Engineering team responsible for characterizing and modifying core automated workflows, developing equipment documentation and SOPs, recommending advanced automation equipment as well as their acceptance criteria and training users in best practices. As a Factory Service Engineer, Generalist, you’ll be frontline support for all production needs. You will be working in a fast-paced and dynamic interdisciplinary laboratory environment, supporting stakeholders involved in adapting quickly to change and new technical challenges. With your help, we’ll keep our symphony of automated instruments humming in tune. etc. 7/7/2020
178 Eurofins
Austin, TX
EMC Technician
AA, technical school
Exp: 0-2 years
Responsible for setting up and executing, evaluating, and documenting tests. Conduct tests and all related tasks. Serve as lead engineer for projects assigned. Complete related tasks assigned by lab manager. 7/5/2020
179 Eurofins
Piscataway, NJ
Aesthetician-Clinical Research Coordinator
BS/BA in sciences/healthcare
Exp: 1-3 years
Measure physical effects on the bodies of study subjects using high-end instrumentation. Manage Bioinstrumentation and related tests and documentation under the supervision of the manager/P.I. Maintain a professional, courteous and respectful work environment. 7/5/2020
180 Eurofins
Lee's Summit, MO
Laboratory Technician
BS/BA in sciences
Exp: 1 year in lab
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. 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 7/5/2020
181 Eurofins
Austin, TX
RF Test Engineer
BS in electrical engineering
Exp: 1 year RF testing
Test common North American and European regulatory standards for licensed and unlicensed radio devices. Previous experience working in a commercial test laboratory a plus. EMC testing experience also a plus 7/5/2020
182 Exelixis
Alameda, CA
Vivarium Technician II
BS/BA
Exp: 1 year experience
The successful and highly motivated candidate is responsible for animal husbandry and housekeeping of animal holding and support areas. The Vivarium Technician will assist and support the daily activities for the in vivo pharmacology program. Maintains animal husbandry and housekeeping of animal holding and support areas. 7/5/2020
183 Exelixis
Alameda, CA
Temporary Assistant Research Scientist I (Compound Repository)
BS/BA in related
Exp: 1 year in related
The candidate will be responsible for creating daily compound stock solutions to support creation of library screening plates. This job will require the candidate to have excellent organization, communication, and teamwork skills, as well as flexibility and versatility, to meet tight deadlines in a dynamic, fast-moving environment. 7/5/2020
184 Biotechne
Minneapolis, MN
QA Specialist
BS/BA in sciences
Exp: 0-2 years in QA
The responsibilities of this position are to support the Quality Assurance function within Bio-Techne through quality systems development, quality systems auditing, documentation review, and other QA functions. Assist in Quality review of newly written or revised GMP specifications, documents, labels and literature for accuracy and completeness. Write documents as needed. 7/5/2020
185 Biotechne
Minneapolis, MN
Research Associate (Serological Assay)
BS in biological sciences
Exp: 0-2 years of related
The responsibilities of this position are to perform ELISA assays to check for quality performance of product, maintain accurate documentation of results, and maintain assay databases. This position will focus on quality control testing of serological assays. This position may also contribute to quality control testing of Quantikine ELISAs, Luminex assays, and/or IVD kits. Perform raw material qualification testing as needed. Calculate data and compile results efficiently. Collaborate with others and perform general lab duties as needed. 7/5/2020
186 Biotechne
Minneapolis, MN
Research Associate (Protein Purification)
BS in biochemistry or equivalent
Exp: 0-2 years in chormatography
The responsibilities of this position is to purify proteins for restock and modify existing protocols to meet the demand of our customers. This position will require assistance with basic lab operations and routine guidance on how to follow SOP’s and purification methods. 7/5/2020
187 Biotechne
Minneapolis, MN
Production Assistant
HS Diploma
Exp: 0-2 years
You will be responsible for assisting in the Clinical Controls Product Finishing Department with the bottling operation and the other activities involved in the product finishing process. Cap vials or tubes, operate the torqueing equipment. Label product, operate the labeling equipment. Assist with monthly cleaning of clean room, including counters, laminer hoods, torque, labeler, sinks, and all work areas. 7/5/2020
188 Exact Sciences
Madison, WI
Production Associate I
Associates in life sciences
Exp: 1 year in lab setting
The Production Associate I is an entry level position and is the starting point to acquire skills and training required for the Exact Sciences Production Operations team. This role will participate in a variety of Production functions, which include bulk reagent production and dispensing, label application, and kitting of finished goods. The position will work within defined protocols and procedures with frequent supervision. 7/5/2020
189 Exact Sciences
Madison, WI
Patient Access Associate I
HS Diploma/Ged
Exp: 3+ months in healthcare
The Patient Access Associate I (PAAI) position is responsible for the accurate and timely filing of insurance claims for Exact Sciences. A PAAI demonstrates medical insurance knowledge by determining initial and/or ongoing eligibility and authorization of insurance including commercial, government, and plan coverage. PAAI communicates insurance information to ancillary departments and ensuring appropriate coverage by utilizing Epic, external portals, and other software. 7/5/2020
190 Exagen
Vista, CA
Research Associate (Flow Cytometry)
BS in biological sciences
Exp: 0-1 years, experience in flow cytometry preferred
The Research Associate assists with the development of new assays for diagnostics and research projects, through various phases of inception, planning and transfer to the clinical lab. Assist with the development, optimization and validation of new diagnostic assays. Perform all aspects of laboratory activities, for example sample preparation, staining, acquisition, and data analysis, with a focus on flow cytometry. 7/5/2020
191 Senes Tech
Phoenix, AZ
Manufacturing Technician
AS/AA in an electro-mechanical discipline
Exp: 1-2 year(s)
Would you welcome a highly responsible role at a revolutionary company? SenesTech, a platform life sciences company, is seeking a Manufacturing Technician to process and package finished goods, operate machines and take responsibility for facilities and planned maintenance. The key responsibilities of a Manufacturing Technician include, but are not limited to: Responsible for making ContraPest® according to SOPs and Batch Record instructions and takes responsibility for manufacturing a quality product. Performing set-up, dismantling, and maintenance of equipment and assuring that equipment is ready for production operations, performing routine sanitization of areas and equipment maintenance such as periodic equipment cleaning, inspection, and filter changes, etc. 7/1/2020
192 Siemens
Elgin, IL
Assembler Associate - 2nd Shift
HS diploma or equivalent
Exp: 1+ year(s)
We are looking for dedicated people with the skills and vision to build a better tomorrow! By joining our manufacturing team, you will be under close supervision, and will be responsible for assembly of wind turbine repair kits! Your Responsibilities. Receive parts from stockroom, document serial numbers and other needed information. Check, skid, package, and tag part per BOM(Bill of Material). Assemble parts per engineering instructions and blueprints and assist in disassembly of gear boxes. Operate overhead crane and other equipment as required. etc. 7/1/2020
193 Siemens
Walpole, MA
Laboratory Technician 2 - QC Systems Improvement
BS in medical technology, immunology, biochemistry or related
Exp: 1+ year(s)
Join our team now at Siemens Healthineers as a Laboratory Technician 2. This position will be responsible for the implementation of the standardization strategy for each individual ADVIA Centaur and Atellica products and the installation of several complex testing instruments within a new lab space. This person will be a part of a small team focused on developing standardization strategies for existing products. This includes developing Anchor and Gold Standards and MDPs when not in existence. In addition, this position will focus on modification to the value assignment process to align with new control system requirements. The position will participate in the execution of the design of experiments. This person will perform material and process validations following written protocols, and help prepare validation and/or test results reports. This person will work with serum and other biological fluids of human and animal origin. etc. 7/1/2020
194 Siemens
Littleton, CO
System Specialist I – Smart Buildings / Automation - Denver
HS diploma/AS/AA
Exp: 1+ year(s)
Responsibilities: Network Technologies: Assist with data back-up from data servers and the creation of automated back-up procedures. Support troubleshooting and resolution of inconsistencies in the functions or sequence of operations. Assist with the set-up and configuration of PC workstations and user interfaces. Support the confirmation of proper network performance. Operational Testing, Verification, and Acceptance: Run routine reports to review system operation. Participate in final inspection and testing. Support customer acceptance. Assist with customer training on system operations. Complete and submit routine written reports. Provide plans and control system documents to engineering for as-built drawings. etc. 7/1/2020
195 Siemens
Shoreview, MN
System Specialist – Smart Buildings/Automation – Level I
HS diploma/AS/AA
Exp: 1+ year(s)
Responsibilities: Network Technologies: Assist with data back-up from data servers and the creation of automated back-up procedures. Support troubleshooting and resolution of inconsistencies in the functions or sequence of operations. Assist with the set-up and configuration of PC workstations and user interfaces. Support the confirmation of proper network performance. Operational Testing, Verification, and Acceptance: Run routine reports to review system operation. Participate in final inspection and testing. Support customer acceptance. Assist with customer training on system operations. Complete and submit routine written reports. Provide plans and control system documents to engineering for as-built drawings. etc. 7/1/2020
196 Siemens
Elgin, IL
Assembler Associate - 1st Shift
HS diploma or equivalent
Exp: 1+ year(s)
We are looking for dedicated people with the skills and vision to build a better tomorrow! By joining our manufacturing team, you will be under close supervision, and will be responsible for assembly of wind turbine repair kits! Your Responsibilities. Receive parts from stockroom, document serial numbers and other needed information. Check, skid, package, and tag part per BOM(Bill of Material). Assemble parts per engineering instructions and blueprints and assist in disassembly of gear boxes. Operate overhead crane and other equipment as required. etc. 7/1/2020
197 Siemens
Grand Prairie, TX
Manufacturing Fabrication Supervisor - 2nd Shift (Entry Level)
BS/BA
Exp: 0-1+ year(s)
Siemens Industry is looking for a Manufacturing Fabrication Supervisor - 2nd Shift for our Grand Prairie, TX facility the heart of the DFW Metroplex. Our growing team has over 700 employees that produce high-quality, engineered and make-to-order power distribution equipment. The Production Supervisor is the key driver of all daily production-related processes and the hub of information transfer between the hourly assembly workforce and Management, Engineering, Quality Control, Purchasing, and Planning. etc. 7/1/2020
198 Siemens
Mishawaka, IN
Biochemist Scientist-Technical Operations
BS in chemistry or related
Exp: Recent graduates considered
The successful candidate will participate in a wide variety of semi-complex technical assignments with respect to systematic troubleshooting and support of manufacturing and supplier issues for paper-based diagnostic tests. The incumbent will be responsible for conducting customer complaint investigations, maintaining the control charting process for production reagents as well as writing and executing validation plans. Other duties include participation in root-cause analysis efforts and aiding in identifying process/equipment improvements as well as other testing as directed. This person must be highly competent in bench-scale solution preparation and willing to learn specialized testing techniques. Must also be able to prepare, analyze, and present coherent data for review and summarize results in a technical report. etc. 7/1/2020
199 Sigilon
Cambridge, MA
Assistant/Associate Engineer, Biomaterials
BS/MS in biomaterials, engineering, biochemistry, or biology
Exp: 1-2 year(s)
Responsibilities: Perform proper sterile technique for tissue culture of primary cells and cell lines. Maintain and set up devices for biopolymer encapsulation systems. Perform established protocols for encapsulation of cells in novel biopolymer systems, cell-based functional assays, and associated biomaterial characterization assays. Work in a matrixed environment to make biomaterials for preclinical studies associated with all developmental cell therapy programs. Make observations, evaluate data, and interpret and document results in a well-maintained laboratory notebook. etc. 7/1/2020
200 Staar Surgical
Monrovia, CA
Quality Engineer
MS in science or engineering
Exp: 1 year
MAIN JOB RESPONSIBILITIES / COMPETENCIES: Support site production, operations, and quality and R&D teams by addressing emergent issues that might arise due to the operation processes. Serve as the quality representative during any product or process investigation. Lead investigations including root cause analysis and health risk assessment of the identified product or process nonconformities. Prepare and execute validations, technical studies, test method validations and other studies / reports as required. This includes preparation of protocols, establishment of test methodology and acceptance criteria, training personnel, execution, data analysis, investigation, and writing final reports. Initiate and lead project teams on non-conformance investigations regarding component failures, finished goods failures, and product returns. This includes but is not limited to performing risk analysis, determining root cause and recommending corrective action. etc. 7/1/2020
201 Staar Surgical
Monrovia, CA
Production Technician (CNC)
HS diploma or equivalent
Exp: 1-2 year(s)
MAIN JOB RESPONSIBILITIES / COMPETENCIES: 1. Thorough knowledge of all applicable SOP's: makes proper decisions in line with applicable SOPs and standards under normal conditions. 2. 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. 3. Troubleshoot issues on equipment and assist with preventative maintenance. 4. Edit equipment programs (as required). 5. Assist in revising procedures related to operation and preventative maintenance. 6. Support qualification activities (as required). etc. 7/1/2020
202 Staar Surgical
Monrovia, CA
Production Operator I
HS diploma or equivalent
Exp: 1-2 year(s)
MAIN JOB RESPONSIBILITIES / COMPETENCIES: 1. Thorough knowledge and appropriate implementation of basic production functions. 2. Completes required production documentation accurately. 3. Consistently meets quality and productivity targets. 4. Appropriately follows company policies, rules, and regulations. 5. Be able to interact well with others and work in a team environment. 6. Maintain work area environment in a clean and orderly manner. 7. Operate production related equipment. etc. 7/1/2020
203 Silverback Therapeutics
Seattle, WA
Lab Operations Assistant
HS diploma/AS/AA
Exp: 1+ year(s)
Silverback Therapeutics, a Seattle-based biopharmaceutical company, is seeking a Lab Operations Assistant to join our team. The successful candidate will support research laboratory operations by completing tasks related to laboratory equipment, stockroom supplies, facilities, and shipping/receiving. Essential Duties & Responsibilities: Promote and facilitate a clean and organized laboratory work area, ensuring the laboratory is well-stocked and functioning smoothly. etc. 7/1/2020
204 Singota Solutions
Bloomington, IN
Material Handler
HS diploma
Exp: 0-1 year(s)
General Description including Skills and Physical Activity Requirements: 1. Must be very customer focused to both internal employees and external clients. 2. Must be able to work within the FDA regulated environment per its specific requirements and those established by internal policy and standard operating procedures. 3. 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. 4. Effectively work within the configuration and rule process set up within an ERP system and bar code scanning environment to accurately manage inventory throughout the business. etc. 7/1/2020
205 Enanta Pharmaceuticals
Watertown, MA
Associate Scientist, Drug Metabolism & Pharmacokinetics (DMPK)
BS in biological sciences
Exp: 0-2 years in lab
The Associate Scientist will work with an experienced Ph. D. scientist to conduct drug permeability and liver / intestine / lung / kidney transporter studies in support of Enanta drug discovery programs. She/he will be an integral member of Enanta’s highly collaborative Pharmacology and DMPK/Bioanalysis Department focused on the discovery of novel therapeutics against liver and viral diseases including nonalcoholic steatohepatitis (NASH), primary biliary cholangitis (PBC), respiratory syncytial virus (RSV), and hepatitis B virus (HBV), etc. 6/28/2020
206 Epic Pharma
Laurelton, NY
Chemist
BS/BA in chemistry or related
Exp: 1 year as chemist or related
Analytical research and development, including analytical method development for assay, related compounds, dissolution for raw materials, in-process and finished products. Carry out method transfer and method validation. Draft validation protocols and reports. Work with different formulation types including tablets, capsules, soft gels, topicals and suspensions. Provide formulation support for research and development where required. 6/28/2020
207 Editas Medicine
Cambridge, MA
Cell Manufacturing Associate I
BS in biological sciences
Exp: 0-2 years in industry/academia
The candidate will contribute as part of a dynamic team to the development of gene-editing based ex vivo cell therapies in multiple disease areas, including hematology and immune-oncology. In this role, the candidate will be responsible for culturing and editing cells for use in Phase I clinical trials and for the creation of cell banks in a GMP environment. 6/28/2020
208 Enzo
Farmingdale, NY
Production Associate
Associates or BS/BA in biological sciences
Exp: 0-2 years in sciences/lab work
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. Assist in all packaging and labeling operations for Manufacturing. Assist in cGMP material inspection and receiving raw materials for Manufacturing. 6/28/2020
209 ERT
Pittsburgh, PA
Sales Associate
BS/BA in business/marketing/communications
Exp: 1-2 years in commercial sales
Identify, research and recommend new products and services for on-going projects based on client recommendations/requests and competitive intelligence. Coordinate with the project management and business development teams to identify, recommend and schedule in-person client visits when appropriate. Communicate with clients regarding services, the customer experience, potential problems, etc. 6/28/2020
210 Eargo
San Jose, CA
Electro-Acoustic Engineer
MS in asoustics/electrical engineering
Exp: 1-2 years in audio product development
The Electro-Acoustic Engineer would be involved in design and engineering development of audio requirements and systems, and related verification and validation of those requirements and systems for Eargo hearing instruments. Measure and validate audio performance at a system & component level. Failure Analysis & Problem solving of Audio Quality, Electroacoustics and Digital Signal processing algorithmic issue pertaining to hearing aids 6/28/2020
211 Element Biosciences
San Diego, CA
Research Associate/Associate Scientist – Chemistry Product Development
BS or MS in chemical or biological sciences/engineering
Exp: 1 year as research associate
Work closely with senior scientific staff to execute reactions that involve multiple complex materials. Optimize chemistry protocols and develop standard operation procedures. Assist troubleshooting problems in experiments in terms of assay design, protocol, reagents and characterization of materials. Prepare reagents, buffers and calibration standards 6/28/2020
212 Rubius Therapeutics
Cambridge, MA
Associate Engineer, Upstream/Downstream Process Development
BS in life sciences or engineering
Exp: 0-2 years
We are seeking an Associate Engineer in the Cell Product Development group, focused on upstream and downstream of bioprocessing for the cellular therapy. They will work directly with a team of scientists to optimize, scale-up, and characterize the novel cell therapy platform to increase productivity and/or advance the clinical pipeline. They will be involved in hands-on manipulation of ex vivo derived cells, and collection and logging of a variety of generated data sets. The right candidate will have experience in laboratory research either in industry or academic settings. etc. 6/25/2020
213 Repligen
Waltham, MA
Manufacturing Associate I - OPUS
BS
Exp: 1-2 year(s)
This position will function in Repligen's OPUS Column Packing groups. Cross training into other departments may be required based on the changing needs of the department. 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. Responsibilities: Experience working in a classified cleanroom, and knowledge of GMP/ISO/document controlled processes would be beneficial. Attention to detail, and the ability to work in a team environment are essential. Ability to read engineering drawings and be familiar with process control software is also highly desirable. etc. 6/25/2020
214 Repligen
Marlborough, MA
QC Technician
AS/AA in biology or other scientific field
Exp: 0-2 years
The QC Technician will report directly to the QC Supervisor and will be primarily responsible for performing in-process testing and data collection of flat sheet membrane and tangential flow filtration cassettes. The analytical equipment you will be using to support this position includes spectrophotometer, balance, pipette, pressure gauges, timers, and stirred cells. The successful candidate will actively follow Repligen ISO 9001 Quality Management System in support of the manufacturing processes and final product testing, including additional laboratory compliance as assigned by the QC Supervisor. etc. 6/25/2020
215 Repligen
Waltham, MA
Manufacturing Associate II - OPUS 2nd shift
HS diploma/BS/BA
Exp: 1-2 year(s)
This position will function in Repligen's OPUS Column Packing groups. Cross training into other departments may be required based on the changing needs of the department. 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. etc. 6/25/2020
216 Repligen
Marlborough, MA
QC Technician - 2nd shift
BS/BA in biology or related
Exp: 0-2 years
The QC Technician will be responsible for performing in-process testing and data collection of flat sheet membrane and tangential flow filtration cassettes. The analytical equipment you will be using to support this position includes spectrophotometer, balance, pipette, pressure gauges, timers, and stirred cells. The successful candidate will actively follow Repligen ISO 9001 Quality Management System in support of the manufacturing processes and final product testing, including additional laboratory compliance as assigned by the QC Supervisor. Training will be on the first shift for approximately 6-8 weeks prior to transitioning to second shift. etc. 6/25/2020
217 Regeneron
Rensselaer, NY
Packaging Process Engineer
BS/MS
Exp: 0+ years
The Fill Finish Engineer will serve as an expert for Packaging equipment and processes directly supporting the operations team. They will support equipment design and selection as well as process development activities. They will be hands-on, solving issues during technology transfer, cGMP start-up and routine manufacturing for Regeneron internal operations. This role will also support validation and training activities for syringe assembly and labeling, auto-injector assembly and cartoning and palletizing equipment and processes. etc. 6/25/2020
218 Regeneron
Tarrytown, NY
R&D Associate - Cardiovascular In-Vivo Pharmacology
BS/MS
Exp: 0-2 years
The Cardiovascular (CV) and Renal Therapeutic Focus Area is currently seeking an entry level R&D Associate to support in-vivo pharmacology studies.. Primary responsibilities will include animal dosing, routine animal procedures, and support for study takedowns across disease indications within the CV Therapeutic Focus Area. Job Duties: Animal husbandry, blood collection, tissue harvesting, basic rodent surgery. Calculate drug dosage and prepare dosing solutions. etc. 6/25/2020
219 Regeneron
Tarrytown, NY
R&D Associate- Clinical Bioanalysis
BS/MS
Exp: 0-4 years
Clinical Bioanalysis is looking for an R&D Associate to join the team. This individual will execute experiments under the direct supervision of a manager, perform routine technical tasks and begin to manage, organize, and interpret data more independently. An ideal candidate should possess a knowledge of the basic principles of immunoassays obtained through academic training and/or relevant industry experience. RESPONSIBILITIES: Train on manual and automated bioanalytical methods and execute methods to perform bioanalysis for clinical studies under supervision. Execute multiple plates within the same day. etc. 6/25/2020
220 Philips
Gainesville, FL
Product Quality Inspection Technician
AS/BS in engineering
Exp: 1+ year(s)
In this role, you have the opportunity to be a part of Philips Health Tech’s Quality Control team in Gainesville, FL. Along with your team, you will be responsible for product inspection to insure that it meets business obligations for product flow while remaining compliant. You will work as a skilled worker preforming a number of non-repetitive product quality inspections. You will operate relatively autonomous within procedures, methods and techniques. etc. 6/25/2020
221 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
222 Prosciento
San Diego, CA
Lab Assistant
HS diploma/BS in a science or health related field
Exp: 3 months
Participates in and assists in supporting the laboratory aspects of human clinical trials under the direction of the Laboratory Supervisor. Performs laboratory procedures while ensuring the integrity of the studies and the safety and well-being of human subjects. Performs duties in accordance with ProSciento’s values, policies, and procedures. Essential Duties and Responsibilities will include the following. Other duties may be assigned at the company’s sole discretion. Participates in day-to-day clinical and laboratory activities and procedures, ensuring efficient workflow, appropriate collection and management of research subjects’ laboratory samples, and adequate care and treatment of research subjects, maintaining quality control of specimen samples. etc. 6/24/2020
223 Prosciento
San Diego, CA
Business Development Associate
BS/BA
Exp: 1-2 year(s)
The Business Development Associate (BDA) works directly with Business Development Directors to increase new account penetration to increase face-to-face meetings and Request for Proposals (RFP). The BDA supports Business Development Directors through research and analysis of industry trends and potential client pipelines through numerous data platforms to develop strategic sales leads. Performs duties in accordance with ProSciento’s values, policies, and procedures. Develops an in-depth knowledge about the scientific and operational benefits of ProSciento services to support Business Development Directors’ communication with perspective clients. Researches and analyzes industry trends and prospective client pipelines across numerous data platforms to generate strategic sales leads for new and ongoing clients for follow-up by Business Development Directors. etc. 6/24/2020
224 Purdue
Wilson, NC
Pharmaceutical Technician, Packaging (2nd Shift: M-Th 4pm-2:30am)
HS diploma or equivalent
Exp: 1-5 year(s)
The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the packaging area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines. Primary Responsibilities: Follow Master Batch Records for the packaging of controlled, oral solid dose (OSD) and other dosage forms when required. Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging. Identify, report, and resolve quality issues. Safely and in compliance with batch records and SOPs, set up, operate, and clean packaging equipment. Perform in-process testing and inspections as required by Master Batch Record. Clean and sanitize packaging rooms including walls, floors, and ceilings per SOPs. etc. 6/24/2020
225 Promega
Madison, WI
Refrigeration / Maintenance Technician 2
AS/AA
Exp: 1+ year(s)
Perform grounds duties, equipment installation, building upkeep, repairs and preventative maintenance. Requiring knowledge of plumbing, electrical, refrigeration, HVAC, building automation systems, and carpentry. Uses experience and judgment to plan and accomplish a variety of complicated tasks. A wide degree of creativity and latitude is expected. ESSENTIAL DUTIES: 1. Perform a wide variety of general building and equipment installation, modification, repair work and preventative maintenance. This includes, but is not limited to electrical, plumbing, drywall, painting, carpentry, floor repair and other general building, varied equipment and systems work. 2. Perform HVAC, boiler, compressed air, refrigeration and other building systems trouble shooting. Identify and recommend the most effective, efficient, and timely course of repair action. etc. 6/24/2020
226 Promega
Madison, WI
Product Finishing IVD Technician - 1st & 3rd Shift (6 month project position)
HS diploma or equivalent
Exp: 1+ year(s)
JOB OBJECTIVE: Technician with a full understanding of the department including dispensing, kitting and labels. Uses technical concepts and depth of knowledge to resolve issues effectively. ESSENTIAL DUTIES: 1. Setup, operate and maintain manual and automated dispensing, capping and labeling equipment. 2. Pull products from inventory and assemble components into kits and kit sub-assemblies using quality system documents, including kit packaging diagrams (KPDs). 3. Accurately complete all required written documentation for batch records. etc. 6/24/2020
227 Discovery Life Sciences
Huntsville, AL
Laboratory Associate - Cell Processing
BS/Ba in biological sciences
Exp: 1-3 years lab experience
To be successful in this job you must be detail oriented, analytical, methodical, responsible, team focused and enjoy learning. You must also have a working knowledge of universal precautions, bloodborne pathogens and handling human biospecimens, proven laboratory experience including basic mammalian cell culture techniques, knowledge of aseptic techniques and excellent computer skills. 6/21/2020
228 Discovery Life Sciences
Huntsville, AL
Feasibility Associate
BS/BA in life sciences
Exp: 0-2 years, research preferred
The individual in this position must keep abreast of oncologic and immunologic diseases. Are you someone with a strong life sciences background who is analytical, decisive, detail-oriented, and an excellent communicator who's looking for a future with a growing biotech company? To be successful in this role, you must have a Bachelor's degree, preferably in life sciences. You must be able to multitask, maintain organized records, efficiently manage several projects simultaneously, think outside of the box and develop creative solutions to problems. 6/21/2020
229 Discovery Life Sciences
Huntsville, AL
Clinical Data Associate
BS/BA in life sciences
Exp: 0-2 years in biotech
To be successful in this role, you must be curious, analytical, detail-oriented, love heavy computer work, and be a team player. A Bachelor's degree, preferably with a major in life sciences is preferred. Previous biotech or medical experience is also preferred. 6/21/2020
230 Discovery Life Sciences
Huntsville, AL
Project Support Associate
Associates or BS in related
Exp: 1-2 years in admin/customer service
We're looking for two (2) standout Project Support Associates who will manage our off-the-shelf inventory projects and provide excellent support to a team of Project Managers, allowing them to remain focused on fulfilling customer expectations. To be successful in this role, you must be highly organized, detail-oriented, be familiar with medical and pathology terminology, have great computer skills, be an excellent communicator and team player. 6/21/2020
231 Diacarta
Richmond, CA
Customer Service & Technical Support Specialist
BS or MS in biology or related
Exp: 1-3 years in life science companay preferred
The customer service & technical support candidate will have strong technical knowledge in molecular biology and cancer diagnostics and will demonstrate technical credibility to effectively consult with customers and internal stake holders. Day to day responsibilities will include, sales order processing, order entry/dispatching/invoicing/post sales inquiries/responding to technical inquiries and trouble shooting. In addition, you will be responsible for dealing with general customer inquiries from new and existing customers, handling incoming leads from our website and update/maintain the lead tracking database. 6/20/2020
232 Diacarta
Richmond, CA
Inside Sales Specialist
BS in biology
Exp: 1-3 years in biotech/industry
The Inside Sales Specialist manages the customer sales process for specific products lines, accounts and/or sales opportunities via phone and e-mail. Includes engaging with existing customers and qualified sales leads, guiding customers to the DiaCarta products that best meet their needs, coordinating with internal resources to address customer questions/objections, providing budgetary pricing, creating and submitting individualized quotes and closing the sales process through the point of order receipt. 6/20/2020
233 Digirad
Mankato, MN
Technologist Assistant
HS Diploma/GED
Exp: 1 month training, CPR certified
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. Demostrates the knowledge and skills necessary to provide care appropriate to the age of the patients served. 6/20/2020
234 Digirad
Houston, TX
Nuclear Medicine Technologist
Degree or certification in nuclear medicine
Exp: 1 year in preforming imaging
The Nuclear Medicine Technologist will work will work under the direct supervision of site physician, performing various duties related to nuclear stress testing. Performs patient care functions related to perfusion imaging and stress testing at customer sites. Perform functional and/or perfusion rest and stress cardiac studies, including processing images for physician review. 6/20/2020
235 Digirad
Novi, MI
Cardiac Stress Technician
Associates or BS in related
Exp: Some experience in medical field/ emergency care preferred
The Cardiac Stress Technician will work under the direct supervision of site physician, performing various professional and administrative duties related to nuclear medicine stress testing. This includes but not limited to patient preparation, administration of exercise and pharmacological stress tests, and application of ACLS measures to patients when directed. 6/20/2020
236 GiscGenitcs
Salt Lake City, UT
Quality Engineer
BS/BA in sciences/engineering/biotechnology
Exp: 1 year in quality engineering
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. Leverages industry expertise and experience to guide and mentor company personnel through GMP/QMS requirements. 6/20/2020
237 Decipher Biosciences
San Diego, CA
Sample Processor I
BS in life sciences
Exp: Entry Level
The Sample Processor’s primary responsibility is to provide front-line support in the procurement of record of loan (ROL) material and manage chain-of-custody of samples received. This individual must support the Decipher internal and external customers in the routine functions to ensure client satisfaction and appropriate records and materials management are consistently maintained. 6/20/2020
238 Pace Analytical
Fargo, ND
Lab Analyst - GMP Micro (Q3/Q4)
BS in biotechnology, microbiology, or related
Exp: 1 year
The Microbiologist will work daily within labs performing tasks associated with GMP services. The Microbiologist is expected to become familiar with all of the products and to be able to perform most tasks associated with the purification of plasmid DNA. Note: We expect to hire for this position in Q3 or Q4 of 2020. RESPONSIBILITIES: Segregation, line clearance, and cleaning of GMP production areas. Planning and submitting inventory requisitions. Planning and preparation for production events including preparing of processing plan memos. etc. 6/17/2020
239 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
240 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
241 Paradigm (Exact Sciences)
Madison, WI
Materials Management Associate I - Monday - Friday, 4:00pm - 12:30am shift
AA/AS in business, operations, or related
Exp: 1+ year(s)
The Materials Management Associate I will assist in a variety of Materials Management functions including but not limited to purchasing, inventory management, packaging, shipping, receiving and distribution of goods and supplies. This position will work within defined protocols and procedures. This is a second shift position with the days and hours of Monday - Friday, 4:00pm - 12:30am shift. Essential Duties and Responsibilities include but are not limited to the following: May receive, verify, inventory or deliver incoming materials. May facilitate shipment of outgoing materials or products. etc. 6/17/2020
242 Paragon Genomics
Hayward, CA
Manufacturing Technician
BS in a biological science or related
Exp: 1 year
Paragon Genomics is a fast-growing life sciences company developing advanced reagents and assay kits for next-generation sequencing (NGS). We’re seeking a temporary Manufacturing Associate with a molecular biology background and basic technical knowledge of manufacturing operations. The ideal candidate has knowledge of and experience with current Good Manufacturing Practice (cGMP) and Standard Operating Procedures (SOPs). The ideal candidate will have wet-lab technical skills in NGS library preparation, target enrichment or molecular biology, in general. There is an opportunity for permanent placement for the candidate who demonstrates competence and a willingness to learn new responsibilities. etc. 6/17/2020
243 PAR Pharmaceutical
Chestnut Ridge, NY
Packaging Operator l - 2nd Shift
HS diploma or equivalent
Exp: 0 years
Learns and performs basic functions relating to the packaging of drug products consistent with established Current Good Manufacturing Practices (cGMP), customer requirements and in conjunction with all Standard Operating Procedures (SOP). Responsible for the safe and efficient execution of job duties, while ensuring product compliance to established standards. Responsibilities: Packaging Operations: Learns and executes under supervision the skills necessary to operate pharmaceutical packaging machinery which may include stamp machines, tape machines, box machines, electronic scales, and other machinery. Learns and executes processes such as: material handling, capping, outserts/med guides, in-process checks, packing, stacking, cartoning, etc. May learn and perform basic equipment set ups. etc. 6/17/2020
244 Perrigo
Covington, OH
QC Chemist II - 1st Shift, 2/2/3 Schedule
BS in chemistry, food science, or biology
Exp: 1-2 year(s)
We are currently looking for a highly motivated QC Chemist who will work 1st shift on a rotating 2/2/3 schedule. Description: Collect samples including raw material, finished product, process equipment and environmental. Test purchased materials and/or Perrigo manufactured products per cGMP requirements and participate in laboratory investigations. Operate laboratory equipment. Participate in internal and external quality audits. Maintain personal laboratory work area and assist with general laboratory cleaning. etc. 6/17/2020
245 Penumbra
Roseville, CA
Manufacturing Engineer 1 (Equipment)
BS in mechanical, biomedical, chemical, or materials engineering
Exp: 0-2 years
The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and that support continuous improvement in production. We are looking for an engineer to play a key role in manufacturing processes, interact between production and cross-departmental engineering groups in resolving problems encountered with equipment, and serve as the subject matter expert for manufacturing equipment. What You'll Work On: Optimize production processes by designing fixtures, acquiring off-the-shelf tooling and equipment, and implementing new fixturing on the production line. Perform equipment qualifications. etc. 6/17/2020
246 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
247 Ora
Andover, MA
Clinical Trial Associate
BS/BA
Exp: 1+ year(s)
At Ora, our Clinical Trial Associates assists project managers in clinical study conduct for clinical projects, supports the oversight of all investigator sites and ensures compliance with protocol/overall clinical objectives. Performs day to day activities under the guidance of the Sr. CTA/Lead, Assistant Project Managers and Project Managers. PRIMARY RESPONSIBILITIES: Ensure trials are conducted in adherence to study protocols, applicable SOPs, EMA, FDA regulations, ICH/GCP guidelines and government regulations. Drafts and/or reviews study-related documents and templates including study protocols, informed consents, source document templates, study plans, study related logs, etc. 6/16/2020
248 OraSure Technologies
Bethlehem, PA
Manufacturing Engineer
BS in chemical, mechanical, or manufacturing engineering
Exp: 1-2 year(s)
Support and optimize the manufacturing and packaging of disposable diagnostic devices. Support projects which may include new products, new equipment, process improvements, and cost reductions. ESSENTIAL DUTIES AND RESPONSIBILITIES: Support production operations by trouble shooting and repairing automated assembly and packaging equipment in conjunction with the Maintenance team. Investigate manufacturing yield or product nonconformance issues, determine root causes, and implement corrective and preventative actions. Develop and revise manufacturing process documentation including material specifications, component and assembly drawings, and work instructions. etc. 6/16/2020
249 Bausch Health
Greenville, SC
Distribution Associate
HS diploma or equivalent
Exp: 1 year
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. etc. 6/16/2020
250 Bausch Health
Tampa, FL
Microbiology Technician III - 2nd Shift
BS in microbiology, biology, or related
Exp: 1-2 year(s)
Objectives: Perform routine testing for release of raw materials, finished products, stability samples and R&D products. Perform Environmental and Utility Monitoring in aseptic areas. Responsibilities: Perform routine assays for endotoxin, potency, sterility, bioburden, microbial limits, and preservative effectiveness on various finished products and/or raw materials. Perform identification of organisms. Maintain laboratory culture collection and preserve cultures. Contribute to the preparation and checking of environmental summaries. Perform testing in conjunction with laboratory investigations. Perform Environmental and Utility monitoring. Perform testing in support of facility Validation activities. etc. 6/16/2020
251 Bausch Health
Rochester, NY
Microbiology Technician IV
HS diploma/BS in a life science
Exp: 1-2 year(s)
Conduct environmental monitoring (EM) per specifications for the Rochester Manufacturing Plant. Support the EM program through analysis and communication by adhering to established guidelines. Contributes as a team member and performs specifically defined work/projects. May participate in quality projects or teams. Responsibilities: Support environmental/water monitoring for the Rochester Plant. Specific responsibilities include scheduling, sampling, testing, and maintenance of supplies. Perform microbiological testing as part of the core competency function. Includes routine testing and validation support to the Rochester Plant and R&D. Initiation of NCR when pre-established levels are exceeded. may assist with root cause investigations/CAPAs when necessary. Preparation/review of memos, reports, SOPs, and protocols. etc. 6/16/2020
252 OraSure Technologies
Ottawa, ON
Lab Technologist, Validation & Compliance
BS/MS in biochemistry or molecular biology
Exp: 1+ year(s)
As part of Research & Development, the Lab Technologist position is responsible for testing as it relates to the DNA Genotek portfolio of products. In this role, the Lab Technologist will be responsible for managing testing timelines, performing hands-on lab work (e.g. extraction and quantification of DNA from biological samples, kinetic enzyme assays), summarizing data, and communicating the results with the team. Responsibilities: Performs experiments to assist in solving scientific problems of interest to the company, with guidance from a Research Associate or Scientist. Executes, and analyzes experiments. Performs hands-on laboratory experimental work. Communicates ideas and participates in scientific discussions. etc. 6/16/2020
253 OraSure Technologies
Bethlehem, PA
Formulation Specialist
BS in chemistry, biochemistry, or equivalent
Exp: 1-3 year(s)
Manufacture the chemical formulations necessary for production of all products. Responsibilities: Coordinate and prepare all chemical formulations according to batch production records (BPR). Responsible for changing documents when necessary (CTN). Assist in writing and performing validation protocols, nonconformance investigations and planned deviation investigations. Evaluate reagents, raw materials and in-process components through visual and performance testing according to specifications. Recommend acceptance or rejection of raw materials, and in-process components based upon established specification and procedures. Be responsible for the accuracy and completeness of material inventory records. Inform supervisor or approved designee to order inventory and supply items as needed. etc. 6/16/2020
254 Nuvasive
Memphis, TN
Associate Sterile Processing Technician
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. 6/16/2020
255 Nuvasive
San Diego, CA
Development Engineer
BS in mechanical or biomedical engineering or related
Exp: 0-2 years
NuVasive is seeking a Mechanical or Biomedical Engineer for our Mechanical Systems Integration team. As a Development Engineer within our team, you’ll be responsible for the design and development of medical devices with enhanced features that allow integration with our navigation and robotics enabling technology platform to treat spinal pathologies in accordance with US and international regulations. You will gain hands-on experience developing innovative mechanical solutions to meet patient and surgeon needs from concept to commercialization. This requires working in cross-functional teams, including marketing, purchasing, regulatory, quality, research and testing, manufacturing, etc., to help manage the product development process, project timeline, and deliverables to ensure designs are safe and effective for clinical use. etc. 6/16/2020
256 Nuvasive
West Carrollton, OH
Material Handler -1st shift
HS diploma or equivalent
Exp: 1+ year(s)
The Associate Distribution Coordinator 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 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. Compiles information on receipt of disbursement of material, equipment, merchandise, or supplies, and computes inventory balance, price, and cost. etc. 6/16/2020
257 Miltenyl Biotec
Auburn, CA
Logistics Associate
HS diploma
Exp: 1 year
As a member of the Miltenyi Biotec team, you will help ensure that the shipping and receiving process runs efficiently for our growing biotechnology organization. You will prepare and process inventory using your Enterprise Resource Planning (ERP) and shipping systems knowledge. In addition, you will record and receive incoming shipments according to established SOPs, as well as prepare and process shipments according to international regulations. There will also be occasion for employing hand-trucks and forklifts in order to move and store certain articles during routine inventory maintenance. etc. 6/16/2020
258 Miltenyl Biotec
Cambridge, MA
Clinical Trial Associate
BS/BA
Exp: 0-2 years
Your Tasks: Collaborate with Clinical Trial Managers to assist in the operational and logistical aspects of clinical trial management tasks. Act as a liaison with CROs and other clinical vendors to ensure deliverables are met. Partner with Investigators and clinical site staff to ensure optimal Sponsor-Site relationships. Proactively Assist in the management of studies to ensure adherence to timelines and identify investigative site risks, proposing corrective actions. Serve as Functional TMF Document Specialist for Clinical Operations, to include submission of documents to and maintenance of the TMF. etc. 6/16/2020
259 CryoLife
Kennesaw, GA
Microbiology Technician II
BS in microbiology or related
Exp: 1-2 years in lab
Perform microbiological testing for human tissue and medical device samples, as well as perform environmental and water monitoring. Monitor cultures for the presence of microbial growth. Hours: Mon, Tues, Wed, Fri from 7am-5:30pm 6/14/2020
260 CryoLife
Kennesaw, GA
DQA Analyst
BS/BA in biological sciences
Exp: 1-2 years in
To coordinate the activities necessary to ensure that all donor records flow through the system with minimal delay. Provide a leadership role for entry level DQA individuals. Ensure that all areas outlined under “Principal Responsibilities” are accomplished in an efficient, professional manner. Read, critique, review and complete DQA form reviews per QA0175, QA0176 and QA0079 as delegated by DQA Management. 6/14/2020
261 CryoLife
Kennesaw, GA
Microbiology Associate
BS/BA in life sciences preferred, HS Diploma minimum
Exp: 1-3 years in lab
Will assist management in the review of Microbiology records to ensure they are compliant with required Standard Operating Procedures. Will ensure that all areas outlined under “Principal Responsibilities” are accomplished in an efficient, professional manner. Interface with Microbiology staff and other applicable personnel to clarify and/or correct the information provided, and to solicit required information. Understand ISO requirements, GTPs and the Quality System Regulations as they pertain to the Laboratory, i.e., nonconformities, Good Documentation Practices, calibration, equipment maintenance, etc. 6/14/2020
262 CryoLife
Kennesaw, GA
Process Engineer I
BS in engineering or life sciences
Exp: 0-2 years
Responsible for providing process engineering support for all product manufacturing departments. Supports manufacturing operations to ensure consistent adherence to the standard operating procedures and business continuity. Initiates process improvement initiatives to improve the efficiency of current manufacturing processes, as well as develop new processes to improve manufacturing efficiency. 6/14/2020
263 Cue
Cambridge, MA
Contract Associate Scientist – Translational Immunology
MS in relevant
Exp: 0-2 years
We are looking for a motivated Contract Associate Scientist to join our Translational Immunology/Immuno-Oncology group to provide key mechanistic, pre-clinical and translational support for Cue Biopharma’s growing pipeline. The Contract Associate Scientist will be part of the company’s TCR Core, a team dedicated to generating and performing key studies with T Cell Receptors – TCR-transduced human cell lines and primary human T cells. This is a temporary contract position that could last up to six (6) months. 6/14/2020
264 Cyanotech
Kailua-Kona, HI
Cultivation Lab Technician
BS in aquaculture, biology, life sciences
Exp: 1 year in lab and/or algal production or aquaculture
This position is responsible for Spirulina production system data and adjustments as necessary to stay within set operating specifications. This position will be responsible for the data necessary to track Spirulina system performance as well as data necessary for operational set point adjustments necessary to stay within system specifications, such as nutrient analyses, pond data, and harvest/processing data. 6/14/2020
265 Corium
Grand Rapids, MI
Operator I - Weekend Days
HS Diploma/GED
Exp: 1-2 years in cGMP environment preferred
Currently, we seek an Operator I to work the weekend day shift at our Grand Rapids facility. The Operator I will set up and operate extrusion equipment to produce products to meet cGMP, customer and internal quality standards for our Grand Rapids facility. As an Operator I, you will: Set-up and operate extrusion equipment. Perform basic maintenance and troubleshooting of equipment. Ensure production crew is on task and focused on safety, quality, and productivity 6/13/2020
266 CRISPR Theraputics
Cambridge, MA
Research Associate/Research Associate II, Immuno-Oncology
BS or MS in biology
Exp: 1-2 years lab biology experience
We are looking for Research Associates (all levels) to join the Immuno-Oncology Groups at CRISPR Therapeutics in Cambridge, MA (oncology). Successful candidates will be integral to developing next generation cellular therapeutics with an emphasis on genetically engineering immune cells to increase their therapeutic potential. Molecular biology skills are required for this position and should have enthusiasm, passion, and a desire to create important new medicines for patients. 6/13/2020
267 Covance
Indianapolis, IN
Medical Technologist I
BS/BA in med technology or clinical lab sciences
Exp: 1 year med tech training program
Resolve technical specimen issues in preparation for analysis and specimen storage and routine and non-routine assay problems. Ensure the validity of test results through the performance of established quality assurance and quality control procedures. Perform experiments, as scheduled, for evaluation of new Calibrator and QC lots. Perform testing, needed to ensure validity of material, prior to being placed into service 6/13/2020
268 Covance
Indianapolis, IN
Medical Technologist I (PRN)
BS/BA in med technology or clinical lab sciences
Exp: 1 year med tech training program
Resolve technical specimen issues in preparation for analysis and specimen storage and routine and non-routine assay problems. Ensure the validity of test results through the performance of established quality assurance and quality control procedures. Perform experiments, as scheduled, for evaluation of new Calibrator and QC lots. Perform testing, needed to ensure validity of material, prior to being placed into service 6/13/2020
269 Covance
Madison, WI
Sample Handling Assistant I
HS Diploma/GED
Exp: 0 years required
Performs a variety of Sample Management and/or Archives responsibilities in compliance with appropriate SOP’s and Good Laboratory Practice (GLP), Good Clinical Practice (GCP) or Good Manufacturing Practice (GMP) regulations (as appropriate) in support of various Business Unit Operations. Ensures that services to both internal and external customers are provided in a timely manner or as agreed in Service Level Agreements. 6/13/2020
270 Covance
Madison, WI
Nonclinical Data Associate
BS/BA in computer sciences/informatics
Exp: 1-3 years, entry level
This is an entry level Nonclinical Data Associate position with a primary function of drafting and finalizing nonclinical datasets. Performing quality control review datasets using industry data standards using (e.g. SEND, SDTM, SENDIG). May compile metadata to populate databases supporting nonclinical safety assessment. May assist with software testing and validation activities: including executing test scripts and maintaining documentation in accordance with Covance Unified Systems Life Cycle (CUSLC) methodology which complies with General Principles of Software Validation issued by the FDA. 6/13/2020
271 Covance
Dallas, TX
Research Nurse I
Associates or BS in nursing with licensure
Exp: 1-2 years in research
As a Clinical Research Nurse for Covance your top priority will be to ensure that the dignity, health, safety, and welfare of participants. This position will be office based in Dallas, TX. This will be a rotating shift to either work Day, mid or overnight shifts as needed. Utilize nursing assessment skills to observe participant general well-being and potential adverse events. Document adverse events and takes appropriate action as needed. 6/13/2020
272 Covance
Indianapolis, IN
Histology Technician
HT(ASCP) certification as histoltechnologist
Exp: 1 year in research/histology
Process daily samples according to written procedures prior to end of day utilizing histology techniques of cryotomy, microtomy, tissue grossing, tissue embedding, routine staining, special staining, immunohistochemistry (IHC) and fluorescence in-situ hybridization (FISH). Maintain accurate documentation and paper work to provide a sample audit trail. Communicate sample enquiries and issues via email to internal and external clients and work well as a part of a team as well as independently 6/13/2020
273 Cardinal Health
Chicopee, MA
Assembler II - Hydra - 2nd Shift
HS Diploma/GED
Exp: 1-3 yearas
Performs a variety of tasks ranging from repetitive to non-repetitive production to put together component parts to make assemblies, sub-assemblies or completed units, using standard operating procedures. May conduct quality inspections on processing line in accordance with quality specifications. 6/13/2020
274 Cardinal Health
Obetz, OH
Associate II, Warehouse Operations (Second Shift)
HS Diploma/GED
Exp: 1-2 years related
Warehouse Operations 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. Also responsible for the efficient flow of products from the point of product receipt from vendors to the shipment of products (via prescribed service parameters) to a variety of internal and external customers 6/13/2020
275 Cardinal Health
La Vergne, TN
Associate II, Warehouse Operations
HS Diploma/GED
Exp: 1-2 years related
Warehouse Operations 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. Also responsible for the efficient flow of products from the point of product receipt from vendors to the shipment of products (via prescribed service parameters) to a variety of internal and external customers. 6/13/2020
276 Cardinal Health
Omaha, NE
Inventory Associate
HS Diploma/GED
Exp: 1-2 years related
Inventory Management is accountable for the design and execution of demand planning and customer forecasting systems, supply planning, product deployment and expediting processes, and the development and implementation of a stocking optimization model to minimize costs and inventory while delivering on service requirements. 6/13/2020
277 Cardinal Health
Charlotte, NC
Lab Technician - Nights
BS/BA in sciences
Exp: 1-2 years in lab
The primary work environment consists of a cyclotron and associated manufacturing facility for the production of PET radiopharmaceuticals, which must be kept clean, orderly, properly lighted and maintained in optimum operating condition. Successfully complete extensive training, including e-learning assignments and hands on components, to demonstrate and maintain proficiency. Manufactures radioactive isotopes (includes synthesis set up, hot cell manipulations, distribution). 6/13/2020
278 Cardinal Health
Crystal Lake, IL
Manufacturing Associate I - C Shift - Contract Conversion
HS Diploma/GED
Exp: 1-3 months training, 0-6 months work experience
Sets up and operates a variety of machine tools to make metal parts, mechanisms, tools, or machines to exacting tolerances and dimensions. determines sequence of operations, number of cuts required, and method of setup. Interprets blueprints, sketches, and engineering specifications. makes standard shop computations relating to dimensions of work, tooling, feeds, and speeds 6/13/2020
279 Cardinal Health
Crystal Lake, IL
Manufacturing Associate II - Syringe - B Shift - Contract Conversion
HS Diploma/GED
Exp: 1-3 years of work/training
Sets up and operates a variety of machine tools to make metal parts, mechanisms, tools, or machines to exacting tolerances and dimensions. determines sequence of operations, number of cuts required, and method of setup. Interprets blueprints, sketches, and engineering specifications. makes standard shop computations relating to dimensions of work, tooling, feeds, and speeds 6/13/2020
280 Natus Medical
Middleton, WI
Repair Technician (I or II)
AA/AS
Exp: 0-6 months
WHAT YOU'LL GET TO DO IN THIS JOB: Test, calibrate and troubleshoot assemblies of our medical devices as well as perform electronic calibration and verify fixtures. Committing to high quality work (less than 2% failure rate on repairs) means delivering an exceptional product to healthcare providers so they can help their patients. Maintain a 10 business day repair turnaround time because getting our customers up and running means we can help more patients faster. Solve challenging problems by developing and/or designing test processes/procedures based on product specifications. Have the opportunity to cross-train to work in other areas to support business needs. etc. 6/10/2020
281 Nelson Labs
Salt Lake City, UT
Development Chemist
BS in chemistry or related
Exp: 1-3 year(s)
Looking for a Development Chemist position with a wide range of experience to work in a fast paced environment. 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). etc. 6/10/2020
282 Nemera
Buffalo Grove, IL
Quality Engineer Quality – Buffalo Grove
Unspecified
Exp: 1-3+ year(s)
Nemera needs a QUALITY ENGINEER to join our team in Buffalo Grove, Illinois. The Quality Engineer is responsible for planning, coordinating and managing through completion, assigned projects to ensure the development and production of products meets customer and internal quality deliverables. Responsibilities will also include coordinating and leading investigations regarding customer complaints, and customer interaction. etc. 6/10/2020
283 Nitto
Cincinnati, OH
Research Scientist I
MS in chemistry or related
Exp: 1+ year(s)
The Research Scientist I is responsible for executing analytical tasks, including method development activities, for one or more projects to support research and development primarily focused on oligonucleotides. Key Responsibilities: Execute testing per method or protocol for development, qualification, verification, validation, and transfer of analytical methods. Analyze test samples, process data, and report results with minimal errors to support research and development primarily focused on oligonucleotides. Provide analytical support to Process Development and Manufacturing. Design and perform method development experiments. Perform GDP and technical peer review. Author technical documentation (e.g. methods, procedures). etc. 6/10/2020
284 Nitto
Cincinnati, OH
Quality Control Analyst I
MS in analytical chemistry
Exp: Not necessary for MS candidates
Key Responsibilities: Provides analytical support to small molecule and oligonucleotide manufacturing groups utilizing various analytical instrumentation techniques including HPLC, UPLC, LCMS and NMR instrumentation. Records and reports results of analyses in accordance with prescribed lab procedures and SOPs. Maintains accurate and complete lab notebooks. Reviews laboratory documentation for calculation, entry and cGMP compliance. Develops and/or modifies test methods. Documents and reports results of development and experimentation in technical reports if needed. Participates in cGMP training and implements cGMP operating procedures. etc. 6/10/2020
285 Nitto
Marlborough, MA
Research Scientist II/III
MS
Exp: 1-4+ year(s)
The Research Scientist II/III is responsible for meeting the analytical testing requirements to support research and development projects primarily focused on oligonucleotides. Design and execute testing per method or protocol for development, qualification, verification, validation, and transfer of analytical methods. Provide analytical support to Process Development and Manufacturing and help develop process controls. Analyze and review project data, correct errors, and report results. Design, review, perform, and improve method development experiments to support research and development primarily focused on oligonucleotides. Develop new analytical applications and technology. Perform GDP and technical review within multiple projects. etc. 6/10/2020
286 Nostrum Laboratories
Kansas City, MO
Packaging Technician
HS diploma
Exp: 1 year
The Packaging Technician performs routine packaging operations for the production of pharmaceutical products; operates packaging line equipment according to established SOPs and department procedures. Duties and Responsibilities: Prepares and cleans room, equipment, facility and documents for manufacturing and packaging process. Verifies calculations, process steps and yield. Ensures that processes, tools, products and materials meet established quality standards and requirements. Notifies management when inventory fails below certain levels. Assists in the assembly and disassembly of process equipment as necessary. Examines sample of finished product per batch record instructions for conformance with specifications. etc. 6/10/2020
287 Novartis
Morris Plains, NJ
Associate Scientist Bioanalytics
BS in biology, chemistry, biochemistry, or related
Exp: 1+ year(s)
In the role of Associate Scientist Bioanalytics you will be responsible for performing Bio-Analytical testing such as Flow, ELISA, cell count, cell viability, residual bead assessment, qPCR. We are looking for an Associate Scientist who follows quality policies, work on shifts covering daytime / evening and one or both weekend days and execute method qualification/optimization of methods as per appropriate protocols. Your responsibilities include, but are not limited to: Contribute to OOS/OOE investigations and deviation investigations. Interface with regulatory agencies during audits. etc. 6/10/2020
288 Novartis
Johns Creek, GA
Manufacturing Technician - Full Time Day & Night Shifts
HS diploma/AS/AA
Exp: No experience required
Manufacturing Technicians participate in all aspects of production processes including but not limited to loading raw materials, operating SPC Lens Inspection, SAP final record review, operating secondary packaging equipment, performing lot changes, improving yields, using calibrated measurement equipment, troubleshooting and using support equipment such as sterilizers and tool drums. Interact closely with lens inspectors to identify defects and perform corrective actions as necessary. Perform minor equipment repairs and adjustments, and conduct Autonomous Maintenance and 5s duties. Coordinate downtime to ensure efficient use for maintenance, corrective actions, and cleaning. etc. 6/10/2020
289 Novartis
Carlsbad, CA
Research Associate
BS/BA
Exp: No experience required
Your responsibilities: Works in a GMP/GCP/GLP/CLIA regulated environment and is responsible for following all applicable regulations. Work in a regulated laboratory following work instructions and SOPs. Provide support for clinical assay development and/or validation activities. May assist in execution of routine testing for clinical specimens using established testing methodologies. Maintain accurate records related to all work with assay development, sample handling and testing, test and project results. Ensuring that Quality Events such as incidents and deviations are proper documented, and for supporting/owning the immediate remediation and preventative actions. Ensuring change requests are properly initiated, completed, and approved prior to the use of the assay, system, instrument, software, etc. being changed. etc. 6/10/2020
290 Novartis
Johns Creek, GA
Lead Production Technician - LS1 Days
HS diploma or equivalent
Exp: No experience required
Coordinate the shipment processes of a natural work area to achieve day to day goals in quality, service, and efficiencies. Actively participate on High Performance Teams to address day-to-day business activities, safety, quality, and training needs. Participate in meeting production goals/product quality. Assure that the goals for product volume and efficiencies are met by: Evaluating negative variances to plan using the MES system and other reports, document these and then determine action plan for correction. Performing shift cross-over w/counter-part at beginning and end of shift. Performing daily 5 minute meetings at the beginning of the shift with area personnel. etc. 6/10/2020
291 Novartis
Fort Worth, TX
Technician III Packaging FWN CLC 1st shift
HS diploma or equivalent
Exp: 0-2 years
Responsible of robust manufacturing process performed under current Good Manufacturing Practices (cGMP) and Health, Safety and Environment (HSE) and support the improvement of the process and deliver efficiency to full satisfaction of our customers. Contribute to maintain a high level of good housekeeping and carrying out operations within accepted GMP and HSE practices -Ensure proper escalation of all matters related with HSE, quality, supply and production, implement decisions and act as responsible for continuity of production -Support senior production operator with problem solving and teamwork and support a high performance teamwork environment. etc. 6/10/2020
292 Novartis
Houston, TX
Molding Operator I
HS diploma or equivalent
Exp: No experience required
Responsible for operating or monitoring tools and equipment on a daily basis used in the molding process. Operates light-duty bench or floor-type machine tools and equipment such as small lathes, power mills, extruding machines, drills or punch presses, power brakes, shears or saws. May set up machining machines and make adjustments, and perform maintenance on machines. Checks work using prescribed gauges, jigs and fixtures to measure close tolerances. Some machines may be numerically controlled. etc. 6/10/2020
293 Novartis
Fort Worth, TX
Scientist (Pre-Clinical Development)
BS/BA
Exp: 0-1+ year(s)
Conduct and maintain in vivo and in vitro exploratory and GLP-regulated preclinical safety studies in support of government submissions. Administers drugs to candidates via a variety of routes including topical ocular, intravitreal, intravenous, etc., to various test systems including nonhuman primates, rabbits, rodents, etc. Assists Study Directors and other senior personnel in the development and validation of new experimental methodologies. Follows study protocols; data will be generated and collected in an accurate and timely manner. Proofreads Data Packages for incorporation into technical reports, and are subject to audits by QAU and various regulatory agencies. etc. 6/10/2020
294 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
295 Cooper Surgical Group
Guilford, CT
Laboratory Technician
BS in biological sciences
Exp: 1-3 years in culture media
We are seeking to hire an laboratory technician for full time employment in a large-scale culture media manufacturing facility. Candidate will be involved in a wide range of process tasks from maintaining an ISO certified cleanroom to final product. 6/8/2020
296 Cooper Surgical Group
San Antonio, TX
Clinical Specialist
BS/Ba
Exp: 1-2 years in sales
As a Clinical Specialist these goals and target accounts are set by both SBU Senior Management and the Regional Manager they are assigned to. Clinical Specialists will be responsible for supporting the sales of all SBU products where appropriate. Individual is required to make sales calls to surgeons of various specialties, operating room management, nursing, supply chain, and administration. 6/8/2020
297 Codexis
Redwood City, CA
Research Associate, Process Development-Downstream
MS in chemical engineering/biochemistry
Exp: 1-2 years in downstream processes
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. Perform protein recovery experiments using unit operations such as homogenization, centrifugation, depth filtration, microfiltration, and ultrafiltration. 6/7/2020
298 Coloplast
Minneapolis, MN
Pricing and Payments Associate
BS or MBA in business/finance
Exp: 0-2 years in analysis
Analyze and model pricing scenarios for Integrated Delivery Network customers (IDNs), dealers and distributors for Requests for Proposal (RFPs). Devise customer incentives with the sales team that are in line with business objectives. Calculate monthly, quarterly, and annual payments for customers including national Group Purchasing Organizations (GPO), Health Systems (IDN), and Key Accounts as indicated by contractual commitments 6/7/2020
299 Color
Burlingame, CA
Clinical Lab Assistant, COVID-19 (Temporary)
BS/BA in sciences/engineering
Exp: 0-2 years in CLIA-cert lab
The Clinical Lab Assistant will be responsible for assisting in routine sample processing in a high complexity CLIA-certified laboratory, and you will be working with other laboratory professionals who have joined Color from UCSF, Stanford, Invitae, Counsyl, and other academic and commercial laboratories. Assist in routine laboratory maintenance, including equipment maintenance, maintaining lab cleanliness and a safe laboratory environment 6/7/2020
300 Complete Genomics
Houston, TX
Field Application Scientist (Houston, TX)
MS in life sciences
Exp: 0-2 years
Coordinate and conduct customer training for MGI NGS products and applications. Troubleshoot issues related to experimental design, data processing, software operation, sample preparation and chemical reaction. Perform preliminary on-site failure analysis to identify root cause and feedback to corresponding company department or personnel. 6/7/2020
301 Complete Genomics
Boston, MA
Field Application Scientist
MS in life sciences
Exp: 0-2 years
Coordinate and conduct customer training for MGI NGS products and applications. Troubleshoot issues related to experimental design, data processing, software operation, sample preparation and chemical reaction. Perform preliminary on-site failure analysis to identify root cause and feedback to corresponding company department or personnel. 6/7/2020
302 Civetta
Cambridge, MA
Research Associate, Protein Biochemistry
MS or BS in biological sciences
Exp: 1-2 years in lab sciences
Perform small-scale and pilot-scale expression trials using robotic liquid handling systems to identify conditions for soluble expression of human proteins in heterologous systems. Scale-up to liter volumes of bacteria in high-density bio-fermentation systems, and of insect cells in shaking incubators. Learn and implement standardized purification workflows for multiple-column purifications of fusion-tagged proteins 6/7/2020
303 Civetta
Cambridge, MA
Research Associate, Molecular Biology
MS or BS in biological sciences
Exp: 1-2 years in lab sciences
Assist in designing and creating expression vectors for use in bacterial and insect cell heterologous expression systems using robotic liquid handling systems. Perform small-scale and pilot-scale expression trials to identify conditions for soluble expression of human proteins in heterologous systems using robotic liquid handling systems. Scale-up to liter volumes of bacteria in high-density bio-fermentation systems, and of insect cells in shaking incubators 6/7/2020
304 Concerto
Remote/Memphis HQ, TN
Quality Control (QC) Reviewer
Associate's degree
Exp: 0-2 years
Concerto HealthAI is looking for a Quality Control (QC) Reviewer who will be responsible for reviewing and ascertaining the quality of curated data across the Data Curation Services (DCS) Division. The QC Reviewer works under the direct management of the Quality Control (QC) Manager. This role can be remote or based out of our Memphis office. 6/7/2020
305 Concerto
King of Prussia , PA
Pharmaceutical Data Analyst – Analytics
BS/BA in related
Exp: 1-4 years in business/data analytics
Writes and reads query language (specifically Microsoft SQL) for purposes of data management, data QC, reporting and analysis. Creates standard and custom reports that provide insight and value for clients using a combination of SQL, Excel, and BI tools. Evaluates internal data sources and processes for quality and integrity, working cross-functionally with other internal teams, Project Managers, and clients to resolve errors. 6/7/2020
306 Concerto
Memphis HQ, TN
Data Abstractor
Associate's degree
Exp: 0-2 years
Access electronic data systems for review of medical records and enter specific data into congruent electronic data systems. Review project specific documents, as needed, to develop familiarity with project goals and with the Abstractor tasks in each project. Use other resources as needed to gain the knowledge required to perform Abstractor work on new projects. 6/7/2020
307 Clinilabs
New York, NY
Clinical Research Assistant/Medical Assistant (PER DIEM) – NY & NJ
HS Diploma/GED
Exp: 1-2 years
The Research Assistant (RA) is responsible for assisting with document management, protocol related clinical assessments of research subjects, laboratory functions and assisting in tasks related to the work of the Clinical Research Coordinators. Assisting in subject visits, including direct contact with subjects, processing of visit data, ensuring the completeness and integrity of source documents and case report forms (CRFs), and other related duties. 6/7/2020
308 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. 6/3/2020
309 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
310 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
311 Cantel Medical
Plymouth, MN
Applications Engineer
Technical degree
Exp: 0-2+ years
At Cantel, preventing infection is our business. As a leading provider of infection prevention products and services in the healthcare market, we are dedicated to delivering high-quality, innovative solutions that improve outcomes and help save lives. We accomplish this mission by delivering our products through the following operating units: Medical: Endoscopy procedure disposables include single-use valves and irrigation tubing. The medical device reprocessing systems, disinfectants, detergents we manufacture and distribute are used to disinfect high-level endoscopes. etc. 6/2/2020
312 LabCorp
Overland Park, KS
Specimen Processor
HS diploma or equivalent
Exp: 1-2 year(s)
Job Duties/Responsibilities: Prepare laboratory specimens for analysis and testing. Unpack and route specimens to their respective staging areas. Accurately Identify and label specimens. Pack and ship specimens to proper testing facilities. Meet department activity and production goals. Properly prepare and store excess specimen samples. etc. 6/2/2020
313 Meridian Bioscience
Cincinnati, OH
Machine Operator- Entry Level
HS diploma or equivalent
Exp: Entry level
The Machine Operator (ImmunoCard Operator I) safely manufactures FDA regulated medical devices in a fast-paced and results-oriented environment, meeting quality standards in accordance with cost, schedule and all standard cGMP operating procedures and guidelines. KEY DUTIES: Perform manual and automated assembly/packaging of commercial diagnostic products. Operate and maintain automated production equipment. etc. 6/2/2020
314 Meridian Bioscience
Cincinnati, OH
Regulatory Affairs Associate
BS in biological science, microbiology, chemistry or related
Exp: 1+ year(s)
This position will be responsible for supporting Meridian’s regulatory and quality processes and ensuring that Meridian’s activities are consistent with applicable quality and regulatory requirements. Assist with product compliance throughout all stages of the product lifecycle as well as work with cross-functional teams to provide support of business objectives. Also assist in assembling timely preparation of documents for domestic and international regulatory submissions, ensuring compliance with applicable regulations. etc. 6/2/2020
315 Meridian Bioscience
Cincinnati, OH
Production Worker- Entry Level
HS diploma or equivalent
Exp: Entry level
The Production Worker (Para-Pak Operator I) safely manufactures FDA regulated medical devices in a fast-paced and results-oriented environment, meeting quality standards in accordance with cost, schedule and all standard cGMP operating procedures and guidelines. Key Duties: Operate manual and automated assembly/packaging of commercial diagnostic products. etc. 6/2/2020
316 Mammoth Biosciences
San Francisco, CA
Research Associate - Sample Prep
BS/MS in biology, chemistry, or related
Exp: 1+ year(s)
Mammoth is seeking a Research Associate experienced in protein and nucleic acid biochemistry techniques to support our research and product development teams. The ideal candidate will have experience with in vitro assay development, nucleic acid extraction and amplification techniques. Further, the candidate will be comfortable working as part of a team, be highly motivated, and display excellent time management skills. Responsibilities: Assist in developing, validating, and improving CRISPR-diagnostic assays. etc. 6/2/2020
317 Cepheid
Sunnyvale, CA
QC Analyst II
AA or technical trade degree
Exp: 1-2 years
The Quality Control Analyst II will perform qualification and manufacturing of template materials used in internal product testing and as raw materials for production according to established procedures. This position will be working in Quality Control to support control reference material production as well as stability program activities in accordance to GMP standards and FDA/ISO regulations. 5/31/2020
318 Sanofi
Framingham, MA
Manufacturing Specialist I
BS/BA
Exp: 1-3 years
The Manufacturing Specialist I uses expert knowledge of compliance and GXP manufacturing processes to manage investigation and improvement initiatives within manufacturing operations. Participates on cross functional teams to drive complex investigation close outs, determine root cause and implement appropriate Corrective and Preventative Action. 5/31/2020
319 Sanofi
Ridgefield, NJ
Aseptic Technician Associate
HS Diploma/GED
Exp: 1-3 years in cGMP environment
Independently performs 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 equipment, glassware, filters, etc. required for production. Assists in process and system validation activities as required. 5/31/2020
320 Sanofi
Framingham, MA
Research Associate
MS in biological sciences
Exp: 0-2 years in cell culture
Responsibilities will include expression vector construction; generation and evaluation of cell lines, including genetic characterization, conducting studies to improve recombinant protein expression and cell line development platforms; development of novel methods for cell line characterization and formal documentation of associated procedures. Manage work assignments, analyze and interpret test results, and conduct necessary troubleshooting; consult with supervisor as needed. 5/31/2020
321 Sanofi
Swiftwater, PA
Production Technician
BS/BA
Exp: 0 years in cGMP or pharma
Performs production in accordance with volume fluctuation, business need, and effective procedures. Must be flexible to ensure staffing for changing business volume and needs. Works with Senior Technicians, leads, and managers to ensure operational area is running as intended to meet all operational goals. Must attend shift change daily to ensure preparedness for workday. 5/31/2020
322 Baxter
Marion, NC
Quality Lab Assoc I
BS/BA in biological sciences
Exp: 0-2 years
Conduct microbiological analyses on raw materials, in-process and finished products. Collect samples related to Environmental Monitoring program at Baxter manufacturing area. Work under minimum supervision. Use laboratory instrumentation and computer systems to collect and record data. 5/31/2020
323 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
324 ChemBio
Medford, NY
Quality Control Laboratory Analyst
BS in biological sciences
Exp: 1-3 years in cGMP environment
Responsible for execution of analytical laboratory tests and evaluations of product performance and processes in the Quality Control Department, in accordance with approved methodologies, policies, and associated regulations. Performing analytical laboratory tests applied by the QC Laboratory for evaluation of raw materials, components, and products at various stages of the manufacturing process. 5/31/2020
325 Cepheid
Sunnyvale, CA
Facility Technician
HS Diploma/GED
Exp: 0-1 years in facilities
The primary function of the M.A.C. Coordinator is the scheduling and implementation of Moves, Adds and Changes from work orders provided by Space Planning. The space planning list will contain the names and destination locations for upcoming new hires as well as those of internal move requests. The M.A.C. Coordinator will reach out to the end user to schedule the implementation. Requests will range from individual staff relocation to furniture systems reconfiguration. 5/31/2020
326 Cepheid
Sunnyvale, CA
Associate Scientist - Infectious Disease
MS in field
Exp: 0-2 years
Perform analytical studies to verify GeneXpert assay performance based on the ability to meet design input requirements. Analyze data using statistical tools such as Microsoft Excel or MiniTab. Handle clinical samples and perform microbiology work of BSL-1 and BSL-2 organisms. Demonstrated ability to apply analytical problem-solving skills to reagent and system integration issues to identify critical performance factors. 5/31/2020
327 Cepheid
Lodi, CA
Manufacturing Technical Trainer
HS Diploma or AA/Trade Degree
Exp: HS: 1-2 years, AA: 0-1 years
Assist Supervisors/Training Specialists in coordinating, delivering, and monitoring training activities that directly affect manufacturing processes, including QSR/GMP compliance. Facilitate and deliver classroom training sessions. Serve as the point of contact for specific learning programs, as assigned. 5/31/2020
328 Cepheid
Sunnyvale, CA
Associate Scientist
BS or MS in biological sciences
Exp: 1-2 years in devices/pharma
This position is in the Biotechnology R&D group and is primarily a bench level job focusing on real time PCR and RT-PCR assay and product development in an FDA-QSR and ISO9001 compliant organization. The candidate will plan and execute laboratory research, demonstrate appropriate technical proficiency, scientific creativity and collaboration with cross-functional departments. 5/31/2020
329 Celsee
Ann Arbor, MI
Laboratory Research Technician
BS in biology/biochemistry
Exp: 1-2 years lab experience
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. 5/31/2020
330 CRISPR Theraputics
Cambridge, MA
Research Associate II, Analytical Development
MS in life sciences
Exp: 0-2 years in assay development
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. 5/30/2020
331 CRISPR Theraputics
Cambridge, MA
Cell Bank Research Associate II, Analytical Development
MS in life sciences
Exp: 0-2 years in assay development
The individual will be responsible for isolating primary cells from donor samples, developing quantitative assays for measuring consistency across donors, and screening donors to ensure reproducibility across cell-based assay runs. The successful candidate will independently design, perform, and analyze experiments for multiple preclinical and clinical programs, and will work independently to support process development and product characterization. 5/30/2020
332 CRISPR Theraputics
Cambridge, MA
Bioinformatics Engineer
MS in computer/biological sciences
Exp: 0-2 years
We are seeking a talented Bioinformatics Engineer with strong programming skills to tackle challenging bioinformatics and computational biology problems. The successful candidate work collaboratively with research groups to build and maintain the tools, algorithms, and pipelines required to support the development of new, transformative CRISPR/Cas9-based gene editing therapies. 5/30/2020
333 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
334 Celgene
Seattle, WA
Research Associate, Viral Vector Process Development

Exp: 
The Research Associate will join our viral vector process development group supporting process development, production and characterization of viral vectors, which are key intermediates in the CAR-T drug product. The candidate will support current programs and advance our capabilities in vector production. 5/30/2020
335 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
336 Capricor
Beverly Hills, CA
Process Development Associate
MS in sciences
Exp: 0-2 years
Independently manage and maintain multiple cell lines in support of process development activities. Design and execute studies to develop and optimize a scalable manufacturing process and analytical assays for production, isolation and characterization of exosomes. Prepare technical summaries to disseminate study results including making detailed observationsand data collection and analysis 5/30/2020
337 Celerion
Lincoln, NE
Sample Management Technician
HS Diploma/GED, Associates preferred
Exp: 0-2 years
Receive and check-in biological samples. Complete all record-keeping required for check-in, samples transfer log for chain of custody and freezer log. Communicate with client or sites as required for sample coordination. Manual entry of sample data 5/30/2020
338 Fujifilm Cellular Dynamics
Madison, WI
Laboratory Technician (#322)
Associate’s Degree in a scientific, engineering or biotechnology
Exp: 1-2 years
FUJIFILM Cellular Dynamics, Inc is recruiting for a laboratory technician to work in our cell manufacturing and research facility in Madison, WI. Provide lab support for scientific personnel and overall operations. Place orders, maintain inventory, and stock laboratory supplies. Work with laboratory staff to maintain and mature organizational structure. 5/30/2020
339 Cellectis
Raleigh, NC
QC Raw Materials Analyst
BS in life/analyatical sciences
Exp: 1-3 years in lab
Ensure compliance with applicable US and European cGMP regulations, corporate policies and company Standard Operating Procedures. Perform cGMP sampling, inspections, distribution of samples, and testing on raw materials and consumables. Review and evaluate timely issuance, review and approval of Raw Material testing results 5/30/2020
340 Cellectis
New York, NY
Research Associate, Immunology
BS or MS in biological sciences
Exp: 1 year lab experience
Design, set up, perform and analyze experiments independently. Maintain cell cultures and perform cell-based and immunological assays (e.g. ELISA, Cytotoxicity, proliferation, apoptosis). Evaluate novel cellular therapies using cellular and molecular biology techniques. Perform and analyze multicolor flow cytometry experiments. 5/30/2020
341 Ajinomoto Bio-Pharma Services
San Diego, CA
Drug Product Inspection Technician
HS diploma or equivalent
Exp: 0-2 year(s)
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. etc. 5/27/2020
342 Ajinomoto Bio-Pharma Services
San Diego, CA
Manufacturing Quality Assistant
HS diploma/BS in a life science
Exp: 0-2 year(s)
Ajinomoto Bio-Pharma Services is currently seeking a MQA Assistant to support our manufacturing. The MQA Assistant ensures completeness and accuracy of information contained in all documents, document files, databases, and documentation systems. This individual has the ability to work independently, within prescribed guidelines, and as a team member. This position promotes a cGMP environment and follows SOPs. Responsibilities: Performs cGMP documentation/data review in support of manufacturing operations (e.g. logbooks, labels, etc.). Performs AQL inspection of final filled product. etc. 5/27/2020
343 Ajinomoto Bio-Pharma Services
San Diego, CA
Environmental Monitoring Assistant
HS diploma/BS in a life science
Exp: 0-2 year(s)
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. etc. 5/27/2020
344 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
345 Alcami
Wilmington, NC
Associate Scientist - Biotech
MS in pharmaceutical science, chemistry, or equivalent
Exp: None required for MS candidates
The Associate Scientist 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 Associate Scientist may also be required to work on method development/method validation projects. For this position 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. 5/27/2020
346 Alcami
Charleston, SC
Manufacturing Tech I - 3rd Shift
HS diploma/AS/AA
Exp: 0-2 year(s)
The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employs acceptable techniques while working in manufacturing environments, including PPE gowning. The Manufacturing Technician I works collaboratively to support other manufacturing areas as required. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies for the role. etc. 5/27/2020
347 Alcami
Charleston, SC
Quality Specialist
MS in chemistry, biology or related
Exp: 1+ year(s)
The Quality Specialist II is accountable for driving results in a fast-paced environment by effectively performing activities of some variety and complexity to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data, conducting basic floor audits and processes inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance training as needed. The Quality Specialist II assists with the development of SOPs or other quality documents as needed. 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. 5/27/2020
348 Alcami
St. Louis, MO
Quality Specialist II
MS in chemistry, biology or related
Exp: 1+ year(s)
The Quality Specialist II is accountable for driving results in a fast-paced environment by effectively performing activities of some variety and complexity to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data, conducting basic floor audits and processes inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance training as needed. The Quality Specialist II assists with the development of SOPs or other quality documents as needed. 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. 5/27/2020
349 Alcami
Wilmington, NC
Quality Specialist II
MS in chemistry, biology or related
Exp: 1+ year(s)
The Quality Specialist II is accountable for driving results in a fast-paced environment by effectively performing activities of some variety and complexity to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data, conducting basic floor audits and processes inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance training as needed. The Quality Specialist II assists with the development of SOPs or other quality documents as needed. 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. 5/27/2020
350 Alcami
Durham, NC
Quality Specialist II
MS in chemistry, biology or related
Exp: 1+ year(s)
The Quality Specialist II is accountable for driving results in a fast-paced environment by effectively performing activities of some variety and complexity to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data, conducting basic floor audits and processes inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance training as needed. The Quality Specialist II assists with the development of SOPs or other quality documents as needed. 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. 5/27/2020
351 Aldevron
Fargo, ND
Downstream GMP Biomanufacturing Operator
AS/BS in a life science
Exp: 1+ year(s)
The Downstream GMP Biomanufacturing Operator works daily within Aldevron’s manufacturing areas, performing tasks associated with Aldevron’s GMP plasmid DNA production services. This role focuses specifically on downstream associated with the purification of plasmid DNA, including lysis, Anion Exchange Chromatography, Hydrophobic Interaction Chromatography (void and enrichment), Thiophilic Absorption Chromatography, diafiltration, and small-scale processing as well as linearization. etc. 5/27/2020
352 Aldevron
Madison, WI
Associate Scientist II, Fermentation
AS/BS in biology, microbiology, biochemistry or related
Exp: 1+ year(s)
The Associate Scientist II, Fermentation supports the execution of 1-L to 1000-L scale microbial fermentations. This role works collaboratively with team members and as an individual contributor. This position requires excellent laboratory skills, attention to detail and excellent documentation practices. Responsibilities: Assist in execution of 1 L 1000 L scale fermentations. Prepare microbiological culture media and other culture reagents. Transform E. coli with plasmid DNA. Harvest E. coli cultures using centrifuges and TFF devices. Prepare and analyze cell lysates (SDS PAGE, Western Blot, Concentration Assays). etc. 5/27/2020
353 Aldevron
Madison, WI
Quality Control Scientist I, Protein
BS in chemistry, biochemistry, genetics, cell biology or related
Exp: 1 year
The Quality Control (QC) Scientist I, Protein, supports production of recombinant proteins. This role is primarily responsible for performing release testing and ensuring that products meet or exceed all quality specifications. This role also supports the management and execution of stability studies. Responsibilities: Accurately record experimental results in real-time; store/save and report data per Aldevron conventions. Work with analytical equipment routinely used to characterize recombinant proteins, including Reverse Phase HPLC, Analytical Size Exclusion Chromatography, SDS-PAGE and Western Blot, UV/Vis and Fluorescence Spectroscopy (cuvette and multi-well plate), ELISA, and Endotoxin Detection Assays. Assist in qualification of test methods, writing and review of documents, internal process reviews, and basic equipment maintenance. etc. 5/27/2020
354 Aldevron
Madison, WI
Shipping and Receiving Specialist
HS diploma or equivalent
Exp: 1-2 year(s)
The Shipping and Receiving Specialist is responsible for supporting the storage and inventory management of materials, the shipping of materials to the clients, and staging materials for client and internal projects. Responsibilities: Responsible for receiving and storing of incoming materials. Performs physical inspection of materials at the time of arrival. Responsible for ensuring purchase orders match items received. Package material for shipment according to established procedures. Performs periodic cycle counts to verify inventory accuracy. etc. 5/27/2020
355 Aldevron
Fargo, ND
Material Handler - 2nd Shift
HS diploma or equivalent
Exp: 1 year
The Material Handler receives and issues inventory to/from the manufacturing operations. This role is responsible for properly identifying and inventorying material all material and equipment from receiving and production. Responsibilities: Receiving and placing material and equipment into stock from Receiving and Manufacturing. Responsible for the receipt of materials into the Raw Materials Management database. Restock picking locations as needed. Tracking and monitoring inventory levels. Conduct regularly scheduled stock counts. Making sure incoming material is labeled. etc. 5/27/2020
356 Aldevron
Fargo, ND
Upstream GMP-Source Biomanufacturing Operator
AS/BS in a life science
Exp: 1+ year(s)
The Upstream GMP Biomanufacturing Operator works daily within Aldevron’s manufacturing areas, performing tasks associated with Aldevron’s GMP-Source plasmid DNA production services. This role focuses specifically on bacterial cell growth, including transformation, subculture, cell banking, fermentation, shake flask growth, wave growth, and harvest. Responsibilities: Plan and submit inventory requisitions. Plan and preparation of production events and process plan memos. Coordinate production events with buffer preparation operators. Perform upstream production events. etc. 5/27/2020
357 Aldevron
Madison, WI
Associate Scientist II, Biomanufacturing
AS/BS in biochemistry. Biotechnology, biology or related
Exp: 0-2 year(s)
The Associate Scientist II, Biomanufacturing role is responsible for duties relating to standard purification of antibodies and proteins. The Associate Scientist II will interact closely with all members of the lab team and will support various lab activities as assigned. Responsibilities: Purify multiple recombinant proteins and/or antibodies using chromatography skid. Using dialysis tube or TFF, perform buffer exchange and final formulation of recombinant protein. Routinely pack, unpack clean, and regenerate resins in chromatography columns for protein purification process. Characterize in-process samples and purified proteins using methods including SDS PAGE, Western Blot, Bradford Assay, and ELISA. etc. 5/27/2020
358 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
359 Alkermes
Wilmington, OH
Process Engineer-OSD
BS in a science or engineering
Exp: 0-3 years
Support and assist in the manufacture of pharmaceutical products for commercial and clinical supplies. Where applicable, the candidate may be tasked with scale-up and transfer of formulations/processes to the commercial production facility, designing and recommending equipment purchases, and writing/executing qualification/validation protocols. Troubleshooting of automated equipment for pharmaceutical manufacturing, identification and implementation of process/equipment improvements to reduce waste and increase process reliability, and cleaning process development are also within the scope of this position. Essential Functions: Troubleshoot and maintain manufacturing systems, processes and equipment. Support development of cleaning processes for the manufacturing area. etc. 5/27/2020
360 Alkermes
Wilmington, OH
Process Engineer I-Bulk
BS in engineering
Exp: 1-2 year(s)
Support and assist in the manufacture of pharmaceutical products for commercial and clinical supplies. Scale-up and transfer formulations/processes to production facility, design and recommend equipment purchases, write and execute qualification/validation protocols. Troubleshoot automated equipment for pharmaceutical formulation and packaging. Identify and implement process/equipment improvements (utilizing Change Control system) to reduce waste and increase process reliability. Support of manufacturing management in periodic review of existing and new revisions to manufacturing documentation in regards to, but not limited to, Operability, Technical accuracy (technical reviews), Compliance, Process Robustness. Perform process and equipment evaluation (FMEA, etc.) to identify risks and weaknesses in new and current processes, etc. 5/27/2020
361 Alkermes
Waltham, MA
Contract Senior Research Associate (In vitro)
MS
Exp: 1-5 year(s)
We are looking for a highly-collaborative temporary stem cell biologist with strong interpersonal and communication skills. We are developing new disease models to build advanced drug discovery assays in immune oncology and neurobiology. This position requires meticulous cell culture abilities, excellent communication skills, and will work in a cross-functional team environment supporting multiple projects. The successful candidate will have experience culturing multiple cell types, including immortalized cell lines and human stem cells with different media and culture requirements. Many of our cultures are maintained in an antibiotic free media. Ideally, this individual will also assist with RNA and DNA purification and setting up next generation sequencing runs on our Ion Torrent sequencers. etc. 5/27/2020
362 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
363 American Regent
New Albany, OH
QA Quality Systems Specialist I
BS/BA
Exp: 1 year
The Quality Systems (QS) Specialist I will be responsible for effectively ensuring non-routine events are investigated and documented in accordance with company SOPs, policies and cGMPs. This is a cross-functional position that interacts with All departments at PharmaForce. The incumbent will participate in organizing the quality systems to meet or exceed the company's quality expectations. 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. Under the direction of the Quality Systems (QS) Manager, the QS Specialist I will: Coordinate specific departmental activities with the goal of maximizing efficiency of management control systems, programs, policies, work methods and procedures. etc. 5/27/2020
364 Aesculap
Irvine, CA
PM Inspector (Excel Packing Pooling)
HS diploma or equivalent
Exp: 1-5 year(s)
Under general supervision, performs visual in-process inspection for quality and packing of finished Excel products. Responsibilities: Essential Duties: Responsible to ensure compliance of product with the quality requirements. Responsible for verifying the documentation/test report and relevant documents of all tests conducted. Responsible for filing, compilation and documentation of the quality batch records. Responsible to update the results. Provides immediate feedback to production line and immediate leadership on all quality related problems. etc. 5/26/2020
365 Aesculap
Irvine, CA
Inspector (Injection Molding ADD/PAB)
HS diploma or equivalent
Exp: 0-4 years
Works under the direction of the Supervisor/Lead Processing Technician/Setup Technician. Using specific methods, inspects plastic molded parts for visual dimensional defects; performs light to medium packaging and product handling functions. Completes documents required to release parts. Performs cleanup of equipment and facilities in the Injection Mold production areas. Attends injection molding machine and subassembly equipment. Does minor trouble-shooting not requiring a maintenance mechanic or process technician (i.e. Lead Processing Technician, Setup Technician, Process Technician). etc. 5/26/2020
366 Agilent
Boulder, PA
Manufacturing Associate
HS diploma or equivalent
Exp: 1+ year(s)
As a Manufacturing Associate, you will check and schedule resources to ensure on-time delivery. Your scientific knowledge and background will be leveraged through your review of formulation documents and active ingredient dilution to ensure that products are manufactured to specification. Responsible for performing a variety of support duties in one or more manufacturing areas. Duties may be related to cleaning, ordering, stocking, preparing, installing, maintaining, repairing and supporting manufacturing equipment and processes. etc. 5/26/2020
367 Agilent
Wilmington, DE
Electronics Technician I
unspecified
Exp: 1+ year(s)
The Electronics Technician I position is required to support the manufacture of GCMS instruments. This position will be responsible for testing, troubleshooting, and reworking instruments within the flow of the GCMS production lines. This role involves working with electronic assemblies in support of shipment of instruments and support parts to meet customer needs. This position works closely with R&D development engineers on NPI products and value engineering improvements. etc. 5/26/2020
368 Agilent
Frederick, CO
Manufacturing Associate - Entry (2nd Shift)
HS diploma
Exp: 1-2 year(s)
As a Manufacturing Associate, you will check and schedule resources to ensure on-time delivery. Your scientific knowledge and background will be leveraged through your review of formulation documents and active ingredient dilution to ensure that products are manufactured to specification. Responsible for performing a variety of support duties in one or more manufacturing areas. Duties may be related to cleaning, ordering, stocking, preparing, installing, maintaining, repairing and supporting manufacturing equipment and processes. etc. 5/26/2020
369 AGC Biologics
, CO
Manufacturing Associate I-IV, Downstream
BS in chemistry or biology
Exp: 1-8 year(s)
The Manufacturing Associate I-IV, Downstream performs GMP manufacturing operations safely, reliably and in compliance with stated processes. We offer a dynamic environment, innovation, operational excellence, and career growth. 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. 5/26/2020
370 AGC Biologics
Bothell, WA
Development Associate I (Upstream) Contract
AS/BS in a life science or engineering
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. etc. 5/26/2020
371 Aesculap
Allentown, PA
Molding Technician (3rd Shift - Injection Molding)
HS diploma or equivalent
Exp: 0 - 6 months
Responsibilities: Essential Duties: Follows established procedures and guidelines to manufacture the organizations products according to specifications and schedules, volume, cost and waste targets, or quality standards. Operates machines and production equipment safely and in accordance with instructions. Monitors the quality of output to identify, discard or remanufacture products. Troubleshoots problems by contributing to team with input, feedback and/or ideas for improvement. etc. 5/26/2020
372 Aesculap
Irvine, CA
Sterilization Product Handler
HS diploma or equivalent
Exp: 6 months
Responsibilities: Essential Duties: Assists supervisor to ensure that production operators have sufficient stock of materials. Collects, checks and keeps records of materials flow to and from production area. The job function listed is not exhaustive and shall also include any responsibilities as assigned by the Supervisor from time to time. etc. 5/26/2020
373 Aesculap
Daytona Beach, FL
QC Inspector
HS diploma or equivalent
Exp: 6 months - 2 years
Responsibilities: Essential Duties: Performs repetitive and routine inspections, checks, tests and sampling procedures of standard parts, units, equipment or materials. Performs inspections of purchased parts, subassemblies or finished company products according to well defined criteria using standard physical, mechanical and/or electrical measurements. Reworks or rejects subassemblies or finished products as required. Performs audits to ensure standards of quality are maintained. etc. 5/26/2020
374 Aesculap
Daytona Beach, FL
Entry Production Technician
HS diploma or equivalent
Exp: 0-6 months
The primary responsibility of a Production Technician is to oversee the operation of production equipment for the manufacturing of pharmaceutical products. This work will include loading & unloading of raw materials, verifying proper machine operation, clearing machine jams when they occur, testing and verifying the quality of the product being produced, and reporting all required data during runs. This individual must possess an overall knowledge of GMP’s, ISO, and OSHA requirements in the manufacturing environment. This position shall operate in accordance with company policies & procedures, FDA regulations, and ISO standards. etc. 5/26/2020
375 Aesculap
Irvine, CA
Set Up Tech (PIC Blow Molding)
HS diploma or equivalent
Exp: 1-2 year(s)
Under the direction of the Supervisor/Lead Processing Technician, set up, operate and perform machine/equipment installations and repairs on plastics equipment to produce quality-molded components. Responsibilities: Essential Duties: Properly set processing equipment and molding tools as instructed by Shift Supervisor, Chief Operator or Scheduler. Set up all operating parameters on above equipment as per process data card (i.e., heaters, times pressures, speeds, type of material and electronic process controllers). Check on the quality of molded products through Process Tech or Quality Inspector or by self-inspection. Variations are communicated with Process Tech or Supervisor to take necessary action. (All Setup Technicians must be able to operate all basic quality control measuring devices.) etc. 5/26/2020
376 Bristol Myers Squibb
New Brunswick, NJ
Associate Process Engineer
BS/BA in biomedical/mechanical engineering
Exp: 0-2 years in pharma/biotech
The Associate Process Engineer provides technical leadership related to new and existing sterile drug products. This position is supports the technical interface with R&D to ensure design and transfer of robust manufacturing processes for new products and key life cycle management products, development of new technology for optimization and continuous improvement in manufacturing operations, providing specialized expertise as necessary to complement site capabilities for critical investigations or process improvements, setting relevant standards and creating and maintaining associated Directives (e.g, for tech transfer, Product monitoring, etc). 5/24/2020
377 Bristol Myers Squibb
Syracuse, NY
Assistant Scientist - Night Shift
BS in sciences
Exp: 0-3 years
Duties include conducting routine and non-routine testing of materials and products using a variety of equipment and test methods upon demonstrating the ability to perform and understand required methods. Each analyst is responsible for capturing data accurately and timely followed by promptly entering testing results within the appropriate data collection system (e.g., LIMS, LES, etc). 5/24/2020
378 Bristol Myers Squibb
Warren, NJ
Associate Bioengineer II – Cell Culture Engineering
BS or MS in biological sciences/engineering
Exp: 0-1 years in industry
With minimal supervision, design and execute experiments to assess impact of cellular metabolism and cytokine signaling on T cell phenotype Optimize cell culture conditions as well as media components that can help improve process performance and achieve desired product attributes Critically analyze and interpret data using statistical methods Summarize experimental results and present them for internal discussions. 5/24/2020
379 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
380 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
381 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
382 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
383 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
384 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
385 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
386 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
387 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
388 BioAgilytix
Durham, NC
Analyst
BS/BA in life sciences
Exp: 1 year in lab
Prepare worksheets with minimal supervision. Prepare plate maps. Serve as lead analyst on sample analysis projects. Troubleshoot assays. Compile/process data (make power export). Prepare summary tables. Participate in assay development and validation 5/24/2020
389 Thermo Fisher Scientific
Cambridge, MA
Cell Culture Lab Support
BS/BA in related field
Exp: 1-3 years
Follows well defined procedures and safety requirements as outlined by Best Practices, SOP’s & work instructions. Take direction from Site Supervisor/Manager (and Team Lead) regarding daily duties. Makes decisions and utilizes available resources to meet customer requirements, independently. Analyzes/maintains/reconciles various customer and Thermo Fisher reports to ensure customer and Thermo Fisher requirements are met. 5/24/2020
390 Cambrex
Malborough, MA
Cleanroom Technician
HS Diploma/GED
Exp: 0-2 years, drivers license
A Cleanroom Services Technician will support the Cleanroom Services team by assisting filed analysts with a wide range of tasks including: equipment setup and stocking supplies, vehicle and equipment maintenance, facility administrative housekeeping. Additionally, this role will be responsible performing work at client sites as needed. 5/24/2020
391 BiorReference Laboratories
Elmwood Park, NJ
Medical Lab Technician
AS in medical/chemical/biological sciences
Exp: 1 year work experience
Follows written lab procedures for the correct handling and processing of specimens. Performs lab procedures of moderate and high complexity in accordance with standards set forth in sectional laboratory procedures. Maintains an up to date working knowledge of all technical procedures in the department and operations of all instrumentation. Reviews all pertinent SOPMs. Manipulate and operate simple and complex laboratory equipment including computers; may perform maintenance and limited tear down and replacement of parts of laboratory equipment; problem-solve equipment malfunctions. 5/23/2020
392 BiorReference Laboratories
Baltimore, MD
Phlebotomist
Phlebotomy certification
Exp:  6 months work experience
The Phlebotomist provides expertise in blood draws and specimen preparation. Their ability to put patients at ease and obtain sufficient samples with minimal discomfort to patients across a wide demographic is critical to our commitment to high quality care for our patients and those of our partners. Experience doing blood draws, labeling specimens, centrifuging specimens, recording maintenance data and decontamination, updating patient information, etc. 5/23/2020
393 BiorReference Laboratories
Elmwood Park, NJ
Medical Lab Technician
AS in medical/chemical/biological sciences
Exp: 1 year work experience
Follows written lab procedures for the correct handling and processing of specimens. Performs lab procedures of moderate and high complexity in accordance with standards set forth in sectional laboratory procedures. Maintains an up to date working knowledge of all technical procedures in the department and operations of all instrumentation. Reviews all pertinent SOPMs. Manipulate and operate simple and complex laboratory equipment including computers; may perform maintenance and limited tear down and replacement of parts of laboratory equipment; problem-solve equipment malfunctions. 5/23/2020
394 BiorReference Laboratories
Melbourne, FL
Specimen Processor
HS Diploma/GED
Exp: 0-2 years
The Specimen Processor must maintain departmental production goals to ensure hourly specimen flow to the labs are consistent. In this role, you will prepare samples for shipping, ensuring they are secure and shipped to the correct laboratory. It will also be your responsibility to handle patient medical records with complete accuracy and confidentiality. 5/23/2020
395 Bio-Techne
San Jose, CA
Manufacturing Technician ( Swing Shift, Wes Cartridge )
AA degree
Exp: 1+ years of lab/manufacturing experience
Operate and maintain robotic and manufacturing equipment. Ability to use hand tools such as small wrenches, pliers, tweezers, etc. Perform in-process QC and record results. Document production batch records/travelers and computer data entry. Maintain and track raw material inventory 5/23/2020
396 Bio-Techne
Minneapolis, MN
Research Associate, Cell Culture and Stem Cell Media Operations and Support Services
BS/BA in biological sciences
Exp: 0-2 years in lab
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for recombinant protein production, media and supplement preparation, and additional duties as assigned. This position requires a Tuesday through Saturday workweek. 5/23/2020
397 Bio-Techne
Minneapolis, MN
Advanced Research Associate, Conjugation
MS in biological sciences
Exp: 0-2 years
This position is responsible for preparing conjugated proteins, antibodies, enzymes, oligonucleotides, and microparticles for both manufacturing and research. In addition, this position will be responsible for the preparation and testing of other chemistry related reagents for company personnel.Prepares conjugated proteins, antibodies, enzymes and microparticles for both manufacturing and research according to written and non written procedures. 5/23/2020
398 Bio-Techne
Minneapolis, MN
Manufacturing Technician
HS Diploma/GED
Exp: 0-2 years
The responsibilities of the Manufacturing Technician are to assist the laboratory staff with the process of building and manufacturing science products. This position will assist with a variety of tasks within a laboratory setting that may include filling containers with product, feeding a production machine, labeling product, recording data, operating equipment, formulation, and plate coating. 5/23/2020
399 Bio-Techne
Minneapolis, MN
Equipment Technician I
HS Diploma/GED
Exp: 1-3 years, 1 year with Associate's degree
As an Equipment Technician I, you will perform preventative maintenance and repair malfunctioning new and existing minor equipment. In doing so, you will manage and document your work orders, respond to supervisory alarms during business hours, and complete routine inspections on equipment. Perform and document scheduled preventative maintenance on minor equipment. Perform minor repairs to malfunctioning equipment per work orders 5/23/2020
400 Bio-Techne
Minneapolis, MN
Research Associate, Cell Culture and Stem Cell Media Operations
BS/BA in biological sciences
Exp: 0-2 years in lab
The main responsibility of this position it to maintain production of mouse embryonic fibroblasts. Additional responsibilities include media and supplement production, QC testing of methylcellulose-containing cell culture media, and cell culture of multiple cell lines. Perform additional duties as assigned. Preferred skills include cell culture, high attention to detail, strong communication and organizational skills. 5/23/2020
401 BioTelemetry
Rochester, NY
Test Engineer (Contract to hire)
BS in engineering, computer/information sciences
Exp: 1-3 years as software test engineer
The Test Engineer I will provide technical testing expertise as part of an Agile development team and be a trusted team member for BioTel Research’s clinical research services. The Test Engineer will refine the product backlog, ensuring the quality and reliability of all functional components used. They will ensure that all systems meet customer requirements in a manner that is consistent with applicable regulatory requirements especially with regard to validation processes outlined in Good Clinical Practice and Good Manufacturing Practice and maintaining Separation of Duties. 5/23/2020
402 BioTel Heart
Linwood, PA
Distribution Quality Technician
HS Diploma/GED
Exp: 1 year in QA
Processing new devices, failed devices and performing QA audits as required. Inspection of incoming goods. Inspection of finished products for final release. Responsible for performing analysis and documentation of all pending failures from out of box, check-in and field failures and generating summary reports at the service center locations. Provide device training when requested. 5/23/2020
403 Biotronik
na, ND
Sales Representative: North Dakota
MS in life sciences or business
Exp: 1 years as clinical specialist
In this role you will gain market share in the cardiac rhythm business by promoting, selling, and servicing Biotronik’s products within an assigned territory. Sales Representatives perform field promotional work to sell and develop new business; this may include work with current accounts, or with customers where product acceptance has not been established. Biotronik seeks candidates who will meet and exceed our customer expectations by striving for the greatest possible reliability and quality in our products, processes and systems by being accountable and taking action. 5/23/2020
404 Biotronik
Los Angeles, CA
Vascular Intervention Sales Representative
MS in life sciences or business
Exp: 1 year in medical industry sales
Conduct sales calls to promote, sell, and service BIOTRONIK products and services to existing and competitive customers. Assists in the utilization of BIOTRONIK products by supporting implant procedures in the Cardiac Catheterization Laboratory. Develop and implement quarterly sales plan to achieve sales goals and objectives. Maintain exceptional knowledge of BIOTRONIK products, changes in the clinical landscape, and of competitors’ product offering 5/23/2020
405 BioVision
San Francisco, CA
Sales Representative
BS or MS in biochemistry or biological sciences
Exp: 1-2 years in life science industry
Meet or exceed sales objectives set by the BioVision management. Learn and master BioVision's product offering and manufacturing capabilities . Establish long-term relationships with the customers and match BioVision's capabilities with customer needs. Identify key contacts and decision makers to maximize the benefits from customer visits 5/23/2020
406 BMG Labtech
Boston, MA
Life Science Capital Equipment Sales Associate
BS or MS in life sciences
Exp: 0-2 years
We are hiring for a Sales Associate position located in the Boston area. This is a home-office based position providing sales, sales-support, service, training and applications support tasks related to operations in the Northeastern U.S. Use your love of science and lab experience to engage with customers in a variety of research labs. Train users in operation and troubleshoot scientific questions 5/23/2020
407 Acumed
Memphis, TN
Sales Associate, Memphis, Tennessee - Future Opportunities
BS/BA in a business or medical discipline
Exp: 0-3 year(s)
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. 5/20/2020
408 Acumed
Philadelphia, PA
Sales Associate, Philadelphia, Pennsylvania - Future Opportunities
BS/BA in a business or medical discipline
Exp: 0-3 year(s)
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. 5/20/2020
409 Adaptimmune
Philadelphia, PA
Quality Assurance Associate- CMC (Deviations & CAPA)
BS/BA
Exp: 1-2 year(s)
This Quality Assurance Associate (Deviations & CAPA) role is for an individual, with entry to intermediate level experience in QA discipline, who will be responsible for the initiation, investigation of process deviations aimed at identification of root cause, and implementation of correct actions to prevent recurrence. This role is expected to work in a Good Manufacturing Practices (cGMP) environment, have some level of working knowledge of manufacturing processes, a professional and expert technical writing capability, be action oriented, and be compliant minded while performing and reviewing investigations and CAPA. This position reports directly to the QA Manager with dotted line reporting to QA Senior Specialist. etc. 5/20/2020
410 Adaptimmune
Philadelphia, PA
Quality Control Associate
Unspecified
Exp: 1-3 year(s)
The Quality Control Associate will be responsible for conducting in-process and finished product testing associated with Adaptimmune clinical trial material. Key Responsibilities: In-process, finished product and stability testing of clinical trial material. Daily maintenance of quality control equipment. Maintenance of Quality Control Protocols, SOP’s and Test Methods. etc. 5/20/2020
411 Adma Biologics
Boca Raton, FL
QA Specialist II - Quality, Engineering, Validation
BS/BA
Exp: 1-5 year(s)
The QA Specialist II-Quality, Engineering, Validation will Perform a wide variety of Quality Assurance activities to ensure compliance with related regulatory requirements. Primarily responsible for the efficacy and compliance of the change control management system, validation and qualification systems, Corrective and Preventive Action reports (CAPA) and Risk Management policies and procedures. etc. 5/20/2020
412 Adma Biologics
Boca Raton, FL
Specialist I QA- Product Release
BS/BA in a life or natural science
Exp: 1-2 year(s)
The Specialist I-Quality Assurance-Product Release will Performs a wide variety of Quality Assurance activities to ensure compliance with related regulatory requirements. Main focus on review of batch records and associated documents for product release. Responsibilities: Perform review and support release of manufacturing batch records (in-house and CMO batches) along with all manufacturing supporting documents including but not limited to logs, charts, specifications, and environmental and WFI data. Perform review and release of all Plasma pools, both for internal use and shipment to customers as required. etc. 5/20/2020
413 Adma Biologics
Boca Raton, FL
QC Lab Support Associate l
BS in biology, chemistry, medical technology, or related
Exp: 1-3 year(s)
The QC Lab Support Associate I will Performs cGMP laboratory support activities including Sample Accessioning, Product Reserve management, Temperature Monitoring of storage chambers, Glassware Cleaning, Supply Inventory management, etc. May also assist with Stability Studies and other QC initiatives. Performs all work under GMP conditions. Provide customer support to QC analysts. etc. 5/20/2020
414 Adma Biologics
Boca Raton, FL
Specialist Supply Chain Plasma Operations
BS in a life science
Exp: Entry Level
The Plasma Operations Supply Chain Specialist will support all Plasma Operation activities, from plasma shipments from approved donation centers to off-site warehousing through to the Boca manufacturing facility. They will also support plasma lookback process for all plasma programs and the Donor Management process, including sample testing in support of RI-002, Nabi-HB and client programs. Assist with vendor relationships with off-site testing labs and off-site plasma warehouse. Document physical supply chain processes, such as plasma shipments, lookbacks and plasma inventory reconciliation. etc. 5/20/2020
415 Adma Biologics
Boca Raton, FL
Specialist I - Supplier Quality Assurance
BS/BA
Exp: 1-3 year(s)
The Specialist I-Supplier QA will perform a wide variety of Quality Assurance activities to ensure compliance with regulatory requirements. Responsibilities: Assists with internal audits of all departments at the ADMA facility that are directly involved with activities described in the cGMPs cGMPs or have an impact on activities described in the cGMPs. Support in managing, receiving and coordinating the vendor notifications process. Assists with the coordination and preparation of the Quality Systems Review Board (QSRB) process. etc. 5/20/2020
416 Adma Biologics
Boca Raton, FL
Materials Technician I
HS diploma or equivalent
Exp: <1 year
We currently have an opportunity available for a Materials Technician centrally located in Boca Raton, FL! Responsibilities: Receive, store and distribute raw materials, intermediate and marketed products in compliance with GMP and company standards. Maintain and order inventory of supplies. Will be working in a cold room environment. etc. 5/20/2020
417 Adma Biologics
Boca Raton, FL
Facilities Building Maintenance Technician
HS diploma or equivalent
Exp: 1 year in a pharmaceutical environment
We currently have an exciting opportunity available for a Facilities Building Maintenance Technician! Responsibilities: This position ensures the proper maintenance and layout changes of all property, buildings, offices, labs and manufacturing areas; takes corrective action and repairs walls, floors, ceilings, exterior buildings, parking lots and landscape as necessary; provides appropriate notification and documentation of all work performed. General maintenance and repairs within a GMP manufacturing facility. etc. 5/20/2020
418 Biotechne
Wallingford, CT
Quality Assurance Specialist
BS/BA
Exp: 0-2 years
The Quality Assurance Specialist role is established to support the Simple Plex Consumables team in the Wallingford facility. Assists Quality Analysts and the QA team in our ISO compliant environment. Provides support for QC / QA activities including: hands-on evaluation of microfluidic cartridge products (see https://www.proteinsimple.com/ella.html), root cause investigations, document control, internal audits, and other common QMS tasks. Understand and follow appropriate quality protocols: Quality Manual. Record Keeping Guidelines. etc. 5/20/2020
419 Biotechne
San Jose, CA
Manufacturing Technician (Finishing)
HS diploma/AS in biotechnology, biology, chemistry or related
Exp: 1+ year(s)
Bio-Techne’s Protein Platform Division is looking for a Manufacturing Technician with a motivation to participate in the growth of a fast-paced company engaged in cutting edge biological research. The successful candidate will work with other members of the Reagent production team to make great products, performing tasks involving plate filling, labeling, vialing, and finishing materials. Operation of semi-automated liquid dispensing equipment is integral to the job. etc. 5/20/2020
420 Biotechne
San Jose, CA
Manufacturing Technician ( Swing Shift, Wes Cartridge )
AA/AS
Exp: 1+ year(s)
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. Key Responsibilities: Operate and maintain robotic and manufacturing equipment. Ability to use hand tools such as small wrenches, pliers, tweezers, etc. Perform in-process QC and record results. Document production batch records/travelers and computer data entry. etc. 5/20/2020
421 Biotechne
Minneapolis, MN
Manufacturing Technician
HS diploma
Exp: 0-2 years
The responsibilities of a Manufacturing Technician are to assist the laboratory staff with the process of building and manufacturing science products. This position will assist with a variety of tasks within a laboratory setting that may include labeling, recording data, operating equipment, formulation and plate coating. This opportunity is second shift with hours from 1:30 PM to 10:00 PM (Monday - Friday). Key Responsibilities: Set up and build product of low complexity. Load machines and move products. Accurately label vials. etc. 5/20/2020
422 Biotechne
Minneapolis, MN
Production Assistant
HS diploma or equivalent
Exp: 0-2 years
The responsibilities of the Production Assistant are to assist the laboratory staff with the process of building and manufacturing science products. This position will assist with a variety of tasks within a laboratory setting that may include filling containers with product, feeding a production machine, labeling product, recording data, operating equipment, formulation, and plate coating. This position offers 1st shift hours of 5:00am-1:30pm. Key Responsibilities: Operate a production machine to fill containers with product. Feed plates into the machines. Batch and label product. etc. 5/20/2020
423 Acumed
Philadelphia, PA
Sales Associate - Lehigh Valley
BS/BA in a business or medical discipline
Exp: 0-3 year(s)
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. 5/19/2020
424 Acumed
Danville, PA
Sales Associate - Danville
BS/BA in a business or medical discipline
Exp: 0-3 year(s)
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. 5/19/2020
425 Acumed
New York, NY
Sales Associate - NYC - Future Opportunities
BS/BA in a business or medical discipline
Exp: 0-3 year(s)
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. 5/19/2020
426 ABEC
Bethlehem, PA
Mechanical Designer
AS/AA
Exp: 1-2 year(s)
The Mechanical Designer works under the direction of the Design Team Leader and also utilize independent judgment to perform the day-to-day project duties of designing, developing and releasing deliverables. This includes detail & assembly drawings and related bills-of material used in the fabrication of equipment for pilot and commercial scale biopharmaceutical manufacturing (largely pressure vessel assemblies for fluid & gas handling and motorized agitation systems). Primary responsibility involves generating design plans utilizing Autodesk Inventor and AutoCAD software. This position requires a high level of attention to detail along with the ability to develop a strong understanding of the ASME/ BPE Bioprocessing Equipment design standards. etc. 5/19/2020
427 BioMarin
Novato, CA
Analyst, QC I (TEMPORARY)
BS in biological/chemical sciences
Exp: 0-2 years
Adhere and follow cGMPs guidelines and procedures at all times. Escalate non-compliance concerns to management. Monitor lab equipment for Calibration needs, monitoring and tracking of issues related to instrumentation. Support the scheduled testing by ensuring the required reagents and glassware are stocked appropriately. Maintain the laboratory in an inspection-ready state 5/17/2020
428 BioMarin
Novato, CA
Research Assistant
BS/BA in biological/physical sciences
Exp: 0-2 years
Primary responsibility is support for the Assay Services subgroup within Analytical Sciences. This position involves performance of a variety of analytical assays with adherence to strict timelines. Assays may include enzyme activity, total protein, cell-based bioassays, chromatography and electrophoresis, done under the supervision of more senior personnel. Assists in the qualification of assay methods and in their transfer to the Quality Control laboratories. Provides major contributions to the evaluation of drug substance and drug product. Receives and records results for Assay Services in support of a variety of different groups including QC, MFG, Cell Culture PD, Purification PD and Formulation. 5/17/2020
429 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
430 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
431 BioMarin
Novato, CA
Analyst, QC In-Process
BS in related
Exp: 0-3 years
The QC In-Process (QCIP) Analyst is responsible for performing microbiological and analytical test methods on in-process intermediates and varying stages of drug products, under minimal supervision and within cGMP guidelines, to support further manufacturing of commercial and clinical therapeutics. This role will involve knowledge that includes but is not limited to the following analyses and concepts: Protein determination by BCA, Bradford, and UV Absorbance, Enzyme activity, Endotoxin detection, Bioburden quantification, HPLC, Total Organic Carbon, microbial identification and challenge studies, aseptic techniques, and method validation. 5/17/2020
432 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
433 BioMerics
Salt Lake City, UT
Injection Molding Machine Operator I, DAY SHIFT
HS Diploma/GED
Exp: 1-2 years
Operate plastic injection molding machines. As the Injection Molding Machine Operator you will set up and operate an injection molding machine in order to shape plastics. You will read and interpret blueprints and diagrams to select, position, and secure machinery. This is a hands-on role. 5/17/2020
434 BioMerics
Salt Lake City, UT
Injection Molding Machine Operator I, NIGHT SHIFT
HS Diploma/GED
Exp: 1-2 years
Operate plastic injection molding machines. As the Injection Molding Machine Operator you will set up and operate an injection molding machine in order to shape plastics. You will read and interpret blueprints and diagrams to select, position, and secure machinery. This is a hands-on role. 5/17/2020
435 Bio-Rad
Hercules, CA
Production Tech I - Temp
HS Diploma/GED
Exp: 0-2 years
Bio-rad is looking for a Production Tech to produce or supports production of instruments or reagents products in compliance with established GMP procedures and ensures products are of consistent high quality. Acts as part of a technical organizational unit. Maintains instrument documentation, operates a variety of lab and/or engineering/manufacturing test equipment, and troubleshoots and repairs instrument products. (6 positions available.) 5/17/2020
436 Bio-Rad
Woodinville, WA
Supply Planner I/II
BS/BA in supply chain, business, management
Exp: 0-5 years in supply planning/management
In this role, you will help drive performance of key inventory metrics as well as service levels. Develops a detailed understanding of the supply strategy as well as the global demand and regulatory constraints for assigned finished goods. Utilize SAP for development and communication of finished goods supply plan. Creation of supply plan while coordinating day to day efforts between warehouse locations 5/17/2020
437 Bio-Rad
Pleasanton, CA
Research Associate or Senior Research Associate, Assay Development Temp to Hire
MS in biological sciences
Exp: 0-2 yeares
You will work in an assay development team on the development of new Research Use Only (RUO) and in vitro diagnostic (IVD) tests for oncology 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. 5/17/2020
438 Bio-Rad
Hercules, CA
Data Analyst I
BS/BA in business admin
Exp: 0-3 years in database management
Bio-Rad is looking for a Data Analyst I. The key business projects will include team activities, data analyses and reports development, validation, training, release in Power BI for all identified Customer-Centric Global Supply Chain metrics. Will also support Technical Lead with data automation strategy and initiatives. 5/17/2020
439 Bio-Rad
Woodinville, WA
Quality Engineer I
BS/BA in sciences
Exp: 0-2 years
Supports project/program activities by performing work with an engineering specialty which involves various types of research, investigations, analysis and interpretation of data. Analyzes nonconformances, complaints and trends to identify and recommend corrective and / or preventive actions. Develops, modifies, applies and maintains methods and procedures for product development, process control, testing and inspection to ensure the manufacturing of safe and effective biotechnological products. 5/17/2020
440 BioMarin
Novato, CA
Research Assistant, Sample Coordinator
BS/BA
Exp: 0-2 years in related
Primary responsibilities will be to support sample tracking, sample submission, and sample testing coordination for the Analytical Sciences group. This position involves documentation of samples received for analysis from QC, Manufacturing, and other groups within Process Sciences and coordinating with the proper personnel in Analytical Sciences to perform analytical assays with adherence to strict timelines. 5/17/2020
441 BioMarin
Novato, CA
Research Assistant
Associates or BS/BA in sciences
Exp: 0-2 years
The Analytical Sciences Department is seeking a Research Assistant that will be responsible for coordinating with lab support service providers and multiple departments such as Facilities, EHS&S, Lab Support, IT, Vendors and Contractors to ensure that Analytical Sciences Department needs are met. Performs good documentation practices with instrument and equipment laboratory logbooks and ensures compliance in their documentation. 5/17/2020
442 Berg Health
Framingham, MA
Operations Lead – Precision Medicine
BS or MS in chemistry or biochemistry
Exp: 1-3 years in industry
Manage project efficiency and timelines across bioanalytical, OMICS, and assay development groups. Coordinate sample extractions and analysis across precision medicine groups. Track and maintain quality control records of instrument analytical performance across groups. Develop project plans and reports for internal and external projects 5/16/2020
443 BioAgilytix
Durham, NC
QA Auditor
BS/BA in biology/chemistry or related
Exp: 1-3 years in industry
Perform Quality Assurance (QA) audits, inspections (internal/external) and monitoring procedures against standard operating procedures, methods, protocols/plans, guidances, and/or regulations, as applicable. Assist in hosting regulatory inspections by acting as scribe and/or reviewing documents and identifying and calling operational staff to answer questions as required 5/16/2020
444 BioAgilytix
Durham, NC
Laboratory Support Technician | Purchasing Agent
Associates in biology/biotechnology
Exp: 1+ years in lab
The Laboratory Support Technician | Purchasing Agent is responsible for laboratory support and purchasing for Operations. This includes processing purchase orders with vendors, matching packing slips with purchase orders, and overall tracking of reagent receipts in NetSuite. 5/16/2020
445 BioAgilytix
Durham, NC
Analyst
BS/BA in biological sciences/technology
Exp: 1 year in lab
Prepare worksheets with minimal supervision. Prepare plate maps. Serve as lead analyst on sample analysis projects. Troubleshoot assays. Compile/process data (make power export) 5/16/2020
446 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
447 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
448 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
449 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
450 BioGX
Birmingham, AL
Reagent Production Technician I
BS in biology or engineering
Exp: 0-2 years
The Manufacturing Technician is responsible for general laboratory duties focused on manual and automated filling andpackaging of standards,controls and panels for commercically avalible nucleic acid tests and other advanced reagents. The Manufacturing Technician is expected to follow standard operating procedures and quality systems documentation in a GMP environment 5/16/2020
451 BioFire
Salt Lake City, UT
Material Handler I
HS Diploma/APICS training
Exp: No experience required
The Material Handler I is responsible for the physical movement, support, and administrative tasks involved in receiving, shipping, storing, and support of raw material used for manufacturing of good. Perform real time daily replenish of material to the floor in a “Just in Time” manner to never run the line dry, yet to also ensure inventory is minimized in the line. Break down, clean, organize, and prep raw material ready for manufacturing in accordance to procedure and production requirements. 5/16/2020
452 Biogen
Cambridge, MA
Engineer I, Purification Process Development, Gene Therapy
BS or MS in biological/chemical engineering or sciences
Exp: 0-2 years
The successful candidate will join a team of engineers/scientists responsible for the development of purification processes used for the clinical and commercial manufacture of adeno-associated viral (AAV) vectors. This individual will be involved in execution of multiple aspects of viral vector purification, including chromatography, filtration and membrane separations (TFF, UFDF, microfiltration, viral filtration, and depth filtration), and validation of viral and contaminant clearance. In addition, the individual may participate in project teams and in the scale-up and technology transfer of purification processes to the manufacturing organizations. 5/16/2020
453 Biogen
Research Triangle Park, NC
Manufacturing Associate (Parenteral Filling Facility)
HS Diploma, BS/BA preferred
Exp: 0-2 years
In this role you will be responsible for performing and documenting daily manufacturing operations in a cGMP environment. This involves operation of process equipment, execution of validation protocols, creating/ revising cGMP documents and other assignments. Applicants will be highly detailed oriented with excellent documentation skills. Applicants will become trained and skilled at most or all unit operations in their area, often leading the execution of procedures, and performs most functions with minimal supervision. 5/16/2020
454 Biogen
Research Triangle Park, NC
Patient Services Coordinator  
BS/BA
Exp: 1-2 years
The primary role of the Patient Service Coordinator is to facilitate the customer lifecycle by assisting patients, healthcare providers and others with activities related to starting and staying on therapy. Patient base includes both newly diagnosed and existing Alzheimer patients. Daily interactions involve contact via phone not only with patients but also health care providers, Biogen field force representatives, business service partners, nursing services and other internal work groups. 5/16/2020
455 Vividion
San Diego, CA
Research Associate, Molecular and Cellular Biology
BS/MS in cell biology
Exp: 0-3 years
The successful candidate will have extensive hands on experience and expertise in basic molecular biology, mammalian cell culture techniques, and cellular and biochemical assay development. They will support the validation of novel drug targets via multiple mechanisms, including testing the effects of compounds on proteins in cellular and biochemical settings. They will utilize the development and/or use of new technology to support drug discovery. etc. 5/13/2020
456 Xellia
Cleveland, OH
EM Specialist I - Night Shift (12 Hours)
BS in microbiology or other science
Exp: 1-5 year(s)
The Aseptic Environmental Monitoring Specialist I position works closely with other departments, such as Operations, Maintenance, Quality Assurance, Validation, and Engineering to assure the support of the Environmental Monitoring department on various projects, studies and routine tasks. The individual holding the position of Environmental Monitoring Specialist I shall be responsible for performing routine and non-routine testing. They will be responsible for Environmental Monitoring documentation and corrections. The individual will assist with the training of environmental monitoring personnel on tests and methods. etc. 5/13/2020
457 Xellia
Cleveland, OH
Microbiologist - 2nd Shift
BS in biology, biochemistry, biotechnology, or related
Exp: 0-2 years
The Microbiologist supports the testing in the Microbiology laboratory at the Xellia Cleveland site. In this role, the Microbiologist I is responsible for will be responsible for all aspects of the Microbiology laboratory operations, such as sample receipt, sample testing, data generation, data analysis and summarization and other QC lab supporting activities. Uses good documentation practices in the collection of data/records. Authors and executes qualification documents, SOPs, protocols, and investigations. Recommends corrective actions or process improvements that will eliminate the potential for laboratory deviations. etc. 5/13/2020
458 Xellia
Cleveland, OH
Sterile Operations Supervisor - RTU Manufacturing
BS
Exp: 0-5 years
Position is primarily the direct supervision of manufacturing Aseptic Operators; ensuring sterile injectable pharmaceuticals are manufactured in strict adherence to cGMPs ensuring safety, quality, and potency of the product produced. Sterile Operations Supervisor is also the first level of management that ensures adherence to the production plan and delivery of On Time In Full targets. etc. 5/13/2020
459 Xellia
Cleveland, OH
Manufacturing Quality Assurance Specialist I
AS/BS in a life or physical science
Exp: 1+ year(s)
The Manufacturing Quality Assurance (MQA) Specialist I is responsible for providing quality oversight to all manufacturing and packaging areas to ensure product quality and SOP/GMP compliance at the Cleveland Manufacturing Facility. Works closely with Production personnel to complete on-the-floor, in process batch record review, resolve all batch related issues or escalate to the Quality Assurance Supervisor as appropriate, and ensure good documentation practices are being followed. etc. 5/13/2020
460 Xellia
Cleveland, OH
Aseptic Operator I - 12 Hour Shift
HS diploma/AS
Exp: 0-1 year(s)
The contents contained in this job description are the minimum requirements required to be met for the aforementioned position. Under the direction of area management or designee, the Aseptic Operator I is responsible for performing all necessary tasks both in and outside of the classified manufacturing suites in support of manufacture of safe and effective sterile (injectable) pharmaceutical products at the Xellia Cleveland plant. etc. 5/13/2020
461 Xellia
Cleveland, OH
Aseptic Operator II - 12 Hours
HS diploma/AS
Exp: 1-2 year(s)
The contents contained in this job description are the minimum requirements required to be met for the aforementioned position. Under the direction of area management or designee, the Aseptic Operator II is responsible for performing all necessary tasks both in and outside of the classified manufacturing suites in support of manufacture of safe and effective sterile (injectable) pharmaceutical products at the Xellia Cleveland plant. etc. 5/13/2020
462 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
463 WuXi AppTec
King of Prussia, PA
Scientist I Downstream Process Development
BS/MS
Exp: 0-5 years
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. etc. 5/13/2020
464 WuXi AppTec
Cranbury, NJ
Associate Scientist II
MS/MA
Exp: 0 years
Essential Job Functions: Under minimal supervision, individual performs routine laboratory techniques and more difficult procedures, including but not limited to weighing the chemical, preparing the stock solution and standard calibrator/QC in biological fluids, extracting the samples, analysing the samples, summarizing the data, and etc. Receives specific instructions on assigned task and expected results. Delivers accurate results on assigned tasks within the expected timeframe. May assume the duty as a trainer to new hires. Has a thorough understanding of the study and method; troubleshoots unexpected results. etc. 5/13/2020
465 WuXi AppTec
King of Prussia, PA
Scientist, Upstream Process Development
BS/MS
Exp: 1-2 year(s)
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. Keep accurate record of cell culture parameters and results into datasheets and/or laboratory notebooks. etc. 5/13/2020
466 WuXi AppTec
St. Paul, MN
Facilities Technician
HS diploma or equivalent
Exp: 1-2 year(s)
Performs facilities duties in compliance with applicable procedures, regulations, and industry standards to support building/laboratory infrastructure and testing/manufacturing operations. Supports continuous improvement initiatives at the Saint Paul, MN facility. Responsibilities: Essential Job Functions: Complete preventative maintenance of equipment, systems, and buildings. Complete non-routine (troubleshooting, repair) maintenance of equipment, systems, and buildings. etc. 5/13/2020
467 WuXi AppTec
Philadelphia, PA
Laboratory Technician II
BS in a biological science or related
Exp: 1-2 year(s)
Performs virology, safety, and gene therapy assays according to testing records and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), and Standard Operating Procedures (SOPs). Responsibilities: Maintain cell cultures in accordance to SOPs and testing records. Conduct assays and lab procedures as outlined in testing record and regulatory guidelines. Conducts PCR and ELISA assays. Works in BSL2 lab setting using virus positive controls. 5/13/2020
468 WuXi AppTec
Cranbury, NJ
Associate Scientist I
BS
Exp: 1+ year(s)
We are searching for an Associate Scientist to join our growing HTS and in vitro screening team. Responsibilities: Requiring daily supervision to participate in the processes of in vitro assay screening and high throughput screening (HTS) of a wide array of protocols for a diverse client base that includes pharmaceutical and biotechnology companies. Works on assignments with a diverse team of scientists to facilitate all aspects of performing in vitro screening and running an HTS laboratory. etc. 5/13/2020
469 WuXi AppTec
San Diego, CA
Analytical Lab Assistant
HS diploma/BS in chemistry or biochemistry
Exp: 1 year
The Analytical Lab Assistant is responsible for providing support to scientists with lab tests and research. The incumbent receives, stores and distributes supplies, assists with pre-analytical, analytical and post-analytical test processes, and other related tasks. Responsibilities: Orders, receives, stores and distributes supplies. Keeps work areas stocked and cleaned. etc. 5/13/2020
470 Eurofins
Cambridge, MA
Laboratory Operations Associate
BS
Exp: 0-2 months
Job Description: Performing routine lab operations including maintenance, tracking, and life cycle management of laboratory equipment. Monitoring of equipment alarm system and coordinating equipment preventive maintenance/repairs with asset management and scientific staff. Assisting in general lab housekeeping. Interfacing with EHS, Facilities, Asset Management, and scientific staff on routine operations and on continuous improvement efforts for optimal operating efficiency. Participating in lab inspections to ensure compliance and safety. Assisting with new equipment assessment and installation and on additional lab related projects as they arise. etc. 5/13/2020
471 Eurofins
Nashville, TN
HPLC Technician
MS in chemistry
Exp: 1-2 year(s)
Employee Responsibilities: Support the analytical testing for process development. Chemical labeling of biological samples, HPLC separation, and data analysis. Preparing buffers, setting up, sterilization, sampling, and cleaning of systems. Document laboratory activities manually and electronically and enter process data into database. Troubleshoot equipment and perform minor repairs. Perform review and peer review of analytical data. etc. 5/13/2020
472 Eurofins
West Point, PA
PCR Assay Scientist
BS/BA in biology, chemistry, biomedical engineering or related
Exp: 6+ months
Assay Scientist responsibilities include, but are not limited to, the following: The development and performing of assays to support biopharmaceutical testing. Prepare and pipet small volume solutions. Maintain records and test results following good manufacturing practices (GMP). Document work clearly and perform tests accurately. Perform tasks in a repeatable and efficient manner. Communicate effectively with team members and client staff. etc. 5/13/2020
473 Eurofins
Lancaster, PA
Molecular and Cell Scientist II: Method Development and Validation
MS in molecular or cell biology or related
Exp: 1-2 year(s)
Job Description: Perform a wide range of analyses (routine and non-routine)to support biopharmaceutical testing. Analyses are primarily, but not limited to, cell-based assays and ELISA's (kit-based and de novo). Meet TAT for assigned testing/projects and work independently. Review and evaluate raw data for acceptability. Assist other technical staff in evaluation of raw data for acceptability. Contribute to the development and validation of methods used within the department.. Be able to plan and organize work week and communicate schedule to management when required. Attend client facing meetings as needed. etc. 5/13/2020
474 Eurofins
Lancaster, PA
Associate Stability Project Management Specialist/Scientist
BS/BA in science, business, or related
Exp: Not necessary for BS/BA candidates
Job Description: Manage all aspects of stability studies submitted by assigned clients. Take responsibility for quality and TAT of assigned studies. Writing stability protocols. LIMS entry for stability studies. Potential to move into a lab role within 12 months as workload shifts. etc. 5/13/2020
475 Eurofins
Indianapolis, IN
Analytical Chemist - Night Shift
BS in chemistry, biology, or related
Exp: 3+ months
Employee Responsibilities: Perform biochemical testing on proteins and antibodies including, but not limited to, CE, IC, HPLC, SEC, SDS-PAGE, UV, Protein A titer, ELISA, and Particulates. Working as part of a team in a rotating night shift role (shift pattern of 3-2-2-3) which includes working weekends and holidays when they fall within shift pattern. Enter data into LIMS. Ability to work independently and as part of a team in a GMP environment. Participate in conducting investigations. etc. 5/13/2020
476 VRL Eurofins
Centennial, CO
Warehouse Associate
HS diploma or equivalent
Exp: Not required
Headquartered near Denver, Colorado, with satellite laboratories in or near Los Angeles, Dallas, Boston, Atlanta, and Minneapolis, VRL Eurofins is continuing to expand throughout the United States and is seeking a highly motivated and detail oriented Warehouse Associate to work in Centennial, CO. Job Description: Warehouse Associate responsibilities include, but are not limited to, the following: Oversee all inbound supply deliveries. Performs receipt inspections and enters received goods into receiving system per SOP. etc. 5/13/2020
477 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
478 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
479 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
480 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
481 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
482 Veeva
Toronto, ON
QA Engineer - Andi
BS in engineering, math, computer science or related
Exp: 1-4 year(s)
Veeva is looking for a QA Engineer that likes to figure out how things work and make sure they are working correctly. This is a hands-on position for delivering a quality SaaS based product. You should want to be part of fast-paced team who takes pride in building great software and making customers successful. Come join us in building a game-changing product to help deliver real-time insights and suggestions via Artificial Intelligence. What You’ll Do: Ensure that all assigned project deliverables meet quality objectives in functionality, performance, stability, security, accessibility and data quality. etc. 5/6/2020
483 ThermoFisher Scientific
High Point, NC
Machine Operator (Encapsulation) - (Nights C shift)
HS diploma or equivalent
Exp: 1 year
Responsibilities: Reads job specifications from the Batch Production Record to determine machine adjustments and material requirements. Observes machine operation. Makes adjustments as needed. Takes samples of product and performs in process testing. Performs all checks as required and documents activities. Is responsible for maintaining all required documentation in accordance with the Work Instructions of Patheon / Thermo Fisher Scientific. Assists Set-Up person to set up machine, empty basket and clean and prepare machine for changeover. Also assists with the actual changeover. etc. 5/6/2020
484 ThermoFisher Scientific
High Point, NC
Printing Associate
HS diploma or equivalent
Exp: 1+ year(s)
What will you do? Set up printing equipment by installing carrier bars, brushes, stripper plate, blow off tubes, gravure roll, rubber roll, ink pan and doctor blade. Set up the vision equipment (install proper belt/color, load appropriate recipe, install proper target, train the cameras, verify background) and trouble-shoot as needed. Work safely to prevent on the job accidents and injuries by observing moving equipment and adhering to all job safety procedures such as wearing PPE. Document work performed by completing forms and logs accurately. etc. 5/6/2020
485 ThermoFisher Scientific
High Point, NC
Medicine Associate
HS diploma or equivalent
Exp: 1 year
Manufacture a quality fill material for use in encapsulation utilizing multiple types of equipment and processes to accomplish this. Works safely to prevent on the job accidents and injuries by observing moving equipment; adhering to all job safety procedures; attending plant safety training; shift safety meetings; adhering to lockout/tag out procedures; wearing appropriate personal protective equipment (PPE) such as captive clothing, steel-toe shoes, respirators, and additional gowning if necessary. Able to be adaptable to a dynamic work environment. At batch initiation and during batch processing performs the following: check lot numbers; check weights; check raw material lot numbers; check part numbers; ensure expiration dates are within acceptable range by comparing the various print-outs and labels with the batch processing record (BPR). Follows BPR instructions as guided. etc. 5/6/2020
486 ThermoFisher Scientific
Middletown, VA
Manufacturing Operator (2nd Shift Fill/Label/Pack)
HS diploma or equivalent
Exp: 1 year
Manufacturing Operators work alone or with other operators to perform filling and/or packaging of products by complying with GMP (Good Manufacturing Practices), ISO 13485 guidelines and company Standard Operating Procedures (SOPs). What will you do? Perform duties on production line to prepare, assemble and pack products as required. Must be able to complete and understand production paper work with minimal to no errors, up to and including product reconciliation, label reconciliation, labor sheets, product fill checks, torque checks, etc. Cleans and sanitizes work areas, machines, glassware or equipment as needed or directed, if required in work area. etc. 5/6/2020
487 ThermoFisher Scientific
Durham, NC
Proposals Specialist
BS/BA in science or business
Exp: 0-2+ years
The Associate Drug Product Commercial Proposal Specialist will take customer provided technical information along with reasonable assumptions and estimate the cost and pricing for late phase transfer programs as well as ongoing commercial supply for pharmaceutical products. This position will then write the related bid proposals that will be issued to the customer through the sales team. This position will support the sales efforts related to the opportunities that they quote on as well as manage the relevant quote records in Salesforce.com. etc. 5/6/2020
488 ThermoFisher Scientific
Mississauga, ON
Proposals Specialist
BS/BA in science or business
Exp: 0-2+ years
The Associate Drug Product Commercial Proposal Specialist will take customer provided technical information along with reasonable assumptions and estimate the cost and pricing for late phase transfer programs as well as ongoing commercial supply for pharmaceutical products. This position will then write the related bid proposals that will be issued to the customer through the sales team. This position will support the sales efforts related to the opportunities that they quote on as well as manage the relevant quote records in Salesforce.com. etc. 5/6/2020
489 Unity Biotechnology
South San Francisco, CA
Research Associate 1/2, in vivo Pharmacology
MS in biology, physiology, bioengineering, or related
Exp: 1-2 year(s)
The candidate should be creative and have both a passion for biology and an interest in using animal models to study human disease. The position requires a self-motivated individual seeking a hands-on, lab-based role using in vivo animal models and in vitro methodologies to contribute to specific project goals as part of a dynamic team. The duties of the job include animal handling/dosing, experimental design and execution, analysis/interpretation of data, downstream sample generation/ samples processing, and presentation (verbal/written) of findings at team meetings. etc. 5/6/2020
490 Unity Biotechnology
South San Francisco, CA
Research Associate in-vivo Pharmacology
MS in cellular biology, physiology, or related
Exp: Not necessary for MS candidates
We are seeking to hire a research associate to join the in vivo pharmacology team at Unity. This position will afford the successful individual an opportunity to discover clinical candidates for an emerging and exciting biology and the potential to translate our science into a pipeline of differentiated medicines. The ideal candidate will be enthusiastic, innovative, and possess a diverse technical skill set having worked on a variety of in vivo models. At Unity, this experience will be applied towards the successful discovery of novel small molecules for the selective elimination of senescent cells in diseases associated with aging. etc. 5/6/2020
491 Baxter
Marion, NC
Technician, Formulation
HS Diploma/GED
Exp: 1 year in manufacturing
Perform and document scheduled cleaning activities which include using a ladder and safety harness to climb into mixing tanks in order to clean the inside of the vessel. Inspect, clean and re-palletize raw materials received from the warehouse. Following standardized formulas, apportion, measure, weigh, label and stage raw materials. 5/3/2020
492 Baxter
Marion, NC
Quality Lab Assoc I
BS in microbiology or biological sciences
Exp: 0-2 years
Conduct microbiological analyses on raw materials, in-process and finished products. Collect samples related to Environmental Monitoring program at Baxter manufacturing area. Use laboratory instrumentation and computer systems to collect and record data. Perform advanced assays requiring precise analytical skills and understanding of microbiological principles. 5/3/2020
493 Baxter
Round Lake, IL
Manufactuirng Supervisor I, 2nd Shift
BS/BA
Exp: 1 year experience
The supervisor position is responsible for implementing and supervising daily activities in a specific production area to ensure manufacturing goals and project deadlines are met while maintaining compliance with current good manufacturing practices (GMPs), environmental health and safety (EHS) guidelines and any other regulations that could apply.May monitor and control labor. 5/3/2020
494 Baxter
Round Lake, IL
Quality Lab Associate I
BS in microbiology or 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 5/3/2020
495 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
496 Baxter
Round Lake, IL
Quality Lab Associate I
BS in microbiology or 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 5/3/2020
497 Baxter
Round Lake, IL
Quality Lab Associate I
BS in microbiology or 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 5/3/2020
498 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
499 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
500 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
501 BD
Sandy, UT
Process Specialist
HS Diploma/GED
Exp: 1-2 years in manufacturing
The Process Specialist Operates high speed automated manufacturing equipment in the Surgical Scrub department. Operates high speed automated manufacturing equipment. Ensures that correct doses of the active ingredients are dispersed. Responsible for readying production equipment and materials during product changeovers. Responsible for set-up of work stations and bringing in materials for production order. 5/3/2020
502 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
503 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
504 Bayer
Indianola, PA
Assembler I - 2nd Shift 2:00pm - 10:20pm
HS Diploma/GED
Exp: 0-1 years working
Assemble and package various products; Perform rework and inspection on the product;Be aware of quality standards and ability to identify defects in products; 5/3/2020
505 Bayer
Pittsburgh, PA
Machine Operator I - D2 6am-6pm
HS Diploma/GED, Associates Preferred
Exp: 0-2 years
Understand the potential hazards and safe equipment operating practices in a manufacturing environment; Understand the quality systems and guidelines that impact areas of responsibility including component specifications, equipment operating parameters, data collection and cleanliness requirements; Ensure all potential equipment deficiencies and component defects are properly identified throughout areas of responsibility to ensure adherence to quality guidelines; 5/3/2020
506 Bayer
Muscatine, IA
Packaging Tech
HS Diploma/GED, Associates Preferred
Exp: 1 year in electrical/mechanical work
Operate, maintain, and repair packaging equipment as well as troubleshoot problems associated with equipment, process, or systems; Perform mechanical maintenance and preventative maintenance on packaging equipment; Complete equipment repair notifications and work directly with Maintenance Technicians on any repairs requiring their assistance; 5/3/2020
507 Bayer
Marshall , MO
Seed Technician
HS Diploma/GED
Exp: 0-2 years
Operate equipment in the production sites and leveraging real time data to maximize existing procedures; Perform preventive maintenance and inspections; troubleshooting problems associated with equipment, processes and systems as needed; Support areas across the plant in driving the adoption of continuous improvement practices and programs (5S, Lean, Six Sigma) conducive to an organized and clean work environment; 5/3/2020
508 Beckman Coulter
Minneapolis, MN
Human Resources Representative I
BS/BA in human resources
Exp: 0-2 years
The selected individual will provide counsel and assistance to broad employee populations, including front-line associates and senior managers. In support of these client groups, this role will be responsible for end-to-end human resources work including recruitment, training facilitation, employee relations, management consulting, metrics reviews, and all applicable annual processes. 5/3/2020
509 Beckman Coulter
Chatsworth, CA
Field Service Engineer - Chemistry/Automation: Northern LA
Associates
Exp: 1-3 years
Under minimal supervision, serve as lead to assigned customers; complete troubleshooting, installation, validation, maintenance, and service repair needs on designated equipment. May assist and/or train newer Field Engineers. Provide excellent and efficient service to Beckman Coulter’s customers, along with technical training on products 5/3/2020
510 Beckman Coulter
Chaska, MN
Software Engineer I - Diagnostic Instrument
BS/BA in computer science, biomedical engineering, or related
Exp: 0 years required
As part of the software development team, you’ll work with a variety of technologies to bring new products to market. We develop product software with primarily a C#/.NET windows-based technology stack. As an R&D software engineer, you could be writing code to control mechanical systems, design UIs, and interact with databases and web services. 5/3/2020
511 Avid Bioservices
Tustin, CA
Biomanufacturing Technician (Buffer/Media Support)
AA or HS Diploma
Exp: 0-1 year in life science industry
The Manufacturing Technician provides support for: Production Operations and multiple aspects of cGMP contract cell culture manufacturing in strict compliance with cGMP, under Standard Operating Procedures in a multi-product manufacturing facility, including, but not limited to: production, documentation, writing reports, requesting and purchasing materials, and scheduling equipment services and calibrations 5/2/2020
512 Avid Bioservices
Tustin, CA
Biomanufacturing Associate/Technician (Downstream Purification)
BS/BA in life sciences
Exp: 0-1 years (technicial level)
As a Biotech Manufacturing Associate / Technician, you play an integral role in ensuring the on-time delivery of quality biopharmaceutical products. You get to participate in a variety of tasks including purification of biologics, keeping up-to-date GMP documentation, writing reports, ordering materials, and scheduling equipment services. 5/2/2020
513 Avid Bioservices
Tustin, CA
Shipping Clerk, Supply Chain (Entry-Level)
AA or HS Diploma
Exp: 0-2 years in shipping
Schedule shipments with carrier including waybill and commercial invoice if needed. Complete sample packaging and shipping duties. Organize all shipping supplies in an easy to locate and count fashion. Coordinate the efficient movement of samples with QC, Manufacturing and other departments under cGMP standards 5/2/2020
514 Azzur Group
Waltham, MA
Validation Engineer (Consultant)
BS in engineering/sciences
Exp: 1-7 years in manufacturing environment, regulated
Development and editing of technical documentation including: Standard Operating Procedures, User Requirements and Design Specifications, Commissioning and Qualification Protocols. Development of project plans, as appropriate. Execution of validation test procedures 5/2/2020
515 Avexis
Longmont, CA
Quality Control Technician (Microbiology)
BS/BA in microbiology or related
Exp: 0-1 years
This position will work with the Quality Control team in supporting our efforts in this exciting new area of gene therapy. This position will be responsible for environmental monitoring, product and raw material testing, and other general QC microbiology sampling and testing processes. Perform environmental and utilities monitoring in clean rooms and subsequent analyses. 5/2/2020
516 Avexis
Libertyville, IL
Training Associate
BS/BA
Exp: 1-3 years in training
The Training department is responsible for developing the skills and knowledge of site employees, allowing development within their current role, as well as enhancing careers within AveXis. The Training Associate is responsible for the day-to-day operation of the Learning Management System (LMS), monitoring and reporting compliance to the program, and assisting with the identification and development of training content. 5/2/2020
517 Avexis
Libertyville, IL
Quality Control Technician (Microbiology-Day Shift)
BS/BA in microbiology or related
Exp: 0-2 years
This position will work with the Quality Control team in supporting our efforts in this exciting new area of gene therapy. This position will be responsible for environmental monitoring, product and raw material testing, and other general QC microbiology sampling and testing processes. Perform environmental and utilities monitoring in clean rooms and subsequent analyses. 5/2/2020
518 Avexis
Durham, NC
Quality Control Investigations Specialist
BS/BA
Exp: 1-3 years in quality
As part of the Manufacturing organization, the Quality Control (QC) Investigations Specialist will be responsible for the investigation and completion of laboratory investigations and non-conformances aimed at identification of root cause, assessing potential impact and implementation of corrective and preventive actions. The QC Investigations Specialist will help determine the validity of data, and determination of out of specification results. 5/2/2020
519 Azzur Group
Waltham, MA
Operations Engineer I
BS/BA in sciences
Exp: 1-2 years in similar role
Identifying and executing project actions to improve the Inventory Control System or the Computerized Maintenance Management System used to support Facility operations. Support the execution of equipment qualification and commissioning studies for shipping, facility utilities and equipment used in client process operations and in facility operations. Execute protocols and help resolve protocol deviations/discrepancies, analyze study data and write summary reports. 5/2/2020
520 Serepta Therapeutics
Cambridge, MA
Specialist I, Patient Affairs
BS/BA
Exp: 1-3 year(s)
The Operations Specialist I focus primarily on performing the day-to-day operations within the Patient Affairs team and streamlining Patient Affairs’ processes within our department, in addition to how we work with our internal, cross-functional partners. This role can improve the overall function of our department while also gaining exposure (and ultimately helping to drive the execution) of work across the team to partner with the patient/caregiver community externally and internally drive patient voice across Sarepta’s global sites. This role works primarily with Patient Affairs, in addition to policy, legal & compliance, marketing, corporate communications, information technology (IT), and regulatory. etc. 4/29/2020
521 Serepta Therapeutics
Dublin, OH
Research Associate I, Histology
BS in chemistry or a physical or biological science
Exp: 1 year
The Research Associate, Histology provides laboratory support of day-to-day GCLP/GLP testing on muscle/nerve and other tissue types using complex histology methods in accordance with the requirements of approved protocols. The RA has strong histology laboratory expertise and utilizes this experience to train others, maintain records of experiments, assist in analyzing data, and prepare laboratory reports. The RA participates in development, GCLP/GLP qualification, and validation of histology related assays to support clinical trials and clinical development decision-making. etc. 4/29/2020
522 Serepta Therapeutics
Durham, NC
Research Associate I
BS in biochemistry, immunology, bioengineering or related
Exp: 1-3 year(s)
The Research Associate I provides laboratory support, performs experiments and collects data on in vitro, ex vivo, and/or in vivo studies to investigate the effects of CRISPR-based gene editing on gene and protein expression, tissue pathology, and disease phenotype in animal models of neuromuscular disorders. The RA participates in development, GCLP/GLP qualification, and validation to support preclinical development, clinical trials and clinical development decision-making. 4/29/2020
523 Serepta Therapeutics
Burlington, MA
IT Support Specialist I
HS diploma/BS/BA
Exp: 1-3 year(s)
Level I Specialist primary duties include Tier 1 technical support, including software/hardware installation, troubleshooting, hardware break/fix, VoIP phone support and asset management. Primary Responsibilities Include: Provide Tier 1 technical assistance for computer hardware, software systems, and printers/copiers. Respond to inquiries via email, phone, walk-up or ticketing system. etc. 4/29/2020
524 Serepta Therapeutics
Andover, MA
Associate I, Quality Control
BS in chemistry or related
Exp: 1-2 year(s)
This individual will support quality control activities conducted both internally and at the Contract Test Laboratories (CTLs). The individual will be responsible for generating and reviewing release data, writing technical reports, and supporting analytical method validation and qualification activities conducted internally, as well as supporting the above tasks at the CTLs as needed. This individual will assist in transferring assays to and from domestic and overseas vendors and monitoring, compiling and reviewing data. The individual will also assist in managing laboratory investigations, quality events, data trending, review of quality documents originated at the testing laboratories as well as internally at Sarepta. etc. 4/29/2020
525 Sedia
Portland, OR
QC Technician
HS diploma/AS/AA
Exp: 1-3 year(s)
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. 4/29/2020
526 Sedia
Portland, OR
Manufacturing Technician
HS diploma/AS/AA
Exp: 1+ year(s)
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. 4/29/2020
527 Sekisui
Charlottetown, PE
Associate Scientist
BS
Exp: 0-2 years
The Associate Scientist will be responsible for designing, executing and interpreting experiments and analytical procedures under general supervision. Initiates, directs and executes pre-clinical scientific research and/or development strategies in research and/or development. Investigates the feasibility of applying a wide variety of scientific principles and concepts to potential inventions, products and problems. Plans and executes laboratory research. Maintains broad knowledge of state-of-the-art principles and theories. May participate in development of patent applications. Interfaces with various departments. etc. 4/29/2020
528 Sekisui
San Diego, CA
Maintenance Technician II
HS diploma/AS/AA
Exp: 1-2 year(s)
The Maintenance Technician II performs preventative and/or corrective maintenance for all manufacturing and facility equipment according to the specifications and procedures. Executes electrical and mechanical troubleshooting to determine problems in non-functioning equipment used in the manufacturing process. Diagnoses, adjusts, repairs, tears-down and re-assembles equipment. Uses test and diagnostic equipment to perform inspections. Completes maintenance records in accordance with Good Manufacturing Practices. Coordinates with vendors to ensure work is conducted in a timely and safe manner. etc. 4/29/2020
529 Sekisui
Kansas City, KS
Research Assistant
BS in a biological and chemical science
Exp: 1+ year(s)
SEKISUI XenoTech, LLC is currently hiring for an entry level Research Assistant to the 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 experiments. Maintains laboratories and equipment. etc. 4/29/2020
530 Seracare
Cumberland Foreside, ME
Manufacturing Chemist I
BS in biology, chemistry, or medical technology
Exp: 0+ years
The Manufacturing Chemist I prepares reagents, buffers, stocks and other solutions relying on established procedures within a controlled production environment. This role also performs the analysis and interpretation of test results within pre-established guidelines. The Manufacturing Chemist at this level is familiar with: Basic laboratory equipment and techniques. etc. 4/29/2020
531 SomaLogic
Boulder, CO
Laboratory Technician I/II
AS in a physical, biological, or medical science
Exp: 6 months
SomaLogic is a rapidly growing privately owned biomedical science company that has developed a revolutionary proteomics technology capable of measuring thousands of proteins in a single sample. We are a dedicated team of science-based colleagues working to build new tools based on our technology that will change the way life science research is done and healthcare is delivered. The Laboratory Technician I, II, or Associate I position in our U.S. Regulated Clinical Laboratory, located in Boulder, CO. The primary role of this position is to perform routine testing of patient samples using robotic liquid handling systems. etc. 4/29/2020
532 Sorrento Therapeutics
San Diego, CA
Manufacturing Associate I
BS in the life sciences
Exp: 1+ year(s)
We are currently seeking a Manufacturing Associate who will be responsible for performing and supporting Downstream manufacturing tasks. Including but not limited to: Maintain GMP compliance in clean rooms. Responsible for Downstream GMP processing activities: buffer preparation, antibody purification, and drug substance formulation. Support material inventory control for downstream activities. etc. 4/29/2020
533 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. 4/29/2020
534 Steris
Reno, NV
Field Service Technician
AS/BS in electronics, mechanics, or related
Exp: 1+ year(s)
At STERIS, our Field Service Technicians act as the face of our company by ensuring top-notch service for our customers. In this field-based, customer-facing role, you will travel to hospital and surgical facilities to maintain, troubleshoot, service, and provide calibration and installation support for steam sterilizers, medical equipment washers and other STERIS products as needed. In addition, you will be responsible for building positive relationships with customers and colleagues, as well as completing necessary administrative tasks. etc. 4/29/2020
535 Steris
Minneapolis, MN
Installation Technician
AS/AA in electronics, mechanical, or related
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. etc. 4/29/2020
536 Steris
Toronto, ON
Field Service Technician
AS/BS in electronics, mechanics, or related
Exp: 1+ year(s)
At STERIS, our Field Service Technicians act as the face of our company by ensuring top-notch service for our customers. In this field-based, customer-facing role, you will travel to hospital and surgical facilities to maintain, troubleshoot, service, and provide calibration and installation support for steam sterilizers, medical equipment washers and other STERIS products as needed. In addition, you will be responsible for building positive relationships with customers and colleagues, as well as completing necessary administrative tasks. etc. 4/29/2020
537 Steris
Richmond, VA
Technician I
HS diploma or equivalent
Exp: 1-3 months
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. Travel requirements may vary by location. etc. 4/29/2020
538 Steris
Clifton, NJ
Installation Technician
AS/BS in electronics, mechanics, or related
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. etc. 4/29/2020
539 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
540 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
541 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
542 Stryker
Plainfield, IN
Quality Control Technician
unspecified
Exp: 1-2 year(s)
Responsibilities: 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. etc. 4/29/2020
543 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
544 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
545 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
546 Sunrise Pharma
Rahway, NJ
Regulatory Affairs Associate
MS in pharmaceutical manufacturing, regulatory affairs, quality assurance or related
Exp: 6 months
Pharmaceutical Manufacturing seeks a Regulatory Affairs Associate. Resp. include creating & implementing labels for OTC & ANDA submissions, assist in ANDA submissions using eCTD submission software, prepare & maintain annual reports, SOP, deviations & OOS reports, review product complaints & queries & support in developing regulatory strategies & launch OTC products. etc. 4/29/2020
547 T2Biosystems
Lexington, MA
Research Associate II
MS in microbiology or molecular biology
Exp: 1-2 year(s)
This position will join our growing Microbiology team and will provide aid and expertise in the development of laboratory protocols for the cultivation and characterization of pathogenic organisms. The individual will work with other Microbiology team members 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 team. This role consists of hands-on execution in the laboratory and data analysis within the Microbiology group and is based in Lexington, MA, reporting directly to the Director of Microbiology, R&D. etc. 4/29/2020
548 Tandem Diabetes Care
Boise, ID
Complaint Management Associate
BS in biology or chemistry
Exp: 1-2 years
What you’ll be doing: You’ll be working closely with your team to provide a high level of administrative support. This will involve drafting & filing Medical Device Reports to the FDA, maintaining our databases, and supporting departmental audits. The right person for this position will be a quick learner who is detail-oriented. etc. 4/29/2020
549 TechLab
Radford, MA
Quality Assurance Officer 1
AS/AA/BS/BA
Exp: 0-1 year(s)
An employee in this position can expect to perform the following duties: Release pre-raw, raw materials and components to departments for use. Create, review, and apply QA Release Labels. Issue and review Master Batch Records (MBRs) in support of Production and BMP schedules. Issue, confirm and approve Expiration Dates of Raw Materials, Components and Finished Products. Review QC results detailed per SOPs, RMSs, and PRSs. Ensure approved documents are issued and controlled. Ensure Controlled Records are controlled and easily retrievable. etc. 4/29/2020
550 Tecomet
Kenosha, WI
Maintenance Technician
HS diploma or equivalent
Exp: 1-2 year(s)
Essential Duties and Responsibilities: Installs, repairs, overhauls and maintains electronic, electrical, hydraulic, pneumatic, mechanical and/or electro-mechanical machinery and equipment. Observes and tests operation of electronic, electrical, electro-mechanical, hydraulic, pneumatic and/or mechanical devices in order to evaluate and identify operating problems. Fabricates replacement components with direction from section managers/supervisors and/or team leaders in order to affect in-house repairs and/or modify machinery and equipment to improve efficiency. Dismantles equipment and machinery in order to identify, remove, repair and/or replace damaged or deteriorated components, and reassemble equipment. etc. 4/29/2020
551 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
552 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
553 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
554 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
555 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
556 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
557 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
558 Scholar Rock
Cambridge, MA
Senior Associate Scientist - IHC
BS/MS in biology or related
Exp: 1-3 year(s)
Scholar Rock seeks a highly motivated associate with a background in immunohistochemistry to join our research team. The successful candidate will be responsible for supporting and maintaining all aspects of our histopathology workflow, with a strong emphasis on automation. This person will play a key role in our translational science team as they will help establish IHC / IF / ISH assays to characterize drug targets and measure disease endpoints in both patient samples and preclinical models. This position also provides an opportunity to learn new techniques in digital analysis and algorithm development. etc. 4/29/2020
559 Takeda
Cambridge, MA
Manufacturing Technician II
AS in a life science or engineering
Exp: 1 year
This position reports to Days, 6:00 am – 6:30 pm, 2-2-3, 12.5 hours shift, off every alternate weekend. Due to business need, on select occasions, employees may be required to work overtime. Primary Duties: With general supervision the individual will perform routine and critical manufacturing operations, including but not limited to work functions in Cell Culture, Purification, Solution & Equipment Prep areas. Operates production equipment according to SOPs for the production of clinical and/or commercial products. Responsibilities: This individual will carry out cGMP manufacturing operations utilizing Standard Operating Procedures (SOP), Batch Records and Form Preps. etc. 4/29/2020
560 Boston Scientific
Minnetonka, MN
Quality Engineer I Job
BS/BA in engineering or related
Exp: 0-2 years in related
This role will assist in developing and refining failure analysis methodologies as a means of advancing comprehensive understanding of product performance to improve patient outcomes. This position will identify, analyze, investigate, monitor and document patterns and trends in complaint data. Communicate and educate management, R&D, Design Assurance, Ops Quality, Marketing, Sales and other departments about product performance and escalations. Ensure that information and insights gained from product investigations and corrective actions is fed back to the R&D, Design Assurance and Marketing organizations as part of the risk management and design input process. 4/25/2020
561 Boston Scientific
Minnetonka, MN
Product Analyst I Job
BS/BA or MS
Exp: BS: 0-2 years, MS: 0 years
Investigates and resolves product complaints of all products. Maintains complaint databases and complaint files, runs trend reports. Facilitates product complaint investigations. Confirms complaint, follows up to get additional information when needed. Makes initial MDR decision, under supervision. Reviews file for completeness, closes and files the complaint folder. Interfaces with various internal and external entities such as Manufacturing and R&D to assist with obtaining complete information or product complaint analysis. 4/25/2020
562 AvantGen
San Diego, CA
Laboratory Assistant
HS Diploma/GED
Exp: 0 years, college coursework
The scope of work for this position includes general lab support operations, such as stocking lab supplies, cleaning and autoclaving glassware, prepararation of media and buffers, and perform basic molecular biology experiments, such as PCR, cloning, and plasmid preps. 4/25/2020
563 Avantor
Chandler, AZ
JIT Technician
HS Diploma/GED
Exp: 1-2 years in customer facing environment
The Technician is responsible for providing a high level of accuracy, and contributing to a culture of safe work and superior customer service. Accurately records and communicates information to internal and external teams. Shares with team any changes in demand to maintain appropriate service levels. Builds positive relationships with both internal and external customers 4/25/2020
564 Avantor
Fort Worth, TX
Lab Support Technician
HS Diploma/GED
Exp: 1-2 years in lab setting
The laboratory technician prepares and weighs samples for testing and analysis. May setup and conduct tests, assays, and other protocols under the direction of a laboratory services manager, researcher, or scientist. Follow Standard Operating Procedures (SOPs) and Good Laboratory Practices (GLPs). Ensure all laboratory equipment and work areas are clean, sterile, and in proper working order. May be responsible for calibration of instruments and also involved in media prep. 4/25/2020
565 Avantor
Rensselaer, NY
Inventory Technician
HS Diploma/GED
Exp: 1-2 years in customer facing environment
The Technician is responsible for providing a high level of accuracy, and contributing to a culture of safe work and superior customer service. Accurately records and communicates information to internal and external teams. Shares with team any changes in demand to maintain appropriate service levels. Builds positive relationships with both internal and external customers 4/25/2020
566 Avantor
Rensselaer, NY
Inventory Technician
HS Diploma/GED
Exp: 1-2 years in customer facing environment
The Technician is responsible for providing a high level of accuracy, and contributing to a culture of safe work and superior customer service. Accurately records and communicates information to internal and external teams. Shares with team any changes in demand to maintain appropriate service levels. Builds positive relationships with both internal and external customers 4/25/2020
567 Avantor
Devens, MA
Cleanroom Assembly Technician, 1st shift
HS Diploma/GED
Exp: 0-2 years in cleanroom
Under direction of the cleanroom lead and the area supervisor, the Cleanroom Assembly Technician will build a wide-range of Single-Use assemblies that meet or exceed customer requirements. Uses a variety of manufacturing and measuring equipment such as tube cutters, rulers, oetiker tools, and heat sealers. Follows engineering drawings, products work instructions, standard operating processes to accurately and efficiently build product and maintain associated data throughout the process. 4/25/2020
568 Avantor
Radnor, PA
B2B Assoc Tech Proj Mgr, eBusiness (US)
College degree in related
Exp: 1-3 years app. Experience
The Associate Technical Project Manager will be responsible for managing small to medium internal customer eProcurement integration projects. This role will also assist in developing standards and documentation for external integrations to VWR systems, analyzing current business processes and technologies, and driving improvements within the customer Procure to Pay life cycle. 4/25/2020
569 Avantor
Rensselaer, NY
Inventory Technician
HS Diploma/GED
Exp: 1-2 years in customer facing environment
The Technician is responsible for providing a high level of accuracy, and contributing to a culture of safe work and superior customer service. Accurately records and communicates information to internal and external teams. Shares with team any changes in demand to maintain appropriate service levels. Builds positive relationships with both internal and external customers 4/25/2020
570 Arrowhead Pharma
Madison, WI
Associate Scientist, Discovery Analytical Chemistry
BS/BA in chemistry or biology
Exp: 1 year in preping biological samples
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 4/24/2020
571 Arrowhead Pharma
Madison, WI
Associate Chemist, CMC
MS in chemistry/biochemistry
Exp: 0-3 years
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. 4/24/2020
572 Arrowhead Pharma
Madison, WI
Associate Production Chemist
HS Diploma/GED
Exp: 0-5 years in similar position
Arrowhead Pharmaceuticals is seeking a highly motivated individual to become a part of its scientific team. We have an immediate opening for an Associate Production Chemist in the Chemistry, Manufacturing, and Controls Group. The successful candidate will be expected to: Follow batch records, SOPs, and work instructions to detail. Document all operations in batch records and notebooks. Comply with GMP protocols 4/24/2020
573 Arthrex
Cleveland, OH
Vet Sales Associate
BS/BA
Exp: 1 year in outside sales
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. 4/24/2020
574 Arthrex
Ave Maria, FL
Labeling Systems Technician - Ave Maria
Associates Degree preferred
Exp: 0-2 years in industry
Troubleshoots hardware and software problems related to labeling operations, including, but not limited to, barcode scanners, labeling systems, labels, and printers. Performs equipment calibration, maintenance, and qualification activities. Participates in the execution of Arthrex validation protocols related to labeling operations, including, but not limited to, label printing, barcode scanning, and barcode inspection. Helps determine process capability of new equipment through execution of approved protocols and assures defined parameters are incorporated into respective operating procedures. 4/24/2020
575 Arthrex
Sandy Springs, SC
Clean Room Assembler
HS Diploma/GED
Exp: 0-2 years in manufacturing/packaging
Performs manual and fixture assisted device assembly and packaging on medical device components, kits, convenience packs and / or any clean room specific device assembly as assigned. Performs placement of components onto the blister trays and die cut restraints. Performs label application onto packaging constructs. Performs supplemental label application, blister loading, pouch and blister sealing and visual seal inspection 4/24/2020
576 Arthrex
Sandy Springs, SC
Engineer - Packaging
BS/BA in engineering (packaging, industrial, etc.)
Exp: 1-3 years in process/packaging engineering preferred
Responsible for supporting Packaging Operations and Packaging and Manufacturing Process Engineers on the development and execution of sterile packaging processes including material, design, and equipment validations. Assist in the selection, installation, and validation of medical device packaging equipment. Write and execute engineering studies/DOEs, validation IOQ/PQ protocols, gage R&Rs for packaging equipment processes, tools/fixtures, and inspection apparatus including: pouch sealing, blister tray sealing, burst testing, pull testing, dye penetration testing, print & apply, etc. 4/24/2020
577 ArunaBio
Athens, GA
 Biomanufacturing Associate
BS/BA in biological sciences or engineering
Exp: 0-2 years in industry
The Biomanufacturing Associate supports the the manufacturing efforts of ArunA Bio, and must work collegially and collaboratively as part of a larger team. The position requires the individual to carry out complex stem cell manufacturing with an advanced degree of detail, and in accordance with established SOPs, cGMPs, and safety regulations. The individual will work as a member of a team responsible for performing all bioprocessing workflows. 4/24/2020
578 ArunaBio
Athens, GA
Research Associate I – Preclinical R&D Team
BS/BA in biological sciences
Exp: 1-2 years in lab
The successful candidate would participate in a wide variety of research activities including animal care, animal technical procedures, animal health evaluations, and research data collection.Perform routine, pre-operative, and post-operative care of research animals. Assist during and/or perform surgical and other technical procedures with rodents 4/24/2020
579 ArunaBio
Athens, GA
Research Associate I – CNS Targeting and Drug Delivery
BS/BA in biological sciences or engineering
Exp: 1-2 years in lab
The Research Associate I will perform cell culture, execute analytical and functional assays to characterize exosome modifications and assist with in vivo procedures. Perform mammalian cell culture using sterile technique. Use a variety of equipment such as pipettors, balances, ultracentrifuges, laminar flow hoods, incubators, microscopes, centrifuges, plate readers, and nanoparticle tracking analysis equipment such as NanoSight 4/24/2020
580 Arvinas
New Haven, CT
Laboratory Assistant, Formulation R&D
BS in sciences
Exp: 1-3 years in pharma R&D
In the role as a laboratory assistant, you will prepare pharmaceutical formulations used in animal pharmacology and pharmacokinetic studies, and will work closely with compound management and in-life colleagues to make sure that dosing materials are available as needed. When issues related to formulation arise, you will serve as a primary problem-solving Formulation R&D contact for those in other disciplines. 4/24/2020
581 AskGene Pharma
Camarillo, CA
Associate Scientist / Scientist – Cell Line Development
MS in biological/chemical science or engineering
Exp: 1-3 years
In this role you will primarily be responsible for CHO cell line generation and process development. Plasmid DNA preparation. CHO cell line development for expression of monoclonal antibodies, bispecific antibodies, Fc-fusions and other therapeutic proteins. CHO cell culture process development 4/24/2020
582 AskGene Pharma
Camarillo, CA
Associate Scientist – Upstream Process Development
MS in biological/chemical science or engineering
Exp: 1-3 years
Reporting to the director of the upstream process Development team, you will be responsible for the cell line/upstream process development to support process development and manufacturing activities (e.g. stable cell line generation and characterization and various bioreactors operation). You will also involve in tech transfer, process scale up and CMO management. This is an entry level hands-on scientist position. You will design and carry out experiments, perform general laboratory activities that include the routine maintenance of equipment and will keep an accurate laboratory record (lab notebook) of all experiments. You will also write technical reports when needed. 4/24/2020
583 Associates of Cape Cod
East Falmouth, MA
Technical Services BET Specialist (2 openings)
BS/BA in chemistry/biology
Exp: 0-2 years in related
Provide technical support for endotoxin and glucan detection products. This includes answering questions, troubleshooting for current ACC customers. Troubleshoot/triage issues, problems and complaints in a timely manner, documenting them in CRM and providing trending to manager. Frequent follow up on all issues ensuring timely resolution of the customer’s issue. Knowledge of relevant instrumentation and softwares used for endotoxin and glucan detection by the end users 4/24/2020
584 Associates of Cape Cod
East Falmouth, MA
Qjuality Control Analyst I
BS in sciencecs
Exp: 0-2 years lab experience
In this role you will perform chemical and/or biological assays of commercial product raw materials, production intermediate and bulk samples, finished product, environmental monitoring samples, process and cleaning validation samples. Assays are qualitative, quantitative and investigational in nature and are performed in compliance with cGMP, ACC SOPs, and FDA Analyst has working knowledge of relevant QC techniques, policies and procedures to perform QC tasks and document results 4/24/2020
585 Associates of Cape Cod
East Falmouth, MA
Production Technician I (Saturday - Wednesday)
HS Diploma/GED
Exp: 0-2 years in related
In this position you will perform routine manufacturing operations for the manufacture of ACC and SKK commercial products. You will carry out cGMP manufacturing operations based on Standard Operating Procedures. You would need to come onboard initially Monday thru Friday for a few months to train in gowning, filling, crimping, lyo, oven operation, and autoclave operation 4/24/2020
586 Astrazeneca
Gaithersburg, MD
R&D Associate II/Associate Scientist I - Formulations - BPD
MS in chemistry/biological science or engineering
Exp: 0 years
Laboratory activities include buffer and protein solution preparation, pipetting and aseptic operations in a biosafety cabinet. Analytical methods that are used routinely include HPLC (reversed-phase, size-exclusion, and ion-exchange chromatography), UV-visible spectroscopy, HIAC and MicroFlow Imaging for sub-visible particle counting.The candidate will work under general supervision and his/her work will be reviewed for accuracy and soundness of technical approach. The candidate will make detailed observations, summarize results in tables and figures, document data into lab notebooks, and analyze data and interpret results. 4/24/2020
587 Astrazeneca
Gaithersburg, MD
Associate Scientist I/II
MS in mechanical/biomedical/chemical engineering, or pharma sciences
Exp: 0-2 years
The candidate will be a part of Dosage Form Design and Development group working on combination device characterization and functionality, development of novel technologies, and transforming scientific knowledge / analysis into practical implementations. Innovate, develop and evaluate device characterization techniques and technologies as they relate to device development requirements. Perform test method qualification and method transfer to GMP testing group in support of device verification & validation testing. 4/24/2020
588 Astrazeneca
Gaithersburg, MD
Pilot Production Technician I/II - BPD
Associates or Bachelors
Exp: BS: 0 years, AS: 1-2 years
As a pilot production associate in the Clinical production team within Biopharmaceutical Development, you’ll build broad knowledge of bioprocessing in a cGMP environment to launch your career in the biopharmaceutical industry. In this role you will take an adaptable, science driven approach to everything you do. You will become an integral part of process development, accelerating product candidates into the clinic and gaining knowledge and experience in cell culture, purification and critical support activities. 4/24/2020
589 Astrazeneca
Gaithersburg, MD
Associate Scientist I, Purification Process Sciences
MS in related
Exp: 1 year in protein/viral vector purification
Develop and characterize purification processes for the manufacture of biopharmaceuticals (viral vectors, antibodies and other proteins) in early stage clinical development. Be responsible for a portion of a purification process development project. Make observations, analyze data and interpret results. Maintain accurate records of experimental results, review, analyze, and interpret experimental data. 4/24/2020
590 Astrazeneca
Frederick, MD
Production Technician I - Night Shift - Operations
BS/BA
Exp: 0-1 yearas
Operation of upstream / downstream / central services processing equipment according to established SOPs. This equipment includes but is not limited to bioreactors, TFF skids, biological safety cabinets, incubators, chromatography skids, UFDF skids, autoclaves, washers, and product hold tanks. Upstream / downstream / central services processing according to established manufacturing production records (MPRs & SPRs) in accordance with cGMPs. 4/24/2020
591 Astrazeneca
Frederick, MD
Production Technician II - Day Shift - Operations
BS/BA
Exp: 1-3 years
Proven ability to perform all process steps of upstream / downstream / central services production operations and act as the primary trainer of those with less experience (and may act as interim Lead as required). Ability to generate SOPs, MPRs, and SPRs for equipment and procedures used in the manufacture of biological based products. Execution of validation protocols as required as well as the ability to execute projects with minimal instruction and strategic direction. 4/24/2020
592 Astrazeneca
Frederick, MD
Production Technician I - Day Shift - Operations
BS/BA
Exp: 0-1 years
Operation of upstream / downstream / central services processing equipment according to established SOPs. This equipment includes but is not limited to bioreactors, TFF skids, biological safety cabinets, incubators, chromatography skids, UFDF skids, autoclaves, washers, and product hold tanks. Upstream / downstream / central services processing according to established manufacturing production records (MPRs & SPRs) in accordance with cGMPs. 4/24/2020
593 Astro Pak
Downey, CA
Associate Technician - Ontario
1 year technical training/certification course
Exp: 1 year in related
The Associate Technician performs entry-level Field Services duties to gain knowledge and understanding of cleaning and passivation of vessels and piping. Under supervision, Associate Technicians work together to complete the process in a safe and expedient manner to prevent unnecessary down time of the customer equipment. Proper calculations and installation of Astro Pak equipment plus vigilant operation of said equipment is necessary. 4/24/2020
594 Astro Pak
Raleigh, NC
Associate Technician - North Carolina
1 year technical training/certification course
Exp: 1 year in related
The Associate Technician performs entry-level Field Services duties to gain knowledge and understanding of cleaning and passivation of vessels and piping. Under supervision, Associate Technicians work together to complete the process in a safe and expedient manner to prevent unnecessary down time of the customer equipment. Proper calculations and installation of Astro Pak equipment plus vigilant operation of said equipment is necessary. 4/24/2020
595 ATEC Spine
Carlsbad, CA
Material Handler
HS Diploma/GED
Exp: 1-3 years in inventory Control
This position is responsible for creating purchase orders and shipping inventory for outside processing. Counts and verify parts for outside processing. Packages parts safely for shipping. Creates purchase order for outside processing. Files all work and purchase orders. Delivers products to vendors when needed. 4/24/2020
596 Athenex
Clarence, NY
Warehouse Associate
HS Diploma/GED
Exp: 1-3 years in warehouse environment
The Warehouse Associate is responsible for the physical process of goods pertaining to the receipt, storage and shipment in and out of the warehouse. This includes site inventory of raw materials, work-in-process and finished goods as well as the maintenance, repair and operating supplies. Inventory must be current and accurate in status, warehouse, quantity, lot ID and warehouse location. 4/24/2020
597 Atomwise
San Francisco, CA
Research Associate in Biochemistry
MS in biological/chemical science or engineering
Exp: 1-3 years
Atomwise is looking for a Research Associate to support our scientific and business development teams by performing literature and database analyses and providing insightful reports and research plans. Search scientific literature, databases and biochemical structural data. Prepare scientific research plans. Understand the experimental design and methodologies in life science publications 4/24/2020
598 Atreca
South San Francisco, CA
Research Associate I/II, Target ID (Temporary)
BS in biology
Exp: 1-2 years in lab
In this position, the successful candidate will apply her/his skills and expertise to support Atreca’s oncology team in discovering the unique targets of patient-derived antibodies. In particular, the successful candidate contributes by maintaining in-vitro cell cultures and operating robotics for high throughput target-ID assays. 4/24/2020
599 Quotient Sciences
Garnet Valley, PA
Project Coordinator
BS/BA
Exp: 1-2 year(s)
Due to growth and expansion, we have an exciting opportunity for a Project Coordinator to join the Project Management Department. As the Project Coordinator, you will work on multiple projects with Project Managers and be responsible for coordinating project activities internally and externally with customers and vendors. Tasks and responsibilities will include: Assist with the development and maintenance of project plans. Assist with the organization of meetings, development of meeting agendas, minutes and action items. etc. 4/22/2020
600 Quotient Sciences
Boothwyn, PA
Analytical Scientist II
MS in chemistry
Exp: 0-2 years
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: HPLC/UPLC. Dissolution apparatus. Karl-Fisher water content titrator. GC. FTIR. UV. Other analytical instruments as directed. Follow analytical test methods, compendial methods, experimental procedures and SOP’s. etc. 4/22/2020
601 Quotient Sciences
Boothwyn, PA
Analytical Scientist I
BS in chemistry
Exp: 0-3 years
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. etc. 4/22/2020
602 Quotient Sciences
Garnet Valley, PA
Recruitment Coordinator
unspecified
Exp: 1+ year(s)
The Recruitment Coordinator position is a critical addition to the US recruitment function and the Human Resources team. The successful candidate will engage in scheduling, planning and executing recruitment activities throughout 3 US based sites located in the greater Philadelphia, Pennsylvania region and Miami, Florida. This highly visible position allows for both local and global visibility and will assist in shaping the future initiatives within the talent acquisition function. etc. 4/22/2020
603 Regeneron
Tarrytown, NY
R&D Associate-VI Next - Oligonucleotides
MS/MA
Exp: 1-2 year(s)
We are seeking a highly skilled and motivated associate to join our new group devoted to the drug discovery and technology development specifically in the area of oligonucleotide therapeutics such as antisense oligonucleotides and siRNAs. The responsibilities of this position include designing and screening of oligonucleotide candidates as well as carry out research on technology development to improve chemistry and delivery of nucleic acid therapeutics (siRNA/ASO). Candidates are expected to work independently in a creative, collaborative, and dynamic team environment, with strong support for skill and career development. etc. 4/22/2020
604 Rejuvenate Bio
San Diego, CA
Research Assistant
BS/BA in biology, biochemistry, biomedical engineering or related
Exp: 1+ year(s)
Rejuvenate Bio is looking for a highly-motivated individual to join our energetic team and accelerate the development of our therapies. There search assistant position will directly support efforts to drive forward our future commercial offerings working with other RA's and scientists. The applicant will be performing standard molecular biology procedures as well as more advanced cell culture and virus creation. The role reports to senior or principal scientists at Rejuvenate Bio. 4/22/2020
605 Renaissance
Lakewood, NJ
Compounder, 2nd shift
HS diploma or equivalent
Exp: 1-3 year(s)
Entry level position to Compounding Department with emphasis on ensuring that equipment used to process aseptic and non-aseptic products has been cleaned, sanitized or sterilized, as required by specific documentation or procedures. This entails performing automated and manual equipment cleaning prior to sterilization, placing cleaned equipment into autoclaves, starting and monitoring autoclaves, unloading equipment from autoclaves, and delivering equipment to areas of use. etc. 4/22/2020
606 Renaissance
Lakewood, NJ
Compounder, 3rd shift
HS diploma or equivalent
Exp: 1-3 year(s)
The Compounder's primary responsibility is for the execution of bulk product batch processing, inclusive of all process related and administrative activities, as well as Equipment Preparation activities as declared in Compounder 1. Hours are 11:00 pm - 7:30 am. Responsibilities: Follow manufacturing procedures to process bulk product. Batches to be made right the first time. Follow manufacturing procedures specific to the task being performed. etc. 4/22/2020
607 Rheos Medicines
Cambridge, MA
Research Associate
BS in cellular or molecular , immunology, or related
Exp: 0-5 years
The Research Associate is responsible for initiating, designing and executing experiments that support scientific projects relevant to different immune related diseases. Ability to perform a variety of immune cell based in vitro assays utilizing both cellular and molecular biology techniques. Effectively communicate results and conclusions to cross-functional project teams. etc. 4/22/2020
608 Ribon Therapeutics
Cambridge, MA
Research Associate/Senior Research Associate – Biological Sciences
MS in biology, biochemistry or related
Exp: 1-3 year(s)
The successful candidate will serve as an integral member of a multidisciplinary drug discovery project team developing novel small molecule inhibitors for monoPARPs and NADome targets. This position by will be reporting to a scientist in the Biological Sciences group to support target validation. He or she will employ a variety of molecular and cell biology techniques to understand target biology and develop cell-based assays for small molecule inhibitors. etc. 4/22/2020
609 Roche
Mansfield, OH
Field Engineering Specialist - Molecular Diagnostics
BS in chemistry or biomedical, mechanical or electrical engineering
Exp: 1-2 year(s)
The Roche Support Network group is committed to providing industry-defining support to its customers. As a Field Engineering Specialist, you will have the opportunity to travel and demonstrate your expertise as a technical repair and/or installation specialist for Roche assigned product lines, and provide valued service to your laboratory customers in an assigned territory. The Field Engineering Specialist, Clinical Chemistry in the Roche Support Network, position serves as a technical repair or installation specialist for Roche products for assigned product lines and geographies. etc. 4/22/2020
610 Roche
Tuscon, AZ
Technician Instruments
AS/AA in electronics, electrical engineering, or related
Exp: 1-3 year(s)
A Technicians responsibilities include testing of Company products following documented procedures to assure conformance to specifications and standards, completing written records of work done, and identifying and documenting non-conformances in piece parts, assemblies and test results. In addition, an Associate Technician must be able to effectively troubleshoot routine test failures to the subassembly level, consulting with more experienced technicians as needed. Responsibilities may also include assembly of Company products. etc. 4/22/2020
611 Roche
Branchburg, NJ
Scientist
BS in the life sciences, engineering, or related
Exp: 0-1 year(s)
The ‘Case Investigation and Resolution’ department is the Center of Excellence for the resolution of global product complaints. The Scientist (CIR) is responsible for effective and timely resolution of global cases, including complaint investigations, risk assessments, case documentation, trending analysis and preparing reports, ensuring regulatory compliance and optimal levels of customer satisfaction. Also participates in the On-Boarding of new employees by providing product and process training and support. The ideal candidate has strong technical knowledge, expertise of assay workflow and system functionality, enjoys troubleshooting, and has a problem solving mindset. etc. 4/22/2020
612 Roche
Tuscon, AZ
Instrument Assembler
HS diploma or equivalent
Exp: 0-1 year(s)
Responsibilities: Ensure accurate assembly of components and subassemblies per production drawings and documents while maintaining accurate manual and electronic records. Adhere to manufacturing schedule in order to meet deadlines while sustaining quality, cost, delivery, and safety metrics. Control accurate inventory on assembly line. Adhere to company policies in order to ensure successful manufacturing goals. etc. 4/22/2020
613 Roche
Branchburg, NJ
Diagnostic Tech Associate (2nd shift)
HS diploma or equivalent
Exp: 0-2 years
Job requirements will include ability to perform in the aseptic environment. Wear personal protective equipment, such as eye, foot, lab coat, mask, gowning coveralls. DIAG TECH ASSOCIATE- 2nd shift: For our Second Shift we are looking for someone who is willing to work Monday to Friday with normal hours from 3:00PM until 11:30PM. etc. 4/22/2020
614 Roche
Indianapolis, IN
Maintenance Technician (2nd Shift)
HS diploma or equivalent
Exp: 1 year
As a Maintenance Technician, you will dismantle, adjust, repair and assemble equipment according to drawings, operation and maintenance manuals, or sketches. You will assist in the determination of the root causes of failures and provide input on preventive/predictive options to eliminate/limit like failures. You will work under the guidance of your supervisor or experienced team members, perform simple electrical and mechanical troubleshooting to determine problems with equipment used in the manufacturing process. etc. 4/22/2020
615 Roche
Branchburg, NJ
Diagnostic Technician Associate 1st Shift Final Packaging
HS diploma or equivalent
Exp: 0-2 years
Responsibilities: Assembles totes, cartons, platforms, and associated packaging and filling components. Under direction of area supervision, assist in setting up Packaging/Filling lines, and staging for production activities. Perform visual inspection for visible defects of components produced in the Filling Area and components being placed into kits in the Packaging Area. Place components (filled vials, inserts, barcode clips ect.) into totes and or kits per instructions in applicable SOPs and Production Records. etc. 4/22/2020
616 Rocket Pharma
Cranbury Township, NJ
Manufacturing Associate 1
BA/BS in biotechnology, chemical engineering, or a life science
Exp: 0-2 years
This technical position is a key role in manufacturing operations. The ideal candidate will have less than 2 years of experience performing large scale cGMP clinical or commercial manufacturing of viral vectors, biologics or monoclonal antibodies at a leading pharma or biotech organization. Candidates with no previous experience who meet the educational requirements are encouraged to apply. As a Manufacturing Associate, you will be responsible for large scale manufacture of viral vector therapies. Additional responsibilities include set-up, operation and cleaning of equipment, equipment and process monitoring, upkeep of cGMP equipment and manufacturing area, completing cGMP batch documentation, and receiving cGMP materials from the warehouse. etc. 4/22/2020
617 Sangama Therapeutics
Brisbane, CA
Development Associate II
BS in pharmaceuticals, biology, or related
Exp: 1-2 year(s)
We are seeking a motivated and hard-working Research Associate I/II for our Technical Operations Analytical Development Group. In this role, you will perform key gene- and cell-based potency and strength assays to support AAV gene therapy; 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 biolab equipment maintenance and minimal supply ordering. This position requires experience in good laboratory and documentation practice. etc. 4/22/2020
618 Renaissance
Lakewood, NJ
Materials Coordinator I, Temporary
HS diploma or equivalent
Exp: 0-2 years
The Materials Coordinator will assist in the efficient receipt, storage, movement and inventory of items throughout the Warehouse. This is a temporary position. Responsibilities: Perform several tasks simultaneously. Must be able to organize and prioritize work in order to accomplish tasks assigned. Picks and stages raw materials/ components as required to support work orders on the production schedule. Complete material returns and issue materials to orders in ERP system. Assist with receiving of materials. etc. 4/22/2020
619 Repligen
Waltham, MA
Manufacturing Associate II- Biomanufacturing 2nd Shift
BS in a biological science
Exp: Not necessary for BS candidates
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. Candidates must be willing and able to learn new manufacturing processes as the company grows and also to work overtime. etc. 4/22/2020
620 Repligen
Rancho Dominguez, CA
Assembler-I
HS diploma or equivalent
Exp: 0-1 year(s)
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. Perform manual assembly of complex fiber, membrane, and polycarbonate components.​ Follow detailed manufacturing and assembly procedures.​ etc. 4/22/2020
621 Repligen
Waltham, MA
ELISA Manufacturing Associate Level 2
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. Responsibilities: Plate coating, conjugate production, buffer preparation and kit assembly. Dispensing, capping, labeling and packaging of reagents. etc. 4/22/2020
622 Repligen
Waltham, MA
Manufacturing Associate I - OPUS 2nd shift
unspecified
Exp: 1-3 year(s)
This position will function in Repligen's OPUS Column Packing groups. Cross training into other departments may be required based on the changing needs of the department. 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. etc. 4/22/2020
623 Regeneron
Tarrytown, NY
R&D Associate - VI Next
MS in immunology, molecular biology, biochemistry or related
Exp: 0-2+ years
We are seeking a R&D associate with a strong foundation in immunology to join our VI Next group. The candidate must have experience with animal handling, injections and tissue harvesting. Experience designing flow cytometry panels and FACS analysis software is strongly preferred. This position will involve work on multiple projects simiulataneously, so excellent record-keeping and time management are very important. etc. 4/22/2020
624 Regeneron
Tarrytown, NY
Process Development Associate II - Cell Culture Data Analytics
BS/BA in chemical engineering or computer science or engineer
Exp: 0-5 years
The Cell Culture Development group of the Process Development organization is actively searching for a motivated person with a record of accomplishment and/or a strong interest in analyzing bioprocessing data. This position presents the opportunity for statistical and data science innovation to enhance the efforts of a dynamic and data driven group. Starting level would be determined by background experience. etc. 4/22/2020
625 Regeneron
Tarrytown, NY
R&D Associate - Protein Biochemistry
BS/MS in biochemistry, biophysics, chemical engineering. Or related
Exp: 0-2+ years
We are seeking an R&D Associate with demonstrated experience using different biophysical and biochemical methods to quantify the physicochemical properties of proteins. The qualified candidate will be responsible for providing in-depth characterization of therapeutic proteins to support research, developability assessments, and early development programs through IND. The candidate is expected to participate in method development and technology innovation efforts aimed to enhance our understanding of biotherapeutic proteins and specifically address both upstream research and late-stage program needs. etc. 4/22/2020
626 Quotient Sciences
Garnet Valley, PA
Recruiter
BS/BA
Exp: 1+ year(s)
Reporting into the Senior Manager, Talent Acquisition, this Recruiter will be a key figure in the US expansion of our rapidly growing team. This individual will have the opportunity to support a broad number of professional functions across 3 sites in Pennsylvania and Florida. Main tasks and responsibilities: Assists the Senior Manager, Talent Acquisition in delivering recruitment strategy through Full-Life cycle recruitment of candidates by partnering with hiring managers and other appropriate managers when a vacancy arises. Supports the generation and maintenance of internal and external job postings; determines effective advertising mediums; places appropriate advertisements. etc. 4/22/2020
627 Santa Cruz Biotechnology
Dallas, TX
Customer Service Representative
AA/BA/BS in biology or business administration
Exp: Entry level
SCBT has an immediate opening for an entry level Customer Service Representatives at its Dallas, TX Headquarters campus. This position performs telephone customer support, order processing, and data entry functions. The current shift available for this position is the early afternoon to early evenings shift, Monday through Friday. This is a full time position with career advancement opportunities within the company. Santa Cruz Biotechnology, Inc (SCBT) is a world leader in the development of products for the biomedical research market. For the past twenty-five years, SCBT has focused on the development of research antibodies, biochemicals, labware and it has more recently expanded into animal health care products. etc. 4/22/2020
628 Santa Cruz Biotechnology
Dallas, TX
Technical Sales Representative
BS in biology, chemistry, or related
Exp: 1-2 year(s)
A Technical Sales Representative is responsible for inside sales activities with customers via phone, email and live chat. The ideal candidate will actively make outgoing calls to speak to customers and build relationships with the goal of increasing sales. This is a full time position. Training on our extensive product line and related protocols is provided. etc. 4/22/2020
629 Santa Cruz Biotechnology
Paso Robles, CA
Animal Health Marketing and Sales Representative
BS/MS in animal science or related
Exp: Entry level
SCAH/SCBT has an immediate opening for an entry level Animal Health Sales Representative at our Paso Robles, CA campus. This is a full time position with career advancement opportunities within the company. Some intermittent weekend work is required. Required Skills: Ability to work independently to achieve sales growth for the Santa Cruz Animal Health product line in the U.S. Ability to professionally receive inbound customer calls regarding orders and technical questions. Capacity to identify and source new products to broaden our product line. etc. 4/22/2020
630 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
631 Quidel
San Diego, CA
Process Analyst I
BA/BS in chemistry, biology, or related
Exp: 0-2 years
Under general supervision, the Process Analyst I is responsible for analyzing device and subassembly testing data and ensuring continuity of data entry. The position is responsible for developing methods/reports to analyze data to predict product quality and summarize product performance periodically. The position is also responsible for assisting in product quality improvements, supporting resolution of field-reported performance issues, transferring and validation of new products, and implementation of product improvements which increase quality, lower cost, and increase manufacturing capacity. etc. 4/21/2020
632 Quidel
San Diego, CA
Production Chemist (Particle Chemistry)
MA/MS
Exp: Not necessary for MS/MA candidates
Quidel is searching for a Production Chemist to work in our Particle Chemistry Lab in the Mira Mesa area of San Diego. Under close supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP, under the direction of senior staff. ESSENTIAL FUNCTIONS: Purification sof various antbodies via different liquid chromatography procesuders. Conjugation of antibodies. etc. 4/21/2020
633 Quidel
San Diego, CA
Quality Assurance Specialist
BS/BA in science
Exp: 1-3 year(s)
Under the supervision of the Supervisor/Manager, the scope of this position is responsible for carrying out the daily operations of the Batch Record Department as defined by the Quidel Quality Management System and within defined company policies, procedures and regulatory requirements. ESSENTIAL FUNCTIONS: Responsible for managing throughput of all QA reviewed Device History Records, and others as assigned. Responsible for reporting of monthly trending metrics, and developing weekly priorities. Work with groups within the organization to get corrections and clarifications to Device History Records. etc. 4/21/2020
634 Quanterix
Billerica, MA
Research Associate - Accelerator
BS in chemistry, biochemistry, or life science
Exp: 1-3 year(s)
To continue our solid growth, we are seeking a talented and highly motivated Research Associate to join our growing organization. This position will be part of our Accelerator Laboratory Services team. In this role, you will be developing, optimizing and troubleshooting new biomarker assays for Quanterix's proprietary Simoa technology. Key Responsibilities: Apply your laboratory skills and experience to generate high quality data in support of a diversity of projects, which will include both immunoassay development and validation as well as testing and analysis of clinical samples using commercial kits. etc. 4/21/2020
635 Quanterix
Billerica, MA
Manufacturing Associate
BS in chemistry, biology, or related
Exp: 1+ year(s)
To continue our solid growth, we are seeking a talented and highly motivated Manufacturing Associate to join our growing organization. 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. Key Responsibilities: 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. etc. 4/21/2020
636 Quanterix
Billerica, MA
Quality Control Analyst I
BS in chemistry, biochemistry, or biology
Exp: 1+ year(s)
To continue our rapid growth, we are seeking a talented and highly motivated Quality Control (QC) Analyst to join our growing organization. This position will be part of our Quality Control team, responsible for a variety of activities including immunoassay testing on automated and semi-automated platforms, advanced data analysis, and prioritization and coordination and new product launch readiness in accordance with current Good Laboratory Practices (cGLPs). Key Responsibilities: Perform QC testing of incoming consumables and raw materials per compendial and non-compendial methods for GMP use in manufacturing. etc. 4/21/2020
637 Qiagen
Germantown, MD
Contract Technical Associate - Kit Assembly Operations
HS diploma or equivalent
Exp: 1-3 year(s)
Position Description: 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. etc. 4/21/2020
638 Pyramid Laboratories
Costa Mesa, CA
Labeling and Packaging Technician
BS/BA
Exp: 1 year
Under general supervision and instructions, responsible for the labeling and packaging of pharmaceutical products following cGMP, and Safety standards while maintaining a teamwork attitude to effectively manage production needs and meet the production schedule. PRINCIPAL DUTIES: Perform printing, labeling and final packaging execution activities as assigned per appropriate procedures using appropriate automated systems in place with a focus on quality and efficiency. etc. 4/21/2020
639 Applied Medical Technologies
Brecksville, OH
Order Puller/Packer- 1st Shift
HS Diploma/GED
Exp: No experience necessary
Process work orders by filling orders with raw materials for production floor. Package finished goods for shipment. Unload raw materials from truck. Responsible for quality control. No damaged product is sent out. No damaged raw material is accepted in. 4/19/2020
640 Applied Molecular Transport
South San Francisco, CA
Research Associate
BS or mS in biological/chemical sciences
Exp: 1-5 years
Applied Molecular Transport, Inc. is looking to hire a research associate in analytical method development and quality control (AD & QC) for its therapeutic programs. Perform analytical method development for LC based assays such as SEC, IEX and reversed-phase HPLC, and other protein-based analysis (i.e. SDS-PAGE, western blot, A280). Provide testing support for the in-house manufacture of drug substance and drug product. Execute stability studies to evaluate and characterize protein degradation during storage 4/19/2020
641 Arbor Biosciences
Ann Arbor, MI
Resarch Associate - Next Generation Sequencing
BS/BA in related field
Exp: 1 year in molecular biology
Routine activities of this role will involve evaluating client-provided DNA/RNA samples, converting them to NGS sequencing libraries, enriching them with hybridization probes, and amplifying them with PCR.  Research & development activities using the same skills are also common. Fundamental understanding of the concepts and methods of PCR, ligation and other enzymatic reactions, strong laboratory skills, organizational skills, note-taking diligence, and attention to detail are key. 4/19/2020
642 ArcherDX
Boulder , CO
Quality Control Associate I
BS/BA in sciences
Exp: 0-2 years in lab
Evaluates and implements protocols and methods to inspect and test raw materials, in-process materials and finished products to ensure that they are in compliance with internal safety and quality standards for distribution as a Research Use Only (RUO) In-Vitro Diagnostic. Performs analysis and identifies trends in QC data and recommends corrective actions when necessary. Develops processes and tests with LEAN concepts in mind to determine that appropriate quality control analysis is being performed. 4/19/2020
643 ArcherDX
Boulder , CO
Quality Assurance Specialist I/II
BS/BA in sciences
Exp: 1-3 years in quality role
The Quality Assurance Specialist will provide support in the quality system area of Change Control Additionally, the Quality Assurance Specialist may provide support to one or more additional quality system area(s). Provide support for the maintenance of the change control management program. Assist with internal and external audit activities. Assist with management of Nonconformance Reports, Temporary Deviations, and Corrective and Preventive Action Reports, as applicable. 4/19/2020
644 ArcherDX
Boulder , CO
Manufacturing Associate I
BS/BA in sciences
Exp: 1-2 years in FDA regulated manufacturing experience
Associate level position for manufacturing medical devices in accordance with controlled procedures (SOPs) in compliance with Good Manufacturing Practice (GMP) regulations and current GMP (cGMP) guidelines. Manufactures solutions, labels and fills containers, labels and assembles kits. Compiles auditable electronic or paper records of manufacturing, maintains equipment logs and monitors supplies. 4/19/2020
645 ArcherDX
Boulder , CO
Facilities Assistant
HS Diploma/GED
Exp: Previous facilities experience preferred
The facilities assistant will be responsible for maintaining daily operations of the facility. The position will support facilities staff by preforming Facility maintenance duties such as furniture moves, simple electric projects, spot painting and/or cleaning, light constructions and exterior cleanup. The facilities assistant will also work with outside contractors on building and equipment repairs. 4/19/2020
646 Arcus Biosciences
Hayward, CA
Bioanalysis Research Associate
BS/MS in chemistry/biochemistry
Exp: 1-4 years
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. Develop, troubleshoot, and validate LC-MS/MS based bioanalytical methods. Analyze, summarize and report preclinical pharmacokinetic and toxicokinetic results 4/19/2020
647 Arcus Biosciences
Hayward, CA
Research Associate/Sr. Research Associate
BS/BA in biology, immunology or related
Exp: 1-2 years research experience
The role will be responsible for executing a variety of experiments including handling and analysis of ex vivo samples as well as performing in vitro assays to understand mechanism of action and pharmacodynamic properties of drug candidates. A successful candidate will contribute as part of a multidisciplinary team in a fast-paced environment to plan and execute experiments and subsequently collate, document, interpret, and present data internally. 4/19/2020
648 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
649 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
650 Argonaut Manufacturing
Carlsbad, CA
Quality Control Assistant
BS/BA in life sciences
Exp: 1-2 years in GMP QC
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. 4/19/2020
651 Arrakis Therapeutics
Waltham, MA
Research Associate, Biophysics and Assay Development
BS in biochemical sciences/chemistry
Exp: 0-1 years in research
The position requires good working knowledge of binding, thermodynamics and equilibrium, and kinetics. Contribute to screening of small-molecule and RNA interactions by SPR, MST, FP, and other assays as needed. Be motivated to independently analyze and report data from 100-1000s of small molecule candidates on a routine basis and report progress to team. 4/19/2020
652 Pfizer
Sanford, NC
Bioprocess Technician BPT IV
BS/BA
Exp: 0 years
The incumbent is a skilled manufacturing technician/operator with knowledge of microbial Fermentation, Purification, Chemistry and Process Support processes in the production of microbial vaccines and bulk intermediates. The incumbent is knowledgeable of required processing unit operations and control systems needed for operations. The incumbent performs scientific and operational tasks related to commercial manufacturing. The incumbent is a skilled manufacturing technician/operator with knowledge of microbial Fermentation, Purification, Chemistry and Process Support processes in the production of microbial vaccines and bulk intermediates. The incumbent is knowledgeable of required processing unit operations and control systems needed for operations. The incumbent performs scientific and operational tasks related to commercial manufacturing. 4/19/2020
653 Pfizer
McPherson, KA
Chemist I - AB2 shift/12 hour night schedule
BS in chemistry/biochemistry
Exp: 0-1 years in lab
Performs chemical analysis on purchased raw materials, in-process preparations, pure drug substances and finished pharmaceutical products to determine that they meet official compendial and/or Pfizer requirements. Perform standard qualitative and quantitative analysis on purchased raw materials, in-process products, pure drug substances, finished pharmaceutical preparations, stability samples, and contract manufacturing samples utilizing accepted gravimetric and spectrophotometric procedures, in accordance with approved testing procedures Pfizer, the National Formulary (NF), and the United States Pharmacopeia (USP). 4/19/2020
654 Pfizer
Lake Forest, IL
CQ Lab Analyst
BS/BA in sciences (chemistry or biology
Exp: 0-1 years in QC or R&D
The primary responsibility of this role includes using Functional/Technical skills to perform analytical testing and data processing in accordance with procedure, regulatory guidelines (FDA, MHRA, TGA, ICH, and DEA). This individual will need to seize accountability by assuring accurate laboratory records are kept in accordance with procedures and cGMPs. This individual will also be required to perform peer review of other’s laboratory solution notebooks. 4/19/2020
655 Pfizer
Sanford, NC
Bioprocess Technician IV (Gene Therapy)
BS/BA
Exp: 0-2 years
The incumbent is a skilled manufacturing technician/operator with knowledge of any of the following: solution preparation, upstream processing, downstream processing and Drug Product filling. The incumbent is knowledgeable of required processing unit operations and control systems needed for operations. The incumbent performs scientific and operational tasks related to commercial manufacturing. 4/19/2020
656 Arraystar
Rockville, MD
Lab Assistant - Molecular Biology
BS/BA in biological sciences
Exp: 1-2 years wet lab experience
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. 4/19/2020
657 Arrowhead Pharmacueticals
Madison, WI
Associate Chemist, Bioconjugation
BS or MS in chemistry/biochemistry
Exp: 1-2 years
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. Perform bioconjugation, purification, and characterization of oligonucleotide conjugates. Identify critical issues/steps in a conjugation and solve the problems in a timely fashion 4/19/2020
658 Arbor Biotechnologies
Cambridge, MA
Software Engineer - Research
MS in engineering
Exp: 1-2 years in industry
At Arbor, you will be at the cutting edge of biodiscovery, systematically searching through nature’s diversity to discover and engineer new technologies for improving human health and sustainability. As a Software Engineer in Research, you will focus on building a search engine from the ground up. You will have significant latitude towards ideation, problem definition, and finding novel uses of machine learning. 4/19/2020
659 AMPAC Fine Chemicals
Rancho Cordova, CA
Process Engineer I
BS in chemical engineering
Exp: 1-3 years in manufacturing
Under general supervision and following established policies, performs professional assignments requiring full use and application of standard engineering principles, theories, concepts and techniques. Monitor existing processes, ensuring that batch records are maintained, variances are investigated, and day to day activities are properly planned. Activate and qualify facilities and equipment. 4/18/2020
660 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
661 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
662 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
663 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
664 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
665 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
666 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
667 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
668 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
669 Angiex
Cambridage, MA
Research Associate – Biology
MS in biological/health sciences
Exp: 1-3 years in lab
Angiex is seeking a talented, creative, self-motivated research associate to join in (1) cell biology investigations of novel cellular pathways in endothelial cells and tumor cells, and (2) the evaluation of drugs specific to those pathways in cells in vitro and mice in vivo. 4/18/2020
670 AngioDynamics
Marlborough, MA
Regulatory Affairs Specialist I
BS in sciences/technical field
Exp: 1+ years in regulatory affiars
Responsible for determining the path to market for new and modifications to existing products in compliance with Regulations of intended market territory and for guiding teams on the required deliverables to support the Regulatory status of products distributed by AngioDynamics Inc. Under minimal supervision, acts as company representative, developing and maintaining positive relationships with device reviewers through oral and written communications regarding pre-submission strategy/regulatory pathway development, testing requirements, clarification and follow up of submissions under review 4/18/2020
671 Anika
Sarasota, FL
IT Support Specialist
BS/BA in computer science preferred, HS Diploma minimum
Exp: 1-3 years in end-user management role
The position is primarily responsible to provide local and remote hardware and software support for desktops, laptops, printers, and other peripherals. This position interacts with all levels of employees and candidates must be able to maintain a courteous, professional manner. Provide hardware and software support for all desktop, laptop, and other mobile users, to established standards and IT Service Level Agreement 4/18/2020
672 Aphena
Easton, MD
Machine Operator- 2nd Shift (Night Shift)
HS Diploma/GED
Exp: 1 year in machine operation
Change material rolls of various sizes. Clean and maintain ink printers. Change gears, sprockets and chains. Maintain jaws and replace tape as needed. Etc 4/18/2020
673 Aveva
Miramar, FL
Engineering Technician
BS/BA
Exp: 0-3 years
This person is responsible for the installation of new equipment including mechanical assembly and electrical, pneumatic, and thermal control fluid connections. Oversee and verify all operating aspects of new equipment at installation. Utilize detailed knowledge of mechanical components along with general knowledge of electrical equipment and controls, pneumatics, hydraulics, and plumbing to assemble and setup equipment. 4/18/2020
674 Aveva
Miramar, FL
Manufacturing Operator I
HS Diploma/GED
Exp: 1-3 months
Assists in the manufacturing of Aveva’s transdermal products.Coats blends and adhesives to produce laminate.Prepares finished and slit laminate rolls.Documents operational parameters for manufacturing equipment. 4/18/2020
675 Aveva
Richmond Hill, ON
Lab Assistant, Microbiology (10 Month Contract)
Associates or BS/BA
Exp: 0-2 years
Responsible for maintaining a constant inventory of clean laboratory glassware and a clean wash up area. Preparation of sanitizing and cleaning agents. Support of Microbiology laboratory, as required, in autoclaving of waste and preparation of microbiological media as per current procedures. Check glassware for cleanliness prior to restocking clean, dry glassware in storage areas in laboratory. Maintain a constant inventory of clean glassware and cleaning supplies. 4/18/2020
676 Applied Medical
Rancho Santa Margarita, CA
CNC Machine Operations Engineer
BS/BA in mechanical, industrial, manufacturing engineering
Exp: 1-2 years in engineering
As a CNC Machine Operations Engineer, you will use skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. Develop and sustain manufacturing processes. Debug manufacturing processes and equipment via root cause analysis. Develop and update engineering documents such as process maps, process FMEA, Manufacturing/Quality Instructions, test methods, drawings, and test reports 4/18/2020
677 Applied Medical
Rancho Santa Margarita, CA
Associate Engineer
Associates in engineering or sciences
Exp: 1 year in engineering
As an Associate Engineer, you will be responsible for working within the framework of a team and performing the following activities: Develop and update engineering documents such as manufacturing instructions, drawings and test procedures. Review and evaluate non-conforming materials, address customer experience reports, perform root cause analysis, and propose corrective/preventive actions. 4/18/2020
678 Applied Medical
Rancho Santa Margarita, CA
Mechanical Engineer - Packaging
BS in mechanical engineering
Exp: 1 year in engineering
As a Mechanical Engineer- Packaging you will be responsible for working within the framework of a team and performing the following activities: Design of product packaging and automated equipment using custom or off the shelf machinery to improve existing manufacturing processes. Generate documentation such as drawings, test protocols, reports, and troubleshooting guides, manufacturing instructions 4/18/2020
679 Applied Medical
Rancho Santa Margarita, CA
Quality Engineer II
BS/BA in engineering/STEM
Exp: 1-2 years work experience
As a Quality Engineer II, you will use your skills to support medical device quality through design controls, process validations and documentation as part of a cross-functional team. Conduct experiments to prove hypotheses. Create and validate test methods for design verification and manufacturing inspection testing by using measurement system analysis, gauge R&R and other relevant techniques. 4/18/2020
680 Ani Pharmaceuticals
Baudette, MN
Operator I - Production (1st, 2nd and 3rd Shift)
HS Diploma/GED
Exp: 1-2 years
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. 4/18/2020
681 Ani Pharmaceuticals
Baudette, MN
QC Chemist
BS/BA in biological sciences or chemistry
Exp: 1-3 years
Perform review of data collected under approved test methods and investigational plans and protocols, in accordance with governing SOPs. Provide accurate assessment of data integrity, and document findings. Perform calibrations, preventive maintenance and repairs as needed on instrumentation. Qualify new equipment as assigned. Perform cGMP tasks such as laboratory housekeeping, auditing documentation and ordering supplies. Perform other duties as assigned or requested. 4/18/2020
682 ARL Bio Pharma
Oklahoma City, OK
Research & Development Scientist I
BS/BA in chemistry or related
Exp: 0-2 years industrial experience
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. 4/18/2020
683 ARL Bio Pharma
Oklahoma City, OK
Laboratory Technician - Chemistry Lab
Associates or BS/BA in chemistry
Exp: 0-2 years
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. 4/18/2020
684 Amphastar Pharma
Inland Empire, CA
Machinist
1 year certification from college/tech school
Exp: 0-4 years
Sets up and operates conventional, special purpose, and numerical control (NC) machines and machining centers to fabricate metallic and nonmetallic parts by performing the following duties. Studies blueprints, sketches, drawings, manuals, specifications, or sample part to determine dimensions and tolerances of finished work-piece, sequence of operations, and setup requirements. 4/18/2020
685 Amphastar Pharma
Rancho Cucamonga, CA
Validation Technician
BS required
Exp: 0-4 years
Validates and maintains validation records of pharmaceutical product manufacturing equipment and processes by performing the following duties. Performs validations on equipment and process such as autoclaves, ovens, aseptic processes, product assembly lines, filling machines, sterilization processes, and cleaning process. 4/18/2020
686 Aphena
Cookeville, TN
Facilities Maintenance Technician
HS Diploma/GED
Exp: 1-2 years in facilities maintenance
Coordinate with other departments and team members for preventive maintenance work and repairs. Record and fill out work orders in accordance to company’s policy. Perform basic electrical work (replacing outlets, switches, light bulbs, ballast, light fixtures, reset breakers, etc.). Perform preventive maintenance program tasks related to facilities and plant services 4/18/2020
687 Aphena
Cookeville, TN
Production Technician
HS Diploma/GED
Exp: 0-1 years in manufacturing
Read and understand labels and batch records. Visual and Physical Checks on Product and Machine. Ensure compliance with all approved standard operating procedures based on regulatory and internal requirements. Review batch records to examine potential for corrective action 4/18/2020
688 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
689 Catalent (Paradigm Diagnostics)
Gaithersburg, MD
Manufacturing Associate II
BS in a scientific or engineering field
Exp: 1-3 year(s)
The Manufacturing Associate II is responsible for supporting the overall GMP manufacturing process, through the application of broad knowledge of theories and principles utilized to solve operational, as well as routine tasks in the production of bulk biologics from microbial and cell culture systems for Phase I/II & commercial GMP manufacturing. The Role: Completes Batch Production Records under cGMP, and documents in detail through the use of SOPs and BPRs for the processes and manufacturing steps. Support initiation and closure of deviations; may serve as the lead in the departmental investigation and be responsible for closing out deviations and CAPAs. etc. 4/15/2020
690 Catalent (Paradigm Diagnostics)
Harmans, MD
Manufacturing Associate II, Upstream
BS in a scientific or engineering field
Exp: 1-3 year(s)
The Manufacturing Associate II, Upstream is responsible for supporting the overall GMP manufacturing process, through the application of broad knowledge of theories and principles utilized to solve operational, as well as routine tasks in the production of bulk biologics from microbial and cell culture systems for Phase I/II & commercial GMP manufacturing. The Manufacturing Associate II Upstream role is critical to our patients. Manufacturing life-saving medicines right the first time for themselves and their team with patient safety in mind is our priority. Quality, safety and on-time delivery is a must to be successful in this role! etc. 4/15/2020
691 Catalent (Paradigm Diagnostics)
Baltimore, MD
Manufacturing Associate I
BS/BA
Exp: 0-1 year(s)
The Manufacturing Associate I perform 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 is critical to our patients. Manufacturing life-saving medicines right the first time with patient safety in mind is our priority. Quality, safety and on-time delivery is a must to be successful in this role! etc. 4/15/2020
692 Catalent (Paradigm Diagnostics)
Rockville, MD
Associate Scientist II - Analytical Development
MS
Exp: 0+ years
The Associate Scientist II, Analytical Development will be responsible for process and product development within a dynamic project team. The ideal candidate will demonstrate strong technical knowledge, initiative, and scientific commitment, and make significant scientific and technical contributions within the Analytical Development Group as well as their project teams. The Associate Scientist, II Analytical Development role is critical to our patients. We generate high-quality tests/assays to provide patients with the best materials possible, with patient safety in mind, executing with efficiency always. Quality, safety, and on-time delivery is a must to be successful in this role! etc. 4/15/2020
693 Catalent (Paradigm Diagnostics)
Bloomington, IN
Manufacturing Associate
AS/AA
Exp: 0-2 years
A manufacturing associate’s primary duty is to perform variety of operational tasks in accordance with current GMP’s. Responsibilities include: Follow accurately all GMP documents (Batch records, SOP’s. Protocols, etc.), safely operate production equipment, operate in a clean room environment within required gowning, aseptic behaviors, and proper flow procedures, must work effectively in a team environment to achieve company goals, must adhere to company compliance, safety and attendance required. etc. 4/15/2020
694 Catalent (Paradigm Diagnostics)
Bloomington, IN
Associate Manufacturing Technology Specialist
BS/MS in a scientific or engineering field
Exp: 0+ years
The Role: Provide technical training as necessary to operators. Provide on-the-floor oversight of the manufacturing process, as necessary. Interact with client technical representatives, including Person in Plant observers on manufacturing floor. Monitor process data, identify trends, present data, and propose action as necessary. Perform technical troubleshooting and investigations of process issues. This includes documenting formal deviation investigations as needed. etc. 4/15/2020
695 Catalent (Paradigm Diagnostics)
Woodstock, IL
Production Associate II - B Shift
HS diploma or equivalent
Exp: 1+ year(s)
The position is responsible for packaging and inspecting pharmaceutical products in accordance with packaging instructions, Standard Operating Procedures (SOP), and current Good Manufacturing Practices (cGMP) while adhering to health and safety requirements. The Production Associate II role is critical to our patients. They oversee all inspection of our products with safety in mind, executing with efficiency always. The Role: Monitor and direct employee position rotations on the line. Assist team lead in the coordination of OJT. etc. 4/15/2020
696 Paragon Genomics
Hayward, CA
Quality Assurance Specialist
BS in molecular biology, chemistry, or other life science
Exp: 1+ year(s)
We are seeking a Quality Assurance (QA) Specialist that can build out and implement a Quality Management System (QMS) from the ground up, focusing initially on ISO 9001 certification and transitioning to ISO 13485 certification. The QA Specialist ensures compliance with policies and procedures, serves as the main point of contact for customer quality audits and provides quality system performance reports to management. This position will be expected to take a hands-on approach to activities in production and other processes, in order to identify and recommend opportunities for improvement. etc. 4/15/2020
697 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
698 PBS Biotech
Camarillo, CA
Research Associate, BioprocessR&D
MS in chemical or biochemical engineering, or a life science
Exp: Not necessary for MS candidates
We are seeking a full-time, highly motivated Research Associate to join our growing bioprocess R&D team. This position is an invaluable opportunity to gain experience working with cutting edge technology and a variety of cell types that are significant to the rapidly emerging cell and gene therapy market. Responsibilities and Tasks: 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. etc. 4/15/2020
699 PCI Sequens Research
Devens, MA
Process Chemist R&D
BS/MS in chemistry
Exp: 0-5 years
The successful candidate is expected to be able to participate in a chemical synthesis program with the objective to develop a chemical process that can be safely performed on large scale. This involves being able to design, adapt and execute synthetic procedures and purification methods on a laboratory scale to fit the requirements of the development or scale-up plant. etc. 4/15/2020
700 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
701 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
702 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
703 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
704 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
705 Personalis
Menlo Park, CA
Laboratory Assistant
BS in molecular biology or related
Exp: 0-2 years
We are looking for a team-oriented Laboratory Assistant to join our operations team. The ideal individual must have the ability to think on their feet and troubleshoot issues. 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. Responsibilities: Adhere to the laboratory's quality control policies. etc. 4/15/2020
706 Personalis
Menlo Park, CA
Research Associate - Operations
BA/BS in a biological discipline
Exp: 0-2+ years
Located in Menlo Park, CA, we are seeking a talented and highly motivated Research Associate to join our Operations Team. You will participate in the daily activities of the laboratory in order to effectively maximize turnaround time, equipment, and material utilization within budgetary constraints while adhering to quality technical standards. Responsibilities: Participates in a hands-on fashion to the daily lab activities in one of the following areas by performing and assisting in laboratory tests, processes and analyses according to the laboratory’s standard operating procedures. etc. 4/15/2020
707 FCX Performance
Plymouth, MI
Instrument Technician
HS diploma/AS in process instrumentation
Exp: 1-3+ year(s)
Essential Functions & Responsibilities: Respond to customer inquiries & requests to perform maintenance, repair, installation, and calibration on various types of high-end industrial electronic and standard instrumentation & measurement devices. Perform data collection and analysis of the various technologies; including but not limited to Vibration, Motor Circuit, Oil, and/or Power Quality Analysis. Report job activity as well as maintain detailed logs about service calls, parts, and orders. Identify opportunities for upgrades at the customer facility. etc. 4/15/2020
708 Pharmaron
Germantown, MD
Laboratory Technician, Accelerator Mass Spectrometry
BS/BA in related field
Exp: 6-12 months
We are looking for a Laboratory Technician to work on a full-time basis in our Germantown, MD facility. 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: To work to the Company’s quality procedures in accordance with GLP and GCP regulations and be involved in working to and generating a culture of continuous improvement. To comply with the Company’s Health and Safety, MOSH and ionizing radiation procedures. To participate in the day‐to‐day operation of the Laboratory, the analysis of samples and associated duties. etc. 4/15/2020
709 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
710 Pharmaron
Germantown, MD
Associate Bioanalytical Scientist, Accelerator Mass Spectrometry
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: 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. Prepare/review data tables and reports within Laboratory Information Management System (LIMS). etc. 4/15/2020
711 PLDevelopments
Copiague, NY
Process Operator I – Copiague, NY
HS diploma or equivalent
Exp: 1 year
POSITION RESPONSIBILITIES: Reports process or equipment problems to supervisor; performs general troubleshooting. Ensures batch records, equipment log books, and other relevant records are current; performs batch record reconciliation. Sets up and operates equipment for processing operations. Cleans and maintains processing rooms and equipment. Monitors process and equipment and makes necessary adjustments to maintain batch record specifications. etc. 4/15/2020
712 Poseida Therapeutics
San Diego, CA
Lab Technician
BS/BA
Exp: 6 months+
Poseida is seeking an outstanding candidate to join our Research Operations team. The Lab Technician is responsible for providing broad support for research personnel by maintaining lab facilities, carrying out basic lab equipment maintenance, washing and autoclaving glassware, coordinate collection of biohazard/chemical waste, and replenishing lab supplies. Responsibilities: These may include but are not limited to: Set up and carry out daily operational maintenance of lab equipment, including incubators, water baths, biosafety cabinets, centrifuges, and cold storage units. etc. 4/15/2020
713 Precision Biosciences
Durham, NC
Associate Process Engineer/Process Engineer, Downstream
MS in chemical engineering, biological engineering, or relevant science
Exp: 0-2 years
Precision BioSciences is currently seeking to fill the role of Associate Process Engineer or Process Engineer. This position will be a critical part of the team charged with developing a world-class manufacturing process for making an mRNA-based active pharmaceutical ingredient (API). The candidate will participate in all aspects of process development, including in-vitro transcription, downstream purification and testing of products and intermediates. Responsibilities: Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position. This list contains the major duties and requirements of the job and is not all-inclusive. Incumbent(s) may be expected to perform role-related duties other than those contained in this document. Set up and run transcription reactions at small and large scale. Assist in the development of downstream purification operations appropriate to the scale of the process. Collaborate with the Analytical team to perform in-process and final product testing. etc. 4/15/2020
714 Precision
Frederick, MD
Processing Technician I/II - Biological Samples
BS in biology, chemistry, or other life science
Exp: 1-2 year(s)
Our Processing Technician I receive and inventory all incoming fresh biological samples into LIMS database, perform cell isolations and/or separate whole blood and body fluids into various components, perform cryopreservation of all isolated cells, prepare reagents used in lab, perform cell thawing and counting, create and perform first key of data collection sheets. In addition to the above, the Processing Technician II perform plate based assays such kit based ELISAs for clinical patient specimen samples, QC analyses for controls and standards utilized in the plate based assays to ensure that results meet specifications, isolation and cryopreservation of intact RNA, miRNA and DNA from clinical patient specimen samples of all tissue and types, quantification and QC evaluation of nucleic acid samples including Picogreen assays and QC analyses (RNA/DNA integrity analysis, Real-Time PCR) to ensure that results meet specifications and perform equipment preventive maintenance. etc. 4/15/2020
715 PRESCOS
San Diego, CA
Vivarium Assistant
HS diploma or equivalent
Exp: 0-1 year(s)
We are looking for a full-time Vivarium Assistant to perform husbandry tasks such as the changing and cleaning of animal cages, feeding/watering of animals, and the sanitation/ cleaning of the animal facility. Essential functions: Perform cage changes (provide food/water and change bedding) and routine daily health monitoring. Washing and sterilizing of laboratory caging, supplies and equipments. Maintain and upkeep documentations such as animal cage cards, duty log sheets, animal computer database, and sanitation logs. etc. 4/15/2020
716 Prevail
New York, NY
Lab Associate - Process Development
MS
Exp: 1-2 year(s)
Reporting to the Director of Process Development, the Lab Associate of Process Development will play a critical role in our efforts to advance the development of AAV gene therapy pipeline drugs for neurodegenerative disorders. We are looking for an enthusiastic, self-motivated, hands-on lab associate with excellent interpersonal skills who is comfortable working in an open environment spanning multiple functions. As an early hire at a new company, you will have exposure to senior management, to all activities at Prevail, and you will be influential in championing and developing our culture. etc. 4/15/2020
717 Propharma Group
Montreal, QC
Biologics Validation Engineer - Consultant
BS/BA in a related field
Exp: 1-10 year(s)
Job Description: Preparing and executing validation documents in a biologics environment. Project execution for multiple systems validation. Understanding the hours budgeted for completion of each task on a specific. Individuals must represent the company and division at client sites and interact confidently with clients, contractors, management, and peers. Develop Installation, Operational and simple Performance qualification documents. etc. 4/15/2020
718 ProSciento
San Diego, CA
Clinical Research Associate
BS in a life science
Exp: Not necessary for BS candidates
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. Ensures the protection of study subjects by verifying that informed consent procedures have been followed and protocol requirements are adhered to according to applicable regulatory requirements. Monitors, tracks, and follows up on all Adverse Events (AEs) and Serious Adverse Events (SAEs). Ensures all SAEs are reported to sponsor and regulatory authorities within required timelines. 4/15/2020
719 Promega
Madison, WI
Product Finishing IVD Technician 1
HS diploma or equivalent
Exp: 1+ year(s)
Technician with a full understanding of the department including dispensing, kitting and labels. Uses technical concepts and depth of knowledge to resolve issues effectively. ESSENTIAL DUTIES: Setup, operate and maintain manual and automated dispensing, capping and labeling equipment. Pull products from inventory and assemble components into kits and kit sub-assemblies using quality system documents, including kit packaging diagrams (KPDs). Accurately complete all required written documentation for batch records. etc. 4/15/2020
720 Performance Validation
Unspecified, IN
Level 1 Staff Validation Engineer
BS in mechanical, chemical, or biomedical engineering
Exp: Entry level
Performance Validation is seeking full-time Level 1 Validation Engineer/Specialists in the following locations: Indiana, Michigan, Illinois, and Kansas. The Level 1 Validation Engineer/Specialist is an entry level position and reports directly to the Division Director or Manager and is assigned to one or more project teams to perform work for Performance Validation’s customers. etc. 4/15/2020
721 Performance Validation
Unspecified, IN
Level 1 Staff Validation Specialist
BS in the life sciences
Exp: Entry level
Performance Validation is seeking full-time Level 1 Validation Engineer/Specialists in the following locations: Indiana, Michigan, Illinois, and Kansas. The Level 1 Validation Engineer/Specialist is an entry level position and reports directly to the Division Director or Manager and is assigned to one or more project teams to perform work for Performance Validation’s customers. etc. 4/15/2020
722 PRA Health Sciences
Charlottesville, VA
Safety Assistant
HS diploma/BA/BS
Exp: 1-2 year(s)
You’ve been working as a pharmacy, lab or medical technician and want to utilize your skills in a new environment that allows for long-term career growth opportunities. Or, as a new graduate or early-career professional, you’ve been wondering how to put your degree in biology, chemistry, or other life sciences to practice in a meaningful way. Are you incredibly detail-oriented to ensure the accuracy and reliability of your work? Do you want to impact the lives of others through research – helping to develop cutting edge, safe pharmaceuticals that will extend the life of or cure others? If so, you are an emerging drug safety professional! etc. 4/15/2020
723 PRA Health Sciences
Salt Lake City, UT
Lab Associate PRN
BS/BA in a medical, laboratory, or life science
Exp: 1-2 year(s)
The Lab Associate is part of the operational team within the sample preparation laboratory. The Lab Associate ensures the appropriate collection, processing, storage and shipment of samples. Daily tasks may involve maintenance of equipment, processing and shipment of samples. The Lab Associate is part of the study team that is responsible for the execution of the study. etc. 4/15/2020
724 PRA Health Sciences
Salt Lake City, UT
Medical Research Associate FT Nights - Salt Lake City
BS/BA in a clinical or health related area
Exp: 1-2 year(s)
Who are you? Are you a recent Medical Assistant Grad looking for experience? Or maybe a skilled CNA, EMT, or Phlebotomist, looking to use your skills in an ever-changing environment? Or, a healthcare professional looking for a career that can impact the lives of millions? Still with me? Good! Then an opportunity as a Medical Research Associate in our Clinical Research Organization is the career for you! Clinic Tasks: Screen potential subjects. 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 etc. 4/15/2020
725 PRA Health Sciences
Charlottesville, VA
Safety Assistant 2
HS diploma/BA/BS
Exp: 1-2 year(s)
You’ve been working as a pharmacy, lab or medical technician and want to utilize your skills in a new environment that allows for long-term career growth opportunities. Or, as a new graduate or early-career professional, you’ve been wondering how to put your degree in biology, chemistry, or other life sciences to practice in a meaningful way. Are you incredibly detail-oriented to ensure the accuracy and reliability of your work? Do you want to impact the lives of others through research – helping to develop cutting edge, safe pharmaceuticals that will extend the life of or cure others? If so, you are an emerging drug safety professional! etc. 4/15/2020
726 Poseida Therapeutics
San Diego, CA
Research Associate, Immuno-Oncology
MS in immunology, molecular biology, or related
Exp: 0+ years
Poseida is seeking an outstanding candidate to join our immuno-oncology team. The Research Associate will support the development chimeric antigen receptors (CAR-T) cellular therapies against cancer and will involve bench work, laboratory studies, and the coordination of research projects with the assistance of a senior lab member and/or lab director. Responsibilities: These may include but are not limited to: Support the development of CAR-T cellular therapies. Studies may include work with molecular biology and cloning techniques, tissue culture of human cell lines, isolation of cells from blood products, virus production, in vitro human cell-based immunoassays, and cell separation techniques. etc. 4/15/2020
727 Pharmaron
Germantown, MD
Associate Bioanalytical Scientist, Small 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: 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. Prepare/review data tables and reports within Laboratory Information Management System (LIMS) etc. 4/15/2020
728 Nova Biomedical
Waltham, MA
Reagent Packager I
HS diploma or equivalent
Exp: 1+ year(s)
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. 4/8/2020
729 Nova Biomedical
Waltham, MA
Chemical Filling Operator - First Shift
Unspecified
Exp: 0-2 years
The Filling Operator is responsible for the proper filling, sealing and labeling of various reagents. Responsibilities include: monitoring and maintenance of the filling equipment during operation, recording necessary data into procedures, inspection of product, loading/unloading product from equipment and movement of materials. Requirements: High School Diploma or equivalent. Must be able to lift up to 50 pounds and be able to work alternately in a seated or standing procedure. Must have basic mechanical aptitude and the ability to read, write and comprehend English. Ability to wear cartridge type respirator. Will work with hand tools and gages to properly operate filling equipment such as bottle fillers and pouch fillers. Ability to operate electric and manual pallet jacks. Requires 0 to 2 years’ experience as a machine operator. Entry level knowledge of Quality System Regulations, Good Manufacturing Practices, and OSHA safety standards desirable. Hours: Monday – Friday, 6:45 AM – 3:15 PM. 4/8/2020
730 Nova Biomedical
Waltham, MA
Replenishment Associate
HS diploma
Exp: 1 year
The Receiving Replenishment Associate's is responsible for maintaining raw inventory within the raw material warehouse area. As part of the Receiving Team, the Replenishment Associate will be responsible for (1) the moving of raw material from the Receiving dock to the warehouse, (2) the consolidating of raw material in the warehouse, and (3) the picking and delivering of raw materials to the manufacturing floor. The Replenishment Associate will use documented procedures and good judgement to ensure inventory is stocked in an optimum manner, controlled, and ready for picking. Essential Responsibilities: 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.). etc. 4/8/2020
731 Novo Nordisk
Durham, NC
Maintenance Technician (Packaging)- OFP
AA/AS in a relevant field
Exp: 1 year
Position Purpose: Improve systems & equipment reliability on assigned process, reduce system/equipment downtime on assigned process & support operation of assigned process. Accountabilities: Follow all safety & environmental requirements in the performance of duties. Follow Standard Operating Procedures in performance of assigned duties. Support the development & establishment of maintenance procedures, maintenance plans & spare parts lists for processes assigned. Perform corrective & preventative maintenance on assigned process in a timely manner. etc. 4/8/2020
732 Novo Nordisk
West Lebanon, NH
Quality Control Microbiologist I
BS in a scientific discipline
Exp: 0-2 years
This position carries out routine microbiological testing to support the manufacturing facility. All work is carried out in a Quality Control (QC) Good Manufacturing Practice (GMP) environment where the highest level of compliance and attention to detail is necessary. Role focuses on routine activities such as utility and facility monitoring, data reporting, general laboratory support and activity coordination. This individual works with supervision/instruction on routine work and detailed instruction for new activities. Main Job Tasks: Duties include but are not limited to: Conducts routine microbiology assays following Standard Operating Procedures (SOP’s) such as bioburden and endotoxin testing. Collects Environmental Monitoring samples including high quality water systems, cleanroom environments and gases in the field (manufacturing, utilities and laboratory locations). etc. 4/8/2020
733 Novo Nordisk
West Lebanon, NH
Facilities Equipment Technician
AS/AA
Exp: 1 year
The Facilities Equipment Technician will be responsible for routine maintenance and troubleshooting of equipment – such as diaphragm valves, centrifugal pumps, pressure regulators, autoclaves, Clean in Place (CIP) systems, centrifuge, and homogenizer. This role will assist in the coordination and execution of manufacturing equipment maintenance, improvement programs, and quality responses for process equipment as needed. Main Job Tasks: Perform preventive maintenance (PM) of manufacturing related equipment. Perform trouble shooting, repair and corrective maintenance (CM) of manufacturing related equipment. etc. 4/8/2020
734 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
735 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
736 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
737 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
738 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
739 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
740 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
741 Nuventra Pharma Sciences
Durham, NC
Regulatory Publishing Associate
BS/BA
Exp: 1-2 year(s)
We seek an experienced eCTD publisher for a growing regulatory operations team. The ideal candidate will be self-motivated, detail-oriented, and will have eCTD publishing experience in both US and global markets. This is an office-based position in Durham, NC. Responsibilities: Use Microsoft Word and Adobe Acrobat to format and compile submission-ready documents. Build electronic (eCTD) regulatory submissions, including INDs, NDAs, and BLAs, utilizing industry-standard publishing software. Perform quality control reviews of submissions within publishing software. etc. 4/8/2020
742 OraSure Technologies
Bethlehem, PA
Manufacturing Technician - 2nd Shift
HS diploma or equivalent
Exp: 0-2 years
Operate equipment for the assembly of medical diagnostic tests. Schedule for this position will be Monday-Friday 3:30 PM-12 AM. Responsibilities: Operate semi-automated and automated equipment in the production area at a sufficient rate and quality level. Perform on-line inspection of all components/parts produced. Take corrective action and/or make recommendations to the supervisor. Complete all paperwork and equipment logbooks and review other operator's paperwork for accuracy and completeness as required. etc. 4/8/2020
743 Organogenesis
Norwood, MA
Materials Handler
HS diploma or equivalent
Exp: 1 year
KEY RESPONSIBILITIES: Receives and labels incoming materials. Delivers materials to internal customers. Produce labels for finished products. Product labeling and packaging. Assist in the daily scheduling of activities. Prepare and package outgoing product shipments. Print and prepare documentation. Complete cycle counts and inventory checks in a timely and accurate manner. etc. 4/8/2020
744 PACT Pharma
South San Francisco, CA
Clinical Immunology Research Associate
BS/MS
Exp: 1+ year(s)
We are currently recruiting for Research Associate in Clinical Immunology. This position will be based in South San Francisco. Who you are: A person eager to contribute to new understanding of T cell and cancer biology by preparing and analyzing samples from patients in our clinical trial. A detail-oriented person who takes pride in producing high-quality, accurate data. A person who prefers clear and consistent job responsibilities and objectives. etc. 4/8/2020
745 PACT Pharma
South San Francisco, CA
Molecular Biologist Research Associate I / II
MS
Exp: 1+ year(s)
The ideal candidate should be experienced in the latest molecular cloning techniques and in mammalian cell culture. 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. What you will do: The candidate will be generating plasmids expressing patient-derived T cell receptors using an established molecular cloning protocol. He/she will also be responsible for genome engineering human T cells to express the patient-derived T cell receptors. etc. 4/8/2020
746 PACT Pharma
South San Francisco, CA
Research Associate
BS/BA
Exp: 0-2 years
We are currently recruiting for a Research Associate who will report to the Scientist and continue advancing PACT’s cutting edge engineered cell product. This will be a unique opportunity to see your ideas rapidly translate into the clinic and impact patient lives. What you will do: Support the Protein Production pipeline with high-throughput DNA Prep, cloning, protein expression and purification. Expression and purification of recombinant proteins in mammalian host system. etc. 4/8/2020
747 PACT Pharma
South San Francisco, CA
Research Associate Protein Sciences
BS/BA
Exp: 1-2 year(s)
We are currently recruiting for a Research Associate Protein Sciences who will report to the Associate Director of Protein Sciences and continue advancing PACT’s cutting edge engineered cell product. This will be a unique opportunity to see your ideas rapidly translate into the clinic and impact patient lives. The individual will be responsible for the execution of high-throughput cloning, protein expression and purification and will be involved in the critical path for the discovery of neoEpitope and corresponding cognate TCRs. The position involves a considerable amount of bench work in a GMP-like environment and will on protocols and SOP executions to support our clinical trial. The ideal candidate should have keen attention to details, be highly organized and should enjoy operating in an exceptionally dynamic and collaborative environment. etc. 4/8/2020
748 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
749 OraSure Technologies
St. Paul, MN
Software Engineer
BS in computer science
Exp: 6 months
We are looking for a team member who can contribute to our high-throughput data tracking and analysis applications. We generate terabytes of genomic data per week and need to ensure efficient and accurate tracking is completed along with quick, accurate, and reproducible data analysis. By facilitating fast and easy data access for our clients, we expedite advances in scientific knowledge. Our new software engineer will join a development team of highly-motivated, passionate and inclusive engineers. If you’re looking for a position that will directly improve human health and the environment, we want you! etc. 4/8/2020
750 OraSure Technologies
Bethlehem, PA
Quality Control Specialist I
AS in chemistry, biology, medical technology or related
Exp: 1 year
Quality Control Specialist I personnel perform procedures that include evaluation of raw materials, in-process components, finished products, stability testing, equipment quality control, and equipment maintenance in compliance with guidelines established by Orasure Technologies and regulatory agencies. Responsibilities: Perform all procedures accurately and according to written Work Instructions and SOPS as indicated in the Quality Control procedures and other applicable facility procedures. Perform testing at all levels of production including raw materials, in-process components, finished products and stability testing. Perform visual finished product inspections. etc. 4/8/2020
751 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
752 Nanosyn
Santa Clara, CA
Research Associate / Screening and Compound Profiling
BS in biology, biochemistry, or related
Exp: 0-2 years
We are currently seeking a highly motivated screening and compound profiling research associate to join our biology department in Santa Clara, CA. 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. The ideal candidate should have good organizational skills, possess good problem solving, communication and interpersonal skills and to adapt rapidly to new challenges. We are currently seeking a highly motivated screening and compound profiling research associate to join our biology department in Santa Clara, CA. 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. etc. 4/7/2020
753 Nanosyn
Santa Clara, CA
Associate Scientist / Analytical Chemist
BS/MS in chemistry
Exp: 1+ year(s)
Nanosyn is currently seeking a highly motivated candidate to join the analytical and compounds management team in Santa Clara, CA. The candidate will play a key role in the organization by being responsible for the planning and timely execution of characterization, purification, QC, data processing, etc. for Nanosyn’s chemistry/biology services. She/he will be responsible for consistently generating high quality data and meeting agreed upon timelines. Applicants must have at least 1 year of relevant experience, very strong organizational skills, the ability to work on multiple projects simultaneously, and be productive both independently and as part of a team. etc. 4/7/2020
754 NantKwest
San Diego, CA
Research Associate - Analytical
MS
Exp: 1 year
Major Job Objective and description of responsibilities/milestones/key objectives: Assist in the running of the laboratory including purchasing, set up and maintenance of equipment; maintenance of reagent inventories; preparation and management of standard operating procedures. Support the scientific operation of the laboratory by maintaining mammalian cells in cultures and generating cell banks in GXP setting. Assist in the design and execution of in vitro experiments to isolate, expand and characterize NK cells and target cell lines. Assist in the development and validation of bioassays to determine the in vitro efficacy of NK cells against various target cell lines. etc. 4/7/2020
755 Nephron Pharma
West Columbia, SC
Microbiology Analyst I
BS in biology, microbiology, or other life science
Exp: 1 year
Position Summary: 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. Additional work duties or responsibilities as evident or required. Performs other duties as assigned or apparent. NOTE: The Primary Accountabilities and Knowledge, Skills and Abilities below are intended to describe the general content of and requirements of this position and are not intended to be an exhaustive statement of duties. Incumbents may perform all or most of the primary accountabilities listed below. Specific tasks or responsibilities will be documented in the incumbents' performance objectives as outlined by the incumbents' immediate supervisor or manager. 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. etc. 4/7/2020
756 NeuMoDx
Ann Arbor, MI
Manufacturing Specialist Reagent
BS/BA in chemistry or other science
Exp: 1 year
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. In this position, Manufacturing Specialists, will maintain manufacturing equipment, create work instructions, train others, often be asked to contribute to or lead projects, be cross functionally trained to work in several areas as needed. etc. 4/7/2020
757 Neurocrine
San Diego, CA
Associate Scientist, In Vivo Biology
BS/BA in biology or related
Exp: 1 year
We are seeking a highly motivated and collaborative scientist to join the In Vivo Biology group. This is a hands-on role in which the successful candidate will execute behavioral experiments in both genetic and pharmacological rodent models to evaluate novel treatments for psychiatric, neurodevelopmental, and neurodegenerative disorders. Within a dynamic and engaging environment, you will interact with scientific investigators to plan and execute preclinical rodent studies. Strong technical skills and excellent communication ability are required. etc. 4/7/2020
758 New England Biolabs
Ipswich, MA
Materials Handler
HS diploma
Exp: 1+ year(s)
The Shipping Department at New England Biolabs (NEB) is inviting candidates for the position of Part-Time Shipping Clerk. The hours of this job are Monday through Friday from 3:00 pm - 8:00 pm. Primary Responsibilities: Efficiently and accurately pick and pack customer orders for shipment. Process product shipments utilizing electronic SAP/ ERP system. Support end of day procedures and ensure all customer packages are ready for delivery. Maintain and organize the shipping and warehouse area. Manage inventory and restocking of finished goods materials. Work closely with the Monarch Kit Team. etc. 4/7/2020
759 Newport Laboratories
Worthington, MN
Technician II, Bio/Pharm Prod - Media Preparation
BS/BA
Exp: Not necessary for BS/BA candidates
In this position, the incumbent will be trained in the set-up, operations, and troubleshooting of the equipment in the production areas, with focus on media preparation and equipment cleaning and sterilization. Additional duties will include documentation of work and specific computer functions. Must integrate company initiatives into work practices. Responsible for safely producing vaccines which meet all product specifications in accordance with current Good Manufacturing Practice standards. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. etc. 4/7/2020
760 Nitto
Milford, MA
Equipment Maintenance Technician
HS diploma/AS/AA
Exp: 0-10+ years
The Equipment Maintenance Technician is responsible for performing maintenance activity on process and process support equipment in accordance with departmental schedules. Key Job Responsibilities: Responsible for execution all assigned work as described by written procedures (SOPs, PM work orders, or equipment manuals). Responsible for performing all work using all prescribed safety procedures. Responsible for periodic inspections of equipment to ensure they are operating properly and safely. Assist with installation of equipment and write basic safety and maintenance procedures. Must serve on rotation for on call support and be able to respond as required. etc. 4/7/2020
761 Nobel Life Sciences
Woodbine, MD
Animal Care Tech
BS
Exp: 1+ year(s)
The Animal CareTech is a key position within the organization with significant prospects for career growth as the company continues to increase the breadth and scope of its business. This position reports directly to the Vivarium Manager. Responsibilities include but are not limited to: 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 logs. Ensure that all animals are fed the proper diet and have adequate water within the date and time requirements. Clean and disinfect animal holding rooms daily. Assist Study Director with the performance of animal related procedures, as needed. etc. 4/7/2020
762 Nobel Life Sciences
Woodbine, MD
Animal Lab Tech
BS
Exp: 1+ year(s)
The Animal Lab Tech is a key position within the organization with significant prospects for career growth as the company continues to increase the breadth and scope of its business. This position reports directly to the Vivarium Manager. Responsibilities include but are not limited to:Perform duties in accordance with relevant study protocols and the Standard Operating Procedures (SOPs).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. etc. 4/7/2020
763 Nobel Life Sciences
Woodbine, MD
QC Associate
BS
Exp: 1+ year(s)
The QC Associate is a key position within the organization with significant prospects for career growth as the company continues to increase the breadth and scope of its business. This position reports directly to Sr. Vice President and a Consulting Quality Assurance Unit. Responsibilities include but are not limited to: 1. Become and maintain intimate familiarity with all applicable FDA and EPA GLP and other appropriate regulations and guidelines as well as with the company SOPs and other QA systems. 2. Supervise day to day quality control operations and documentation. 3. Assist in writing and reviewing standard operating procedures, study protocols and reports. etc. 4/7/2020
764 Nordson
Salem, NH
Production Associate I (Balloon) Third Shift
HS diploma or equivalent
Exp: No experience 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. This position requires direct contact with medical grade components. etc. 4/7/2020
765 Nordson
Chippewa Falls, WI
Assembler
Unspecified
Exp: 1-3 year(s)
Essential Job Duties and Responsibilities: Review bills of materials and insure parts are available in the assembly area to meet customer delivery date. Prep assembly parts according to customer order. Prep die bodies after chrome plating by stoning the bodies. Study blueprints and/or specifications to plan sequences of operations for fabricating tools, dies, or assemblies. Lift, position, and secure machined parts on worktables using hoists and/or vises. Fit and assemble parts to make dies, using machine tools and hand tools. File, grind, shim, and adjust different parts to properly fit them together. etc. 4/7/2020
766 Norwich Pharma Services
Norwich, NY
MDAS Research Assistant
BS in chemistry or related
Exp: 1-2 year(s)
The Method Development and Analytical Services (MDAS) Research Assistant is a technical resource in performing the analytical testing necessary to support development and commercialization of new pharmaceutical products. The MDAS Research Assistant is responsible for performing the bench chemistry testing for release, stability and product characterization. The MDAS Research Assistant will work under the supervision of more experienced technical staff. ORGANIZATION STRUCTURE: The Research Associate typically reports to a Group Supervisor/Leader, Manager or Director. RESPONSIBILITIES: Hands-on laboratory bench work and sample testing supporting development of pharmaceutical products. This includes but not limited to performing assay, related compounds testing, dissolution, uniformity, and other tests to characterize and demonstrate product performance. Perform laboratory bench work to develop, optimize, and troubleshoot analytical methods for testing raw materials and products (semi-finished and finished) under the guidance of senior staff. etc. 4/7/2020
767 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
768 B. Braun
Fremont, CA
IV Tech I
National Pharmacy Tech certification
Exp: 1 year in related
Prepares compounded sterile products and performs related activities under the direction of a pharmacist. Assists in the set up of the compounding room, equipment, and supplies for preparation of compounded sterile solutions, using aseptic technique. Performs general cleaning and maintenance duties as directed. 4/5/2020
769 AGC Biolgics
Seattle, WA
QC Associate I
BS/BA
Exp: 1-3 years relevant experience
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. 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 4/5/2020
770 AGC Biolgics
Bothell, WA
Process Transfer Technical Writer
BS in sciences/engineering
Exp: 0 years
The Process Transfer Technical Writer is a role for individuals with a STEM background that provides the opportunity to learn and support biotechnology manufacturing operations. Working under the direction of departmental staff, individuals in this role take part in generating key manufacturing documentation, resolving technical issues, and providing training to manufacturing operators. Generating process instructions and batch records from pre-established templates, using source data and information provided, and as instructed and guided by Process Transfer Staff 4/5/2020
771 AGC Biolgics
Bothell, WA
Manufacturing Associate I-IV, Downstream
BS in chemistry/biology
Exp: 1-8 years in aseptic processing
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. 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 4/5/2020
772 AGC Biolgics
Bothell, WA
Manufacturing Associate, Downstream
BS in chemistry/biology
Exp: 1-8 years in aseptic processing
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. 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 4/5/2020
773 AGC Biolgics
Bothell, WA
Associate Business Development Partner
BS or MS in biological sciences
Exp: 1-3 years in pharma, cdmo, or biotech
As Associate Business Development Partner, you will transform customer Request for Proposals (RFP) into winning proposals and be very involved during the sales process by providing technical/operational expertise. The individual selected will interact intensively with both business development and technical colleagues and senior management and will work in a dynamic and fast-paced environment. 4/5/2020
774 AGC Biolgics
Bothell, WA
Accounting Specialist I/II
AA in accounting preferred, HS Diploma/GED
Exp: 0-2 years in accounting
Input vendor invoices into the system in a timely and accurate manner (including 2 way/3 way match). Assist in the preparation of the weekly check runs. Oversee the maintenance of our expense reporting tool (Acubiz) including user maintenance, recording expenses in the GL, and expense report approvals. Ensure all invoices/payments are properly filed 4/5/2020
775 AGTC
Gainesville, FL
QA Specialist I/II/III
BS in sciences
Exp: 0 years in QA
The Quality Assurance (QA) Specialist provides quality oversight of internal and external activities, documentation and processes to assure compliance with company procedures and FDA regulations and assists with tasks necessary to achieve departmental and company goals. 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 4/5/2020
776 AGTC
Gainesville, FL
Process Development Associate, Downstream
BS in biological sciences/engineering
Exp: 1 year in biologics
The PD Associate is responsible for performing downstream process development activities as needed, working independently, with minimal supervision, and on a timely basis, in order to achieve department and/or company goals. Conduct downstream unit operations, including hands-on work with column chromatography and filtration techniques, for the optimization of downstream process unit operations. Collect, analyze, record, and summarize data in the course of biologics production and processing. 4/5/2020
777 Ajinomoto Bio-Pharma
San Diego, CA
Facilities Assistant
HS Diploma/GED
Exp: 0-2 years
The facilities assistant is responsible for general maintenance of facility areas including office, conference room, and utility areas. The position provides general support including cleaning, painting, uncrating and assembly, and ordering and stocking of facility supplies, spare parts, and equipment. Maintain facility in a presentation-ready, clean state. Assist with maintenance activities as overseen by a senior member. 4/5/2020
778 Ajinomoto Bio-Pharma
San Diego, CA
Drug Product Manufacturing Assistant – 1st and 2nd Shift Opportunities
HS Diploma/GED
Exp: 0-2 years in lab or manufacturing
The Drug Product Manufacturing Assistant is responsible for implementation of routine production and manufacturing procedures to optimize processes and regulatory requirements. Performs various routine manufacturing tasks under the guidelines of established SOP’s and cGMP regulations. Implements production and manufacturing procedures. Performs visual inspection. 4/5/2020
779 Ajinomoto Bio-Pharma
San Diego, CA
Aseptic Cleaning Technician
HS Diploma/GED
Exp: 0-2 years in aspectic/GMP cleanroom
The Aseptic Cleaning Assistant performs tasks of the production operation specific to aseptic cleaning and sterilization of processing equipment, parts and rooms. The Assistant maintains batch record documentation and logs as required by corporation and regulatory agencies. This role prepares, according to procedures, various stock solutions and buffers as required by the production process. In addition, this position is responsible for operating general production equipment (such as autoclaves). 4/5/2020
780 Aklesogen
Peachtree Corners, GA
Research Associate
BS/BA in clinical, health or life sciences
Exp: 1 year in lab
This individual is a Research Associate who will work with a team of research associates and scientist at AKESOgen. The Research Associate will work under the general direction of a Team Lead. This individual will perform extractions on a variety of sample types, genotyping on Affymetrix and/or Illumina platform equipment maintenance, solution and reagent preparation in addition to other tasks in laboratory. Operate automated liquid handling platforms for sample processing, DNA/RNA extraction and quantification instruments. 4/5/2020
781 Akorn
Somerset, NJ
Sanitization Associates
HS Diploma/GED
Exp: 1 year in pharma/aspectic manufacturing
All Sanitization Associates are responsible for all activities associated with the manufacturing and filling operations, required to produce sterile drug products under aseptic conditions. Compliance with associated SOPs and training requirements. Removal of used scrubs and coveralls into appropriate bins. Stocking of consumable items, such as bouffant hats and beard covers 4/5/2020
782 Alamo Pharma Services
Baltimore, MD
Pharmaceutical Sales Representative - Dermatology
BS/BA
Exp: 1 year in b2b sales
The Specialty Dermatology Pharmaceutical Sales Representative is accountable and responsible for her/his territory achieving or surpassing sales goals on a monthly basis. Takes ownership and demonstrates the ability to drive monthly sales results through superior selling skills - meeting and exceeding all performance goals. Proven ability to observe and identify market opportunities and challenges and subsequently develop, plan, implement, and follow through with action plans to positively influence opportunities and challenges. 4/5/2020
783 Alamo Pharma Services
Los Angeles, CA
Pharmaceutical Sales Representative - Dermatology
BS/BA
Exp: 1 year in b2b sales
The Specialty Dermatology Pharmaceutical Sales Representative is accountable and responsible for her/his territory achieving or surpassing sales goals on a monthly basis. Takes ownership and demonstrates the ability to drive monthly sales results through superior selling skills - meeting and exceeding all performance goals. Proven ability to observe and identify market opportunities and challenges and subsequently develop, plan, implement, and follow through with action plans to positively influence opportunities and challenges. 4/5/2020
784 Alamo Pharma Services
Austin, TX
Pharmaceutical Sales Representative - Dermatology
BS/BA
Exp: 1 year in b2b sales
The Specialty Dermatology Pharmaceutical Sales Representative is accountable and responsible for her/his territory achieving or surpassing sales goals on a monthly basis. Takes ownership and demonstrates the ability to drive monthly sales results through superior selling skills - meeting and exceeding all performance goals. Proven ability to observe and identify market opportunities and challenges and subsequently develop, plan, implement, and follow through with action plans to positively influence opportunities and challenges. 4/5/2020
785 Alcami
Wilmington, NC
Process Engineer I
BS in engineering/pharmacy/chemistry
Exp: 0-2 years
The Process Engineer I/II is accountable for driving results in a fast-paced environment by providing technical support for the of tablets and capsules for commercial distribution and clinical use. The Process Engineer I/II in this position will provide technical assistance including but not limited to the following: transfer of new process and technologies into the company and writing appropriate documentation to support process transfer and validation activities, sourcing and qualification of equipment and components, troubleshooting current validated processes, initiate process deviations and conduct investigations. 4/5/2020
786 Alcami
Charleston, SC
Process Engineer
BS in engineering/pharmacy/chemistry
Exp: 0-2 years in technical support of sterile manufacturing
The Process Engineer I (Sterile) for our parenteral site in Charleston, SC is accountable for driving results in a fast-paced environment by providing technical support for the manufacturing facility, including, troubleshooting validated processes, process deviations and investigations, transfers of new processes and technologies into the site and preparation of documentation to support validation and process transfer activities. 4/5/2020
787 Alcami
Wilmington, NC
Metrology Calibration Technician I
AS or AAS
Exp: 1-3 years in calibration/instrumentation
The Metrology Calibration Technician I is accountable for driving results in a fast-paced environment by performing scheduled and unscheduled calibration, preventive maintenance (PM), and repair tasks in support of typical analytical and/or process instrumentation prevalent within the bio-pharmaceutical industry. Examples of instrumentation supported include but are not limited to: temperature and pressure measuring instruments, micrometers, calipers, torque testers, hardness testers, balances 4/5/2020
788 B. Braun
Fremont, CA
IV Tech I
National Pharmacy Tech certification
Exp: 1 year in related
Prepares compounded sterile products and performs related activities under the direction of a pharmacist. Assists in the set up of the compounding room, equipment, and supplies for preparation of compounded sterile solutions, using aseptic technique. Performs general cleaning and maintenance duties as directed. 4/5/2020
789 AGC Biolgics
Seattle, WA
QC Associate I
BS/BA
Exp: 1-3 years relevant experience
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. 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 4/5/2020
790 AGC Biolgics
Bothell, WA
Process Transfer Technical Writer
BS in sciences/engineering
Exp: 0 years
The Process Transfer Technical Writer is a role for individuals with a STEM background that provides the opportunity to learn and support biotechnology manufacturing operations. Working under the direction of departmental staff, individuals in this role take part in generating key manufacturing documentation, resolving technical issues, and providing training to manufacturing operators. Generating process instructions and batch records from pre-established templates, using source data and information provided, and as instructed and guided by Process Transfer Staff 4/5/2020
791 AGC Biolgics
Bothell, WA
Manufacturing Associate I-IV, Downstream
BS in chemistry/biology
Exp: 1-8 years in aseptic processing
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. 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 4/5/2020
792 AGC Biolgics
Bothell, WA
Manufacturing Associate, Downstream
BS in chemistry/biology
Exp: 1-8 years in aseptic processing
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. 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 4/5/2020
793 AGC Biolgics
Bothell, WA
Associate Business Development Partner
BS or MS in biological sciences
Exp: 1-3 years in pharma, cdmo, or biotech
As Associate Business Development Partner, you will transform customer Request for Proposals (RFP) into winning proposals and be very involved during the sales process by providing technical/operational expertise. The individual selected will interact intensively with both business development and technical colleagues and senior management and will work in a dynamic and fast-paced environment. 4/5/2020
794 AGC Biolgics
Bothell, WA
Accounting Specialist I/II
AA in accounting preferred, HS Diploma/GED
Exp: 0-2 years in accounting
Input vendor invoices into the system in a timely and accurate manner (including 2 way/3 way match). Assist in the preparation of the weekly check runs. Oversee the maintenance of our expense reporting tool (Acubiz) including user maintenance, recording expenses in the GL, and expense report approvals. Ensure all invoices/payments are properly filed 4/5/2020
795 AGTC
Gainesville, FL
QA Specialist I/II/III
BS in sciences
Exp: 0 years in QA
The Quality Assurance (QA) Specialist provides quality oversight of internal and external activities, documentation and processes to assure compliance with company procedures and FDA regulations and assists with tasks necessary to achieve departmental and company goals. 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 4/5/2020
796 AGTC
Gainesville, FL
Process Development Associate, Downstream
BS in biological sciences/engineering
Exp: 1 year in biologics
The PD Associate is responsible for performing downstream process development activities as needed, working independently, with minimal supervision, and on a timely basis, in order to achieve department and/or company goals. Conduct downstream unit operations, including hands-on work with column chromatography and filtration techniques, for the optimization of downstream process unit operations. Collect, analyze, record, and summarize data in the course of biologics production and processing. 4/5/2020
797 Ajinomoto Bio-Pharma
San Diego, CA
Facilities Assistant
HS Diploma/GED
Exp: 0-2 years
The facilities assistant is responsible for general maintenance of facility areas including office, conference room, and utility areas. The position provides general support including cleaning, painting, uncrating and assembly, and ordering and stocking of facility supplies, spare parts, and equipment. Maintain facility in a presentation-ready, clean state. Assist with maintenance activities as overseen by a senior member. 4/5/2020
798 Ajinomoto Bio-Pharma
San Diego, CA
Drug Product Manufacturing Assistant – 1st and 2nd Shift Opportunities
HS Diploma/GED
Exp: 0-2 years in lab or manufacturing
The Drug Product Manufacturing Assistant is responsible for implementation of routine production and manufacturing procedures to optimize processes and regulatory requirements. Performs various routine manufacturing tasks under the guidelines of established SOP’s and cGMP regulations. Implements production and manufacturing procedures. Performs visual inspection. 4/5/2020
799 Ajinomoto Bio-Pharma
San Diego, CA
Aseptic Cleaning Technician
HS Diploma/GED
Exp: 0-2 years in aspectic/GMP cleanroom
The Aseptic Cleaning Assistant performs tasks of the production operation specific to aseptic cleaning and sterilization of processing equipment, parts and rooms. The Assistant maintains batch record documentation and logs as required by corporation and regulatory agencies. This role prepares, according to procedures, various stock solutions and buffers as required by the production process. In addition, this position is responsible for operating general production equipment (such as autoclaves). 4/5/2020
800 Aklesogen
Peachtree Corners, GA
Research Associate
BS/BA in clinical, health or life sciences
Exp: 1 year in lab
This individual is a Research Associate who will work with a team of research associates and scientist at AKESOgen. The Research Associate will work under the general direction of a Team Lead. This individual will perform extractions on a variety of sample types, genotyping on Affymetrix and/or Illumina platform equipment maintenance, solution and reagent preparation in addition to other tasks in laboratory. Operate automated liquid handling platforms for sample processing, DNA/RNA extraction and quantification instruments. 4/5/2020
801 Akorn
Somerset, NJ
Sanitization Associates
HS Diploma/GED
Exp: 1 year in pharma/aspectic manufacturing
All Sanitization Associates are responsible for all activities associated with the manufacturing and filling operations, required to produce sterile drug products under aseptic conditions. Compliance with associated SOPs and training requirements. Removal of used scrubs and coveralls into appropriate bins. Stocking of consumable items, such as bouffant hats and beard covers 4/5/2020
802 Alamo Pharma Services
Baltimore, MD
Pharmaceutical Sales Representative - Dermatology
BS/BA
Exp: 1 year in b2b sales
The Specialty Dermatology Pharmaceutical Sales Representative is accountable and responsible for her/his territory achieving or surpassing sales goals on a monthly basis. Takes ownership and demonstrates the ability to drive monthly sales results through superior selling skills - meeting and exceeding all performance goals. Proven ability to observe and identify market opportunities and challenges and subsequently develop, plan, implement, and follow through with action plans to positively influence opportunities and challenges. 4/5/2020
803 Alamo Pharma Services
Los Angeles, CA
Pharmaceutical Sales Representative - Dermatology
BS/BA
Exp: 1 year in b2b sales
The Specialty Dermatology Pharmaceutical Sales Representative is accountable and responsible for her/his territory achieving or surpassing sales goals on a monthly basis. Takes ownership and demonstrates the ability to drive monthly sales results through superior selling skills - meeting and exceeding all performance goals. Proven ability to observe and identify market opportunities and challenges and subsequently develop, plan, implement, and follow through with action plans to positively influence opportunities and challenges. 4/5/2020
804 Alamo Pharma Services
Austin, TX
Pharmaceutical Sales Representative - Dermatology
BS/BA
Exp: 1 year in b2b sales
The Specialty Dermatology Pharmaceutical Sales Representative is accountable and responsible for her/his territory achieving or surpassing sales goals on a monthly basis. Takes ownership and demonstrates the ability to drive monthly sales results through superior selling skills - meeting and exceeding all performance goals. Proven ability to observe and identify market opportunities and challenges and subsequently develop, plan, implement, and follow through with action plans to positively influence opportunities and challenges. 4/5/2020
805 Alcami
Wilmington, NC
Process Engineer I
BS in engineering/pharmacy/chemistry
Exp: 0-2 years
The Process Engineer I/II is accountable for driving results in a fast-paced environment by providing technical support for the of tablets and capsules for commercial distribution and clinical use. The Process Engineer I/II in this position will provide technical assistance including but not limited to the following: transfer of new process and technologies into the company and writing appropriate documentation to support process transfer and validation activities, sourcing and qualification of equipment and components, troubleshooting current validated processes, initiate process deviations and conduct investigations. 4/5/2020
806 Alcami
Charleston, SC
Process Engineer
BS in engineering/pharmacy/chemistry
Exp: 0-2 years in technical support of sterile manufacturing
The Process Engineer I (Sterile) for our parenteral site in Charleston, SC is accountable for driving results in a fast-paced environment by providing technical support for the manufacturing facility, including, troubleshooting validated processes, process deviations and investigations, transfers of new processes and technologies into the site and preparation of documentation to support validation and process transfer activities. 4/5/2020
807 Alcami
Wilmington, NC
Metrology Calibration Technician I
AS or AAS
Exp: 1-3 years in calibration/instrumentation
The Metrology Calibration Technician I is accountable for driving results in a fast-paced environment by performing scheduled and unscheduled calibration, preventive maintenance (PM), and repair tasks in support of typical analytical and/or process instrumentation prevalent within the bio-pharmaceutical industry. Examples of instrumentation supported include but are not limited to: temperature and pressure measuring instruments, micrometers, calipers, torque testers, hardness testers, balances 4/5/2020
808 B. Braun
Irvine, CA
QC Microbiology Assoc I
Associates or HS Diploma/GED
Exp: 0-2 years related
Performs routine functions and analysis (dependent upon experience) as required by the specific laboratory requirement in compliance with B. Braun and cGMP specifications. Responsible for microbiological sample receiving/labeling/preparation/sampling/test/ counting/checking and recording of data analysis on finished products, stability test samples and any other test requisitions as directed. Supports the department in ensuring laboratory equipment performance, i.e. scheduling and execution of equipment qualification (IQ/OQ/PQ), calibration, maintenance and trouble shooting. 4/5/2020
809 B. Braun
Irvine, CA
QC Microbiology Assoc I
Associates or HS Diploma/GED
Exp: 0-2 years related
Performs routine functions and analysis (dependent upon experience) as required by the specific laboratory requirement in compliance with B. Braun and cGMP specifications. Responsible for microbiological sample receiving/labeling/preparation/sampling/test/ counting/checking and recording of data analysis on finished products, stability test samples and any other test requisitions as directed. Supports the department in ensuring laboratory equipment performance, i.e. scheduling and execution of equipment qualification (IQ/OQ/PQ), calibration, maintenance and trouble shooting. 4/5/2020
810 B. Braun
Irvine, CA
QC Microbiology Assoc I
Associates or HS Diploma/GED
Exp: 0-2 years related
Performs routine functions and analysis (dependent upon experience) as required by the specific laboratory requirement in compliance with B. Braun and cGMP specifications. Responsible for microbiological sample receiving/labeling/preparation/sampling/test/ counting/checking and recording of data analysis on finished products, stability test samples and any other test requisitions as directed. Supports the department in ensuring laboratory equipment performance, i.e. scheduling and execution of equipment qualification (IQ/OQ/PQ), calibration, maintenance and trouble shooting. 4/5/2020
811 B. Braun
Irvine, CA
QC Microbiology Assoc I
Associates or HS Diploma/GED
Exp: 0-2 years related
Performs routine functions and analysis (dependent upon experience) as required by the specific laboratory requirement in compliance with B. Braun and cGMP specifications. Responsible for microbiological sample receiving/labeling/preparation/sampling/test/ counting/checking and recording of data analysis on finished products, stability test samples and any other test requisitions as directed. Supports the department in ensuring laboratory equipment performance, i.e. scheduling and execution of equipment qualification (IQ/OQ/PQ), calibration, maintenance and trouble shooting. 4/5/2020
812 B. Braun
San Diego, CA
IV Tech I
National Pharmacy Tech certification
Exp: 1 year in related
Prepares compounded sterile products and performs related activities under the direction of a pharmacist. Assists in the set up of the compounding room, equipment, and supplies for preparation of compounded sterile solutions, using aseptic technique. Performs general cleaning and maintenance duties as directed. 4/5/2020
813 B. Braun
San Diego, CA
IV Tech I
National Pharmacy Tech certification
Exp: 1 year in related
Prepares compounded sterile products and performs related activities under the direction of a pharmacist. Assists in the set up of the compounding room, equipment, and supplies for preparation of compounded sterile solutions, using aseptic technique. Performs general cleaning and maintenance duties as directed. 4/5/2020
814 B. Braun
Irvine, CA
Mixing Tech I (Mixing)
HS Diploma/GED
Exp: 1-2 years in related
Perform daily, weekly and monthly clean-up of equipment, plumbing and facilities in the Mixing complex to censure that they are cleaned and properly sanitized to meet government and industry standards. Assist Mixing Technician II with elementary mixing tasks. Performs technical and manual duties required to mix chemical and physical formulation of products. Includes all steps of production from receiving raw materials to providing solutions for production lines. 4/5/2020
815 B. Braun
Irvine, CA
Mixing Tech I (Mixing)
HS Diploma/GED
Exp: 1-2 years in related
Perform daily, weekly and monthly clean-up of equipment, plumbing and facilities in the Mixing complex to censure that they are cleaned and properly sanitized to meet government and industry standards. Assist Mixing Technician II with elementary mixing tasks. Performs technical and manual duties required to mix chemical and physical formulation of products. Includes all steps of production from receiving raw materials to providing solutions for production lines. 4/5/2020
816 B. Braun
Beltsville, MD
IV Tech I
National Pharmacy Tech certification
Exp: 1 year in related
Prepares compounded sterile products and performs related activities under the direction of a pharmacist. Assists in the set up of the compounding room, equipment, and supplies for preparation of compounded sterile solutions, using aseptic technique. Performs general cleaning and maintenance duties as directed. 4/5/2020
817 B. Braun
Beltsville, MD
IV Tech I
National Pharmacy Tech certification
Exp: 1 year in related
Prepares compounded sterile products and performs related activities under the direction of a pharmacist. Assists in the set up of the compounding room, equipment, and supplies for preparation of compounded sterile solutions, using aseptic technique. Performs general cleaning and maintenance duties as directed. 4/5/2020
818 LaunchCOde
Plano, TX
Entry Level Mainframe Systems Engineer
HS Diploma/GED
Exp: Entry Level
Selected candidates will be required to attend both virtual, at-home training and a series of in-person training beginning in Pittsburgh, PA. After training is completed, you will continue your learning journey as a Mainframe Systems Engineer in one of the hiring company’s locations across 20+ cities. 4/5/2020
819 LaunchCOde
Plano, TX
Entry Level Mainframe Systems Engineer
HS Diploma/GED
Exp: Entry Level
Selected candidates will be required to attend both virtual, at-home training and a series of in-person training beginning in Pittsburgh, PA. After training is completed, you will continue your learning journey as a Mainframe Systems Engineer in one of the hiring company’s locations across 20+ cities. 4/5/2020
820 Acutus Medical
Carlsbad, CA
UX Designer/Researcher
BS in sciences/engineering
Exp: 1 year related work
The User Interface Designer/Researcher conducts iterative design activities to help build best-in-class customer experiences across all Acutus hardware and software platforms and touchpoints. The UX Designer/Researcher is responsible for driving the user experience across a wide array of projects. This role collaborates with customers, product managers, software/system design leads, and various engineering leads to ensure the design deliverables successfully and efficiently move each feature from concept to final product. 4/4/2020
821 Acutus Medical
Carlsbad, CA
IT Specialist
BS/BA in related
Exp: 6 months in computer support
Responsible for providing technical assistance and support related to computer systems, printers, AV equipment, hardware or software. Responds to queries, runs diagnostic programs, isolates problem and determines and implement solutions. Maintain and support IT system security in the organization to ensure safety of data and IT systems. Deploy and maintain computer work stations and printers 4/4/2020
822 Adaptimmune
Philadelphia, PA
Manufacturing Cell Therapy Specialist
BS/BA in biological sciences/engineering
Exp: 1 year in lab
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. Inputting and uploading of manufacturing data in real time to existing database. 4/4/2020
823 Adaptive Biotechnologies
Seattle, WA
Research Assistant, Research & Development
BS/BA in biological sciences/engineering
Exp: 1-2 years in research lab
The Research Assistant will perform regular upkeep and maintenance of lab equipment and reagents for the R&D labs at Adaptive. They will work with people across multiple departments, including the environmental health and safety officer, facilities & equipment specialist, and material handling team, in addition to closely working with the multiple teams within MRI and Molecular Product Development, to create a safe and well-prepared lab environment. Successful candidates will be able to proactively assess and address the needs of the team, while being a positive and approachable source of information regarding safe lab practices, and acquisition of materials for experiments. 4/4/2020
824 Adaptive Biotechnologies
Seattle, WA
Research Assistant, Research & Development
BS/BA in biological sciences/engineering
Exp: 1-2 years in research lab
The Research Assistant will perform regular upkeep and maintenance of lab equipment and reagents for the R&D labs at Adaptive. They will work with people across multiple departments, including the environmental health and safety officer, facilities & equipment specialist, and material handling team, in addition to closely working with the multiple teams within MRI and Molecular Product Development, to create a safe and well-prepared lab environment. 4/4/2020
825 Adaptive Biotechnologies
Seattle, WA
Research Assistant, Molecular Product Development
BS/BA in genetics, immunology, bioengineering or related
Exp: 1-3 years in diagnostic/med devices
This successful candidate will be responsible for performing various tasks to support the laboratory technical staff including equipment maintenance and calibration, monitoring and stocking of supplies and reagents, and overall cleanliness of the laboratory work-spaces within the Molecular Product Development (MPD) laboratory. Perform routine instrument calibration, assist facilities with IQ/OQ of instruments (PQ as needed), and track and schedule instrument maintenance. 4/4/2020
826 Adaptive Biotechnologies
Seattle, WA
Biological Sample Management Specialist II
Associates or BS/BA
Exp: 1 year in clinical lab
The BSM Specialist II position will join the Biological Sample Management (BSM) group at Adaptive Biotechnology’s Seattle laboratory. The primary function of this role is to support sample management and chain of custody for Adaptive’s immunosequencing services that includes research, clinical projects, and diagnostic testing. Primary responsibility is to receive and accession samples into the Laboratory Information System (LIMS) used by BSM AND/OR perform sample discards and returns per standard retention times, or by request. 4/4/2020
827 Adaptive Biotechnologies
Seattle, WA
Lab Associate I, Antigen Map
BS/BA in biological sciences
Exp: 1-2 years in research lab
As a member of the Antigen Map Production Lab, you will contribute to the generation of the samples required to generate this TCR-Antigen. Monitor inventory levels and formulate reagents as needed. Stock and stage materials to support operations. Handle biohazardous and chemical waste. Support cell isolation, expansion and stimulation as requested 4/4/2020
828 Adaptive Biotechnologies
Seattle, WA
Research Associate I
BS/BA in biological sciences
Exp: 1-3 years lab experience
Adaptive is seeking a research associate I with an aptitude for learning to join our dynamic and collaborative R&D team. You will partner with other researchers and computational biologists in the development of new and optimization of existing assays for transition into a service lab and/or kit. Work in tandem with team to develop PCR-based assays for immune system profiling by next generation sequencing. DNA/RNA extraction from large number of samples. 4/4/2020
829 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
830 Adare Pharmaceuticals
Vandalia, OH
Operator I
HS Diploma/GED
Exp: 1 year in manufacturing
This is an entry level position at Adare Pharmaceuticals, Inc. (Adare) and the skills learned during training will enable the new operator to perform essential job functions. The essential job function are to produce specified products by the mixing, blending, and combining of raw materials as specified by written procedures. This position is night shift working 12 hours shifts on a 2-2-3 schedule, for example working Monday and Tuesday off Wednesday and Thursday and working Friday, Saturday and Sunday then off Monday and Tuesday. 4/4/2020
831 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
832 Adarza Biosystems
Maryland Heights, MO
Research Associate – Research and Development
BS to relevant sciences
Exp: 0-2 years lab experience
Responsibilities will broadly include supporting the development of new biomarker assays with Adarza’s proprietary AIR™ technology on the ZIVA platform. You will work as part of a team utilizing your laboratory skills to develop and validate immunoassays, as well as provide routine analysis of biological samples for early access clients. The successful candidate will be responsible for reagent preparation, specimen processing, developing and running AIR™ assays. Candidates will be asked to communicate previous work experience successes during the interview process to demonstrate their abilities and the relevance of their experience 4/4/2020
833 Adma Biolgics
Boco Raton, FL
Technician I, Manufacturing Purification
BS/BA in chemistry/life sciences
Exp: 0-2 years
This position is under direct supervision of the Group Leader. It is mainly responsible for the manufacturing of plasma products through protein precipitation/separation and other tasks involving plasma receipt, plasma pooling, and protein separation. The Protein Purification Manufacturing Technician will also clean and sanitize equipment before and after use, make and verify connections on flow panels, perform pH and conductivity measurements, performs chemical and buffer additions and may assist Group Leader in training other tech positions. 4/4/2020
834 Adma Biolgics
Boco Raton, FL
Document Assistant - Temporary
College enrolled or recent graduate
Exp: 1-2 years in document management
The Document Assistant will Create, format, revise and proof read controlled documents such as Standard Operating Procedures (SOPs), Forms, Validations, etc. from departments including but not limited to Quality Assurance, Manufacturing, Facilities, and Quality Control. Perform general office duties such as photocopying, word processing, filing, scanning, physical inventory, ordering supplies. 4/4/2020
835 Adma Biolgics
Boco Raton, FL
QC Lab Support Associate l
BS in biological/chemical/medical sciences
Exp: 1-3 years in regulated lab
The QC Lab Support Associate I will Performs cGMP laboratory support activities including Sample Accessioning, Product Reserve management, Temperature Monitoring of storage chambers, Glassware Cleaning, Supply Inventory management, etc. May also assist with Stability Studies and other QC initiatives. 4/4/2020
836 Adma Biolgics
Boco Raton, FL
Chemist I
BS in biological/chemical sciences
Exp: 0-3 years in lab setting
The Chemist I will Perform quality control testing of raw materials, in-process and final products; following general instructions on routine work and detailed instructions on new assignments. Perform quality control chemistry and/or Immunoassays for raw materials, in-process and final products according to approved Standard Operating Procedures (SOP’s). Perform instument calibration or qualification according to written procedures. 4/4/2020
837 Admera Health
South Plainfield, NJ
Associate Scientist I-PM (Non-Lab Position)
BS or MS in biological sciences
Exp: 1+ years in lab
Relay standard information on next generation sequencing applications to customers. Standard communication with prospective, current, and past customers. Co-coordinating multiple genomic projects with excellent documentation skills and communication to customers. Materials purchasing support for laboratory team 4/4/2020
838 Admera Health
South Plainfield, NJ
Regional Sales Manager-East Coast
BS/BA in biological/life sciences
Exp: 1 year with genomics/gemonics related
Achieve annual sales goals within defined territory/accounts through development, maintenance, and enhancement of customer accounts development, maintenance, and enhancement of customer accounts. Responsibility for managing all business accounts in assigned region/territory including implementing strategies in developing new growth of accounts. Drive the marketing process for the territory by creating a marketing plan, registering/planning/ attending local vendor shows, creating and working with Marketing and PM team to execute email campaigns 4/4/2020
839 Biotechne
Minneapolis, MN
Laboratory Production Assistant
HS Diploma/GED
Exp: 0-2 years
You will be responsible for assisting in the Clinical Controls Product Finishing Department with the bottling operation and the other activities involved in the product finishing process. Label product, operate the labeling equipment. Upon release of product by QA lab, count, verify and record number of finished products. Assist with monthly cleaning of clean room, including counters, laminer hoods, torque, labeler, sinks, and all work areas. 4/4/2020
840 Biotechne
Minneapolis, MN
Administrative Support / Shipping Assistant
HS Diploma/GED
Exp: 0-2 years
The responsibilities of this position are to support the DD OEM Accounts / Shipping Manager and Shipping Department’s activities by performing order processing, proofing, set assembly, shipping and other related duties. Order processing in our ERP System. Assist in preparing final shipping documents for OEM, International, Survey and Domestic shipments. Assist with maintaining Distributor, OEM and Survey customer orders and shipping records 4/4/2020
841 Biotechne
Minneapolis, MN
Lab Assistant
HS Diploma/GED
Exp: 0-2 years
The responsibilities of this position include processing raw biological materials for the use in manufacturing our products, maintaining and cleaning production equipment and containers, and completing required paperwork. Perform other duties as needed. Processes raw biological materials for the use in manufacturing our products. Maintains production equipment and containers 4/4/2020
842 Biotechne
Minneapolis, MN
Research Associate, Cell Culture and Stem Cell Media Operations
BS/BA in biological sciences
Exp: 0-2 years in lab
The main responsibility of this position it to maintain production of mouse embryonic fibroblasts. Additional responsibilities include media and supplement production, QC testing of methylcellulose-containing cell culture media, and cell culture of multiple cell lines. Perform additional duties as assigned. Preferred skills include cell culture, high attention to detail, strong communication and organizational skills. 4/4/2020
843 Acutus Medical
Carlsbad, CA
UX Designer/Researcher
BS in sciences/engineering
Exp: 1 year related work
The User Interface Designer/Researcher conducts iterative design activities to help build best-in-class customer experiences across all Acutus hardware and software platforms and touchpoints. The UX Designer/Researcher is responsible for driving the user experience across a wide array of projects. This role collaborates with customers, product managers, software/system design leads, and various engineering leads to ensure the design deliverables successfully and efficiently move each feature from concept to final product. 4/4/2020
844 Acutus Medical
Carlsbad, CA
IT Specialist
BS/BA in related
Exp: 6 months in computer support
Responsible for providing technical assistance and support related to computer systems, printers, AV equipment, hardware or software. Responds to queries, runs diagnostic programs, isolates problem and determines and implement solutions. Maintain and support IT system security in the organization to ensure safety of data and IT systems. Deploy and maintain computer work stations and printers 4/4/2020
845 Adaptimmune
Philadelphia, PA
Manufacturing Cell Therapy Specialist
BS/BA in biological sciences/engineering
Exp: 1 year in lab
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. Inputting and uploading of manufacturing data in real time to existing database. 4/4/2020
846 Adaptive Biotechnologies
Seattle, WA
Research Assistant, Research & Development
BS/BA in biological sciences/engineering
Exp: 1-2 years in research lab
The Research Assistant will perform regular upkeep and maintenance of lab equipment and reagents for the R&D labs at Adaptive. They will work with people across multiple departments, including the environmental health and safety officer, facilities & equipment specialist, and material handling team, in addition to closely working with the multiple teams within MRI and Molecular Product Development, to create a safe and well-prepared lab environment. Successful candidates will be able to proactively assess and address the needs of the team, while being a positive and approachable source of information regarding safe lab practices, and acquisition of materials for experiments. 4/4/2020
847 Adaptive Biotechnologies
Seattle, WA
Research Assistant, Research & Development
BS/BA in biological sciences/engineering
Exp: 1-2 years in research lab
The Research Assistant will perform regular upkeep and maintenance of lab equipment and reagents for the R&D labs at Adaptive. They will work with people across multiple departments, including the environmental health and safety officer, facilities & equipment specialist, and material handling team, in addition to closely working with the multiple teams within MRI and Molecular Product Development, to create a safe and well-prepared lab environment. 4/4/2020
848 Adaptive Biotechnologies
Seattle, WA
Research Assistant, Molecular Product Development
BS/BA in genetics, immunology, bioengineering or related
Exp: 1-3 years in diagnostic/med devices
This successful candidate will be responsible for performing various tasks to support the laboratory technical staff including equipment maintenance and calibration, monitoring and stocking of supplies and reagents, and overall cleanliness of the laboratory work-spaces within the Molecular Product Development (MPD) laboratory. Perform routine instrument calibration, assist facilities with IQ/OQ of instruments (PQ as needed), and track and schedule instrument maintenance. 4/4/2020
849 Adaptive Biotechnologies
Seattle, WA
Biological Sample Management Specialist II
Associates or BS/BA
Exp: 1 year in clinical lab
The BSM Specialist II position will join the Biological Sample Management (BSM) group at Adaptive Biotechnology’s Seattle laboratory. The primary function of this role is to support sample management and chain of custody for Adaptive’s immunosequencing services that includes research, clinical projects, and diagnostic testing. Primary responsibility is to receive and accession samples into the Laboratory Information System (LIMS) used by BSM AND/OR perform sample discards and returns per standard retention times, or by request. 4/4/2020
850 Adaptive Biotechnologies
Seattle, WA
Lab Associate I, Antigen Map
BS/BA in biological sciences
Exp: 1-2 years in research lab
As a member of the Antigen Map Production Lab, you will contribute to the generation of the samples required to generate this TCR-Antigen. Monitor inventory levels and formulate reagents as needed. Stock and stage materials to support operations. Handle biohazardous and chemical waste. Support cell isolation, expansion and stimulation as requested 4/4/2020
851 Adaptive Biotechnologies
Seattle, WA
Research Associate I
BS/BA in biological sciences
Exp: 1-3 years lab experience
Adaptive is seeking a research associate I with an aptitude for learning to join our dynamic and collaborative R&D team. You will partner with other researchers and computational biologists in the development of new and optimization of existing assays for transition into a service lab and/or kit. Work in tandem with team to develop PCR-based assays for immune system profiling by next generation sequencing. DNA/RNA extraction from large number of samples. 4/4/2020
852 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
853 Adare Pharmaceuticals
Vandalia, OH
Operator I
HS Diploma/GED
Exp: 1 year in manufacturing
This is an entry level position at Adare Pharmaceuticals, Inc. (Adare) and the skills learned during training will enable the new operator to perform essential job functions. The essential job function are to produce specified products by the mixing, blending, and combining of raw materials as specified by written procedures. This position is night shift working 12 hours shifts on a 2-2-3 schedule, for example working Monday and Tuesday off Wednesday and Thursday and working Friday, Saturday and Sunday then off Monday and Tuesday. 4/4/2020
854 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
855 Adarza Biosystems
Maryland Heights, MO
Research Associate – Research and Development
BS to relevant sciences
Exp: 0-2 years lab experience
Responsibilities will broadly include supporting the development of new biomarker assays with Adarza’s proprietary AIR™ technology on the ZIVA platform. You will work as part of a team utilizing your laboratory skills to develop and validate immunoassays, as well as provide routine analysis of biological samples for early access clients. The successful candidate will be responsible for reagent preparation, specimen processing, developing and running AIR™ assays. Candidates will be asked to communicate previous work experience successes during the interview process to demonstrate their abilities and the relevance of their experience 4/4/2020
856 Adma Biolgics
Boco Raton, FL
Technician I, Manufacturing Purification
BS/BA in chemistry/life sciences
Exp: 0-2 years
This position is under direct supervision of the Group Leader. It is mainly responsible for the manufacturing of plasma products through protein precipitation/separation and other tasks involving plasma receipt, plasma pooling, and protein separation. The Protein Purification Manufacturing Technician will also clean and sanitize equipment before and after use, make and verify connections on flow panels, perform pH and conductivity measurements, performs chemical and buffer additions and may assist Group Leader in training other tech positions. 4/4/2020
857 Adma Biolgics
Boco Raton, FL
Document Assistant - Temporary
College enrolled or recent graduate
Exp: 1-2 years in document management
The Document Assistant will Create, format, revise and proof read controlled documents such as Standard Operating Procedures (SOPs), Forms, Validations, etc. from departments including but not limited to Quality Assurance, Manufacturing, Facilities, and Quality Control. Perform general office duties such as photocopying, word processing, filing, scanning, physical inventory, ordering supplies. 4/4/2020
858 Adma Biolgics
Boco Raton, FL
QC Lab Support Associate l
BS in biological/chemical/medical sciences
Exp: 1-3 years in regulated lab
The QC Lab Support Associate I will Performs cGMP laboratory support activities including Sample Accessioning, Product Reserve management, Temperature Monitoring of storage chambers, Glassware Cleaning, Supply Inventory management, etc. May also assist with Stability Studies and other QC initiatives. 4/4/2020
859 Adma Biolgics
Boco Raton, FL
Chemist I
BS in biological/chemical sciences
Exp: 0-3 years in lab setting
The Chemist I will Perform quality control testing of raw materials, in-process and final products; following general instructions on routine work and detailed instructions on new assignments. Perform quality control chemistry and/or Immunoassays for raw materials, in-process and final products according to approved Standard Operating Procedures (SOP’s). Perform instument calibration or qualification according to written procedures. 4/4/2020
860 Admera Health
South Plainfield, NJ
Associate Scientist I-PM (Non-Lab Position)
BS or MS in biological sciences
Exp: 1+ years in lab
Relay standard information on next generation sequencing applications to customers. Standard communication with prospective, current, and past customers. Co-coordinating multiple genomic projects with excellent documentation skills and communication to customers. Materials purchasing support for laboratory team 4/4/2020
861 Admera Health
South Plainfield, NJ
Regional Sales Manager-East Coast
BS/BA in biological/life sciences
Exp: 1 year with genomics/gemonics related
Achieve annual sales goals within defined territory/accounts through development, maintenance, and enhancement of customer accounts development, maintenance, and enhancement of customer accounts. Responsibility for managing all business accounts in assigned region/territory including implementing strategies in developing new growth of accounts. Drive the marketing process for the territory by creating a marketing plan, registering/planning/ attending local vendor shows, creating and working with Marketing and PM team to execute email campaigns 4/4/2020
862 Biotechne
Minneapolis, MN
Laboratory Production Assistant
HS Diploma/GED
Exp: 0-2 years
You will be responsible for assisting in the Clinical Controls Product Finishing Department with the bottling operation and the other activities involved in the product finishing process. Label product, operate the labeling equipment. Upon release of product by QA lab, count, verify and record number of finished products. Assist with monthly cleaning of clean room, including counters, laminer hoods, torque, labeler, sinks, and all work areas. 4/4/2020
863 Biotechne
Minneapolis, MN
Administrative Support / Shipping Assistant
HS Diploma/GED
Exp: 0-2 years
The responsibilities of this position are to support the DD OEM Accounts / Shipping Manager and Shipping Department’s activities by performing order processing, proofing, set assembly, shipping and other related duties. Order processing in our ERP System. Assist in preparing final shipping documents for OEM, International, Survey and Domestic shipments. Assist with maintaining Distributor, OEM and Survey customer orders and shipping records 4/4/2020
864 Biotechne
Minneapolis, MN
Lab Assistant
HS Diploma/GED
Exp: 0-2 years
The responsibilities of this position include processing raw biological materials for the use in manufacturing our products, maintaining and cleaning production equipment and containers, and completing required paperwork. Perform other duties as needed. Processes raw biological materials for the use in manufacturing our products. Maintains production equipment and containers 4/4/2020
865 Biotechne
Minneapolis, MN
Research Associate, Cell Culture and Stem Cell Media Operations
BS/BA in biological sciences
Exp: 0-2 years in lab
The main responsibility of this position it to maintain production of mouse embryonic fibroblasts. Additional responsibilities include media and supplement production, QC testing of methylcellulose-containing cell culture media, and cell culture of multiple cell lines. Perform additional duties as assigned. Preferred skills include cell culture, high attention to detail, strong communication and organizational skills. 4/4/2020
866 Adarza Biosystems
Maryland Heights, MO
Manufacturing Technician
BS to relevant sciences
Exp: 0-2 years in pharma
The position requires the ability to use and maintain delicate microarray equipment, training will be provided. Preferred candidates will have experience with laboratory automated systems, with a strong preference to individuals with silicon wafer processing and metrology systems (Cleaning, Etching, Optical Inspection and Ellipsometery) or experience in a related science discipline (biology, chemistry, biomedical engineering, or biochemistry). 4/4/2020
867 Adarza Biosystems
Maryland Heights, MO
Manufacturing Technician
BS to relevant sciences
Exp: 0-2 years in pharma
The position requires the ability to use and maintain delicate microarray equipment, training will be provided. Preferred candidates will have experience with laboratory automated systems, with a strong preference to individuals with silicon wafer processing and metrology systems (Cleaning, Etching, Optical Inspection and Ellipsometery) or experience in a related science discipline (biology, chemistry, biomedical engineering, or biochemistry). 4/4/2020
868 Merieux NutriSciences
Visalia, CA
Laboratory Technician Micro
AS/BS
Exp: 1+ year(s)
The incumbent prepares sample for processing and maintains documentation of process to facilitate analysis procedures. Job Duties: Read plates and tubes, as required, to determine the number of organisms in the sample. Record findings on worksheet for verification. Write identification onto plates so that client and sample number can be tracked. Pipette sample solution into tubes or plates according to the analysis process being performed. Pour the agar into plates or tubes to begin the growth process. Prepare sample for analysis by recording, weighing, and blending. Collect plates and place them in the incubator for the specified amount of time and temperature. Prepare media and broth for use in pathogen testing as required. etc. 4/1/2020
869 Merieux NutriSciences
Crete, IL
Customer Care Representative
BS/BA
Exp: 1+ year(s)
Be the primary interface for customers. Is responsible for a select group of accounts with responsibility for properly setting up and welcoming them, ensuring proper and timely communications are in place, and timely resolution of issues. Acts as the liaison between Customers and our labs, Technical Sales Managers and other functions as needed and assist in identifying new opportunities with existing customers and ensure new leads are properly routed to the Sales function. Job Duties: Provide exceptional Customer Service while following Mérieux NutriSciences’ policies and best practices. Build and maintain productive collaborative relationships within the department and across the organization to effectively support the customer. etc. 4/1/2020
870 Merit Medical
South Jordan, UT
Biological Safety Engineer I
BS in biomedical engineering or related
Exp: 1 year
Performs biological safety related tasks and assists with biomaterials characterization and analysis in our R&D environment. DAY TO DAY: Assists with developing test strategies and test plans for biomaterials used in Merit Medical products. Assists with writing biocompatibility sections of 510(k)s, PMAs, IDEs, etc. for regulatory submissions, both in the U.S. and global markets. Assists with writing no-test rationales for well known and understood biomaterials. Maintains database of scientific literature references and testing. Works with R&D teams and engineers. etc. 4/1/2020
871 Merit Medical
South Jordan, UT
Technician II
AS/AA
Exp: 1 year
Performs routine technical tasks including assembling or constructing simple or standard equipment or parts, and may service or repair simple instruments or equipment. ESSENTIAL FUNCTIONS PERFORMED: Conducts a variety of tests using established and clearly defined methods. 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. etc. 4/1/2020
872 Merit Medical
South Jordan, UT
Molding Operator II
HS diploma or equivalent
Exp: 1 year
This position is responsible for cosmetic part quality, dimensional charting, paperwork completion, and submission of molded component lots to Quality Assurance for final audit approval. ESSENTIAL FUNCTIONS PERFORMED: Performs start-up dimensions, as required. Submits daily lots to Quality Assurance for final audit. Packages and weighs the product and makes labels. Completes paperwork. Inspects parts visually and using measuring tools; documents results and ensures compliance to drawings and specifications; performs testing of products, as required. etc. 4/1/2020
873 Meso Scale Diagnostics
Gaithersburg, MD
Research Associate I, Immunoassay Development
BS in a life science
Exp: 1+ year(s)
A Research Associate I (RA I) is responsible for carrying out reagent and assay development activities in the laboratory, under supervision, working to achieve development project goals including data analysis and assay qualification. This is a laboratory position performing protein-based immunoassays on a routine basis with relatively high throughput (3-10 plates per day). Some degree of professional latitude, creativity and self management is expected. DUTIES AND RESPONSIBILITIES: Analyze and prepare reagent and product documentation, organize and procure reagents, perform experiments, analyze data and document results. Presentation of results. Participation in general lab maintenance including maintaining laboratory supplies and equipment. etc. 4/1/2020
874 Meso Scale Diagnostics
Gaithersburg, MD
Cell Culture Specialist I
BS in biology, chemistry, engineering or related
Exp: 6+ month(s)
Lab & Equipment: Manage and manipulate multiple cell lines (both adherent and suspension), which are primarily high maintenance mouse hybridoma cell lines for the production of monoclonal antibodies and other cell based products. Execute transfections for the production of recombinant QRM antibodies. Use, maintain and troubleshoot the following cell culture equipment: Hemocytometer, Biological Safety Cabinet, Automated Cell Counter, Plate Readers (for ELISA and BCA assays), LN2 Freezers, Humidified Incubators, Water Baths, CO2 Tanks, and Controlled Rate Freezer. Use, maintain and troubleshoot AKTA purification systems. Occasionally handle BSL2 reagents. Provide general cell culture laboratory maintenance. Keep process areas stocked with essential equipment and supplies. etc. 4/1/2020
875 Meso Scale Diagnostics
Gaithersburg, MD
Engineer I, Manuf
BS in engineering or related
Exp: 1+ year(s)
In this entry-level position, the candidate will develop and implement optimal, cost-effective manufacturing processes and methods in accordance with product specifications and quality standards; this will include recommendation for and implementing improvements to production designs, tools/fixtures, processes, methods and controls. The incumbent will coordinate and/or assist manufacturing launch for new or revised products. DUTIES AND RESPONSIBILITIES: Develop and implement optimal, cost-effective manufacturing processes and methods for company products in accordance with product specifications and quality standards. Recommend and implement improvements to production designs, processes, methods and controls. Coordinate the manufacturing launch of new/revised products including establishing goals, generation of assembly documentation, training of team members and evaluating results. etc. 4/1/2020
876 Analytical Lab Group
Concord, CA
Sample Receiving Technician
HS diploma or equivalent
Exp: 0-1 year
The Sample Receiving Technician performs tasks such as Certificate of Analysis preparation, sample pickup and sample log-in. Technical support is performed in accordance with standard operating procedures and adheres to documentation practices in accordance with ALG-West policies. Sample Receiving personnel are responsible for reporting any adverse or unusual events to management, as well as participates in process improvement activities as needed. etc. 4/1/2020
877 Analytical Lab Group
Concord, CA
Virology Associate
BS in a biological science or related
Exp: 1+ year(s)
The Virology Associate is responsible for sample chain of custody, sample processing, testing and data reporting using a variety of virology, cellular and molecular biology methods and techniques. The position requires excellent organizational skills along with good written and verbal communication skills in English. Testing is performed in accordance with standard operating procedures. The Virology Associate is capable of the following work tasks with minimal supervision: Maintains working knowledge of lab equipment and methodologies necessary to monitor operation and service condition of equipment. etc. 4/1/2020
878 Analytical Lab Group
Concord, CA
EM Technician
AS/BS
Exp: 1+ year(s)
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. Duties: Perform air sampling in cleanroom or laboratory areas. Collect and test microbial and chemical water samples. Collect and test compressed gas samples. Chemical cleaning and sanitization of equipment. etc. 4/1/2020
879 Midwest Institute for Clinical Research
Indianapolis, IN
Medical Research Study Coordinator
unspecified
Exp: 1-3 year(s)
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. 4/1/2020
880 Midwest Institute for Clinical Research
Indianapolis, IN
Medical Research Coordinator Associate
unspecified
Exp: 1-3 year(s)
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. 4/1/2020
881 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
882 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
883 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
884 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
885 Mizuho
San Antonio, TX
Field Service Engineer
AS/AA in an electrical or applied science
Exp: 1-2 year(s)
The Field Service Engineer (FSE) is primarily responsible for technical support, repairing and servicing Mizuho products in the field throughout the United States. The Field Service Engineer provides, highly visible, customer support through the performance of independent on-site service and repair of complex equipment and systems. To include but not limited to installation, troubleshooting, repair, and performance of preventive maintenance as required. Responsible for the inspection and operational quality and safety of Mizuho OSI products. May also instruct customers in the operation and maintenance of the system. Serves as company liaison with customers on administrative and technical matters for assigned projects. Interprets customers’ needs and assigns the responsibility for problem resolution to the appropriate resource. etc. 4/1/2020
886 Moderna
Cambridge, MA
Sr./Research Associate, Rare Diseases Research
BS/MS in biology, biochemistry, molecular biology or related
Exp: 0-3 years
Moderna is seeking a self-motivated and adaptable Research Associate/Sr. Research Associate with experience in performing in vitro and in vivo analyses to support the development of novel mRNA therapeutics. The candidate will support preclinical and clinical programs through the development and execution of biological and bioanalytical assays, and interface with internal as well as external partners and collaborators. This position will contribute to the Rare Diseases therapeutic area through the performance and development of laboratory-based assays for early research through development candidates of novel therapies. The individual will work with scientists within Rare Disease and other parts of the company to ensure the highest level of quality of the work. etc. 4/1/2020
887 Moderna
Norwood, MA
Research Associate, Pilot Development Lab
BS in a life science or engineering
Exp: 1-3 year(s)
Moderna is seeking a Research Associate for the Pilot Development Lab, based at their Norwood, MA site. The individual in this role will be part of a cohesive team responsible for producing Drug Substance, Drug Product and Sterile Fill production for development and toxicology. The successful candidate must demonstrate the ability to quickly master new processes and must have the drive to be part of a dynamic, fast paced, and highly motivated team. Ideally, the candidate will have training in chromatography, TFF, aseptic and sterile drug product filling techniques and proven ability to work with custom automation. This position will require excellent communication and organizational skills, as well as a focus on operational excellence and process optimization. Candidates are expected to collaborate between technical development groups, Preclinical, GMP Manufacturing and Supply chain. etc. 4/1/2020
888 Moderna
Norwood, MA
Sr/Research Associate, Process Development
BS in chemical engineering, chemistry, or related
Exp: 0-3 years
Moderna is working to develop first-in-class messenger RNA (mRNA) based medicines. Moderna is seeking a highly skilled and motivated process development research associate residing in Moderna’s Technical Development organization. This role will support the process development of Moderna’s first-in-class messenger RNA (mRNA) based medicines to enable our clinical supply. The applicant should have strong communication and collaboration skills, along with multiple examples of a strong technical background. The successful candidate must be able to work in a fast paced and highly dynamic environment, will have relevant academic and or industrial experience in large molecule bioprocessing, and will be able to contribute to both process development and commercialization related activities. etc. 4/1/2020
889 Moderna
Norwood, MA
Sr/Research Associate, Analytical Development
MS in biophysics, cell biology, chromatography or related
Exp: 1 year
Moderna is seeking a Research Associate/Sr. Research Associate for a position based at their Norwood, MA site. The individual in this role will be a highly skilled, talented and motivated analyst. He/she will participate in performing biochemical and biophysical characterization (HPLC, cIEF, light scattering, particle characterization, spectroscopy, calorimetry) of lipid nanoparticles, lipids and mRNA. He/she will also participate in the coordination of characterization/comparability studies and compile the data packages into reports to support advancement of Moderna’s development candidates. The individual will work with other RAs and Scientists within the Analytical Development, Analytical Operations, and Platform Analytics teams. etc. 4/1/2020
890 Moderna
Norwood, MA
Sr. /Research Associate, Molecular Biology
BS/MS in molecular biology, biochemistry, chemical engineering or related
Exp: 1-3 year(s)
Moderna is seeking a curious, detail-oriented research associate for a position based at their Norwood, MA site. The individual will participate in the synthesis and analysis of research scale material using novel processes in support of Moderna’s mRNA platform. Here’s What You’ll Do: Synthesize mRNA at different scales to support research activities throughout Moderna. Develop and apply novel processes for mRNA synthesis. Perform analyses using various types of instrumentation (HPLC, mass spectrometry, etc.). Perform research to support new assays and process improvements. Maintain scientific records of experiments and clearly communicate results. Maintain a clean and organized lab bench. Maintain equipment and instruments. etc. 4/1/2020
891 Moderna
Cambridge, MA
Sr./Research Associate, Process Development
BS in chemical engineering, chemistry, or related
Exp: 0-3 years
Moderna is working to develop first-in-class messenger RNA (mRNA) based medicines. Moderna is seeking a highly skilled and motivated process development research associate residing in Moderna’s Technical Development organization. This role will support the process development of Moderna’s first-in-class messenger RNA (mRNA) based medicines to enable our clinical supply. The applicant should have strong communication and collaboration skills, along with multiple examples of a strong technical background. The successful candidate must be able to work in a fast paced and highly dynamic environment, will have relevant academic and or industrial experience in large molecule bioprocessing, and will be able to contribute to both process development and commercialization related activities. We seek applicants that are proactive, enthusiastic, and show a passion for process development. etc. 4/1/2020
892 Moderna
Cambridge, MA
Workday Associate
unspecified
Exp: 1 year
Reporting to the Manager, Human Resources you will be responsible for supporting our HR Workday needs and processes. Are you someone who loves supporting business processes and pulling reports? Do you want to work in a highly digitalized environment? Do you enjoy simplifying people processes with technology? Then Moderna is the place for you. We are seeking someone who has previously used Workday and is a fantastic communicator. This person must understand that successful business processes within Workday matter and that these processes are integral to the success of Moderna! Here's What You’ll Do: Partner with the HR team to understand their Workday needs. Help optimize Workday Business Processes, so they are simple and easy to understand. etc. 4/1/2020
893 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
894 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
895 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
896 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
897 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
898 Mylan
Morgantown, WV
Associate Electronic Submissions
AS/AA
Exp: 1+ year(s)
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: Performs moderately complex submission building, compilation, publishing and validation of receipt associated with generating hard copy and electronic (eCTD, NeeS, etc.) submissions to global health authorities. Prepares and completes a variety of simultaneous submission compilation activities including utilization of publishing tools (e.g. Lorenz docuBridge, ISIToolbox) for electronic and paper submission generation, scanning, QA/QC for document standards, and electronic/paper archiving. etc. 4/1/2020
899 MyoKardia
Brisbane, CA
Scientist I, Pharmacology
MS in physiology, pharmacology, biochemistry, or related
Exp: 0-2 years
ESSENTIAL DUTIES AND RESPONSIBILITIES: Work with colleagues in pharmacology to gain an understanding of primary and secondary pharmacologic mechanisms, biomarkers, translational potential, and safety for discovery- as well as development-stage programs. Implement appropriate clinically-relevant in vivo small animal models to study cardiovascular physiology and pharmacology. Design, execute, and summarize results from studies with novel small molecules that demonstrate detailed proof of mechanism. Establish PK/PD relationships in non-clinical species. Conduct and document studies to support proposed clinical indications (i.e. combination studies, label expansion). Serve as a pharmacology representative for cross functional project teams. etc. 4/1/2020
900 NAMSA
Irvine, CA
Microbiolgy Technologist
BS/BA
Exp: No experience necessary for BA/BA candidates
Principal Duties and Responsibilities: May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. Accurately collects and records raw data in logbooks and on worksheets. 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. May be required to operate autoclave, depyrogenation oven or other specified laboratory equipment. etc. 4/1/2020
901 NAMSA
Brooklyn Park, MN
Animal Care Technician
HS diploma or equivalent
Exp: 0-2 years
Principal Duties and Responsibilities: Primarily involved in the welfare and husbandry activities of animals, including sanitation of equipment and the vivarium. Receives, identifies, and acclimates laboratory animals. May euthanize animals. May administer medications under the direction of a Veterinarian. Follows the Quality Manual, all NAMSA SOPs, and Process documents. Documents all required tasks. May administer treatments as directed by staff veterinarian. etc. 4/1/2020
902 NAMSA
Northwood, MA
Animal Care Technician
HS diploma or equivalent
Exp: 0-2 years
Principal Duties and Responsibilities: Primarily involved in the welfare and husbandry activities of animals, including sanitation of equipment and the vivarium. Receives, identifies, and acclimates laboratory animals. May euthanize animals. May administer medications under the direction of a Veterinarian. Follows the Quality Manual, all NAMSA SOPs, and Process documents. Documents all required tasks. May administer treatments as directed by staff veterinarian. May conduct training on husbandry tasks for other Associates and update training records. etc. 4/1/2020
903 NAMSA
Northwood, MA
Chemist
MS
Exp: No experience necessary for MS candidates
Principal Duties and Responsibilities: Independently conduct testing according to written instructions. May be requested to conduct more involved studies. May perform USP and EP monograph testing activities using wet chemical and analytical instrumentation. May conduct routine testing per NAMSA SOPs as well feasibility, protocol driven methodology, and/or method verifications on at least one of the following instrument types: HPLC, GC, or ICP, etc. Works with management to ensure large studies are completed on or before the due date. Prepare and maintain the reagents required for testing. May mentors and train staff in general laboratory testing as well as offering more complex instrumentation training. etc. 4/1/2020
904 Merck KGaA
Urbana, IL
Production scientist, associate
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. etc. 4/1/2020
905 Merck KGaA
Carlsbad, CA
Quality Analyst 1
BS/BA in life sciences
Exp: 1 year
As a Quality Analyst 1, you will support the comprehensive quality activities, including entering, tracking and trending Environmental Monitoring (EM) data, managing timelines while ensuring the production environment is in a state of readiness. The role will entail operating in a fast-paced, highly dynamic environment with multifunctional groups/departments, including both internal and external stakeholders as needed. As a Quality Analyst, you will support the daily operations of the Microbiology/EM and Manufacturing processes and fills. You will need to complete documentation, data entry, and data review for EM data in a timely manner. Ensure that all required documentation including records and log books, is complete and entered in the timely manner and accurate according to the current GMP rules. etc. 4/1/2020
906 Miltenyi Biotec
Gaithersburg, MD
Accounting Associate - Accounts Payable
AS/AA
Exp: 1-3 year(s)
As a member of the Miltenyi Biotec Accounting team, you will work closely with Accounting leadership to assist in a variety of accounting functions focused on Accounts Payable. Your duties would include reconciling back-up documents to invoices, processing invoices through receipt and account verification, maintaining vendor and accounting files. 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. etc. 4/1/2020
907 Miromatix
Eden Prairie, MN
R&D Operations Technician
HS diploma or equivalent
Exp: 1-2 year(s)
Miromatrix is a biotechnology company on a mission to save and drastically improve countless lives by eliminating the organ transplant waiting list. Through our proprietary perfusion decellularization and recellularization technology, we are bioengineering human livers and kidneys to solve the large unmet clinical need that exits today. Miromatrix has an immediate opening for a highly motivated R&D Operations Technician at our Eden Prairie, MN facility. Primary duties include: Works with facility manager/supervisor to ensure clean room facilities are cleaned according to cGMP requirements. Performs various support functions using proper procedures to meet cGMP cleaning requirements. Maintains and cleans equipment and the facility; maintains and restocks supplies; strong attention to detail is essential while dealing with multiple tasks. Additional cleaning (i.e.,emergency cleanups, construction cleanups, and room set-ups) will need to be performed on an as needed basis. etc. 4/1/2020
908 Aiomed
Danvers, MA
Clinical Research Associate I
BS/BA in life sciences
Exp: 1 years in field monitoring
Reporting to the Manager of Clinical Research Associates, the person in this role is responsible for the management of day-to-day aspects of investigational site activities on assigned clinical trials. The CRA should ensure compliance with international guidelines, local regulations and corporate policies and procedures. Conduct reviews of documentation needed for internal and external audits to ensure all essential clinical Trial Master File (TMF) documents are compliant with Good Documentation Practices, Abiomed internal SOPs, and US and OUS regulations 3/29/2020
909 AbSci
Vancouver, WA
Purification - RA I/II
BS or MS in biochemsitry
Exp: 1+ years in industry
The Research Associate I/II will join our purification team and will play a significant role in purification of protein biologics. Core responsibilities include maintaining and operating chromatography instrumentation, (e.g., AKTA Pure, HPLC, etc.),conducting hands-on research for development of new techniques, and supporting ongoing protein purification activities. Develop and execute techniques to extract and purify protein biologics from SoluPro, AbSci’s proprietary E. coli expression platform 3/29/2020
910 Accelerate Diagnostics
Tucson, AZ
Research Associate, Quality Control
BS in chemical/biological sciences
Exp: 1+ years in lab/research
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. 3/29/2020
911 Accelerate Diagnostics
Tucson, AZ
Manufacturing Technician
HS Diploma/GED
Exp: 1 year in manufacturing
The Manufacturing Technician will perform a variety of processing duties according to Batch Records (BRs) and Manufacturing Work Instructions (MWIs) in a cGMP environment for the Consumable Manufacturing Department including, but not limited to: Cleaning/recovery of classified area and work spaces, components preparation . Aseptic filling . Final Consumable Inspection 3/29/2020
912 AccuraGEn
Menlo Park, CA
Research Associate/Senior Research Associate
BS/MS in biological sciences
Exp: 1+ years in industry/academia
Plan, execute and interpret experiments; Analyze data, evaluate results, form conclusions, and recommend future experiments; Ensure accurate and consistent recording of experiment methods, materials and results; keep a high-quality laboratory notebook; Communicate and work efficiently with other groups within R&D team; 3/29/2020
913 Accuray
Madison, WI
Production Technician
Associates Degree
Exp: 1-3 years in manufacturing or engineering
The Production Technician is responsible for producing and testing components by assembling parts and subassemblies in manufacturing that will allow Accuray to provide products that meet customer needs and in accordance with regulatory requirements. Prepares work to be accomplished by gathering parts, subassemblies, tools, and materials required per job order. Assembles components per work instructions and tests product as required using test equipment and fixtures. 3/29/2020
914 Acell
Columbia, MD
Biotechnician
HS Diploma/GED
Exp: Entry LEvel
This is an entry level position for a Biotechnician. Employee will carry out manufacturing practices in a cGMP biotechnical facility. The job involves the manual processing of porcine urinary bladders, which includes all aspects from collection of raw materials to packaging of the final product. Following training, work will be expected to be performed independently to a high degree of standard in biomaterial handling. 3/29/2020
915 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
916 Acorda Therapeutics
Chelsea, MA
Process Mechanic - HVAC
HS Diploma/GED
Exp: 0-2 years
The Process Mechanic HVAC I is responsible for performing and documenting the required maintenance and monitoring of the facility, systems, and equipment in a cGMP facility. The required duties include preventative and corrective maintenance on the facility’s mechanical system, operation of the facility's HVAC, installation of new equipment, general plumbing, electrical work, building grounds work and other duties as assigned. 3/29/2020
917 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
918 Aurolife Pharma
Dayton, NJ
QA Documentation Associate
BS/BA
Exp: 1-2 years in GMP related industry
Person will be responsible for the activities related to QA Documentation department related to Batch record issuance, Reconciliation of documents, Issuance of Control documents, file training record in company wide training folder of each employee. Maintain the Manufacturing and Packaging Batch Record Master Hard copy and Pdf soft copy. 3/29/2020
919 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
920 Aurolife Pharma
East Windsor, NJ
Automation Engineer
BS or MS in electrical/mechanical engineering
Exp: 1-2 years
The role of the AutomationEngineer is to ensure that all the Automated Storage and Retrieval System (ASRS), the associated features, and procedures of the Warehouse Control System are aligned and operational to ensure business continuity. The position works closely with key functional groups of Warehouse Operations and Projects to work on the new requirements and enhancements and take up continuous improvement projects to drive the operational efficiencies of the system. Apart from warehouse operations the position should work on the L3, L4 systems integration of DSCSA (Drug Supply Chain Security Act) Serialization requirements with the packaging team. 3/29/2020
921 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
922 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
923 Abeona Therapeutics
Cleveland, OH
Associate, Inventory Control
BS/BA in biological sciences
Exp: 1 year in manufacturing
The Inventory Control Operator is a critical role supporting the GMP Manufacturing, Process and Assay Development and Quality Control functions at Abeona. This individual will support and lead the organization and management of inventory encompassing the receiving, quarantine and release spaces. The ICO will ensure adequate inventories of all supplies (several hundred different SKUs) for Manufacturing during clinical trials, initial commercial process, for process and assay development activities, cleaning of Manufacturing facilities and gowning of Manufacturing associates. 3/29/2020
924 Abeona Therapeutics
Cleveland, OH
Associate, Quality Control
BS in biological sciences
Exp: 0-4 years
Abeona is looking for a Quality Control Associate to join our team in Cleveland, OH. The successful candidate is a key part of our growing QC Team and will be primarily responsible for performing routine laboratory activities in support of GMP testing for Quality Control. Testing includes raw material, packaging components, environmental monitoring, in-process and finished product. Interacts with employees internal and external to Quality Control. 3/29/2020
925 Abzena
San Diego, CA
Lab Services Associate
HS Diploma/GED
Exp: 1 year in lab
Provides maintenance of laboratory equipment. Maintains proper laboratory cleanliness and organization. Operates to the highest ethical and moral standards. Complies with Abzena’s policies and procedures.Adheres to all safety standards and protocols. 3/29/2020
926 Aurolife Pharma
East Windsor, NJ
Manufacturing Operator
Associates in engineering/STEM
Exp: 1-3 years in batch manufacturing
Manufacturing Associate is to perform all required Batch manufacturing, equipment cleaning, area cleaning, in- process testing & sampling for Manufacturing batches. Perform maintenance and troubleshooting of the equipment and machinery. Perform verifications using special instruments (pH meter, DO meter, Balance, etc.) Other Job Duties: Provide on-going technical support for manufacturing operations after project installation. 3/29/2020
927 zPredicta
San Jose, CA
Laboratory Technician
BS/BA in life sciences
Exp: 0-1 years in lab
To be successful, you have to be excited to support the fast-paced environment of a start-up, be engaged while performing multiple roles, and possess a desire to learn. Responsibilities include: Cell culture, Maintenance of lab safety records, Purchasing and procurement 3/28/2020
928 Zymergen
South San Francisco, CA
Chemistry Associate, Polymer Characterization
BS in polymer/material sciences
Exp: 1-2 years in polymer characterization
The ideal candidate has a strong technical background in polymer science with industrial materials R&D experience in polymer characterization. Familiarity with automation of data analysis and development of application testing for polymers is a strong plus. Execute our polymer characterization R&D efforts focused on our film products. Support lab safety, maintain and promote safe work practices 3/28/2020
929 Zymo Research
Irvine, CA
Research Associate
MS in life sciences
Exp: 0-2 years
The incumbent will have demonstrated clear leadership potential with ability to efficiently multi-task and manage a scientific research project, starting from the initial idea through to completion and publication in a peer-reviewed journal. Duties include: Assist in experimental design. Conduct complex, high-level scientific research activities. Interface with Principal Investigator to analyze experiments. Optimize experimental procedures. 3/28/2020
930 Zymo Research
Irvine, CA
Customer Service Associate
HS Diploma/GED
Exp: 0-2 years
The Customer Service Associate mainly processes orders via online, phone, fax, and emails. Other non- ordering job functions include interaction with customers to provide and process information in response to inquiries, concerns and requests about products and services. Receive and process customers’ orders - Main job function 3/28/2020
931 Zymo Research
Irvine, CA
Technical Manufacturing and QC Associate
BS in life/biological sciences
Exp: 1-2 years in research
Assist in the manufacturing of various chemicals, buffers, and other product-related components to ensure consistent product performance. Responsible for conducting quality control tests on various chemicals, buffers, and other product-related components. Initiate and implement appropriate experiments according to the SOP in order to accept or reject the release of product(s) and other related product components. 3/28/2020
932 Zynex Medical
Queens, NY
Medical Device Sales 1121 - Addressing the Opioid Crisis
BS/BA
Exp: Previous sales experience a plus but not necessary
We are seeking individuals who are self-confident, self-starting, resourceful, assertive, and persuasive. Must be able to build loyalty with clinicians and doctors developing a prescription-based stream of business. You will generate prescriptions from physical therapists and doctors for our NexWave pain management device, which is an alternative to opioid pain medication. This is an autonomous position that requires you to be independent and dedicated to becoming an outstanding medical device sales representative that services physical therapy clinics, pain management clinics, orthopedic surgical groups and other medical providers. 3/28/2020
933 Zynex Medical
Pasadena CA, 
Medical Device Sales 2027 - Addressing the Opioid Crisis
BS/BA
Exp: Previous sales experience a plus but not necessary
We are seeking individuals who are self-confident, self-starting, resourceful, assertive, and persuasive. Must be able to build loyalty with clinicians and doctors developing a prescription-based stream of business. You will generate prescriptions from physical therapists and doctors for our NexWave pain management device, which is an alternative to opioid pain medication. This is an autonomous position that requires you to be independent and dedicated to becoming an outstanding medical device sales representative that services physical therapy clinics, pain management clinics, orthopedic surgical groups and other medical providers. 3/28/2020
934 Zynex Medical
Buena Park, CA
Medical Device Sales 2038 - Addressing the Opioid Crisis
BS/BA
Exp: Previous sales experience a plus but not necessary
We are seeking individuals who are self-confident, self-starting, resourceful, assertive, and persuasive. Must be able to build loyalty with clinicians and doctors developing a prescription-based stream of business. You will generate prescriptions from physical therapists and doctors for our NexWave pain management device, which is an alternative to opioid pain medication. This is an autonomous position that requires you to be independent and dedicated to becoming an outstanding medical device sales representative that services physical therapy clinics, pain management clinics, orthopedic surgical groups and other medical providers. 3/28/2020
935 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
936 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
937 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
938 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
939 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
940 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
941 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
942 Abbott
Plymouth, MN
Operator I
HS Diploma/GED
Exp: 6 months or more in medical company
We are seeking an experienced, high caliber Operator I. This position is responsible for the production of high quality medical devices within a manufacturing cell. This position includes detailed assembly and operation of various equipment and machinery. Ensure that relevant job documentation for cell operations and functions is accurate and up to date - Troubleshooting skills - Interpersonal skills such as conflict resolution, active participation, active listening, Interpreting, cooperation and flexibility to allow for a successful self-managed team 3/28/2020
943 Abbott
St. Paul, MN
Quality Engineer I - Operations
BS in engineering or technical field
Exp: 0-2 years
This position is responsible for developing and maintaining quality engineering methodologies and providing quality engineering support within new product development, manufacturing, or system/services support. Identify and implement effective process control systems to support the development, qualification, and on-going manufacturing of products to meet or exceed internal and external requirements. Lead in the implementation of assurances, process controls, and CAPA systems designed to meet or exceed internal and external requirements 3/28/2020
944 Abbott
Alameda, CA
Quality Assurance Specialist
BS in engineering or life/physical sciences
Exp: 1-2 years in pacing industry
Working under direct supervision, provides education support to the Technical Service staff. Provides training to department for new hires, progression training, product launches, and field corrective actions. Provides periodic quality reviews of department calls and documentation. Identifies and routinely uses the most effective, cost efficient and best business practices to execute processes; continually evaluates their effectiveness and appropriateness. Exercise judgment in planning, organizing and performing work; monitors performance and provides solutions for performance improvement. 3/28/2020
945 Abbott
Sylmar, CA
Operator I
HS Diploma/GED
Exp: 6 months
Briefly state the main purpose and scope of the job. Working under close supervision, may perform a combination of assembly, weld, x-ray, repair, and test operations on pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical device assemblies. Performs routine assignments according to specified and/or standardized procedures. Work is closely and continually reviewed. 3/28/2020
946 Abbott
St. Paul, MN
R&D Engineer, I
BS in mechanical engineering, material science, or related
Exp: 1-2 years in design/manufacturing
The R&D Engineer I will use multidisciplinary engineering knowledge to contribute to a team designing and developing innovative medical devices or components/subsystems in the dynamic structural heart space where Abbott is a leading provider of solutions. Candidate will be responsible for providing engineering support in the creation and development of new medical device products as well as the support of established commercial medical device platforms in the heart valve space. 3/28/2020
947 Abbott
Sylmar, CA
Electrical Development Quality Engineer I
BS in electrical/system engineering, or physics
Exp: 0-2 years
Responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success by protecting patient/user safety and meeting business needs. Support and ensures the proper prediction of, and the ultimate product performance of the electrical system. Support on-time execution of Quality Plans for internal development, OEM-based and design change projects. Evaluates product design to identify potential design issues and drive technical decisions 3/28/2020
948 Abbott
Alameda, CA
Complaint Investigation Technician
HS Diploma/GED
Exp: 1-2 years
Safely perform routine testing and receiving of returned products due to customer complaints and be able to document investigation activities clearly and accurately in a timely manner. Adhere to procedures and work instructions throughout. Be able to handle multiple tasks effectively and efficiently. Understand the priorities of investigation as outlined in the procedures and as assigned by the laboratory supervisor. 3/28/2020
949 Abbvie
Lake County, IL
Associate Scientist I/II, Engineering - Technical Operations
BS or MS in chemical engineering
Exp: 0-3 years
This position will serve as a liaison between the Process Research and Development scientific functions and the API Pilot Plant organization. The successful candidate will assist in the optimization and scale-up of synthetic processes and facilitate the implementation of the processes and new technologies in to the API Pilot Plant. The Scientist will also provide technical oversight during production campaigns and will support technical transfer to the ultimate commercial manufacturing site. 3/28/2020
950 Abbvie
South San Francisco, CA
Associate I/Associate II, In Vivo Pharmacology
BS or MS
Exp: 0-3 years in industry
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. 3/28/2020
951 Abcam
Cambridge, MA
Logistics Technician
HS Diploma/GED, BS/BA preferred
Exp: Entry Level
Process incoming shipments from suppliers, ensuring accuracy of all product data. Aliquot product into vials and assemble kits for customer orders and global stocking. Work with colleagues across the business to resolve discrepancies quickly. Maintain accurate inventory levels using both manual and automated systems. Fulfill customer orders using internal systems and processes, ensuring accuracy of all products in all orders. 3/28/2020
952 Abcam
Cambridge, MA
Lab Technician - Protein Scientist
Associates Degree
Exp: 1 year
Abcam is looking for a Lab Technician to join our team in Cambridge MA, working to support the Protein Science team in the development of standalone recombinant products at Abcam. Perform routine laboratory tasks, including glass wash, autoclaving, media and buffer preparation, centrifugation, ordering/inventory management, and vialing/labeling of protein samples. Communicate clearly with team members within the Protein Sciences Group, providing delivery dates and the necessary documentation as for activities. 3/28/2020
953 Abcam
Milpitas, CA
Molecular Research Associate
BS in molecular sciences or related
Exp: 1 year in lab
Following the acquisition of gene editing platform and oncology product portfolio of Applied StemCell Inc, we are now looking to expand the team as we look to become a leader in the cell engineering field. With this in mind, we are recruiting for a Research Associate to join our Molecular team. Conduct projects and experiments for genotyping and gRNA validation using multiple approaches, including PCR, Sanger sequencing, NGS, QPCR, ddPCR, Surveyor Assay, or any other assays as needed 3/28/2020
954 Abcam
Milpitas, CA
Cell Science Research Associate
BS in cell biology
Exp: 1 year in lab
Following the acquisition of gene editing platform and oncology product portfolio of Applied StemCell Inc, we are now looking to expand the team as we look to become a leader in the cell engineering field. With this in mind, we are recruiting for a Research Associate to join our Cell Engineering team. Perform cell engineering using CRISPR technology for service type cell-based projects. Generate and maintain modified cancer, iPSC and other cell lines in BSL-2 level laboratory environments 3/28/2020
955 Abcam
Eugene, OR
Batch Production Research Associate
BS in biological sciences
Exp: 1 year in biotech
Our facility in Eugene is responsible for the replenishment of a catalog of more than 2000 products for customers that expect high quality and a high degree of consistency between batches. Follow documented manufacturing work instructions. Comply with our Good Documentation Practices (GDP). Maintain physical and digital raw material, intermediate, bulk, and finished good inventory. 3/28/2020
956 Abcam
Branford, CT
Research Associate
BS in biological sciences
Exp: 1-3 years lab experience
The Custom Services Department is responsible for the development of best in class antibodies using wide variety of antibody discovery pipelines and extensive suit of antibody characterization assays. Execute experiments under direction of supervisorWork as part of the team to implement experimental plans support data management: ensure the recording and analysis of all processed data in a timely manner, with appropriate population of laboratory notebooks and data management systems 3/28/2020
957 3T
Menlo Park, CA
Research Associate
MS in life sciences
Exp: 0-2 years
Protein engineering to support TCR-T cell programs, and identify compounds with optimal therapeutic index. TCR engineering for improved efficacy, and specificity. Performing cell-based assays to test prospective optimized leads. Discovery of TCR mimetic (mTCR) compounds that bind selectively to pMHC targets identified at 3T. Improvement of existing yeast display platforms and development of next-generation pMHC libraries. 3/28/2020
958 MabPlex
San Diego, CA
Process Development Engineer/Associate
MS in a science or engineering discipline
Exp: 1+ year(s)
This is an intermediate experienced engineer/associate position that will play an important role in developing stable cell lines and robust cell culture processes to be used in clinical manufacturing. Experience will dictate the exact title. The position will report to the Manager of Cell Line Development. Essential Job Responsibilities: Develop stable cell lines. Host cell transfection with target plasmid. Minipool screening and single-cell cloning. Shake flask fed-batch studies to support stability studies and top clone selection. etc.This is an intermediate experienced engineer/associate position that will play an important role in developing stable cell lines and robust cell culture processes to be used in clinical manufacturing. Experience will dictate the exact title. The position will report to the Manager of Cell Line Development. Essential Job Responsibilities: Develop stable cell lines. Host cell transfection with target plasmid. Minipool screening and single-cell cloning. Shake flask fed-batch studies to support stability studies and top clone selection. etc. 3/25/2020
959 Mallinckrodt Pharmaceuticals
Hobart, NY
Packaging Operator I
HS diploma or equivalent
Exp: 3-12 months
Packaging Line Operator is responsible for tending machines and conveyors at various stages of the packaging line to maintain efficient, continuous packaging of the product for shipment. Essential Functions: Components are in Place and Filled: Sets up assigned station(s) on the line including assembly of basic equipment and preparing materials needed (e.g. bottles, caps, cotton, etc.). Tends/operates station(s) during production run to insure proper operation and keep station filled with supplies or product. Weighs product at various stages of the packaging process. Performs checks/tests required for applicable station(s). Adjusts containers/materials for proper placement and remove defective pieces. Starts and stops equipment when required. Performs hand-packaging and material-handling functions. Collects all process related hazardous wastes and transports to accumulation drums. etc. 3/25/2020
960 Mallinckrodt Pharmaceuticals
Hobart, NY
Blending Technician I - C shift
HS diploma or equivalent
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. etc. 3/25/2020
961 Mallinckrodt Pharmaceuticals
Hobart, NY
Blending Technician I - D shift
HS diploma or equivalent
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. etc. 3/25/2020
962 Mallinckrodt Pharmaceuticals
Hobart, NY
Manufacturing Assoc I - 3rd Shift
HS diploma or equivalent
Exp: 3-12 months
Processes active compound materials into final tablet form performing quality control checks to maintain consistency of product according to manufacturing specifications. 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 Manufacturing Associate 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. etc. 3/25/2020
963 Mallinckrodt Pharmaceuticals
Hobart, NY
Manufacturing Assoc I - 2nd Shift
HS diploma or equivalent
Exp: 3-12 months
Processes active compound materials into final tablet form performing quality control checks to maintain consistency of product according to manufacturing specifications. 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 Manufacturing Associate 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. etc. 3/25/2020
964 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
965 MaxCyte
Gaithersburg, MD
Research Associate
BS in a biological science
Exp: 1 year
The Research Associate is part of a team that works on cell loading technologies with applications that include gene and cell therapy and protein production. This individual executes a variety of laboratory procedures to ensure timely completion of the company's scientific objectives and customer requirements. This individual also provides lab support to scientists working with customers in the field. Works under general supervision. Job Duties: Performs general molecular techniques such as plasmid purification, gel-electrophoresis, DNA/RNA isolation, Western blot, Elisas, basic cell transfection experiments, and basic flow cytometry. etc. 3/25/2020
966 McGuff Pharmaceuticals
Santa Ana, CA
Manufacturing Technician - Evening Shift
unspecified
Exp: Entry level
McGuff Pharmaceuticals, Inc. currently has an opening for a Manufacturing Technician within our production facility located in Santa Ana, CA. This position reports to the Production Supervisor. The candidate must be detail-oriented, results-oriented, possess good communication and writing skills, capable of performing assigned production duties and flexible in adapting to changing work priorities. etc. 3/25/2020
967 MedPace
Cincinnati, OH
Compensation Analyst
BS/BA in business administration, accounting, human resources or related
Exp: Entry level
Medpace is a Clinical Research Organization (CRO) that is rapidly growing across the world. Due to our recent growth, we are in need of qualified and focused driven individuals, like yourself. This is a critical role in our continuously-growing Human Resources department, where you will be part of a dynamic, fast-paced work environment. As a Compensation & Benefits Analyst, you will be able to use your finely tuned skills to help accomplish task that are instrumental to the company’s growth. etc. 3/25/2020
968 MedPace
Cincinnati, OH
Audit Associate
AS/AA in a business related field
Exp: Not necessary for AS/AA candidates
Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach. We leverage local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 2,700 people across 36 countries. etc. 3/25/2020
969 MedPace
Cincinnati, OH
Automation Test Engineer
unspecified
Exp: 1+ year(s)
Voted a Top Cincinnati Workplace for 4 years running, Medpace is growing rapidly, and we are currently seeking a full-time, office-based Software QA Tester to join our Information Technology (IT) team. The Software QA Tester position is a vital role whose success relies upon your knowledge, experience, and dedication. The Medpace IT department delivers software solutions that enable and empower both internal and external customers to manage their business processes most effectively and efficiently. Our Software QA Testers ensure these custom solutions are designed, built, and implemented correctly. etc. 3/25/2020
970 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
971 LabCorp
Miami, FL
Technologist [University of Miami]
BA/BS in biology, chemistry, medical technology, or related
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 Technologist in Miami, FL. In this position, you will work in a fast paced, customer focused, and challenging environment. etc. 3/25/2020
972 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
973 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
974 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
975 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
976 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
977 Merieux Nutrisciences
Allentown, PA
Microbiologist I
unspecified
Exp: 1-2 year(s)
We are looking for a Microbiologist I. 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. Follow appropriate methods and SOPS on all tasks. Maintain quality control records. Read, calculate, record data in Laboratory Information Management System. Perform rapid test methods. etc. 3/25/2020
978 Merieux Nutrisciences
Allentown, PA
Lab Assistant
unspecified
Exp: No experience necessary
The Technician we are looking for has… - The ability to work collaboratively, as a member of a team, to achieve a common goal. - A desire to protect themselves, their friends and family, and the entire world from illness caused by foodborne pathogens. - The flexibility and productivity to work in a fast paced, often varied environment. - A strong sense of pride in achieving accurate, timely, and consistent results in their work. etc. 3/25/2020
979 Merieux Nutrisciences
Columbus, OH
Micro Tech
unspecified
Exp: Entry level
We are looking for a Micro Tech. Your missions will be to: Prepare samples for processing and maintains documentation of process to facilitate analysis procedures. This position requires weekend work. The Laboratory Technician we are looking for has… - The ability to work collaboratively, as a member of a team, to achieve a common goal. - A desire to protect themselves, their friends and family, and the entire world from illness caused by foodborne pathogens. - The flexibility and productivity to work in a fast paced, often varied environment. - A strong sense of pride in achieving accurate, timely, and consistent results in their work. etc. 3/25/2020
980 Merieux Nutrisciences
Allentown, PA
Microbiology Technician
unspecified
Exp: Entry level
Prepares sample for processing and maintains documentation of process to facilitate analysis procedures. Job Duties: Read plates and tubes, as required, to determine the number of organisms in the sample. Record findings on worksheet for verification. Write identification onto plates so that client and sample number can be tracked. Pipette sample solution into tubes or plates according to the analysis process being performed. Pour the agar into plates or tubes to begin the growth process. Prepare sample for analysis by recording, weighing, and blending. Collect plates and place them in the incubator for the specified amount of time and temperature. etc. 3/25/2020
981 Merieux Nutrisciences
Madison, WI
Microbiology Technician
unspecified
Exp: Entry level
Mérieux NutriSciences is dedicated to improving food safety and quality though nutritional research, scientific excellence and innovation at every step of the food supply chain. Our team of scientists and technicians is committed to providing our clients with accurate results, delivered on time, with uncompromising ethics, honesty, personal integrity and confidentiality. NO PREVIOUS LABORATORY EXPERIENCE REQUIRED. Your Mission: 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. etc. 3/25/2020
982 Merieux Nutrisciences
Stone Mountain, GA
Micro Tech
unspecified
Exp: No experience necessary
We are looking for a Micro Tech: The ability to work collaboratively, as a member of a team, to achieve a common goal. A desire to protect themselves, their friends and family, and the entire world from illness caused by foodborne pathogens. The flexibility and productivity to work in a fast paced, often varied environment. A strong sense of pride in achieving accurate, timely, and consistent results in their work. etc. 3/25/2020
983 Mammoth Biosciences
San Francisco, CA
Research Associate - Genome Editing
BS in a relevant field
Exp: 1+ year(s)
Mammoth is seeking a Research Associate with experience in tissue culture and genome editing. The ideal candidate will have experience working with genome editing technologies. Strong candidates for this role will also have experience with molecular biology and cloning. Understanding of CRISPR systems and their applications is a plus. Responsibilities: Work directly with Scientists and Research Associates to develop new CRISPR tools. Establish and maintain mammalian cell lines. Analyze genome editing outcomes with NGS and flow cytometry. etc. 3/25/2020
984 Mammoth Biosciences
San Francisco, CA
Research Associate - Assay Development
BS/MS in biology, chemistry, or related
Exp: 1+ year(s)
Mammoth is seeking a Research Associate experienced in protein and nucleic acid biochemistry techniques to support our research and product development teams. The ideal candidate will have experience with in vitro assay development, nucleic acid extraction and amplification techniques. Further, the candidate will be comfortable working as part of a team, be highly motivated, and display excellent time management skills. etc. 3/25/2020
985 Maverick Therapeutics
Brisbane, CA
Research Associate, Cell Biology & Assay Development
BS/MS
Exp: 0-3 years
This position will involve the development of in vitro assays to characterize lead clinical candidate molecules in drug development. It will primarily focus on developing both immunochemical assays and cell-based assays to support the development of preclinical pipeline products. Additional responsibilities may include testing early pipeline molecules in established in vitro assays and/or developing novel in vitro assays to support mechanism of action studies. Key Responsibilities: Execute assigned tasks following appropriate laboratory/technical procedures under minimal supervision. etc. 3/25/2020
986 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
987 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
988 Lipocine
Salt Lake City, UT
Associate Scientist
BS/MS in a life science, chemical engineering, or related
Exp: 1-3 year(s)
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. 3/24/2020
989 Liquidia Technologies
Morrisville, NC
Associate Scientist
BS in relevant scientific field
Exp: 0-2 years
This is a laboratory-based position where the candidate will have the opportunity to leverage Liquidia’s PRINT® technology in the development of new pharmaceutical products. In this role, the candidate will be responsible for supporting preclinical and early clinical formulation development focusing on inhalation powders. Specific Duties, Activities, and Responsibilities: Work with manager and team members to design and evaluate new product formulations. Use experimental design principles to optimize formulation composition and identify early manufacturing process. Support manufacture of material for formulation development as well as preclinical and early clinical studies. etc. 3/24/2020
990 Liquidia Technologies
Morrisville, NC
Manufacturing Technician - Temporary to Permanent
BS
Exp: 0-2 years
The Manufacturing Technician (Temporary to Permanent) will perform routine running of manufacturing equipment to support production and R&D efforts. This role will provide feedback to engineering and scientific staff on process performance and ideas for process improvement. Responsibilities: Responsible for running manufacturing equipment to support production and R&D efforts. Collect samples for in-process testing and complete test and inspection activities. Monitor the manufacturing process, recording observations and key run parameters as needed, and adjusting the process as necessary within the defined process window. etc. 3/24/2020
991 Locus Biosciences
Research Triangle Park, NC
Research Associate
BS/MS in microbiology, synthetic biology, genetic engineering, or related
Exp: 6-24 months
Locus Biosciences is seeking a highly motivated and entrepreneurial applicant to join our research and development team as a full-time Research Associate. This position is well suited for those that can accomplish defined work, as well as assist in approaching and solving complex scientific problems. This individual will be responsible for assisting in the generation, production and characterization of novel antimicrobial products. The ideal candidate will be able to independently conduct general microbiological and molecular biology research, and assist in the development of our broader research goals. This individual must be able to communicate effectively in formal and informal settings and be able to work well within a team. Candidates should have prior laboratory experience and be competent at basic molecular biology techniques. etc. 3/24/2020
992 Locus Biosciences
Research Triangle Park, NC
Data Analyst
BS/MS in bioinformatics, computational biology, or data science
Exp: 6-24 months
Locus Biosciences is seeking a highly motivated and entrepreneurial applicant to join our research and development team as a full-time Data Analyst. This individual will be responsible for assisting in the generation, production and characterization of novel antimicrobial products. Primary responsibilities include maintaining and leveraging data acquired from automated and high-throughput instruments. The ideal candidate will be able to drive the automation of data acquisition from lab instruments, maintain a data warehouse, and derive meaningful insights from large datasets. This individual must be able to communicate effectively in formal and informal settings and be able to work well within a team. Candidates should have a passion for data-driven decision making and bringing life-saving therapeutics to patients. etc. 3/24/2020
993 LogicBio
Cambridge, MA
Animal Care Technician
AS/AA in biology, pharmacology, or related
Exp: Entry level
LogicBio is seeking a highly motivated animal care technician to join our in vivo pharmacology group. The successful candidate will support preclinical development by ensuring the proper care of our research animals and assist in our vivarium operations. If you share our passion and sense of urgency for finding a lasting cure for patients, and are looking for a dynamic, collaborative and fulfilling work environment, we invite you to join our team. etc. 3/24/2020
994 LogicBio
Cambridge, MA
Research Associate, Discovery Biology
BS in biology, biochemistry, molecular biology, or related
Exp: 1-2 year(s)
LogicBio is seeking an entry level Research Associate to join our Discovery Biology team. The successful candidate will support the team in performing assays to assess protein expression and function of new targets in our growing pipeline. This role will work closely with other teams internally and externally, and support the analysis of preclinical studies to evaluate therapeutic candidates. Primary Responsibilities: Perform molecular and cellular-based assays to assess protein expression and activity. This includes, and is not limited to ELISAs, SDS-PAGE, BCA protein, and immunoblotting assays. Support assay development team in developing, optimizing and validating assays. Work closely with in vivo pharmacology and R&D teams to support sample analyses. Maintain and update detailed electronic notebook of experiments. Prepare, review and deliver scientific presentations for internal/external use. etc. 3/24/2020
995 LGC
Novato, CA
GMP Manufacturing Technician
BS/BA in a related field
Exp: Not necessary for BS/BA candidates
The GMP Manufacturing Technician I position is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements as directed by the departmental supervisor, manager or director. Areas of Responsibility: Perform manufacturing activities according to written protocols, as directed by the departmental supervisor, manager or director. Maintain batch records, equipment logs and other production records as directed per company procedures. Maintain a clean an orderly laboratory environment. Perform routine maintenance of equipment used in manufacturing. etc. 3/24/2020
996 LGC
Petaluma, CA
Chemical Production Support Technician I
College-level chemistry coursework
Exp: Not necessary with coursework
In our Genomics Division, we use our expertise in DNA extraction, genotyping, sequencing and PCR to enable scientists and companies to feed, cure and protect the world’s population. We supply genomic services from our UK, Germany and US laboratories, to global customers in agricultural biotechnology, molecular diagnostics, research, pharma/biotech, applied and clinical markets. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. etc. 3/24/2020
997 LGC
Manchester, NH
Kitting Assistant I/Chemical Repackager I
HS diploma/AS
Exp: 0-1 year(s)
The Production Department at LGC Standards in Manchester, NH produces an extensive line of analytical single and multi-element reference standards both in oil and aqueous matrices. The kitting group supports production by packaging standards used together in a kit. We are ISO 9001, ISO 17025, and ISO 17034 accredited. The main function of this role is to bottle and assemble private label kits in a clean and safe lab environment. The secondary function of this role is to package bulk product into finished goods bottle with the downstream production group. Key responsibilities and accountabilities: Label and package kits for private label customers. Clean labware and prepare vials/bottles per instructions. Repackage product from bulk containers to final product packaging as needed. Leak test final packages, apply labels and celoms, and check labels for accuracy. etc. 3/24/2020
998 Xellia Pharmaceuticals
Cleveland, OH
Aseptic Operator II - All shifts available
HS Diploma/GED
Exp: 1-2 years in cGMP environment
Perform job functions with in compliance of 21CFR part 210 and 211, FDA, OSHA and other regulatory agencies. Ensure that the current requirements for Environmental, Health, Safety (EHS) issues are met within the production operations. Ensure training compliance for assigned curriculum prior to performing any work task. Set-up, Operation, and troubleshooting of key manufacturing equipment: including (but not limited to) lyophilizer, autoclave, parts washers, filler, capper, CIP/SIP skid, etc. 3/22/2020
999 Xellia Pharmaceuticals
Cleveland, OH
Compliance Quality Assurance Specialist
BS in life/physical sciences
Exp: 1-5 years
The Compliance Quality Assurance (CQA) Specialist is responsible for providing quality oversight to all Doc Control, Change Control, Deviation Management, APR’s, Auditing, Laboratory, Complaints, Reprocess, Recalls and Supplier Qualification to ensure product quality and SOP/GMP compliance at the Cleveland Manufacturing Facility. Works with the aforementioned departments to resolve all quality issues or escalate to the Quality Assurance Manager as appropriate, and ensure good documentation practices are being followed. 3/22/2020
1000 Xellia Pharmaceuticals
Cleveland, OH
Aseptic Operator I - All shifts available
HS Diploma/GED
Exp: 0-1 years in cGMP environment
Perform job functions with in compliance of 21CFR part 210 and 211, FDA, OSHA and other regulatory agencies. Ensure that the current requirements for Environmental, Health, Safety (EHS) issues are met within the production operations. Ensure training compliance for assigned curriculum prior to performing any work task. Set-up, Operation, and troubleshooting of key manufacturing equipment: including (but not limited to) lyophilizer, autoclave, parts washers, filler, capper, CIP/SIP skid, etc. 3/22/2020
1001 Xellia Pharmaceuticals
Cleveland, OH
Aseptic Operator, IV Bag Manufacturing II
HS Diploma/GED
Exp: 1-2 years in cGMP environment
Perform job functions with in compliance of 21CFR part 210 and 211, FDA, OSHA and other regulatory agencies. Ensure that the current requirements for Environmental, Health, Safety (EHS) issues are met within the production operations. Ensure training compliance for assigned curriculum prior to performing any work task. Set-up, Operation, and troubleshooting of key manufacturing equipment: including (but not limited to) lyophilizer, autoclave, parts washers, filler, capper, CIP/SIP skid, etc. 3/22/2020
1002 Xellia Pharmaceuticals
Cleveland, OH
Microbiologist - 2nd Shift
BS/BA in sciences
Exp: 0-2 years in lab
In this role, the Microbiologist I is responsible for will be responsible for all aspects of the Microbiology laboratory operations, such as sample receipt, sample testing, data generation, data analysis and summarization and other QC lab supporting activities. Uses good documentation practices in the collection of data/records. Authors and executes qualification documents, SOPs, protocols, and investigations. 3/22/2020
1003 Xellia Pharmaceuticals
Cleveland, OH
Inside Sales Representative
BS/BA
Exp: 1-3 years in pharma/biotech/medical
As a part of Xellia’s growing, energetic, and innovative pharmacy injectables Sales Team, the Inside Sales Representative will reach customers via telephone and sell our newly patented Vancomycin RTU IV bags to new customers. While meeting established individual and organizational sales objectives, the Inside Sales Representative will build and maintain valuable sales skills, cross-functionally learn about all facets of the business, and help develop a pathway for growth opportunities and career advancement. 3/22/2020
1004 Xellia Pharmaceuticals
Cleveland, OH
CCA Material Handler
HS Diploma/GED
Exp: 1-2 years, must be able to use forklift
The CCA Material Handler is responsible for receiving, stocking, issuing, and delivering material required to support the Cleveland manufacturing operations. Responsible for receiving all items for this location and working with Warehouse and Quality to ensure all material is ready for production use. Locates product and material and transfers to CNC and CCA as applicable. Performs all transactions to confirm the issuance, transfer or destruction of materials that have been picked, transferred or destroyed. 3/22/2020
1005 Yokogawa
Sugar Land, TX
ESTIMATOR I
BS in engineering or math
Exp: <2 years experience
Responsible for overall estimation and order processing activities associated with the successful completion of assigned Systems Parts quotations including technical and commercial review and compliance, product selection, costing and support to achieve the division’s short-range and long-term business objectives of providing accurate, timely and precise information for all customer quotations. 3/22/2020
1006 Yokogawa
Newnan, GA
ASSEMBLER I
HS Diploma/GED
Exp: 1 year in manfacturing/soldering
To assemble product in accordance with shop orders and established production procedures. To produce a product in high quality by utilizing the necessary tools and equipment provided. Work using the NYPS philosophy and 6's. Have the ability to perform with speed and accuracy in all processes of the job. Determine type of instrument, parts necessary and production procedure to be followed for the required instrumentals by reading shop orders or work card. 3/22/2020
1007 Yokogawa
Newnan, GA
Rotational Engineer
BS/BA in engineering
Exp: Entry Level
Yokogawa’s Emerging Engineering Talent Rotational Program is an 18 month program designed to grow high potential talent by accelerating their development through technical and professional training and different engineering assignments. The program is composed of three rotational assignments designed for its members to gain hands-on experience while working on challenging projects, and gaining leadership exposure through targeted training and intentional engagement with Subject Mater experts and organizational leaders. 3/22/2020
1008 ZeteoTech
Sykesville, MD
Electrical Engineer - Software Systems
BS in electrical/computer engineering
Exp: 1-5 years in data analysis/data sciences
Actively participate in the design, development and implementation of data/information processing and analysis systems. Work with the Zeteo team and customers at all stages of the development process to ensure successful commercialization. Support development, implementation and testing of signal and information processing algorithms 3/22/2020
1009 ZeteoTech
Sykesville, MD
Electrical Engineer - Embedded Sensors
BS in electrical/computer engineering
Exp: 1-5 years in embedded systems
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 hands-on hardware and software engineering expertise to conceive, design, build, test and commercialize products. Actively participate in the design, development and implementation of embedded systems, including platform selection, programming, and testing. Work with the Zeteo team and customers at all stages of the development process to ensure successful commercialization. 3/22/2020
1010 ZeteoTech
Sykesville, MD
Chemist
BS in chemistry
Exp: 1-5 years
Conduct chemical experiments, tests, and analyses using techniques such as MALDI-TOF mass spectrometry, gas chromatography mass spectrometry, and microscopy. Conduct chemical and physical laboratory tests to assist scientists in refining MALDI-TOF MS equipment. Compile and interpret results of tests and analyses. Prepare chemical solutions for products and processes following standardized formulas, or create experimental formulas 3/22/2020
1011 ZeteoTech
Sykesville, MD
Electrical Engineer
BS in electrical/computer engineering
Exp: 1+ year in embedded systems
Our ideal candidate is interested in working in an entrepreneurial environment, developing game changing solutions to healthcare and national security challenges. You'll use your hands-on hardware and software engineering expertise to conceive, design, build, test and commercialize products. 3/22/2020
1012 ZeteoTech
Sykesville, MD
Microbiologist
BS/BA in biological sciences
Exp: 1-5 years lab experience
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. Prepare media and reagents required for conduct of microbiological analyses, while practicing aseptic techniques. Perform routine and non-routine sampling and testing of decontamination approaches. 3/22/2020
1013 Zimmer Biomet
Irvine, CA
Clean Room/ Packaging Operator
AS/AA in biotech/med/life sciences
Exp: 0-2 years
Performs drug product formulation, filling, crimping, sterilization, Visual inspection, labeling and Packaging. May be required to perform all or a combination of the duties listed below. Buffered solution preparations according to Standard Operating Procedures (SOP’s). Chemical Reactions and RODI Purification of reaction precipitate. 3/22/2020
1014 Zimmer Biomet
Warsaw, OH
Quality Engineer
BS in engineering
Exp: 0-3 years
Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. Interacts with many different functional departments, suppliers, and experts outside Zimmer Biomet to implement Zimmer Biomet Quality goals. Formulates procedures, specifications, and standards for Zimmer products and processes. Develops and implements corrective/preventative action plans. 3/22/2020
1015 Zimmer Biomet
Scottsdale, AZ
Quality Engineer
BS in engineering
Exp: 0-3 years
Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. Interacts with many different functional departments, suppliers, and experts outside Zimmer Biomet to implement Zimmer Biomet Quality goals. Formulates procedures, specifications, and standards for Zimmer products and processes. Develops and implements corrective/preventative action plans. 3/22/2020
1016 Zimmer Biomet
Memphis, TN
Product Assur Coordinator (602436) - 2nd Shift position
HS Diploma/GED
Exp: 1-3 years mechanical inspection
The Product Assurance Specialist is responsible for inspecting parts at all stages of processing (acceptance, clean, package, and label) and deciding whether or not the parts conform to visual and dimensional specifications and documenting these decisions and supporting data. The Specialist must work with minimal supervision and be capable of evaluating and judging level of conformance with defined requirements. 3/22/2020
1017 Zimmer Biomet
Warsaw, OH
Contract Associate Specialist
BS/BA in business or related
Exp: 0-3 years
Responsible for administering and analyzing contracts with regional buying groups, medical surgical distribution companies, integrated health systems, and individual facilities while assisting with national group purchasing organizations. Thoroughly understands and applies good contract management principles. Administers contract maintenance process to ensure sales transactions are accurate and recorded timely. Strong analytical skills are required for position. 3/22/2020
1018 Zimmer Biomet
Warsaw, OH
Manufacturing Engineer
BS/BA in engineering
Exp: 0-3 years in engineering
The manufacturing engineer is responsible for providing manufacturing engineering services to support efficient manufacturing processes. Engineering services may include cell management, process development, project management, process validation, tool design, and trouble shooting. Maintaining and improving controlled technical documents such as prints, procedures, bill of materials and routers. Supporting a wide variety of processing applications such as machining, finishing, forging, casting, cleaning, heat treating, bonding, molding, etc. 3/22/2020
1019 Vividion
San Diego, CA
Research Associate, Molecular and Cellular Biology
BS/MS in cell biology
Exp: 0-3 years
The successful candidate will have extensive hands on experience and expertise in basic molecular biology, mammalian cell culture techniques,and cellularand biochemical assay development. They will supportthe validation of novel drug targets via multiple mechanisms, including testing the effects of compounds on proteins in cellular and biochemical settings. They will utilize the development and/or use of new technology to support drug discovery. 3/21/2020
1020 Vodori
Chicago, IL
DevOps Engineer
BS/BA in computer sciences/engineering
Exp: 1-2 years in devops, system engineering/software develoment
Our platform is based on open source technologies, so if you have a passion for Linux server administration (CentOS), Web server configuration (Apache & Tomcat), Database administration (MySQL & MongoDB), and Infrastructure management and automation (Puppet, Docker, and Kubernetes), you would be a great fit for this role. In this role, you will automate tasks using Python, Bash, or other scripting technologies. You will find it very helpful to have previous experience with AWS (Amazon Web Services) in cloud networking and working with SaaS software in cloud environments. 3/21/2020
1021 Voyager Therapeutics
Cambridge, MA
Research Associate, Vector Engineering
BS in molecular/cellular biology
Exp: 1-3 years in research
This is an ideal position for an individual with experience in in vitro molecular biology assays, who thrives in a team-oriented, fast-paced, and cross-disciplinary start-up biotech environment. The individual will work in the laboratory and be responsible for experimental execution for research studies supporting cutting edge therapeutic programs and platform discovery research in neurodegenerative disease areas. We are looking for a candidate with hands-on experience with molecular clonings and downstream analysis (e.g. RT-qPCR, ELISA, tissue sectioning, immunohistochemistry and western blot). 3/21/2020
1022 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
1023 Wake Research
Raleigh, NC
Clinical Research Patient Recruiter
HS Diploma/GED
Exp: 6 months in call center
The Clinical Research Patient Recruiter will 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. 3/21/2020
1024 Waters Milford Machining
Milford, MA
Quality Engineer I - Machining Operations
BS in engineering
Exp: 0-3 years in manufacturing
Quality engineering support will include nonconformance management, process improvement, programming of automated inspection equipment, fixture design, and statistical analysis of process qualification data. The ideal candidate shall be comfortable communicating with machine operators, mechanical inspectors, process engineers, operations management, and quality systems staff, and shall possess knowledge of design and manufacturing principles. 3/21/2020
1025 Waters
Golden, CO
Assembly/Production Technician II - ASR
HS Diploma/GED
Exp: 0-2 years in quality
This position will join a team which has responsibilities for production, assembly, inventory control, labelling, kitting, transporting, and Quality Control of products. It includes completing documentation and review to meet Waters Analytical Standards & Reagents (ASR)specifications. Quality and attention to detail are top priority. 3/21/2020
1026 Waters
Milford, MA
Electronics Technician
AS/AA or apprenticeship
Exp: 1 year as electronic technician
This position involves performing all aspects of support, repair and maintenance to electrical/mechanical systems in a state-of-the-art Instrument development group. Record data with equipment such as a DVM, O-scopes, logic analyzers, and other electric measuring/monitoring devices. Collaborate with engineers and other professionals on technical tasks. Service, maintain and troubleshoot electrical problems on both new and legacy Water Liquid Chromatography (LC) systems. 3/21/2020
1027 WCCT Global
Cypress, CA
Clinical Research Technician
Medical assistant or CPT1
Exp: 1 year clinical research experience
The Clinical Research Technician (CRT) works directly with the Clinical Trial Director (CTD), Clinical Trial Manager (CTM), Clinical Research Coordinator (CRC), or Assistant Clinical Research Coordinator (ACRC) in the preparation, collection, compilation, and documentation of clinical research data by performing administrative and clinical duties. 3/21/2020
1028 Westat
Rockville, MD
Research Assistant
BS/BA in social sciences/educaton
Exp: 1 year in research or education
We have an immediate opening for a research assistant who will work with a research team to support the data collection for the National Assessment of Educational Progress, (NAEP), an innovative digital educational assessment also known as “The Nation’s Report Card.” 3/21/2020
1029 Westat
Rockville, MD
Research Assistant
BS/BA in social sciences
Exp: 1-3 years in research
Westat is seeking a research assistant with strong quantitative skills to contribute to education research and evaluation projects. Developing code in statistical software to manipulate data, produce descriptive statistics, and conduct inferential analysis (e.g., multiple regression). Creating data visualizations with Microsoft Excel or other tools. 3/21/2020
1030 Westat
Rockville, MD
Research Assistant
BS/BA in social sciences/educaton
Exp: 1 year working
We have an immediate opening for a research assistant who will work with a multidisciplinary research team to support the data collection for the OECD’s Programme for International Student Assessment (PISA), the world’s largest international education assessment involving more than 85 countries and economies. 3/21/2020
1031 Westat
Rockville, MD
Research Assistant
BS or MS in social sciences with quantitative experience
Exp: 1 year working
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. 3/21/2020
1032 Westat
Rockville, MD
Research Analyst
MS in social sciences
Exp: 1 year
Westat is seeking a Research Analyst to work on survey research projects, defining and processing survey data and metadata from collection through delivery to Westat’s clients. Data review, data operations specifications and file documentation writing are part of the role. Write technical specifications for programming survey instruments and analytic variables. 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. 3/21/2020
1033 Westat
Rockville, MD
Medical Records Abstractor
HS Diploma/GED
Exp: 1 year in medical terminology
The primary role of the medical record abstractor (MRA) is to review medical records in a sampled hospital's emergency department(s), abstract specific information from the patient's chart following the project's case identification protocol, and entering the information into a data collection tool. 3/21/2020
1034 Worldwide Clinical Trials
San Antonio, TX
PRN Research Technician I
HS Diploma/GED
Exp: 0-2 years as lab technican
The PRN Research Technician 1, works under the direct supervision and guidance of the Assistant Supervisor, Laboratory Services, and the Supervisor, Laboratory Services performing technical and laboratory procedures following Worldwide Clinical Trials Clinical (WCT) procedures and study protocol requirements. 3/21/2020
1035 Worldwide Clinical Trials
Morrisville, NC
Evidence Clinical Research Associate (CRA)
BS/BA in medical/health/physical sciences
Exp: 0-2 years
The Clinical Research Associate (CRA), Evidence is responsible for managing the research activities at sites participating in Worldwide’s clinical research projects, which are predominantly registries and other types of non-interventional studies. The CRA, Evidence will typically be involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and negotiating contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the sites activities during study maintenance, and closing down research activities at the sites once the study has concluded. 3/21/2020
1036 Worldwide Clinical Trials
Morrisville, NC
Clinical Operations Assistant
BS/BA in medical/health/physical sciences
Exp: 1 year in clinical research
The Clinical Operations Assistant is a full-time position responsible for completing all assigned projects for Clinical Operations in a timely and accurate manner while interfacing directly with in-house personnel and field employees. Key functions include management of essential document submission to Trial Master Files, supporting field personnel with Microsoft Office, and providing additional administrative support when time permits. 3/21/2020
1037 Wright Medical
Kent, WA
Hub Material Handler II - Kent, Washington
AS/AA
Exp: 1-3 years
This role will ensure the timely processing of kits/sets in the Hub. This could include, but is not limited to, checking in sets, verifying completeness, restocking, creating new kits from sterile implant skus, and other basic set maintenance. The Hub Material Handler II is required to function with minimal supervision to ensure that work flow is uninterrupted and that all customer requirements are met within the functional area. The Hub Material Handler II will be cross-trained on other Hub positions in order to ensure that all Hub functions are carried out timely and as needed. 3/21/2020
1038 Wright Medical
Indianapolis, IN
Associate Sales Representative, Upper Extremities - Indianapolis, IN
BS/BA
Exp: 0-2 years
This role will initially support our Hand, Wrist, Elbow and Biologics portfolio and may grow into selling the shoulder portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. 3/21/2020
1039 Wright Medical
Worthington, OH
Hub Material Handler II
AS/AA
Exp: 1-3 years
This role will ensure the timely processing of kits/sets in the Hub. This could include, but is not limited to, checking in sets, verifying completeness, restocking, creating new kits from sterile implant skus, and other basic set maintenance. The Hub Material Handler II is required to function with minimal supervision to ensure that work flow is uninterrupted and that all customer requirements are met within the functional area. The Hub Material Handler II will be cross-trained on other Hub positions in order to ensure that all Hub functions are carried out timely and as needed. 3/21/2020
1040 Wright Medical
Philadelphia, PA
Material Handler I - Philadelphia, PA
HS Diploma/GED
Exp: 1+ year in delivery
The Hub Material Handler I is responsible for making pickups and deliveries of implants and instruments to and from local hospitals, surgery centers, clinics/doctor’s offices, the airport, bus station, and other locations for expedited shipments. Excellent communication must be maintained with adaptability to the needs of the customers, sales management/reps, and both corporate and office personnel to ensure timely transportation of goods for surgical procedures. This position has responsibilities to be the liaison between the field office and Wright Medical customers for coordinating activities relating to the efficient use of company assets. 3/21/2020
1041 Wright Medical
Dover , DE
Associate Sales Representative, Upper Extremities
BS/BA in related
Exp: 0-2 years in sales
This is an entry level sales position that will require you to learn our products, market and industry. This role will initially support our Hand, Wrist, Elbow and Biologics portfolio and may grow into selling the shoulder portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. This is an entry level sales position that will require you to learn our products, market and industry. This role will initially support our Hand, Wrist, Elbow and Biologics portfolio and may grow into selling the shoulder portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. This is an entry level sales position that will require you to learn our products, market and industry. This role will initially support our Hand, Wrist, Elbow and Biologics portfolio and may grow into selling the shoulder portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. 3/21/2020
1042 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
1043 WuXi AppTech
St. Paul , MN
Associate Quality Assurance Specialist
BS/BA
Exp: 0 years
The Associate Quality Specialist is responsible for ensuring GLP studies, GMP testing, and GMP manufacturing activities are executed in accordance with the appropriate regulatory bodies and internal procedures. Ensures compliance to Good Laboratory Practices (GLP) and current Good Manufacturing Practices (cGMP). Perform job specific tasks in compliance with applicable Regulations, International Standards, and WuXi AppTec Policies and Standard Operating Procedures. 3/21/2020
1044 WuXi AppTech
King of Prussia, PA
Assocaite Scientist Upstream Process Development
BS or MS in relevant field
Exp: 0-2 years
The successful candidate will be responsible for conducting experiments to support client based processes with a focus on vaccine upstream cell culture processes. 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. Support technical transfer of processes into the non-GMP pilot plant or GMP production facility. 3/21/2020
1045 WuXi AppTech
King of Prussia, PA
Assocaite Scientist Upstream Process Development
BS or MS in relevant field
Exp: 0-2 years
The successful candidate will be responsible for conducting experiments to support client based processes with a focus on vaccine upstream cell culture processes. 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. 3/21/2020
1046 WuXi AppTech
Philadelphia, PA
Associate Scientist - Process Development, Downstream
MS in biological sciences/engineering
Exp: 0-2 years
Scientist contributing to the development of early and late stage clinical manufacturing processes and commercial manufacturing processes for Cell and Gene Therapies. This position will work with a team of scientists and technical specialists responsible for process development, technology transfer and GMP manufacturing to ensure the application of well-designed unit operations for inclusion in routine manufacturing operations supplying clinical and commercial materials. Responsible for supporting development project leads in the development, scale-up/out, and verification of clinical and commercial manufacturing processes. Contributes to operations of development team, and may support tech transfer activities as necessary. 3/21/2020
1047 WuXi AppTech
Philadelphia, PA
Associate Raw Material Specialist
MS in biological sciences/engineering
Exp: 1+ years in GMP manufacturing/QA
Maintains current knowledge of regulatory guidelines and requirements related to control and testing of raw materials for advanced therapy manufacturing. Authors and revises controlled documents to support material onboarding and risk management. Performs verification of Material Item Masters and works cross-functionally with Supply Chain and Quality Assurance. Creates and maintains end-user resources and tools. Supports delivery of client-specific material risk control and assessment documents as needed. 3/21/2020
1048 Kite
Oceanside, CA
Manufacturing Associate I
BS in biology or related
Exp: 0-1+ year(s)
We are seeking a highly motivated Manufacturing Associate to support our new Viral Vector biotechnology facility in Oceanside, CA. Under minimal supervision, in this role you will be accountable for and focused on front line manufacturing of viral vectors. Responsibilities (include, but are not limited to): Assist with startup activities of a new cGMP facility by collaborating with PD, MSAT, Engineering and Quality departments. Perform all tasks associated with the manufacture of viral vectors following batch records and standard operating procedures (SOPs) to ensure safe and compliant operations. Work as part of a team to execute GMP runs in close collaboration with Process Development and Quality. etc. 3/18/2020
1049 Kite
El Segundo, CA
QC Microbiology Tech I
BS in microbiology
Exp: 1+ year(s)
We are seeking a highly motivated individual to join us as a QC Microbiology Technician in our commercial cell therapy production center located in El Segundo CA. You will work with the Quality Control team in supporting our efforts in this exciting new area of cancer immunotherapy. This position provides Quality Control microbiological testing for clinical and commercial manufactured product, responsible for product testing, utility testing and environmental monitoring. Responsibilities (include but are not limited to): Perform environmental monitoring of cleanrooms. Collect water samples. Perform microbiological assays such as Gram Stain, Endotoxin, Sterility, Microbial Identification, Growth Promotion, Bioburden and Plate Reading. etc. 3/18/2020
1050 Krystal Biotech
Pittsburgh, PA
Computer Systems Validation (CSV) Analyst
unspecified
Exp: 1-3 year(s)
Krystal Biotech, Inc is seeking a highly motivated Computer Systems Validation (CSV) Analyst. This role will have responsibility to support CSV activities of systems and programs requiring system and/or software qualification and testing. This will include the validation of new GxP computer systems used in the QC labs and within Manufacturing production. The analyst will be responsible for the development of validation documentation, including User Requirements Specifications (URS), Functional Requirements Specifications and Test Protocols to ensure that the system is fit for its intended use. etc. 3/18/2020
1051 KVK Tech
Newtown, PA
Sample Management Associate
AS/BS
Exp: No experience necessary
Sample Management Associate provides support to Sample Coordinator and performs administrative tasks in the Sample Management Department. Follows SOPs, and fulfills laboratory requests with minimum direct supervision. JOB RESPONSIBILITIES: Performs duties and training to acquire the skills required for sample and standard handling in support of the laboratory. Handling of samples received in Quality Control Laboratory. Follows SOPs, and fulfills laboratory requests with minimum direct supervision. Quality Control related tasks like receiving, documenting, distributing and reconciliation of all samples received in the laboratory. etc. 3/18/2020
1052 KVK Tech
Newtown, PA
Analytical Chemist
BS/MS
Exp: 1-4+ year(s)
Perform analytical testing of raw materials, in-process materials, stability samples, finished products and product development products using different analytical techniques. JOB RESPONSIBILITIES: Operation, Calibration, Qualification, Preventive maintenance and routine trouble shooting of analytical instruments like UPLC, HPLC, GC, AAS, UV spectrophotometer, Dissolution apparatus, Laser Diffraction Particle Size analyzer, etc. Evaluate existing, develop and validate new analytical methods of drug products and drug substance as per FDA, USP and ICH guidelines by different analytical techniques. Document all performed analysis as per cGMP, USFDA and 21CFR211.194 guidelines. etc. 3/18/2020
1053 LakePharma
Worcester, MA
Scientist I/II
MS in biology or related
Exp: 1+ year(s)
We are rapidly growing and seeking a talented individual to join our Vector Technology Team as a Scientist I/II. 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
1054 LakePharma
Hopkinton, MA
QC Analyst 1
BS in a life science
Exp: 6-24 month(s)
LakePharma is the leading US-based biologics contract research, development, and manufacturing organization (CRDMO). The company has developed a range of technologies and capabilities in antibody discovery, protein engineering, cell line development, protein optimization, and GMP manufacturing. With comprehensive technologies, integrated platforms, and five facilities located in key biopharma hubs on both the East and West Coast, LakePharma enables and supports the discovery and development of the biologics of tomorrow. Position Summary: Perform supportive activities for general lab readiness, laboratory equipment qualification and method transfers. etc. 3/18/2020
1055 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
1056 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
1057 LakePharma
Hopkinton, MA
Associate Scientist/Scientist Pharma Assays and Analytics
BS/MS in biochemistry or related
Exp: 1-5 year(s)
We are seeking a talented individual to join our team as an Associate Scientist/Scientist, based in our Hopkinton, MA facility, supporting the Pharma Assay and Analytics group in the execution of R&D workflows. Essential Duties and Responsibilities: Validate and Perform Cell-based and Enzyme-based assays and related procedures using manual and automated liquid handling equipment, including but not limited to: Enzyme Activity Analysis. Cell-Based Assays. Viral transduction Workflows (BL1/BL2). etc. 3/18/2020
1058 Lampire Biological Laboratories
Everett, PA
Small Animal Technician
HS diploma/BS in life sciences or related
Exp: 1 year
The primary responsibility of this individual is to maintain the overall health and well-being of the rabbits including cage and facility maintenance. This would include the feeding and watering of rabbits, administering treatments, as well as swapping, cleaning, disinfecting, and sanitizing all animal housing units and animal facilities. Responsibilities Include (but are not limited to): Feeding, watering, and administering treatments, including observing and reporting any signs of disease/illness and help to treat minor cases of such findings. Scraping, chipping, and dusting, animal caging units. etc. 3/18/2020
1059 Lampire Biological Laboratories
Coopersburg, PA
Laboratory Technician
HS diploma/BS
Exp: 1-2 year(s)
To facilitate daily operations at the Coopersburg Laboratory by supporting the whole blood, plasma/serum, anticoagulant, brokered and abattoir departments as necessary. Responsibilities Include (but are not limited to): Prepare formulations and products according to established batch records and work orders. Maintain lot number, batch and equipment logbooks in accordance with established procedures. Perform on-line inspection of components/product and immediately notify supervisor of any problems. etc. 3/18/2020
1060 Lampire Biological Laboratories
Everett, PA
Purification Technician
BS in a scientific field
Exp: Not necessary for BS candidates
This position will be responsible for the purification of antibodies at the Everett facility. Responsibilities Include (but are not limited to): Routine buffer preparation for all processes being performed in the department. Protein A and Protein G purification of Normal igGs and other antibodies. Write and revise Standard Operating Procedures (SOP’s) and Batch Records (BR) as needed. Assist in filing, labeling and finished product good inspection. Operate basic Laboratory and Analytical equipment. etc. 3/18/2020
1061 Latham BioPharm Group
Elkridge, MD
Associate / Senior Associate / Consultant, Quality Assurance
BS in a scientific or engineering field
Exp: 1-2 year(s)
At Latham BioPharm Group, Inc., you will support multiple clients to assure their development phase programs meet or exceed industry cGMP requirements by assisting in the creation and implementing corporate Quality Manuals, Quality Policy’s, SOP’s and training programs. In addition, perform batch record; review, approval and disposition of lots and labels. Manage deviations and CAPA identification to closures. Furthermore, you will provide audit support by assisting in conducting vendor qualification through routine scheduled audits. The ideal candidate must be able to work independently and have excellent interpersonal relationship skills with flexibility to adapt to fast pace environment with changing priorities. etc. 3/18/2020
1062 Leidos Biomedical Research
Frederick, MD
Research Technician
BA/BS in a related field
Exp: Not necessary for BS/BA candidates
We are looking for a Research Technician to join our dynamic, interactive, multidisciplinary research team working on AIDS pathogenesis and development of vaccines for prevention of HIV infection and AIDS, working with non-human primate models. The successful candidate will be able to work in a close team environment, consistently follow detailed protocols and instructions, and keep careful records. Specific duties will include: Processing of potentially infectious blood and tissue specimens from non-human primates. Preparation/formulation of drug compounds. Operation of laboratory equipment. Updating and maintaining detailed sample databases. etc. 3/18/2020
1063 Leidos Biomedical Research
Frederick, MD
Research Technician
BA/BS
Exp: No experience necessary
KEY ROLES/RESPONSIBILITIES: Processing blood and body fluids from HIV-infected patients. Performing complete blood cell counts and blood cell differential counts on a Sysmex XNL 350i hematology instrument. Performing manual blood cell differential counts. Documenting results. Performing basic data analysis. Performing quality control evaluations. Monitoring equipment for optimum performance and basic instrument troubleshooting. etc. 3/18/2020
1064 Leidos Biomedical Research
Frederick, MD
Glassware Processor
HS diploma or equivalent
Exp: 1+ year(s)
The Basic Science Program (BSP) pursues independent, multidisciplinary research programs in basic or applied molecular biology, immunology, retro-virology, cancer biology or human genetics. Research efforts and support are an integral part of the Center for Cancer Research (CCR) at the Frederick National Laboratory for Cancer Research (FNLCR). BSP provides procurement and logistical assistance in support of the research activities of the CCR. Operating as a component of the BSP, the Central Glassware Service performs the daily pick up, washing, sterilizing and delivery of laboratory related items and glassware to research facilities located at the FNLCR. KEY ROLES/RESPONSIBILITIES: Picks up soiled glassware items from laboratories, plastic tanks containing disinfectant. Processes dirty glassware by machine washing, drying and sterilizing in a central kitchen facility. Restocks laboratory glassware cabinets with appropriate quantities of standard laboratory glassware. etc. 3/18/2020
1065 Leidos Biomedical Research
Frederick, MD
Manufacturing Associate, Fermentation
BA/BS
Exp: No experience necessary
KEY ROLES/RESPONSIBILITIES: Complete assigned tasks supporting manufacturing laboratory functions. Maintain bacterial and mammalian cell cultures. Perform microscopic technique/cell counting. Operate advanced buffer/media skid, SU and fixed large scale, chromatographic skid equipment, GMP autoclaves and associated equipment, basic lab equipment operation. Follow Standard Operating Procedures. Complete Batch Production Records under current Good Manufacturing Practices. etc. 3/18/2020
1066 LakePharma
Hayward, CA
Lab Assistant / Associate Scientist, Process Development & Manufacturing
BS in biochemistry, biology, or related
Exp: 0-5 years
We are rapidly growing and seeking a talented individual to join our Process Development & Manufacturing - Cell Line Development Team. The successful candidate will be able to execute hands-on laboratory work in cell culture including planning and executing stable cell line development, shake flask production, and bench scale purifications experiments. 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
1067 Intersect ENT
Menlo Park, CA
Technician I, Quality Engineering
AS/AA
Exp: 1 year
Support Quality Engineering department on various tasks used to support production and development of medical products used in the treatment for ear, nose and throat disorders. DUTIES AND RESPONSIBILITIES: Work with QE and ME in developing procedures, test methods, qualification protocols, and reports. Perform QA investigation testing on returned product/field complaints, NCMR/CAPA or manufacturing line issues. Assist in performing complaint investigations and return goods evaluation as assigned. Perform QA related data entry and data analysis. Perform responsibilities for NCMR coordinator. Assist QE in providing manufacturing line support including routine observation. etc. 3/17/2020
1068 Invenra
Madison, WA
Research Associate - Cell Biology
BS in a biological science
Exp: 1+ year(s)
Invenra is seeking a highly motivated Research Associate with a strong background in cellular biology. This individual will support the Invenra antibody discovery platform. Aspects of the job entail mammalian cell culture and assays, analytical flow cytometry, ELISAs, and immunofluorescence/luminescence assays. In addition, the position will involve general ordering and stocking of lab supplies as well as upkeep of standard cell biology equipment (i.e. incubators, biosafety cabinets, etc.). The position requires strong communication and organizational skills as well as attention to detail. etc. 3/17/2020
1069 Invicro
Doylestown, PA
Data Management Associate
BS in a life science
Exp: 1-2 year(s)
The Data Management Associate plays an essential role in the establishment and maintenance of database standards, the efficient design of sponsor databases, the integration and reporting of data from multiple sources, and the reporting and analysis of key study data metrics. The incumbent will recommend and drive solutions for efficient database design and data reporting. This role is critical for meeting sponsor study data specification requirements. etc. 3/17/2020
1070 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
1071 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
1072 Invitae
Cambridge, MA
Bioinformatics Engineer, Algorithm
unspecified
Exp: 1+ year(s)
As part of the pipeline engineering team, you will be responsible for maintaining, improving, and adding to our catalog of production bioinformatics pipelines across an expanding set of modern assays. You will be responsible for scaling our pipelines as we work toward our goal of providing low-cost genetic answers to billions of people. You will work and learn among an extraordinary set of peers: bioinformaticians, molecular biologists, and software engineers. Your work will directly improve the quality of our product and positively impact each tested patient. 3/17/2020
1073 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
1074 Jubilant Life Sciences
Spokane, WA
Associate, Regulatory Affairs
HS diploma/AS/BS
Exp: 1 year
The Regulatory Affairs Associate/Specialist supports the regulatory compliance programs by coordinating the scheduled activities of state and federal reporting, as well as medical complaint handling, ensuring compliance with US and International regulatory agencies. Essential responsibilities include but are not limited to: Associate: Compliance: Oversees state and federal certification and registration requirements to ensure compliance with reporting obligations. Conducts project research and gathers supportive materials. Conducts document fact checking/comparisons, log updates, and tracking/archiving/filing backup. etc. 3/17/2020
1075 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
1076 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
1077 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
1078 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
1079 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
1080 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
1081 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
1082 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
1083 KBI Biopharma
Boulder, CO
Research Associate I/II Particle Core
BS/BA in chemical engineering, chemistry, biochemistry, or related
Exp: Not required
KBI’s Particle Characterization Core is looking for a scientist or engineer to become our next colleague and learn the fine art of particle characterization. Our new associate will have an active role in a dynamic laboratory environment that will include learning cutting-edge analytical techniques, development of data analysis tools, establishing direct relationships with clients, and continuing to build a world-class specialty analytical business. If you are eager to learn and want to jump start a career in pharmaceutical analytics, you might be the person we are looking for! etc. 3/17/2020
1084 KBI Biopharma
Durham, NC
Manufacturing Associate I-Upstream (Night Shift) (temp to hire)
BS/BA
Exp: 0+ 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. Job Description: 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. Use equipment and techniques related to support, mammalian cell culture and/or harvest and purification. Responsible for completing paperwork for each task, cleaning procedures, aseptic processing techniques, Good Manufacturing Practices (GMP) and laboratory safety practices and procedures. etc. 3/17/2020
1085 KBI Biopharma
Durham, NC
Manufacturing Associate I/II-Downstream
BS/BA
Exp: 0+ years
Job Summary: Coordinate and perform cGMP manufacturing operations for manufactured biopharmaceutical products. Ensure the effective use of material, equipment and personnel while making products at high quality levels. Job Description: Assist in execution of procedures for cell culture manufacturing, purification, or support area of manufacturing using SOP's and batch records. Use equipment and techniques related to support, mammalian cell culture and/or harvest and purification. Responsible for completing paperwork for each task, cleaning procedures, aseptic processing techniques, Good Manufacturing Practices (GMP) and laboratory safety practices and procedures. 3/17/2020
1086 Klus Pharma
Cranbury, NJ
Research Associate, Antibody Discovery
BS in cell biology, immunology, or related
Exp: 1+ year(s)
We are currently seeking a highly motivated individual to join the KLUS Pharma to support therapeutic antibody programs. Key Responsibilities: Have interest in implementing process improvement technologies, exhibit initiative, work independently, be technically proficient in the processes assigned to them, and be flexible in a start-up environment. Responsible for the antibody screening and antibody identification, activities include but not limited to cell culture and cell cryopreservation, cell fusion, hybridoma subcloning/expansion and supernatant harvesting, high throughput screening large panels of antibodies derived from immunizations and hybridoma pools with ELISA and flow cytometry. etc. 3/17/2020
1087 KemPharm
Coralville, IA
Laboratory Assistant
BS in a life science or biotechnology
Exp: Not required for BS candidates
The Laboratory Assistant requires a recent graduate, or student currently pursuing a biotech-related degree, who will utilize basic biological, chemical, physical, and life science laboratory skills to perform the following responsibilities: Reports directly to the Senior Group Leader, Chemistry, and indirectly to the EVP, Research & Development, and supports the entire R&D team. Follows standard operating procedures (SOP) for maintaining laboratory equipment and facilities. Assists in the preparation and/or prepares solutions, reagents, starting materials. Performs routine laboratory tests, chemical reactions, and isolation/purification procedures. Coordinates and/or conducts laboratory equipment maintenance and calibration. Keeps laboratory supplies up-to- date and using Quality Assurance techniques and assists with inventory, ordering, receiving and stocking of laboratory supplies and equipment. etc. 3/17/2020
1088 Perkin Elmer
Austin, TX
Associate Lab Technologist
HS Diploma/GED
Exp: 1+ years in lab/research
Seeking candidate who will work as part of the production team to manufacture Next-Gen Sequencing library kits. Job duties include but are not limited to: Making and testing kit components. Quality Control. Pipetting reagents. Labeling tubes 3/16/2020
1089 Perkin Elmer
Upper Providence, PA
Research Specialist (Tech)
BS/BA in biology
Exp: 1-3 years in lab environment
Perform weekly checks on balances (mix of top loader, analytical, and micro balances) in UP09. Perform daily checks on pH meters in UP09. Preparation of recipe based media, including dissolution, mobile phases, and diluents in accordance with protocols/instructions uploaded into Labware • Data review required; data review is performed by the requestor. 3/16/2020
1090 Perkin Elmer
Waltham, MA
Associate Inside Sales Representative
BS/BA
Exp: 0-2 years in telemarketing
The Associate Inside Sales Representative will act as a lead generation professional working closely with a team of Key Account Sales Specialists, Inside Sales Representatives and the Regional Sales Manager. They will plan and conduct outbound calling and/or email correspondence to targeted prospects and clients, and qualify leads generated by the Marketing team. Position partners closely with the regional sales team to effectively drive business in the region. 3/16/2020
1091 Perkin Elmer
San Diego, CA
Lab Concierge
BS/BA
Exp: 1 year in administrative/lab services
Primary liaison for SAP and Maximo work order requests and tracking initiating work order requests and tracking. Check-in and check-out service providers on-site. Expedite service from OEM and third-party service provides and execute escalation procedures as necessary. Ensure required PM and validation calls are assigned as per SOW. Review, verify, and confirm SAP and Maximo are in sync. 3/16/2020
1092 ViaCyte
San Diego, CA
R&D Engineer I
BS or MS in material, chemical, mechanical, or biomedical engineering
Exp: 1 year in med device/research
As a member of the Combination Product Engineering group, the engineer shall support product development, process development, and manufacturing activities involving the combination product. Under direction from more senior team members, the employee shall utilize R&D methods and engineering techniques to develop processes, generate test systems, and improve manufacturing procedures with respect to the combination product manufacturing line. With guidance, the engineer shall write and execute engineering protocols, document reports, and all elements necessary to launch combination products through design control. 3/16/2020
1093 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
1094 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
1095 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
1096 Vigene Biosciences
Rockville, MD
Upstream Manufacturing Associate – Level II/III
BS/BA in sciences or engineering
Exp: 1-3 years with upstream biologic production
The Upstream Manufacturing Associate applies a broad knowledge of biological, bioprocess, and mechanical principles to execute complex operations that result in clinical and commercial stage medicines to dramatically improve the human condition through gene therapy. Perform basic to complex activities in seed train, bioreactor, transfection and recovery operations for both suspension and adherent cultures using SOPs and Batch Production Records. 3/16/2020
1097 Vigene Biosciences
Rockville, MD
Downstream Manufacturing Associate – Level II/III
BS/BA in sciences or engineering
Exp: 1-3 years with downstream biologic production
The Upstream Manufacturing Associate applies a broad knowledge of biological, bioprocess, and mechanical principles to execute complex operations that result in clinical and commercial stage medicines to dramatically improve the human condition through gene therapy. Perform downstream purification activities such as Chromatography, TFF, Ultracentrifugation, and Final Formulation steps. Perform various filter integrity tests throughout the process 3/16/2020
1098 Vigene Biosciences
Rockville, MD
Fill/Finish Manufacturing Associate – Level II/III
BS/BA in sciences or engineering
Exp: 1-3 years with biologic production
Perform basic to complex activities in dispensing of Drug Substance and final fill-finish of Drug Product using SOPs and Batch Production Records. Performing critical downstream activities in preparation of fill finish of Drug Product. Document all activities in Batch Records, Logbooks, Forms, etc. Exercise intellectual curiosity by identifying and escalating events and subtle variances that deviate from normal operation. 3/16/2020
1099 Vigene Biosciences
Rockville, MD
Research Associate
BS/BA in chemical/biomolecular engineering, life sciences, etc.
Exp: 0-3 years in R&D
As a part of the Upstream Process Development Team, the Research Associate is responsible for working with clients in evaluation of upstream processes, sourcing reagents, equipment, and materials for specific projects. Working with clients in evaluation of upstream processes, sourcing reagents, equipment, and materials for specific projects and ensuring proper technology transfer from client. Process demonstration using bench-top bioreactors. 3/16/2020
1100 Viiv Healthcare
Rockville, MD
Data Science – Future Leaders Program, US – 2020
BS/BA in data/computer sciences/engineering or related
Exp: 2020 Graduate
Our Data Science Future Leaders Graduate Program will challenge and support you to grow professionally and personally. You will receive a generous personal training budget and be supported by a technical mentor. You’ll get to meet senior leaders and network with other graduates. You’ll also improve your technical skills while gaining valuable leadership expertise. It all adds up to a role that’s designed to transform talented graduates into key, senior figures. 3/16/2020
1101 Viracor Eurofins
Lee's Summit, MO
Laboratory Technician
BS/BA in biological/physical/chemical sciences
Exp: 1 year in lab
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. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Document remedial action, troubleshooting, quality assurance activities and instrument maintenance 3/16/2020
1102 Viracor Eurofins
Lee's Summit, MO
Laboratory Specimen Processor I, II or III
HS Diploma/GED
Exp: 1 year in data entry
The Laboratory Specimen Processor Associate is primarily responsible for performing duties related to accessioning and data entry with a high degree of proficiency. Demonstrate data entry proficiency with the Laboratory Information Management System (LIMS) and/or other specimen tracking system. Examine samples for accuracy and other requirements (sample type, volume, etc.) 3/16/2020
1103 Viracor Eurofins
Lee's Summit, MO
Clinical Laboratory Scientist I
BS/BA in biological/physical/chemical sciences
Exp: 1 year in lab
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. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. 3/16/2020
1104 Viracor Eurofins
Lee's Summit, MO
Clinical Laboratory Scientist I
BS/BA in biological/physical/chemical sciences
Exp: 1 year in lab
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. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Perform laboratory assays in accordance with Viracor-IBT’s standard operating procedures 3/16/2020
1105 Viracor Eurofins
Lee's Summit, MO
IT Business Analyst I
BS/BA in biological/physical/chemical sciences
Exp: 1-2 years
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. 3/16/2020
1106 Viveve
Englewood, CO
Quality Associate
Associates minimum, BS/BA preferred
Exp: 1-3 years in medical devices quality
Responsible for supporting the company’s quality compliance activities as part of the Quality System to ensure that these activities are performed in full compliance with the Company Quality System, FDA, QSR and any other appropriate international quality system requirements. 3/16/2020
1107 Viveve
Englewood, CO
Regional Sales Representative
BS/BA
Exp: 1-3 years in B2B sales
Manage the sales performance of assigned region recurring revenue placement goal. Achieve assigned recurring revenue placements. Provide comprehensive reports on sales activity and other pertinent department activity to assist management in strategic planning. Develop sales techniques for obtaining new business and execute strategies consistent with corporate sales plan. 3/16/2020
1108 Vir Biotechnology
San Francisco, CA
RESEARCH ASSOCIATE – IMMUNOLOGY/ T CELL BIOLOGY
BS or MS
Exp: 1-5 years in immunology or infectious disease
The successful candidate will join Vir’s efforts in discovery research aimed at development of novel therapeutic programs. This person will have significant interactions with both the discovery and clinical development teams. Experience in T cell immunology with a focus on antigen recognition is required. The candidate will also be expected to contribute to the discovery of novel T cell immunomodulators for infectious disease. Experience in human immunology with a focus on T cell assays as well as antibody development is desirable. 3/16/2020
1109 Berry Wehmiller
Portland, OR
Project Accountant (Design Group)
BS/BA in finance/accounting/business admin
Exp: 0-3 years
As part of the Design Group financial team, you will provide project finance support, oversight and analysis focused specifically with supporting the local offices and region. Project finance oversight includes, but is not limited to: Reviewing Project Manager project forecasts and entering the finalized version into EMS, ensuring that project revenues and margins are accurately reflected in the system. Preparing and reviewing client invoices and issuing them accurately & timely according to the client agreement to ensure positive project cash flow. 3/14/2020
1110 Berry Wehmiller
Baltimore, MD
Electrical Assembler (BW Papersystems - Baltimore)
HS Diploma/GED
Exp: 0-2 years
Under direct supervision, perform installation and wiring of electrical components on company produced equipment. Read and interpret basic wiring diagrams, specifications, and work orders to determine materials requirements or assembly instructions. Assemble basic electrical or electronic systems or support structures and install components, units, sub-assemblies, wiring, or assembly casings using rivets, bolts, and soldering equipment. 3/14/2020
1111 Berry Wehmiller
Baltimore, MD
Mechanical Assembler (BW Papersystems - Baltimore)
HS Diploma/GED
Exp: 0-2 years in automotive maintenance
Plan and perform a normal range of operations connected with the assembly and erection of company-produced machines.  Responsible for the mechanical assembly of box-making machines comprised of feed, printing, cutter, scorer-slotter sections and related units in accordance with design specifications.  Work involves working from complex drawings and a considerable number of component parts that require skill and care to align, fit, and assemble into units and obtain exacting operating performance and appearance. 3/14/2020
1112 Berry Wehmiller
Portland, OR
Project Engineer (Design Group)
BS/BA in chemical engineering
Exp: 0-2 years in chemical engineering/mechanical facilities engineering
Interacting with project team, client, and vendors designing and specifying production line and facility layouts. Working directly with vendors specifying equipment. As-building facilities 3/14/2020
1113 Berry Wehmiller
Sacramento, CA
Project Engineer (Design Group)
BS in mechanical/electrical engineering
Exp: 1-5 years in project engineering
Accountability for all aspects of project execution including line layout engineering, mechanical design, vendor/contractor management, equipment procurement, schedule management, project finances, site management and installation support. Simultaneously organize and successfully execute multiple project responsibilities. Maintaining and growing solid client relationships. 3/14/2020
1114 Berry Wehmiller
St. Louis , MO
Entry-Level Controls Engineer (Design Group)
BS in electrical/computer engineering
Exp: Entry Level
The Controls/Automation Engineer will design, program, and troubleshoot packaging machinery and line control systems. This person will travel to top clients across the country to assist in the design of manufacturing processes, help manage projects, develop facilities, and impact the world by conducting themselves with integrity in pursuit of individual and enterprise goals. Create user applications to monitor and control the production of consumer goods, to satisfy various regulatory agencies, using modern industry standards 3/14/2020
1115 Berry Wehmiller
Romeoville, IL
Entry-Level Project/Process Engineer (Design Group)
BS in mechanical/chemical engineering
Exp: Entry Level
The Project/Process Engineer will be accountable for all aspects of project execution including line layout engineering, mechanical design, vendor/contractor management, equipment procurement, schedule management, project finances, site management and installation support. This person will travel to top clients across the country to assist in the design of manufacturing processes, help manage projects, develop facilities, and impact the world by conducting themselves with integrity in pursuit of individual and enterprise goals. 3/14/2020
1116 Vapotherm
Exeter, NH
Warehouse Associate I
HS Diploma/GED
Exp: 1-3 years in warehouse environment
A Warehouse Associate is responsible for proper receipt, handling, storage, count accuracy, transfer, packaging, and shipment of products in and out of the warehouse. 3/14/2020
1117 Varex Imaging
Salt Lake City, UT
entry Level Production Operator - Day Shift
HS Diploma/GED
Exp: 0-1 years
Assembles/processes product, parts and assemblies using hand tools, customized tooling, and/or semi-automated equipment. Follows written process/assembly documentation. Inspects and tests parts, assemblies and product using precision measuring and testing equipment. Adjusts process within defined ranges based on measured results. 3/14/2020
1118 Varex Imaging
Salt Lake City, UT
Entry Level Production Operator - Day Shift
HS Diploma/GED
Exp: 0-1 years
Assembles/processes product, parts and assemblies using hand tools, customized tooling, and/or semi-automated equipment. Follows written process/assembly documentation. Inspects and tests parts, assemblies and product using precision measuring and testing equipment. Adjusts process within defined ranges based on measured results. 3/14/2020
1119 Varex Imaging
Salt Lake City, UT
Manufacturing Engineer I
BS/BA
Exp: No experience necessary
Develops, implements and maintains methods, operation sequence and processes in the manufacture or fabrication of parts, components, sub-assemblies and final assemblies. Interfaces with design engineering in coordinating the release of new products. Estimates manufacturing cost, determines time standards and makes recommendations for tooling and process requirements of new or existing product lines. Maintains records and reporting systems for coordination of manufacturing operations. 3/14/2020
1120 Varex Imaging
Franklin Park, MA
Manufacturing Engineer
BS/BA
Exp: No experience necessary
Develops, implements and maintains methods, operation sequence and processes in the manufacture or fabrication of parts, components, sub-assemblies and final assemblies. Interfaces with design engineering in coordinating the release of new products. Estimates manufacturing cost, determines time standards and makes recommendations for tooling and process requirements of new or existing product lines. Maintains records and reporting systems for coordination of manufacturing operations. 3/14/2020
1121 Varex Imaging
Palo Alto, CA
Research Associate, Molecular Biology and Radiobiology
BS/BA or MS in life sciences
Exp: 0-4 years in research
The Research Associate, Molecular Biology and Lab Management, is an experienced individual responsible for performing molecular biology assays supporting Varian’s radiobiology and drug-radiotherapy screening investigations and managing laboratory equipment and purchasing for the Global Translational Science team. 3/14/2020
1122 Varex Imaging
Palo Alto, CA
Research Associate: Molecular Biology
MS in biological sciences
Exp: 0-2 years
The Research Associate, Molecular Biology, is responsible for planning and executing experiments in support of Varian’s scientific objectives. Reporting to the Manager of the Global Translational Science Team, the Research Associate, Molecular Biology is responsible for planning and executing experiments related to human and mouse IHC in support of Varian’s scientific objectives. 3/14/2020
1123 Veeva
Pleasanton, CA
Associate Automation Engineer
BS/BA in computer/information sciences
Exp: 0 years, recent graduate
Identify automatable test cases that are most likely to catch issues in SaaS CRM product used by end users around the globe. Refine test cases to make for robust automation, make configuration settings and design automation datasets. Develop software for automation testing in Windows OS, Apple iOS, and web browser environments. Maintain/tune automation suites 3/14/2020
1124 Veeva
Toronto, Ca
Associate Performance Engineer
BS/BA in computer science/engineering/math
Exp: 0 years, recent graduate
The Vault Performance Engineering Team works within the Vault Development Team and participates in all phases of the software development life cycle. 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 3/14/2020
1125 Veeva
Fort Washington, PA
Associate Data Analyst
BS/BA in computer science/engineering/math
Exp: 0 years, recent graduate
The Associate Data Analyst will be responsible for all aspects of the data analytics process and will be tasked with helping the Data Operations team innovate with a scalable framework for data collection, extraction, reporting, and analysis. Assist in the building of web scraping systems to crawl, extract, and ingest data using common web scraping tools. Understand how to translate high-level design Proof of Concept ideas into actionable tasks and specifications designed to accomplish the goal 3/14/2020
1126 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
1127 Vericel
Cambridge, MA
QC Analyst I
BS/BA
Exp: 1 year in cGMP lab
Quality Control (QC) is responsible for incoming inspection of components and raw materials, plus quality testing (e.g. analytical, microbiological) of intermediate, stability and final product samples to demonstrate that all products manufactured meet standards required for cGMP operations. Various techniques (e.g. assay transfers, validation and qualification of new instrumentation) are utilized within the Quality Control Laboratory to ensure cGMP compliance. 3/14/2020
1128 Vericel
Cambridge, MA
Manufacturing Technician
BS/BA
Exp: 0-2 years in cGMP lab
Responsible for the execution of process steps to manufacture commercial cell therapy products meeting internal and regulatory requirements. Perform manufacturing procedures inside an ISO Class 7 clean room in accordance to established SOPs, cGMPs, and safety regulations. Perform aseptic manipulations of cell culture lots and final product assemblies. Document production operations in corresponding batch records and log sheets according to cGMPs and established SOPs. 3/14/2020
1129 Vericel
Cambridge, MA
Lab Assistant
HS Diploma/GED
Exp: 0-1 years
The Research and Development (R&D) group within Vericel supports the continuing development, characterization and validation of manufacturing methods, novel assays, new technology and operational improvements. This group manages technology transfers, clinical manufacturing, training, database development, trending analysis and stability. The R&D team plays an important role in commercial manufacturing troubleshooting, root cause investigation, process optimization and product life cycle management. 3/14/2020
1130 Vericel
Cambridge, MA
Engineer, Validation I
MS in life sciences
Exp: 1+ years validation experience
The Validation department performs equipment, utility, cleaning, sterilization, software, and process validation activities to ensure compliance with company procedures and industry standards in support of Operations and Quality Systems for cell therapies products. The department also functions as the liaison with the Metrology department and performs all equipment ownership and quality assurance review responsibilities associated with site calibration activities. 3/14/2020
1131 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
1132 VGXI
Woodlands, TX
Manufacturing Support Technician
HS Diploma/GED
Exp: 1-3 months
Responsible for the maintenance, cleaning, and sterilization of manufacturing equipment, manufacturing support equipment, supplies, and production areas. Wash all glassware and plastic supplies in a washer or by hand, as needed. Sterilizes materials as requested to ensure the purity of research and GMP materials. 3/14/2020
1133 VGXI
Woodlands, TX
Process Technician
BS or Associates
Exp: 0-3 years
Responsible for the implementation of cGMP in the pilot plant. Write and review SOPs and production batch records. Implement production processes for the manufacture of plasmid DNA. Conduct cGMP production of plasmid products on an ongoing basis. 3/14/2020
1134 Veeva
New York, NY
Associate Product Manager - New Products
BS/BA in computer science/engineering/math
Exp: 1-2 years in project management/technical services
Own and design product features start to finish, including UX design, user stories, specifications, UAT with QA, and customers conversations to ensure effective design. Author high-quality design specifications within an agile methodology based upon industry and customer requirements. Support release and sprint planning to ensure product enhancements support customers at the right time and the right sequence 3/14/2020
1135 Veeva
Columbus, OH
Associate, Sales Support
BS/BA
Exp: 0-2 years in customer service/sales
We are looking for a Sales Support associate to join our team. You will be a partner to the Sales team and manage the operational steps required to effectively engage, retain and support our existing customers ongoing needs related to their Veeva software subscriptions. Our ideal candidate is a motivated, goal oriented, recent college graduate who is interested in developing sales support and customer service best practices. 3/14/2020
1136 Veeva
Indianapolis, IN
Associate Software Engineer
BS/BA in computer science/engineering/math
Exp: 1+ years in client-side or server-side programing
Drive the implementation and delivery efforts for our cloud-based features and products. Write clean, testable, readable code in a team setting using design patterns and object-oriented principles. Create and enhance rich user experiences. Write quality code with high unit and integration test coverage 3/14/2020
1137 Veeva
Columbus, OH
Associate Automation Engineer
BS/BA in computer/information sciences
Exp: 0 years, recent graduate
Identify automatable test cases that are most likely to catch issues in SaaS CRM product used by end users around the globe. Refine test cases to make for robust automation, make configuration settings and design automation datasets. Develop software for automation testing in Windows OS, Apple iOS, and web browser environments. Maintain/tune automation suites 3/14/2020
1138 InBios
Seattle, WA
Research Associate II - (Molecular Biology - antibody engineering)
MS n molecular biology, biochemistry, or related
Exp: Not necessary for MS candidates
We are seeking a motivated individual with experience in molecular biology techniques to join our molecular biology/antibody engineering team. If you enjoy a busy workday, a mix of computer and bench work, and enjoy working both independently and as part of a friendly and motivated team, then we encourage you to apply for this position. Experience and knowledge needed to be successful in this position: In-depth theoretical understanding of molecular biology and strong molecular biology wet lab technique. Experience with DNA sequencing, PCR amplification and plasmid construction. etc. 3/10/2020
1139 Incube Labs
San Jose, CA
Mechanical Designer
BS in mechanical, manufacturing or related engineering fields
Exp: 1-3 year(s)
The Mechanical Designer is a temporary position for a minimum of three months with possibility of extending to six months if needed. The primary responsibility is to provide design and drafting of tools and equipment and their documentation including ECO submission. This position works closely with Engineering, Quality and Manufacturing teams. Major Duties and Responsibilities: Create 3D models and detail drawings by reverse engineering existing tools and fixtures. Work closely with the Engineering and Manufacturing teams to understand design intent and incorporate Geometric Dimensioning and Tolerancing (GD&T). etc. 3/10/2020
1140 Incyte
Wilmington, DE
Research Scientist, Cell Line Development
MS in molecular or cell biology, chemical engineering, or related
Exp: 1-3 year(s)
Our Global BioPharmaceutical Development Group is looking for a Research Scientist, Cell Line Development. This position develops commercially viable cell lines that are used in the production of therapeutic recombinant proteins such as fusion protein, monoclonal and bispecific antibodies. Key responsibilities: Execute experiments to support Cell Line development, including transfection, routing cell passaging and maintenance, secure freeze. Design and execute high throughput assays to screen mAb or BsAb clones, ensure production, product quality, and genetic stability of cell lines. Operate Ambr 15 Fed-batch study to evaluate pools and clones. Execute studies to ensure production, product quality, and genetic stability of cell lines. Qualify single cell plating and imaging workflow to ensure the monoclonality. assessments meet regulatory expectations. Create and maintain research cell banks. etc. 3/10/2020
1141 Innogenix
Amityville, NY
Quality Control Chemist
MS in chemistry
Exp: 1 year
Perform quality control/development activities. Develop, validate and test analytical methods. Analyze raw materials, in-process and finished product samples using modern QC techniques and advanced analytical equipment. Assist Scientists in developing/implementing quality systems and activities. Perform in-process inspections and document results. Assist Scientists in developing and implementing quality systems and related activities. 3/10/2020
1142 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
1143 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
1144 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
1145 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
1146 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
1147 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
1148 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
1149 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
1150 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
1151 Integral Molecular
Philadelphia, PA
Biotechnology Sales Associate
BS in biology, chemistry, or other life science
Exp: 1+ years
We are seeking a Sales Associate to join our University City, Philadelphia-based sales, marketing and business development team. Are you a biologist at heart, but want to explore opportunities outside of typical bench work? Are you a team player who likes to meet new people, build professional relationships, and contribute to the success of a growing biotech company? If you answered “Yes!”, to all the above, then this may be the position for you! Opportunities: Be a key part of the sales, marketing, and business development team of a biotech company. Work with senior management in the planning, strategy, and execution of product development. etc. 3/10/2020
1152 Integral Molecular
Philadelphia, PA
Laboratory Technician
AS/BS in biology, chemistry, medical technology, or related
Exp: 6 - 24 months
We seek an entry level Laboratory Technician to perform vital laboratory tasks to support the continued success of our research teams. The candidate will be part of a lab management team that works in a unified and collaborative manner to ensure the efficient operation of the laboratory. Responsibilities: Coordinate multiple tasks with team members to provide needed supplies. Prepare reagents including buffers, chemicals solutions, complex reaction mixtures and media according to established methods and standard operating procedures (SOP). etc. 3/10/2020
1153 Integral Molecular
Philadelphia, PA
Research Associate I
BS in biology, bioengineering, or related
Exp: 1-2 year(s)
We seek a Research Associate I, who will work with a dedicated group of scientists on the development and commercialization of biomedical technologies. Responsibilities: 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). etc. 3/10/2020
1154 Intellia Therapeutics
Cambridge, MA
Associate Scientist, RNA Oligonucleotide Chemistry
BS/MS in chemistry, biochemistry, or related
Exp: 1-4 year(s)
Intellia Therapeutics is seeking an individual to work closely with the RNA Chemistry Team responsible for synthetic oligonucleotides. This individual will be involved in a complete production process for the identification, implementation & fulfillment of synthesis, purification and reaction scheme analytical characterization and method development of oligonucleotides. RESPONSIBILITIES: Hands-on position in an oligonucleotide chemistry lab inclusive of operating, maintaining & calibrating synthesis platforms and other scientific equipment. Synthetic oligonucleotide method and process development participation. Perform semi-preparative and analytical HPLC and LC-MS quality control processes. Solid decision-making on product path with the ability to work independently and collaboratively while problem-solving. etc. 3/10/2020
1155 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
1156 Intersect
Menlo Park, CA
Technician I, Quality Engineering (Swing Shift)
AS/AA
Exp: 1 year
Support Quality Engineering department on various tasks used to support production and development of medical products used in the treatment for ear, nose and throat disorders. DUTIES AND RESPONSIBILITIES: Work with QE and ME in developing procedures, test methods, qualification protocols, and reports. Perform QA investigation testing on returned product/field complaints, NCMR/CAPA or manufacturing line issues. Assist in performing complaint investigations and return goods evaluation as assigned. Perform QA related data entry and data analysis. Perform responsibilities for NCMR coordinator. Assist QE in providing manufacturing line support including routine observation of manufacturing activities to ensure compliance with manufacturing process instructions and procedures. etc. 3/10/2020
1157 Immunomedics
Morris Plains, NJ
Manufacturing Specialist I
AS/BS in a science or engineering field
Exp: 0-1 year(s)
This position will be 2nd Shift (4PM-2AM) Monday-Thursday. Responsible for pharmaceutical manufacturing in compliance with current Good Manufacturing Practice (cGMP). Responsibilities: Ensures consistent completion of all the planned manufacturing activities assigned to him/herself. Minimize waste of the resources (worktime, materials, and components). Organize workplace to maximize the throughput and minimize risks of errors. Follow well defined procedures closely, with attention to detail. Practice strong aseptic technique. Document activities accurately and clearly as per GDP. Operate manufacturing equipment according to well defined procedures. Daily monitoring of the process. etc. 3/10/2020
1158 Insmed
Bridgewater, NJ
Senior Research Associate - Medicinal Chemistry
MS in chemistry
Exp: 0+ years
The candidate will work with a multidisciplinary team of scientists focused on the discovery, formulation development, and, characterization of novel drug candidates to treat rare lung diseases. Specifically, the candidate will assist with medicinal chemistry efforts including chemical synthesis, purification, and characterization of small molecule drug targets. Responsibilities: Conduct chemical synthesis, purification, and characterization of small molecule drug targets under the direction of a supervising scientist in Insmed’s research labs. Plan and execute assigned experiments, with increasing independence, in support of project goals. etc. 3/10/2020
1159 Guardant
Redwood City, CA
Client Services Associate
BS/BA
Exp: 1+ year(s)
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. Responsibilities: 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. Keeping precise and clear documentation of all phone communications and follow up activities. Adhering to Standard Operating Procedures (SOP’s) pertaining to data entry and data verification requirements. Ability to enter and qualify new customer information into Salesforce.com and LIMS. Contact physicians and other medical personnel to obtain missing information required to complete the order entry process. 3/9/2020
1160 Guardant
Redwood City, CA
DevOps Engineer
BS/MS in computer science or related
Exp: 1-3 year(s)
We are building a unique software stack to manage an ecosystem of microservices, RESTful APIs, and data integrations with internal and external systems to deliver useful and elegant user experiences in the extraordinarily complex oncology diagnostic and therapeutic landscape. We connect patients with clinical trials, help clinicians order our test and receive our clinical reports, and deliver valuable genomic datasets to researchers to help uncover important insights into treatment paradigms and drug discovery. Our technology stack reflects our views of using the best tools for the job, employing Java, Python, Ruby along with Kubernetes, Docker, Mule, MySQL, MongoDB, high-performance computing clusters (HPC), and a variety of AWS services to analyze and disseminate vast volumes of genomic data. 3/9/2020
1161 Guardant
Redwood City, CA
Scientist I -II , Reagent Development
MS in molecular biology, genetics, bioengineering, biochemistry, or related
Exp: 1-5 year(s)
To enable Guardant Health to lead the disruption of cancer treatments through non-invasive cancer screening, the Technology Development Team is seeking a highly motivated Scientist I - II to help develop, test, and improve sample preparation technologies for rare variant studies with next-generation sequencing. At Guardant, we leverage the most advanced technologies and work with leaders in many different fields to create the most impactful and meaningful technologies for cancer management. etc. 3/9/2020
1162 Helmer Scientific
Noblesville, IN
Assembler Level I 2nd Shift
HS diploma or equivalent
Exp: 1-3 year(s)
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. Promotes Helmer values as demonstrated in personal productivity and quality of work, management of internal/external relationships, actively seeking out and participating in Continuous Improvement practices, and willingness to engage and support team initiatives. Comply with workplace safety procedures. 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. etc. 3/9/2020
1163 Helmer Scientific
Noblesville, IN
Assembler I - Clean & Pack
HS diploma or equivalent
Exp: 1-3 year(s)
Responsibilities: The Assembler I - Clean & Pack: 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. 3/9/2020
1164 Hitachi Chemical Advanced Therapeutics Solutions
Allendale, NJ
Associate Scientist, MSAT
BS in a life science or engineering field
Exp: 1+ year(s)
The Associate Scientist, MSAT performs process and analytical experimental studies as part of a team that is effectively delivering cell therapy services to clients in accordance with defined scope of work, timelines, and budgets. This includes supporting clients in process development, technology transfer and continuous improvement of our client's novel manufacturing processes. Our goal is to support our clients in developing commercially viable cell therapy products, so that they can become accessible to all. etc. 3/9/2020
1165 Homology Medicines
Bedford, MA
Research Associate - Molecular Analytical Development (6 Month Contract)
MS in a biological science
Exp: 0-4 years
Homology Medicines is seeking a Research Associate to aid in operational support for methods to characterize AAV vector products. The individual in this role will be a talented and motivated technician who will focus on the analysis of research/development-grade vector samples using multiple AAV-specific analytical methods. This is a largely laboratory-based position with a focus on providing analytical support for characterizing research-grade vectors. Responsibilities: Plans and executes AAV-specific characterization assays, including vector genome quantification by qPCR and ddPCR, viral capsid quantification by ELISA, protein analysis by SDS-Page gels, endotoxin testing, and additional assays as needed. etc. 3/9/2020
1166 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
1167 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
1168 ICON
Raleigh, NC
Clinical Research Associate
BS in a life science
Exp: 1+ year(s)
ICON is currently hiring Clinical Research Associates with at least 1 year of independent monitoring experience in any therapeutic area! You will be supported with manageable sites & protocols, a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, vacation, and eligible for the annual performance bonus. Additionally, we have innovative technology and provide excellent training to ensure better outcomes. 3/9/2020
1169 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
1170 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
1171 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
1172 Immune Technology Corp.
New York, NY
Untitled Sales Position
BS in a life science
Exp: 1 year
Full/part time position, responsible for ensuring customer retention through account management and increasing revenue through marketing activities and generation of sales leads. JOB RESPONSIBILITIES: 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. Attending tradeshows, exhibits, and industry functions a few times per year. Prospecting sales leads through exhibits and trade shows. etc. 3/9/2020
1173 Helmer Scientific
Noblesville, IN
Electromechanical Design Technician I
AS/BS in engineering or engineering technology
Exp: 1-5 year(s)
Responsibilities: The Electricromechanical Design Technician: Promotes Helmer values as reflected in personal productivity and quality of work; maintains positive internal/external relationships; seeks & considers diverse perspectives; is committed to individual development and achievement of company goals/objectives. Complies with workplace safety procedures. Assembles and update prototype units for new and existing product including mechanical cabinet, electrical wiring and thermal control system. etc. 3/9/2020
1174 Harpoon Therapeutics
South San Francisco, CA
Clinical Trial Assistant
BS in a biology related field
Exp: 1+ year(s)
We are seeking a highly motivated CTA to be responsible for the coordination of activities (primarily administrative tasks) associated with Clinical Trial startup and maintenance 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. Key Responsibilities: Maintain and/or accelerate timelines for achieving clinical operational milestones. File, track and maintain study activity. Manage and ensure the paper and electronic Trial Master File (eTMF) meets FDA/ICH/GCP requirements. Coordinate execution of Non-Disclosure and Confidentiality Agreements (NDAs and CDAs) with study sites. etc. 3/9/2020
1175 Harpoon Therapeutics
South San Francisco, CA
Research Associate, Biology
BS/MS in cell biology, biochemistry, or related
Exp: 1+ year(s)
The Research Biology group at Harpoon Therapeutics seeks a Research Associate to join our team. Responsibilities include testing of samples in support of both preclinical development and clinical programs, assay development and optimization, and collection of data in support of regulatory filings. Applicants should be capable of working flexibly and expeditiously in a collaborative, innovative and inspiring environment. The ideal candidate will have experience with mammalian cell culture, stable cell line generation, luciferase assays, flow cytometry, and bioassay automation. Good communication skills, good planning, and an ability to meet deadlines are essential. 3/9/2020
1176 Harpoon Therapeutics
South San Francisco, CA
Research Associate, New Technologies (Assay Development)
BS/MS in biology or related
Exp: 1+ year(s)
We are seeking a highly motivated Research Associate to join the New Technologies group at Harpoon. Our growing team is focused on the development of novel, conditionally active biologic prodrugs. These prodrugs are designed to be preferentially active in the tumor, and thus, enable the safe targeting of previously intractable therapeutic targets. The successful candidate will be expected to design and execute experiments to help develop new biologic prodrug candidates, work collaboratively in a cross-functional environment, and have a strong desire to learn new techniques and the underlying scientific rationale. etc. 3/9/2020
1177 Harpoon Therapeutics
South San Francisco, CA
Research Associate, New Technologies (Immunology)
BS/MS in biology or related
Exp: 1+ year(s)
We are currently seeking a Research Associate to join the New Technologies group at Harpoon. Our growing team is focused on the development of novel, conditionally active biologic prodrugs, including our protease-activated T cell engager platform (ProTriTAC). These prodrugs are designed to be preferentially active in the tumor, and thus, enable the safe targeting of previously intractable therapeutic targets. The successful candidate will be expected to design and execute experiments to help develop new biologic prodrug candidates, work collaboratively in a cross-functional environment, and have a strong desire to learn new techniques and the underlying scientific rationale. 3/9/2020
1178 Jubilant
Spokane, WA
Validation Associate
Associates in sciences
Exp: 6-12 months in industry
The Validation Associate works closely with the Validation Specialist in support of capital, contract, and compliance projects. This position is responsible for executing a variety of validation studies, including performance qualifications and/or requalification’s for terminal and component sterilization work. 3/8/2020
1179 Jubilant
Salisbury, MD
Manufacturing Process Operator
HS Diploma/GED
Exp: 1 year in manufacturing
The Process Operator runs, performs set-ups, maintain safe operations, and cleanings of the production equipment. Operates production machinery and follows the procedures per both company & FDA requirements. Meets the requirements for use of manufacturing equipment and other commonly used equipment per standard operating procedures (SOPs). 3/8/2020
1180 TriLink Biotechnologies
San Diego, CA
Manufacturing Associate I
BS in life sciences
Exp: 1-3 years
This position will produce research and clinical grade components and products within ISO 5 and greater environments. The candidate will participate in the set-up, cleaning, operation, and maintenance of laboratory equipment; perform chemical and enzymatic reactions following asceptic procedures. The candidate must document all actions using GMP Good Documentation Practices. This position requires a candidate that can excel as a leader in the laboratory space. 3/8/2020
1181 Tris Pharma
Monmouth Junction, NJ
Sales Operation Associate
BS/BA
Exp: 1 year in office/manfacturing
The Sales Operations Associate assists the generic sales and marketing efforts by providing analytical and operational support to both internal commercial departments and external clients. Collaborating closely with the President, Generic division, the incumbent supports various and diverse sales operations, analytics, and business development projects and on-going tasks. She/he also works closely with the Sales Operations Representative to contribute to, and support, the building, maintaining and enhancing of client business relationships with assigned customers as well as cross functionally with internal departments and external resources on sales operations issues. 3/8/2020
1182 Tris Pharma
Monmouth Junction, NJ
Technician/Laboratory Assistant – Product Development
HS Diploma/GED
Exp: 0-2 years in lab/manufacturing
The Lab Technician assists the Product Development department by performing routine preformulation and formulation development activities per the given instructions of Scientists. Carries out responsibilities in accordance with the organization’s policies, procedures, and state, federal and local laws Preparation drug-excipient compatibility studies and other Preformulation studies, as instructed 3/8/2020
1183 Twist Biosciences
South San Francisco, CA
Research Associate
BS or MS in biological/chemical sciences
Exp: 1-5 years in research
We are seeking an outstanding, innovative, and creative Research Associate to join our R&D team to develop world-class Next Generation Sequencing (NGS) Products. This Research Associate will play multiple roles within the R&D group and will work within a small team responsible for development of NGS Products with an emphasis on library preparation and target enrichment applications. 3/8/2020
1184 Twist Biosciences
South San Francisco, CA
Manufacturing Associate, Gene Production
Bachelors/Associates in life sciences
Exp: 0-2 years in manufacturing environment
The Manufacturing Associate, Gene Production will be accountable for following scheduled tasks, operating automated liquid handling devices in a safe and efficient manner, Exhibit detail-oriented documentation skills for updating batch records and logs, cleaning and restocking the lab, and practice good lab bench techniques to ensure high quality and consistent products. Manufacture high quality custom oligo containing products in a high throughput MFG lab according to established SOPs. Daily use of traditional molecular biology processes and techniques especially PCR, DNA quantitation and handling, DNA purification 3/8/2020
1185 Twist Biosciences
South San Francisco, CA
Manufacturing Associate, Custom Vector Onboarding
Bachelors/Associates in life sciences
Exp: 0-2 years in manufacturing environment
The Manufacturing Associate will be responsible for the production of custom gene based products and/or various intermediates according to established SOPs and complete manufacturing batch records to contribute to the daily production schedule. Manufacture high quality custom oligo containing products in a high throughput MFG lab according to established SOPs. Operation of robotic laboratory equipment and traditional lab equipment (bioanalyzers, centrifuges, sealers, thermocyclers, spectrometers, HPLCs, Next Gen Sequencing etc.) 3/8/2020
1186 UCB
Boston, MA
Research Associate - Cell Line Generation
BS in biological sciences
Exp: 1-3 years in lab
For our Bedford laboratory, we are seeking a highly-motivated full-time Research Associate to perform a variety of complex technical duties involving mammalian cell engineering for signal transduction and reporter assay development. The successful candidate will be responsible for transgene design, generating a variety of disease relevant cell culture models, designing and executing experiments to test engineered cell lines, analyzing data, and communicating results to UCB colleagues. 3/8/2020
1187 Ultivue
Cambridge, MA
Biomanufacturing Technician
BS in chemical/life sciences
Exp: 0-3 years
This individual will focus on applying his/her technical expertise to perform approved manufacturing and analytical processes to make and test reagents for use in kit products and for company internal use. Make, QC test and deliver on-time, high quality and highly reproducible reagents. Perform incoming QC on purchased antibodies and other raw materials. Working in a team, use established protocols to conjugate antibodies, prepare solutions, and produce nucleic acid reagents 3/8/2020
1188 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
1189 United Therapeutics
Research Triangle Park, NC
Materials Associate
HS Diploma/GED
Exp: 1+ years in warehouse/manufacturing environment
The Materials Associate will be responsible for processing incoming material receipts, control and issuance of materials and preparation of product shipments. This individual will be responsible for performing warehouse activities in accordance with UT policies and procedures. 3/8/2020
1190 United Therapeutics
Research Triangle Park, NC
Seasonal Support Associate - Clinical Operations (Clinical Oversight)
BS/BA
Exp: 0-1 years
Support the Clinical Oversight, Training and Standards team with harmonization of clinical development SOPs, study plans, and processes, as well as deployment and maintenance of clinical systems and training. Provide administrative support related to Clinical Oversight, Training and Standards activities 3/8/2020
1191 United Therapeutics
Research Triangle Park, NC
Research Associate I/II - Bioscaffolds/Lung Function
BS or MS in life sciences/engineering
Exp: 1-3 years lab work
Conduct and assist in product development and research efforts for tissue-based regenerative medicine products for treatment of pulmonary hypertension and other lung diseases. More specifically, support decellularization process development and focus on material and functional characterization of lung scaffold and RegenLung construct. 3/8/2020
1192 United Therapeutics
Silver Spring, MD
Research Software Engineer I
MS in computer science, engineering or math
Exp: 0-2 years
As an important part of this effort in your role as a Research Software Engineer, you will integrate models from multiple scales (organ-level to molecule-level) and guide your team members on how to optimize the efficiency of simulations that further our MedicinesForLife® mission. Work with computational biologists to translate mathematical descriptions of physiological and molecular processes into high-performance computer simulations. Develop and analyze complex integrated systems of differential equations and rule-based models at multiple space and time scales 3/8/2020
1193 United Therapeutics
Research Triangle Park, NC
Bioprocess Technician - Cell Biology
AAS/BA/BS in Biology, Cell and Molecular Biology, or Biomedical Sciences
Exp: 1+ year in life sciences
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. Assist with generation and maintenance of all master and working cell banks. Routinely perform bioanalytical assays to phenotypically and functionally characterize cells (such as flow cytometry and plate-based assays) 3/8/2020
1194 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
1195 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
1196 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
1197 Utah Med
Midvale, UT
Quality Control Engineer - Midvale, Utah
BS
Exp: 1 year
Manages complaint handling system. Schedules and conducts or reviews internal quality audits. Reviews and maintains records of internal audits and internal corrective actions, and participates in MRB. Responsible for Quality Assurance review of R&D and manufacturing projects. Gathers, prepares and presents appropriate Company Quality Assurance-related reports. As assigned: develops defect criteria for use in existing products/raw materials, analyzes/investigates defect causes, inspects/tests products/raw materials to determine compliance, failure mode, etc., and participates in company-wide quality-improvement efforts. 3/8/2020
1198 Vanda
Grand Rapids, MI
Associate Neuroscience Specialty Sales Representative (Grand Rapids, MI)
BS/BA or higher
Exp: 0-1 years with internship/part-time experience
As an Associate Neuroscience Specialty Representative, you will be responsible for: Becoming knowledgeable of disease state, product and competitive market knowledge. Educating Healthcare providers on Vanda's product portfolio. Developing relationships with Healthcare providers in order to understand their needs. 3/8/2020
1199 The Ritedose Corporation
Columbia, SC
Packaging Specialist
2 year technical degree
Exp: 12 months
The Packaging Specialist is responsible for operating and maintaining the equipment on their respective shift and support of the overall department’s performance goals. They are responsible for the completion of operations on a daily basis. This includes meeting the daily packaging output goals, following the procedures as defined by SOP’s, and executing specific verbal directions from their direct leadership 3/7/2020
1200 West Pharmacuetical Services
Exton, PA
Associate Packaging Engineer
BS/BA in packaging, chemical, mechanical engineering or related
Exp: 1-3 years
Provide project support for the development of new packaging, products, and technologies. Contribute to the selection of materials, create specifications, and manage tasks associated with the development of unique and functional packaging that enhances and preserves the value of West’s products. Perform packaging process development activities and equipment setup as appropriate in laboratory and production environment following all appropriate cGMPs and company policies and procedures. 3/7/2020
1201 West Pharmacuetical Services
Tempe, AZ
Lab Quality Auditor & Inspector
HS Diploma/GED
Exp: 1-3 years
In this role, you will provide total manufacturing quality inspection services including: manufacturing inspection, quality inspection, quality control, sampling inspection, documentation and record keeping. You will also complete and maintain all documentation necessary to ensure conformity to specifications and traceability of records. 3/7/2020
1202 West Pharmacuetical Services
Kinston, NC
Extruder Operator
HS Diploma/GED
Exp: 1-3 years cGMP experience
Ideal candidates are quick thinking and confident to ensure consistent processing and foresight to know the next task required. It is the responsibility of this individual to ensure that product/customer specifications are followed always. Ideal candidates have previous cGMP experience. Duties include: Extrude quality stock of enough quantities required to run our molding presses to produce molded parts that meet our customer’s specifications. Set up Dispersion Enhanced Systems (DES) with a screen pack and Breaker Plate for formulas to be ran while maintaining traceability for all formulations running on the extruder. 3/7/2020
1203 West Pharmacuetical Services
Tempe, AZ
Mold Technician (Day Shift)
HS Diploma/GED
Exp: 0-3 years
Performs labor along a production line. Operates, inspects, and troubleshoots production line machinery and /or assemblies. Ability to work from verbal instructions or from drawings and sketches to plan, construct, alter, assemble, or rebuild a variety of tooling, test fixtures, tools, mold and die components, or related assemblies or equipment. Check work quality continuously, making equipment adjustments and other related changed if necessary, after consulting with Lead person. 3/7/2020
1204 West Pharmacuetical Services
Tempe, AZ
Operator (Multiple Shifts)
HS Diploma/GED
Exp: 1-3 years in manufacturing
West is looking for a motivated operator to join our top-quality production team. In this role, you will perform labor along a production line. Operates, inspects, and troubleshoots production line machinery and /or assemblies. Visually inspects, ensures, and assembles parts in process to quality specifications, being aware of critical visual and dimensional defects and determines acceptability of the parts, based on customer specifications. Assures accuracy of product packaging and tractability as required, including generating labels, the correct labeling of containers, and accurate part count. 3/7/2020
1205 West Pharmacuetical Services
Scottsdale, AZ
Calibration Technician
HS Diploma/GED
Exp: 1-3 years in calibration/maintenance
In this role, you will oversee, coordinate, and execute equipment and facility calibrations in accordance with ISO 13485 requirements. Oversees the maintenance and execution of the calibration program to ensure compliance to standards, including ISO 13485 and FDA 21CFR820. Maintains calibration schedule for facility and equipment – including, but not limited to, logs, records, files, and other documentation for both internal and external calibrations. 3/7/2020
1206 West Pharmacuetical Services
Tempe, AZ
Associate Manufacturing Engineer
BS/BA in engineering or sciences
Exp: 0-3 years
In this role, you will support the manufacture and startup new Plant equipment and equipment upgrades as assigned. Assist with providing engineering support with hands on expertise and practices in projects from conception through production. Interact with engineering, management, site and corporate team members and/or vendors to develop engineering specifications for new equipment or required process improvements; maintain drawings; maintain project timelines; continuously evaluate projects from the tasks, resource and costs perspective, ensure delivery of the projects on time and within budget; and actively install, start-up, and validate equipment or tooling. 3/7/2020
1207 The Weinberg Group
Washington, DC
Researcher
BS/BA in life sciences
Exp: 1-2 years
Is an expert at identifying sources and searching for relevant information. Retrieves, researches, and compiles data to support client projects. Conducts analysis of scientific data and regulatory information. Summarizes regulatory information and pertinent scientific literature for assigned projects. 3/7/2020
1208 TherapeuticsMD
Boca Raton, FL
Help Desk Technician
HS Diploma/GED
Exp: 1-2 years in computer related work
Primary responsibility is to work the queue of Help Desk tickets from users within the company and resolve their requests or escalate to other staff for more complex requests. Respond to and log requests received via the Help Desk system, email, phone, or other avenues. Build/repair PCs and other computer equipment. 3/7/2020
1209 Theravance Biopharma
South San Francisco, CA
Research Associate I/II, Biology & Pharmacology
BS/MS
Exp: 1-4 years pharma research experience
This individual will join a multi-disciplinary team to develop, automate and conduct biochemical and cell-based assays to help drive lead optimization and obtain mechanistic insights for all research programs. Will play a key role in developing, optimizing, and automating new assays. Will conduct compound screening for SAR support and perform quality data analysis. 3/7/2020
1210 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
1211 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
1212 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
1213 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
1214 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
1215 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
1216 Tolmar
Windsor, CO
Manufacturing Operator I - Derm; 1st Shift, Monday - Friday
HS Diploma/GED
Exp: 1 year in GMP manufacturing
The Manufacturing Operator I performs routine activities related to supporting the dermatology team, while ensuring that products are made with quality for our patients. Perform routine sampling and inspections for product attributes (fill weights, product sealing, labeling) of filled products. Assist in the setup/operation/disassembly and cleaning of production filling equipment. 3/7/2020
1217 Tolmar
Fort Collins, CO
QA Associate I - Process 2nd shift
HS Diploma/GED, Associates preferred
Exp: 1-3 years
The Quality Assurance Associate I is responsible for the inspection, testing, record keeping and overall quality assurance support to manufacturing. Follow procedures to determine status or disposition, and properly document results on records and in lab notebooks.Inspect material, components, and finished product against specified requirements. 3/7/2020
1218 Tolmar
Windsor, CO
Process Development Engineer I
BS in engineering, chemical or mechanical preferred
Exp: 1 year in engineering environment
Assists with the design and implementation of aseptic manufacturing processes, instrumentation and equipment from the laboratory through pilot plant and commercial manufacturing scale-up. Understand and improve process and equipment by working with formulation scientists, other engineers, and manufacturing personnel.Assist other Process Development Engineers as needed to refine batch records, implementing changes when necessary to address manufacturing considerations including processing, manufacturability and scale-up. 3/7/2020
1219 Tolmar
Windsor, CO
Manufacturing Operator I - Aseptic
HS Diploma/GED
Exp: 1 or more year in GMP manfacutring
The Aseptic Operator I performs routine activities related to supporting the injectable team, while ensuring that products are made with quality for our patients. Perform job responsibilities in accordance with standard operating procedures (SOPs) and production records with an expectation of "Right the First Time". Assist in setup and manufacture (bulk, fill, stopper, label, and package) clinical supplies and commercial pharmaceutical products in an aseptic environment in accordance with production batch records. 3/7/2020
1220 Torque
Cambridge, MA
Associate Scientist, T cell Immunotherapy Characterization
BS or MS in biological/engineering sciences
Exp: 1-5 years
The successful candidate will contribute to assay development and process/product characterization efforts supporting the development of our Deep-Primed™ cell therapy platform. This lab-based role will work closely in a cross-functional team of immunologists, analytical chemists, and process engineers to support analytical method development/optimization, product characterization, formulation development, and process development efforts. Primary responsibilities include experimental design and execution, data analysis, documentation, and verbal and written communication of results to the team. 3/7/2020
1221 Toxikon
Bedford, MA
Histology Research Associate
BS/BA in life sciences
Exp: 0 years
Toxikon is currently seeking a full-time Histology Research Associate. Qualified candidates should be a team player, have a willingness to learn, be detail oriented, proficiency with computers and have well-developed time management skills. Trimming of tissues and organs harvested at necropsy. Embedding and processing of tissues. Microtomy Routine H&E staining, other stains as required. Maintain and/or create GLP documentation as necessary, including relative SOPs and histology records, Maintain wet tissue archive. 3/7/2020
1222 Toxikon
Bedford, MA
Research Associate, Extraction
BS in sciences
Exp: Entry Level
The successful candidate will work hand in hand with our study directors, quality assurance and sponsors/clients to ensure all medical device preparation aspects are performed per scientific and regulatory standards. Prior to being tested in clinical trials, medical devices are required by the FDA, EU, Japan, China etc. to perform pre-clinical safety testing referred to as biocompatibility. As most medical devices cannot be directly dosed or applied to the test system, they are extracted using common vehicles and solvents which mimic the conditions found in the human body (blood, muscle, lipids etc.). It is these “extracts” which pull compounds out of the devices, which the body would naturally, and these solutions are dosed as equivalent alternative to the original, whole device. This Medical Device Extraction Research Associate position is responsible for the preparation of the medical devices and creating the required dose solutions (extracts). 3/7/2020
1223 Toxikon
Bedford, MA
Quality Assurance Associate, Micro
BS/BA in life sciences
Exp: 1-3 years in testing environment
In this quality assurance role, the appropriate candidate will be responsible for the implementation, functioning, and monitoring of quality assurance activities. This includes monitoring biological and chemical studies, and creating reports in conformance with GLP practices. Candidates will review GMP, GLP and non-GLP reports for accuracy with reference to protocols, Quality Assurance Standards, Standard Operational Procedures, laboratory precision and accuracy limits, as well as reviewing all protocols for compliance and accuracy. 3/7/2020
1224 Toxikon
Bedford, MA
Laboratory Assistant, In-Vivo
HS Diploma/GED
Exp: Entry Level
Toxikon is seeking an entry level lab assistant to work in the In Vivo Biocompatibility department. The successful candidate will haveinteraction with In Vivo Research Associates, In Vivo Study Directors, Vet Care staff and interface with laboratory management regarding all day-to-day activities of the studies. They will be responsible for providing logistical support for the studies being conducted. As a laboratory assistant, you will be responsible for preparing animals for the studies conducted, including shaving, weighing and identification. 3/7/2020
1225 Toxikon
Bedford, MA
Laboratory Assistant, Extraction
Associates in biotechnology/life sciences
Exp: Entry Level
We are seeking a self-motivated and quality focused individual to join our Extraction team as a Lab Assistant. This position will be responsible for preparing medical devices by extraction using common vehicles and solvents for pre-clinical safety testing. Routine mathematic principles, such as surface area calculations, are required to be able to prepare medical devices and create the required dose solutions. 3/7/2020
1226 Toxikon
Bedford, MA
Clinical Pathology Laboratory Assistant
As or BS in biological/chemical sciences
Exp: 
Toxikon is looking for a self-motivated and quality first lab assistant to join our clinical pathology lab. The successful candidate with work hand in hand with our lab staff, study directors, veterinarians and pathologists to process data and samples. This position offers great possibilities for growth as exposure to test methods and sample analysis will occur with experience in the lab. You will be joining a fast growing team and will be selected based on both experience, aptitude and a dynamic personality.  Toxikon is looking for a self-motivated and quality first lab assistant to join our clinical pathology lab. The successful candidate with work hand in hand with our lab staff, study directors, veterinarians and pathologists to process data and samples. This position offers great possibilities for growth as exposure to test methods and sample analysis will occur with experience in the lab. You will be joining a fast growing team and will be selected based on both experience, aptitude and a dynamic personality.  Toxikon is looking for a self-motivated and quality first lab assistant to join our clinical pathology lab. The successful candidate with work hand in hand with our lab staff, study directors, veterinarians and pathologists to process data and samples. This position offers great possibilities for growth as exposure to test methods and sample analysis will occur with experience in the lab. You will be joining a fast growing team and will be selected based on both experience, aptitude and a dynamic personality.   3/7/2020
1227 ThermoFisher
Lexington, MA
Associate I, Manufacturing
BS/BA in life sciences
Exp: 0-3 years
The Manufacturing Associate 1 is an associate with little to moderate level of technical expertise and experience. An MA1 may independently perform routine operations commensurate with their experience and training. An MA1 participates in the day to day operation of a cGMP compliant Manufacturing facility. Responsibilities include performing basic to moderately complex activities related to operating bioprocess manufacturing equipment, completing the associated documentation of those activities, monitoring assigned processes using automated production systems and controls. 3/7/2020
1228 Fluidigm
South San Francisco, CA
Research Associate
unspecified
Exp: 1-3 year(s)
Fluidigm is looking for a Research Associate to join our Group. The successful candidate will characterize antibodies for use on Fluidigm’s new Imaging Mass Cytometry platform. Description: Perform antibody-metal tag conjugations for a multitude of antibody/tag combination for use in multiplex assays. Perform verification studies on new metal-conjugated antibody products for use with our Mass Cytometry and Imaging Mass Cytometry (IMC) technology. etc. 3/4/2020
1229 Fluidigm
Markham, CA
Reagent Manufacturing Associate
BS in biology, biochemistry, or other life science
Exp: 1-2 year(s)
Fluidigm is seeking a Reagent Manufacturing Associate. The Reagent Manufacturing Associate is a member of our Proteomics Reagent Operations team. The scientist will be accountable for QC testing of raw materials, in-process materials and finished goods for release. This individual will also be a subject matter expert in the development and testing of new QC procedures. etc. 3/4/2020
1230 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
1231 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
1232 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
1233 Fresenius Kabi
Boston, MA
Manufacturing Technician I
HS diploma or equivalent
Exp: 0-2 years
Key Accountabilities include: Execution of routine production operations, labeling, quality control, inventory management, continuous improvement, maintenance of clean room equipment, carry out work in a safe manner while notifying management of safety issues and risks, assumes other duties and responsibilities as directed by supervisor. This is a 1st shift position; however, the hours vary each week depending on which task you are assigned for that week. etc. 3/4/2020
1234 Freudenberg
Jeffersonville, IN
Manufacturing Associate - 1st Shift
HS diploma or equivalent
Exp: None required
Your tasks: Hand assemble manufactured medical components. Complete required documentation for work performed. Quality inspect work performed. Follow defined work procedures. Provide your suggestions and ideas of continuous improvements. 3/4/2020
1235 Freudenberg
Jeffersonville, IN
Manufacturing Associate - 2nd Shift
HS diploma or equivalent
Exp: None required
Your tasks: Hand assemble manufactured medical components. Complete required documentation for work performed. Quality inspect work performed. Follow defined work procedures. Provide your suggestions and ideas of continuous improvements. 3/4/2020
1236 Freudenberg
Jeffersonville, IN
Manufacturing Associate - Weekend Shift
HS diploma or equivalent
Exp: None required
Your tasks: Hand assemble manufactured medical components. Complete required documentation for work performed. Quality inspect work performed. Follow defined work procedures. Provide your suggestions and ideas of continuous improvements. 3/4/2020
1237 Freudenberg
Jeffersonville, IN
Manufacturing Associate - Part Time
HS diploma or equivalent
Exp: None required
Your tasks: Hand assemble manufactured medical components. Complete required documentation for work performed. Quality inspect work performed. Follow defined work procedures. Provide your suggestions and ideas of continuous improvements. 3/4/2020
1238 Frontage
Exton, PA
Scientist- Bioanalytical Services-ICP-MS
MS in analytical chemistry, biochemistry, pharmacology or related
Exp: 1+ year(s)
Scientist / Bioanalytical Services Essential Functions Run sensitive, reliable and efficient LC-MS/MS bioanalytical assays for TK/PK assessment. Candidates with experience in ICP-MS and/or ICP-MS/MS for bioanalytical or other applications are preferred. Duties: Perform high-volume sample analysis and/or data analysis, data QC, and data interpretation. Maintain schedule of projects and timelines. Coordinate study activities with Principle Investigator to ensure efficiency and quality. Aid in the preparation of study summaries and/or reports. etc. 3/4/2020
1239 Gliknik
Baltimore, MD
Laboratory Research Associate
BS in cell biology, microbiology, immunology, biochemical engineering, or related
Exp: Entry level
Gliknik Inc. is seeking motivated, energetic, individuals with an interest in biopharmaceutical drug discovery to learn and conduct laboratory techniques as a laboratory research associate. This position is an entry-level role at Gliknik, located at the UMB BioPark in Baltimore, MD, which discovers and develops innovative large molecule therapeutics for oncology and autoimmune diseases. etc. 3/4/2020
1240 Grail
Menlo Park, CA
Clinical Laboratory Associate - Accessioning
BS/BA in molecular biology or related
Exp: 1 year
The Clinical Laboratory Associate (CLA) - Accessioning will assist in building and establishing GRAIL’s Clinical Laboratory, performing specimen testing and supporting the daily operations of the Clinical Laboratory. The focus of the CLA - Accessioning will be on the receipt, triage, accession, and centrifugation of patient samples submitted to the CLIA laboratory for testing. You Will: Assist in pre-analytical testing activities including specimen processing, quality control, preparation and aliquoting of reagents. etc. 3/4/2020
1241 Grail
Menlo Park, CA
Core Services Research Associate 1/2
BS
Exp: 1+ year(s)
GRAIL is seeking Research Associates I/II for the LabOps Core Services team, who will be primarily responsible for ensuring the efficient execution of GRAIL assays in support of Research and Development activities. The ideal candidate is a detail-oriented, dynamic team player with experience in both automated and manual NGS assay execution. The candidate will be expected to partner with many functions of our organization - Automation, Product Development, LIMS, Quality, Supply Chain, Biosample Operations, and Clinical Lab - to ensure the successful completion of R&D projects and general Operational support. etc. 3/4/2020
1242 Grail
Menlo Park, CA
Quality Control Research Associate 1
BS
Exp: 1+ year(s)
GRAIL is seeking a Research Associate for the LabOps Manufacturing Sciences andTechnology team (MSAT), who will be primarily responsible for materials quality control (QC) and associated tasks. The ideal candidate is a detail-oriented, exceptional team player with hands-on laboratory experience. The candidate will be expected to partner with many functions of our organization - Automation, Product Development, LIMS, Quality, and Clinical Lab - to identify systems limitations, implement process improvements, write documentation, and be instrumental in the implementation and operation of an internal QC system. etc. 3/4/2020
1243 GreenLight Biosciences
Research Triangle Park, NC
Research Associate – Plant Biology
BS in biology
Exp: 1-2 year(s)
GreenLight Biosciences is seeking a highly motivated and collaborative Research Associate to join our Crop Protection team. Greenlight is developing cutting edge RNA technologies that address key challenges in global Crop Protection. In this role you will be integrally involved in the discovery and development of novel biopesticides by developing and executing bioassays for crop pests. The ideal candidate will also have molecular biology skills applicable to RNA interference and gene expression analyses. Strong technical, organizational, and communication skills, as well as the ability to maintain a commitment to excellence and high-quality work in a fast-paced milestone driven company, are essential. etc. 3/4/2020
1244 GreenLight Biosciences
Research Triangle Park, NC
Research Associate Entomology - Contract
BS in entymology
Exp: 0-3 year(s)
GreenLight Biosciences is seeking a highly motivated and collaborative Research Associate to join our Crop Protection team. Greenlight is developing cutting edge RNA technologies that address key challenges in global Crop Protection. In this role you will be integrally involved in the discovery and development of novel biopesticides by developing and executing bioassays for crop pests. The ideal candidate will also have molecular entomology skills applicable to RNA interference and gene expression analyses. Strong technical, organizational, and communication skills, as well as the ability to maintain a commitment to excellence and high-quality work in a fast-paced milestone driven company, are essential. etc. 3/4/2020
1245 Grifols
Johnson City, TN
Biomedical Technician
HS diploma/AS/BS in biology, anatomy, or physiology
Exp: 6-12 month(s)
Primary Functions and Duties (actual tasks performed based on task-specific training identified on Job Training Requirements Matrix: At all times follow Standard Operating Procedures, and responsible for remaining current regarding SOP changes. 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. Provide a positive customer experience by providing health information as per standard operating procedure (SOPs) or as directed by the center Medical staff , explaining fees schedules and bonus programs, instruct donors regarding the importance of plasma donation and explains the uses of the products made from donated plasma. etc. 3/4/2020
1246 Grifols
Kingsport, TN
Biomedical Technician
HS diploma/AS/BS in biology, anatomy, or physiology
Exp: 6-12 month(s)
Primary Functions and Duties (actual tasks performed based on task-specific training identified on Job Training Requirements Matrix: At all times follow Standard Operating Procedures, and responsible for remaining current regarding SOP changes. 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. Provide a positive customer experience by providing health information as per standard operating procedure (SOPs) or as directed by the center Medical staff , explaining fees schedules and bonus programs, instruct donors regarding the importance of plasma donation and explains the uses of the products made from donated plasma. etc. 3/4/2020
1247 Grifols
Hattiesburg, MS
Biomedical Technician
HS diploma/AS/BS in biology, anatomy, or physiology
Exp: 6-12 month(s)
Primary Functions and Duties (actual tasks performed based on task-specific training identified on Job Training Requirements Matrix: At all times follow Standard Operating Procedures, and responsible for remaining current regarding SOP changes. 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. Provide a positive customer experience by providing health information as per standard operating procedure (SOPs) or as directed by the center Medical staff , explaining fees schedules and bonus programs, instruct donors regarding the importance of plasma donation and explains the uses of the products made from donated plasma. etc. 3/4/2020
1248 Grifols
Clayton, NC
Principal Automation Engineer
MS in an engineering, computer, industrial, or automation field
Exp: 1 year
The Validation Automation Engineer II is a junior level professional who is responsible for using technology to improve and streamline a manufacturing process through automation validation. Depending on their specific assignment, this person provides automation validation support for projects or within a specific area. The Validation Automation Engineer II will also integrate into supporting a large scale project. He/she is recognized as proficient in their field such as specific control systems, instrumentation, process, utilities, or qualification testing. He/she meets customer needs in support of business goals. In addition, the incumbent will collaborate with other automation and validation engineers. etc. 3/4/2020
1249 Grifols
Bristol, VA
Biomedical Technician
HS diploma/AS/BS in biology, anatomy, or physiology
Exp: 6-12 month(s)
Primary Functions and Duties (actual tasks performed based on task-specific training identified on Job Training Requirements Matrix: At all times follow Standard Operating Procedures, and responsible for remaining current regarding SOP changes. 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. Provide a positive customer experience by providing health information as per standard operating procedure (SOPs) or as directed by the center Medical staff , explaining fees schedules and bonus programs, instruct donors regarding the importance of plasma donation and explains the uses of the products made from donated plasma. etc. 3/4/2020
1250 Grifols
Research Triangle Park, NC
Sr. Assoc. Research Scientist I
MS in biology, chemistry, or toxicology
Exp: 1 year
The selected candidate provides analytical testing support for process characterization, developmental stability studies, and release of preclinical or clinical batches for internal research projects. The individual selected for this position will conduct testing of non-routine sample types in support of process development, characterization, and/or validation and compile data for the generation of multi-user interactive analytical databases. The analyst may participate in development, implementation and validation of new analytical techniques. etc. 3/4/2020
1251 Grifols
Dothan, AL
Biomedical Technician
HS diploma/AS/BS in biology, anatomy, or physiology
Exp: 6-12 month(s)
Primary Functions and Duties (actual tasks performed based on task-specific training identified on Job Training Requirements Matrix: At all times follow Standard Operating Procedures, and responsible for remaining current regarding SOP changes. 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. Provide a positive customer experience by providing health information as per standard operating procedure (SOPs) or as directed by the center Medical staff , explaining fees schedules and bonus programs, instruct donors regarding the importance of plasma donation and explains the uses of the products made from donated plasma. etc. 3/4/2020
1252 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
1253 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
1254 Guardant
Redwood City, CA
Research Associate, Technology Development
BS/MS in molecular biology, bioengineering, or biochemistry
Exp: 1-3 year(s)
As a Research Associate supporting product and technology development, you will work with members within the team and interface with multiple functions including process engineering, clinical operations, research operations, and bioinformatics. You will be hands on in the molecular biology lab; designing, implementing, and validating new technologies related to liquid biopsy sequencing assays for the early detection and monitoring of oncology biomarkers. You will be utilizing your analytical skills to undertake root cause analyses and identify solution spaces for continuous improvement. etc. 3/4/2020
1255 Guardant
Redwood City, CA
Research Associate, LUNAR
BS/MS in molecular biology, bioengineering, or biochemistry
Exp: 1+ year(s)
The Lunar Research Team focuses on developing and implementing new technologies to improve early cancer detection. We are seeking a highly motivated Research Associate to be hands on in the lab and assist with the planning, developing and use of new molecular assays. You will handle samples from various sources and work with members within the team as well as interface with multiple teams such as process engineering, Tech Ops, and Bioinformatics. etc. 3/4/2020
1256 Guardant
Redwood City, CA
Research Associate, Tech Ops (Contract)
BS
Exp: 1-3 year(s)
As a Research Associate supporting product and technology development, you will work with members within the team and interface with multiple teams including process engineering, clinical operations, research operations, and bioinformatics. You will be hands on in the lab and be required to use existing assays and/or assay prototypes to generate data in support of new technologies related to liquid biopsy sequencing assays. etc. 3/4/2020
1257 Guardant
Redwood City, CA
Automation Engineer
MS
Exp: 1+ year(s)
In this role, you’ll be part of a team that is responsible for automating and scaling complex workflows and implementing processes for a state of the art sequencing lab. You will wear multiple hats and support the development of all parts of a state of the art robotics facility. Your customers will be licensed clinical operators; your goal is to use software and automation to help them focus on extensive screening. The Process Engineer will be involved in all aspects of assay automation development from concept, requirements definition, and manual assay development to adaptation, optimization, troubleshooting and validation. etc. 3/4/2020
1258 GenapSys
Redwood City, CA
Machine Learning Engineer/Scientist
MS in computer science, mathematics, physics, or engineering
Exp: 1-4 year(s)
Machine learning approaches are at the core of GenapSys' methods for generating high quality DNA sequencing data. As a machine learning engineer, you will join forces in the development of cutting-edge machine learning methods that solve key problems in the DNA sequencing, base calling, and variant calling processes. You will work closely with a cross-functional team of life scientists, bioengineers, and data scientists to identify areas where machine learning can make a difference, to conceptualize and develop biological datasets using cutting edge, high throughput platforms, and to analyze these data sets using the best machine learning methods, applied at scale. 3/4/2020
1259 GenapSys
Redwood City, CA
Research Associate, Clonal Amplification
MS in molecular biology, biochemistry, or related
Exp: Not necessary for MS candidates
We are looking for a Research Associate to join in our clonal amplification team to develop a novel clonal amplification platform for the GenapSys sequencer. You will plan and execute experiments, and analyze data under the guidance of Senior Scientist. You must be motivated, organized and detail-oriented with a strong molecular biology foundation and experience in nucleotide assay development. Responsibilities: Develop a novel clonal amplification platform for Genapsys sequencer. etc. 3/4/2020
1260 GenapSys
Redwood City, CA
Research Associate, Development
MS in molecular biology, biochemistry, or related
Exp: 1+ year(s)
We are looking for a Research Associate, Development who will help to drive the development of reliable high-quality DNA sequencing products. The ideal candidate for this role will have some hands-on experience working in a development environment, including developing and optimizing reagents for R & D, developing QC methods and setting specification that correlate with performance, and carrying out stability studies. Experience with DNA Sequencing technology or similar instrumentation is a plus. If this opportunity sounds exciting, and you have the desire to redefine the current paradigm of DNA sequencing, please apply. etc. 3/4/2020
1261 Fujifilm
College Station, TX
Associate Scientist – Analytical Method Transfer
BS/MS in chemistry, biology, or other laboratory science
Exp: 1 year
Essential Functions: Execute method transfers/qualifications/validations based on regulatory guidelines and industry best practices. Perform assays to evaluate the accuracy, precision, specificity, linearity, robustness, and detection/quantitation limits of analytical methods. Maintain laboratory instrumentation and assist with vendor qualifications. Develop expertise on a subset of analytical methods and participate in method troubleshooting activities. Maintain awareness of project timelines and milestones and openly communicate scheduling challenges. etc. 3/4/2020
1262 Fujifilm
College Station, TX
Associate Scientist, Bioassay Development Associate Scientist, Bioassay Development Associate Scientist, Bioassay Development
BS
Exp: 1+ year(s)
The Bioassay Development group is seeking an energetic Associate Scientist with protein chemistry experience to become an integral member of a high performing development team supporting process and formulation development groups. The successful candidate will primarily perform sample analysis using bioassay based techniques such as qPCR, ELISA or plate-based potency assays for the characterization and testing of recombinant protein pharmaceuticals. etc. 3/4/2020
1263 Fujifilm
College Station, TX
Associate Scientist – Downstream Process Development
MS in chemistry, biology, or other laboratory science
Exp: 1 year
Essential Functions: 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). Operation of centrifugation equipment. Operation of filtration equipment. Participate in developing and carrying out experimental protocols. etc. 3/4/2020
1264 Fujifilm
College Station, TX
Associate Scientist/Scientist I, Analytical Development
MS
Exp: 1+ year(s)
The Analytical Development group is seeking an energetic Associate Scientist or Scientist I with protein chemistry experience to become an integral member of a high performing method transfer team supporting protocol based activities including technical transfer of methods from donor labs as well as training of colleagues for internal transfer, and qualification, validation and verification of methods. The successful candidate will primarily execute biochemistry based techniques such as UPLC/HPLC (SEC, IEX, RP, glycan, affinity, etc.), capillary electrophoresis (icIEF, CE-SDS), gel electrophoresis, UV, western blot (SDS-Page), plate based assays and spectrophotometry (SoloVPE) for the characterization and testing of recombinant protein pharmaceuticals. etc. 3/4/2020
1265 Fujifilm
College Station, TX
Automation Engineer
BS in electrical, mechanical, or chemical engineering
Exp: 1 year
Essential Functions: Provide support on a daily basis to process control system, building management systems and data historian systems. Perform system software updates, security updates and upgrades to newer version. Support and enforce the data integrity program. Support and maintenance of computerized systems. OSI Soft PI Historian and reporting system configuration and maintenance. Maintain Functional Specifications, Database Design Specifications and Hardware Design Specifications for automation systems. etc. 3/4/2020
1266 Fujifilm
College Station, TX
Cell Biology Analyst I
BS in biology or related
Exp: Not necessary for BS candidates
Essential Functions: Assist with quality control analytical testing of samples provided to the QC laboratory. Assist with executing test qualification and validation of QC test methods. 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. etc. 3/4/2020
1267 Fujifilm
College Station, TX
Drug Product Operations – Technician I
AS in biology, chemistry, engineering or related
Exp: 0-1 year
Essential Functions: Responsible for the operation of Vanrx SA25 Vial Filling Isolator. Responsible for assisting in the formulation of the bulk drug product in accordance to procedures. Responsible for visual inspection and labeling of filled bulk drug product vials in accordance to procedures. Assist in writing, reviewing, and/or updating Standard. Operating Procedures (SOPs) and Batch Production Records (BPRs). Document and maintain activity records according to cGMP regulations and ensure junior team members are trained. etc. 3/4/2020
1268 Tecomet
Woburn, MA
Machine Operator -Entry
HS Diploma/GED
Exp: 0-2 years machining experience
Under the direction of the Director, Operations, maintains the Quality system as directed. Majority of tasks performed under the supervision of an experiencedmachinist or the Production Manager. Takes direction to learn basic machine operation, setup and maintenance. Duties and tasks are simple andrepetitive. 3/1/2020
1269 Tecomet
Woburn, MA
Photo Etch Operator - 1st Shift
HS Diploma/GED
Exp: Entry Level
The Photo Etch Operator is responsible for processing metal parts in small batches through various chemical baths and rinsing tanks in compliance with Tecomet standards. Process metal parts in small batches through various chemical baths and rinsing tanks. Process panels through conveyorized etch systems per given instructions. Perform in-process visual inspection of chemically cleaned and stripped panels. 3/1/2020
1270 Tedor
Cumberland, RI
Production Technician
HS Diploma/GED
Exp: 1-2 years in production
The Production Technician position performs all tasks involved in the pharmaceutical process following cGMP’s and SOP’s such as wet granulation, dry granulation, tablet compression, encapsulation, tablet coating, packaging and finished product, put product on stability. The position follows standard work methods and practices safe work habits to ensure production is as efficient and safe as possible. 3/1/2020
1271 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
1272 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
1273 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
1274 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
1275 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
1276 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
1277 Tergus Pharma
Durham, NC
Associate Scientist, IVRT
AS or BS in chemistry/biology/pharma sciences
Exp: 0 years
Conducts experiments under limited supervision and maintains excellent notebook documentation in a GMP/GLP laboratory following Good Documentation Practices and ALCOA principles. Performs In Vitro Release Testing (IVRT) for topical formulations such as Gels, Creams, Ointments, Films and Ophthalmic Solutions as per customer needs. Prepares solutions for IVRT and High Performance Liquid Chromatography (HPLC) analysis such as Receiving Media and Mobile Phase. 3/1/2020
1278 Terumo
Campbell, CA
R&D Technician II
AS/AA or BS/BA
Exp: 0-3 years
ob Details: 1. Assemble prototype products per design specifications, drawing and/or engineering direction. 2. Assemble parts by using small instruments with or without a microscope, and through the operations of automated/semi-automated equipment. 3. Troubleshoot and suggest creative solutions to design and process issues. 3/1/2020
1279 Terumo
Elkton, MD
Quality Engineer I
BS/BA in engineering or life sciences
Exp: 1-3 years in med devices
Job Summary: This position is responsible for investigating, planning, and implementing improvements in and/or additions to current products and manufacturing processes that directly affects safety, quality, and productivity with the end result of producing a better quality product more efficiently. Ensure compliance to Terumo’s quality policy, respond to customer complaints, perform audits, develop test methods, and/or write procedures for material characterization. 3/1/2020
1280 Terumo
Elkton, MD
NPD Engineer I
BS/BA or higher in engineering
Exp: 0-3 years
Job Summary: This entry level engineering position is responsible for providing engineering support to Terumo Interventional Systems (TIS) new product development activities as defined in Terumo Medical Corporation (TMC) QA101 Product Development Process & Design Controls under the direction and oversight of senior engineering personnel. Key activities may include: collection of voice of customer (VOC) data; development of concepts for feasibility analysis; development of product specifications; new product design, development, verification and validation; preparation of design control documentation; risk management studies and analyses; process development and prototype fabrication; and support of commercialization activities. 3/1/2020
1281 Terumo
Elkton, MD
NPD Quality Engineer I
BS/BA in engineering or life sciences
Exp: 1-3 years in med devices QA
As part of a project team and with the assistance of the manager, the NPD QE I will be responsible for developing sound Design History File deliverables, including, but not limited to, Quality Plans, Supplier Qualification Strategies/Quality Agreements, Manufacturing Quality Plan, Design Verification protocols and reports, and conducting Design History File Verifications at the end of each design control phase. In addition, the NPD QE I will actively participate in design characterization, risk management activities, and design and process validation. 3/1/2020
1282 Terumo
Elkton, MD
Facilities Technician I
HS Diploma or Associates or Trade School Cert
Exp: Entry Level
This position is an entry level position in the Facilities Engineering department. Associate will be expected to perform maintenance on equipment and plant facilities to ensure functional accuracy and completeness, under the guidance and direction of Senior / Lead Facilities Engineers. 3/1/2020
1283 Terumo
Somerset, NJ
Clinical Research Associate (CRA)
BS/BA in life sciences
Exp: 1-3 years in monitoring
Job Summary: PURPOSE: Ensure clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements by engaging with assigned sites. JOB DETAILS: • Perform site selection, start-up/regulatory, initiation, monitoring and close out visits in accordance with contracted scope of work, using good clinical practices, applicable regulations, SOPs and work instructions. • Complete appropriate therapeutic, protocol and clinical research training to perform job duties. • Administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues. 3/1/2020
1284 Teva
Tacoma, WA
Neuro / Psychiatry Sales Representative - Tacoma, WA
BS/BA in related field
Exp: 1 or more in business to business sales
Teva is searching for an experienced Neuro / Psych Sales Representative to join our team in the Tacoma, WA area! As a Sales Representative you will establish and maintain professional relationships with targeted physician groups to maximize new business opportunities. Build rapport and relationships by interacting effectively with employees and external contacts (i.e. HCP and office staff) at all levels, demonstrating the awareness of their needs and responding with the appropriate action. Provide healthcare product demonstrations, physician detailing and in-servicing of products to current and potential customers. 3/1/2020
1285 Teva
Rome, GA
Neuro / Psychiatry Sales Representative - Tacoma, WA
BS/BA in related field
Exp: 1 or more in business to business sales
Teva is searching for an experienced Neuro / Psych Sales Representative to join our team in the Tacoma, WA area! As a Sales Representative you will establish and maintain professional relationships with targeted physician groups to maximize new business opportunities. Build rapport and relationships by interacting effectively with employees and external contacts (i.e. HCP and office staff) at all levels, demonstrating the awareness of their needs and responding with the appropriate action. Provide healthcare product demonstrations, physician detailing and in-servicing of products to current and potential customers. 3/1/2020
1286 Teva
Toledo, OH
Neuro / Psychiatry Sales Representative - Tacoma, WA
BS/BA in related field
Exp: 1 or more in business to business sales
Teva is searching for an experienced Neuro / Psych Sales Representative to join our team in the Tacoma, WA area! As a Sales Representative you will establish and maintain professional relationships with targeted physician groups to maximize new business opportunities. Build rapport and relationships by interacting effectively with employees and external contacts (i.e. HCP and office staff) at all levels, demonstrating the awareness of their needs and responding with the appropriate action. Provide healthcare product demonstrations, physician detailing and in-servicing of products to current and potential customers. 3/1/2020
1287 Teva
Olive Branch, MS
Warehouse Operator
HS Diploma/GED
Exp: 1 year in warehouse work
As a Warehouse Operator I, you will have the opportunity be a part of a growing team dedicated to serving our customers-in-need by driving day-to-day Anda warehouse operations. You will be responsible the picking, packing and shipping of products to our customers in a manner that meets company standards. Additionally, you utilize RF scanning equipment to ensure accuracy in movements. 3/1/2020
1288 Teva
Shreveport, LO
Sales Represnetitive I
BS/BA in related field
Exp: 1 or more in business to business sales
Teva is searching for an experienced Neuro / Psych Sales Representative to join our team in the Tacoma, WA area! As a Sales Representative you will establish and maintain professional relationships with targeted physician groups to maximize new business opportunities. Build rapport and relationships by interacting effectively with employees and external contacts (i.e. HCP and office staff) at all levels, demonstrating the awareness of their needs and responding with the appropriate action. Provide healthcare product demonstrations, physician detailing and in-servicing of products to current and potential customers. 3/1/2020
1289 Teva
Salt Lake City, UT
Compliance Specialist I
BS/BA in sciences/engineering
Exp: 0-3 years
This position will be responsible for vendor management, supporting annual product reviews (APRs)/product quality reviews (PQRs), and providing audit support for Regulatory Agency Inspections, Teva Global Regulatory Audits (GRA), internal audits and Partner audits. The candidate will support and perform tasks related to key compliance processes, including but not limited to, document changes, investigations, CAPAs, change control, metrics, quality agreements, notifications to management (NTMs), FAR submissions, market renewals/submissions, and other related activities. This position will also interact with Partners on occasion under the direction of the department manager. 3/1/2020
1290 Teva
North Wales, PA
Material Handler I - 1st Shift
HS Diploma/GED
Exp: 6 months in industrial environment
Utilizes radio frequency (RF) system and operates fork-lift to receive and put-away inbound (IB) receipts - includes physically breaking down and creating optimal sized pallets prior to put-away into inventory. Utilizes RF system and operates fork-lift to move inventory throughout the warehouse for the purpose of managing inventory and replenishing picking locations. Performs tote picks via tote management system (Pick-to-light module) - includes deployment of totes on PTL module, using PTL module to accurately pick orders from shelf to tote 3/1/2020
1291 TRC
Columbia, SC
Packaging Specialist
HS Diploma/GED
Exp: 12 months experience
The Packaging Specialist is responsible for operating and maintaining the equipment on their respective shift and support of the overall department’s performance goals. They are responsible for the completion of operations on a daily basis. This includes meeting the daily packaging output goals, following the procedures as defined by SOP’s, and executing specific verbal directions from their direct leadership. The Packaging Specialist is responsible for maintaining and ensuring their training is complete. Each Specialist is hired into a minimum level that they are required to attain. 3/1/2020
1292 Tempus
Chicago, IL
Cell Culture Research Associate (11 am – 7 pm)
MS in lab or biological sciences
Exp: 0-2 years
Responsibilities include: Receive and process patient tumor samples for our patient-specific biological modeling. Plate cells to grow tumor organoids and maintain cell cultures. Plate tumor organoids for assays. Cryopreserve tumor tissue and tumor organoids to create the most comprehensive organoid biobank 3/1/2020
1293 Teligent
Buena, NJ
Compounder I – 1st Shift
AS/AA
Exp: 1 year in pharma
Perform functions relating to the processing of Topical products (creams, ointments, lotions, solutions) ensuring product compliance to established current Good Manufacturing Practices (cGMPs), customer requirements, and in conjunction with all Standard Operating Procedures (SOPs). Perform functions relating to the cleaning and sanitization of compounding process equipment and compounding facility to facilitate GMP compliance, quality, safety, and schedule attainment. Follow standard operating procedures to complete tasks, some of which may vary in scope, sequence, complexity and timing. 3/1/2020
1294 Syros
Cambridge, MA
Research Associate/Senior Research Associate, Medicinal Chemistry 
BS or MS in life sciences
Exp: 1 year in small molecule drug discovery
Syros Pharmaceuticals is seeking an experienced, motivated, and energetic Medicinal Chemist to join the discovery research group. Assist in development chemistry plans, strategy, and tactics to efficiently deliver high quality drug development candidates (DCs). Contribute to the design, synthesis, and characterization of novel molecules targeting diverse protein targets. Carry out integrated analysis and interpretation of multi-faceted biological data (activity, selectivity, kinetics, DMPK, physical properties, etc.). 2/29/2020
1295 Syros
Cambridge, MA
Research Associate I/II, Molecular and Cellular Biology
BS or MS in life sciences
Exp: 1-2 years
This lab-based position will focus on performing high throughput screening assays to support drug discovery for oncology projects. The successful candidate will genetically and chemically interrogate cellular systems, perform and eventually develop cell-based screening assays to support discovery and development of small molecule oncology drug candidates. This individual will have the opportunity to learn and master various cutting-edge techniques including FACS, high-content imaging, Meso Scale Discovery (MSD) etc. to support programs as they progress and should be an enthusiastic learner with the ability to pick up things quickly without repeated training. 2/29/2020
1296 System Bioscience
Palo Alto, CA
Customer & Technical Support Representative (CSR/TSR)
BS in life sciences
Exp: 1-2 years in life sciences
The ideal candidate will have a B.S. degree in the life sciences and will support an existing group of customer support personnel taking telephone orders from customers, logging into a CRM system, printing packing slips, sales orders, and shipping documentation, and assist with packaging of life science reagents for shipment to worldwide customers. This position will also provide support to the Commercial Team. 2/29/2020
1297 t2 Biosystems
Lexington, MA
Software Quality Engineer - Contract
BS in computer sciences/engineering
Exp: 1-3 years in device testing
We are seeking an experienced software quality engineer who is excited about the work we do at T2 and will work as part of our Engineering team to verify, validate and release software updates, in compliance with our Quality System. This position reports to the Director of Software Engineering and is based in Lexington, MA. The ideal candidate will have strong organizational and communication skills (verbal and written), a meticulous, detail-oriented work approach and be comfortable following a regulated, formal development and release process.  2/29/2020
1298 Tactiva Therapeutics
Buffalo, NY
Senior Lab Technician
MS in life sciences
Exp: 18 months in research lab
The senior laboratory technician designs and optimizes assay processes including sample preparation, workflow automation, and analytic detection, as well as provides data for critical review of test development. The senior laboratory technician provides direct scientific and analytic support to the laboratory director(s) and monitors timelines to meet production goals and objectives. 2/29/2020
1299 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
1300 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
1301 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
1302 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
1303 Talis
Menlo Park, CA
Research Associate
MS in life sciences
Exp: 0-5 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. Work with senior scientists and run hands-on experiments for microbiology, sample preparation, nucleic acid extraction and amplification. Perform detailed data analysis of experiments using Minitab or similar tools and develop summaries for the Assay Development group. 2/29/2020
1304 Tango
Cambridge, MA
Associate Scientist, Immunology
BS or MS in immunology or related
Exp: 0-8 years in industry
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. Culture and engineer primary human T cells, murine T cells, and tumor cells using genetic tools. Assessment of T cell phenotype and function by multicolor flow cytometry, ELISA and gene expression analysis 2/29/2020
1305 Tanvex
San Diego, CA
Research Associate, Analytical Sciences - #1214
BS or MS in biological/chemical engineering or sciences
Exp: 0-3 years
The Research Associate will perform analytical tests using HPLC, Spectrophotometry (RP, IEX, SEC, HILIC etc.), CE, mass with high quality and efficiency; provides analytical support in R&D settings for samples from various process scales; writes experiment summaries and development reports; and assists during document review comprising of but not limited to: batch records, standard operating procedures and assay protocols. 2/29/2020
1306 Tanvex
San Diego, CA
Research Associate, Analytical Sciences - #1189
BS or MS in biological/chemical engineering or sciences
Exp: 0-3 years
The Research Associate will perform analytical tests using HPLC, Spectrophotometry (RP, IEX, SEC, HILIC etc.), CE, mass with high quality and 2/29/2020
1307 Target Health LLC
New York, NY
Biostatistician
MS in statistics/bio statistics
Exp: 1-3 years is a plus
Provide statistical support for study design, data transfer, analysis, verification, interpretation of results in clinical trials. Program datasets used for analysis according to CDISC standard, along with data define documentation and data reviewer’s guide. Create and verify listings/tables/figures based on data collected in clinical trials. Work closely with data management, clinical and regulatory departments. 2/29/2020
1308 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
1309 TE Connectivity
Middleton, PA
Software Systems Engineer I
BS or higher in computer science/engineering
Exp: 0-2 years
TE Connectivity’s Software Systems Engineering Teams provide functional and empirical analysis related to the design, development, and implementation of software operating/automation systems, including, but not limited to, utility, development, and diagnostic software. They perform technical planning, system integration, verification and validation, cost, risk, supportability and effectiveness analyses for total systems. 2/29/2020
1310 TE Connectivity
Bellville, TX
PRODUCT ENGINEER I
BS/BA in mechanical/electrical engineering
Exp: 0-2 years
Actively lead & contribute to New Product Development activities. Provide Sustaining Engineering support for existing product lines. Exercises considerable latitude in determining objectives and approaches to assignment. Drives results primarily through collaboration and influence, not through direct reporting relationships 2/29/2020
1311 TE Connectivity
Maple Plain, MN
Extrusion Technician
HS Diploma/GED
Exp: 1-2 years a extruder operator
General setup, operation and maintenance of PTFE extrusion equipment and tooling to support manufacturing and development efforts in a clean room environment. Facility cleaning, shipping & receiving, QA support as needed, Customer Service support as needed. Overall a multi-functional individual that will wear several hats during our growth needs. 2/29/2020
1312 Synthego
Redwood City, CA
Research Associate
MS in life sciences
Exp: 0-2 years
The Research Associate will pair their scientific skill sets with laboratory and process intuition to figure out new and better ways of performing our work.  Our team runs large, automated research campaigns for key customers and internal clients. We are building a new business function at Synthego and you can be a part of it. 2/29/2020
1313 Synthego
Redwood City, CA
Shipping Associate, CRISPRevolution
HS Diploma/GED
Exp: 1 year in shipping
Synthego is looking for a shipping associate to execute our daily order fulfillment activities, ensuring quality and customer satisfaction are top priorities. Coordinate with manufacturing and commercial operations to ensure daily orders are picked, packed, and shipped on-time. Inspect finished product for defects and verify accuracy of order contents and documentation prior to packaging and shipment 2/29/2020
1314 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
1315 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
1316 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
1317 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
1318 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
1319 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
1320 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
1321 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
1322 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
1323 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
1324 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
1325 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
1326 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
1327 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
1328 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
1329 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
1330 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
1331 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
1332 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
1333 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
1334 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
1335 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
1336 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
1337 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
1338 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
1339 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
1340 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
1341 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
1342 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
1343 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
1344 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
1345 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
1346 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
1347 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
1348 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
1349 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
1350 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
1351 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
1352 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
1353 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
1354 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
1355 Synexus
Pinellas Park, FL
Clinical Research Coordinato
BS/BA in health sciences
Exp: 1 year in clinical research
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. Coordinate and conduct patient care visits (drawing blood, collecting vital signs, performing ECG’s and processing specimens) and assure all procedures are conducted in compliance with the clinical protocol. 2/23/2020
1356 Synexus
Dalas, TX
Clinical Research Study Nurse
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
1357 Synexus
Columbus, OH
Patient Services Assistant
HS Diploma/GED
Exp: 1 year as receptionist/office coordination
Manages the front desk activities of the site office. Schedules subjects for study visits, enters information in clinical conductor system, and conducts appointment reminders; Provide support for filing, mailings, copying, collating, ordering, etc. 2/23/2020
1358 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
1359 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
1360 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
1361 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
1362 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
1363 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
1364 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
1365 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
1366 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
1367 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
1368 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
1369 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
1370 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
1371 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
1372 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
1373 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
1374 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
1375 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
1376 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
1377 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
1378 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
1379 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
1380 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
1381 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
1382 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
1383 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
1384 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
1385 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
1386 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
1387 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
1388 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
1389 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
1390 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
1391 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
1392 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
1393 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
1394 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
1395 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
1396 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
1397 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
1398 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
1399 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
1400 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
1401 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
1402 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
1403 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
1404 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
1405 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
1406 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