Links to 542 Entry-Level Biotechnology & Life Science Jobs

We are looking for someone with expertise in classifying diseases/conditions by medical specialty to do drug pipeline confirmation tasks. Contract work on a task basis. Must be able to accept payment by PayPal or Venmo. Also must be able to function in the world without using ChatGPT, because if we thought AI could do the task well, you would not be reading this job posting. Please send a message through the contact form if interested.

The Advanced Cell Technologies, Screening, and Sequencing (ACTS) group in Discovery Neuroscience, in Cambridge, MA, is seeking a highly motivated scientist to join our team. This position is responsible for performing molecular biological research focused on target identification and validation, supporting early drug discovery efforts for neurodegenerative diseases and neuropsychiatric disorders. The ideal candidate will be collaborative, productive, and have strong hands-on experience with molecular biology techniques. The successful candidate will be expected to support multiple neuroscience pipeline projects that require both molecular and transcriptomic validation, as well as target identification for the exploratory projects.

Biotherapeutics and Genetic Medicine (BGM), a part of Discovery Research within AbbVie’s R&D, is a global organization dedicated to the discovery and optimization of innovative drug candidate molecules for biotherapeutic modalities (monoclonal antibodies, multispecifics, proteins, conjugates, etc.) and genetic medicines (AAV, LNPs, siRNA, etc.) across all therapeutic areas. We are seeking a highly motivated and forward-thinking scientist with demonstrated expertise in data engineering to develop and optimize automated lab data capture workflows, as well as create dynamic visualization dashboards supporting biologics discovery.

Performs functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components and final materials. Uses sophisticated programs (such as LIMS, SAP, automated control systems, etc.) to collect and evaluate operating data, which can be used to conduct on-line adjustments to products, instruments or equipment. Determines and may assist in developing methods and procedures to control or modify the manufacturing process.

Abeona is looking for a Manufacturing Associate to join our team in Cleveland, OH. The successful candidate will be responsible for Manufacturing initiatives supporting multiple product pipelines. The candidate will be an integral part of a fast-paced group responsible for the manufacture of retroviral vector, autologous gene-corrected cell therapies, and clinical AAV gene therapies. Responsibilities will include executing protocols and manufacturing clinical material across multiple products as well as supporting process optimization work and document generation. The ideal candidate will have experience in production of biologics in a controlled cGXP setting. Strong aseptic and cell culture technique as well as collaborative work in a team is an integral part of this position.

We are seeking entry-level applicants for the Clinical Research Assistant role at our Philadelphia location (Zipcode: 19104). This role is ideal for entry-level candidates interested in learning clinical research operations, contributing to study execution, and developing foundational skills in patient interaction, data management, and regulatory compliance. The Clinical Research Assistant (RA) provides foundational support in the conduct of clinical trials at the site level. Working under the direct supervision of a CRC II, CRC III, or Site Manager, the RA assists with operational, administrative, and participant-facing tasks to ensure studies run smoothly and in accordance with ICH-GCP, regulatory requirements, and protocol guidelines. This role is an ideal entry point for individuals seeking to gain hands-on experience in clinical research.

We are seeking experienced applicants for the Clinical Research Coordinator I role at our Philadelphia location (19104). This role is ideal for early-career coordinators with some prior research exposure, looking to develop hands-on clinical and protocol management experience. The Clinical Research Coordinator I is responsible for supporting and performing routine clinical research activities under the guidance of a CRC II or CRC III. The CRC I may independently manage lower-complexity trials (e.g., maintenance studies, extension studies) and serves as a secondary coordinator on high-enrolling screening trials. This role represents the first step in assuming ownership and accountability in study execution.

The Microbiologist I, Quality Control Product Testing, performs quality control testing of raw materials, in process samples and final products.

This role is accountable for designing, stabilizing, and continuously improving end-to-end manufacturing process flow. The Manufacturing Process Engineer focuses on how work moves through the system — people, materials, information, and controls — to ensure predictable, compliant, and efficient production of orthopedic medical devices.

We are seeking a highly effective, motivated recent graduate to join our team. You will experience all facets of building a startup at a cutting edge biotech company in San Carlos! You will work with an experienced team of founders and scientists running lab experiments and assays. You are a good fit for this role if you resonate with our values, namely if you work hard, are ambitious, creative, and honest, write python scripts to solve your problems, and will do whatever it takes to win.

Provides guidance and expertise to ensure process, data and product quality meet requirements. May lead and help drive improvements. Provides quality-related review to quality control data. Reviews product and process quality data to ensure adherence to internal and external requirements. Works on quality department assignments with clearly defined objectives. This role will focus on quality assurance support working closely with manufacturing personnel working on the floor. Individual will provide in-depth support of QC Operations and GMP experience, and the ability to work independently, while collaborating with cross-functional departments.

We are seeking a detail-oriented and experienced Quality Control Microbiology Analyst to join our growing Quality team. In this role, you will support product release, stability testing, environmental monitoring, and cleaning verification activities under cGMP and GLP conditions. You’ll play a key part in ensuring the quality and safety of pharmaceutical products while maintaining strict compliance with FDA, ICH, and international regulatory standards.

As a Field Service Engineer for Agilent, you will work at a variety of labs, so having an appetite for continuously learning about new instruments, software, and consumables is key. Applying your communication skills, creativity, and can-do attitude is essential. The ability to help customers solve problems and a commitment to delivering the highest levels of customer service are key to driving customer success. You will be responsible for supporting our customers with on-site installation, preventive maintenance, and repair of Agilent Chromatography systems. Our product lines include hardware, software, networking products, and operating systems.

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 assist with method development/method validation projects. For this position, UV-Vis, FTIR, HPLC, GC, Titration, and/or AA based methodologies are commonly employed in the described testing.

The Quality Specialist will provide site quality support in a fast-paced environment by effectively performing activities of substantial variety to ensure quality and compliance with applicable regulatory requirements and is proficient in all document and protocol approvals applicable to the respective processes executed at the respective lab or manufacturing facility. Activities include reviewing documents and data, supporting audits and 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 position develops SOPs or other quality documents as needed.

The Scientist II - Chemistry (ICP) is accountable for driving results in a fast-paced environment by performing analytical routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. For this Scientist II (Chemistry) position, ICP, GC-MS, LC-MS, HPLC, TOC, UV, osmolality, density, and pH are commonly employed in the described testing in addition to other key methodologies such as KF and titration. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company) and may also assist with method development / method validation projects.

As a Research Associate / Associate Scientist, you will work within the Genetic Medicine team in Waltham, MA. You will also collaborate with internal/external partners on nucleic acid drug discovery projects to ensure timely execution of the experiments, and delivery of high-quality data. This role will have an autonomy owning various stakeholders, projects, and tasks in a dynamic start-up environment while keeping up the pace of Alloy.

We are seeking an associate scientist-II to join our protein sciences team to contribute to our protein production and conjugation efforts. The candidate must be independent, goal oriented, technically competent, and able to efficiently work across multiple projects. We are searching for enthusiastic, innovative, and highly motivated individuals, with scientific background in protein expression, purification, and analytical techniques, who are comfortable working in a fast-paced entrepreneurial environment. The successful candidate will be part of cross-functional teams including biologists, chemists, and pharmacologists and will contribute to advancing research programs across multiple therapeutic modalities

We are seeking a Technician II to join our Traverse city, MI location, supporting chemical analysis in a regulated laboratory environment. This role is ideal for candidates who are eager to grow their technical expertise, develop hands‑on analytical skills, and build a long‑term career in laboratory science. Our lab offers structured training, mentorship, and clear pathways for professional development.

NSF is looking to add experienced Chemistry Scientists II, to our HPLC Group. Persons with good lab skills and the ability to work well in a team environment.

Let’s do this. Let’s change the world. In this vital role you will work in a highly dynamic in vivo pharmacology team executing in vivo preclinical disease models and in vitro assays in the vivarium and lab supporting pipeline programs. Key Responsibilities: Perform hands-on in vivo work primarily mice, possibly rats in the vivarium daily. Provide technical support for studies, dosing, sample/tissue collection, health checks, study setup and take down. Work side-by-side with Scientists/Senior Scientists to execute and help design experiments. Run concurrent studies, stay organized and detail-oriented to meet study timelines. Participate in weekend/evening dosing rotations as needed. Support in vitro assays as required. Communicate results to immediate team and follow established protocols and safety procedures. Work in a flexible team-oriented environment. Weekend and evening work may be required.

Maravai LifeSciences is seeking a #MiracleMaker to join our Quality Assurance team as a Temporary QA Resource. As a Temporary QA Resource, you will be responsible for reviewing and approving material release specifications, raw materials, intermediates and consumables in compliance with cGMP regulatory requirements and ISO standards. Provide support for other functions performed by QA operations group.

We are seeking a highly motivated and detail-oriented Research Associate to join our dynamic Next-Generation Sequencing (NGS) product development team. In this hands-on role, you will support the evaluation, optimization, and advancement of cutting-edge NGS solutions. You will perform high-quality laboratory experiments, contribute to critical data generation, and help drive successful internal and external adoption of our products. This position is ideal for someone passionate about molecular biology and eager to grow their expertise in NGS workflows, product development, and applications.

As a Manufacturing Associate I, Fill Finish (2nd Shift), you’ll play a hands‑on role in producing sterile drug products that patients and families depend on. You'll support fill‑finish operations by operating equipment, preparing materials, completing cGMP documentation, and maintaining a clean, compliant production environment. This role is ideal for someone who takes pride in precision, follows procedures with care, and enjoys being part of a collaborative manufacturing team where quality and safety come first. The Manufacturing Associate I, Fill Finish (2nd shift) provides process support for the production of drug products under strict adherence to cGMP, OSHA, and United Therapeutics policies and regulations in the Silver Spring, Maryland facility.

As a Bioprocess Technician I on our Bioscaffolds team, you’ll support the processes that help turn innovative science into engineered lung tissue. You’ll work directly with tissue preparation, decellularization systems, and bioanalytical assays—contributing to meaningful progress in regenerative medicine. This role is ideal for someone who enjoys hands‑on lab work, takes pride in precision, and wants to grow their skills while being part of something bigger. Conduct and assist in research efforts to develop tissue-based regenerative medicine products for the treatment of pulmonary hypertension and other lung diseases.

As a Manufacturing Engineer at Varda, you will have the opportunity to utilize your experience to scale manufacturing from a few bespoke vehicles to many consistent, concurrent builds. Manufacturing engineers will be a vital part in increase Varda's build cadence working directly with design engineers and technicians for a broad array of processes (structures, thermal protection systems, propulsion, and avionics components) required to manufacture our vehicles. The focus of the job is to implement incremental improvement for every vehicle Varda produces.

The Thermal Hardware Engineer is the Responsible Engineer (RE) for the hardware design of vehicle thermal and fluid systems. This role encompasses the development of tubing, valves, pumps, MLI, thermal straps, thermal switches, phase change materials, etc., used in passive and active thermal control systems. Day-to-day responsibilities will be focused in CAD design, drawings, GD&T, manufacturing, testing, procurement, and analysis. This is a great opportunity to grow your engineering skills with exposure to all aspects of spacecraft analysis and design. A proactive problem-solving approach and commitment to meeting tight schedules are critical to supporting Varda's goals of expanding manufacturing capabilities and reentry systems.

We are looking for an awesome electrical systems engineer to join our research and development department. We are creating and introducing a new series of electronics into our x-ray product offerings in the marketplace. You will be joining a diverse R&D group that develops and integrates a high voltage imaging chain for major and developing OEM partners and has a lot of fun doing it. If you can handle challenging product requirements and deadlines, work with a broad range of technical backgrounds, handle success and failure with an indomitable spirit, and work through the rigors of R&D work - we would love to talk to you!

The Distribution Technician I is responsible for maintaining a high level of inventory accuracy and integrity in accordance with company Policies and procedures. Ensures that Distribution Operations are in Compliance with Federal Regulations and AATB Standards. Promotes Lean Behaviors across the organization (This includes Participating in Try storming, Brainstorming and Lean Related Initiatives). Resourceful in completing deadlines and can multitask effectively. Directly impacts On-Time Delivery to customers.

The Process Engineer I is responsible for evaluating and improving manufacturing processes to reduce cost, improve yields, and reduce variation. This position performs new process design and implementation, process validations and process qualifications. Process Engineers also participate in technology transfer to ensure the processes necessary for new products are effectively translated to manufacturing from R&D. Process Engineer I makes use of statistical analysis methods, critical thinking, process development, and scaling principles to achieve the objectives mentioned above.

The Quality Control Microbiologist I is responsible for performing microbiological testing and managing results of incoming raw materials, in-process samples, and final product samples. Review and analyze testing data to ensure internal specifications are met in accordance with standard operating procedures requirements. Ensure testing results are accurate, and results are available in a timely manner. Performs all functions in accordance with standard operating procedures, all applicable federal and state regulatory and accrediting standards requirements.

Vyriad is a clinical stage biotechnology company based in Rochester MN. We are developing the next generation of targeted genetic medicines for cancer therapy. The Bioproduction Technologist will be responsible for upstream and/or downstream process development and GMP manufacturing of oncolytic viruses, lentiviral vectors and other biologics for clinical trials. The Bioproduction Technologist plays a vital role in the day-to-day process development projects and manufacturing operations in compliance with cGMP standards. Virus and gene therapy manufacturing operations involve aseptic processing in a pharmaceutical cleanroom facility, large-scale cell culture in shake flasks and bioreactors, vector generation, purification, concentration, and fill and finish operations, according to established standard operating procedures (SOPs). In addition, staff are responsible for the daily operations and environmental monitoring of the GMP facility to ensure compliance with applicable regulations.

In this role you will perform routine and non-routine testing to support product release, including but not limited to environmental monitoring, water testing, and other laboratory functions as needed.

We’re looking for a detailed engineer who enjoys learning and taking on challenges. This role blends manufacturing engineering and design engineering – you’ll create and maintain product drawings and BOM’s, develop processes, maintain product compliance and work with other manufacturing engineering groups to ensure the manufacturing lines maintain high-quality execution.

Responsible for Document Control, Learning Management System and Equipment Control. Support Audit activities and incoming inspection. Interacts with many different functional departments, suppliers, and experts outside Zimmer Biomet to implement Zimmer Biomet Quality goals.

Zymo Research is looking for a dynamic individual to join our Microbiomics Research & Development Team! In this role, you will play a vital part in developing new sample preparation systems and molecular assays, utilizing your skills and expertise in a laboratory set-up and in a highly dynamic team. Your contributions will be essential for the development of new products and services that drive microbiome-related discoveries and applications.

This position works out of our Columbus, Ohio plant location in the Abbott Nutrition Division. Our Nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow to keeping adult bodies strong and active. Millions of people around the world count on our leading brands – including Similac®, PediaSure®, Pedialyte®, Ensure®, and Glucerna® – to help them get the nutrients they need to live their healthiest lives.

This position works out of our Columbus, OH location in the Nutrition Division. In Research & Development, our ambition is providing innovative high-quality products, creating sustainable value, delivering superior user experience, and enhancing health outcomes at all stages of life.

This position works out of our Altavista, VA location in the Abbott Nutrition division. Our Nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow to keeping adult bodies strong and active. Millions of people around the world count on our leading brands – including Similac®, PediaSure®, Pedialyte®, Ensure®, and Glucerna® – to help them get the nutrients they need to live their healthiest lives. Altavista, Va., is one of Abbott’s largest nutrition manufacturing plants equipped with advanced technology to ensure efficient production. Working here will make you feel like you’re part of a family that works together to make a difference and help nourish millions of families around the world.

This position works out of our Columbus, Ohio plant location in the Abbott Nutrition Division. Our Nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow to keeping adult bodies strong and active. Millions of people around the world count on our leading brands – including Similac®, PediaSure®, Pedialyte®, Ensure®, and Glucerna® – to help them get the nutrients they need to live their healthiest lives.

Independently generate precise, reliable and reproducible data in a timely manner. Demonstrate experimental precision and strong data interpretation skills and should possess understanding of core discipline. We are seeking a talented and motivated Mechanical Engineer with instrumentation or systems development experience to join the Madison Peptide Therapeutics (MPT) Engineering team. This individual will work with engineers and scientists to maintain and enhance our fleet of Peptide Array Synthesizers in a biotech research environment.A successful individual for this position would develop a strong understanding of scientific, medical, or laboratory instrumentation and utilize their mechanical engineering expertise to support and enhance internally developed laboratory equipment. This person would often design, modify, or integrate hardware components, including sensors, actuators, pumps, motors, cameras, manifolds, and other devices to perform coordinated, reliable activities. They work collaboratively in a team environment to design and develop high quality systems and workflows that increase throughput, reduce cost, and improve the quality of the product.

In this role, you will help design, maintain, and continuously improve a quality management system that supports regulatory approval and business growth across global markets. You’ll collaborate across functions to ensure quality processes are not only compliant, but practical, efficient, and future‑ready.

The Manufacturing Engineer contributes to medical device product design, development, manufacturing, and testing in accordance with the company’s Quality System. Helps generate design outputs where required through interface with cross-functional team members.

We are searching for motivated, enthusiastic, and hands-on individuals interested in advancing science through the manufacturing of our CRISPR regulated products. As a Lab Associate at Synthego, you will join our Clinical operations team and have direct responsibility for the synthesis and purification of our sgRNA products in the INDe and GMP factories. This role requires a strong attention to detail, a desire to learn and adapt to new processes, and familiarity with safe laboratory practices. This role will combine hands-on laboratory protocols with advanced automation to ensure the timely delivery of high quality products to our customers.

The Quality Engineer 2, Manufacturing independently executes quality engineering activities that support the development and maintenance of compliant manufacturing processes. This role contributes to product and process quality throughout the product lifecycle, with emphasis on process validation, test method validation, regulatory compliance, and quality system support. The QE2 works collaboratively with manufacturing, engineering, and cross-functional partners to implement quality initiatives that promote consistent process execution, operational efficiency, and product reliability. The QE2 applies working knowledge of quality systems and industry regulations to support manufacturing readiness, risk-based decision making, and continuous improvement.

Work within a cutting-edge genomics workflow to provide quality control support in a high-volume molecular laboratory. Create and implement equipment functionality and reagent processes for use by Tempus R&D, clinical, and modeling lab staff while maintaining CLIA/CAP/NYS-DOH/ISO compliance. Complete, schedule, and track Performance Qualifications (PQs), Preventive Maintenance (PM), relocation, and routine maintenance for all laboratory equipment. Organize and prepare reagents prior to quality control evaluations and use. Execute and record quality control evaluations for new reagent lots for laboratory use. Collect and analyze QC data including phase ins, PQs, and monitoring of metrics. Investigate issues and facilitate the implementation of corrective and preventative actions. Liaise with lab management and personnel to provide training, troubleshoot issues, and prioritize QC activities. Report significant findings/deviations and system deficiencies to lab management, as appropriate. Update Standard Operating Procedures (SOPs) and equipment records within the document control system, including drafting, revision, and review of internal SOPs and other quality documentation, including but not limited to: reagent lot verifications, equipment repair field service reports, and maintenance logs. Navigate filing and database systems to retrieve and accurately record QC results and data. Participate in lab audits with QA/Pharma/regulatory bodies as needed. Monitor and respond to laboratory temperature excursions. Maintain a clean working environment and contribute to maintaining an organized laboratory.

Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications.

We are seeking an Analytical Scientist II with exceptional problem-solving skills to join our Research and Development team in High Point, NC, United States. As an Analytical Scientist III, you will have a crucial role in advancing our research initiatives and contributing to the development of innovative scientific solutions.

Initiate and maintain the lifecycle of multiple analytical instruments used in testing synthetic molecules. The lifecycle includes initial qualification, calibration, preventative maintenance, troubleshooting and repair, and decommissioning of analytical instrumentation. Provide support to multiple laboratories by ordering supplies, managing inventories, coordinating vendor visits, and helping to maintain GMP status for analytical instrumentation. Provide documentation support in the form of proof-reading, formatting, document control (Condor), and technical writing. Document Control Specialist will support documentation needs for controlled documents throughout the creation, revision, and final approval process. Act as a change owner (Trackwise/Veeva) to create change control records for analytical equipment and documents, and review of proposed changes to documents to ensure traceability throughout the document change control process. Ensure on-time completion of all routine activities related to instrument lifecycle (e.g., preventative maintenance activities) and change records. Ensure all work is completed efficiently under GMP compliance to maximize operations. Help ensure laboratory compliance by performing routine walk-throughs to detect and mitigate potential environmental, health and safety issues.

Provides basic business/system support of software systems and/or laboratory instrumentation. Works with staff of various departments and the client to initiate and complete performance qualification (PQ) validation activities. Facilitates the validation process and implementation of system upgrades, including guiding, testing, and supporting the introduction, as well as ongoing support of software systems.

The Manufacturing Operations Engineer I provides technical support for manufacturing processes for specialty injectable and aseptic products while ensuring those products are made with quality for our patients. The Manufacturing Operations Engineer I assists with protocols and changes for the Manufacturing Department and provides hand-on and technical support for other department projects when dealing with Manufacturing. Owns Quality Event investigations and supports equipment troubleshooting / updating / installing. Manufacturing Operations Engineers are system owners for the Electronic Batch Records (EBR) and Freeweigh systems and serve as the manufacturing technical point of contact for Enterprise Resource Planning (ERP) projects.

At QuidelOrtho, we’re advancing the power of diagnostics for a healthier future for all. Join our mission as our next Instrument Verification and Validation Engineer to support our Instrument Systems team. This role provides Instrument Verification and Validation (V & V) support for new products, assay / instrumentation integration, technology transfer and other instrument V & V activities. Integrates engineering theory and practice within the areas of new product development, manufacturing, and marketing support.

Our Production Technician I – Formulation plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical product. Once you complete our training, your responsibilities will include supporting daily manufacturing activities for non-sterile and sterile bulk/CSP operations. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.

Our Microbiologist I plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete training, you will be required to perform individual hands-on work in the sterility testing and/or endotoxin testing programs. This person provides scientific guidance and interpretation of microbiology results to QC and production management. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.

Our Production Technician I – Formulation plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical product. Once you complete our training, your responsibilities will include supporting daily manufacturing activities for non-sterile and sterile bulk/CSP operations. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.

As an R & D Category Assistant at Reckitt, you will thrive in our fast-paced environment alongside a team of expert scientists dedicated to ensuring product safety and efficacy. Your meticulous attention to detail will be crucial in supporting technical dossier management and analytical lab compliance.

We are seeking a highly motivated Associate Scientist – Flow Cytometry to join our Research Flow Cytometry Core (RFCC). The RFCC facility provides sorting, analysis and maintenance services to all of Regeneron’s Research Departments. In this exciting role, you will perform sorting experiments for the research staff. You will also maintain analytical instruments that are located in the various buildings on Regeneron’s campus, as well as data analysis using various flow cytometric software programs.

Regeneron’s Cell Culture Development Group within Preclinical Manufacturing and Process Development (PMPD) is looking for a motivated Process Development Engineer I to work as part of the late stage development team to develop production processes of monoclonal antibodies in a non-GMP process development laboratory. In this role, they will perform studies at bench scale in support of clinical or commercial manufacturing production.

Repligen is a global, publicly traded company seeking an Associate Scientist to join our dynamic team. The ideal candidate will support our team in testing affinity resins derived from Avitide’s proprietary affinity ligand discovery platform, with emphasis on developing and optimizing downstream processes for the purification of biopharmaceutical products. This position offers an exciting opportunity to contribute to the advancement of novel therapies and medicines that impact global health.

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team, you will join other outstanding Revolutionaries in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

We are seeking a dedicated Associate Clinical Lab Scientist 1 to join our Pittsburgh state-of-the-art omics laboratory, where you'll begin your career making a meaningful difference in patient care. Working within our biochemical and immunological analysis departments, you'll contribute to our mission of delivering precise diagnostic results that help healthcare providers improve patient outcomes. This position offers the opportunity to develop your laboratory skills while working with cutting-edge technology and being part of a team committed to scientific excellence and quality patient care.

BioLegend is looking for a Product Development associate who will be responsible for performing all essential functions related to antibody-fluorescence conjugation, including following SOPs and batch records and maintaining and analyzing lot histories. The Product Processing Associate will be an integral member of a team that ensures the highest quality of our finalized antibody products. This position offers the opportunity to gain experience with different types of conjugation chemistries and different chromatography methods to purify conjugated antibodies and offers the opportunity to work in small scale to large scale product projects and to learn to utilize the (Enterprise Resource Planning) ERP database to track production schedules and deadlines and to enter production results. This position will also perform troubleshooting of problematic products, including continuous improvement methodologies for efficiency.

The Biochemist I – GMP position will be responsible for the different stages of manufacturing various BioLegend’s regulated product produced in our US FDA registered cGMP manufacturing facility. This role will be responsible for formulating and vialing, completing batch records, putting away finished good inventory (FGI), data entry, equipment maintenance and supply inspections & storage. Other responsibilities include buffer preparation and inspection of incoming buffers into the GMP suite, as well as material preparation for Lyophilization and post lyophilization processes. This role will prepare product/project related documentation and maintain the device history records for all the regulated products and will work closely with product development on new products in order to establish a smooth transition into manufacturing.

Reporting to the Manager, Manufacturing Chemistry, the Associate Manufacturing Chemist support the optimization and performance of silicone formulation processes in our manufacturing operations. In this role, you will assist with process monitoring, data collection, and material management while working closely with senior engineers and production teams. This is an excellent opportunity to gain hands-on experience in a fast-paced manufacturing environment and contribute to the improvement of Si-kit performance and consistency.

The Quality Control Scientist, EM & Microbiology will be responsible for maintaining the EM/Micro program at Serán BioScience. This role supports manufacturing through performing routine monitoring testing, utility testing, and cleaning process verifications testing. Work performed must be in accordance with US-FDA, EU and other applicable regulations. Preference will be given to those with regulatory knowledge and experience in a pharmaceutical manufacturing environment. Those with a background in microbiology and environmental monitoring in an adjacent industry are encouraged to apply.

The Quality Specialist provides quality oversight, GMP guidance and support and makes quality related decisions for the designated functional areas within Sharp Commercial sites. They work closely with internal teams daily and occasionally represent Sharp Quality in customer interactions. The Quality Specialist is responsible to support, design and implement GMP initiatives and continuous improvement opportunities within the Quality Operations organization through data analysis, training, motivation and coaching in collaboration with internal and external stakeholders. Must possess a working knowledge of FDA regulations pertaining to Pharmaceutical /Pharmaceutical Packaging Operations. Scope of the position includes Allentown, Macungie and/or Conshohocken. The impact of decisions relating to customer interface, quality inspections, and documentation requirements could expose the company to significant risk or economic loss.

The Supplier Engineer will be responsible for providing technical support to the contract manufacturers and component suppliers on the implementation and validation of manufacturing lines for Shockwave products. Including evaluation and building of prototypes, pilot, and production equipment or tooling as appropriate, troubleshooting and implementing changes to improve manufacturing quality and product performance.

As a Product Development Engineer, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by: Working with Commercialization and Product Engineering teams to ensure laboratory testing for development and sustaining activities is completed based on project needs. Collaborating with cross-functional global teams composed of members from manufacturing, quality, regulatory, application engineering, business, clinical, and multiple other functions to maintain product continuity. Driving impactful product development experiments for New Product Introduction (NPI) teams and design changes to existing commercialized projects to maximize customer satisfaction and promote business success. Integrating new products into sustained operations by consulting with New Project Introduction (NPI) teams during Scale Up through design ownership transfer

The Quality Specialist is responsible for ensuring compliance with the US and International Quality System requirements. Areas of focus are sustaining Quality Management System (QMS) processes, process improvement, quality control inspections, and document control.

The Process Manufacturing Engineer in our Plymouth, Minnesota Provide Manufacturing Engineering support to Operations through line support, continuous improvement, capacity improvements and new product transfers. Improve the overall efficiency of the manufacturing operation while optimizing human work factors, quality control, material flow, etc. by identifying areas for improvement through use of statistics and root cause analysis tools.

As an Associate Scientist I you will work within the Sustaining microbiology team with several strains of BSL-1 organisms and employ numerous microbiology methodologies for testing including but not limited to aseptic technique, plate colony counting, inoculation and recovery of test articles and serial dilutions. In this role you will also support testing of current STERIS biological products for both the STERIS Healthcare and STERIS Life Science sectors. The position will require accurately maintaining, recording and reporting of test data. Additionally, as an Associate Scientist I you must possess the ability to perform and accurately document tasks according to established work instructions and written protocols in a timely manner, while working both independently and within a team on multiple studies at different stages of the process.

The QC Technician I is responsible for performing inspections and testing at various stages of production of the product from raw materials, sub-assemblies, and final assemblies to assure product quality and conformance to specifications and procedural requirements.

Join us as an entry-level Scientist I in the Volatiles department, where you'll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory.

Join us as a Lab Technician I in our Metals Prep, where you'll put your love of science to work in the sample preparation department of our environmental testing laboratory. You'll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®.

Wound Care Microbiologist. A candidate for this role will support the development of new healthcare products and applications as well as complete quality control testing in the wound care space. They will perform a variety of biological and microbiological preparations and analyses using excellent aseptic techniques.

Pacific Biosciences is seeking a talented Research Associate / Senior Research Associate, Quality Control, to join our Chip Manufacturing Team. This position reports to the Manager, Senior Manufacturing.

We are looking to fill a Scientist 1 - Solution Prep and Lab Support - Large Molecule position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in Rahway, NJ. This Parexel position offers full benefits, sick time, 401K, paid holidays, and paid time off. This role does not offer sponsorship. We are seeking a motivated candidate who can support the laboratory areas for our solution preparation team. The position will provide an opportunity for learning and development in a professional lab setting, contributing to development and commercialization of life-saving therapeutics. The primary responsibility for this position will be the support of the solutions prep team.

We are looking to fill an Engineer position working as a full-time employee of Parexel FSP on assignment onsite at one of our clients located in West Point, PA. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer sponsorship. One of our clients’ research laboratories Bioprocess Clinical Manufacturing and Technology (BCMT) Equipment Engineering Team is seeking a specialist Equipment Engineer position. This person will perform various activities regarding equipment maintenance and engineering supporting the Good Manufacturing Practice (GMP) manufacture of bulk clinical supplies. Candidate is expected to work in a team atmosphere in close collaboration with plant personnel, Engineering Maintenance and Utilities personnel, Quality, Environmental, and Safety groups. Some extended hours will be required as well as occasionally supporting off-hour manufacturing. There is the potential for limited weekend work requests to respond to emergencies or time critical operations (less than five times per year).

We are looking for a Scientist III - Analytical Chemistry and Molecular Biology to work as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in Rahway, NJ. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This role does not offer sponsorship.

We are looking to fill a Scientist III - Analytical Chemistry & Molecular Biology position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in Rahway, NJ. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer any sponsorship. Support of routine bioanalytical testing of samples from cell-line development, in-process, process development/characterization, forced degradation, release & stability, and pre-formulation. Other potential opportunities include method development/optimization, workflow optimization, and template development.

The Manufacturing Associate I is responsible for executing GMP production of injectable pharmaceuticals by following all applicable SOP's. Manufacturing associates are responsible for preparing equipment and materials for GMP aseptic production and operating equipment such from glasswashers, autoclaves, depyrogenation ovens and automated filling machines.

Project Engineers (PE) and Senior Project Engineers (Senior PE) are fully billable roles that will work collaboratively with clients, vendors, contractors, and other Team Members to support projects related to biomanufacturing across the entire engineering lifecycle. PEs and Senior PEs are responsible for delivering high quality work, forming and maintaining valuable, long-term relationships with our clients, and continually strengthening their technical and industry knowledge. They will maintain a strong focus on Project Farma’s Patient Focused and People First mindset.

Project Engineers (PE) and Senior Project Engineers (Senior PE) are fully billable roles that will work collaboratively with clients, vendors, contractors, and other Team Members to support projects related to biomanufacturing across the entire engineering lifecycle. PEs and Senior PEs are responsible for delivering high quality work, forming and maintaining valuable, long-term relationships with our clients, and continually strengthening their technical and industry knowledge. They will maintain a strong focus on Project Farma’s Patient Focused and People First mindset.

Project Engineers (PE) and Senior Project Engineers (Senior PE) are fully billable roles that will work collaboratively with clients, vendors, contractors, and other Team Members to support projects related to biomanufacturing across the entire engineering lifecycle. PEs and Senior PEs are responsible for delivering high quality work, forming and maintaining valuable, long-term relationships with our clients, and continually strengthening their technical and industry knowledge. They will maintain a strong focus on Project Farma’s Patient Focused and People First mindset.

At Personalis, we are transforming the active management of cancer through breakthrough personalized testing. We aim to drive a new paradigm for cancer management, guiding care from biopsy through the life of the patient. Our highly sensitive assays combine tumor-and-normal profiling with proprietary algorithms to deliver advanced insights even as cancer evolves over time. Our products are designed to detect minimal residual disease (MRD) and recurrence at the earliest timepoints, enable selection of targeted therapies based on ultra-comprehensive genomic profiling, and enhance biomarker strategy for drug development. Personalis is based in Fremont, California.

The Power Distribution and Automation Systems Engineer provides technical competency in assuming liaison and/or control responsibility for various multidisciplinary activities supporting the overall site operations and colleagues for the Global Workplace Experience (GWE) –Pearl River, NY Research and Development site. This entails a diverse range of accountabilities including oversight and direction of vendor and contractor work performed on building systems and assets, new designs and installations, operations and maintenance activities, modifications, and modernization technologies, as well as the protection of physical facilities and process equipment. Additional accountabilities include the creation and monitoring of the site’s power distribution and automation strategies for all facility operations and facility/critical utilities as well as providing strategic input for the site’s capital program. The role requires the development and maintenance of close working relationships with colleagues and contracted resources to define facility requirements, analyze needs, provide recommendations, and execute plans and options that align with overall GWE goals and supported business line objectives and strategies.

The QC Microbiologist will play a critical role in ensuring the microbiological quality and compliance of raw materials, in-process samples, finished products, and the manufacturing environment in accordance with cGMP and regulatory standards.

The Laboratory Scientist is responsible for supporting and executing experimental work to complete analytical service projects, for supporting the development of chemical and biopharmaceutical testing equipment and innovative applications, and for distributing our expertise in the form of demonstrations and training.

We are seeking a skilled and detail-oriented Protein Purification Associate Scientist to join our US Protein Department. This role involves executing downstream processing activities including protein purification, characterization, and documentation. The ideal candidate will have a solid background in biochemistry, biotechnology, or a related field, along with hands-on experience in protein purification techniques in a laboratory or manufacturing setting.

We're seeking a creative, passionate, and detail-oriented individual to join our Technology Development team. You will work at the intersection of biology, automation, and data to advance cutting-edge research. Your primary responsibility will be the high throughput screening of gene editing enzymes in mammalian cells. Your work will provide foundational datasets for building, training, and optimizing protein design algorithms. On a monthly basis, you will be responsible for the execution, quality, and tracking of plate-based gene editing experiments. On a day to day basis this includes but is not limited to, preparation of plasmid DNA from bacterial culture, maintenance of mammalian cell cultures, roboticized plate-based transfections, PCR-based sample preparation, and data and sample tracking. To accomplish this at scale you will rely heavily on automated liquid handling instruments and our laboratory information management system. We welcome candidates from diverse backgrounds who share our commitment to revolutionizing biology, driving meaningful innovation, and making a lasting impact on global healthcare. This role offers a unique opportunity to shape the future of AI-driven protein design while collaborating with a dynamic, interdisciplinary team of experts in machine learning, protein engineering, cell biology, and gene editing.

This is the entry level position in the Clinical Trials Quality Assurance track. Exercises judgement within defined areas of responsibility. Works on problems of limited scope; performs all duties and responsibilities with direct supervision.

Responsible for developing, characterizing and validating manufacturing processes to produce biochemical assay plates and related consumables.

Assist in the upstream and downstream biochemical/bioanalytical and biological analysis of oligonucleotides. Preparation of reagents and buffers for biochemical/bioanalytical and biological experiments by measuring the weight of organic compounds and the volume of solutions. Preparation of buffer solutions of specified molarity for Liquid Chromatography (LC) analysis of oligonucleotides. Assist in the physicochemical experiments (thermal denaturing Tm experiment of Oligo’s oligonucleotides. Assist in the operation of Liquid Chromatography Mass Spectrometry (LCMS) system and be able to learn and work on the system. Maintain a report of experimental procedures and findings in electronic lab notebooks. Use of pH meter, Nanodrop to record data

As a QC Analyst within the Bioassay team at Moderna’s Norwood site, you will play a critical role in ensuring the quality of raw materials, drug substance, and mRNA drug products through robust in-process and release testing. You’ll collaborate closely with management and technical teams to uphold high-quality standards in compliance with cGMP, contribute to laboratory operations and method implementation, and support both commercial and clinical programs. This is a high-impact opportunity for a technically skilled professional seeking to strengthen Moderna’s QC operations while working at the forefront of mRNA science. You will also have the opportunity to work closely with Generative AI tools as part of ongoing digital transformation and innovation initiatives within the QC organization.

Modulo Bio is seeking a Stem Cell Scientist to develop and scale an induced-pluripotent stem cell (iPSC)-based in vitro model of the neuroimmune system. Modulo Bio is building a proprietary immune cell modeling platform, which incorporates human genetics, functional genomics, molecular biology, cellular and tissue profiling, disease model engineering, and advanced computational models.

As the System Packaging Engineer, you will support the engineering team with 3D modeling system layouts, proposal design solutions, and customer negotiations that influence Size, Weight, and Power. The products of Moog generally are unique for each customer. Therefore, most new applications require a special, tailored design, even though adaptation of existing designs always should be considered. Understanding of assembly and test methods if critical for early requirements definition and proposed solutions. This brings a regular supply of new and different challenges engaging all engineering disciplines early in the design life cycle. There will be support across multiple Moog BU’s and at times component level drawings as needed. The majority of the work is engaging with the design team and the customers to provide rough solutions that can meet complex requirements and mission objectives.

Our SDG team in Salt Lake is eagerly looking for an Associate Quality Engineer to join their dynamic team. You will join the Quality Engineering team, reporting directly to our Missiles Site Quality Manager and be tasked with applying knowledge and understanding of manufacturing processes, quality requirements, and procedures to provide direction and support related to defense products and contracts. This is an on-site, collaborative working environment that offers a 9/80 schedule to include every other Friday off! (Typical schedule is M-Th, 7am-4pm, every other F 7am-3pm)

Moog Space and Defense Group is the operating group with the longest heritage at Moog. The ever-evolving markets we serve require innovation and allow for constantly developing career opportunities. Our expansive defense portfolio is aligned with U.S. military priorities and our mission of “equipping those who defend freedom.” We are also “revolutionizing the way to space” by supporting the return of humans to the Moon and NASA's deep space exploration programs. Our team in Space and Defense - Power & Data is looking for an Electronics Engineer to join them. You will report to the Electrical Engineering Manager and will have an onsite work schedule in Blacksburg, Virginia.

Schedules and oversees daily operations of assigned laboratory area. Monitors work, coordinates resources, and communicates with other functional areas within NAMSA to address client expectations. May perform various testing independently in accordance with SOPs and utilizing applicable work instructions, standards or guidelines. Performs routine calculations and may participate in analyzing and interpreting results. Maintains all test equipment and supplies for various testing and may assist with procurement of test equipment. Clean glassware and prepare reagents for use in laboratory testing. Perform routine disposal of laboratory waste including disposal of test articles. Assist with making solutions and preparing reagents. Assist in the preparation of items for testing. May have direct client contact as needed. Monitors raw materials and final finished media for conformance with applicable material specifications and SOPs and resolve issues and non-conformances. May be responsible for extractions, which may include: test article and control preparation, animal holding and preparation and solution preparation. May be responsible for chain of custody, delivery of samples, filing and sample distribution/shipping. Accurately collect and record raw data in logbooks and on worksheets. Maintain clean workspace, testing supplies, and equipment. May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms in accordance with criteria outlined in Standard Operating Procedures. May be required to operate specified laboratory equipment as applicable. Other duties as assigned.

Assists in analyzing specimens and maintains equipment in good operating condition.

Support the activities for reagents used in the Operations Department’s Clinical Laboratories. Executes the preparation and qualification of molecular diagnostic reagents. Performs Quality Control tests on new incoming shipments of raw materials and small-scale manufacturing procedures (formulations and dispensing) reagent. Reviews data obtained for compliance to specifications and reports abnormalities. Maintains and improves QC documentation pertaining to raw material specification, reagent qualification, and QC testing. Support Incoming Quality Control activities as needed.

The Quality Engineer is responsible for providing Quality Engineering support to ensure compliance with FDA and ISO 13485. This also includes supporting the manufacturing quality function of the company during ongoing production and shipment of Neocis products to the field.

Under the direct supervision of licensed personnel, or within a training environment, the Laboratory Technician will assist with responsibilities associated with processing specimens for clinical testing and will provide general support for the laboratory following established policies and procedures. This is the entry level for the Laboratory Technician job category. The employee works in a learning capacity while performing a range of laboratory technician assignments under close supervision.

As a Design Controls Engineer, your primary responsibility will be to design, implement, and continuously improve software-focused design control systems with regulatory compliance embedded into their architecture. You will build systems that eliminate ambiguity, reduce manual effort, and enable rapid and reliable development of regulated medical device software. These systems will support the full software lifecycle, from requirements definition through verification, validation, risk management, and release. You will continuously optimize these systems to improve speed, traceability, and audit readiness while supporting aggressive development timelines and frequent design changes.

The Quality Assurance (QA) Specialist will work with Neuralink's teams to ensure that the appropriate governing body regulations are followed. This includes, but is not limited to, adherence to ISO standards, Good Laboratory Practices (GLP), clinical guidelines, manufacturing protocols, and quality control practices.

We’re looking for a Manufacturing Engineer to help scale the manufacturing of consumables used in our robotic surgeries. These consumables include the Needle Cartridge (the end effector that inserts electrodes into the cortex) as well as other complex mechanical assemblies and surgical proxies, like the one being assembled here. In this role, you will help expand our team’s capabilities by supporting the build-out of a new manufacturing site in Texas while sustaining production at existing sites. You’ll work hands-on to troubleshoot manufacturing issues, analyze data, improve processes, and design fixtures. You will collaborate closely with hardware designers, machinists, quality engineers, and the surgery team to ensure parts are built correctly, released on time, and delivered where they’re needed. You will contribute to technical solutions for complex manufacturing problems and help design processes that scale as production ramps. This role is well suited to someone who enjoys working closely with hardware, learning how products move from development to production, and operating in a fast-paced environment.

As part of a $60M+ manufacturer of surgical solutions for the medical industry, Manufacturing Engineer I (Disposables) is responsible for supporting manufacturing processes across disposable product lines. This role is expected to independently complete assigned tasks on time, resolve daily production issues, and support engineering projects. The Engineer I work closely with cross-functional teams to ensure process stability, product quality, and equipment performance. During this stage, the engineer is developing the ability to lead larger initiatives and is actively learning the tools and systems used to deliver engineering solutions in a regulated medical device environment.

This role is responsible for the completion of the work assigned to your and will contribute to the overall success of the Quality Control (QC) Department. Under limited supervision and following established procedures and guidelines, this position supplies assistance and support to the manufacturing operations (consumables or Reagent department areas) and R&D groups. You will be self-motivated and responsible for performing the Real Time Inspection of the Reagent Department filling and packaging, review of Device History Records (DHR), the inspection of labels / final products, the performance of line clearances, and possibly the processing of Non-Conforming Materials in support of Manufacturing’s schedule. You will be highly experienced in the inspection of consumables and fluid manufacturing products. You will electronically transact product to Finished Goods and will generate and maintain certification for all released products. You will be familiar with retrieving various DHRs per established procedures. You will train other Review & Release Inspectors.

The Production Automation Associate is responsible for operating, monitoring, and supporting a variety of automated production equipment to ensure efficient, accurate, and safe manufacturing workflow. This role involves setting up automated systems, performing routine equipment checks, dispensing buffers, observing equipment performance, and responding to basic operational issues.

This is an entry level position. The Associate will perform all activities involved in the aseptic processing of a living product (Dermagraft), under the direct supervision of the Dermagraft Team Leader/Dermagraft Supervisor/Manager. The Dermagraft Associate will support the Dermagraft Manufacturing department by performing the tasks that will assure the safe and timely processing of Dermagraft, working in both a ISO 7 and ISO 8 cleanrooms.

This is an entry level position. The Associate will perform all activities involved in the aseptic processing of a living product (Apligraf), under the direct supervision of the Apligraf Team Leader/Apligraf Supervisor/Manager. The Apligraf Associate I will support the Apligraf Manufacturing department by performing the tasks that will assure the safe and timely processing of Apligraf, working in both a Class 100 and Class 10K cleanroom.

The Manufacturing Engineer I is responsible for providing manufacturing engineering support to Product Development teams. The Manufacturing Engineer is also responsible for designing, developing, testing, and implementing processes, manufacturing work instructions, tooling, and fixtures for products in the Product Development process.

The Manufacturing Process Specialist is a technical expert supporting the manufacturing of biological products both on the site and across the network. Provides technical expertise to ensure that atypical event and non-conformance investigations relating to production and the testing of materials and products are completed in compliance with all applicable procedures and regulations. Monitors and trends key process parameters. Troubleshoots manufacturing problems as required and provide primary technical support. Identifies and implement process improvements both locally and across the network. Supports capital projects, site wide initiatives or other projects as needed in the capacity of a project manager or a subject matter expert. Conducts technical and validation studies. This position requires strong organizational, communication and project management skills.

We are searching for the best talent for Lentivirus Manufacturing Operator. Be part of the manufacturing operations team responsible for production of Lentivirus vector for the autologous CAR-T products in a controlled current Good Manufacturing Practice (cGMP) cleanroom environment.

Determine the acceptability of manufactured products for final release by reviewing production and QA documentation to ensure compliance with product specifications.

Coordinate and perform cGMP manufacturing operations for manufacturing biopharmaceutical products. Ensure the effective use of material, equipment, and personnel while making products at high-quality levels.This position is overnight shift 6pm to 6:30am and operates on a 2-2-3 rolling schedule.

The Manufacturing Associate I will perform Upstream or Downstream production activities for early and late-phase Cell Culture programs in a GMP environment. Responsibilities include executing tasks per SOPs, batch records, and GMP/GDP/GLP standards, ensuring compliance and accuracy. The role involves various unit operations such as media/buffer preparation, bioreactor operations, aseptic techniques, chromatography, ultrafiltration, and drug substance filling. Candidates must maintain process ownership, facility upkeep, and thorough documentation review to ensure compliance. The ideal candidate should have a basic understanding of cell culture, fermentation, or purification unit operations, with preference given to those experienced in single-use platform technology. Strong written and verbal communication skills are essential. The role requires an energetic, motivated, and dynamic individual who is highly organized and capable of maintaining efficiency and a positive demeanor in a fast-paced, multitasking environment

The Microbiology Associate II will be part of the Microbiology Department responsible for the testing and support for the Microbiology Laboratory in support of a Contract Manufacturing biotechnology facility and Process Development. The position will be a first shift, 10-hour/shift position, located at the Hamlin Road facility. Responsibilities include laboratory support, program testing, reporting of results, execution of protocols.

Are you ready to be a part of our remarkable journey? We're looking for someone exceptional to join our growing team as an Associate Scientist II in the Analytical Development group. This isn't just a job; it's an opportunity to contribute to groundbreaking therapies, to be part of a company's inception, and to make a transformative impact on patients' lives. If you're passionate about scaling a company from the ground up, making a real difference, and shaping the inclusive culture we're proud of, this opportunity is tailor-made for you. Join us and be a driving force in achieving excellence in viral engineering.

​​The QA Specialist I provides quality oversight and compliance support for operations including equipment and material preparation, aseptic compounding, filling, inspection, and packaging activities. This role applies knowledge of cGMP and regulatory standards to review documentation, monitor processes, and support investigations. QA Specialist I collaborates with cross-functional teams to maintain compliance and contribute to continuous improvement initiatives.

Under minimal supervision, the main accountabilities are focused on the front line technical support of manufacturing operations while closely collaborating with the Quality and Product Sciences Unit.

Krystal Biotech is seeking a highly motivated Process Validation Associate (1+ years’ experience) or Engineer (3+ years’ experience) to support process validation planning, design, and execution. This person will be responsible for risk assessments, process improvements, investigations, and other projects. They will also play a pivotal role in technology transfer and ensuring processes transition properly from site to site.

Krystal Biotech, Inc is seeking a highly motivated and dynamic Bioprocess Engineer to support our product manufacturing at our Pittsburgh GMP facility. This role is critical to our make a meaningful difference in the lives of underserved patient populations having rare diseases. Quality, safety and on-time delivery is a must to be successful in this role! The ideal candidate will have foundational experience in upstream and/or downstream biologics or gene therapy manufacturing.

Supporting executing a variety of technical projects and/or programs. Define, develop, and execute the validation lifecycle following GAMP5® principles – including requirement specifications and qualification protocols (e.g., URS, FRS, DDS, DR, IQ, OQ, PQ, TM) in support of Commissioning & Qualification (C&Q) activities. Collaborating with Engineering and Quality professionals. Commissioning and Qualification of GMP facilities, utilities, and equipment. Provide technical project leadership and contributions to CQV projects, including managing schedules, support staff, and project execution. Provide review and input on areas of subject matter expertise. Review and summarize data for presentation to quality and regulatory professionals.

The Manufacturing Engineer contributes to medical device product design, development, manufacturing, and testing in accordance with the company’s Quality System. Helps generate design outputs where required through interface with cross-functional team members.

The primary focus area and scope of this position is characterization of biological materials and providing support to manufacturing with timely and accurate in-process and final product testing. The business departments (outside the immediate team) that this role will be working closely with on a regular basis are manufacturing, disease state procurement, and materials management.

The Manufacturing Support Engineer works within cross-functional teams to support internal manufacturing operations. Provides technical support to the engineering of novel particles for drug delivery during bulk manufacturing as well as manages manufacturing deviations and CAPA’s. This role is for 1st shift support (5am - 2pm, M-F).

As a member of the Protein Science team, this individual will set up transfections to express proteins in mammalian cells followed by their purification and characterization to support the Biologics discovery pipeline.

Ensures processes and products conform to established company and regulatory standards. Reviews, analyzes and reports on quality discrepancies related to manufacturing and testing of product and company systems. Investigates problems and recommends disposition and corrective actions for recurring discrepancies. Uses predetermined methods, operations and procedures to inspect and test raw materials, work-in-process, finished product as applicable. This is a 2nd Shift position. Hours are from 2:00pm to 10:30pm.

As a Mechanical Engineer at MMT, you’ll be at the forefront of innovation, designing and testing everything from custom machines to robotics. You’ll collaborate with a talented design team, bring your ideas to life using CAD software, and see your work go from concept to production.

As a Design Quality Engineer II, you will play a critical role supporting the design quality, risk management, and U.S. launch of innovative surgical robotics and instrumentation, including the Hugo™ platform. This design‑focused quality role works at the intersection of R&D, manufacturing, supplier quality, and regulatory, supporting medical device designs from early development through manufacturing transfer and post‑launch support. You will translate design and risk requirements into effective manufacturing controls, ensuring quality is built into the product from the outset, while operating with a high degree of autonomy and cross‑functional influence.

The QA Specialist I in Finishing Operations supports the quality systems as they relate to the manufacturing and testing of cGMP drug products. Provides quality oversight for terminal sterilization, visual inspection, labeling and packaging of parenteral drugs. Performs the quality release of incoming materials. Reviews documentation and quality records.

Support the quality systems as they relate to the manufacturing and testing of cGMP drug products. Provide quality support of GDP for terminal sterilization, visual inspection, labeling and packaging Operations of parenteral drugs. Provide oversight and general support for deviation and CAPA systems, batch record review, SOP creation and revision, and review of quality documents, such as COAs.

The EHS Coordinator is an entry-level role responsible for supporting day-to-day Environmental, Health, and Safety (EHS) activities within a biomedical or pharmaceutical manufacturing, laboratory, or research environment. This position works closely with EHS leadership and cross-functional teams to help maintain regulatory compliance, promote a strong safety culture, and ensure safe work practices are followed during off-shift hours. Flexibility exists surrounding the exact off shift hours worked and may vary based on business needs. This role is ideal for candidates with a background in biomedical sciences, pharmaceutical operations, laboratory environments, or related fields who are interested in developing a career in EHS. The position focuses on hands-on support, data tracking, inspections, training coordination, and employee engagement while gaining exposure to OSHA, EPA, and industry best practices.

The Biospecimen Associate I supports the management of patient samples and provides the link between the Clinical Operations and Client Services teams. The Biospecimen Associate I is responsible for receiving, unpacking, processing, and recording samples sent for laboratory testing under the supervision of the Biospecimen Management Supervisor. The Biospecimen Associate I has demonstrated an understanding of laboratory workflow.

Hologic is dedicated to enabling healthier lives everywhere, every day—and the quality of our on‑market medical devices is central to that mission. We’re looking for a Senior Product Quality Engineer to lead post‑market product quality efforts by driving complaint investigations, root cause analysis, and implementation of corrective and preventive actions. In this role, you’ll own complex investigations, perform health risk assessments, lead cross‑functional teams to implement design and process changes, and provide data‑driven insights that improve product performance in the field. If you’re a technically strong, proactive engineer who enjoys solving real‑world quality issues and partnering across the business, this role is for you.

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 costs, 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. Learns to use professional concepts. Applies company policies and procedures to resolve routine issues. Normally receives detailed instructions on all work. Works on problems of limited scope. Follows standard practices and procedures in analyzing situations or data from which answers can be readily obtained. Builds stable working relationships internally.

The Product Development Engineer 2 applies strong technical expertise and customer-centric design principles to support new product development from concept through production. This role requires the ability to work both independently and collaboratively to solve moderately complex engineering challenges, contribute to project documentation, and support manufacturing transfer activities.

We are seeking a Part-time In Vivo Technician to provide weekend and holiday support for our In Vivo lab. Execution of drug formulation protocols. Drug administration via multiple routes (IV, IP, SC, PO). Observes, records, and reports atypical findings to senior personnel.

The Design Quality Engineer plays a key technical role within Highridge Medical to ensure spinal implant and instrument systems meet all applicable regulatory, safety, and performance requirements. The Design Quality Engineer partners closely with Development, Research, Regulatory Affairs, Marketing, and others to guide design decisions, establish robust design inputs/outputs, develop verification and validation (V&V) strategies, establish risk management files, and maintain compliance to external regulations and internal procedures.

The Quality Assurance Specialist will coordinate and ensure compliance of various elements of the ICU Medical Quality System such as (but not limited to) – CAPAs, NCMRs, SCAR Review Boards, Data Analysis, Management Reviews, Change Orders, Sample Analysis, QA Verification Activities, among others. A successful candidate will have good project management, communication and collaboration skills and be able to work in a dynamic and fast-paced manufacturing environment to support the Operations Quality Engineering team.

Seeking an entry level mechanical engineer to contribute to the next generation of genome sequencing systems. This position involves working on projects that lay the foundation for future product platforms. A driven creativity, a willingness to learn and a passion for solving difficult problems in cross-disciplinary teams are crucial.

The optical engineer will be part of a dynamic and talented engineering group focused on innovative optical system development for next generation sequencing. The engineer will be responsible for testing and integration in an interdisciplinary team environment. The preferred candidate will be a self-starter, with a hands-on, detail-oriented and analytical approach to testing and integration.

The Technical Services and Manufacturing Sciences (TSMS) Operations Engineer will provide direct technical support to manufacturing operations on the production floor in accordance with current good manufacturing practices (cGMP) for clinical and commercial programs. This role will work closely with manufacturing operators and supervisors to ensure smooth production operations, troubleshoot technical issues, and support process execution as specified.

The Technical Services and Manufacturing Sciences (TSMS) Technical Transfer Engineer will be responsible for supporting all facets of Tech transfer, Process Validation, GMP Floor Support, and Continued Process Verification in accordance with current good manufacturing (cGMP) for clinical and commercial programs. This role will provide strong technical oversight to the production to ensure robust and reliable production processes are established.

INCOG BioPharma is seeking a highly motivated individual with subject matter expert (SME) capabilities in sterile pharmaceutical manufacturing process controls and industrial automation of inspection and packaging equipment. The Equipment Specialist has a key technical role within INCOG BioPharma Operations. The ideal candidate must have experience in pharmaceuticals and/or biologics, GMP manufacturing, or within highly regulated industries. The Equipment Specialist’s primary responsibility is to efficiently and safely set up and operate various pieces of production equipment within the facility. They will be expected to work hands-on, be actively involved in continuous process improvements while taking ownership of the quality and quantity of product produced. The ideal candidate should possess a strong mechanical aptitude with strong trouble shooting skills on manufacturing equipment. They should demonstrate mentor and leadership skills to motivate manufacturing personnel, drive timely production activities and inspire problem solving & solution driven thinking. The ideal candidate must thoroughly understand and be able to adapt to the changing needs of a manufacturing environment while providing high level support to the process engineering and operations team in troubleshooting, repair and preventative maintenance of manufacturing equipment and processes.

This position must provide expertise and leadership in the areas of post market surveillance, including root cause analysis, risk assessment, failure mode determination, product reliability and monitoring. This position will work with Development, Operations, Manufacturing, other Quality functional areas along with the global field teams to ensure work is completed in accordance with Inspire procedures and geographic regulations. In addition, this role must be flexible for changing priorities and able to work without direct supervision.

Our close-knit, medium-sized company is composed of smart, curious, diverse scientists who take an active interest in the scientific and technical development of our team members. We seek a Research Associate I to join our dedicated group of scientists. A desirable candidate will have the skills to culture mammalian and/or bacterial cells, perform DNA mini-preps, and complete bacterial transformations or cell transfections.

Engineer I is the entry level engineering position for manufacturing engineering. The engineer will work under the direct supervision of a manager and/or more experienced team members, to support the improvements in manufacturing quality, capacity, and stability through solving problems, developing solutions, and executing strategies. The position is intended to prepare engineers new to the medical device industry for advancement to the next level of Engineer II.

We are seeking a Laboratory Associate- Flow Cytometry to join IQVIA’s laboratory business at Valencia, CA. Shift: Saturday-Wednesday, 4PM - 12:30 AM. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.

iRhythm is currently seeking an Electrical Test Engineer to join our Product Development team. Engineers at iRhythm work passionately to deliver innovative solutions that improve the quality of healthcare and the patient experience. In this role you will contribute directly to near and long-term commercialization efforts for our next-generation wearable bio-sensors, collaborating alongside a small team of multi-disciplinary engineers experienced in bringing medical devices to market. You will gain exposure to the testing approach required to release Class 2 compliant hardware in the medical device industry. Your tasks will be to test, analyze, design, evaluate and debug circuits to support exciting additions to our product line. This is a fantastic opportunity to get hands on experience with a cutting-edge product within the medical device space.

Determines project scope, develops a preliminary plan of investigation, and determines project specifications such as cost, time, and sample requirements by analyzing client input, available supplemental data, and product construction. Projects may include travel to conduct or witness tests at client sites. Initiates communication with clients to promote and explain the benefits of new and existing services. Follows up on contacts from clients. Communicates with clients to discuss technical issues, explain UL procedures and requirements, convey project cost, and negotiate completion date and sample requirements. Acts to address client concerns and to resolve client issues. Provides technical assistance to clients in reference to product inspection and follow-up services. Establishes appropriate test programs by reviewing files and manufacturer's information, examining samples, and applying UL requirements. Is familiar with applicable standards, company manuals and appropriate technical literature. Examines samples for compliance with UL requirements and notifies client of any areas in which the product is not in compliance or of any changes in project scope or specifications. Coordinates laboratory activities by preparing data sheets and instructions to technicians, scheduling and reviewing work of laboratory technicians and engineering assistants and establishing completion dates. Coordinates administrative aspects of project management. May serve as Project Handler of record and/or Reviewer of record as assigned. Communicates project status and results to clients through frequent contact and by preparing reports. Prepares Follow-Up Service Procedures and information pages. Integrates continuous improvement concepts and techniques into all aspects of the job. Resolves engineering issues associated with Variation Notices by analyzing and reporting on the acceptability of the variations. Assists in the development of UL requirements. Assists in developing special test methods and test equipment. Analyzes test program for adequacy and sequence. May coordinate and/or perform File Reviews, as directed. May represent UL at industry related functions such as seminars and trade shown. Read and follow the Underwriters Laboratories Code of Conduct and follow all physical and digital security practices. Performs other duties as directed.

UL Field Engineering Team is hiring in the Huntsville, Alabama area. A Field Engineer performs safety and non-safety certification inspections, audits of quality systems and field evaluations in accordance with the required performance standards and requirements.

We’re looking for a Regulatory Affairs Specialist to join our mission-driven Regulatory Affairs team. In this role, you’ll support, develop, and drive the timely preparation of regulatory submissions and product updates necessary to obtain and maintain regulatory approvals for Endologix products. This position will support the regulatory strategy, review of design changes, manufacturing changes and specification changes.

The Laboratory Technician I, using general laboratory methods, techniques, equipment, and instrumentation in compliance with Eurofins Environment Testing America’s Quality Assurance programs and standard operating procedures, supports laboratory operations through general maintenance of laboratory and supply storage areas, equipment, instruments, and supplies.

The position will be responsible for performing analytical testing on raw materials, intermediates, finished products, and to ensure compliance of all product quality attributes as defined in approved specifications. The incumbent will also participate in investigations (CAPA) and Deviation investigations when appropriate. This role will provide the opportunity to work within laboratory setting, giving exposure to different types of analysis. The successful candidate will have experience working within a GMP/GDP environment and possess excellent communication skills.

Understand and follow Quality System documents relevant to responsibilities, e.g., Quality Manual, SOPs, and Methods. Adhere to appropriate quality measures to meet or exceed the standards set by ISO/IEC 17025, government regulatory (cGMP, GLP), and company requirements relevant to assigned duties. Adhere to all health, safety, and environmental regulations relative to assigned analytical work; maintain and assist others in maintaining a clean, safe work environment. Demonstrate proficiency in at least one core method and ability to conduct at least one other assigned method with no more than 25% supervision. Demonstrate ability to operate all required basic lab equipment within department. Set up batches of samples to weigh and weigh samples. Perform timely and accurate analysis of samples to meet customer commitments, including but not limited to, preparing samples for analysis, using appropriate analysis methods and techniques, and applying appropriate data reduction. Maintain a neat and accurate record system; keep accurate records of work performed on a daily basis and as needed for quality control tests or regulatory purposes; record test data and results for samples in logbook, record book or BookMaster and enter the data or results into eLIMS either manually or through automatic export in a timely and accurate manner.

This position will inspect materials before, during and after production including filling and/or packaging to measure the characteristics of materials and ensure that they conform to specifications.

To support our extraordinary teams who build great products and contribute to our growth, we’re looking to add a Document Control Analyst located at our site in Columbia South Carolina. Reporting to the Manufacturing Engineering Manager, the Document Control Analyst responsible for controlling and maintaining the engineering change and documentation tracking process with emphasis on Bills of Material (BOM’s), parts masters, specifications, drawings and documentation to ensure appropriate changes are documented.

To support our extraordinary teams who build great products and contribute to our growth, we’re looking to add a Quality Engineer located in Salt Lake City, UT. In this role, the potential candidate will be maintaining quality engineering programs, standards and improvements within the organization helping the supplier quality side.

Conducts Quality audits of products assuring company standards are maintained and product integrity is preserved. Consults with management to resolve quality, production, and efficiency problems. Functions as an information source to employees when quality issues occur.

Implementation of digitization initiatives and projects according to Connected Factory strategic objectives and targets in horizontal cooperation with corporate areas. Supervision of internal and external projects in the field of digitalization and automation. Planning and technical implementation of production & testing machinery PLC retrofits, PLC programming for machine connectivity (OT, fieldbus/PLC layer). Integration of the location into MES System (MSCADA). Further development and improvement of process data acquisition at the location. Strengthen the FST digitization network. Development of methods and tools to stabilize data recording. Support of internal SME structure regarding digitalization

This position will support experiment design, data collection, analysis, troubleshooting, and data reporting within the DMPK department. This includes gathering data on pre-clinical compound parameters using a variety of techniques, organizing and processing the data using statistical and analytical methods to reach meaningful conclusions, and reporting observations to clients and other decision-makers.

The laboratory technician performs a variety of laboratory procedures as required by the study protocol. Laboratory technicians are responsible for assisting the Laboratory Manager, Principal Investigator, Clinical Research Coordinators, and other medical professionals in the preparation and handling of specimens, analyzing results, and maintaining laboratory equipment. Laboratory Technicians ensure accuracy, quality control, and adherence to safety protocols, contributing directly to scientific research, development of new products, or medical diagnostics.

As Research Associate Senior, you are responsible for conducting research, development, and manufacturing laboratory experimentation and other scientific activities to support Ventana projects. You are exercising technical expertise, independent judgment, methods and techniques in the design, execution, and interpretation of experiments that contribute to project strategies obtaining results.

Responsible for supporting projects from advanced laboratory techniques related to viral vector production and analytics to routine performance of upstream and downstream manufacturing operations including aseptic cell culture technique, preparing solutions and media, molecular biology techniques, chromatography, TFF and general cleanroom sanitization/area maintenance. The position requires working independently, but also under the supervision of experienced personnel.

As a Sr. Research Associate, you will participate a multi-disciplinary drug discovery team through the design and synthesis of new molecules. The successful candidate will have an excellent track record and a commitment to tackling drug discovery challenges through organic synthesis.

The Associate Project Engineer will be responsible for all engineering functions of their product lines. This includes bringing a product from idea/concept through design, prototyping, development testing, design verification and validation, manufacturing, FDA approvals, product introduction and post introduction monitoring. This individual will work with spine surgeons and all other functions of the company to ensure high quality and on-time product introductions.

As a Quality Engineer, you will design, implement and maintain quality assurance protocols and methods for processing materials into finished products. Guide the compliance of manufacturing and production processes with internal and external safety, quality, and regulatory standard requirements for worldwide distribution. Inspect, test and evaluate the precision and accuracy of production processes and equipment. Support the analysis of reports and production data to help identify trends and recommend updates or changes to quality standards and procedures. Uphold the company's quality standards and testing systems to reflect efficiency, reliability and performance. Assist in the creation of documentation to report issues and errors relating to the production process.

As an Associate Quality Engineer, you will design, implement and maintain quality assurance protocols and methods for processing materials into finished products. Support the compliance of manufacturing and production processes with internal and external safety, quality, and regulatory standard requirements for worldwide distribution. Inspect, test and evaluate the precision and accuracy of production processes and equipment. Assist in report production for trend analysis. Uphold the company's quality standards and testing systems to reflect efficiency, reliability and performance.

The Process Development Engineer will focus on optimizing distribution center operations through labor standard improvements, workflow and layout design, time studies, ergonomic assessments, and productivity analysis. The position supports cost-reduction initiatives, quality improvements, and root-cause analysis while maintaining accurate BOMs, routings, capacity models, and manpower planning. It requires strong cross-functional collaboration to design flexible manufacturing cells, develop data-driven solutions, and ensure compliance with industry standards and company policies.

This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations.

This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations.

This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations.

Perform complex testing and data evaluation such as TGA. Perform complex Liquid/Gas Chromatography, UPLC, and other testing, and, as needed, troubleshoot issues. Participate in or assist with test method validations. Evaluate data for trends. Support supervisors in OOS Investigations and complete CAPA requirements. Interact with outside departments including attending meetings, providing updates, etc. Coordinate testing performed at outside testing labs, raw materials, etc. Maintain a detailed and accurate recording of activities and results on paperwork. Execute, author, and review SOPs, reports, protocols, investigations, change controls, and data summaries. Understand and use basic risk assessment and root cause tools. Train upon and understand methods, equipment and standard operating procedures. Provide training to others as needed. Attend internal and external training on related subjects, including both intra- and inter-departmental cross-training on new techniques and procedures. Support equipment upkeep. Prepare and order supplies, as necessary. Enter data into relevant data management systems. Perform tracking and trending of data as requested. Compile data and provide data summaries to management. Utilize a thorough understanding of regulatory and compliance guidelines for the pharmaceutical industry. Interact with other departments within the company for testing needs and scheduling. May lead departmental projects with the opportunity to participate in or lead cross-functional teams, including continuous improvement projects and new customer teams. May lead stability program including management of test points, reporting of data, and investigations of out of specification or aberrant stability results.

The Procurement Specialist responsibilities include ensuring materials are available for production according to schedule, ensuring inventory is minimized and assisting with cash management optimization. Global Procurement projects require functional alignment to provide an efficient implementation process for early recognition of savings. Sourcing and negotiations are to be conducted at a country level with local suppliers or as designated by Procurement Management.

Perform complex testing and data evaluation such as TGA. Perform complex Liquid/Gas Chromatography, UPLC, and other testing, and, as needed, troubleshoot issues. Participate in or assist with test method validations. Evaluate data for trends. Support supervisors in OOS Investigations and complete CAPA requirements. Interact with outside departments including attending meetings, providing updates, etc. Coordinate testing performed at outside testing labs, raw materials, etc. Maintain a detailed and accurate recording of activities and results on paperwork. Execute, author, and review SOPs, reports, protocols, investigations, change controls, and data summaries. Understand and use basic risk assessment and root cause tools. Train upon and understand methods, equipment and standard operating procedures. Provide training to others as needed. Attend internal and external training on related subjects, including both intra- and inter-departmental cross-training on new techniques and procedures. Support equipment upkeep. Prepare and order supplies, as necessary. Enter data into relevant data management systems. Perform tracking and trending of data as requested. Compile data and provide data summaries to management. Utilize a thorough understanding of regulatory and compliance guidelines for the pharmaceutical industry. Interact with other departments within the company for testing needs and scheduling. May lead departmental projects with the opportunity to participate in or lead cross-functional teams, including continuous improvement projects and new customer teams. May lead stability program including management of test points, reporting of data, and investigations of out of specification or aberrant stability results.

As a Healthcare Operations Manager (Facility Administrator) at DaVita, you’ll be a part of a Team that values work-life balance and where your personal and professional growth is a top priority. DaVita has an open position for a Healthcare Operations Manager (Facility Administrator) who must be an ambitious, operationally-focused and results-driven leader. You will directly impact patient care as the trusted front-line leader in an outpatient clinic setting. Health care experience is not required!

We are seeking a dedicated and detail-oriented Inventory Control Analyst to join our team. The successful candidate will play a crucial role in managing inventory and ensuring smooth spare part and asset management operations across shifts; while supporting attendants, engineers, and technicians.

Provides functional expertise with the use of smart devices with Dexcom’s CGM system. Designs and implements new methodologies, materials, machines, processes, or products. Develops new concepts from initial design to market release. Conducts feasibility studies of the design to determine ability to function as intended. Maintains detailed documentation throughout all phases of research and development. Coordinates activities with outside suppliers and consultants to ensure the delivery of supplies or services needed to meet scheduled timelines.

Develop and conduct analytical methods including UPLC/HPLC, dissolution, GC, DSC/TGA, KF titration and UV/Vis. Perform data analysis and troubleshoot methods and instrumentation. Prepare data for presentations and assist in generating technical reports. Interact with internal and external groups. Initiate and perform investigations, as needed. Write protocols and technical reports and transfer methods internally and externally

As a Manufacturing Engineer – Robot, you will support the build, test, and continuous improvement of Capstan’s robotic system across all phases of manufacturing – from sub-assemblies (eg. actuator stack) through full system integration. This is a hands-on, onsite role ideal for an early-career engineer who thrives in troubleshooting complex electro-mechanical systems and learning by doing. You will work closely with senior manufacturing engineers and cross functional partners to debug issues on the manufacturing line, execute testing, analyze build and test data, and document non-conformances. Over time, you will grow your ability to independently investigate failures, improve processes, and contribute to scalable manufacturing solutions for our novel surgical robotic platform. If you are eager to use your mechanical, electrical and software superpowers to make a difference, come join us!

Join our dynamic laboratory team supporting critical pharmaceutical clinical testing. We are seeking a detail‑oriented and motivated Biochemistry Laboratory Associate who thrives in a regulated environment, enjoys hands‑on bench work, and values accuracy, collaboration, and continuous learning.

eGenesis is seeking an innovative QC Microbiology Technician to lead and provide the technical and strategic oversight of eGenesis’s environmental monitoring program. In this position you will be responsible for hands-on environmental monitoring sampling, testing, reporting and trending of eGenesis GMP manufacturing facilities in Northwest, IN. You will ensure activities are executed in a cGMP compliant manner and have the opportunity to work collaboratively on implementation and maintenance of our contamination control program. The ideal candidate will be independently motivated, a strong communicator and demonstrate proficiency in regulatory compliance.

We are looking for a driven and team-oriented Associate Scientist to join our Immunology Discovery group in Boston. In this role, you will help uncover and validate new therapeutic targets by combining in vivo models, cellular assays, molecular approaches, and immunological expertise to advance early discovery research. You will play a vital role in developing treatments for autoimmune and inflammatory disease patients by designing and conducting in vivo experiments, running in vitro assays, analyzing results, and collaborating closely with colleagues across multiple disciplines.

We are looking for a driven and team-oriented Associate Scientist to join our Immunology Discovery group in Boston. In this role, you will help uncover and validate new therapeutic targets by combining in vivo models, cellular assays, molecular approaches, and immunological expertise to advance early discovery research. You will play a vital role in developing treatments for autoimmune and inflammatory disease patients by designing and conducting in vivo experiments, running in vitro assays, analyzing results, and collaborating closely with colleagues across multiple disciplines.

Lilly’s Synthetic Molecule Design and Development (SMDD) is involved in key activities for the development of active pharmaceutical ingredients and formulated drug products from pre-clinical phases through commercialization of drug substances and drug products for small molecules, synthetic oligonucleotides, and synthetic peptides. Our scientists develop key technical and business solutions across the portfolio using their deep technical expertise to speed up testing of the clinical hypothesis and overall drug development. SMDD tackles this diversity of responsibilities by recognizing that an even greater diversity of talents and cultures is necessary to deliver the next generation of life changing medicines to patients.

The mission of Technical Services/Manufacturing Sciences (TS/MS) is to provide scientific leadership and technical support for manufacturing to make medicine today and tomorrow. The Visual Inspection Scientist provide technical support to achieve the reliable and compliant manufacture of parenteral drug product to predetermined global quality standards via a detailed set of manufacturing instructions and procedures. This person interacts daily with a wide variety of people, including customers, other personnel and site management.

The Quality Engineer in Danvers, MA, is crucial to the success of both the Quality and Manufacturing teams at our production site. Key responsibilities of the role include, but are not limited to, utilize root cause analysis tools to complete product and process related investigations. Lead and support risk assessments utilizing FMEA. Review and improve standard operating procedures and other production documentation. Support customer-facing improvement projects that incorporate evolving customer and industry requirements. Conduct internal GMP and ISO audits. Support deviation resolution in production and corrective action implementation. Assure products are manufactured in compliance with regulatory requirements and manufacturing plans are monitored for compliance to ISO, GMP, and MilliporeSigma standards. Monitor and trend process performance and drive continuous improvement. Lead projects with cross functional teams to improve in-process quality, reduce customer complaints, and increase production efficiency.

As an Associate Scientist 2 – In Vitro, your activities will support assay development through commercial application of new and innovative service offerings within the biosafety testing space. You are responsible for the scientific integrity of technical work performed in the laboratory, and are required to make scientific observations, maintain detailed workbooks/documentation and ensure all documentation fulfills generally accepted professional/industry standards. Requirements also include maintaining a thorough understanding of company testing services, technical principles and applications as they apply to your position.

The Process Engineer at the Lenexa, KS site, will play a crucial role in monitoring and supporting the Dry Powder Manufacturing process within our 24/7 media manufacturing plant. The Process Engineer will be responsible for gaining a comprehensive understanding of the Dry Powder Media manufacturing process, including blending, pin milling, dispensing/packaging, and the cleaning and drying of equipment. The incumbent will also navigate the process control systems for the equipment, ensuring a thorough understanding of how these systems interface and store data within the OSI PI historian. This role is essential for maintaining high-quality production standards and driving continuous improvement initiatives within the manufacturing environment.

The Quality Associate, Microbiology is responsible for performing routine environmental and utilities monitoring of the cGMP manufacturing facilities. Conducts microbiological and chemical testing including endotoxin, bioburden, total organic carbon (TOC), and conductivity to support product release and facility compliance. Additional responsibilities include assisting with data trending, supporting method validation activities, and contributing to the drafting of protocols, reports, and SOPs related to microbiological operations. The role also involves timely and compliant reporting of test results and participation in investigations as needed.

As a Metrology and Calibration Quality Engineer II at Boston Scientific’s Maple Grove site, you will ensure the accuracy, reliability, and compliance of the equipment that makes our manufacturing possible. You’ll collaborate with technicians, manufacturing partners, and quality teams to maintain a world‑class calibration system, support audits, and develop high‑quality calibration documentation that enables safe and effective product production. This role directly contributes to patient safety, operational continuity, and site readiness.

The Protein Assembly Technician will support the organization by overseeing the day-to-day tasks and administrative needs of business operations. The responsibilities include completing various administrative tasks, performing lab functions, and adhering to the organization’s policies and standards. This position works with various departments across the organization to ensure all administrative and operational tasks are completed as needed.

The Specialist, Validation Engineer I supports the successful implementation of manufacturing, and laboratory equipment alongside facilities and utilities at multi-use sites through interaction with internal customers and external service providers. The incumbent is tasked with qualifying new equipment, facilities, utilities and maintaining equipment systems in a qualified / validated state according to established policies and procedures. The individual participates in projects and ongoing work activities of low to moderate complexity. With minimum supervision and given general instructions, this individual carries out routine tasks and functions, and uses basic analytical skills to recognize and solve common problems of limited scope. As a developing team player, the incumbent interacts with their immediate supervisor and personnel within their own work group to achieve team goals while building trust and collaborative relationships outside the immediate organization.

The Support Engineer, GxP is responsible for the technical design, planning, implementation, and support of enterprise systems and laboratory equipment to ensure that these are operating at optimum levels. You will serve as the technical expert in systems administration for specialized manufacturing, development, and quality control systems and recommend the redesign, configuration, recovery, and continuity plans of the operational and information technology and applications for these systems. You will analyze the feasibility of system requirements and develop system specifications and will support project leadership and management in the identification, development, and adoption of technology and processes to deliver quality reliable solutions in the support of our core manufacturing and quality control operations.

We are seeking a Chemical Production Lead to serve as the on-site expert in chemical processing and distillation. This role is highly hands-on at a small site, requiring deep technical knowledge to manage day-to-day operations while also handling documentation, data analysis, analytical testing lab experience, equipment / process troubleshooting, and cross-department collaboration. You’ll also support the development of less experienced staff through mentoring and knowledge-sharing, while ensuring safety, quality, and efficiency in daily operations.

The Production Engineer will be a Operations technical expert and responsible for reviewing documentation for Operations to implement projects for the manufacture of APIs, bulk intermediates, and other products from development through piloting and/or commercial production.

The ideal candidate will have a degree in chemical engineering with experience and a passion for developing new process technology. The candidate should enjoy building equipment and carrying out process development and manufacturing activities in a laboratory or kilo-laboratory environment. The candidate should be well versed in process development and scale-up activities, including common reaction, separation and purification techniques, such as working with 10-100L batch reactors, liquid-liquid extractions, vacuum distillation, filtration, and crystallization. Experience with the development of reactions in flow is preferred but not required. Candidates must possess strong written and oral communication skills.

As a Manufacturing Technician, you’ll be a vital part of Capricor’s efforts in delivering therapies for patients in need. Supporting critical clinical trialscommercial production, you’ll perform meticulous production tasks and documentation to uphold our quality and compliance standards. This role places you in a cleanroom environment, where precision and attention to GMP standards are essential. You’ll be instrumental in ensuring that each production step is performed with accuracy, ultimately contributing to Capricor’s therapeutic success.

We are seeking a highly organized, meticulous self-starter who loves bringing order to records and ensuring every document is perfect, on time, and inspection-ready. This dedicated Document Control role will spend the vast majority of the day issuing, tracking, reconciling, filing, and archiving the controlled records that keep our clinical manufacturing running smoothly and compliantly. This position is located at Capricor’s headquarters in San Diego, CA.

As a Manufacturing Engineer – Robot, you will support the build, test, and continuous improvement of Capstan’s robotic system across all phases of manufacturing – from sub-assemblies (eg. actuator stack) through full system integration. This is a hands-on, onsite role ideal for an early-career engineer who thrives in troubleshooting complex electro-mechanical systems and learning by doing. You will work closely with senior manufacturing engineers and cross functional partners to debug issues on the manufacturing line, execute testing, analyze build and test data, and document non-conformances. Over time, you will grow your ability to independently investigate failures, improve processes, and contribute to scalable manufacturing solutions for our novel surgical robotic platform. If you are eager to use your mechanical, electrical and software superpowers to make a difference, come join us!

The Validation Engineer is responsible for the regulation and support of equipment and systems. Assists in equipment selection, specification, and negotiating fees. Maintains all records related to qualification and validation. Works on projects where data analysis requires evaluation of defined factors to broad concepts. Utilizes independent judgment within broad parameters to determine an appropriate solution. Prepares validation reports, suggests and assists in determining specifications, and makes recommendations for modifications as necessary. The Validation Engineer reports to the Validation Supervisor.

If you are passionate about developing innovative medical devices, we are seeking an Associate Product Development Engineer to support new product development and sustaining engineering activities. In this role, you will contribute to the design, verification, and validation of spinal implants and instruments; support documentation and quality system requirements; and collaborate with cross-functional teams and surgeon advisors to translate clinical needs into effective product solutions. This role reports to the Group Manager, Product Development.

The Associate QA Auditor will perform audits of quality control testing data for routine assays, incoming and in-process materials, process documentation and labeling to assure accuracy and compliance with Good Manufacturing Practice Regulations (GMP) and Standard Operating Procedures (SOP). Additional responsibilities include: Review of Accessory Batch Records, participating in team activities such as pre-audit walkthroughs, data reporting, and additional tasks as needed.

Perform audits of basic records and reports and inspections of routine processes to assure compliance with applicable regulatory requirements, international standards, and corporate policies and procedures.

A Technician 1 – Clinical Pathology is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to conduct a study, which may include biological sample management including labeling, delivery, aliquoting, processing, and verification; cleaning of lab and equipment; preparation, staining, and consolidation of slides. The technician is working under close supervision to gain proficiency.

The following are responsibilities related to the Research Analyst I:The Immunology and Immunochemistry disciplines support large molecule drug development using ligand binding assays (LBA), such as enzyme-linked immunosorbent assay (ELISA), to measure large molecules and their immune responses. The main types of assays include Pharmacokinetic (PK) assays to measure drug and Immunogenicity assay to measure anti-drug antibodies (ADA) and neutralizing antibodies (NAb). Other assay types also performed are branched DNA (bDNA) and cell-based assays. An array of platforms are used to support these assays that include spectrophotometer, Meso Scale Discovery (MSD), Luminex and Gyrolab. Utilizing these platforms/assays, the teams are responsible for the method development, validation and routine sample analysis in both the regulated and non-regulated space of non-clinical and clinical studies.

Perform first piece and daily visual and dimensional analysis of finished product at required intervals as specified on the inspection plans. Perform first article inspection and evaluation. Perform floor audits of paperwork, materials, finished product, and control plan at required intervals as specified on the inspection plans. Control of Non-Conforming Product - Perform inspection of non-conforming product, Initiate containment activities, execute control of non-conforming product procedures and documentation of results. Work together with other team members to ensure all required work is completed each day. Escalate issues, as needed, to Lead Quality Inspector. Be able to effectively operate equipment as required. Maintain a clean and safe work environment. Follow and communicate to others all plant Health, Safety and Quality guidelines and GMP. ISO13485 additional position responsibilities: Provide support and guidance to operations on the floor with respect to ISO 13485 and cGMP requirements. Other duties as assigned.

Quality Control Lab Technician I role at Cord Blood Registry (CBR) is responsible for analyzing and documenting test results from our cord blood and cord tissue processed samples, releasing raw materials, supporting the analytical and processing equipment maintenance program, conducting environmental monitoring, and providing a wide range of critical functions that support the cryogenic storage of our client's final product. This position is also responsible for providing our internal customers with technical expertise while maintaining the highest quality services possible. The Quality Control Lab Technician I directly supports manufacturing to ensure the Product Operations function is provided with adequate equipment and materials to support stem cell processing activities. At the Technician I level, the individual performs critical daily activities involving high complexity testing, equipment maintenance and troubleshooting, interfacing with service providers, reagent testing, executing quality control assays and environmental monitoring activities. The role is also involved with supporting and executing validations, verifications, and projects within the Quality Control department.

The Research Associate (RA) at Crown Bioscience North Carolina will support the execution of in vivo research studies, contributing to the advancement of oncology and pharmacology research. The RA will work closely with scientists and senior research staff to carry out experiments, maintain animal models, collect and analyze data, and assist in the development of novel research techniques. This position plays a critical role in ensuring the quality and integrity of preclinical studies.

Under routine supervision, primarily responsible for the enhancement of existing products on our sustaining team. Involved in creating concepts and modeling and drafting designs utilizing 3D CAD software. Other responsibilities include drafting of design history file documents, development of test plans to assess designs, and assisting in the development processes for Manufacturing, Quality Control, Regulatory and Planning for their particular project.

August Bioservices is seeking to hire experienced manufacturing technicians to support our growing formulations and filling teams. Headquartered in Nashville, TN – one of the fastest-growing and most exciting cities in the United States – August Bioservices is a privately-owned, high-growth, and high-impact Contract Development Manufacturing Organization (CDMO).  As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our work is instrumental in helping to develop molecules today that can become the life-changing therapies of tomorrow. For those seeking dynamic opportunities, rewarding career paths and a chance to make a difference in global health, come grow with August!

Carry out Molecular Biology, Microbiology, Protein experiments following established SOPs and/or guidance of laboratory management. Perform DNA/RNA extraction, quantification, and gel QC. Perform PCR setup for qualitative and quantitative analysis. Report experimental results to project managers in a timely manner. Follow established quality management policies and GLP and GMP practices.

In this role, you will report to the Onsite Supervisor and will work closely with the Avantor’s Advanced Laboratory Services professionals to serve our customers by performing customized, mission-based lab work and research protocols that help return time back to science.

The Support Engineer, GxP is responsible for the technical design, planning, implementation, and support of enterprise systems and laboratory equipment to ensure that these are operating at optimum levels. You will serve as the technical expert in systems administration for specialized manufacturing, development, and quality control systems and recommend the redesign, configuration, recovery, and continuity plans of the operational and information technology and applications for these systems. You will analyze the feasibility of system requirements and develop system specifications and will support project leadership and management in the identification, development, and adoption of technology and processes to deliver quality reliable solutions in the support of our core manufacturing and quality control operations.

As a Sr. Microbiologist, Quality Control, you will lead the way in ensuring compliance with environmental regulations and Good Manufacturing Practices (GMP) by performing microbiological testing in a biopharmaceutical manufacturing organization. You will utilize state-of-the-art technology to monitor air, water, and surfaces for potential contaminants, inoculate microbial cultures for growth promotion testing, and perform bioburden testing. You will also review and trend data, generate charts, and maintain inventory of supplies. Your work will contribute to the production of life-saving biopharmaceuticals, making a positive impact on public health and the environment.

The Microbiologist I conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols.

The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development.

The Environmental Monitoring Microbiologist conducts cleanroom monitoring activities to ensure the air, surfaces, and critical utilities utilized for pharmaceutical product manufacturing meet cGMP requirements. These samples are collected according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures.

Responsible for all microbiological and some analytical testing of production materials under GMP conditions. Responsible for process and equipment validation (autoclave and depyrognenation oven) in cooperation with Engineering and R&D (New Product Sterility and LAL validation.)

Senior Systems Engineer uses state-of-the-art techniques to achieve Infusion System device designs that meet customer needs. Guides technical team in resolving difficult problems in a collaborative environment. Applies standard risk management principles, methods, and techniques to ensure products meet medical device design control best practices. Plans, and executes engineering assignments under the guidance of the Product Risk Management Owner.

As a Senior Mechanical Engineer, you will be at the forefront of product development, working on both new and existing infusion systems. Your responsibilities will include: Defining Design Requirements: Collaborate with customers and users to translate their needs into clear design requirements and hardware specifications. Architecting Mechanical Systems: Contribute to the development and documentation of innovative mechanical system architectures that push the boundaries of technology. Designing Complex Assemblies: Create and develop intricate designs for mechanical assemblies, mechanisms, and component parts of electro-mechanical medical devices, ensuring they meet performance objectives. Conducting In-Depth Analysis: Perform detailed mechanical analysis, including tolerance analysis (GD&T), load and fatigue life analysis, and thermal modeling, to guarantee consistent performance in safety-critical applications. Utilizing FEA Tools: Leverage advanced tools like SolidWorks Simulation and Abaqus for structural analysis, both linear and non-linear, to validate your designs. Integrating Designs: Ensure seamless integration of mechanical design elements with electrical and consumable components, collaborating with cross-functional teams. Troubleshooting and Problem Solving: Engage in troubleshooting efforts related to mechanical design aspects, working closely with other design constituents to resolve issues. Transitioning to Manufacturing: Effectively transition products to manufacturing, ensuring robust designs and processes that meet production standards. Optimizing Designs: Continuously improve mechanical and electro-mechanical designs to enhance production efficiency, reliability, regulatory compliance, and cost-effectiveness. Defining Testing Protocols: Establish and orchestrate testing protocols to validate the safety and effectiveness of your designs, ensuring they meet the highest standards.

The Quality Assurance Scientist II is responsible for Reagent Manufacturing Quality Assurance, encompassing tasks such as approvals for nonconformances and other quality documentation. Key responsibilities also include attending Material Review Board (MRB) meetings and providing general floor support.

Administer and implement Environmental, Health and Safety (EHS) programs and procedures in collaboration with the Division EHS Manager. Follows established procedures to support BD Distribution Center personnel to maintain compliance with facility/corporate EHS policies, agency regulations, and best management practices. Works on problems of limited scope where analysis of procedures and policies is necessary to select appropriate methods and techniques for obtaining satisfactory solutions.

BD (Becton Dickinson and Company), a leading global medical technology company, is seeking a Research and Development Engineer II to work on the sustainability and development of medical devices for BD’s healthcare products. They assume the technical role of projects and champion technical and architectural excellence. The candidate should be passionate about solutions to clinician and patient unmet needs, and enjoy the details involved with the long-term outlook of technological solutions to clinical needs. The position is an exciting opportunity to make a meaningful, positive impact on patients throughout world by leveraging cutting edge technologies.

The Regulatory Affairs (RA) Specialist will provide primary RA support for one or more product lines and/or region(s), including independent participation on new product development teams and continued RA support through the lifecycle of the product. The RA Specialist will also prepare regulatory submissions required to market new or modified medical devices in global markets. The RA Specialist is able to interpret and communicate regulatory issues to ensure the business is aware of opportunities, risks, and concerns.

BioLegend (a division of Revvity, Inc.) is seeking a highly motivated Quality Assurance Coordinator. The Quality Assurance Coordinator will be a multi-faceted and integral part of the Quality Assurance team and will perform and administer Quality Assurance (QA) activities at BioLegend, in accordance with BioLegend Vision, Mission, Quality Policy and Quality Objectives for implementation, maintenance and improvement of BioLegend's Quality Management System (QMS) and support the upcoming ERP system deployment. The QA Coordinator will be responsible for processing document control requests as well as assisting with the ongoing ERP project as needed, while supporting document control duties and training processes within current eQMS system (Smartsolve) as needed. Responsible for working with one or more of the following quality system processes: document control and training. Interacting with other QA departments and processes: change management, nonconformance, complaint management, CAPA management, supplier quality management, internal audits, post-market surveillance and vigilance management, risk management, QA product release and QA design control responsibilities. The QA Coordinator is responsible for ensuring quality systems procedures are followed and records are compliant in their applicable areas of responsibility. This role requires some work experience and knowledge of standards and regulations such as MDSAP, ISO 13485 and country and region-specific regulations (i.e. FDA 21 CFR 820, EU IVDD).

This is a dynamic role as part of a team of engineers and scientists developing a novel intradermal biosensor technology. It is a hands-on, laboratory role which straddles R&D and pilot-scale production, making extensive use of proper laboratory practices, including preparing solutions, designing and running experiments, and recording and analyzing data. You will have the opportunity to assist the scientific team perform experiments and collect data to validate biosensor performance.

Join Bio-Rad as our Quality Engineer and work in our Woodinville, WA site! Working in this Quality Assurance role, you will attend cross functional Daily Management meetings and represent Quality Assurance following up on blocking issues and implementing counter measures. You will manage the Material Review Board and ensure thorough data-driven documentation of non-conformities and risk based determination of CAPA. You will review data for trends, manage corrections and corrective action and support Global Supply Chain and business partners as requested.

This position will support system validation and product release processes, ensuring compliance with industry standards and regulatory requirements. You will play a key role in contributing to the development and improvement of validation procedures and driving overall product excellence. This is an entry-level, remote position. Successful candidates have a bachelor’s degree within an engineering discipline, a passion for technology, and exposure to system/software testing in the life science industry.

As a Field Service Engineer for Agilent, you will work at a variety of labs, so having an appetite for continuously learning about new instruments, software, and consumables is key. Applying your communication skills, creativity, and can-do attitude is essential. The ability to help solve customer problems and a commitment to delivering the highest levels of customer service are how you will build customer success. You will be responsible for supporting our customers with on-site installation, implementation, maintenance, and repair of Agilent Liquid Chromatography /Molecular Spectroscopy systems. Our varied product lines include hardware, software, networking products, and operating systems.

You're passionate about science and want to be in a hands-on role supporting our transgene analysis team. The Research Associate I will assist with basic Molecular Biology techniques and will focus on generating protein expression data from cell and tissue samples.

The Scientist II - Chemistry (ICP) is accountable for driving results in a fast-paced environment by performing analytical routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. For this Scientist II (Chemistry) position, ICP, GC-MS, LC-MS, HPLC, TOC, UV, osmolality, density, and pH are commonly employed in the described testing in addition to other key methodologies such as KF and titration. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company) and may also assist with method development / method validation projects.

The Manufacturing Technician II (Compound/Fill/Finish) is accountable for results in a fast-paced environment and assists with the manufacturing of sterile injectable products in vial and syringe configurations for clinical/commercial distribution. The Manufacturing Tech II is a key role responsible for executing advanced production tasks involving compound, fill and finish processes for sterile injectable pharmaceutical products executed via aseptic isolator technology. This position entails a high level of technical expertise in aseptic processes requiring single-use components, ability to troubleshoot, and responsibility for maintaining quality and compliance with Good Manufacturing Practices (GMP). The Manufacturing Tech. II performs 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 Tech. II employs acceptable techniques while working in manufacturing environments, including PPE gowning. The candidate must have the ability to learn specific department procedures, have a general understanding of Good Documentation Practices (GDP) and GMP, and follow directions from leadership/peers to ensure manufacturing goals are met.

The successful candidate will be responsible for process development, process characterization and scale-up of small molecules and oligonucleotide drug candidates. The candidate will work closely with cross-functional teams and contract manufacturing organizations on process development, process transfer and oversight of manufacturing processes.

Let’s do this. Let’s change the world. In this vital role, you will have the outstanding opportunity to support the start-up of the Amgen North Carolina (ANC) manufacturing facility. This is a manufacturing support role responsible for the generation of electronic documentation, for tracking of EBR metrics and for communication between the operations teams and the various functional groups working through start-up activities. During start up, Manufacturing Senior Associates will have oversight of electronic batch records operational readiness activities in multiple manufacturing areas such as: Dispensing, Buffer/Media Preparation, Upstream Cell Culture, Harvest, Downstream Purification, Analytical Testing, and Column Packing. Manufacturing Senior Associates can also support Standard Operating Procedure (SOP) creation, review, and approval; design of job aids and work instructions, advancement of digital tools to support manufacturing operations, and training of staff.

Let’s do this. Let’s change the world. In this vital role you will partner with cross-functional teams—including Engineering, Quality, Process Development, and Operations—to implement process improvements, support new technology introductions, and maintain robust GMP manufacturing performance. Your work will directly contribute to Amgen’s ability to deliver life-changing therapies to patients worldwide.

The Validation Engineer I provides support in performing equipment, facility and utility qualification activity and re-qualification activity to ensure compliance to cGMP and Amneal's quality requirements.

A primary focus of this role is creating and modifying LIMS test plans to support QC activities while adhering to regulatory and data integrity guidelines. The LIMS Coordinator is responsible for tracking and managing laboratory inventories within the LIMS system and to perform and verify daily verification of laboratory data for accuracy and completeness, ensuring compliance with GxP standards before submission for review.

Responsible for all microbiological and some analytical testing of production materials under GMP conditions. Responsible for process and equipment validation (autoclave and depyrognenation oven) in cooperation with Engineering and R&D (New Product Sterility and LAL validation.)

We are seeking a Laboratory Technician to join our team, reporting directly to a supervising scientist or research associate. This multifaceted role involves maintaining lab cleanliness, procuring consumables and reagents, managing stock inventories, and overseeing product deliveries. The candidate will execute analytical and molecular biology procedures, including ELISA, SDS-PAGE, miniprep/midiprep, and agarose gel electrophoresis, along with antibody purification and in-vitro experiments under guidance. Proficiency in MS Office, particularly Excel, meticulous record-keeping, effective communication, and the ability to meet deadlines in a fast-paced environment are essential. Flexibility for occasional late hours and a capacity to thrive in a self-directed team environment are also required, with the possibility of undertaking additional duties as needed.

Join Applied Medical and be at the forefront of precision medical device manufacturing. As a Manufacturing Design Engineer, you’ll merge engineering creativity with hands-on design expertise, developing equipment and automation solutions to support sub-assembly workflows product integration. In this dynamic, production-facing role, you’ll collaborate with PPD teams, machinists, and cross-functional engineers—applying your CAD skills and mechanical intuition to design tooling, prototype components, and support the build and validation of custom equipment that enhances throughput, quality, and manufacturability across the floor.

Responsible for a basic knowledge of all phases of the production operation from weighing through coating. On each shift, each Manufacturing Technician will be responsible for one of the following production operations: weighing, mixing, coating, or slitting, as assigned by the Manufacturing Operations Supervisor or Shift Lead.

The Manufacturing Technician II/III is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The Manufacturing Technician is expected to fully participate in both departmental projects and any quality working teams which may be applicable. existing procedures. All of the specific requirements presented in this job description are applicable to the functional area in which it resides.

Join a company where you can make a difference from day one and help make the world a better and safer place. ARL Bio Pharma provides analytical and microbiological testing for the pharmaceutical industry. Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug manufacturers, and raw material suppliers bringing excellence to pharmaceutical sciences and making pharmaceuticals safer. This position is a fantastic stepping-stone for those with some basic experience looking to expand their career in the interesting world of the pharmaceutical industry. 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.

The position requires the performance of variety of task including assisting project managers in a timely manner with administrative tasks, being the primary point of contact between the clients and R&D lab and working closely with project managers to create plans concerning resources, tracking and project timelines.

This position will involve assisting in the synthesis and subsequent purification steps of large scale oligonucleotides. The operator must comply with GLP/GMP protocols and be able to follow all association SOPs and work instructions when performing and documenting operations.

Arrowhead is seeking a highly motivated Associate Scientist to join our growing Discovery Chemistry team at our San Diego site. This individual will primarily focus on oligonucleotide bioconjugation, peptide synthesis, purification, and analytical chemistry. As a discovery chemist, you will play a key role in the development and optimization of siRNA-based therapeutics by applying your expertise in bioconjugation strategies and peptide chemistry.

The Quality Control Associate supports all product release testing activities from raw material to finished good products and product stability. This role involves in process testing of incoming raw materials, analytical testing, bulk functional testing, and kit lot release testing in accordance with ISO 13485 GMP requirements.

The Manufacturing Engineer assists in the plan, design, and maintenance of manufacturing processes. Ensure systems are running according to specifications and within regulations in the production of quality product. Determine parts and tools required for Manufacturing to achieve their goals of producing quality products. The need to meet GMP and ISO standards when developing these procedures is a must. This position requires close collaboration with the Formulation & Filling, Packaging, Materials, Q.C. and R&D departments. The ability to set project schedules and meet appointed deadlines is required.

We are seeking a highly motivated and detail-oriented Research Associate to join our dynamic Next-Generation Sequencing (NGS) product development team. In this hands-on role, you will support the evaluation, optimization, and advancement of cutting-edge NGS solutions. You will perform high-quality laboratory experiments, contribute to critical data generation, and help drive successful internal and external adoption of our products. This position is ideal for someone passionate about molecular biology and eager to grow their expertise in NGS workflows, product development, and applications.

You're passionate about science and want to be in a hands-on role supporting our transgene analysis team. The Research Associate I will assist with basic Molecular Biology techniques and will focus on generating protein expression data from cell and tissue samples.

As an Integration and Test Engineer, you will have a broad role scope owning vehicle systems, integration, and test. Ultimately, engineers are responsible for the vehicle and ensuring all systems are ready for launch and operations. To accomplish this, engineers need knowledge of system design, manufacturing, test, and operations. This role interfaces with all engineering departments and Integration and Test Engineers must be able to drive conflicting requirements to implemented solutions.

Vaxcyte is looking for an energetic and talented Associate Engineer II to contribute to the Polysaccharide Upstream Pilot Plant as this person will be responsible supporting design and execution of experiments at pilot scale of polysaccharide production and scale down model experiments of process operations, contributing towards the process characterization of the polysaccharide process. The successful candidate will have knowledge and practical laboratory upstream process experience in executing, supporting, or developing processes such as fermentation, clarification processes (centrifugation experience is a plus), and tangential flow filtration. In addition, the candidate must have experience in performing plate-based colorimetric assays (Bradford and Lowry assays are a plus).

We are seeking a motivated and detail-oriented Research Associate with strong hands-on experience in chromatographic analysis to support QC release and stability testing. The successful candidate will perform routine cGMP QC testing using HPLC methods (RP-HPLC, SEC, IEX), Agilent HPLC systems, and additional supporting assays in a fast-paced, collaborative environment. This is a unique opportunity to be part of an emerging early-phase clinical company bringing innovative technology to the global market.

The Scientist role within the Chemical Development group will focus on the synthesis, process development, and analytical strategy for protected phosphoramidite precursors used in therapeutic oligonucleotide API manufacturing. This position is key to building Veranova’s commercial capability in producing high-quality oligonucleotide building blocks. The ideal candidate will have strong expertise in phosphoramidite chemistry, including impurity profiling and customer-specific requirements. This role will also collaborate closely with the Analytical Team to establish robust characterization and control strategies that ensure exceptional product quality.

Review in-process batch records finished product batch records (Pharm, and/or MPD), and intermediate analytical records. Release intermediate materials. Assess the manufacturing operations and process documentation for compliance to GMP’s and Standard Operating Procedures. Participates in the evaluation and triage of events, deviations, and unplanned activities that impact processes and/or materials. Assure deviations are appropriately reported. Identifies improvement opportunities and participates on project teams geared toward continuous improvements for the various elements of the quality system. Perform annual retain inspections. Assists with the revision of SOP’s, QF’s and training modules as needed. Attends training classes and seminars as needed.

The Clinical Trial Assistant (CTA) will provide administrative support to the Clinical Operations Team in full spectrum of clinical trial activities related to study start up, study maintenance, study closure and vendor management in compliance with Good Clinical Practice (GCP), Standard Operation Procedures (SOPs), and all applicable regulations governing the conduct of clinical trials.

The QC Labeling Inspector is responsible for maintaining a high level of inventory accuracy and integrity within the Tissue Bank. Performs final product labeling and inspections, manages transport and storage of quarantine tissue, and maintains labeling supplies. Promotes Lean Behaviors across the organization (This includes Participating in Try storming, Brainstorming and Lean Related Initiatives). Promotes Usage of Problem Solving. Ensure that Labeling Operations are in Compliance with the State and Federal Regulations and AATB Standards.

Vyriad is a clinical stage biotechnology company based in Rochester MN. We are developing the next generation of targeted genetic medicines for cancer therapy. The Bioproduction Technologist will be responsible for upstream and/or downstream process development and GMP manufacturing of oncolytic viruses, lentiviral vectors and other biologics for clinical trials. The Bioproduction Technologist plays a vital role in the day-to-day process development projects and manufacturing operations in compliance with cGMP standards. Virus and gene therapy manufacturing operations involve aseptic processing in a pharmaceutical cleanroom facility, large-scale cell culture in shake flasks and bioreactors, vector generation, purification, concentration, and fill and finish operations, according to established standard operating procedures (SOPs). In addition, staff are responsible for the daily operations and environmental monitoring of the GMP facility to ensure compliance with applicable regulations.

The Scientist I, Analytical Development position is responsible for the development and implementation of analytical characterization methods for a range of pharmaceutical dosage forms to support formulation, process, and specification development. This position collaborates with product development scientists in developing therapeutic drug products utilizing the company's proprietary XeriSol® and XeriJect® platform technologies. This position also supports Quality Control and CMC functions in establishing product specifications, stability programs, material qualification, method validation, method transfer, and process validation.

Yokogawa is seeking an Analytical Systems Engineer with responsibility for delivering customer satisfaction through the application of specialized chemical engineering knowledge and professional judgment in the analysis, design, and implementation of analytical systems. This includes the use of advanced engineering tools and methodologies such as gas chromatographs, continuous emission monitoring systems (CEMS), process gas analyzers, and sample conditioning systems. The role requires autonomous execution of complex engineering tasks, including the development and optimization of analytical strategies, integration with control systems, and compliance with environmental and safety regulations. The Analytical Systems Engineer acts as a Subject Matter Expert (SME) in chemical process analysis, often leading technical decisions and providing engineering solutions that align with industry standards and client requirements.

The Specialist Mfg Tech works out of our Abbott Park (Lake Bluff), IL location in the Core Diagnostics Division. Our diagnostic solutions are used in hospitals, laboratories, and clinics around the globe. The crucial information derived from our tests, instruments and informatics systems are often the first step in patient care decision making for hundreds of health conditions from heart attacks to blood disorders to infectious diseases and cancers.

The CRA will ensure quality, accuracy, and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials according to the Code of Federal Regulations, ICH GCP, and ISO14155. This position is onsite in our Alameda, CA location.

Perform production line duties required to meet production goals while complying with quality standards and safety requirements. Operate production equipment and complete documentation in accordance with cGMP’s and department SOP’s while monitoring product to ensure quality standards are maintained.

Perform production line duties required to meet production goals while complying with quality standards and safety requirements. Operate production equipment and complete documentation in accordance with cGMP’s and department SOP’s while monitoring product to ensure quality standards are maintained.

We are seeking a Lab Technologist to grow with the company, contributing to our company goals and meeting customer needs. The Lab Technologist will perform hands-on commercial sample assays, support production activities by developing QC protocols and maintain/establish Standard Operation Procedures (SOPs) with compliance with ISO 9001 and 17025 standards.

This position is responsible to ensure all center activities are performed in accordance with standard operating procedures (SOPs) and the center is ready for inspection by regulatory agencies at any time. The Quality Assurance Specialist (QAS) assists in the development of policies, procedures, and processes to ensure the necessary requirements and controls are appropriately addressed in an effort to reduce or eliminate the potential of errors. This may be identified through scheduled audits, performance observations, or record review. This position assists in the gathering and compilation of data and information to provide appropriate monitoring of all quality initiatives and programs. The QAS is responsible for ensuring an appropriate investigation of any deviations from process or procedure is complete. The investigation may require root cause analysis and effective corrective or preventative actions. Monitoring for the recurrence or the potential for recurrence is a critical component of data analysis.

Aether is looking for a hands-on Research Associate to join our Materials Development team. You will play a central role in how our materials are printed, tested, and understood - operating our fleet of 3D printers, running mechanical and thermal characterization, and generating high-quality data that drives product development and customer success. This is a junior, execution-focused role with significant room for growth. You’ll start as a generalist across printing and testing workflows, and over time develop a deep intuition for 3D printing behavior and materials performance. As our R&D capabilities expand beyond FFF and FDM, you will have opportunities to help build novel testing workflows and support application development.

Responsible for supporting customers through on-site activities such as installation, implementation, maintenance and repair of company and multi-vendor systems solutions which may include hardware, software and networking products as well as operating systems. Installs and optimizes hardware/software/network products and configurations at customer sites. Diagnoses and resolves product performance problems. Performs maintenance and repair services. Ensures customer satisfaction by advising customers on preventive maintenance and configurations, which may impact product performance. Proactively responds to potential equipment or software issues to prevent unplanned interruption of customers' business. Delivers (does not design) fully integrated solutions, which may include peripherals, communications, operating systems and applications software. Serves as an internal resource on technical issues and manages product escalations Collaborates with Agilent teams such as Support, Sales, Marketing and R&D to provide solutions to customers. May have knowledge of third-party products. May deliver internal technical training and maintenance seminars and workshops for field engineers or customers. May train other field engineers or customers. May calibrate equipment on-site for large volume customers. May qualify leads. Must consent to participate and meet Agilent approved customer/vendor credentialing requirements necessary to gain access to customer sites. Requirements may include, but are not limited to, proof of identification, proof of certification to perform the work required, customer health and safety requirements, etc.