Links to 621 Entry-Level Biotechnology & Life Science Jobs

The Tech Transfer Engineer II will be joining the Pfizer Andover Clinical Manufacturing Facility (ACMF) team. The ACMF is a facility located on the Pfizer Andover, MA campus and is responsible for cGMP production of phase I/II clinical drug substance supporting the Pfizer Biotherapeutics portfolio. The ACMF resides within the Research and Development organization. The ACMF Technology Transfer Team is responsible for incoming product site assessment, preparatory activities, campaign readiness, and overall product/project ownership to support ACMF manufacturing of clinical drug substance.

Your technical skills will help us keep our plants, utility systems, buildings and equipment up and running. Pfizer relies on you for maintenance, redesign, and repair of utilities in our plants, such as electrical, plumbing, carpentry, air conditioning, heating, painting and general maintenance. You will be relied on to take the necessary preventive and corrective steps for setting priorities, forecasting and allocating resources in the maintenance tasks. As a Senior Mechanical Engineer, your breadth of knowledge on internal or external business challenges will help us improve our engineering products, processes and services. You will manage projects by meeting objectives and preparing forecasts for resource requirements. Your risk-taking ability will help us advance new concepts and methodologies. You will provide technical guidance and oversight to team members and help in problem solving.

The Facilities Electrical Engineer provides electrical and controls expertise to support site operations at the Pearl River, NY R&D site. This role is primarily focused on planning, oversight, and vendor management for facility electrical, power distribution, and automation systems (rather than day‑to‑day hands‑on electrical work). You will partner closely with internal teams and external contractors to ensure safe, reliable, and compliant facility operations, while contributing to capital planning, modernization efforts, and long‑term site strategies. This role offers strong opportunities for growth and development within Pfizer. You'll build new skills and gain diverse experiences within Pfizer’s dynamic environment.

Polysciences technical operations and scientific laboratories offer custom synthesis, contract manufacturing and packaging, and laboratory products. We are proud to offer a broad range of products and tailored solutions for the life sciences, bioprocessing, microparticles, medical device, specialty chemical and eChem industries. We adhere to ISO13485:2016, FDA cGMP 21 CFR 820 regulations, and SOCMA’s ChemStewards® Management System. We believe the best scientific innovations are built through collaborations. The QC Analyst I is responsible for performing incoming raw materials, in-process samples, intermediate products, and final products analytical analysis per approved internal and customer specifications following associated procedures to support both product manufacturing and commercial product release. Will work under the supervision of more experienced analysts and follow established procedures and protocols.

We are seeking a Quality Assurance Specialist to help establish, implement, and maintain Quality processes and policies for Precision Neuroscience. In this role you'll collaborate with physicians, neuroscientists, and software, hardware and machine learning engineers to develop the next-generation human-ready Brain-Computer Interface (BCI).

The (Sr) Technician, Upstream Process will work within the Upstream Processing group and performs the following activities while executing upstream operations: Preparation of stock solutions, buffers and media. Filtration of stock solutions, buffers and media. Set-up and operate disposable fermenters / bioreactors and other disposable bioprocess equipment including depth filtration. Passage and expansion of microbial and mammalian cell lines The (Sr) Technician, Upstream Process supports relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate.

The Associate Scientist (Management Trainee) – Molecular Biology, Gene Production Department position is designed for recent graduates with strong learning agility, leadership potential, and an interest in laboratory operations and team management. This role provides structured training in gene synthesis production, laboratory operations, continuous improvement, and leadership development. The successful candidate will work closely with experienced team leaders and supervisors to develop the technical and managerial skills required for future leadership positions within the organization.

We are seeking a motivated and creative Research Associate to join our Therapeutic Translation Team. In collaboration with members of the Therapeutic Translation, Cellular Models and Automation teams, you will design, validate and execute high-throughput experiments to characterize and optimize therapeutic gene editing proteins. Your work will be foundational for expanding our gene editing toolbox and translating these advances to new therapeutic opportunities. The ideal candidate will have experience with molecular biology, mammalian cell culture and NGS preparation workflows. This is an excellent opportunity to work cross-functionally with a diverse team of experts across machine learning, protein design, cell biology, gene editing and laboratory automation

The Manufacturing Specialist, Cell Processing at ProKidney is responsible for supporting cell processing operations, ensuring compliance with cGMP guidelines in the development and production of regenerative medicine therapies. This role involves setting up and operating production equipment, including control rate freezers, orbital shakers, and other equipment, while contributing to efficient processing, freezing, and storage of cell therapy products.

The Quality Assurance Document Control Specialist is responsible for day-to-day administration, maintenance, and continuous improvement of the organization’s document control within the Quality Management System (QMS) in a regulated pharmaceutical and medical device environment. Ensuring that QMS components are accurate, current, revised, approved, accessible and archived in a compliant manner. The Quality Documentation Control Specialist ensures ProMed’s brand, philosophy, systems, policies, and procedures are properly implemented and observed.

Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. Our Validation specialists will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The validation specialist will evaluate the equipment/utility/system/procedures used in development, production, and holding of pharmaceutical products and determine a validation approach. The individual should have experience with current US and international regulations, guidance, industry best practice in one of the following areas of validation: facilities, utilities, and equipment qualifications, process validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the validation specialist must be approved by the client.

We are seeking a motivated Research Associate to support troubleshooting and continuous improvement of immunoassay-based products within Technical Operations. This lab-based role focuses on investigating manufacturing and quality issues, identifying root causes, and implementing data-driven solutions to improve assay performance and reliability. In this role, success is defined by your ability to independently troubleshoot assay issues, perform laboratory experiments and data analysis, and implement improvements that enhance product performance and customer experience.

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.

The responsibilities of this position, Scientific Support Associate (SSA), are to respond to incoming technical inquiries from the Bio-Techne commercial team and Bio-Techne's North American customers, providing first-tier technical and sales assistance for R&D Systems, Tocris, and Novus products. Completes all customer requests including e-mail responses and simple quotes. Maintains technical resources. Backs up Customer Service and Sales departments as necessary. Continues training to stay up to date on technical information for old and new products. Performs additional duties as assigned.

Bio-Techne’s GMP Process Development team is responsible for the development of Bio-Techne's various product lines, with a focus on the high-quality recombinant protein products. We seek a highly motivated and creative individual to participate in the development, optimization, and technology transfer of protein purification procedures for recombinant proteins expressed in E.coli cell lines to our GMP production facility. In addition, you will develop procedures and processes in the feasibility stages of the development cycle. This is a great opportunity to gain experience with cutting-edge biotech development/manufacturing processes & practices while working in a collaborative laboratory environment.

This position is responsible for purifying polyclonal/monoclonal antibodies in a GMP Lab, following GMP guidelines. This includes, but is not limited to GMP, natural, and other products used by pharma and IVD customers. Purifies polyclonal/monoclonal antibodies by column chromatography, using a variety of techniques and equipment. Filter, aliquot, and bottling of product using aseptic techniques, and submits to bulk inventory. Documents batch records following GMP guidelines.

Responsible for developing controls, calibrators, working solutions, and intermediates according to approved standard operating procedures in an invitro diagnostics environment. Responsible for developing quality products on schedule. General knowledge and basic application of concepts, theories, terminology, and practices that apply to research in a laboratory environment.

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Scientist to join our Therapeutic Protein department to support ongoing programs by purifying and biochemically characterizing protein reagents and antibodies. You will work in a fast-paced, collaborative lab environment, ensuring high-quality outputs and clear, timely communication of results.

Regeneron is seeking a highly motivated and passionate Associate Scientist to join our Product Biochemistry team. In this exciting role, you will play a critical part in implementing innovative biophysical assessment strategies to support a wide range of drug candidate modalities.

Regeneron is seeking an Associate Scientist working in the field of Allergy to join a highly collaborative Immunology & Inflammation team. This individual will have the opportunity to support a broad pipeline by executing in vivo experiments in mice as well as in vitro assays. Candidate should prefer working in a team-driven environment, possess organizational skills and communicate openly and frequently with manager and team members.

The System Support Engineer – Level 1 provides frontline technical support for Talis Clinical’s software and hardware solutions. This role focuses on learning core systems, responding to customer issues during business hours, executing defined troubleshooting workflows, and developing foundational skills in medical device integration, QA testing, and database operations. Level 1 engineers work under close guidance and are expected to follow documented procedures while building the knowledge required to progress to more independent support responsibilities.

We are looking to fill a Scientist III – Potency Assay 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 is a laboratory-based role.

We are looking for a Scientist III – Liquid Chromatography – Mass Spectrometry (LC-MS) and Analytical Support 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 position does not offer any sponsorship. This is a laboratory-based role that maintains and operates open access LC-MS instrumentation and performs other tasks as assigned by the client.

We are looking to fill a Scientist 1 - Biologics Downstream Process Development 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 role does not offer sponsorship.

We are looking to fill a microbiologist position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients in West Point, PA. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer any sponsorship.

We are seeking a skilled Manufacturing Reliability Process Engineer to join our manufacturing team. Responsibilities include ensuring equipment reliability, implementing maintenance strategies, and driving continuous improvement initiatives for enhanced performance.

As a QC Technician within the Microbiology team is responsible for supporting microbiological testing and routine laboratory operations within a cGMP-regulated environment. This role ensures timely and compliant execution of testing, environmental monitoring, and general lab upkeep to maintain a state of inspection readiness.

The Analytical Chemist/ Process Development (PD) Chemist is responsible for developing and optimizing manufacturing processes in the Chemistry production area, meeting specific quality, schedule, and cost requirements, following all applicable safety and regulatory requirements.

The Scientist I QC is responsible to perform a large variety of routine and complex Quantitative and Qualitative procedures in the analysis of raw materials for cell culture media by various testing techniques including but not limited to FTIR, UV-Vis, purity and water determination by auto titrator, Polarimetry, GC and HPLC. Follow and adhere to GLPs, cGMPs, SOPs and all safety regulations as they apply to the laboratory and work areas. Subject matter expert for testing methodologies, providing technical expertise for raw material release decisions, and serving as a key point of contact for internal site teams and off-site testing partners.

Under direct supervision, this position may investigate, author, coordinate, and revise deviations, corrective and preventative actions, complaints, and other cGMP documents such as Master Production Batch Records. The Manufacturing Investigator I supports simple write-ups and the resolution of issues or risks related to Manufacturing. This role works with multiple departments, and may coordinate the review, revision, and approval of procedures and associated documentation.

The Scientist I position supports the efforts of the Process Development department within a fast-paced, expanding CDMO. This job will require extensive laboratory work, testing, and strategic client support of pharmaceutical development projects.

This position is responsible for supporting manufacturing at PCI Pharma Services. The Microbiology Associate I may focus on a specialized area and provide routine analysis and testing according to standard operating procedures in any of the following areas: in process and final product testing and microbiology assays including TOC, conductivity, bioburden, endotoxin, and growth promotion.

The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and that support continuous improvement in production. Project opportunities are designed to develop professional work knowledge and abilities and to support the efforts and projects that have global importance to the success of the business. Area of work involves manufacturing processes with interaction between production and cross-departmental engineering groups in resolving problems encountered on the production floor and across the business. Evaluates, selects, and applies exciting engineering techniques, procedures, and criteria, using judgment in developing and implementing adaptations and modifications on the production line and to quality systems.

As a Quality Engineer I, you will be charged with the quality behind Penumbra's game-changing medical devices used to address some of the world's toughest disease states! Unlike quality engineering roles in other companies, at Penumbra, we provide our quality engineers with highly technical problems to solve. Your efforts will directly impact the safety of patients around the world who use our products. You will apply your passion for creative problem solving throughout all stages of the process, from concept to commercialization and into continuous improvements.

Performance Validation is seeking a full-time Level 2 Validation Engineer/Specialist to join our team in Raleigh, NC The Level II Validation Engineer/Specialist reports directly to the Site Manager and will be assigned to one or more project teams headed by a Project Leader.

You will join a team of dedicated cell biologists to participate in the development and management of a best-in-class cell services program. You will have the opportunity to leverage and develop your skills in cell culture following industry best practices. You will liaise with scientists and support staff under the direction of the Technical Laboratory Services Leader to ensure that scientist projects are returned in a timely manner. Bring your experience working in a regulated environment to manage customer cell inventory. You will be a key partner for the Research and Development internal stakeholders.

The successful candidate will be able to work in a safe and efficient manner in accordance with current GLP’s, SOP’s, analytical methods, and work instructions. Excellent communication skills, attention to detail, and the ability to work both independently and as part of a team are desired. A thorough understanding of aseptic technique is essential. Microbiological testing is performed on raw materials, in-process samples, finished products, water samples, and environmental swab samples.

This role offers the opportunity to gain experience in a fast paced cutting edge clinical lab environment. The Sample Accessioner will work in a team environment which includes project managers and clinical lab ops specialists. As an Accessioner, daily tasks will involve patient specimen intake, accessioning and fulfilling client requests for returns or destructions. This will entail following SOPs and working with Laboratory Information Management System (LIMS) and other software. This role will also perform shipping / receiving, recording and inventorying of samples sent for laboratory testing.

The qualified candidate will join the Analytical R&D organization in Andover, MA, to enable development of biological therapeutics.  Within Analytical R&D the candidate will join the Characterization and Analytical Sciences – Andover Group focused on monoclonal antibodies/fusion proteins/synthetic peptides and other biological modalities.  This group develops analytical methodologies and strategies needed to progress biotherapeutic products in the pipeline; this includes method development, process support, formulation and stability support, product characterization and method qualification.  

The successful candidate will be part of a dynamic team of experts who form Pfizer’s Environment, Health, & Safety (EHS) division. Due to the importance of this team for Pfizer’s employees and patients, the organization relies heavily on its team members’ timely actions and efficiency. You will contribute to delivering excellence, ensuring that Pfizer's medicines reach those who need them most with greater efficiency and safety than ever before. This dedicated team is committed to maintaining superior safety protocols, enabling the swift and secure distribution of our products. By joining us, you become part of a forward-thinking group focused on excellence and innovation, driving the mission to provide safe and effective medicines to patients worldwide. As an EHS Senior Associate, your ability to meet team targets will help in completing important deliverables on time. Your innovative use of communication tools and techniques will make it easy to manage difficult issues and help in establishing consensus between teams. It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.

Moderna is seeking a Senior Research Associate to join the Protein Design team at its Cambridge, MA site. This role will primarily support protein expression screening and characterization for the Infectious Disease Research. The candidate will be responsible for utilizing mammalian cell culture techniques for protein expression, applying chromatographic methods for protein purification, and performing biophysical characterization of proteins to support the development of vaccines and therapeutics. Strong collaboration and problem-solving skills are essential, as the candidate will align on project goals and deliver high-quality results to drive the progress of multiple research programs. This is an exciting opportunity to contribute to cutting-edge vaccine and therapeutic development in a fast-paced and innovative environment.

Moog’s Military Aircraft Group is seeking an Associate Manufacturing Engineer for their team. This position offers a 2nd shift schedule and is located at our Aerospace plant in East Aurora, NY. As an Associate Manufacturing Engineer, with Moog Aircraft Group’s Electronics Operations Engineering Team, you will be assigned direct engineering responsibility for a variety of production programs. Work assignments require some originality and unreviewed action. You will receive program and technical guidance from the department supervisory personnel, project, senior product, or product engineers. This role supports the Mechanical and Industrial Process aspects found in Moog Military Aircraft Electronics A&T. Electronics manufacturing expertise is preferred. Candidates with experience that could be applied and motivated to work in a high-paced production environment will be considered.

Fueled by partnerships and increasing demand for internal R&D, we will be looking to you to develop and perform high-throughput and multiplex assays for evaluating antibody function. This will include: Designing and performing high-efficiency DNA library cloning and construction. Implementing high throughput cloning workflows. Executing yeast display selections coupled to MACS/FACS and NGS to characterize libraries of protein and antibody variants. Optimizing therapeutic candidates in lead programs to have desired affinity and developability properties. Working together with our dry-lab and other wet-lab scientists to establish a rapid and seamless production and testing pipeline for characterizing machine learning generated antibody designs

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. Maintain all test equipment and supplies for various testing. 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. Monitor raw materials and final finished media for conformance with applicable material specifications and SOPs. 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 as applicable and in accordance with criteria outlined in Standard Operating Procedures. May be required to operate specified laboratory equipment as applicable. Maintains an efficient workflow process relative to sample prioritization. Other duties as assigned.

nanoComposix, a wholly owned subsidiary of Fortis, develops innovative nanomaterials for research and commercial markets. We manufacture hundreds of different variants of metal and metal-oxide core/shell nanocomposites for a wide range of applications including biosensors, medical devices, clinical diagnostics, and optical effects. Our mission is to help our clients bring nano-enabled products to market. We are currently seeking a Manufacturing Lab Associate II (Production Chemist) for a full-time, onsite position in San Diego, CA.

The Assoicate CQV Engineer is responsible for the service and support of laboratory equipment and instrumentation utilized in the Operations laboratory. The scope of support includes installation, calibration, maintenance, and repair of both simple (e.g., plate sealers) and complex (e.g., liquid handling robotics) instrumentation in the laboratory. The Instrument Service Engineer will be the primary point of contact for production lab personnel when equipment and instruments are not operating or not meeting operational specifications. This is a contract position for three months.

We are seeking a highly motivated and skilled Research Associate I to join our dynamic team in the sample management. In this role, you will be responsible for the management of biological samples, ensuring their integrity, overseeing quality control, and supporting research projects that rely on biological specimens. The ideal candidate will have a strong background in bio sample management, research methodologies, and data analysis, with an interest in contributing to cutting-edge scientific research.

The Global Specimen Specialist I supports Pharma projects by performing foundational Project Support tasks under direct supervision. Responsibilities include receiving and accessioning specimens, preparing samples for laboratory testing, and assisting with sample data management, including the completion of quality control checks as trained. This role supports the preparation of reports, data transfers, sample shipping, and the archiving of samples and documentation in accordance with established procedures. The Administrator I follows defined processes, maintains accurate records, and develops proficiency in laboratory systems and workflows while contributing to the timely and accurate execution of Project Support activities.

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.

This position will be responsible for ensuring the efficient design, optimization, and maintenance of manufacturing systems and processes to meet quality, safety, and regulatory standards. This role plays a key part in driving continuous improvement in production operations, working closely with cross-functional teams to enhance production efficiency, reduce costs, and maintain product quality.

As a Quality Systems Engineer (dedicated towards Design Controls), 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.

As a Software 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 Research Scientist I is responsible for meeting the analytical testing requirements to support research and development projects primarily focused on oligonucleotides.

Reporting directly to the Automation Supervisor or the Lead Automation Engineer. The Automation Engineer will be primarily engaged in the development, implementation, modification, and validation activities of the plant vision, control, motive, and communications systems.

We are seeking a Quality Engineer I – Disposables to support the Quality Management System (QMS) and ensure the quality and compliance of electronic components and medical devices throughout their lifecycle. This role provides hands-on support for manufacturing, investigations, and quality processes while developing foundational skills in validation, risk management, and problem-solving. The QE I works closely with cross-functional teams including Manufacturing, Engineering, R&D, Regulatory, and Supply Chain to support product quality and continuous improvement initiatives in a regulated environment.

This role will be in support of Robotics & Automation’s Optical Encoder Product Line. As a Quality Engineer, you'll ensure product quality and reliability. The ideal candidate will have some quality experience in mechatronic and electronic systems. The Quality Engineer will have a strong customer focus and have the desire to drive quality investigations and improvements, and to be a major contributor to new product development programs. They will be self-starting, with a strong desire to succeed, collaborate and grow with others in the organization. The candidate will demonstrate passion and rigor needed to develop/deliver a product to market and sustain released products. Key responsibility for the overall management of incoming, in-process and final inspection, along with RMA activities and projects and support Supplier Quality activities as well. This individual will be responsible for processing and analyzing incoming RMAs from the field and drive the process through to customer closure. The Quality Engineer will have a strong customer focus and have the desire to drive quality investigations and improvements, and to be a contributor to new product development programs.

The Quality Control (QC) Analyst I, Raw Materials is responsible for performing routine and non-routine testing of raw materials to ensure compliance with internal specifications, regulatory requirements, and industry standards. This role involves analytical testing, documentation, and collaboration with cross-functional teams to support manufacturing and supply chain operations.

The Specialist, Quality Assurance position is a key role in meeting the quality policy through their management of the different quality systems, including production records and deviation system management. The ideal candidate will be responsible for managing the quality systems, including deviations, change control, corrective and preventive actions (CAPA), and document management. Additionally, this role involves making timely batch disposition decisions to ensure quality standards are met before product release, supporting the rapid processing times required by our product. You will have the unique opportunity to make a difference in the lives of many patients as Orca Bio develops next-generation cell therapies.

As a Design Engineer on our Product Development Team, you'll collaborate with other engineers and work cross-functionally with our Marketing, Regulatory, Manufacturing, and Quality teams to create and modify designs for spine implants and surgical instruments. This is a great way for you to leverage your engineering degree to gain experience in design feasibility, testing, engineering analysis, design control documentation, and design for manufacturing. You’ll have the opportunity to tackle projects where you can provide solutions to a variety of technical problems related to complex spine products that ultimately impact patients’ lives.

Join us as a Scientist 2 in our Metals department and put your passion for science to work in our environmental testing laboratory. In this role, you’ll conduct hands-on analysis within our laboratories, helping ensure the integrity and quality of environmental data that impacts communities and ecosystems.

The Microbiologist I will perform routine microbiological testing and environmental monitoring in support of sterile and oral solid dosage manufacturing. This role ensures testing is performed in compliance with cGMP and data integrity principles to maintain product quality and contamination control. The ideal candidate will have foundational microbiology knowledge, strong attention to detail, and the ability to apply aseptic techniques in both laboratory and cleanroom environments.

This a role that supports both engineering project execution and the engineering group operations related to financial reporting and document management. This position will use the current set of capital reporting tools to establish capital project accounts, publish financial status reports for capital projects in progress, and assist management in procurement and invoice/cashflow tracking and reporting. This position will execute small projects as directed by other project engineers or by the department manager. This position will support the creation, revision, issuance, and archival of controlled documents (i.e. specifications, drawings, turnover packages) both for engineering department records and if required for quality/compliance records. This position is based in Massachusetts and requires a presence on-site, and open to applicants authorized to work for any employer within the United States.

We are seeking a motivated and detail-oriented Associate Engineer to join our high-throughput Research Operations team. In this role, you will focus on hands on materials synthesis of various powders and porous medias as well as characterization of materials using spectroscopy and microscopy techniques. You will gain hands-on experience with state-of-the-art automation technologies while contributing directly to projects that drive our company’s growth. This is an excellent opportunity for candidates excited to learn engineering principles, work with advanced laboratory automation, and develop a strong foundation in scientific operations in a dynamic, shift-based environment.

Lila is seeking a dedicated and skilled Research Associate, Protein Sciences to join our high through-put Cell-Free Expression platform. As a Research Associate, you will play a vital role in our interdisciplinary research efforts focused on building and automating artificial intelligence-driven processes across a variety of valuable applications.

The Associate Scientist, Quality Control is an entry-level, hands-on laboratory role responsible for performing analytical testing in support of in-process, and product release. This position operates within a cGMP-regulated Quality Control laboratory and plays a critical role in ensuring data integrity, compliance, and timely product disposition. The Associate Scientist works closely with senior QC staff, Quality Assurance, Manufacturing, and other cross-functional teams to ensure laboratory activities meet internal quality standards, regulatory requirements, and established procedures.

The Associate Scientist, QC Raw Materials is an entry-level, hands-on laboratory role responsible for performing analytical testing to support raw material release in a cGMP-regulated Quality Control laboratory. This role is responsible for executing testing in accordance with approved methods, ensuring data integrity, and supporting timely and compliant material disposition. The position requires strong attention to detail, adherence to procedures, and the ability to work in a fast-paced, team-oriented environment.

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.

As a Mechanical Engineer - Design, you will help bring a future generation of LSI products to market. You will be part of a team to further improve our current products that are already available by iterating on the innovative design. Working in a cross functional team, you will take ownership of all things related to the form, fit, function, and feel of the product. Other tasks include, stack up analysis, failure analysis, improvements for manufacturability, communicating design intent and inspection requirements with 3D and 2D CAD, and other tasks.

Perform hands-on laboratory assays using automated liquid handling workflows to support sample analysis, method development, and validation. Generate high-quality data and documentation that meet turnaround time expectations and regulatory and corporate requirements.

The Part-Time Clinical Trial Assistant (CTA) provides administrative and operational support to Lumicell’s Clinical Affairs organization. This role supports regulated clinical documentation, clinical systems administration, and cross-functional coordination across Clinical Affairs, Clinical Operations, Regulatory Affairs, Quality Assurance and Medical Affairs. We are looking for a self-starting and collaborative team member to support multiple aspects of a post-market and investigational drug/device combination product.

We’re looking for a Controls Engineer I to join our Pennsauken, NJ team. In this role, you’ll be at the heart of designing and implementing servo motion controllers, automation systems, and other critical components for our specialized machinery. From programming and prototyping to testing and customer collaboration, you’ll help bring high-performance systems to life that exceed client expectations.

We are seeking a committed professional to join our team, required to reside within the territory and drive to multiple accounts throughout the region. A valid driver's license is essential for this role, which also involves ~25% amount of travel outside the territory, presenting opportunities for broader engagement. As an AiBLE Clinic Engineer I, you will deliver clinical, technical, and sales support to surgeons, hospital staff, and sales representatives, helping design patient-specific implants and drive post-operative data analytics. This role offers a unique opportunity to serve as a key technical liaison between Medtronic and the medical community. You will operate in a highly collaborative environment and handle sensitive information with professionalism, discretion, and sound judgment.

Manage global registration and TOI activities including shipping coordination, planning, and scheduling of shipments. Follow up with customers after shipments to confirm shipping conditions and to resolve temperature excursions. Manage internal and global analytical method transfer activities including shipping coordination. Collaborate with commercial manufacturing teams to support facility start-up activities and provide analytical support both within the company's network and at contract manufacturing organizations (CMOs) or contract testing laboratories (CTLs). Lead assignment execution against accelerated, critical-path timelines in a right-first-time manner. Author and/or review technical documents to support analytical issues. Support GFLS teams from a shipping and logistics perspective. Support various vaccine and biologics registrations, launches, and troubleshooting activities external to the US, including documentation preparation and coordinate supply of critical reagent shipments.

The Nonclinical Drug Safety (NDS) group at the West Point, PA site is seeking a highly motivated individual with strong technical and communication skills and attention to detail to join the Central Pharmacy laboratory within the Toxicological Sciences group. Central Pharmacy is responsible for the preparation of vehicle and test article dosing formulations to support Good Laboratory Practices (GLP)-compliant and exploratory nonclinical studies. Additional study support activities include maintaining documentation in an electronic document management system, coordinating collection of samples of dosing formulations for analysis, authoring the test and control article information section of study reports, and receiving and shipping materials to support internal and Contract Research Organization studies. Scientists also maintain the pharmacy’s test and control article, chemical, GLP reserve sample, and controlled substance inventories.

The Quality Control Associate provides support to the Bioanalytical Laboratory (BAL) staff for sample testing studies, including those performed under applicable elements of Good Laboratory Practices (GLP) and/or Good Clinical Laboratory Practices (GCLP), under direct supervision. This includes, but is not limited to, performing Quality Control review of study data and all laboratory and study-related documentation for accuracy and adherence to applicable plans, protocols, and policies.

As a member of the Biotechnology Quality Control team at our Ewing facility, you will support our Life Science business unit. You will be responsible for testing bulk produced and final packaged products to ensure that they meet our high-quality standards. Daily activities will be centered around testing raw materials and products using a wide variety of analytical techniques including PCR / molecular biology techniques, biochemical analysis, immunoassays, cell culture and testing, microbiology methods. This is primarily a lab-based role, but you will also support routine quality management and process improvement projects within the quality organization. You will train on and independently perform a variety of analytical testing methods and general lab support activities.

An exciting new opportunity has arisen to join our company as Formulation & Packaging Tech (m/f) Life Science.The Formulation & Packaging Tech’s primary function is to coordinate and prioritize assigned production activities through review of the weekly production schedule and to liaise with the Manager, other Team Leads and Project Coordinator as necessary to optimize productivity and target smooth lab operation.

In the Analytical Scientist role, you’ll be working in the Contract Testing, Development, and Manufacturing Organization (CTDMO) within the Life Sciences group of MilliporeSigma in St. Louis, MO, and will serve as an individual contributor in the Process and Analytical Development organization.  You will be working in a lab setting on analytical method development and optimization for external customers in the field of Antibody Drug Conjugates (ADC).  The role will include problem solving, working within project timelines, and contributing to documentation for method qualification and transfer into GMP manufacturing and quality control organizations.

The Quality Control Analytical Associate I serves as a support role in clinical and commercial production. The QC Analytical Associate I will assist with process check point, stability, and release analytical testing to ensure that quality standards are upheld for all products produced at the facility.

As Systems Engineer you will be part of a small, agile team; responsible for medical device development projects starting from technology exploration, product definition, to guiding integration with software controlled electromechanical systems; ending with product and release testing. We develop a broad spectrum of products from sterile disposables to complex capital equipment using a customer-centric, collaborative, innovation driven approach. We value ownership, calculated risk-taking, and tolerance for ambiguity as we build future devices and improve existing products.

The Manufacturing Engineer, Electrical provides daily support of the manufacturing assembly operation for all hardware products and certain disposable test processes. With minimal supervisory oversight, this highly collaborative role will continuously develop, maintain and improve the manufacturing and test processes aimed at driving efficiency and quality. This position is responsible for complying with the Quality System requirements and carrying out responsibilities outlined in the environmental, health, and safety policies.

INCOG BioPharma is seeking a highly motivated individual with subject matter expert (SME) capabilities in sterile pharmaceutical manufacturing process controls and industrial automation. The Equipment Specialist is a key technical role within INCOG BioPharma Operations. This candidate must have experience in pharmaceuticals and/or biologics, GMP manufacturing, or within highly regulated industries.

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.

The primary purpose of this job is to perform non-routine assignments of substantial variety and complexity. Develops, designs, installs and maintains new processes, tests and/or control systems. Conduct research or development projects associated with the design and the development of new products or models. Investigates and resolved technical problews involving product performance. Coordinates development and design problems to find create soultions with products not released to the manufacturing side. Follows up on the building of design and life test models, analyzing the test results. Follows through on laboratory and field tests and develops new ideas based on results

Integral Molecular is a close-knit, medium-sized biotech company focused on developing and applying innovative technologies that advance vaccines and antibody therapeutics targeting difficult proteins. Over the past year, we implemented and optimized an electronic Quality Management System to streamline the maintenance of our products and services at a consistent, high-quality standard. We are actively seeking a Quality Assurance Associate to own our Quality Management System (QMS), ensure compliance, drive data-informed improvements, and keep the company aligned with ISO 9001 standards. If you thrive in a detail-oriented, cross-functional environment and are energized by making strong quality systems even better, we encourage you to apply.

The Process Engineer I is responsible for supporting the development, execution, and documentation of processes and experimental workflows for an oligonucleotide synthesis platform and supporting process equipment. This position reports to the Senior Manager of Emerging Technologies and is part of Emerging Technologies, Platform Development group located in Sunnyvale, CA and will be a full-time, on-site role.

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. The Engineer I role is responsible for day-to-day production support, developing, maintaining and improving production processes. This role will be responsible for supporting and optimizing injection molding processes for plastic components used in manufacturing operations. This role ensures high-quality production, cost efficiency, and compliance with industry standards while driving continuous improvement initiatives.

Iovance Biotherapeutics is an immuno-oncology company focused on the development and commercialization of novel cancer immunotherapies based on tumor infiltrating lymphocytes (TIL). The Aseptic Manufacturing Technician I, role is crucial for the autologous cell therapy manufacturing program. This position requires a broad understanding of theories, techniques, and principles to support manufacturing processes. As an Aseptic Manufacturing Technician I, you will primarily be responsible for the following tasks: suite preparation for cell processing, material transfer, environmental monitoring, BSC runner duties, final product inspection, and final product cryopreservation in controlled rate freezers, for commercial and clinical use. This position works across different shifts. Depending on your assigned shift, you may be required to work overtime, weekends, and holidays to ensure the manufacturing process is completed. As this person will be a key member of the autologous cell therapy manufacturing program, a background in cell culture, aseptic gowning and qualifications, as well as ISO class 5 (Grade A) cleanroom operations is strongly desired.

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Conduct qualitative and quantitative lab procedures under minimal supervision, following safety and GLP protocols Prepare samples for analysis and accurately document experimental workflows. Operate and maintain laboratory instruments; assist with troubleshooting technical issues. Analyze results and report findings to contribute to project meetings and deliverables. Ensure consistent compliance with SOPs and customer requirements. Collaborate with researchers and technical teams to meet performance objectives. Contribute to continuous improvement of lab practices and data integrity. Support additional duties as assigned in a fast-paced laboratory setting

Ensure compliance with all federal, state, and local regulations concerning all environmental rules, protocols, regulations and appropriate guidelines. Create ways to keep workers and the general public safe from harm and design safe workspaces. Ensure that proper personal protective equipment [PPE] is available to all employees for all operations Maintain recordkeeping and tracking of all safety metrics and incidents. Develop, implement, and manage safety programs & corporate safety programs (not limited to): Lockout/tagout, Fall Protection, Electrical Safety, Fire Prevention, Laser and Radiation Safety, Emergency Action Plan, Lab Safety and Hazard Communication, Respiratory Protection Machine Shop Safety, etc. Support environmental reporting and permitting requirements: SPCC, Tier II reporting, Triennial Reporting, Oil Spill Prevention Plan, Flammable Storage Permit, etc. Oversee and surveille Hazardous Waste Management Plan. Ensure regulatory agency compliance i.e. labeling, containment, proper disposal, employee training, and documentation, universal waste program. Support occupational health programs. Respond to emergency situations, coordinating with emergency responders. Instill a proactive safety culture by implementing behavioral based safety initiatives including determining risks, potential hazards and development of mitigation controls. Develop, prepare, and deliver classroom instructions and "hands on" training (online and virtual training development). Investigate all incidents and injuries to identify root causes and implement corrective actions. Support contractor safety program and safe work permitting. Support industrial hygiene programs and conduct sampling as necessary for chemical and noise hazards. Provide Field Team safety guidance such as radiation safety, respiratory protection program, training, etc., while being the point of contact for field inquiries

We are searching for the best talent for a R&D Engineer 2 to support our Electrophysiology business. This role will work onsite in our Irvine, CA office. A Level 2 Mechanical/Mechatronics Engineer contributes to the design, development, verification, and transfer-to-manufacturing of electrophysiology (EP) and ultrasound catheter products. The role works on cross-functional project teams to deliver safe, reliable, and manufacturable catheter shafts, steerable mechanisms, electromechanical subsystems, and miniaturized ultrasound transducer assemblies used in EP or Structural Heart procedures.

Supports the processes involved in releasing finished goods to distribution. Performs testing on finished products ensuring conformance to company requirements. Performs analysis for special test requests to provide continuous improvement in the areas of quality, technology and processes. These tests include utilizing analytical instrumentation such as HPLC, GC, UV-Vis and refractometer. Ability to distinguish color variation required Adheres to environmental policy and procedures and supports department environmental objectives. Ability to pay special attention to detail with degree of accuracy. Excellent interpersonal, organizational and communication skills. Must be familiar with GMP, GLP, SOP and ISO. Requires some initiative and judgment. Actions checked periodically.

The Sr. Site Transfer Manufacturing Engineer leads and executes product and process transfers between manufacturing sites (domestic and international), ensuring successful, compliant, and timely ramp of on-market products. This role is the primary technical lead for multi-site transfers, coordinating cross‑functional teams (R&D, QE, Regulatory, Supply Chain, Production, and External Partners) to deliver validated, robust manufacturing processes at the receiving site.

As a Reagent Manufacturing Associate I, you will support the production of critical reagents used in Karius’ NGS-based infectious disease diagnostic assays. This role is hands-on and process-focused, with responsibility for manufacturing and qualifying reagents, supporting RUO and IVD product workflows, performing quality testing, and maintaining accurate documentation in an ISO 13485-compliant environment. You will work closely with scientific and operational teams to support equipment readiness, material management, troubleshooting, validation activities, and continuous process improvement. The ideal candidate is detail-oriented, reliable, and comfortable working with chemical and biological materials in a fast-paced manufacturing setting where quality, consistency, and patient impact are central to the work.

The Manufacturing Associate I/II - Nights 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 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.

Are you detail-oriented and passionate about quality and compliance? Join our team as a Quality Assurance Specialist and help ensure the safety and integrity of life-saving plasma products. In this role, you’ll be a key player in upholding regulatory standards and supporting continuous improvement across the center’s operations. As a Quality Assurance Specialist, you’ll work closely with the Quality Assurance Manager and center leadership to monitor compliance, review documentation, and support training and audit readiness. Your work will directly impact donor safety and product quality.

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.

The Accessioning Technologist III performs critical sample receipt and data entry functions in FMI’s CLIA-certified clinical laboratory. Specifically, the Accessioning Technologist receives all incoming samples and ensures that necessary information has been received to move forward with processing. This role is involved in both independent and collaborative work that includes the use of account or patient demographic data entry.

Responsible for representing the sites quality initiatives and compliance objectives in the development of methods, procedures, validations and quality planning for the facility.

The ideal candidate will have experience in handling biological samples, chemicals, sample logistics and sample tracking, experience in regulated environments (GLP, SOPs, etc..), and strong written and oral communication skills.

Frontage Laboratories Inc. is hiring Manufacturing Associate. The Manufacturing Associate will support GMP manufacturing operations, perform hands‑on production activities, assist in facility and equipment setup, and ensure compliance with cGMP standards. Responsibilities include executing GMP manufacturing of drug products, documenting activities, maintaining equipment cleanliness, and supporting raw material handling.

The Imaging Specialist is responsible for performing Quality Control functions on all cases and taking digital microphotographs on designated cases for final pathology report. The Imaging Specialist will follow the direction of the supervisor while taking initiative in performing and promoting quality and efficiency within the department. The Imaging Specialist will be trained in the expected task in order to meet the competency set by the department.

Generate Biomedicines is seeking a Research Associate II/Senior Research Associate to join our CryoEM Group in generating large-scale protein structural datasets. This role offers the opportunity to work at the intersection of protein biochemistry and cutting-edge structural biology, contributing to our mission of accelerating drug discovery through advanced imaging technologies.

GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. Genscript is seeking Senior Lab Technicians for our Production team in Piscataway, NJ.

Small Molecule Formulation and Process Development (FPD) provide formulation, process, and manufacturing support and technical expertise throughout research and development, from pre-exploratory to commercialization. A Sr. Research Associate within FPD may support teams conducting compounding screening to enable drug candidate selection, drug substance physio/chemical property assessment and form selection, development of clinical formulations and manufacturing processes, small molecule drug product manufacturing tech transfer and scale-up at internal and external sites, oversight of small molecule drug product manufacturing, and establishment a robust DP formulation and optimized manufacturing process to enable commercial production. FPD formulation scientists develop the small molecule formulation and manufacturing process control strategies and authors technical reports, risk assessments, and regulatory filings from IND to NDA. FPD supports DP manufacturing process validation and provides technical expertise throughout post-approval commercial manufacturing and life-cycle management.

Conduct GMP testing for release, stability, and method transfer for clinical drug substances and products. Conduct GMP testing for raw materials, raw material intermediates, in-process control, and cleaning samples in support of pilot plant manufacturing. Analyze samples using various analytical techniques such as Ultra-Performance Liquid Chromatography/High-Performance Liquid Chromatography (UPLC/HPLC), Gas Chromatography, Ion Chromatography, Dissolution, Karl Fischer, Differential Scanning Calorimetry, Particle Size Distribution, X-Ray Powder Diffraction, UV-Vis spectroscopy, etc. Perform verification and data review to ensure compliance to appropriate Standard Operating Procedures (SOPs), test methods, specifications, and protocols. Perform stability data trending, conduct laboratory investigations for suspect results, and troubleshoot instruments and test methods. Author/Review laboratory investigation records (issues and investigations), deviations, and Corrective and Preventive Action (CAPA). Provide on-the-job training of analytical techniques or other Good Manufacturing Practice (GMP) training to new hires or junior staff. Write/Revise protocols, methods, SOPs, reports, etc. Participate in laboratory housekeeping activities and report any concerns to a laboratory lead and/or manager. Lead projects and support cross-functional activities (e.g., instrument/system upgrade activities, method validation, etc.). Serve as a Subject Matter Expert in analytical techniques or processes, participate in working groups, assess pharmacopeial changes, and support internal audits and regulatory inspections, as appropriate

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.

The Equipment Engineer I will be responsible for supporting the development and documentation of return-to-service procedures following maintenance, repairs, or major modifications to advanced laboratory equipment, all in alignment with applicable regulatory requirements.The supported equipment spans a broad range, including next-generation sequencing (NGS) platforms and automated liquid handling systems. The engineer will work closely with Engineering Operations, Process Engineering, Automation Engineering and Quality Assurance. Success in this position requires strong interpersonal skills, effective technical writing, and exceptional troubleshooting abilities.

Provides quality support to both internal and external projects, including the on-boarding of new clients / client projects, capital expenditures (CAPEX), continuous improvement initiatives, and as required in routine manufacturing and finishing operations. This position works closely with Project Managers, Filling and Finishing Operations, Quality Assurance Operations, Analytical Technical Services, Manufacturing Science & Technology, Validation, and QC Analytical and Microbiology departments. This is not a remote role.

Hologic is seeking a Senior Quality Systems Specialist to strengthen and sustain our Quality Management System (QMS) and quality operations. In this role, you’ll work across engineering, supply chain, regulatory, marketing, and other functions to investigate process, product, and system issues, support audits and inspections, and help develop and refine quality procedures. You’ll use data-driven tools to analyze trends, support continuous improvement, and ensure our systems are audit-ready. If you enjoy solving diverse quality challenges, partnering cross-functionally, and owning impactful quality system initiatives in a regulated environment, this role is a strong fit.

Join Hologic as a Quality Engineer in a regulated medical device environment, responsible for ensuring products, processes and systems meet internal quality requirements and external regulatory standards (e.g., FDA, ISO). The position supports Operations, Engineering and R&D, focusing on defect prevention, continuous improvement, and robust manufacturing practices.

Hologic is seeking a Systems Engineer to join our Research and Development team in Newark, Delaware. In this role, you will contribute to the development of advanced medical imaging systems and electromechanical subsystems that help improve clinical outcomes. This position requires regular onsite presence in Newark, DE to collaborate closely with cross‑functional engineering teams and support hands‑on system integration, testing, and troubleshooting. You will work alongside electrical, mechanical, and software engineers, scientists, and product owners to support the design, integration, verification, and validation of medical imaging technologies.

As a Systems Design Engineer at HighRes Biosolutions, you will be heavily involved with all elements of our custom systems product life cycle. You’ll work closely with the sales and applications team to turn a customer’s needs into an automated solution. Additionally, you’ll work closely with the operations team to turn your designs into fully functional systems. The systems you design will be used by top pharmaceutical and biotech companies around the world to help improve human health. The qualified candidate will have strong design capabilities with SolidWorks. A product development background for lab, medical or consumer products is beneficial.

Highridge Medical creates the world’s most innovative spinal solutions across the spectrum from Motion Preservation to MIS to Bone Healing to Core Spine. Working at Highridge Medical is not just work. Life at Highridge Medical is purpose driven. Every day, you have the privilege of using your talents to demonstrate Confidence in your work and restore Confidence for our patients. Confidence that moves. The Post Market Surveillance Quality Engineer ensures post market surveillance activities including, complaint processing, health authority reporting and post-production performance reports are completed in a timely and compliant manner. Coordinates quality planning, identifies and solves product and process problems and supports various operational groups.

This position is responsible for manufacturing and product Quality activities. This role is within Mfg/Ops Quality organization and is accountable for supporting day to day sustaining activities in a manufacturing environment. The position requires exceptional communication, interpersonal, and project management skills to effectively coordinate activities and deliver results. This position will have direct interaction with Manufacturing and Process Engineering groups to support manufacturing sustaining activities, continuous improvement, and manufacturing capacity expansion. The position may also have quality oversight for more than one manufacturing area. The position will be responsible to support change management activities, Nonconformances, equipment lifecycle, meeting facilitation and other ad hoc sustaining manufacturing requests.

Set up and maintain electrical engineering laboratory equipment, including but not limited to oscilloscopes, power supplies, signal generators, and measurement instruments. Collaborate with engineers and researchers to design and assemble experimental setups for various projects. Conduct tests, experiments, and measurements under the supervision of senior engineers. Troubleshoot and repair printed circuit cards assemblies. Assemble prototype hardware and cable harnesses to engineering specifications. Manage the calibration and verify the accuracy of test equipment to maintain high-quality standards. Assist in the development and improvement of laboratory procedures and protocols. Provide technical support to engineering staff and researchers as needed. Writing technical documents such as rework and test procedures and reports. Stay updated on industry trends, advancements, and emerging technologies in electrical engineering.

Our Quality team has an immediate opening at our flagship Buena, NJ plant for a Quality Engineer who is ready to take their career to the next level. As a Quality Engineer at Comar you will be a critical member of the team bringing new products to market, continuously improving our processes, and ensuring the highest quality standards are met in support of our customers and the patient or end user of our products. Are you an Engineer looking to make a difference with a company that values teamwork, innovation, and professional growth? One of our Core Values is “Work Together, Win Together.” Come work and win with us today!

The Manufacturing Engineer I at CooperSurgical is responsible for driving manufacturing excellence and optimizing production processes for our medical device and fertility products. The Manufacturing Engineer I plays a critical role in implementing lean principles, improving process efficiency, and fostering a culture of continuous improvement.

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 Quality Assurance (QA) Specialist II is responsible for maintaining Quality databases and providing an on-the-floor QA presence and oversight to operations. This role includes identifying compliance risks in the operation prior to and during execution, avoiding deviation whenever possible as well as managing immediate corrective action. The QA Specialist II primarily works in the cGMP areas to manage adherence to the quality system and assist in and/or initiate the resolution of deviations.

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 Quality Assurance (QA) Specialist II is responsible for maintaining Quality databases and providing an on-the-floor QA presence and oversight to operations. This role includes identifying compliance risks in the operation prior to and during execution, avoiding deviation whenever possible as well as managing immediate corrective action. The QA Specialist II primarily works in the cGMP areas to manage adherence to the quality system and assist in and/or initiate the resolution of deviations.

The QC Lab Technician is responsible for conducting routine and non-routine analysis of raw materials, in-process, and finished goods, creating and maintaining databases to ensure consistent quality metrics and maintaining the QA laboratory. This position reports to the QA Manager and is part of the Quality Assurance Department located in Pensacola, FL and will be an on-site role.

The QC Batch Review Technician is responsible for timely, accurate and compliant review of raw material, intermediate and finished good records to ensure compliance with ISO 9001 and Cytiva QMS standards. Supports timely product release by resolving documentation issues and coordinating with Production & Supply chain to drive cross-functional cooperation and improvements. Collects raw material samples, performs basic product testing and supports compliance audits at GEMBA. This position reports to the Quality Value Stream Manager and is part of the Quality Department located in Pensacola, FL and will be an on-site role.

We are seeking a Packaging Medical Device Engineer II to join our innovative team. The ideal candidate will have experience in designing and developing systems that ensure the robust hermetic sealing and/or sterility, safety, and integrity of high volume packaging products medical devices. This role requires an understanding of a complete medical device packaging system that includes the hermetic seal and/or sterile barrier and sub-level systems, such as the protective packaging to maintain the safety and integrity of our cutting-edge medical device products while ensuring regulatory compliance. This role requires an understanding of the interaction of sub-level primary, secondary, and tertiary packaging systems to ensure that the full system remains hermetically sealed/sterile and intact until it reaches the end user, while also meeting regulatory requirements and industry standards. If you are passionate about creating solutions that enhance patient safety and product performance, we invite you to apply and contribute to our mission of empowering people to take control of their health management.

This Quality Engineer will support, perform, and/or complete assigned complaint investigations that include (but are not limited to) product failure analysis and complaint documentation review (device history record, complaint history, products instructions, risk management, etc.), and prepare technical investigation reports.

Element has an upcoming opportunity for an Analytical Chemist (Environmental Testing) to join our growing team in Fort Wayne, IN. The Analytical Chemist (Environmental Testing) prepares and analyzes environmental and drinking water samples using standard analytical techniques according to approved scientific and EPA methodologies in compliance with Element Materials Technology quality assurance programs and standard operating procedures (SOPs). This position can be a physical job that may require standing for long periods, working with organic solvents, laboratory glassware and specialized equipment.

Eli Lilly and Company seeks a Chemist (R2-R4) to perform compound synthesis, purification, and characterization under the direction of senior scientific staff. Design new molecules to address hypotheses and issues in portfolio projects. Design and implement multi-step synthetic routes towards targeted compounds. Independently set up and complete a variety of organic chemistry reactions, including those with air sensitive and hygroscopic reagents. Perform routine purification of synthetic intermediates and final products and characterize reactions products. Rigorously document laboratory experimentation and employ safe laboratory practices. Actively contribute to a multi-disciplinary drug discovery research team in a fast-paced lab environment. Integrate emerging analytical chemistry, computational design technologies, automation chemistry, and biophysical methods into drug discovery.

The Process Engineer provides technical assessment and support for production operations in the areas of developing and sustaining process knowledge, process and equipment support, process optimization, equipment capability and asset management, and engineering business systems. This role is to serve as a process engineer supporting drug substance active pharmaceutical ingredient (API) manufacturing for biologics, oligonucleotide, peptide, and bioconjugate purification.

The Manufacturing Scientist provides the technical support required to achieve the reliable and compliant manufacture of the Active Pharmaceutical Ingredient External Manufacturing (API EM) portfolio which includes raw materials, intermediates, enzymes and bulk drug substances. The API EM Manufacturing Scientist executes technical projects (experimental, modeling and/or production data analysis) to improve and optimize process control, yield, purity, and/or productivity. In addition, the manufacturing scientist should be capable and technically independent in setting up and executing a variety of experiments at the laboratory scale and conduct research on manufactured product for process improvements and troubleshooting in the technical services and manufacturing sciences laboratory.

The Regulatory Affairs Specialist is responsible for the development and implementation of the regulatory strategy (as applied to new product development projects, process, and/or product) and partners with internal stakeholders to align on an optimized regulatory strategy to achieve business objectives.

Performing physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products (tablets, capsules, parenterals, devices, liquids, creams, and gels) and animal health products. Preparing standards and samples for analysis; running the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, HPLC, and dissolution apparatus. Executing method transfer protocols. Performing monthly maintenance of laboratory equipment. Working efficiently, documenting work clearly, and performing tests accurately. Ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations. Reads and understands analytical procedures (compendial and client supplied) and internal SOPs. Processes data, generates reports, and evaluates data. Trains others in laboratory procedures. Performs laboratory maintenance. Communicates with vendors and repair personnel. Writes investigations. Leads project/test areas and perform method transfers/feasibility studies. Preparing standards and samples for analysis; running the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, HPLC, and dissolution apparatus.

The Formulation Scientist will support the Client Sterile and Specialty Products team at the Rahway site. This role is primarily project-based and focused on sterile product development. Responsibilities include formulation composition and process development support, as well as the design, preparation, testing, and documentation of formulations and processes.

Performs work in a laboratory setting, meeting the physical job requirements of a lab role. Prepares and manages inventory of buffers, reagents, media, semi-finished and finished goods. Maintain and culture multiple cell lines, ensuring consistency, sterility, and experimental reproducibility in a BSL2 environment. Execute and optimize cell-based assays to support drug discovery programs in ADMETox, BioMAP® Services, Ion Channel Services, BioMarker Services, OncoPanelTM Services and/or BioTherapeutics. Identify opportunities to improve workflows, efficiency, or data quality. Perform compound dosing, serial dilutions, and plate-based assay workflows. Understands and complies with requirements for work performed at a GxP site. Completes required training and supports 100% of Employee Health and Safety requirements. Demonstrates proficiency with, care and maintenance of lab equipment and department assets. Conducts responsible use of confidential IT and business systems, as required. Adheres to department SOPs and documentation requirements, maintains accurate data management and reporting records. Troubleshoot assay variability and identify root causes of inconsistent results. Contribute to improving assay robustness, scalability, and throughput. Record, organize, and analyze experimental data using tools such as Microsoft Excel and GraphPad Prism. Perform basic statistical analysis and generate graphs (e.g., dose-response curves, bar charts) to support data interpretation. Perform routine laboratory calculations, including molarity, dilutions, and concentration conversions. Use Microsoft Office (Excel, Word, PowerPoint) to organize and analyze data, generate reports and visualizations, and effectively communicate experimental results. Work cross-functionally with biology, chemistry, and project management teams. Supports unit goals and demonstrates Eurofins’ competencies, as defined in the job plan. Provides training to colleagues and external end users, when required. Stay current on advancements in scientific technologies and drug discovery trends. Works effectively in a team environment, under minimum direction, to achieve business production, project timelines, and quality objectives. Adjusts work hours and provides cross-functional support to other departments, as required, and maintains accountability in delivering to client needs/timelines. Routinely communicates project updates to internal and external clients.

The Scientist III, Bioconjugation (ADC) Process Development, will have an opportunity to contribute to Exelixis’ Antibody Drug Conjugates (ADCs) technology platforms. The successful candidate will be responsible for the development of scale-able and robust downstream ADC processes and support technology transfer efforts, leading to clinical GMP manufacturing of ADCs.

Serve as a bridge between the Engineering team and the Millipore Sigma Life Science business to execute both high-level strategic and immediate tactical projects. Own the continuous improvement of production processes, specifically targeting gains in efficiency, quality, and performance. Provide hands-on, day-to-day troubleshooting and technical guidance for manufacturing issues or process changes. Define and deploy improvement strategies on the production floor using Lean SixSigma methodology to reduce waste and boost efficiency. Focus on implementing sustainable solutions that prevent recurrence and ensure a stable manufacturing environment. Manage and execute process improvement projects within stipulated timeframes and budget constraints, ensuring they meet intended design specifications as per the capability of Project Excellence. Conduct comprehensive process analysis and develop solutions for optimal process performance, ensuring integration of new technologies and analytics tools as needed. Develop and implement standardized production systems that facilitate easy maintenance, minimize downtime, and reduce maintenance costs based on the design for maintenance capability. Contribute to the execution of the Life Science strategy and strive for technological advancement by evaluating effective, sustainable, and state-of-the-art solutions in line with applicable safety and quality requirements.

The Quality Engineer II will provide Quality Engineering support for Arden Hills Manufacturing lines and New Products Introduction ensuring delivery of the highest quality result to the customer while supporting continuous improvement projects and quality initiatives. The person in this role will partner with manufacturing engineers for line support activities and with product development teams to ensure development of robust new products. In a fast-paced and dynamic environment, the Quality Engineer II will be responsible for several manufacturing processes on the manufacturing line, working cross-functionally with manufacturing engineering and production teams to achieve business unit goals. The person in this role will be comfortable interfacing with downstream internal customers and providing quality leadership to a production team.

This position is responsible for returns processing activities within the CRM and EP Returns Processing (Post-Market Quality) team at Arden Hills, Minnesota. This position is intended to be focused on returned product decontamination, with opportunities to support additional returned product activities as needed.

RayzeBio is looking for an Associate Scientist to support in the development of novel therapeutics in preclinical stages. Candidates will work as part of a team of scientists to synthesize and design both small molecules and peptide analogs to optimize potency, pharmacokinetics, and in vivo efficacy of potential drug candidates. This position offers a challenging and rewarding work environment within a thriving company.

Our Manufacturing Associate, Cell Therapy team manufactures human blood-derived components per Batch Record and Standard Operating Procedures in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Job duties are performed within a team according to an assigned, production shift schedule. Communication of production deviations and assistance with quality investigations are required, as applicable.

Responsible for supporting QC testing for in-process, final product, and stability samples. May assist with documentation, deviations, investigations, and continuous improvement efforts.

As a Manufacturing Technologist, you'll work in our production department with a team of technicians and engineers responsible for manufacturing the Hysitron product line of instrumentation. This position offers the opportunity gain hand-on skill with cutting edge technology and opens the door to an exciting future in mechanics and engineering. Under the appropriate guidance, you will be responsible for building electro-mechanical components and devices that are used in our line of nanoindentation products. You will have opportunities to work with advanced scientific tools including the Hysitron scanning probe nanomechanical test systems.

The Field Service, System, and Applications position within the service organization is an ambassador of Bruker Nano Surfaces and Metrology Division. Bruker Nano Surfaces and Metrology manufactures the world's leading Cryo Dry Cleaning systems, Atomic Forces Microscopes, Stylus profilers, X-Ray Metrology (XRR, XRD, XRF, XRI, TXRF), Mask Repair, non-contact 3D optical microscope instrumentation, and Tribology systems. This technical role is responsible for customer direct post-sale instrumentation and application support including: installation, basic user and application training, instrument diagnostics/fix, and post-sale developed applications support. Individual must be customer focused with strong industry background and technical experience capable of independent judgement that enables our customers to maintain their instrument at peak performance and maximize productivity for their intended use case.

As a Mechanical Manufacturing Engineer at Bruker AFM, you’ll play a pivotal role in sustaining engineering, championing supply chain initiatives, resolving end-of-life challenges, and ensuring peak performance of production test equipment. If you’re ready to make a significant impact in electrical manufacturing, we encourage you to apply and become part of our innovative family.

As a Manufacturing Associate I, you’ll be a vital part of Capricor’s efforts in delivering therapies for patients in need. Supporting critical clinical trials and exosome development, 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 Quality Assurance Associate II to join our team. This role is critical in scaling clinical production activities, ensuring compliance with cGMP and regulatory standards. The position will assist in batch record review, deviation investigations, label issuance, and management of controlled documentation across GLP/GCP/GMP systems. The ideal candidate is detail-oriented, organized, and passionate about driving quality excellence in a fast-paced environment.

The Pathologist Associate is responsible for supporting and assisting the Pathology and Pathology Operations departments in their daily operations. This position will perform tasks needed to be completed in the day-to-day operation. This position also includes performing the tasks of Macrodissection and Microdissection.

The qualified candidate will be working in the Assay Development and Validation Department. The individual will play a critical role in supporting the development, validation, transfer, establishment and successful launch of new molecular assays, instrumentation, and methodologies into the clinical laboratory. Candidate will be responsible for assisting with planning, designing, and performing various laboratory experiments, documentation, reagents receiving, storing and tracking, data analysis, summarization and presentation, transfer of knowledge to other team members and to other departments, training clinical personnel, as well as additional functions fit for the position. Development Associates are expected to contribute both technically and intellectually to optimize quality and efficiency for Caris' pipeline of development projects.

The Process Engineer plays a critical role in optimizing operations across packaging, labeling, storage and distribution, and continuous improvement, collaborating with cross‑functional teams to drive efficient, compliant, high‑quality production. In this highly autonomous role, you’ll influence daily operations by supporting production scheduling, resolving capacity constraints, investigating deviations, contributing to client audits, and serving as a subject matter expert on equipment and systems. This position offers the chance to lead meaningful, site‑wide initiatives, strengthen your technical and operational expertise, and make a visible impact on reliability, quality, and customer experience—giving you a unique opportunity to grow your career while shaping the future of our operations.

Catalent Pharma Solutions in Madison, WI is hiring an Associate Scientist II - Quality Control. This position requires a variety of skills necessary for biotech company operations. The position is an entry level laboratory role with the expectation that the candidate is able to be trained on technical procedures and once trained, execute them consistently and reliably. Additionally, this position may support preventative maintenance and basic laboratory maintenance activities while maintaining a GMP quality system.

Catalent Pharma Solutions in Madison, WI is hiring an Associate Scientist I - Quality Control, Sample Management. This position requires a variety of skills necessary for biotech company operations. The position is an entry level laboratory role with the expectation that the candidate can be trained in technical procedures and once trained, execute them consistently and reliably. Additionally, this position may support preventative maintenance and basic laboratory maintenance activities while maintaining a GMP quality system.

Catalent Pharma Solutions in Madison, WI is hiring Facilities Engineer. This position will work on complex facility-related problems requiring in-depth data analysis to determine appropriate action. The Engineer is expected to have extensive ongoing communication with employees and cross-functional group managers/departments on facility-related issues.

Cellipont Bioservices is growing, and we are looking for a QA Technician I, Operations who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The QA Technician I, Operations will be responsible for monitoring systems and procedures to ensure compliance where applicable. The QA Technician I, Operations is responsible for providing Quality Assurance support real-time for GMP Manufacturing of Cell Therapies. This individual will be responsible for providing QA on the Floor during manufacturing including observing critical processes, review executed GMP documentation, and supporting other QA functions as needed.

Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP’s and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents.

The Scientist, Quality Associate position is responsible for the cGMP analytical laboratory analysis in the Quality Control department of MilliporeSigma. Analysis may consist of all/some of the following: incoming raw material analysis, in-process testing, final product analysis, method validation/qualification, cleaning, reference standard requalification, and environmental monitoring to support Quality Control activities at the Madison and Verona sites. Analysis includes techniques specific to, but not limited to: HPLC, GC, KF, DSC, TGA, IR, MS, NMR and XRPD among other tests and instruments. Other responsibilities may include initiation and review of deviations, OOS/OOT’s, change controls, and CAPA’s. Additionally, participation in process improvement initiatives, working in a team environment, maintaining a clean and safe work area, and supporting the department in maintaining the laboratory in an audit ready state are other duties. The Scientist, Quality You will exhibit a willingness to contribute to the overall success of the company by assisting in many areas beyond specific job duties.

Serve as a bridge between the Engineering team and the Millipore Sigma Life Science business to execute both high-level strategic and immediate tactical projects. Own the continuous improvement of production processes, specifically targeting gains in efficiency, quality, and performance. Provide hands-on, day-to-day troubleshooting and technical guidance for manufacturing issues or process changes. Define and deploy improvement strategies on the production floor using Lean SixSigma methodology to reduce waste and boost efficiency. Focus on implementing sustainable solutions that prevent recurrence and ensure a stable manufacturing environment. Manage and execute process improvement projects within stipulated timeframes and budget constraints, ensuring they meet intended design specifications as per the capability of Project Excellence. Conduct comprehensive process analysis and develop solutions for optimal process performance, ensuring integration of new technologies and analytics tools as needed. Develop and implement standardized production systems that facilitate easy maintenance, minimize downtime, and reduce maintenance costs based on the design for maintenance capability. Contribute to the execution of the Life Science strategy and strive for technological advancement by evaluating effective, sustainable, and state-of-the-art solutions in line with applicable safety and quality requirements.

The Chemistry Technician IV supports the development and ongoing improvement of contact lens and lens care products by conducting analytical testing and product evaluations. The Chemistry Technician IV is integral to ensuring product stability, performance, and compatibility, working closely with R&D teams to support both new innovations and existing products throughout their lifecycle.

Our Engineering Team is dedicated to quality. Delivering life-saving products is about getting them right, and our technical expertise and experience working in a manufacturing environment empower us to meet that challenge. When you join us, you will work with a team of committed individuals who trust each other to deliver on the tasks at hand. We support innovation and out-of-the-box thinking balanced with collaboration across functions and other teams. Our leadership understands the need for continuous education and provides opportunities for further development. As an Engineering Technologist, you will have the opportunity to lead by example, and enjoy mentoring and learning from others. Here, you are trusted to manage your own time and are given opportunities to grow your career as you wish.

Perform routine quality control testing of protein, peptide or antibody products using standard operating procedures to determine lot status, product release and product stability. Tests include: concentration determination, SDS-PAGE with densitometry, endotoxin assay, TOC, conductivity and other testing as assigned. The position requires routine documentation, analysis and communication of results within the department and across different groups. Other duties include instrument calibration and maintenance, record keeping, and lab support. Within this job function, the Research Associate must also pursue annual goals that aim to facilitate innovation, efficiency, productivity and team building across the QC Department or the entire company. Perform additional duties as assigned.

We are seeking a motivated R&D Technologist to support the development and optimization of molecular diagnostic assays in a laboratory research environment. This role is ideal for an early-career scientist with a strong foundation in molecular biology who enjoys hands-on laboratory work and contributing to assay development projects. The R&D Technologist will perform routine and semi-routine laboratory experiments, support assay development and validation activities, and work closely with scientists and cross-functional teams. This position operates under direct to general supervision and provides opportunities to build technical expertise in sequencing-based diagnostic workflows.

Manages day to day manufacturing activities to ensure goals areaccomplishedand communication occurs within the group and across all functions/shifts.  This includes providing leadership inday to daymanufacturing operation activity, employee career development, and overall coaching support to the manufacturing team.

Primary focus of this position is to support in developing, optimizing, implementing, and validating components/elements of a medical device. The candidate will perform hands-on testing in optimization of a device; conduct process development activities to understand process inputs and outputs; assist/write technical documents, validation protocols and reports; prepare work instructions and standard operating procedures; assist in conducting design and process qualification and validation; support equipment development; support other activities from R&D, Quality, Operations, and Regulatory Affairs.

Reporting to the EHS manager, Provide technical and operational support to the EHS function by implementing and maintaining programs related to industrial hygiene, occupational safety, incident prevention, and regulatory compliance. Support key elements of the PSM system as needed to help ensure a safe and compliant operation.

We're seeking a dynamic Operational Technology (OT) Systems Specialist to revolutionize our sterilization and operations infrastructure! In this role, you'll orchestrate the installation and ongoing support of cutting-edge Operational Technology systems, ensuring our technology not only meets but exceeds application requirements while maintaining rigorous corporate security standards. You'll be at the forefront of implementing manufacturing IT initiatives spanning cybersecurity, network infrastructure, telecommunications, database and server administration, virtualization, storage networks, and disaster recovery protocols. The technology guardian we seek possesses exceptional communication abilities, meticulous attention to detail, and demonstrates agility in adapting to rapidly evolving technologies.

BigHat Biosciences is seeking a self-motivated individual for a Research Associate I/II, Production, role to power our high-throughput, automated platform for antibody production and deep molecular characterization.

The Microbiology Laboratory Specialist III (MLS III) works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development and clinical affairs activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g. nucleic acid extraction, PCR, serial dilution, bacterial, fungal and parasitic cultures, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and other instructive documents, regulations, safety requirements and the quality system. Work is primarily collaborative and requires the ability to communicate and coordinate with peers and supervisors effectively and respectfully. The position requires basic laboratory technical skills, organizational skills, attention to detail, critical thinking, troubleshooting and problem solving, and dedication to the mission and goals of the department and bioMerieux. A Microbiology Laboratory Specialist III will normally self-direct on routine with minimal instruction and general supervision and will operate with general or detailed instruction and general supervision on new procedures and assignments.

The Sr Tech II performs corrective and preventative calibrations on manufacturing and laboratory analytical instrumentation with limited supervision. Supports manufacturing and laboratory personnel in the use, maintenance and repair of on-site instrumentation and test equipment. Supports Validation and engineering activities when called upon. Authors changes to procedures and job plans when required.

Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; Downstream (Purification), MAs perform these critical steps in a clean environment governed by Current Good Manufacturing Practices (cGMP).

The Associate for BioLegend’s Quality Control group will test products such as antibodies and proteins in the following application(s): flow cytometry, immunohistochemistry, western blotting, ELISA, multiplex immunoassays and/or functional bioassays. The candidate will perform all aspects of the assays following SOPs and ISO requirements. Additional responsibilities include culturing mammalian cell lines, isolating primary cells, and maintaining laboratory equipment and supplies. We are looking for a highly motivated person who loves science and wants to be part of a dynamic and fast paced team.

BioLegend is looking for a Biochemist to be an integral member of a team that manufactures and provides antibodies and reagents to a diverse set of research areas. The Biochemist will report to a team lead and will ensure the highest quality of our finalized products. This is a great opportunity to work in a fast-paced and dynamic environment for you to enhance your knowledge in the biotechnology industry! In this position you will follow Standard Operating Procedures (SOP)s, manufacture and deliver magnetic beads and related products, and cross train on a variety of other supporting tasks. This Biochemist works with Mojo manufacturing team. The main responsibility for this position will be to perform manufacturing and protein coating of magnetic nanobeads, prepare and formulate related beads and antibody reagents according to established Standard Operating Procedures (SOPs) for cell separation applications. Other duties will include completion of appropriate batch record forms, updating relevant databases and other lab duties.

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.

Biolog is seeking a Manufacturing Associate to support in-house manufacturing of Biolog consumable products within our Operations Consumables Production team in Hayward, CA. Under the direction of the Senior Manager of Operations, this role is responsible for executing methods and protocols for chemical formulation of reagents, manufacturing workflows, and final packaging of finished goods. This position may also support shipping-related activities as needed. The ideal candidate is detail-oriented, dependable, and capable of working independently while maintaining high standards for safety, documentation, and product quality.

BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.

Bionova is seeking for Manufacturing Associate, to support plasmid DNA production through upstream and downstream unit operations. This role executes GMP manufacturing processes, documents activities accurately, and supports a safe, compliant manufacturing environment.

QC Specialist will come in and perform suitability testing to verify QC equipment performance is acceptable prior to starting any Functional Process Order testing on multiple Bio-Rad product lines. Equipment and Sample preparation will occur in the Lab throughout the day and completion of needed paperwork, results recording in SAP, and performance monitoring in shared Minitabs will be done and submitted for review and then turned into QA for product release. Any Non-conformances discovered during testing will follow our Out of Specification process and will determine if a Non-Conformance is required.

As a Production Chemist, you will formulate products and intermediates utilizing biologicals and chemicals of varying properties and characteristics in order to meet specifications.

Let’s do this. Let’s change the world. At Amgen, our mission is simple yet powerful: to serve patients. At our Ohio site, you’ll play a critical role in ensuring the highest standards of quality in the products that impact lives around the world. We’re looking for a Senior Associate in Quality Assurance who brings energy, precision, and a passion for excellence to our growing team. If you thrive in a fast-paced, regulated environment and enjoy solving complex challenges, this is your opportunity to make a meaningful difference. As a Sr. Associate in QA, you will be a key player in maintaining compliance and driving quality across manufacturing operations.

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.

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.

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.

Works on complex problems requiring in-depth analysis and evaluations of factors, and on assignments that are required to be performed according to defined procedures and practices. Exercises considerable judgment and initiative within broadly defined practices and policies in selecting methods and techniques. Normally receives no instruction on routine work, general instructions on new assignments.

We are currently offering a fantastic career opportunity for a highly motivated and Lab Technician to join Antharis Therapeutics, a pre-clinical company based in San Diego. The company is committed to discovering and developing novel immunotherapeutics (monoclonal antibodies and antibody-drug conjugates) for an array of disease states. The approaches for antibody discovery, including hybridoma technology, aim to streamline the development of lead candidates for entering the clinic in an expedited fashion. 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.

The Laboratory Technician I supports Applied Medical’s Biological Sciences operations by performing essential laboratory activities that enable testing, experimentation, and data generation in a regulated environment. This role contributes to product quality and compliance by maintaining laboratory readiness, executing established laboratory procedures, and supporting cross functional scientific teams. The Laboratory Technician I plays a critical part in ensuring accurate data collection, safe laboratory operations, and consistent support for biological testing and development initiatives.

The Complaint Evaluation Engineer plays a critical role in Applied Medical’s post-market quality and patient safety efforts by investigating returned medical devices and evaluating real-world product performance. This hands-on, laboratory-based engineering role focuses on device teardown, functional and mechanical testing, and recreation of reported product issues to determine root cause and support continuous improvement. Working closely with cross-functional engineering and quality teams, the complaint evaluation engineer contributes to regulatory compliance, technical documentation, and post-market surveillance activities in alignment with Food and Drug Administration standards, International Organization for Standardization (ISO) 13485 requirements, and Medical Device Reporting expectations. This position is well-suited for engineering professionals seeking experience in medical device investigation, failure analysis, and post-market quality engineering.

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.

Under the supervision of the laboratory supervisor the Microbiologist I provides a high level of quality pharmaceutical microbiology testing as well as effective customer service to ARL Bio Pharma clients. This is a safety sensitive position as defined by state and federal laws that will require working with hazardous materials and/or handling medicine.

The Associate Manufacturing Scientist I (second shift) role 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.

Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for an Engineer II – Laboratory Operations and Process. This individual will be responsible for managing operations and efficiencies of the Orthopedic Research Biomedical Engineering Laboratory and ensure the procedures, equipment, and personnel are compliant under the Quality Management System. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better™.

Responsible for providing process engineering support for all product manufacturing departments. Supports manufacturing operations to ensure consistent adherence to the standard operating procedures and business continuity. Initiates process improvement initiatives to improve the efficiency of current manufacturing processes, as well as develop new processes to improve manufacturing efficiency. Supports new product launches by collaborating with other functional areas and providing process engineering expertise during the implementation of processes or equipment.

The Regulatory Affairs (RA) Specialist is responsible for supporting day-to-day manufacturing, preparing U.S. and international submission content, and obtaining and maintaining approval for products to markets worldwide based on direction from RA management. Additionally, the RA Specialist is responsible for assessment of regulated product changes for regulatory implications and for performing regulatory activities in support of implementation. The RA Specialist will work independently and manage their own regulatory projects.

The Analytical Chemist 1 performs routine analytical testing under supervision, supporting the generation of quality data to advance pharmaceutical development and manufacturing.

The Manufacturing Associate Support provides support for: Production Operations and multiple aspects of cGMP contract cell culture manufacturing in strict compliance with cGMP, under Standard Operating Procedures in a multi-product manufacturing facility, including, but not limited to production, documentation, writing reports, requesting and purchasing materials, and scheduling equipment services and calibrations. The Manufacturing Associate will play an integral role in ensuring the production and on-time release of quality products. The Manufacturing Associate will conduct themselves in a manner representing the core values (Integrity, Adaptability, Innovation, Teamwork, and Passion) of the company with the common purpose of improving patients’ lives by consistently delivering high-quality biopharmaceutical products.

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 Quality Control Specialist I supports the Operations department by being responsible for reviewing laboratory derived data to ensure a high standard of scientific and data integrity for all services and products provided. In addition, the individual in this role assists management in ensuring quality and regulatory requirements for good laboratory practice (GLP) are met, when specified.

The QC Microbiologist 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 Scientist II sets up Extractables & Leachables studies and conducts quantitative and qualitative analyses according to FDA, cGMP, and Boston Analytical Inc. Standard Operating Procedures. Duties include analysis of extract and pharmaceutical product samples using LC-MS, GC-MS, and/or ICP-MS. A Scientist II will also develop and validate leachables methods for these techniques.

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.