Abzena | Careers / Vacancies

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Senior Associate, Downstream

Key Responsibilities: Designs and executes process development experiments to develop a thorough understanding of operating and performance parameters and identifies promising areas for process improvements. Effectively analyses experimental results and designs and executes follow-up experiments that build upon previous results. Guides and oversees the work of the Process Development (PD) Associates and junior personnel to […] Read more

Location: San Diego, CA

Project Manager

Abzena Pennsylvania Inc. is seeking a Project Manager in Bristol, PA. Duties Provide plans and feedback on analytical techniques, troubleshooting and approval of analytical documents. Provide orthogonal testing and characterization of the material by analytical chemistry. Provide technical feedback on manufacturing, analytical and quality assurance. Review the documents, provide feedback to the teams and clients for […] Read more

Location: Bristol, PA

Senior Facilities Mechanic

Overall Responsibilities: This position is responsible for the continuous operation of the Abzena San Diego campuses and associated utilities.  This function requires a detailed understanding of cGMP practices and procedures.  Computerized systems will be utilized to oversee routine maintenance and organize repairs.  Daily interaction with other professionals to improve production facilities, reduce the incidence of […] Read more


Senior Scientist Process Development

At Abzena, you will have the opportunity to work in a dynamic and rewarding work environment. The scientists’ at Abzena conduct research on the cutting edge of science and deliver meaningful results in the pharmaceutical industry. The Chemistry and GMP Manufacturing group at Abzena has an opening for a Senior Scientist to conduct process development/optimization […] Read more


Senior GMP Analytical Scientist

Overall Responsibility The principle responsibility of the GMP Analytical Scientist/Senior GMP Analytical Scientist is analytical support for GMP manufacturing and process development. The GMP Analytical Scientist/Senior GMP Analytical Scientist may also provide analytical services for discovery and R&D projects as needed. This is a hands-on laboratory position with additional technical, supervisory, and management responsibilities dependent […] Read more

Location: Bristol, PA

Manager, Quality Control Microbiology (QCM)

The Manager of Quality Control Microbiology will have responsibility over QC environmental monitoring and microbiological/safety testing activities supporting GMP manufacturing.  Practical knowledge in all aspects of product development from investigational phase to commercial launch. Experience working in GMP regulated environment.   This position is deputy to the Sr. Director of Quality Control/Analytical Method Development for […] Read more

Location: Bristol, PA


We have a vacancy for an experienced scientist to join our busy Cell Line Development team in Cambridge (UK) site as a Scientist.  In this role you will work as part of a team on client-facing projects and have the opportunity to learn new techniques in a fast-paced but supportive environment. At Abzena we recognise […] Read more

Location: Cambridge, UK

Sr. Scientist Analytical Method Development

Overall Responsibilities The Sr. Scientist Analytical Method Development will develop direct execute and document Scientific development projects in support or product development programs at Abzena San Diego. Specifically, the individual will develop and optimize analytical methods to support process development, in-process monitoring, drug substance and drug product testing, specifications, method qualification/validation protocols and reports.   […] Read more

Location: San Diego, CA

Validation Associate

Overall Responsibilities: Develop validation/qualification documents for simple to complex manufacturing, laboratory and facilities equipment systems, including any associated software. Execute simple to complex system validations/qualifications. Review simple to complex system validations/qualifications submitted by other in-house personnel or by outside vendors. Participate in, and potentially take a lead role in, cross-functional teams to establish system requirements […] Read more

Location: San Diego, CA

Computer Software Validation Engineer

Overall Responsibilities: Author and/or maintain Computer Software Validation Master Plans. Independently develop validation/qualification documents for computerized systems. Execute computerized system validations/qualifications, as needed. Independently review computerized system validation/qualification documents that are submitted by other in-house personnel or by outside vendors . Lead cross-functional teams to establish system requirements and to apply risk management techniques to […] Read more

Location: San Diego, CA

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