Associate, Process Development; Cells
Listed on 2026-10-27
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Research/Development
Research Scientist, Clinical Research, Medical Science -
Healthcare
Clinical Research, Medical Science
We are seeking a highly enthusiastic Associate, Process Development (Cells) to join our process development team focused on developing bioprinted tissue therapeutics for cell therapy applications. You will support the production, qualification, and scale-up of multiple cell lines to drive the development of bioprinted tissue therapeutics (BTT). You’ll be joining a company committed to developing regenerative medicines that deliver life-changing, functional cures for patients living with serious diseases.
Responsibilities- Independently support the production and supply of various cell types to Aspect’s CMC and R&D groups for downstream bioprinting and assay development.
- Independently complete all stages of cell culture processing including cell isolation from cadaveric tissue, cell thawing, expansion, media change, aggregation, cryopreservation, and banking.
- Assess and interpret in vitro viability and functional assays for cell characterization.
- Optimize and contribute to the scale-up processing of therapeutic cells.
- Contribute to the development of release Certificate of Analysis (CoA) for internal cell lines to document post-production characterization and ensure quality cell products.
- Complete internal IQ/OQ/PQ of new cell processing and manufacturing equipment.
- Work closely with R&D, CMC, quality, and regulatory teams to support non-GMP technology transfer(s) of culture processes in compliance with regulatory requirements.
- Perform data collection and analysis to contribute insights for cell culture process improvement.
- Assist with reagents and buffers preparation, and complete periodic inventory checks.
- Collaborate with cross functional teams (preclinical R&D, CMC, Therapeutic Cell Platforms) to refine bioprocessing methods.
- Create, review, and maintain documentation such as standard operating procedures (SOPs), Batch Production Records (BPRs), protocols, reagent preparation forms, and experimental reports in Good Documentation Practices (GDP).
- Develop subject matter expertise and work with other CMC teams to ensure technical compliance and adherence.
- Education +
Experience:
BSc (with 2+ years of experience) or MSc in Cell Biology, Biotechnology, Biomedical Engineering, or a related field with demonstrated experience working aseptically with mammalian cell culture preferably in an industry setting. - Knowledge: Experience with cell isolation from human or animal tissue, 3D cell culture, primary cell culture, immortalized insulinoma cell lines, primary or stem cell derived insulin-producing cells will be an asset.
- Go-Getter: You work with a sense of urgency, are results-driven, and thrive in a fast-paced, interdisciplinary, and entrepreneurial environment. You are willing to roll up your sleeves and do what it takes to get the job done.
- Collaborative: You thrive in a multi-disciplinary team environment and believe that we can get further, faster by working together. You take direction well and ask for clarification when necessary.
- Effective Communicator: You are an active listener who can communicate to different audiences in diverse situations.
The hiring range for this role is $64,000 - $72,000, annually. Our ranges are based on market data. Offered salaries will be based on a combination of factors including, but not limited to, job-related knowledge, skills, education, and experience. For candidates who exceed role requirements, we are open to exploring above-range offers. Note that base salary is just one part of the overall compensation bers of the Aspect team also receive a comprehensive benefits package, and support for continuous learning and career progression.
WhoWe Are
Aspect Biosystems is a biotechnology company pioneering the development of a novel category of…
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