Sr. Associate Scientist Vector Process Development - Contract - Cambridge, MA
Advance next‑gen cell therapies by shaping smarter, scalable viral vector processes.
Proclinical is seeking a Sr. Associate Scientist for Vector Process Development in Cambridge, MA. In this position offers the opportunity to support pipeline programs, engage in process development and CMC activities, and drive innovation in next-generation vector processes.
Primary Responsibilities:
The successful candidate will contribute to the development of scalable and efficient lentiviral vector manufacturing processes for cell therapy programs.
Skills & Requirements:
- Hands-on experience with bioreactors, control software, and process analytical technology is strongly preferred.
- Familiarity with process development and pharmaceutical manufacturing; experience with scale-up and pilot plant operations is a plus.
- Background in vector process development and manufacturing is advantageous.
- Strong problem-solving skills, attention to detail, and ability to work independently.
- Effective communication and interpersonal skills, with the ability to thrive in a fast-paced, cross-functional team environment.
- BS/MS in Bioengineering, Chemical Engineering, Biology, Cell Biology, or related biological sciences.
- Proven experience in biotechnology or pharmaceutical industry (2 years for MS or 4 years for BS).
- Solid understanding of cell biology and hands-on experience with mammalian cell culture.
The Sr. Associate Scientist Vector Process Development's responsibilities will be:
- Conduct routine viral vector production operations at bench and pilot scales, including media preparation, culture initiation, seed train maintenance, and bioreactor operations.
- Perform experiments to evaluate process changes and new technologies for advancing lentiviral vector production.
- Develop experimental plans, interpret scientific results, and provide statistical analysis as needed.
- Maintain laboratory equipment and inventory while performing general lab tasks.
- Support technology transfer activities to manufacturing partners as an upstream subject matter expert (SME).
- Organize and manage critical data, ensuring proper documentation practices.
If you are having difficulty in applying or if you have any questions, please contact Mike Raletz at m.raletzproclinical.com
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
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