
Senior Engineer II, Downstream Development, Viral Vector Product Development
- Cambridge, MA
- Permanent
- Full-time
- Lead bench-scale early and late phase process development activities and optimization of AAV purification process steps (chromatography, filtration, UF/DF)
- Enhance the lab-based purification development strategy and implement next-generation tools to increase throughput and efficiency
- Design and execute OFAT and DoE-directed experiments to identify key and critical process parameters and recommend acceptable ranges for process scale-up large-scale manufacturing
- Participate on CMC program teams as a process development functional representative, providing updates and ensuring process development milestones are met
- Serve as SME for scale-up and GLP manufacturing planning and execution up to 200L scale
- Provide mentorship to junior lab members to improve team skills around experimental design and lab techniques
- Lead tech-transfer of manufacturing processes to external partners, providing person-in-plant (PIP) support when necessary
- Author development reports, tech transfer documents, and other relevant process/regulatory documents for pipeline programs and research collaborations
- Engage in platform development for the evaluation and implementation of novel technologies to improve purification efficiency and product quality
- BS, MS, or PhD in Chemical Engineering, Biochemistry, or related discipline with 10+ years (BS), 8+ years (MS), or 2+ years (PhD) of relevant experience in the biotech industry
- Extensive experience developing biologics purification process steps (Clarification, chromatography, UF/DF, NFF)
- Experience developing high-throughput purification screening techniques and novel technology evaluation
- Experience managing scale-up, tech-transfer, and implementation of purification processes at internal and external manufacturing partners
- Expertise with statistical analysis and design of experiment (DOE)
- Experience authoring technical documents (process development, tech transfer, batch records, IND supporting documents) and supporting drafting of CMC sections of regulatory submissions (IND, IMPD, BLA)
- Proficiency with statistical analysis and design of experiment (DOE) using software tools such as JMP
- Ability to work comfortably in a controlled lab environment with biological, infectious, and hazardous materials; lift/carry 15/30 pounds unassisted/assisted; gown/degown PPE; use a computer; engage in communications via phone, video, and electronic messaging; engage in problem-solving and non-linear thought; collaborate with others; maintain general availability during standard business hours
- Experience developing AAV-specific purification processes
- Experience with participation in project teams and regulatory documentation
- Understanding of molecular or physical biology analytical techniques (qPCR, ELISA, HPLC) is a plus