Principal Scientist, Late Stage Upstream Process Development (San Francisco, CA)

Cedent; San Francisco (CA); On-site; USD 120,000 - 160,000; Full time

Job summary

A leading biotech company in San Francisco is searching for a Principal Scientist to lead late-stage upstream cell culture process development for large molecule programs. This role requires a PhD with at least 7 years of biotech experience in process development and regulatory compliance. The ideal candidate will manage scale-up and tech transfer activities, ensuring successful collaboration across various teams. Candidates should have excellent communication skills and a strong understanding of regulatory expectations for process validation.

Qualifications

• Minimum 7 years of cell culture process development experience in biotech/biopharma.
• In-depth understanding of CHO-based fed-batch processes.
• Experience with late-stage upstream process development and BLA authoring.

Responsibilities

• Lead scale-up and tech transfer of upstream processes to manufacturing.
• Collaborate with cross-functional teams for process performance qualification.
• Author and review relevant CMC documentation.

Skills

Cell culture process development

Technical writing

Leadership

Cross-functional collaboration

Statistical tools

Education

PhD in biology, biochemistry or related field

BS/MS with 12+ years of experience

Job description

Principal Scientist, Late Stage Upstream Process Development (San Francisco, CA)

Client is seeking an experienced and driven scientist/engineer to lead late-stage upstream cell culture process development activities for clinical and commercial-stage large molecule programs. This individual will serve as the upstream lead for scale-up and tech transfer to manufacturing sites, establishing process validation (PV) strategy and PPQ/post-approval process support.

Key Accountabilities/ Core Job Responsibilities

• Lead scale-up and tech transfer of the upstream process to manufacturing sites, ensuring alignment with control strategy and regulatory filings.
• Serve as the technical lead, responsible for upstream process activities for a late-stage large molecule programs including commercial manufacturing support
• Author and review relevant CMC documentation including PV protocols/reports and regulatory sections (e.g., BLA, IND amendments).
• Develop and execute strategies for process performance qualification (PPQ) and continued process verification (CPV).
• Collaborate cross-functionally with MSAT, Downstream, Analytical Development, CMC management, Manufacturing Operations, QA, QC, Regulatory, and Contract Manufacturers
• Represent upstream function in regulatory strategy, technical meetings, and CDMO interactions.
• Provide technical support for upstream process-related investigations, product impact assessments, change control assessments, CAPA assessments etc.

Qualifications/Skills

• PhD in biology, biochemistry, chemical engineering or related scientific discipline with minimum 7 years of cell culture process development experience in the biotech/biopharma industry; or BS/MS with 12+ years of experience.
• In-depth understanding of CHO-based fed-batch processes, scale-up/scale-down principles, and statistical tools.
• Thorough understanding of cell culture bioreactors including microbioreactors, bench-scale and pilot-scale bioreactors, and scaleup/tech transfer activities
• Demonstrated experience with late-stage upstream process development, PPQ strategy, tech transfer and BLA authoring
• Strong knowledge of regulatory expectations for process validation and control strategies.
• Excellent communication, leadership, and cross-functional collaboration skills.
• Demonstrated ability for taking initiative, creativity, and innovation in problem solving
• Experience working with novel large molecule formats such as bispecific antibodies and Fusion proteins/enzymes is a plus
• Demonstrated technical writing, critical thinking, scientific problem-solving and communication skills