Meet Life Sciences
Overview
Meet has partnered with a clinical-stage biopharmaceutical company that leads the development, manufacturing, and lifecycle strategies of biologic drug products, ensuring production quality, regulatory compliance, and clinical supply. Collaborates cross-functionally to manage technology transfers and formulation development, while providing strategic guidance to internal teams and external partners.
Base pay range
$150,000.00/yr - $175,000.00/yr
Candidates need to work a hybrid model in San Diego, CA - 3 days in office.
Responsibilities
- Lead drug substance and product manufacturing at CMOs, including validation, PPQ, stability, and GMP runs.
- Provide scientific and technical leadership across development, clinical supply, and commercialization stages.
- Drive technology transfer, scale-up, and final product assembly at CDMOs, managing documentation and execution.
- Collaborate with QA and Regulatory Affairs to ensure compliance, manage complaints, and support risk mitigation.
- Oversee CRO/CMO coordination, review data and reports, author regulatory documents, and assist with budgeting.
Qualifications
- 7+ years working in pharma/biotech, focused on biologics and combination products like autoinjectors and prefilled syringes.
- Strong skills in formulation, process development, and scaling up drug products.
- Experienced with analytical tools (like HPLC) and writing regulatory documents (IND, BLA).
- Knows global regulations (FDA, EMA, ICH) and works well in fast-paced teams.
- Motivated, independent, and great at managing multiple projects and presenting to senior leaders.
Please reach out to Martin Wenzel if you're interested in learning more:
Seniority level
- Mid-Senior level
Employment type
- Full-time
Job function
- Science
Industries
- Staffing and Recruiting, Biotechnology Research, and Pharmaceutical Manufacturing