Associate Director, Quality Assurance (Emeryville)
Scientific Search, Emeryville, California, United States, 94608
Location:
Emeryville, CA (Onsite)
Engaging Summary
My client — a fast-scaling biologics CDMO — is searching for a bold, detail-obsessed QA leader who thrives where science meets execution. As Associate Director of Quality Assurance, you’ll be the guardian of GMP excellence, shaping quality operations that support cutting-edge antibody development. If you’re energized by the pace of biotech, love owning QA systems end-to-end, and want to influence the full product lifecycle, this role is built for you.
Why You Should Apply
Lead QA operations in a high-impact CDMO environment Own batch review, lot disposition, QMS execution, and key quality systems Partner cross-functionally in biologics development and tech transfer Competitive salary + strong benefits + onsite visibility Shape Quality culture as the site continues expanding
What You’ll Be Doing
Maintaining site GMP compliance and documentation Overseeing deviations, CAPA, change control, quality agreements Leading batch record review & timely lot disposition Supporting regulatory submissions and audits Working closely with manufacturing, QC, facilities & external labs
About You
BS + 7 years pharma/biotech experience; 5 years QA Strong biologics/GMP background Skilled reviewer, communicator, and collaborator CMOs/CTOs experience strongly preferred
How To Apply
Send resume to
ava@scientificsearch.com
with
Job # 19698.
Emeryville, CA (Onsite)
Engaging Summary
My client — a fast-scaling biologics CDMO — is searching for a bold, detail-obsessed QA leader who thrives where science meets execution. As Associate Director of Quality Assurance, you’ll be the guardian of GMP excellence, shaping quality operations that support cutting-edge antibody development. If you’re energized by the pace of biotech, love owning QA systems end-to-end, and want to influence the full product lifecycle, this role is built for you.
Why You Should Apply
Lead QA operations in a high-impact CDMO environment Own batch review, lot disposition, QMS execution, and key quality systems Partner cross-functionally in biologics development and tech transfer Competitive salary + strong benefits + onsite visibility Shape Quality culture as the site continues expanding
What You’ll Be Doing
Maintaining site GMP compliance and documentation Overseeing deviations, CAPA, change control, quality agreements Leading batch record review & timely lot disposition Supporting regulatory submissions and audits Working closely with manufacturing, QC, facilities & external labs
About You
BS + 7 years pharma/biotech experience; 5 years QA Strong biologics/GMP background Skilled reviewer, communicator, and collaborator CMOs/CTOs experience strongly preferred
How To Apply
Send resume to
ava@scientificsearch.com
with
Job # 19698.