CQV Engineer: GMP Commissioning & Qualification
20blocThousand Oaks, CA
CQV Engineer: GMP Commissioning & Qualification
20blocThousand Oaks, CA
yesterday
Industries
Pharmaceutical Preparation ManufacturingBiological Product (except Diagnostic) ManufacturingResearch and Development in Biotechnology (except Nanobiotechnology)About the role
20BLOC INC. in Thousand Oaks, CA seeks a CQV-focused professional to create and execute IQ/OQ/PQ protocols and related documentation for GMP equipment and systems. The role emphasizes field execution, risk assessment, and close collaboration with Engineering, Manufacturing, and Quality teams. Ideal candidates have 2–5 years of CQV or GMP experience, a technical degree, and strong technical writing skills. This is an on-site, full-time role offering competitive compensation and benefits.
Matching similar jobs
JOB OVERVIEW
Experience level
Lead
Location
Thousand Oaks, CA
Occupation
Validation Engineers
Industry
Pharmaceutical Preparation Manufacturing
Posted
yesterday
Tired of running searches?
Rank the roles you'd take once, and matches like these arrive on their own.
CREATE PROFILE