CPC Scientific in Rocklin, CA is seeking a QA Director for a full‑time, on‑site role. You will lead the strategic QA governance for the new peptide CDMO site, oversee batch release, CAPA, and data integrity, and drive regulatory
CPC Scientific is seeking a QA Director for their Rocklin, CA site to lead strategic QA planning and operational delivery of all QA functions at the greenfield peptide CDMO manufacturing site. The role requires ownership of
CPC Scientific (CPC) is a globally recognized and leading CDMO specializing in synthetic peptide and oligonucleotide production, with one of the largest research peptide facilities in the world. CPC works directly with leaders in the biotechnology
CPC Scientific is a globally recognized and leading CDMO specializing in synthetic peptide and oligonucleotide production, with one of the largest research peptide facilities in the world. CPC Scientific works directly with leaders in the biotechnology
CPC Scientific (CPC) is a globally recognized and leading CDMO specializing in synthetic peptide and oligonucleotide production, with one of the largest research peptide facilities in the world. CPC works directly with leaders in the biotechnology
Director of Quality Control A growing, highly regulated life sciences manufacturing organization is seeking an experienced Director of Quality Control to provide strategic leadership for its Quality Control function. Reporting to executive leadership, this individual will
Health Plan Correspondence Product Manager Consultant The Health Plan Correspondence (HPC) Content & Composition team, part of Member Experience Transformation, manages controls, requirements, features, prioritization, and sequencing to enhance Blue Shields transactional communications, including ID cards,