Mantell Associates - Quality Control, On-site work

Lead Quality Operations at a premier East Coast CDMO as the site Director of Quality. This senior leadership role requires deep FDA GMP expertise across biologics and small molecules. You will own the site QMS, ensure inspection readiness, and drive a proactive quality culture. Ideal candidate ha...

Join a leading biosimilar developer in Buenos Aires as a Quality Control Consultant. This on-site role requires hands-on review of biological raw data (HPLC, ELISA) in a GMP environment. Ensure data integrity and compliance within a fast-paced biologics manufacturing setting. Ideal candidates hav...

Join a global biosimilars CDMO as a GMP Documentation Analyst in Buenos Aires. You will manage critical GMP documents, including SOPs and Batch Records, ensuring cGMP compliance. The role requires proven pharma documentation experience, eQMS knowledge, and strong organizational skills for this on...

Lead supplier quality audits for a pharmaceutical/biotech leader in California. Ensure cGMP compliance and robust supply chains through on-site evaluations and risk assessments. Ideal candidates have a Life Sciences degree and strong audit experience in a regulated environment. Travel required.