Mantell Associates - On-site work

Join a world-class biologics organization in Buenos Aires as a GMP Manufacturing Analyst. This hands-on role requires direct, large-scale biologics production experience for the technical review of batch records. Your deep process knowledge of upstream/downstream operations is key to ensuring GMP...

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...

Join a global biosimilars CDMO as a Manufacturing Analyst in Buenos Aires. Ensure production excellence and GMP compliance by reviewing Batch Records and QC data. Collaborate cross-functionally to support audits and continuous improvement in a high-performance manufacturing environment.

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.