Mantell Associates - On-site work

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.

Join a leading healthcare logistics firm as a Deviations Consultant. This UK-based contract role is central to GDP quality assurance, focusing on deviation management, root cause analysis, and CAPA systems. Ideal candidates have proven GDP/GMP experience and strong regulatory knowledge. Provide h...

Seeking a visionary Chief Operating Officer for a global Pharmaceutical leader in Switzerland. You will oversee worldwide manufacturing, supply chain, and quality operations, driving strategic growth and operational excellence. This senior role requires extensive pharma industry leadership, P&L r...

Join a leading gene therapy CDMO as a Medical Sales Representative in Brazil. Promote specialized biologic and gene therapy services, building key relationships with research institutions and biotech companies. We seek a Life Sciences graduate with 2-4 years of pharma/biotech sales experience, fl...