Mantell Associates

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 commercial growth as a Business Development Director in Shanghai for a global clinical services leader. Drive revenue by securing new partnerships with pharma and biotech clients across the Asia-Pacific region. This role requires 8+ years of BD experience in CRO/clinical research and a prove...

Lead the global strategy for clinical data management and biometrics in this senior leadership role. You will build and scale a world-class team, ensuring rigorous data delivery for regulatory submissions. Requires deep CDISC expertise and proven experience leading biometrics functions in a bioph...