Overview Are you passionate about quality, precision, and working in a GMP-regulated environment? We are currently seeking a detail-oriented GMP Documentation Specialist (m/w/d) to join our client’s Manufacturing Operations team in a dynamic, fast-paced biopharmaceutical environment.
The GMP Documentation Specialist supports clinical biologics manufacturing by performing operational review of executed batch records and ensuring documentation supports ALCOA+ standards and GMP expectations. The role is part of the Operational Excellence team within Manufacturing