As a Qualified Person (QP) at Catalent, Bathgate, you will provide QA expertise, certify finished products, review GMP documents, investigate batch release improvements, participate in product recalls, ensure regulatory requirements are met, and identify quality improvements. The role requires Sterile and Biological Product experience, Biotech Products knowledge, and compliance with GMP regulations.

Coordinate and drive forward the storing, production, packaging, and distribution of clinical trial medicines for a pharmaceutical company. Manage project plans, lead meetings with clients and internal teams, facilitate project completion, and act as the client advocate. Support Project Management teams and provide training to other project coordinators.