QP/ Qualified Person - Germany - Various Locations
Posted on Mar 17, 2019 by Xplore Pharma
Your tasks: • Certification of batches of medicinal products as a knowledgeable person to the extent defined by law (interim releases and final releases for the clinical trial according to Annex 13) • Participation in the development, production, testing and approval of medicinal products as a qualified person in accordance with §§ 13, 15 AMG • Information and advice to employees, physicians and other healthcare stakeholders through product risk assessment of drugs • Keeping a continuous register with appropriate confirmation of all released batches in accordance with § 19 AMG in conjunction with § 17 AMWHV
My client is a growing, global manufacturing partner to the Life Science industry and have roles in 2 locations in Germany.
Please get in touch for more information to