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QP/ Qualified Person - Germany - Various Locations

Posted on Mar 17, 2019 by Xplore Pharma

Not Specified Germany
15 Mar 2019
Annual Salary
In this role you are responsible for ensuring the quality of the medicines manufactured in the area of ​​responsibility and their release for use in clinical trials.

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

Reference: 672603905