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Quality and Compliance Specialist
vor 1 Woche
We are a diverse and inclusive team of over 100,000 employees across 100 countries, working together to push back the frontiers of healthcare. As a GMP Compliance Specialist, you will be part of the Synthetic Molecules Technical Development team, working closely with key partners in research and early development, as well as commercial counterparts.
The Role DescriptionYou will own and facilitate GMP compliance processes in close collaboration with the global PQS network, participating in global PQS document lifecycle processes and actively influencing authorizing communities. You will also manage local impact assessments and implementation of current PQS requirements.
Requirements- A Master or equivalent degree in chemistry, pharmaceutical sciences, or exceptional experience in a GMP environment within the pharmaceutical industry.
- Experience in synthetic molecule manufacturing and/or quality control is a plus.
- Fluency in German and English and ability to collaborate with diverse international teams.