
Manufacturing Specialist
5 days ago
The ideal candidate will play a key role in the global Process Development organization, supporting manufacturing at various contract manufacturing sites across Europe. This includes new product introductions, lifecycle changes and ongoing commercial production.
Key Responsibilities- Develop expertise in parenteral drug product manufacturing and provide leadership for troubleshooting issues across all processing stages.
- Collaborate with contract manufacturers, Global Operations and drug product process teams to ensure smooth operations.
- Work as a member of cross-site teams to identify and resolve potential issues and implement operational improvements.
- Provide technical expertise for commercial drug product processing in areas such as aseptic processing, process characterization and technology transfer.
- Troubleshoot issues with drug product processing technologies and equipment.
- Support contract manufacturing quality with technical evaluation of nonconformities and visit contract manufacturing sites to observe production operations.
- 5-8 years' pharmaceutical manufacturing experience in either a drug product or drug substance environment.
- Knowledge of current Good Manufacturing Practices (cGMPs) and excellent problem-solving ability.
- Strong academic results in a Bachelor's degree in Science, Engineering or a relevant quality discipline.
- Familiarity with aseptic drug product processes and presentations, as well as quality testing methods and interpretation of results for biological molecules.
- Pharmaceutical Manufacturing
- Opportunity to develop skills in parenteral drug product manufacturing
- Chance to work with experienced professionals in the industry
- Development opportunities in a dynamic company
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