Upstream Process Transfer Specialist
2 weeks ago
We are seeking an experienced Upstream Process Transfer Scientist to join our dynamic department under MSAT unit at AGC Biologics in Copenhagen.
About the RoleIn this role, you will play a key part in the successful transfer of upstream processes from development to manufacturing or form our clients into AGC Biologics manufacturing, ensuring seamless integration and optimal production.
Your Responsibilities- You will collaborate with cross-functional teams to facilitate the transfer of upstream processes from development to manufacturing.
- You will lead and execute technology transfer activities, ensuring alignment with project timelines and quality standards.
- You will provide technical expertise in upstream bioprocessing, including cell culture and fermentation, to optimize manufacturing processes.
- You will conduct risk assessments and troubleshoot issues related to technology transfer and manufacturing.
- You will work closely with development teams to gather and document critical process parameters and data for successful transfer.
- You will collaborate with Quality Assurance to ensure compliance with cGMP and other regulatory standards.
- You will participate in process validation activities and support the resolution of deviations or discrepancies.
- You will contribute to the continuous improvement of technology transfer processes and documentation.
- You have a PhD or M.Sc. within biochemistry, protein chemistry, biotechnology, or a related field.
- You have experience within process development and/or manufacturing within upstream processing.
- You have a flexible approach and desire to take on and drive new tasks and responsibilities.
- You have proven experience in upstream bioprocessing and technology transfer within a CDMO or biopharmaceutical environment.
- You have a strong understanding of cell culture, fermentation, and bioreactor operations.
- You have experience with process optimization and troubleshooting in a manufacturing setting.
- You have knowledge of regulatory requirements for biopharmaceutical manufacturing (cGMP).
- You have excellent English communication and interpersonal skills.
- You are able to work collaboratively in a fast-paced and dynamic environment.
AGC Biologics offers a highly competitive compensation package and a friendly, collaborative culture that values personal initiative and professional achievement. We are an equal opportunity employer and welcome applications from all qualified candidates.
The estimated salary for this role is around $120,000 per year, depending on your level of qualification and experience. The location of the job is in Copenhagen, Denmark.
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