Upstream Process Transfer Specialist

4 weeks ago


Gladsaxe, Gladsaxe Municipality, Denmark AGC Biologics Full time

Unlock a World of Possibilities in Biopharmaceutical Development

We are seeking a talented Upstream Process Transfer Scientist to join our dynamic team at AGC Biologics in Copenhagen. As a key member of our Process Transfer Department, you will play a crucial role in the successful transfer of upstream processes from development to manufacturing, ensuring seamless integration and optimal production.

About the Job

In this exciting career opportunity, you will take part in key upstream process activities across various projects, including microbial and mammalian processing. Your expertise will be invaluable in facilitating the transfer of upstream processes, leading technology transfer activities, and providing technical support to optimize manufacturing processes.

Your Key Responsibilities Will Include:

  • Collaborating with cross-functional teams to ensure efficient transfer of upstream processes.
  • Leading technology transfer activities, aligning with project timelines and quality standards.
  • Providing technical expertise in upstream bioprocessing, including cell culture and fermentation, to enhance manufacturing processes.
  • Conducting risk assessments and troubleshooting issues related to technology transfer and manufacturing.
  • Working closely with development teams to gather and document critical process parameters and data for successful transfer.
  • Collaborating with Quality Assurance to ensure compliance with cGMP and other regulatory standards.
  • Participating in process validation activities and supporting the resolution of deviations or discrepancies.
  • Contributing to the continuous improvement of technology transfer processes and documentation.

You Will Thrive in This Role If You Have:

  • A PhD or M.Sc. in biochemistry, protein chemistry, biotechnology, or a related field.
  • Experience within process development and/or manufacturing within upstream processing.
  • A flexible approach and desire to take on new challenges and responsibilities.
  • Proven experience in upstream bioprocessing and technology transfer within a CDMO or biopharmaceutical environment.
  • Strong understanding of cell culture, fermentation, and bioreactor operations.
  • Experience with process optimization and troubleshooting in a manufacturing setting.
  • Knowledge of regulatory requirements for biopharmaceutical manufacturing (cGMP).
  • Excellent English communication and interpersonal skills.
  • Ability to work collaboratively in a fast-paced and dynamic environment.

We Offer a Competitive Compensation Package and a Friendly, Collaborative Culture That Values Personal Initiative and Professional Achievement. The Estimated Salary for This Role is Approximately €60,000 - €80,000 Per Year, Depending on Experience.



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