*Upstream Process Transfer/MSAT Scientist (12 months temporary position)

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An exciting and diverse career opportunity awaits you in our Process Transfer Department in Copenhagen. We are actively seeking a quality-focused individual with expertise in upstream processing and a proven ability to foster interdepartmental collaboration. This role is initially offered as a 12-month temporary position, with potential for extension or transition to permanent employment based on performance and business needs. Join us in shaping the future of biopharmaceutical development and manufacturing!

Job Description:

AGC Biologics is seeking a talented and experienced Upstream Process Transfer Scientist to join our dynamic department under MSAT unit. In 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.

Depending on your level of qualification, you will take part in key upstream process activities in several projects, both within microbial and mammalian processing. As a Process Transfer Scientist, your key responsibilities will be:

  • Collaborate with cross-functional teams to facilitate the transfer of upstream processes from development to manufacturing.
  • Lead and execute technology transfer activities, ensuring alignment with project timelines and quality standards.
  • Provide technical expertise in upstream bioprocessing, including cell culture and fermentation, to optimize manufacturing processes.
  • Conduct risk assessments and troubleshoot issues related to technology transfer and manufacturing.
  • Work closely with development teams to gather and document critical process parameters and data for successful transfer.
  • Collaborate with Quality Assurance to ensure compliance with cGMP and other regulatory standards.
  • Participate in process validation activities and support the resolution of deviations or discrepancies.
  • Contribute to the continuous improvement of technology transfer processes and documentation.

Qualifications:

  • PhD or M.Sc. within 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 and drive new tasks 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.

About AGC Biologics:

AGC Biologics is a leading Contract Development and Manufacturing Organization (CDMO) dedicated to providing high-quality services for the development and manufacturing of biopharmaceuticals. With state-of-the-art facilities and a commitment to innovation, AGC Biologics empowers clients to accelerate their biologics programs from development to commercialization.

We offer a dynamic working environment and an excellent opportunities for working and growing with a varied array of tasks and challenges. Exciting and challenging assignments will keep coming your way, but you will largely be able to plan your daily work on your own. AGC employees have a flexible attitude, and we help each other to reach deadlines together as one team, compliant with our slogan - Right. On Time.

Want to keep posted about our growth and to learn more about our company?

We also urge you to follow us on our LinkedIn Company Page and give us a quick Like on Facebook !

AGC Biologics (AGC) is a global Contract Development Manufacturing Organization (CDMO) with bio-manufacturing facilities in Europe, Japan, Italy and the USA. The company provides a comprehensive range of commercial and clinical cGMP biologics manufacturing services, from DNA to active pharmaceutical ingredient (API). The company’s team and approach are tailored to each of its client’s needs, whether turnkey manufacturing or sophisticated, stand-alone analytical, formulation and stability services.

Visit www.agcbio.com to learn why AGC Biologics is a World Leader in process development and contract manufacturing.


Information og data

Denne ledige stilling har jobtypen "Forsker", og befinder sig i kategorien "Sundhed og forskning".

Arbejdsstedet er beliggende i København

Jobbet er oprettet på vores service den 25.1.2024, men kan have været deaktiveret og genaktiveret igen.

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Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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  • København
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