Upstream Process Transfer / MSAT Scientist (12 months)

Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market.

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. Join us in shaping the future of biopharmaceutical development and manufacturing!

About the job
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.

You will…

• 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.

You have…

• 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.

Are you up for a challenge?

• Apply with your CV (In English please)
• If we see a match, you’ll have a call with one of our recruiters to share more about what you can bring to the team.
• Are both sides still positive? Then we proceed to the assessment stage to assess key skills required for the job Confidential
• We will be conducting interviews on an ongoing basis and will close the position once the successful candidate has been found.

Our culture at AGC Biologics is defined by the six core values: Knowledge, Trust, Quality, Ingenuity, Accountability and Teamwork. Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe.

AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit www.agcbio.com. Want to keep posted about our growth and learn more about our company? Follow us on LinkedIn and give us a quick Like on Facebook!

AGC Biologics offers a highly competitive compensation package and a friendly, collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances.

Location: Copenhagen Site