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MSAT Process Transfer Engineer

il y a 1 mois


Brainel'Alleud, Wallonie, Belgique UCB S.A. Temps plein

Make your mark for patients

We are looking for an MSAT Process Transfer Engineer who is innovative, detail-oriented, and collaborative to join our MSAT Tech Transfer & Operational Support team, based at our UCB campus in Braine-l'Alleud, Belgium.

About the Role

As an MSAT Process Transfer Engineer, you will contribute to process technology transfer activities for late-stage and commercial biologics, enabling the successful launch of these molecules into internal and external commercial-scale facilities. You will ensure a seamless transition from development to manufacturing and provide operational support during manufacturing campaigns.

Who You Will Work With

You will collaborate with a dynamic and diverse team in the Tech Transfer group of the Mammalian Cells Drug Substance Manufacturing Sciences & Technology (MSAT) team. You'll also partner with stakeholders across Manufacturing, Engineering, QA, and Process Development to drive success in your projects.

What You Will Do

  • You will support the tech transfer of Drug Substance (USP and/or DSP) processes to internal facilities and Contract Manufacturing Organizations (CMOs).
  • You will manage commercial-scale process validations for Downstream Processes in Drug Substance manufacturing.
  • You will provide on-the-floor support during manufacturing campaigns to resolve challenges in real time.
  • You will assist with deviations and investigation processes to maintain quality standards.
  • You will support Continuous Process Verification (CPV) activities and monitor key performance indicators.
  • You will prepare for and participate in regulatory inspections and filings, acting as a Subject Matter Expert for Drug Substance manufacturing processes.

Interested?

For this role, we are looking for the following qualifications, experience, and skills:

  • Relevant experience in upstream and downstream bioprocessing within the biopharma industry.
  • A solid understanding of biopharma operations and GMP principles.
  • Excellent communication skills and the ability to collaborate effectively with cross-functional teams.
  • Strong organizational skills to manage multiple tasks and meet deadlines.
  • A problem-solving mindset with strong analytical and statistical skills.
  • Self-motivation, a can-do attitude, and an innovative, team-oriented approach.
  • Proficiency in English (spoken and written); knowledge of French is a plus.

Ready to make an impact? Join us and help shape the future of biologics manufacturing

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