Process Engineer Cell Culture

☞ Pauwels Consulting

View: 145

Update day: 16-11-2025

Location: Geel Antwerp

Category: Executive management Production / Operation

Industry: Staffing Recruiting

Position: Entry level

Job type: Full-time

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Job content

For a big Biotech company in the region of Antwerp we are looking for an MSAT Process Engineer (Tech transfer support). Your job will involve the following tasks:
  • Technology transfer, initial process validation and process control strategy definition for introduction of new products and processes at manufacturing scale
  • Identification of process improvements to increase yield or process robustness, and generation of a supportive data package leading to implementation at manufacturing scale
  • Supporting and safeguarding existing production processes by data trending and monitoring, generation of scientific/technical study protocols and reports in support of significant changes, product impact assessments upon significant deviations in the production process and provided technical advice to questions of other departments.
Benefits
  • Challenging projects based on your interests and skills
  • Personal follow-up and clear, transparent communication both before and after commencement of employment
  • Possibility to follow extra training
  • Inspiring network events and legendary after work drinks
  • Strong network of industry leading clients
  • Expertise within IT, Engineering and Life Sciences
  • A flying start for every junior, growth opportunities and possibility to share gathered knowledge for more senior employees
Have you got what it takes?
  • You have (preferably) a PhD in Life Sciences, with relevant in process development or MSAT-like functions
  • You have fluent English speaking and writing skills, knowledge of Dutch is a plus
  • You have specific experience with growing mammalian cells in bioreactors; either on lab- or production scale
  • You have an excellent analytical and problem-solving mindset, are accurate with the necessary eye for detail and can handle multiple tasks at once
  • You have excellent writing technical/scientific writing skills (protocols & reports)
  • You are flexible and willing to support both manufacturing scale operations and set up small scale lab studies
  • You have knowledge of cGMP
  • You are a strong communicator, who is able to connect, go in discussion and find compromise with people in other departments or sites
  • You like to work in team and consider yourself to be a good team player.
  • Flexibility, stress resistance, openness to change & innovation and eagerness to meet deadlines are characteristics of you.
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Deadline: 31-12-2025

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