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Senior Bioprocess Technician

  1. Rotterdam
  1. Contract
  1. Life Sciences
Date Posted26 Apr 2021
Senior Bioprocess Technician - 7 Months - Netherlands

 Our client is a fast growing, biopharmaceutical contract development and manufacturing organization (CDMO) focused on viral vector and recombining protein products. They have recently built a state-of-the-art GMP manufacturing facility that is getting filled with exciting new vaccines, antibodies and protein products. They support customers with the development & commercialization of biologics enabling the treatment & prevention of life threatening conditions such as cancer, COVID-19, influenza and other infectious diseases.

If you too would like to contribute to this challenging and fulfilling activity and become  part of an inspiring biotech services company, then this is a perfect opportunity for you!

As a Senior bioprocess technician, you will be working on USP, DSP as well as aseptically fill processes. You will lead the tech transfer from late stage development into GMP production together with a team of Bioprocess Technicians and Operators.

The following tasks and responsibilities are applicable:
  • Preparing the manufacturing processes: cleaning equipment, requesting and checking the manufacturing documentation, reviewing log books, checking the equipment-status  and ordering materials required for the process.
  • Take accurate and prompt action or escalation on quality related issues.  
  • Execution of manufacturing processes of cell cultures, infection of the cells, harvesting, clarification including  downstream processes. All according to GMP/FDA-guidelines, internal procedures, protocols and batch records.
  • Closing out of the manufacturing: line clearance, equipment or area decontamination and change over.
  • Writing and reviewing of manufacturing batch records.
  • Equipment maintenance and qualification
  • Possibly lead a team of Bioprocess Technicians and Operators
 We are looking for technicians with the following qualifications:
  • BSc in biotechnology, microbiology or related fields
  • Minimum of three years’ experience in cell culturing and/ or aseptic processing under GMP/FDA regime
  • Experience with writing quality documents (e.g. batch record documentation, deviations, changes, etc.)
  • Specific experience with USP is highly preferred
  • Specific experience with single use technology for large bio reactors is preferred
If you have the right skills and experience for this role, apply now!

The candidate must have the rights to work in the location stated in the job advert.

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