Specialist Quality Control

4 weken geleden


Hoofddorp, Nederland i-Pharm Consulting Voltijd

Job Title: GMP Specialist – Cell Therapy

Contract Duration: 8 Months

Location: Netherlands, Hoofddorp (On Site)

Shift: Rotational (Morning/Evening Shifts, including Weekends)

Our client is looking for highly motivated and hands-on individuals to join their Production Support Team and Production Team in their Manufacturing Department. As a leading innovator in cell therapy, they are dedicated to developing cutting-edge treatments that have the potential to transform the lives of patients. This is a unique opportunity to be directly involved in the manufacturing of both clinical and commercial products that make a meaningful impact on healthcare worldwide.

Production Support Team

Prepare growth media in cleanroom ‘nest’ environments.
Transfer and submit samples to QC sample management.
Production Team

Execute GMP runs in A and B grade cleanrooms, following batch records and SOPs.
Collaborate with cross-functional teams (Product Sciences, QA, QC) to ensure successful manufacturing outcomes.
Adhere to SOPs and cGMP regulations to ensure high-quality output.
Maintain cleanroom environments in optimal conditions.
Education: MLO/MBO/HBO (MBO Level +) in Life Sciences or a related field.
Prior cGMP experience in a pharmaceutical/biotechnology manufacturing environment is required.
Knowledge of pharmaceutical manufacturing processes for biotechnology products.
Experience working in a cleanroom and aseptic environment is essential.
Excellent communication skills (verbal and written in English.)

This role requires flexibility with a shift schedule, including weekend work.

If you're looking for an opportunity to make a meaningful impact in the field of cell therapy and grow within a dynamic and innovative environment, we encourage you to apply


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