GMP Production Technician, Hoofddorp, Noord-Holland

Location: Hoofddorp, Noord-Holland  |  Sector: Biotechnology  |  Start Date: 4/1/2025  |  Job ref: 54685

About the Company:
This company is a leader in advanced therapies, specializing in the development and production of innovative cell-based treatments. Their focus is on delivering life-changing therapies to patients while maintaining the highest quality standards in a regulated manufacturing environment.

Role Description:
As a Cell Therapy Technician/Specialist, you will be responsible for executing critical steps in the manufacturing of advanced therapies. Working in a GMP-compliant cleanroom environment, you will perform aseptic processing, material preparation, and product handling to support clinical and commercial cell therapy production. This role requires adherence to strict protocols and a keen attention to detail to ensure the highest quality standards.

Key Responsibilities:

  • Execute cell therapy manufacturing processes in Grade A and B cleanroom environments following batch records and standard operating procedures (SOPs).
  • Support production operations by preparing and transferring materials, media, and components to the manufacturing suites.
  • Perform visual inspections, cryopreservation, and sample submissions for quality control.
  • Maintain cleanroom conditions, ensuring compliance with GMP and safety standards.
  • Accurately document processes and contribute to investigations related to deviations and process improvements.
  • Assist in drafting and revising SOPs, batch records, and work instructions to maintain compliance.
  • Troubleshoot processing and equipment issues as needed.
  • Work collaboratively with cross-functional teams, including Quality, Supply Chain, and Process Development.

Requirements:
  • MLO/MBO/HBO (equivalent to Associate’s or Bachelor’s degree) in Life Sciences, Biotechnology, or a related field.
  • Experience in GMP-regulated manufacturing, preferably within pharmaceuticals, biotechnology, or cell therapy.
  • Understanding of aseptic processing and cleanroom operations.
  • Hands-on experience with biological sample handling, media preparation, and visual inspection is a plus.
  • Ability to work in full gowning requirements and follow strict contamination control procedures.
  • Strong attention to detail, compliance mindset, and ability to adapt in a fast-paced environment.
  • Fluency in English (Dutch is not required).

54685

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Since 2012, SIRE Life Sciences is the most innovative and engaged consultancy company for the life sciences industries.

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Our team of knowledgeable professionals provides customized staffing services to clients and candidates, including secondment, direct hire, temporary-to-hire, temporary staffing, brokering, Statement of Work and we approach each type with the same degree of professional assessment. Our refined and collaborative style is unmatched in the staffing industry. We’re able to see beyond the surface to create matches that result in successful careers for our candidates and valuable talent for our clients.

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