GMP Cell Therapy Production Specialist

SIRE LIFE SCIENCES; Haarlem; On-site; EUR 40,000 - 65,000; Full time

Job summary

SIRE LIFE SCIENCES in the Netherlands is seeking a Biomanufacturing Specialist for a Hoofddorf site to support the production of clinical and commercial cell therapy products in a GMP cleanroom. The role sits within the production team or production support team and emphasizes safe, compliant manufacturing, accurate documentation, and driving process improvements.

You will execute production activities, follow SOPs, manage batch records, support aseptic processing, quality control coordination,

Qualifications

• GMP/regulatory environment experience.
• Aseptic cleanroom experience.
• Strong documentation and batch record skills.

Responsibilities

• Execute manufacturing and production support activities in a GMP cleanroom.
• Follow SOPs and cGMP requirements; complete batch records accurately.
• Perform material prep, decontamination, and transfer into cleanrooms.
• Support aseptic processing and ensure consistent process execution.
• Assist visual inspection and cryopreservation activities as needed.
• Coordinate sample submissions with QC/sample management.
• Support deviation investigations and change management.
• Troubleshoot equipment and process issues; escalate as needed.
• Identify opportunities for continuous improvement and support implementation.
• Collaborate with Production Support, Material Management, QA, and QC.

Skills

Communication skills

Attention to detail

Data handling

Education

MBO/MLO/HBO Level 4+ in Life Sciences

Tools

Microsoft Word

Microsoft Excel

Job description

SIRE LIFE SCIENCES in the Netherlands is seeking a Biomanufacturing Specialist for a Hoofddorf site to support the production of clinical and commercial cell therapy products in a GMP cleanroom. The role sits within the production team or production support team and emphasizes safe, compliant manufacturing, accurate documentation, and driving process improvements.

You will execute production activities, follow SOPs, manage batch records, support aseptic processing, quality control coordination,