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QC Microbiology Analyst
Gi Group Perm B.V.
About the role
Job Title: QC Microbiology Analyst (Microbiologist I) Workplace Type: On-site Job Location: Hoofddorp, Netherlands Employment Type: Contract (12 months) — full-time We are hiring a QC Microbiology Analyst (Microbiologist I) for a leading biotech/pharma manufacturing environment in Hoofddorp, Netherlands. In this role you will support GMP Quality Control Microbiology testing and cleanroom environmental monitoring , helping ensure safe, compliant manufacturing of advanced therapies in a fast-paced setting.
What you'll do
Perform environmental monitoring (EM) of cleanrooms (air, surface, water sampling as applicable). Execute microbiological assays including Endotoxin (LAL) , Sterility , Bioburden , and plate reading . Perform data entry , review , and trending of results in line with GMP requirements. Support routine maintenance of lab equipment and lab spaces (cleanliness, checks, basic troubleshooting). Contribute to department projects and continuous improvement activities. Perform other QC microbiology tasks as required by the team lead.
What you'll bring
MLO level 3 / MLO4+ or Bachelor (BSc) in Microbiology (preferred). 0–4 years of QC Microbiology / Environmental Monitoring experience (preferred). Practical experience with microbiological techniques such as air monitoring, water testing, and surface monitoring. Familiarity with aseptic techniques and cleanroom operations . Comfortable with gowning , cleanroom entry and supporting activities; able to lift approx. 12 kg . Knowledge of GMP , regulations, and quality control processes. Proficient with MS Word, Excel, PowerPoint . English communication skills required (minimum B1 ). (Dutch not required.) Able to work flexibly in a changing, fast-paced environment and adjust priorities when needed. Important: Must be willing to focus on sampling activities for the first 12 months . What you can expect Contract: 12 months with potential extension (6 months). Interview process: 30-minute on-site interview. Work environment: GMP QC lab + cleanroom support in a collaborative team (20+ QC analysts). Schedule: 18-week shift schedule (details shared during the process). Agency recruitment: You will be employed via an agency and assigned to our client site.