Your new role
As a QC Microbiology Analyst, you will play a key role in ensuring microbiological quality within GMP-regulated clean room environments used for the manufacture of advanced cell‑based therapies. Working under strict GMP (Good Manufacturing Practice) requirements, you will be responsible for executing microbiological testing and environmental monitoring activities, ensuring reliable results and accurate documentation. Your work directly contributes to product quality, regulatory compliance, and patient safety in a sterile and controlled environment.
Your day-to-day responsibilities
- Perform environmental monitoring of GMP-classified clean rooms
- Conduct microbiological assays, including:
- Gram staining
- Endotoxin testing
- Sterility testing
- Bioburden testing
- Growth promotion testing
- Microbial identification (genus & species)
- Plate reading
- Enter, review, and trend microbiological test results
- Perform routine maintenance of laboratory equipment and QC lab areas
- Support departmental projects and continuous improvement activities
- Follow all GMP, safety, and quality procedures
- Support other QC activities as required
What you’ll need to succeed
The ideal candidate is reliable, quality‑focused, and comfortable working in a regulated, fast‑paced manufacturing environment.
You have:
- MLO level 4 (Vocational Training) or a Bachelor’s degree in Microbiology (preferred)
- 0–4 years of experience in a microbiology laboratory and/or environmental monitoring
- Experience with aseptic techniques and clean room operations
- Knowledge of GMP, regulations, and quality control processes
- Ability to read and follow English SOPs, test methods, and safety documentation
- Proficiency in MS Word, Excel, and PowerPoint
- Willingness to work in a rotating shift schedule
Personal skills
- Strong attention to detail and a quality-driven mindset
- Able to work independently with minimal supervision
- Flexible and adaptable to changing priorities
- Team-oriented, reliable, and well-organised
- Strong verbal and written communication skills in English
Additional requirements
- Physically able and willing to gown for clean room entry and work in controlled areas.
- Able to lift up to approximately 12 kg
- Comfortable working in sterile environments
- Must already reside in the Netherlands
- Visa sponsorship cannot be provided for this role.
What you’ll get in return
You will start in a contract position, with the possibility of extension or longer-term opportunities based on performance and business needs.
You’ll receive:
- €50,400 gross per year, based on full-time employment
- 12.24% shift allowance
- Travel expense reimbursement
- Pension contribution
- 8% holiday allowance and 28 paid holiday days
Your new company
You will be working for a global biopharmaceutical organisation active in the development and manufacturing of advanced cell therapies. Their modern production facility in the Hoofddorp area operates under the highest GMP standards and focuses on delivering innovative treatments for patients with serious diseases.
What you need to do now
If you are interested in the QC Microbiology Analyst position and meet the residency requirements, please apply with your updated CV or contact us directly.
If this role isn’t quite the right fit, but you are open to new opportunities within QC, microbiology, or GMP environments, we welcome a confidential discussion.
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