QC Microbiologist (Senior)
Senior QC Microbiologist voor een leidende biopharmaceutical organisatie in Hoofddorp, tijdelijke opdracht in een GMP-gereguleerd QC-laboratorium, startdatum 26-10-2026.
Bekijk bij SIRE Life Sciences B.V. (opent in een nieuw tabblad)
Eisen
- Experience with aseptic techniques and cleanroom operations
- Bachelor's degree in Microbiology or a related scientific discipline
- Practical experience with air monitoring, water testing and surface monitoring
- Ability to coordinate laboratory activities, guide colleagues and take ownership of quality-related issues
- Experience handling deviations, impact assessments, change controls and CAPAs
- At least 6 years of experience in microbiology laboratory work and/or Environmental Monitoring
- Strong organisational skills and the ability to work effectively in a fast-paced, regulated environment
- Good understanding of GMP, pharmaceutical regulations and Quality Control processes
- Knowledge of microbial genus and species identification and Gram staining
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Volledige omschrijving
About our client: Our client is a leading biopharmaceutical organisation specialising in innovative cell therapies and advanced cancer immunotherapies. By developing personalised treatments for patients with cancer, the organisation is helping advance the future of cancer care. Working in a fast-paced, highly regulated environment, the company combines scientific innovation with high-quality manufacturing and rigorous quality standards to help deliver life-changing therapies to patients.
About the position: We are looking for an experienced QC Microbiologist to join a Quality Control Microbiology team of more than 20 analysts. In this senior position, you will combine hands-on microbiological laboratory work with quality oversight and day-to-day coordination of laboratory activities. You will act as a key point of contact for the team, supporting junior colleagues and taking ownership of deviations, investigations and quality improvement activities.
This role is ideal for an experienced microbiologist who is confident working in a GMP-regulated environment and ready to take on greater responsibility within a pharmaceutical quality control laboratory.
Working hours: Monday to Friday, 08:30–17:00, with one weekend of work every four weeks.
Responsibilities: Lead the initiation, investigation and follow-up of deviations, including impact assessments. Process and monitor INVAs (investigation records, according to site terminology and procedures). Coordinate laboratory activities and act as the first point of contact for the QC Microbiology team. Provide guidance and delegate tasks to Microbiologist I and II analysts. Manage and follow up on change controls and Corrective and Preventive Actions (CAPAs).
Perform and support microbiological laboratory testing and Environmental Monitoring activities. Escalate quality concerns and operational issues to the relevant Team Leads. Ensure laboratory activities are performed in accordance with GMP requirements, applicable regulations and established procedures.
Requirements: Bachelor's degree in Microbiology or a related scientific discipline. At least 6 years of experience in microbiology laboratory work and/or Environmental Monitoring. Practical experience with air monitoring, water testing and surface monitoring. Knowledge of microbial genus and species identification and Gram staining. Experience with aseptic techniques and cleanroom operations. Good understanding of GMP, pharmaceutical regulations and Quality Control processes.
Experience handling deviations, impact assessments, change controls and CAPAs. Ability to coordinate laboratory activities, guide colleagues and take ownership of quality-related issues. Strong organisational skills and the ability to work effectively in a fast-paced, regulated environment.
Bekijk bij SIRE Life Sciences B.V. (opent in een nieuw tabblad)
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