Hoofddorp
Full-time
0-2 years experience
On-site

Key Skills

Environmental Monitoring
Microbiological Testing
Sterility Testing
Microbial Plate Reading
Microbiological Data Analysis
Data Trending
Aseptic Techniques
Cleanroom Practices
GMP Compliance
Quality Control
Laboratory Equipment Maintenance
Microsoft Word
Microsoft Excel
Microsoft PowerPoint
Written Communication
Verbal Communication

Job Description

As a QC Microbiologist, you will join the Quality Control Microbiology team, supporting the manufacture of innovative cell therapies in a regulated GMP environment. Working alongside a diverse team of microbiology professionals, you will be responsible for environmental monitoring activities, microbiological testing, data management, and laboratory support functions that help ensure product quality and compliance. This role offers the opportunity to contribute to the development of life-changing cancer immunotherapies in a fast-paced and collaborative setting. Responsibilities Perform environmental monitoring activities within cleanroom manufacturing areas. Conduct microbiological testing, including sterility testing and microbial plate reading. Accurately enter, review, analyze, and trend microbiological test data. Carry out routine maintenance and upkeep of laboratory equipment and workspaces. Support continuous improvement initiatives and departmental projects. Ensure compliance with GMP standards, laboratory procedures, and quality requirements. Assist with additional quality control microbiology activities as assigned. Requirements MLO Level 3 qualification or a Bachelor's degree in Microbiology or a related scientific discipline preferred. 0-4 years of experience in a microbiology laboratory and/or environmental monitoring environment. Hands-on experience with microbiological techniques, including air and surface monitoring. Understanding of aseptic techniques and cleanroom practices. Knowledge of GMP regulations, quality control processes, and laboratory compliance standards. Proficiency in Microsoft Office applications, including Word, Excel, and PowerPoint. Strong verbal and written communication skills in English (minimum B1 level). Ability to work effectively in a collaborative and multicultural team environment. Comfortable working in a dynamic, fast-paced setting with changing priorities. Capable of gowning for cleanroom entry and lifting materials/equipment up to approximately 12 kg. Willingness to work an 18-week rotating shift schedule, including: Day shifts: 07:30/08:30 to 16:30/17:30 Evening shifts: 15:00 to 23:30

Core Responsibilities

Perform environmental monitoring in cleanroom manufacturing areas and conduct microbiological testing, including sterility testing and microbial plate reading. Manage and trend test data, maintain laboratory equipment and workspaces, and support GMP compliance, continuous improvement, and other quality control activities.

Requirements

A Level 3 MLO qualification or a bachelor's degree in microbiology or a related scientific discipline is preferred, along with 0–4 years of relevant laboratory or environmental monitoring experience. Candidates should have hands-on microbiology and cleanroom skills, knowledge of GMP and quality control, English proficiency at least at B1 level, and the ability to work rotating shifts and meet cleanroom physical requirements.

About SIRE® Life Sciences 🧬

Industry: Biotechnology Research

Company size: 201-500 employees

SIRE® Life Sciences is the market-leading partner for Life Sciences consultancy, project management, and secondment services in the Netherlands. We specialize in connecting expert consultants and project managers with leading biotech, pharmaceutical, medical device, clinical research, and food technology organizations. Our services include: - Life Sciences recruitment & executive search - Interim management & secondment - SOW-based project outsourcing & delivery - RPO (Recruitment Process Outsourcing) - MSP workforce management & vendor-neutral solutions - GMP, GCP, GLP compliance staffing - Clinical research & regulatory affairs resourcing With 100,000+ professionals in our network and 25+ years of experience, SIRE® Life Sciences delivers measurable results for regulated organizations across the Netherlands and Europe. We work with pharma, biotech, medical device, CDMO, CRO, and food technology companies at every stage of the product lifecycle. What sets us apart: - Deep domain expertise in Life Sciences & regulated industries - Full compliance with GxP, ISO, WAADI, and Dutch labour law - Flexible engagement models: permanent, interim, project (SOW), and managed services - Proven delivery track record across Pharma, Biotech, MedTech & Food Science Based in Leiden Bio Science Park, Netherlands. www.sire-search.com

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