SIRE® Life Sciences 🧬 logo

Laboratory Manager

SIRE® Life Sciences 🧬

Utrecht
Temporary
5-10 years experience
On-site

Key Skills

Chemical Inventory Management
Chemical Data Validation
Safety Data Sheet Administration
ChemWatch
LabVantage
CMR/ZZS Substance Management
ADR Compliance
PGS 15 Compliance
Chemical Storage Compliance
Chemical Compatibility Assessment
Chemical Segregation
UN Labeling
Audit and Corrective Action
SOP and Documentation Management
Stakeholder Management
Project Handover

Job Description

The Chemical Safety & Compliance Consultant will provide temporary support to the Lab Safety Manager in strengthening chemical inventory processes, chemical information management systems, and storage compliance. The role focuses on ensuring the accuracy of chemical data, optimizing chemical management platforms, improving access to safety information, and enhancing compliance with applicable regulatory requirements, including ADR and PGS 15. The consultant will work closely with laboratory, safety, facility, operational, and technical stakeholders to implement improvements and ensure sustainable handover of processes and controls. Responsibilities Review and validate the current CMR/ZZS chemical inventory, resolving data integrity and upload issues within LabVantage. Maintain and optimize the ChemWatch database, including chemical records, Safety Data Sheet (SDS) links, system structure, and ongoing maintenance procedures. Develop and implement clear standards for chemical data management, including ownership, governance, and maintenance responsibilities. Enhance emergency access to SDS documentation for laboratory personnel, emergency response teams (BHV), and external emergency services. Evaluate chemical storage areas to ensure compliance with requirements related to chemical compatibility, segregation, storage limits, and labeling. Support remediation of audit observations and strengthen ADR/UN labeling and compliance controls. Establish routine inspection programs and annual chemical inventory clean-up processes. Update relevant SOPs, controlled documentation, templates, and training materials to reflect improved practices. Coordinate implementation activities with key stakeholders and ensure effective knowledge transfer and project handover upon completion. Requirements Bachelor's or Master's degree in Chemistry, Laboratory Sciences, Environmental Health & Safety, or a related scientific discipline. Qualification as an Occupational Hygienist (Arbeidshygiënist), Higher Safety Professional (HVK), or an equivalent internationally recognized certification is highly preferred. Strong expertise in chemical inventory management, SDS administration, CMR/ZZS substances, and chemical classification systems. Solid understanding of ADR, PGS 15, chemical storage requirements, compatibility assessments, segregation principles, and labeling standards. Demonstrated experience conducting data validation, compliance reviews, audits, and corrective action implementation. Capable of working independently and managing priorities effectively within established timelines. Strong stakeholder management, collaboration, and communication skills, with experience engaging laboratory users, EHS functions, Facilities, Lab Operations, IT teams, system owners, and external suppliers. Excellent written and verbal communication skills in English, with Dutch language proficiency required.

Core Responsibilities

Review and improve chemical inventory data and management systems, maintain chemical records and SDS access, and strengthen compliance with storage, labeling, ADR, and PGS 15 requirements. Establish inspection and inventory-cleanup processes, update controlled documentation and training materials, coordinate implementation with stakeholders, and ensure effective knowledge transfer.

Requirements

A bachelor's or master's degree in chemistry, laboratory sciences, environmental health and safety, or a related scientific discipline is required; an occupational hygiene or higher safety professional qualification is highly preferred. Candidates should have strong chemical inventory, SDS, CMR/ZZS, ADR, and PGS 15 expertise, experience with audits and corrective actions, and effective stakeholder and communication skills; Dutch proficiency is required.

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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