Life Sciences Consultancy & Project Management in Netherlands🔒 SSL Verified

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"Whether you are a life sciences organisation looking to strengthen your project and consultancy capabilities or a specialist seeking new opportunities, SIRE Life Sciences provides the expertise, data, and network to make success inevitable. We connect specialist life sciences consultants with projects that drive discovery, production, and healthcare innovation across the Netherlands. that drive discovery, production, and healthcare innovation across the Netherlands. Join the companies and professionals shaping the future of biotechnology, pharmaceuticals, and medical innovation. Empowering Life Sciences through People, Projects, and Performance."

"The Company A leading international food production organization with operations across multiple locations and a strong focus on employee wellbeing, sustainable growth, and operational excellence. The company supports both manufacturing and office environments and offers a collaborative, people focused culture. About the Role As a Casemanager Verzuim, you will guide employees throughout their sickness absence and reintegration journey in accordance with Dutch legislation. You will act as the central point of contact for employees, managers, and site leaders, ensuring a smooth and compliant absence management process. This role combines operational case management with advisory responsibilities and continuous improvement initiatives aimed at reducing absenteeism and improving employee wellbeing. Responsibilities Manage employee sickness absence cases from the first day of absence Ensure compliance with the Wet Verbetering Poortwachter Conduct regular absence and reintegration meetings Translate occupational physician recommendations into actionable plans Advise employees, managers, and plant managers on absence related matters Support employees throughout reintegration processes Manage IVA and WIA application processes Contribute to absenteeism prevention strategies Participate in process improvement projects Travel regularly to multiple locations across Eastern Netherlands Requirements HBO…"

"Company Our client is a leading organisation in the pharmaceutical manufacturing sector. They operate in a highly regulated environment and are committed to delivering safe, high-quality products through strong quality standards, continuous improvement, and a culture where compliance and collaboration are key. Job Description We are looking for a Quality & Compliance Specialist to support day-to-day production by ensuring activities are performed in line with GMP requirements and internal quality standards. The role focuses on deviation support, investigations, CAPA follow-up, and strengthening documentation practices across manufacturing and packaging operations. Responsibilities – Support manufacturing and packaging teams with deviations and quality-related questions. – Assess deviations and advise whether production activities should be paused or stopped when needed. – Monitor production processes and identify deviations from established procedures. – Investigate and document deviations and complaints, ensuring clear, compliant records. – Perform and document root cause investigations and drive CAPA actions to closure. – Propose and support improvements to production methods, processes, and product quality. – Contribute to continuous improvement initiatives, including actions from internal/external audits. – Review and support updates to SOPs,…"

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