Life Sciences Consultancy & Project Management in Netherlands

The Company A global dairy ingredients manufacturer with more than a century of experience transforming milk and whey into high value nutritional products. The organization operates large scale production facilities and focuses on quality, sustainability, operational excellence, and supply chain innovation. Job description We are looking for a Logistics Specialist / Logistics Team Leader to support logistics operations and continuous improvement initiatives at a major manufacturing site in Borculo. This role combines people leadership, logistics optimization, project management, and operational support. You will lead a small dispatch team, drive process improvements, analyze logistics performance, and contribute to both strategic and day to day logistics activities. Responsibilities • Lead and support a team of 4 dispatch employees • Manage logistics improvement projects using DMAIC methodology • Represent the logistics department during daily operational meetings • Participate in site improvement and operational excellence initiatives • Monitor and report logistics KPIs on a monthly basis • Analyze and resolve complex logistics challenges • Drive improvements in safety, quality, sustainability, service, and cost performance • Collaborate with internal and external stakeholders across multiple disciplines…

The Company Our client is a global pharmaceutical organization specializing in specialty medicines and OTC products. The organization operates GMP-regulated manufacturing facilities and focuses on quality, patient safety, automation, and operational excellence. Role Description As a Quality Specialist, you will support GMP compliance and quality processes within a pharmaceutical manufacturing environment. You will work closely with Quality, Production, Engineering, and other teams to maintain high quality standards. Responsibilities – Manage and support deviations, CAPA, and change controls. – Support investigations and implement corrective actions. – Review quality and manufacturing documentation. – Support internal and external audits and inspections. – Monitor GMP compliance and quality performance. – Work with cross-functional teams to resolve quality issues. – Support continuous improvement and quality initiatives. – Promote a strong GMP and quality culture. Requirements – Bachelor’s degree in Life Sciences, Pharmacy, Chemistry, or a related field. – Experience in QA/QC within a GMP pharmaceutical environment. – Strong knowledge of GMP and quality systems. – Experience with deviations, CAPA, and change control. – Experience supporting audits and investigations. – Strong communication, documentation, and analytical skills.…

Company Our client is a large, international organization with multiple sites in the Netherlands. They operate in a dynamic environment where employee wellbeing, sustainable employability, and compliance are taken seriously. The culture is professional and collaborative, and the team values people who work independently, communicate openly, and take ownership. Job Description We are looking for a Absence Case Manager to guide employees and managers through the full sickness absence and reintegration process. The Registered Absence Case Manager is the central point of contact for absence-related questions and ensures that all actions are followed up carefully and in line with Dutch legislation. The role combines case ownership, stakeholder management, and practical follow-up across multiple locations. Responsibilities – Manage sickness absence cases from the first day of absence through reintegration, ensuring timely follow-up and clear documentation – Act as the main contact person for employees, line managers, and site management regarding absence and reintegration – Hold regular absence meetings and guide stakeholders through next steps and expected timelines – Translate occupational physician input into practical actions and clear agreements – Support applications…

Over het bedrijf Onze opdrachtgever is een grote internationale organisatie met medewerkers op verschillende locaties in Nederland. Binnen de organisatie is veel aandacht voor medewerkers, duurzame inzetbaarheid en professionele begeleiding bij verzuim en re-integratie. Functieomschrijving Als Casemanager Verzuim begeleid je medewerkers gedurende het volledige verzuim- en re-integratieproces volgens de Wet Verbetering Poortwachter. Je bent het centrale aanspreekpunt voor medewerkers, managers en plantmanagers en vertaalt adviezen van de bedrijfsarts naar duidelijke en concrete vervolgstappen. Je bent verantwoordelijk voor meerdere locaties in Oost-Nederland en werkt zowel zelfstandig als binnen een team van Casemanagers. Belangrijkste verantwoordelijkheden Begeleiden van medewerkers vanaf de eerste verzuimdag tot en met re-integratie Begeleiden van verzuimdossiers volgens de Wet Verbetering Poortwachter Voeren van regelmatige verzuim- en re-integratiegesprekken Vertalen van adviezen van de bedrijfsarts naar concrete acties Adviseren en ondersteunen van medewerkers, managers en plantmanagers Begeleiden van WIA- en IVA-aanvragen Signaleren van mogelijkheden om langdurig verzuim te voorkomen Bijdragen aan verbeterprojecten rondom verzuim Geven van inhoudelijk advies aan de organisatie Samenwerken met collega’s binnen het team van Casemanagers Vereisten HBO werk- en denkniveau Certificaat Geregistreerd Casemanager: CROV of RCCM/RCMC Minimaal…

The Company A global pharmaceutical manufacturing organization focused on delivering innovative healthcare products through highly regulated GMP facilities. The company invests in advanced engineering, quality, safety, and operational excellence. Job description The Facility Lead will manage facility engineering activities for a high potency secondary packaging project. The role involves overseeing facility design, construction, commissioning, and qualification while ensuring compliance with GMP, safety, and engineering standards. Responsibilities • Lead facility engineering activities for HVAC, utilities, fire protection, CSA, and building systems • Review and approve engineering designs, specifications, and vendor documentation • Coordinate engineering activities across project phases from design through handover • Support risk assessments, GMP reviews, and safety evaluations • Collaborate with operations, quality, EHS, contractors, and project teams • Support commissioning, qualification, and operational readiness activities • Resolve technical issues and manage project risks Requirements • Degree in Mechanical Engineering or related discipline • Experience in pharmaceutical, biotechnology, or GMP regulated environments • Strong knowledge of HVAC, utilities, and facility infrastructure systems • Experience with facility design, construction, and project execution • Understanding of commissioning and qualification activities…