Senior Construction Project Manager, Bedum, GR

About the Company Our client is a global healthcare organization with a newly established lentiviral vector manufacturing facility in Sassenheim. The facility supports commercial production within a highly regulated GMP environment, with a strong focus on technical excellence, quality and continuous improvement. Role Description As Technical Operations Manager, you will lead a team of around 15 technical specialists supporting manufacturing operations. You will oversee technical improvements, equipment and single-use solutions, complex problem solving and cross-functional projects, while ensuring GMP, safety and quality requirements are met. Key Responsibilities Lead and develop the CoE team of technical specialists. Oversee technical changes and equipment and single-use improvement projects. Provide technical expertise and support the resolution of complex process issues. Partner with Operations, QA, QC, MSAT, IT and other functions on technical projects. Drive improvements focused on quality, cost, cycle time and capacity. Support new product and process implementation within manufacturing. Review and approve technical documentation and specifications. Monitor equipment performance, maintenance and recurring technical issues. Allocate resources to deliver projects within agreed timelines and budgets. Promote innovation, Lean and continuous improvement within the facility. Requirements 10+ years of experience in a pharmaceutical GMP production environment. 6+ years of people leadership experience at Supervisor or Manager level. Strong knowledge of GMP and pharmaceutical manufacturing processes. Proven experience delivering Lean projects, both technically and as a leader. Experience with technical projects involving equipment, materials or single-use systems. Knowledge of EHSS and regulatory requirements in a GMP environment. Strong leadership, decision-making and stakeholder management skills. Able to work effectively in a complex, cross-functional environment. Knowledge of JJOS methodology and systems is an advantage.

The Company Our client is one of the leads from the Biotechnology industry who try to improve patients’ lives, by distributing their medicines to hospital and pharmacies in 100 different countries in the world, to over 10 million patients, in Europe, Turkey, Middle East and Africa Regions. Job Description As a Quality Assurance Associate, you will be responsible for the sampling, inspection, review, and release of incoming materials and packaging components in a GMP-regulated pharmaceutical environment. You will ensure quality and compliance requirements are met while working closely with internal teams and suppliers to resolve quality-related issues. Responsibilities Conduct sampling, inspection, review, and approval of incoming materials, including printed and non-printed packaging components Ensure all incoming materials meet procedural and quality requirements for release Collect data and communicate with internal teams or suppliers to resolve issues or deviations Perform additional sampling and damage inspections on received components as needed Provide quality oversight during the receipt and inspection of components to maintain compliance and standards Requirements MBO, Bachelor’s, or Master’s degree in Life Sciences or a related field, or equivalent experience (minimum three years in Quality Assurance or Control) Familiarity with GMP and GDP principles and their practical application Proficiency in English, both written and verbal Experience working with digital systems such as ERP (SAP) is preferred Strong attention to detail, good communication skills, and ability to work collaboratively within a team Other Information Fully onsite in Breda 24 hours per week initially (3 days per week) Candidate can choose 2 of their working days Friday is mandatory, as this is the busiest day for incoming deliveries Working hours are generally around 08:30–17:00, with some flexibility Apply to our vacancy for more information. We look forward to hearing from you!

Company A leading organization in the life sciences and regulated manufacturing sector is expanding its technical operations team in the North of the Netherlands. The site is modern, highly regulated, and focused on keeping production and facility infrastructure safe, compliant, and reliably available. The environment is international and fast-paced, with a strong focus on quality, safety, and continuous improvement. Job Description For an on-site project in Groningen, we are looking for a Maintenance Engineer. This role focuses on supporting and improving site maintenance and facility engineering activities, ensuring technical availability, reliability, and compliance. The Maintenance Engineer works closely with local stakeholders to keep equipment and building services running smoothly and to resolve operational issues quickly and structurally. Responsibilities - Support day-to-day facilities and maintenance engineering activities on-site. - Coordinate and follow up on maintenance-related issues, prioritizing impact on operations, safety, and compliance. - Drive root-cause investigations for recurring breakdowns and propose sustainable improvements. - Align with internal stakeholders and external service providers to plan and execute maintenance work. - Support documentation, reporting, and process improvements linked to maintenance and facility performance. - Contribute to standardization and continuous improvement initiatives within the engineering/maintenance domain. - Communicate clearly with cross-functional teams in an international working environment. Requirements - Strong engineering background with experience in facilities and/or maintenance within an industrial environment. - Must be able to work full-time on-site in Groningen. - Excellent communication skills in English (mandatory) and Dutch (mandatory). - Hands-on mindset with strong problem-solving skills and stakeholder management. - Preference for candidates available as employees rather than freelancers (unless the fit is exceptional). Other Information The Maintenance Engineer is fully on-site in Groningen and requires strong communication skills in both English and Dutch. If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company A leading organization specializing in industrial infrastructure and capital expenditure projects. Known for its innovative approach and commitment to safety and quality, the company delivers complex construction initiatives across various sectors, including chemicals, pharmaceuticals, and other industrial environments. Role Description We are looking for an experienced Senior CAPEX Construction Project Manager to lead the on-site execution of industrial CAPEX projects. You will be responsible for coordinating contractors, managing site activities, and ensuring projects are delivered safely, on time, and within budget. Responsibilities - Lead on-site construction activities in line with project scope, schedule, budget, and quality standards. - Manage contractors, subcontractors, and vendors, ensuring compliance with safety and project requirements. - Coordinate with engineering, procurement, and operations teams to achieve project milestones. - Oversee site logistics, permits, inspections, and daily construction activities. - Monitor progress, manage risks, and resolve on-site issues. - Support mechanical completion, commissioning, and project handover. - Ensure compliance with health, safety, environmental, and quality requirements. - Maintain effective communication with project stakeholders and provide regular progress updates. Requirements - Bachelor’s degree in Civil Engineering, Mechanical Engineering, Construction Management, or a related field. - 5–10 years of experience managing industrial construction/CAPEX projects. - Experience in chemical, pharmaceutical, or other regulated industrial environments is preferred. - Proven experience managing contractors and construction sites. - Strong knowledge of construction methods, safety standards, and project controls. - Excellent leadership, communication, and stakeholder management skills. - Hands-on, results-oriented, and able to work independently. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company Our client is a fast-paced manufacturing organisation with multiple production sites and a strong focus on reliable supply and efficient operations. The planning team works closely with plant stakeholders to ensure customer demand is translated into a realistic, high-quality production plan. Job Description We are looking for a Central Supply Planning Specialist to provide interim support within a central planning team. The Central Supply Planning Specialist will own the weekly supply planning for several production sites and will translate demand into a practical production plan, balancing high customer service levels with efficient factory output. Responsibilities - Own the weekly planning cycle for multiple production plants (typically 3–5 sites). - Translate demand into weekly production plans and align these with plant capabilities and constraints. - Review prior-week production performance and convert learnings into updated weekly planning buckets. - Switch comfortably between short-term operational priorities and mid-term planning horizons (weeks up to roughly a year ahead). - Challenge and align with plant stakeholders to reach the best possible plan and drive clarity in decision-making. - Support continuous improvement in planning ways of working, reporting, and data  quality where needed. -  Temporary Full-Time Contract (4 Months) - (1-2 days Remote) Requirements - HBO degree, preferably in Supply Chain, Logistics, or Business Administration. - 1–5 years of relevant planning experience (junior to mid-level). - Strong data skills and Excel capability. - Comfortable communicating with and challenging stakeholders to reach the best supply plan. - Fluent in Dutch and English. - Experience with Slim4 (SlimStock) is a plus. Other Information The role is based on-site and requires close collaboration with the central planning team and plant contacts. If you are interested and want to apply, please submit your application via the apply button below and contact me.

About the Company: Our client is a leading pharmaceutical manufacturing company that produces high-quality medicines in a clean, modern, and highly regulated production environment. Safety, quality, teamwork, and continuous improvement are key priorities across the organisation. About the Role: We are looking for an Automated Production Technician to join a GMP-regulated manufacturing team. In this role, you will operate and monitor automated production equipment, help resolve technical issues, complete production documentation, and ensure products are manufactured safely and according to quality standards. You will work closely with colleagues from Production, Quality, Engineering, and Maintenance to keep the production process running smoothly and efficiently. Key Responsibilities: -Operate and monitor automated production equipment in accordance with GMP guidelines and standard operating procedures (SOPs). -Identify, troubleshoot, and report equipment or production issues. -Perform basic machine adjustments to support efficient production and minimise downtime. -Accurately record production data and activities in SAP and MES systems. -Monitor the manufacturing process and escalate deviations or quality concerns when required. -Complete production documentation, including batch records and production logs. -Support line setup, product changeovers, and shutdown activities. -Carry out routine cleaning and basic maintenance tasks according to procedures. -Work closely with Production, Quality, Engineering, and Maintenance teams to resolve operational issues. -Participate in shift handovers and communicate important production updates. -Contribute to process improvements that enhance safety, quality, and operational performance. -Maintain a clean, safe, and organised working environment always. Requirements: -Experience working in a manufacturing, production, or operations environment. -Experience operating automated machinery or production equipment. -Experience within a GMP-regulated environment is preferred, ideally within pharmaceuticals, -biotechnology, food, or another regulated industry. -Comfortable following procedures, work instructions, and documentation requirements. -Good technical aptitude and problem-solving skills. -Ability to work effectively within a team environment. -Good communication skills and a good command of English, both written and spoken. -Willingness to work shifts as required. -Familiarity with production documentation and GMP working practices. Other Information: If you are interested in this opportunity and your experience matches the requirements, please apply using the Apply button or contact me directly for a confidential discussion about the role.  

The company Our client is a leading international organisation operating in a highly regulated food and consumer products environment. The organisation has a strong focus on innovation, product safety, sustainability, and the development of packaging solutions for global markets. As part of the global packaging development function, you will work in an international and multidisciplinary environment, collaborating with teams across Research & Development, Regulatory Affairs, Quality Assurance, Procurement, and Supplier Quality Management. Role Description As a Packaging Regulatory & Compliance Specialist, you will be responsible for assessing packaging materials and ensuring compliance with applicable food-contact, packaging, and product safety regulations across international markets. You will provide regulatory and technical advice to internal stakeholders and external customers, review and manage packaging compliance documentation, and support the implementation of new regulatory requirements. The role offers the opportunity to contribute to packaging development projects, sustainability initiatives, and global compliance activities. Responsibilities • Review, assess, and finalise packaging compliance documentation, ensuring alignment with internal standards and applicable regulatory requirements. • Assess packaging materials for food-contact and regulatory compliance across different international markets. • Draft, review, and manage compliance documentation, including Declarations of Compliance and related supporting documentation. • Assess packaging requirements related to PFAS, heavy metals, and other relevant chemical and material compliance standards. • Verify that packaging materials meet applicable local and international regulations in the markets where products are sold. • Advise and support cross-functional stakeholders on packaging compliance, food-contact materials, and regulatory requirements. • Support the resolution of packaging compliance challenges within product and packaging development projects. • Respond to food safety and packaging compliance questions from internal stakeholders and external customers. • Maintain accurate packaging compliance data, specifications, and documentation within relevant systems. • Support the assessment and implementation of Packaging and Packaging Waste Regulation (PPWR) requirements, including compliance checks and related projects. • Collaborate with Regulatory Affairs, Quality, Procurement, Supplier Quality, R&D, and other international teams to ensure effective compliance management. • Participate in regular compliance team meetings and contribute to continuous improvement of packaging compliance processes and standards. Requirement • Bachelor's or Master's degree in Material Science, Chemistry, Packaging, Food Science, Food Technology, or a related discipline. • Approximately 5–7 years of relevant professional experience in packaging compliance, regulatory affairs, technical compliance, food-contact materials, or a similar field. • Strong experience with European packaging and food-contact compliance regulations. • Experience working with packaging materials in the food, food ingredients, food chemicals, or another highly regulated industry. • Knowledge of packaging and food-contact regulations, compliance assessments, and regulatory risk evaluation. • Experience with compliance documentation, including Declarations of Compliance, is highly relevant. • Familiarity with Packaging and Packaging Waste Regulation (PPWR) and related requirements. • Experience with specification management systems; knowledge of SAP PLM is an advantage. • Strong analytical skills with a high level of accuracy and attention to detail. • Proactive, hands-on approach with a strong sense of ownership and willingness to develop new knowledge and processes. • Excellent communication and presentation skills, with the ability to work effectively with both technical and non-technical stakeholders. • Comfortable working in international, cross-functional teams. • Fluent in English; knowledge of Dutch is not required. Other information Looking for a new opportunity in packaging compliance and regulatory affairs? This could be your next challenge! If you're interested, please click the below button to apply for the job.

Company Our client is a global, innovation-driven organisation in the food sector with an international R&D environment. The team works on developing and improving packaging materials and formats for diverse markets worldwide, with a strong focus on product quality, consumer safety, and compliance with evolving regulations. Job Description We are looking for a Packaging Compliance Specialist to support a global packaging team by ensuring packaging materials meet internal standards and regulatory requirements. The focus of this role is to review and finalise compliance documentation, advise stakeholders on food contact compliance topics, and help keep global compliance data accurate and up to date. Responsibilities - Review, assess, and finalise packaging compliance documentation in line with internal requirements and applicable regulations. - Evaluate packaging materials for compliance topics such as food contact requirements and market-specific rules. - Prepare, review, and manage compliance documentation, including Declarations of Compliance. - Support cross-functional stakeholders (e.g., Regulatory Affairs, Quality, Procurement, Supplier Quality) with compliance guidance during development projects. - Respond to packaging compliance and food safety-related questions from internal stakeholders and external customers. - Maintain and improve packaging compliance data and documentation to ensure accuracy and traceability. - Support the assessment and implementation of packaging regulatory changes (including Packaging and Packaging Waste Regulation-related requirements). - Participate in regular team meetings and contribute to continuous improvement of compliance processes. Requirements - Bachelor’s or Master’s degree in Material Science, Chemistry, Packaging, Food Science/Technology, or a related field. - Several years of relevant experience in food contact material regulation and packaging compliance. - Strong understanding of European packaging and food contact regulations and practical experience applying them. - Accurate, analytical, and proactive working style with strong ownership and attention to detail. - Strong communication and stakeholder management skills in an international environment. - Fluency in English. - Experience with specification management systems (preferably SAP PLM) is a plus. -Temporary Full-Time Contract (4 Months) Other Information The selection process typically includes an online interview. If you are interested and want to apply, please submit your application via the apply button below and contact me.

About the Company Join a global healthcare organization at a state-of-the-art manufacturing site in Leiden. As part of the Facilities team, you will play a key role in ensuring the reliability, safety, and compliance of facility infrastructure, utilities, and manufacturing support systems within a highly regulated GMP environment. Role Description As a Facilities Engineer, you will oversee the operation, maintenance, and continuous improvement of building services, utilities, and facility systems. Working closely with Engineering, Maintenance, EHS, Quality, and external contractors, you will ensure equipment reliability, regulatory compliance, and operational excellence while supporting site improvement projects. Key Responsibilities Coordinate the maintenance and operation of facility systems, utilities, and building infrastructure Ensure compliance with GMP, GxP, EHS, and quality standards Lead equipment reliability and preventive maintenance initiatives Support facility upgrades, maintenance projects, and infrastructure improvements Supervise contractors and monitor service quality, budgets, and project progress Identify operational risks and implement mitigation actions Drive continuous improvement initiatives focused on safety, reliability, and efficiency Support CAPA implementation, change controls, and regulatory compliance activities Monitor energy usage and contribute to sustainability and cost-saving initiatives Collaborate with cross-functional teams to support manufacturing operations Requirements 5+ years of experience in Facilities Engineering, Maintenance, or Technical Operations Experience within a GMP-regulated manufacturing environment (pharmaceutical, biotechnology, medical devices, or similar) Strong knowledge of facility utilities, maintenance systems, and infrastructure Experience with preventive maintenance, contractor management, and project coordination Good understanding of EHS, Quality Management Systems, and CAPA processes Strong troubleshooting and problem-solving skills Excellent communication and stakeholder management abilities Fluent in English

Company A leading financial institution in the Netherlands, operating in a highly regulated and complex environment. They invest heavily in building secure, resilient, and modern technology platforms to support critical banking services. Job Description We are seeking a Platform Services Architect to shape the future of the organization’s platform architecture. This role involves translating business needs, regulatory standards, and technology developments into clear, practical solutions. The focus is on designing and improving platform services across operating systems, storage, backup, disaster recovery, and cyber resilience, ensuring the infrastructure remains secure, scalable, and reliable. Responsibilities -Develop and maintain the architecture blueprint for platform services, ensuring it aligns with business goals and regulatory requirements. -Guide architectural decisions related to Linux, Windows, storage, backup, and recovery solutions. -Shape strategies for disaster recovery, cyber resilience, and data protection, balancing security and operational efficiency. -Collaborate closely with Solution Architects and cross-functional teams to ensure architectural -consistency and best practices. -Lead the development of technical roadmaps and communicate architectural vision to stakeholders across the organization. -Act as a trusted advisor for engineering, security, and senior management on complex infrastructure challenges. -Identify opportunities to standardize, improve, and modernize platform services for better efficiency and security. -Co-lead the Platform Services area alongside senior leaders and provide guidance to technical teams. Requirements -Master’s degree or equivalent professional experience in a relevant field. -Extensive experience working in complex IT infrastructure environments, with a focus on enterprise architecture. -Strong knowledge of Linux and Windows operating systems. -Deep understanding of storage, backup, disaster recovery, and cyber security strategies. -Experience with on-premise, cloud, and hybrid infrastructure environments. -Ability to communicate complex technical concepts effectively to both technical and non-technical audiences. -Experience working across multiple teams and stakeholders. -Collaborative and pragmatic approach to architecture and problem-solving. -Fluency in English and Dutch is essential. -Experience within regulated sectors, like financial services, is highly advantageous. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.