Technical Operations Manager, Leiden, Zuid-Holland

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 Overview We are working with a leading organization that specializes in managing complex industrial construction projects. This company is committed to safety, quality, and delivering projects on time and within scope, supporting various sectors including chemical and pharmaceutical industries. Job Description We are seeking an experienced Senior Construction Project Manager to oversee and lead the on-site execution of CAPEX construction projects. The successful candidate will be responsible for ensuring that projects are completed safely, on schedule, and within budget, while coordinating closely with all stakeholders involved. Responsibilities -Lead the on-site construction activities for CAPEX projects, ensuring proper execution according to scope, schedule, and budget. -Manage contractors, subcontractors, and vendors, ensuring compliance with safety, quality standards, and project specifications. -Collaborate with engineering, procurement, and operational teams to meet project milestones and resolve technical issues. -Oversee site logistics, permits, inspections, and quality assurance processes. -Continuously monitor progress, report risks and performance metrics to stakeholders, and adjust plans as necessary. -Support mechanical completion, commissioning, and handover to operations. -Ensure all work complies with environmental, health, and safety regulations, as well as company policies. -Coordinate stakeholder communication, work permits, and daily site meetings, acting independently and confidently while escalating issues when needed. Requirements -Bachelor’s degree in civil engineering, Mechanical Engineering, Construction Management, or related field (or equivalent experience). -Minimum of 5 to 10 years' experience managing industrial construction CAPEX projects. -Proven track record of safely delivering projects on time and within scope. -Strong contractor management and site organization skills. -Knowledge of construction methods, safety regulations, and project controls. -Excellent leadership, coordination, and communication skills. -Ability to work independently and handle multiple stakeholders effectively. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.  

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: A leading organization in the manufacturing sector, dedicated to delivering high-quality products to its customers. The company values efficiency, innovation, and a data-driven approach to supply chain management. Job Description: We are seeking a proactive and detail-oriented Supply chain Coordinator to join our client's team on an interim basis. The successful candidate will oversee the weekly production planning for multiple manufacturing plants, ensuring a seamless balance between customer service and operational efficiency. Responsibilities: - Manage the weekly planning process for 3–5 manufacturing plants - Translate customer demand into actionable production plans - Evaluate last week’s production results to inform future scheduling - Develop weekly production schedules covering several weeks to up to a year ahead - Switch between short-term and mid-term planning as needed to optimize factory output - Collaborate directly with plant contacts, challenging assumptions when necessary to improve supply plans - Ensure production aligns with demand, balancing service levels with manufacturing efficiency Requirements: - Strong data skills and proficiency in Excel, experience with Slim4 or SlimStock is a plus - HBO degree in Supply Chain, Logistics, Business Administration, or related field - 1 to 5 years of relevant experience in supply chain planning or logistics Critical thinking skills, confident in debating and challenging production assumptions - Fluency in Dutch and English Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.

The Company A global organization operating within the pharmaceutical and life sciences sector, focused on developing and manufacturing innovative therapies for patients worldwide. The company operates in a highly regulated environment and is committed to digital transformation, quality excellence, and continuous process improvement across laboratory operations. About the Role We are seeking an experienced Paperless Lab Design Lead to support the deployment, optimization, and maintenance of digital laboratory systems within an Advanced Therapies Quality Control environment in Leiden, Netherlands. This role serves as the subject matter expert for paperless laboratory initiatives, driving method digitalization, standardization, and harmonization while working closely with laboratory SMEs, quality teams, and system stakeholders. Responsibilities -Drive harmonization activities and convert paper based laboratory methods into digital workflows -Create, configure, and maintain method execution templates within the LIMS platform -Support change control impact assessments when required -Contribute to the design and management of master data used in digital laboratory methods -Coordinate master data validation activities -Create and update technical documentation following standardization processes -Manage enhancements and modifications to existing digital methods -Deliver training and support to laboratory personnel on newly deployed digital methods -Serve as the primary contact for laboratory system related questions -Assist with setup, testing, and validation of LIMS instrument interfaces Requirements -Bachelor’s degree in chemical sciences, Life Sciences, or a related scientific discipline -Advanced degree preferred -Minimum 5 years of experience in Quality Assurance, Quality Control, Analytical Testing, IT, or related    functions -Experience in pharmaceutical manufacturing, advanced therapies, or another highly regulated industry -Knowledge of laboratory testing techniques is preferred -Hands on experience with LIMS platforms, preferably Lab Vantage -Experience as a key user, business administrator, or system owner for digital laboratory systems -Understanding laboratory instrument integration with LIMS is an advantage -Experience participating in process improvement projects -Strong communication, stakeholder management, and presentation skills Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.  

Location : Breda, North Brabant, Netherlands (On-site) / 3-5 Shift pattern About the Company Our client is a global biotechnology company dedicated to improving the lives of patients through innovative medicines. Their Breda site is an international manufacturing and supply chain hub where products are packaged, labeled, assembled, and prepared for distribution to patients around the world. Working in a modern GMP-regulated production environment, you'll become part of a diverse team focused on quality, safety, continuous improvement, and operational excellence. Whether you're starting your manufacturing career or already have extensive technical experience, there are opportunities to grow and develop within the organization. About the Role We are recruiting Production / Technical Operator for the manufacturing team in Breda. Depending on your experience and technical background, you will work on manual, semi-automated, or fully automated production lines. You'll help ensure production runs safely, efficiently, and according to strict quality standards. Some positions focus primarily on manual packaging and production activities, while others involve operating equipment, troubleshooting technical issues, and improving production processes. Responsibilities   Execute production and packaging activities according to established procedures. Prepare production lines, perform set-ups, changeovers, and cleaning activities. Supply materials and support smooth production flow. Monitor product quality and report deviations when necessary. Complete production documentation accurately and in compliance with GMP requirements. Operate and monitor production equipment, depending on the role. Troubleshoot production issues and support continuous improvement initiatives where applicable. Maintain a safe, clean, and organized working environment. Collaborate closely with colleagues from production, maintenance, and quality departments. Qualifications   Experience in a production, manufacturing, logistics, packaging, or technical environment. Good command of English. Comfortable working according to procedures and quality standards. Reliable, accurate, and safety-conscious with strong attention to detail. Willingness to work in a shift system (2, 3, and 5 shifts). Technical affinity is an advantage for operators working with automated production lines. Experience in a GMP or other highly regulated environment is beneficial but not essential. Candidates from industries such as food, automotive, electronics, or high-tech manufacturing are also encouraged to apply if they have strong technical skills and a structured way of working. Required Skills   Experience in a production, manufacturing, logistics, packaging, or technical environment. Good command of English. Comfortable working according to procedures and quality standards. Reliable, accurate, and safety-conscious with strong attention to detail. Willingness to work in a shift system (2, 3, and 5 shifts). Technical affinity is an advantage for operators working with automated production lines. Preferred Skills   Experience in a GMP or other highly regulated environment is beneficial but not essential. Candidates from industries such as food, automotive, electronics, or high-tech manufacturing are also encouraged to apply if they have strong technical skills and a structured way of working.