Senior Product developer, Boxtel, Noord-Brabant

Company Our client operates in a complex, international industrial environment where high standards for safety, compliance, and operational excellence are essential. The organisation works with global suppliers, logistics partners, and internal stakeholders to ensure smooth product flows and reliable service to customers. Job Description The Customer Operations & Logistics Coordinator (SAP) is responsible for coordinating daily customer and supplier operations, ensuring that product movements are executed correctly and that all related administration is accurate and on time. This position is central to managing end-to-end processes across order-to-cash (OTC) and purchase-to-pay (P2P), working closely with supply chain, planning, sourcing, and finance teams. Responsibilities - Coordinate daily planning and execution in line with commercial agreements (term and spot), and align closely with internal and external stakeholders. - Organise loading and discharging activities and provide logistics partners with the correct instructions and documentation. - Manage operational follow-up with external terminals, including stock checks and alignment with business requirements. - Ensure timely, accurate handling of customer and vendor requests, enquiries, and complaints, following internal procedures. - Record all product movements accurately in SAP, including goods receipts/issues and checks for deviations. - Support invoice processing and align with finance/credit processes to ensure smooth transaction flow. - Support monthly closing activities by collecting data, validating figures, and coordinating updates required for accurate reporting. - Provide input and documentation for audits (internal and external) and ensure records are archived properly. - Act as back-up for other desks within the team and support cross-training/desk rotation to ensure continuity. Requirements - Fluent in English and German (both required). - Several years of experience in customer operations, customer service, supply chain operations, or logistics coordination. - Strong working knowledge of SAP and confidence working with data, documentation, and process compliance. - Able to prioritise in a high-volume environment and maintain accuracy under time pressure. - Comfortable working with multiple stakeholders in an international, multicultural setting. Temporary Full-Time Contract (5 Months) German and English Mandatory Other Information This is an on-site position in the Rotterdam area. The onboarding process may take longer than usual due to internal procedures, and candidates can only start once the process is fully confirmed. If you are interested and want to apply, please submit your application via the apply button below and contact me.  

The Company  A leading organization in the pharmaceutical and animal health sector, operating across multiple locations in the Netherlands. The company is known for its strong focus on safety, compliance, and innovation within engineering and production environments Role Description: We are seeking a highly experienced Senior Process Engineer to oversee the design, installation, and qualification of advanced manufacturing equipment for a major development project. This role focuses on ensuring the safe, compliant, and efficient operation of production facilities within the Beta Lactam formulation area at our client’s site in Boxmeer, the Netherlands. Responsibilities: -Lead the engineering design and coordination of complex manufacturing equipment, including formulation vessels, isolators, and auxiliary systems. -Act as a subject matter expert for the Beta Lactam formulation process, providing technical guidance throughout all project phases. -Oversee the installation, commissioning, and qualification activities, ensuring all systems meet quality and safety standards. -Collaborate closely with internal teams across disciplines such as automation, process, mechanical, and civil engineering, as well as external vendors and partners. -Support factory acceptance testing (FAT) at vendor locations and manage integration of equipment with existing and new systems. -Maintain strong relationships with project stakeholders, ensuring timely delivery and adherence to project scope. -Manage technical aspects of the project to facilitate a smooth handover and operational readiness. -Ensure all activities comply with GMP guidelines, including EU GMP Annex 1, EHEDG, and ISPE standards. Requirements: -Bachelor’s or Master’s degree in (Bio)Pharmaceutical, Process, Mechanical Engineering, or a related field. -Minimum of 5 years’ relevant experience in pharmaceutical, biotech, or high-tech capital projects. -Proven expertise in complex process engineering, equipment design, and GMP environments. -Experience with hygienic design, powder handling, and Beta Lactam manufacturing is preferred. -Strong knowledge of European GMP regulations and guidelines. -Excellent communication skills in English; Dutch language skills are a plus but not essential. -Willingness to travel to vendor sites and be on-site in Boxmeer at least three days a week; full-time presence expected during installation and commissioning phases. Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.

The Company: Our client is a global, research-driven pharmaceutical company dedicated to discovering, developing, and manufacturing innovative medicines, vaccines, and animal health products. With a strong focus on quality, regulatory compliance, and scientific innovation, the company operates state-of-the-art manufacturing facilities that produce sterile pharmaceutical products for patients worldwide.. Job Description: We are looking for a Process Validation Engineer to join the team in Boxmeer. This project-based role involves the validation of sterilization processes, specifically addressing issues with filtration systems used in the production of sterile medicines. The ideal candidate will investigate current filtration methods and implement modifications to meet strict sterilization requirements. Responsibilities: -Conduct thorough investigations into existing sterilization and filtration processes. -Modify and optimize filtration procedures to ensure compliance with GMP and sterilization standards. -Write and review validation protocols, reports, and statements documenting procedures and findings. -Collaborate with engineering and production teams to implement process improvements. -Ensure all validation activities align with regulatory and quality requirements. -Support the project from start to completion, which is estimated to last approximately 1 to 1.5 years. Requirements: -Minimum of 5–6 years’ experience in the pharmaceutical industry, with a focus on validation and process improvement. -Strong knowledge of GMP standards, sterilization, and filtration processes, with understanding of aqueous and oily solution chemistry. -Proven experience writing validation protocols, reports, and statements. -Fluent in English; basic Dutch language skills are a plus but not required. -Senior-level experience (P3), with the ability to work independently in a project environment. -On-site availability in Boxmeer; full-time (40 hours/week); maximum one day of remote work. 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 manufacturing organization committed to continuous improvement and operational excellence. They focus on integrating innovative solutions to enhance manufacturing processes and site performance. Job Description: We are seeking a highly skilled Site Deployment Lead to oversee the successful deployment of a new ERP system at multiple factory locations. The role is crucial in ensuring all deployment activities are coordinated smoothly, with a focus on timely delivery and stakeholder engagement at the Leeuwarden site. Responsibilities: •    Own the deployment readiness for the site, ensuring all activities are aligned and executed effectively. •    Coordinate local teams across various workstreams, including manufacturing, maintenance, quality, planning, and R&D. •    Lead testing, training sessions, and system cutover activities. •    Monitor project risks, issues, and dependencies, proactively addressing any challenges. •    Act as the primary point of contact for site teams and leadership regarding deployment activities. •    Collaborate closely with process owners, IT teams, external partners, and site leadership to ensure seamless implementation. •    Develop and embed work instructions, and facilitate process testing across departments. •    Influence and manage stakeholders, including plant management and production teams, to drive organizational change. Requirements: •    Minimum of 7 years’ experience in supply chain transformation, ERP deployment, or project management. •    Proven experience with SAP or similar large-scale business transformation projects. •    Manufacturing experience is preferred. •    Strong execution focus with a hands-on mentality. •    Excellent stakeholder management skills across different organizational levels. •    Capable of motivating teams and managing change effectively. •    Willingness to work on-site at the factory locations. Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me. This is an interim assignment, with an expected duration from September 2026 to May/June 2027, specifically at the Leeuwarden site, with potential for additional roles at other locations. Candidates must be comfortable engaging directly with production and logistics teams to ensure successful system implementation. 

About the Company Join a global leader in animal health, developing and manufacturing vaccines and pharmaceutical products for livestock, companion animals, and aquaculture worldwide. Within the Global Engineering Solutions (GES) organization, you will contribute to a major CAPEX project focused on expanding pharmaceutical manufacturing capabilities through the construction of a new state-of-the-art production facility. Role Description As a Senior Process Engineer, you will act as the technical owner for the Beta Lactam Formulation Area within Project BOND. You will oversee the integration, installation, commissioning, and qualification of complex formulation equipment, ensuring systems are delivered safely, compliantly, and ready for commercial manufacturing. This role requires a senior engineer who can independently manage a complex technical scope while coordinating multiple engineering disciplines, vendors, and project stakeholders. Key Responsibilities Act as the technical lead for the Beta Lactam Formulation Area throughout project execution Coordinate the installation, commissioning, qualification, and handover of complex process equipment Oversee formulation vessels, API powder handling isolators, downflow booths, and related process systems Collaborate with Automation, Mechanical, Process, CQV, Construction, and Site Engineering teams Work closely with equipment vendors and support Factory Acceptance Tests (FATs) Resolve technical challenges related to equipment integration and automation Ensure designs and installations comply with GMP, safety, and quality requirements Maintain project documentation, technical assessments, and engineering deliverables Support project planning, risk management, and technical decision-making throughout execution Requirements Minimum 5 years of experience in pharmaceutical, biotechnology, food, or high-tech capital projects Experience with complex process equipment, commissioning, qualification, and equipment integration Strong understanding of GMP regulations, EU GMP Annex 1, ISPE, and hygienic design principles Experience coordinating multidisciplinary engineering projects and external vendors Strong stakeholder management, planning, and communication skills Able to work independently, take ownership, and make technical decisions Fluent in English; Dutch is an advantage Willing to travel occasionally to vendor sites

Validation Analyst III (Engineering, P3) About the Company Our client is a global, research-driven pharmaceutical organization specializing in innovative medicines and vaccines. The Boxmeer site is one of the world's leading manufacturing and development locations for sterile veterinary vaccines, operating in a highly regulated GMP environment with a strong focus on quality, innovation, and continuous improvement. Role Overview We are looking for an experienced Validation Analyst III to support a critical sterilization validation project. You will investigate, validate, and optimize filtration processes used in sterile manufacturing, ensuring compliance with GMP and regulatory standards. Key Responsibilities Lead sterilization and filtration validation activities. Develop and execute validation protocols, reports, and technical documentation. Investigate and improve filtration processes. Ensure GMP compliance throughout validation activities. Collaborate with Engineering, Manufacturing, and Quality teams. Key Requirements Bachelor's or Master's degree in Engineering, Chemistry, Life Sciences, or a related field. Minimum 5–6 years of pharmaceutical validation experience. Strong knowledge of GMP and validation documentation. Experience with filtration and sterilization processes. Understanding of aqueous and oil-based solution chemistry. Fluent in English. If you're interested in this opportunity, click the application link below to apply. We look forward to reviewing your application.  

Company Our client is a large, international manufacturing organisation operating in a regulated, fast-paced environment. The site is part of a wider network of production locations and is currently preparing for a major digital transformation programme impacting core operational and support processes. Job Description For our client, we are looking for a SAP Implementation Lead (Manufacturing) who will take ownership of site deployment readiness for a major ERP transformation. This person will act as the single point of coordination on the plant site, aligning multiple departments and ensuring the organisation is prepared for testing, training, and cutover activities leading up to go-live. Responsibilities - Own overall deployment readiness for the site and keep activities on track across all local workstreams. - Coordinate local execution across functions such as production, maintenance, quality, planning, logistics, and finance. - Drive and support testing activities, ensuring the right people are involved and actions are followed up. - Coordinate training readiness, including alignment with key users and ensuring work instructions are prepared and embedded. - Manage and monitor risks, issues, and dependencies, escalating when needed and ensuring clear decision-making. - Act as the main local point of contact for deployment teams and external implementation partners. - Align site teams and leadership, motivating stakeholders and creating momentum for change and adoption. - Ensure smooth preparation and execution of cutover activities toward go-live. Requirements - Extensive experience in ERP deployment, supply chain transformation, or large-scale project delivery. - Strong exposure to SAP and/or ERP implementations, including go-live and cutover preparation. - Ability to coordinate across multiple departments and stakeholder levels, including shopfloor and site leadership. - Hands-on, execution-driven mindset with strong organisation and follow-up skills. - Experience in a manufacturing environment is strongly preferred. - Strong communication skills and the ability to influence people without direct reporting lines. - Willingness to work on-site to support high-quality execution and adoption. - Temporary Full-Time Contract for 9 Months -Open for Freelancer's Other Information The selection process will include interviews with the hiring team and site leadership. If you are interested and want to apply, please submit your application via the apply button below and contact me.

Over het Bedrijf Sluit je aan bij een innovatieve producent van hartige snacks en werk mee aan de ontwikkeling van de volgende generatie producten. Je komt terecht in een internationale organisatie waar innovatie, samenwerking en continue productontwikkeling centraal staan. Rolomschrijving Als Senior Product Developer ben je verantwoordelijk voor het zelfstandig leiden van innovatieprojecten, van concept tot succesvolle marktintroductie. Je vertaalt markttrends en nieuwe technologieën naar onderscheidende producten en werkt nauw samen met verschillende interne en externe stakeholders. Daarbij zorg je ervoor dat producten voldoen aan kwaliteitseisen, wet- en regelgeving, certificeringen en kostendoelstellingen. Belangrijkste Verantwoordelijkheden Leiden van productontwikkelingsprojecten van concept tot marktintroductie Signaleren van (internationale) trends en ontwikkelen van nieuwe productconcepten Ontwikkelen van nieuwe recepturen en optimaliseren van bestaande producten Verbeteren van productieprocessen en productiemethoden Uitvoeren en begeleiden van fabriekstesten en evalueren van resultaten Samenwerken met Productie, Sales, Quality, Finance en andere afdelingen Onderhouden van contacten met klanten en leveranciers voor innovatieprojecten Opstellen en beheren van productspecificaties, recepturen en technische documentatie Waarborgen dat producten voldoen aan wetgeving, kwaliteitsnormen, IFS-, Halal- en kosteneisen Vereisten HBO-opleiding Voedingsmiddelentechnologie of een vergelijkbare richting Minimaal 5 jaar ervaring als Product Developer binnen de voedingsmiddelenindustrie Ervaring met productontwikkeling en innovatieprojecten Kennis van kaas, kip of vlees(vervangers) is een pré Ervaring met een gestructureerde productontwikkelingsmethodiek, zoals Stage-Gate Sterke projectmanagement- en stakeholdermanagementvaardigheden Innovatief, proactief en ondernemend Uitstekende beheersing van de Nederlandse taal is verplicht, goede beheersing van Engels is een pré Ervaring met werken in een internationale, multidisciplinaire omgeving

About the Company A leading global biotechnology organization focused on developing and manufacturing innovative medicines for patients worldwide. Operating in a highly regulated GMP environment, the company continuously invests in advanced manufacturing technologies, engineering projects, and operational excellence to support its growing product portfolio. Role Description We are looking for a CQV Engineer to support commissioning, qualification, and validation activities within a GMP manufacturing environment. In this role, you will be responsible for developing validation documentation, leading testing activities, and ensuring that new and modified systems are implemented in compliance with internal quality standards and regulatory requirements. The position requires a hands-on validation professional with experience in secondary packaging systems and computerized systems validation. Key Responsibilities Develop and maintain CQV documentation, including plans, protocols, risk assessments, and summary reports. Lead commissioning, qualification, and validation activities for manufacturing systems. Support the implementation of technical solutions in accordance with validation requirements. Perform system risk assessments and requirement traceability activities. Execute and document testing activities within GMP environments. Provide validation guidance to project teams and stakeholders. Ensure compliance with internal procedures and regulatory requirements. Support project delivery from implementation through validation and handover. Requirements Bachelor's degree in Engineering or a related technical discipline. Minimum 3 years of experience in Commissioning, Qualification, and Validation within the pharmaceutical industry. Hands-on experience with secondary packaging equipment and processes. Experience with print and inspection systems such as Systech and Cognex. Strong knowledge of Computerized Systems Validation (CSV). Experience working within GMP-regulated environments. Strong technical writing and documentation skills. Excellent communication, problem-solving, and stakeholder management abilities.

Company A leading pharmaceutical manufacturing company dedicated to producing sterile medicines. The organization specializes in mixing antigens and oils in large vessels and is committed to maintaining the highest standards of quality and safety throughout its production processes. Job Description We are seeking a Senior Validation Specialist to support a key project focused on validating and improving sterilization processes. The successful candidate will play a crucial role in investigating filtration methods to ensure they meet stringent sterilization requirements, ultimately enhancing the safety and efficacy of the products. Responsibilities - Investigate existing filtration processes to identify issues with current filtration efficiency. - Modify and optimize the filtration procedures to meet sterilization standards. - Write detailed protocols, statements, and validation reports in compliance with GMP requirements. - Collaborate with multidisciplinary teams on-site to execute validation activities. - Ensure all documentation and processes align with industry and internal quality standards. - Contribute to the ongoing improvement of sterilization validation projects. Requirements - Minimum of 5–6 years’ experience in the pharmaceutical or biotech sector, particularly in validation or sterilization processes. - Proven ability to write protocols, validation statements, and technical reports. - Strong knowledge of GMP, as well as the chemistry of aqueous and oily solutions. - In-depth understanding of filtration processes used in sterile production. - Fluent in English; proficiency in Dutch is a plus but not required. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.