Product Development Specialist (Dairy), Wageningen, GE

The Company A leading global biotechnology organization, dedicated to developing and delivering innovative medicines to improve patient outcomes. Operating worldwide, the company combines science, technology, and quality-driven processes to ensure safe and effective clinical products.  Role Description We are seeking a dedicated and motivated Manufacturing Technician to join our client's production team. This role involves operating and maintaining production lines within a fast-paced pharmaceutical environment, ensuring that all processes adhere to strict GMP standards. The technician will collaborate closely with team members to meet production goals and uphold safety and quality standards. Responsibilities - Operate production lines in accordance with detailed operating procedures, ensuring products are manufactured safely and efficiently. - Communicate effectively with team members and line leads to achieve daily production targets. - Identify opportunities for process improvements and support initiatives to enhance efficiency and quality. - Escalate issues or deviations promptly to the line lead, maintaining clear and factual reporting. - Take ownership of assigned tasks and ensure all activities are completed accurately and on time. - Participate actively in shift handovers and ensure proper documentation of tasks and results. - Follow all training requirements and maintain up-to-date knowledge of production processes. Requirements -1+ years of experience in a manufacturing environment, preferably in GMP-regulated pharmaceutical or similar industries. - Strong understanding of standard operating procedures and productivity principles. - Good communication skills in English (verbal, reading, writing). - Able to work in a team-oriented, multicultural environment. - Flexibility to work in different shift patterns as needed. - MBO level (level 2) education or equivalent. Other Information Are you Interested? Click on Apply Now.

About the Company Our client is a global leader in healthcare innovation, dedicated to improving lives through advanced medical technologies and high-quality products. The organization fosters a collaborative, science-driven environment focused on quality, innovation, and continuous improvement. Role Description We are seeking an experienced Staff Scientist to lead microbiological quality and sterility assurance activities across product development and manufacturing operations. This role will provide technical expertise in sterilization validation, aseptic processing, contamination control, and regulatory compliance while partnering closely with Quality, R&D, Manufacturing, and Regulatory Affairs teams. Responsibilities - Support New Product Introductions (NPI), including validation activities, protocol/report writing, and regulatory alignment. - Lead sterilisation and aseptic processing validations for new products, manufacturing sites, and external partners. - Drive sterility assurance, contamination control, microbiology, and process improvement initiatives across the product lifecycle. - Support packaging, cleanroom, environmental monitoring, water systems, and manufacturing process validation activities. - Provide technical expertise for investigations, CAPAs, audits, regulatory inspections, and compliance programs. - Collaborate with R&D, Quality, Manufacturing, Regulatory Affairs, and external partners to ensure product quality and patient safety. - Support supplier qualification, change controls, business continuity planning, and long-term sterility assurance strategies. Requirements - Bachelor's degree in Microbiology, Biology, Engineering, or a related field (Master's/PhD preferred). - 8+ years of experience in the medical device or pharmaceutical industry within GMP/ISO-regulated environments. - Strong expertise in microbiology, sterility assurance, aseptic processing, and sterilisation validation. - Experience with sterilisation technologies including EO, Gamma, E-Beam, Heat, and Aseptic Processing. - Proven experience in investigations, CAPA management, audits, and regulatory compliance. - Excellent communication, stakeholder management, and problem-solving skills. - Proficiency in Microsoft Office and relevant analytical software. 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 the world’s largest and most broadly based healthcare company. Their aim is to improve access to a healthier lifestyle for everyone thanks to their research in different health areas including personal care products, MedTech and pharmaceutical products. Role Description The Staff Scientist MQSA (Microbiological Quality & Sterility Assurance) is a global subject matter expert responsible for driving sterility assurance and microbiological quality strategies across the product lifecycle. The role supports new product development, manufacturing, and regulatory compliance, with a focus on aseptic processing, sterilization, and contamination control.     Responsibilities Lead sterility assurance strategy for new product introductions and lifecycle management. Oversee validation and transfer of sterilization processes (e.g., EO, gamma, e-beam, moist/dry heat) and microbiological methods Support manufacturing sites and external partners through audits, supplier selection, and technical assessments. Ensure compliance with global regulations and support regulatory submissions and inspections. Drive contamination control strategies, environmental monitoring, and cleanroom and water system validation. Lead investigations, CAPAs, and continuous improvement initiatives related to sterility risks. Collaborate cross-functionally (R&D, Quality, Manufacturing) and provide technical training and guidance. Represent the organization in industry forums and stay current with evolving standards. Requirements Bachelor’s degree in Microbiology, Biology, Engineering, or related field (MSc/PhD preferred). Minimum 8 years of experience in medical device or pharmaceutical environments (GMP/ISO). Strong expertise in microbiology, sterilization validation, and environmental control. Experience with regulatory inspections, audits, and technical problem-solving. Strong stakeholder management and cross-functional collaboration skills. Ability to lead technical initiatives and influence globally. Excellent communication and organizational skills. Knowledge of global sterility assurance standards and practices. Proficiency in standard office and analytical tools. Other information Apply to our vacancy for more information. Looking forward to getting in touch!

About the Company Our client is a global leader in the medical technology industry, dedicated to developing innovative healthcare solutions that improve patient outcomes worldwide. Operating in a highly regulated environment, the organization combines scientific expertise, advanced manufacturing technologies, and rigorous quality standards to bring life-changing products to market. The company fosters a collaborative and international culture where innovation, compliance, and continuous improvement are central to its success. Role Description We are looking for an experienced Staff Scientist – Microbiological Quality & Sterility Assurance (MQSA) to provide technical leadership across microbiological quality, sterility assurance, aseptic processing, and sterilization programs within a global medical device environment. This role serves as a key subject matter expert supporting new product introductions, manufacturing operations, validation activities, regulatory compliance, and continuous improvement initiatives. Working across international sites and cross-functional teams, you will drive sterility assurance strategies throughout the product lifecycle while ensuring compliance with global regulatory and quality standards. Key Responsibilities Lead microbiological quality and sterility assurance activities for new product introductions, product lifecycle management, and manufacturing operations. Act as the technical SME for aseptic processing, sterilization validation, environmental monitoring, contamination control, and water systems. Support and approve validation activities, including sterilization, microbiological test methods, cleanroom, utility, and environmental qualification programs. Provide technical leadership during investigations, root cause analyses, CAPAs, audits, inspections, and regulatory submissions. Collaborate with R&D, Quality, Manufacturing, Regulatory Affairs, and external partners to ensure compliant and robust sterility assurance strategies. Assess and support contract manufacturers, sterilization providers, laboratories, suppliers, and manufacturing sites through audits and technical evaluations. Drive continuous improvement initiatives related to microbiological quality, contamination control, and sterilization processes. Represent the organization in industry forums, standards committees, and scientific networks related to sterility assurance and microbiological quality. Deliver training, mentoring, and technical coaching to strengthen microbiological and sterility assurance capabilities across the organization. Support global manufacturing sites through risk assessments, validation programs, regulatory inspections, and compliance activities. Requirements Bachelor’s degree in Microbiology, Biology, Engineering, or a related scientific discipline; MSc or PhD preferred. Minimum 8 years of experience within the medical device, pharmaceutical, or other highly regulated GMP/ISO environment. Extensive expertise in microbiology, sterility assurance, aseptic processing, and sterilization validation. Strong knowledge of sterilization technologies such as EO, gamma irradiation, electron beam, moist heat, dry heat, and aseptic processing. Experience with environmental monitoring, contamination control, cleanrooms, water systems, and microbiological testing. Proven experience leading investigations, CAPAs, risk assessments, and validation programs. Strong understanding of global regulatory requirements, GMP standards, ISO standards, and sterility assurance regulations. Excellent stakeholder management, communication, and influencing skills within international organizations. Ability to work effectively across R&D, Quality, Manufacturing, Regulatory Affairs, and external partners. Willingness to travel internationally and work onsite a minimum of three days per week.

Company Our client is a global food organisation with a strong focus on innovation, quality, and sustainable product development. With an international footprint and well-established brands, they invest heavily in R&D and work closely with production sites to bring new ideas to market at scale. Job Description For an innovation centre in Wageningen, we are looking for an R&D Product Development Specialist (Cheese & Dairy). This person will play a key role in developing and improving cheese products, acting as the link between commercial teams and factory implementation. The role involves hands-on development work, cross-functional stakeholder management, and coordinating trials from lab through to production. Responsibilities - Translate business and commercial needs into clear development plans for new products and product changes - Develop and implement technical solutions to maintain and improve the quality of existing products - Plan, set up, execute, and analyse development experiments in line with project goals and food safety standards - Coordinate product testing at lab, pilot, and production scale, including interpretation of results and writing clear reports - Present findings and recommendations to stakeholders and peers - Support scale-up and implementation in the operational environment, following applicable guidelines - Contribute to continuous improvement and value engineering initiatives where relevant - Build and maintain strong working relationships with internal teams (e.g., Marketing, Sales, Operations, Technology, QA) and external partners/suppliers Requirements: - Master’s degree in food technology, Food Science, (Bio)Chemistry, or Chemical Engineering (dairy-related background is a strong plus) - At least 2 years of experience in product development project work (preferably in cheese or dairy) - Experience working in the food industry, ideally with exposure to cheese technology - Strong communication skills in English (basic Dutch is a plus) - Able to work in a structured way and manage multiple stakeholders in a dynamic environment - Comfortable working partly on-site in Wageningen - Once or twice maximum per month a visit to other NL factory (this is going to be discussed with the HM)  - Temporary Full Time Contract. Other Information This role is based in Wageningen, with a hybrid working setup and occasional travel within the Netherlands depending on project needs. 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 global, innovation-driven organisation operating in a highly regulated life-sciences environment. At their modern site in the Netherlands, teams work across supply chain and operational activities to ensure medicines and critical materials are handled, checked, and released to the highest quality and compliance standards. Job Description We are looking for an Incoming Quality Assurance Associate to join the Incoming QA team in Breda. The Incoming Quality Assurance Associate is responsible for sampling, inspecting, reviewing, and releasing incoming materials before they can be used in labelling and packaging operations. This role is hands-on, detail-focused, and requires strong compliance awareness and clear communication with internal stakeholders and suppliers. Responsibilities - Ensure incoming materials meet all procedural and quality requirements prior to release. - Perform sampling, inspection, review, and release of incoming materials, including printed and non-printed packaging components. - Collect and document data accurately and in a timely manner. - Initiate follow-up with internal stakeholders and/or suppliers to resolve issues and support timely release. - Perform additional sampling and inspections when required. - Carry out damage inspections of received components when needed. - Provide quality oversight of the receiving process and support continuous compliance with site procedures. Requirements - MBO, Bachelor’s or Master’s degree in Life Sciences or a related field, or an equivalent combination of education and experience. - Basic to solid knowledge of GMP and/or GDP, with the ability to interpret and apply procedures in routine cases. - Strong attention to detail and good documentation/writing skills. - Confident communication skills and ability to collaborate with different stakeholders. - Comfortable working with digital systems; ERP/SAP experience is a plus. - Fluent in English (spoken and written). -  100% Onsite. Other Information This position is based in Breda and is performed on-site. If you are interested and want to apply, please submit your application via the apply button below and contact me.

The Company A global fast moving consumer goods organization operating a large scale international supply chain network. The company focuses on delivering high quality consumer products through advanced planning processes, strong operational execution, and continuous improvement across markets and manufacturing sites. Role Description This role focuses on short term supply and production planning within an integrated supply chain network. The position ensures product availability across markets within a zero to twelve week horizon while balancing service levels, inventory, cost, and product freshness. You will play a key role in managing supply demand imbalances, driving scenario planning, and collaborating across functions to maintain a robust and responsive supply network. Responsibilities - Maintain accurate production plans and communicate updates to factory schedulers. - Manage short term finished goods availability across assigned markets and product portfolio. - Handle supply and demand imbalances within the zero to twelve week horizon and drive corrective actions. - Collaborate with factories, markets, and suppliers to resolve exceptions and identify root causes. - Evaluate material constraints and communicate impact on production plans. - Escalate capacity or supply issues through planning forums and stakeholders. - Develop and assess production scenarios to resolve planning gaps. - Monitor service levels and inventory and ensure optimal stock allocation. - Track shipments, holds, and overdue elements for assigned products. - Rebalance inventory within the network to improve service and reduce waste. - Support decisions related to slow moving or non performing inventory. - Contribute to seasonal planning and new product introductions. - Drive continuous improvement initiatives using performance insights. - Analyze key metrics related to cost, cash, and customer service. - Ensure accuracy and governance of supply chain master data. Requirements - Minimum 3 years of experience in production planning or supply chain planning. - Strong analytical and problem solving skills. - Ability to manage complex supply and demand scenarios. - Experience with planning systems and data analysis tools. - Knowledge of inventory management and supply planning concepts. - Strong stakeholder management and communication skills. - Experience with performance metrics and continuous improvement. Other Information - Involves collaboration across international markets and manufacturing locations.

About the Company Our client is a leading international biopharmaceutical organization focused on developing, manufacturing, and delivering innovative therapies worldwide. Operating within a highly regulated GMP environment, the company places a strong emphasis on quality, compliance, and continuous improvement across its global supply chain and manufacturing operations. Role Description For the Incoming Quality Assurance team, we are looking for an Associate QA professional who will be responsible for ensuring the quality and compliance of incoming packaging materials before they are used in manufacturing and packaging operations. In this role, you will perform sampling, inspections, reviews, and release activities while working closely with internal stakeholders and suppliers to resolve quality-related issues. This is a hands-on quality position requiring strong attention to detail, GMP awareness, and the ability to operate effectively in a fast-paced supply chain environment. Key Responsibilities Perform sampling, inspection, review, and release activities for incoming packaging materials, including printed and non-printed components. Ensure all incoming materials meet established quality and procedural requirements before release. Provide QA oversight for incoming material receipt and inspection processes. Investigate and follow up on quality issues with internal departments and external suppliers. Conduct additional inspections and damage assessments when required. Support compliance with GMP and quality standards throughout the incoming materials process. Accurately document findings and maintain quality records within applicable systems. Collaborate with cross-functional teams to ensure timely resolution of material-related issues. Requirements MBO, Bachelor's, or Master's degree in Life Sciences or a related scientific field. Experience in Quality Assurance, Quality Control, or a related GMP-regulated environment. Knowledge of GMP and/or GDP regulations and their practical application. Experience working with ERP systems such as SAP. Strong attention to detail and quality-focused mindset. Ability to identify issues, escalate appropriately, and drive resolution. Effective communication skills and ability to collaborate with multiple stakeholders. Fluent in English, both written and spoken. Team-oriented, proactive, and solution-driven approach. Comfortable working within structured procedures and regulated environments

Company Our client  is known around the world for their chocolate bars, which are some of the most popular. Besides that, they are suppliers of multiple popular pet food brands, as well as several other trademarks. The factory in the Netherlands  currently has the biggest production volume of all the factories, besides being one of the biggest chocolate factories in the world.   Job Description As a Production Planning Specialist you will join our client’s team on a temporary basis. This role involves managing short-term production planning, ensuring optimal product availability, and collaborating across functions to resolve supply and demand issues during a period of parental leave.   Responsibilities •    Develop and maintain accurate production plans and communicate them effectively to factory schedulers. •    Manage finished goods availability within the assigned supply network, adjusting plans based on market needs and stock levels. •    Handle all short-term supply and demand exceptions (0-12 weeks), performing root cause analysis and implementing corrective actions. •    Collaborate with material planners and factory teams to address capacity shortages and material supply challenges. •    Evaluate the impact of material issues on the short-term production plan and escalate as needed. •    Run scenario planning and adjust production schedules to balance demand and supply constraints, including product expiry, inventory levels, and priorities. •    Monitor service levels and inventory health, executing replenishments and rebalancing stock across warehouses to improve customer service and reduce waste. •    Participate in decision-making for inventory movements and non-performing stock. •    Lead root cause analyses regarding supply issues, such as case fill rate and product availability, and develop preventative actions. •    Drive continuous improvement initiatives in planning processes and key performance metrics. •    Maintain accurate master data related to products, production, and supply network within systems. •    Provide backup support for fellow planners on leave or during busy periods.   Requirements •    Bachelor's or Master’s degree in Supply Chain or a related field. •    Minimum of 2 years of relevant supply chain planning experience. •    Fluent in English; Dutch language skills are a plus. •    Strong analytical skills, customer-focused approach, and adaptable to changing priorities. •    Availability to work 40 hours per week with at least 2 days onsite in Veghel, with Wednesdays mandatory onsite.   Other Information Apply to our vacancy for more information. Looking forward to getting in touch!