Customer Service Representative, Rotterdam, Zuid-Holland

The Company Our client is dairy cooperative with international presence, formed by dairy farmers in the Netherlands, Belgium and Germany. The company has a large product range including milk, yoghurts, baby and infant nutrition, cheese, butter and several locations in the Netherlands, serving global markets. Job Description As a Project Buyer for CAPEX projects, you will support sourcing and procurement activities across multiple projects and locations. This is a fast-paced interim role where you will manage tenders, suppliers, and stakeholders while ensuring projects are delivered on time, within budget, and according to business needs. Responsibilities Lead sourcing activities and supplier negotiations across multiple projects Manage tenders, supplier selection, and contract processes Handle multiple projects and priorities simultaneously Build strong relationships with suppliers and internal stakeholders Ensure alignment with internal processes and procurement guidelines Identify risks, opportunities, and potential cost savings Work closely with teams across different functions Requirements Degree in procurement, business, supply chain, engineering, or a related field 5+ years of project procurement experience, preferably within an international environment Experience managing projects, tenders, and supplier relationships Able to work independently and adapt quickly Strong communication and stakeholder management skills Fluent in English; additional languages are a plus Organised, proactive, and results-driven Other Information This is an interim position with hybrid working possibilities depending on business needs. If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company Overview: A global leader in biopharmaceuticals that develops innovative products to enhance animal health and wellbeing. With a strong focus on biological R&D, the company operates across multiple locations and employs thousands of professionals dedicated to improving lives through science and technology. Job Description: We are seeking a skilled Transfer Specialist to join the Quality Control team within our Animal Health division. This vital role involves managing the transfer of biological and analytical tests from R&D or other sites to our QC laboratories, ensuring high standards and timely execution. The successful candidate will play a key part in maintaining product quality and supporting ongoing quality improvements. Responsibilities: •    Serve as the expert on various biological and analytical test techniques. •    Manage and ensure the successful transfer of tests according to established transfer methodologies, including new R&D methods and existing tests from other sites. •    Lead or support transfer projects, ensuring they are completed within set timelines. •    Facilitate proper transfer of tests to QC laboratories for commercial batch release. •    Participate in or lead transfer-related activities, including development, implementation, and post-transfer testing. •    Act as the primary contact for deviations, changes, audits, training, and documentation, ensuring compliance with GMP procedures. •    Use Lean Six Sigma tools for problem-solving, process improvements, and continuous quality enhancement. Requirements: •    HBO level education in (micro)biology, analytical chemistry, or similar field. •    Minimum of 5 years’ experience in a biological QC laboratory, preferably within GMP or GLP environments. •    Proven expertise in transfer processes, data analysis, and root cause investigation. •    Experience with change management and project leadership is advantageous. •    Familiarity with SAP, LIMS, and electronic QC data systems. •    Certified Yellow Belt or experienced with Lean/Six Sigma methodologies is a plus. •    Accurate, proactive, and solution-oriented with strong communication skills in English and Dutch. Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company Overview: A leading organization in the pharmaceutical sector dedicated to delivering high-quality healthcare products globally. The company is committed to operational excellence and continuous improvement in its supply chain processes. Job Description: We are seeking a proactive and detail-oriented Supply Chain Coordinator to oversee the import and export activities related to pharmaceutical products. This role involves managing end-to-end shipments, ensuring compliance, and maintaining strong relationships with internal teams and external partners. Responsibilities: •    Coordinate the distribution of pharmaceutical products worldwide, ensuring timely and accurate delivery. •    Process daily supply orders in accordance with company policies. •    Handle export and import documentation to facilitate smooth international shipments. •    Book, track, and monitor shipments, proactively addressing potential issues. •    Resolve service and transportation challenges efficiently. •    Manage return processes, ensuring accurate and compliant handling. •    Collaborate with third-party logistics providers, vendors, and internal departments to optimize the supply chain. •    Maintain strong relationships with internal and external customers, including affiliates and distributors. •    Represent the supply chain team in cross-functional projects and initiatives. •    Identify opportunities for process improvements and contribute to ongoing KPI reporting. •    Stay updated on GMP/GDP regulations and relevant training. •    Review and recommend enhancements to Order-to-Cash policies and procedures. •    Support disaster recovery planning alongside Corporate Planning, Distribution, and Quality teams. •    Perform other duties as required to ensure efficient supply chain operations. Requirements: •    Bachelor’s or Master’s degree, coupled with at least 2 years of supply chain experience within a GMP or GDP regulated environment. •    Strong multitasking abilities and experience working with diverse, international teams. •    Comfortable with computer systems and ERP software. •    Excellent communication skills in English, both written and verbal. •    Customer-focused attitude with a commitment to quality. •    Knowledge of logistics and issue resolution in a supply chain context is preferred. •    Ability to prioritize tasks effectively and solve problems independently. 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 fast-growing European food company specializing in innovative frozen snacks. With a strong focus on quality, sustainability, and consumer trends, GoodLife Foods develops market-leading products enjoyed by customers across Europe Role Description We are seeking a proactive and detail-oriented Production Planning Coordinator to oversee and optimize production schedules. This temporary role involves managing the weekly production plan, ensuring operational efficiency, and aligning production activities with business goals. Responsibilities -Develop and manage the weekly production schedule, working within an 8-week horizon, with the first two weeks locked (“frozen”). -Collaborate closely with production teams to ensure plans are realistic, feasible, and aligned with capacity and staffing levels. -Translate demand and supply guidelines into actionable production plans. Monitor production progress throughout the week and adjust schedules as needed to address delays, disruptions, or changing priorities. -Communicate changes clearly to all relevant stakeholders, including production, logistics, and management. -Document current processes, define planning parameters such as capacity and lead times, and ensure transparency and repeatability of the planning procedures. Requirements -HBO level education, preferably in logistics, supply chain, or production planning. -Experience in a manufacturing environment is a plus. -Strong organizational and analytical skills. -Proficiency with ERP and planning systems, advanced Excel skills. -Logical, structured thinking with a business-oriented mindset. -Independent, proactive, with a passion for optimization. -Excellent communication skills to present insights and recommendations to stakeholders at various levels. 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 organization in the life sciences industry, recognized for delivering high-quality products through advanced manufacturing processes. The company offers a modern working environment with a strong focus on quality, safety, teamwork, and continuous improvement. Role Description We are looking for a Manufacturing Operator to join a production team in a regulated manufacturing environment. In this role, you will operate assembly, packaging and labeling equipment, monitor manufacturing processes, and help ensure products are packaged safely, efficiently, and in line with quality standards. Key Responsibilities Operate and monitor manufacturing equipment. Set up production lines and perform product changeovers. Troubleshoot basic equipment and process issues. Complete production records and required documentation. Follow GMP, safety, and quality procedures. Support routine cleaning and basic equipment maintenance. Work with the team to improve production performance. Requirements 3+ years of experience in a regulated manufacturing/production environment. Familiarity with GMP is a plus.  Technical qualification (MBO, VAPRO, or equivalent) is an advantage. Basic knowledge of SAP, MES, or similar manufacturing systems is a plus. Good communication and problem-solving skills. Fluent in English. Willing to work in a shift-based environment (3 or 5 shifts pattern)  Other Information If you're interested in this opportunity and would like to learn more, click Apply today. We look forward to discussing your experience and helping you take the next step in your career.

Company: A leading pharmaceutical organization dedicated to producing sterile medicines through advanced manufacturing processes. The company specialises in mixing antigens and oils in large-scale vessels, ensuring the highest standards of product safety and quality. Job Description: We are seeking an experienced Senior Validation Specialist to join the team in Boxmeer. This role is focused on the validation of sterilization processes, specifically investigating and improving filtration methods to ensure compliance with sterilization requirements. This is a project-based position with an emphasis on process enhancement and quality assurance. Responsibilities: -Lead the validation of sterilization processes, focusing on filtration methods. -Investigate existing filters and filtration procedures to identify deficiencies and develop improvements. -Modify filtration processes to meet strict sterilization standards. -Write protocols, validation statements, and detailed reports in accordance with GMP guidelines. -Collaborate with cross-functional teams to ensure process compliance and effectiveness. -Document validation activities thoroughly and clearly. Requirements: -Minimum of 5–6 years’ experience in the pharmaceutical industry, particularly in process validation and sterilization. -Strong knowledge of GMP regulations, filtration processes, and the chemistry of aqueous and oily solutions. -Proven experience in drafting protocols, reports, and validation documentation. -Fluent in English; knowledge of Dutch is beneficial but not essential. Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.  

Company Overview A leading international organization specializing in cutting-edge innovation in healthcare and consumer technology. The company provides advanced solutions across medical devices, digital health, and consumer products, operating globally and committed to improving lives through breakthrough innovations. Role Description We are seeking a highly experienced Senior Innovation Program Manager to lead large-scale, cross-business innovation initiatives. This role involves managing complex projects that span hardware, software, AI, regulatory, and supply chain domains. The successful candidate will drive innovative, AI-enabled medical and consumer health solutions from concept through to market launch, ensuring alignment with strategic goals and regulatory requirements. Responsibilities - Lead large, multi-business innovation programs, ensuring successful end-to-end delivery of new platforms and products. - Transform customer, clinical, and consumer insights into innovative solutions, architecture decisions, and value creation strategies. - Oversee the entire innovation lifecycle, including concept development, validation, verification, regulatory readiness, industrialization, and deployment. - Maximize value across multiple Philips businesses by promoting platform thinking and reusable solutions. - Manage program scope, budget, schedule, quality, and risks, ensuring adherence to corporate standards and medical regulations such as FDA, MDR, ISO 13485, ISO 14971, and IEC 62304. - Coordinate cross-disciplinary teams including R&D, Data Science/AI, Design, Supply Chain, Regulatory, and Manufacturing. - Facilitate program governance through steering committees and stakeholder engagement, ensuring clear decision-making. - Integrate AI/ML technologies into products and management workflows, applying system engineering principles across hardware, embedded software, cloud services, and systems. - Ensure cybersecurity, data governance, interoperability, and clinical/consumer workflow integration. - Build strategic external relationships with partners, suppliers, academic institutions, and industry forums. - Lead and develop multidisciplinary teams across diverse locations, fostering a high-performance, collaborative culture. - Contribute to continuous process improvements, tooling, reporting, and capability development within the organization. Requirements - Master’s degree in engineering, technology, biomedical, systems engineering, or related field. - Over 10 years of experience leading complex, multi-site innovation or product development programs. - Proven successful track record in bringing medical devices, digital/AI solutions, or consumer health products from concept to market. - Experience with AI/ML-driven products and leveraging AI tools in program management. - Strong leadership, strategic thinking, and stakeholder management skills. - Project management certifications such as PMP, IPMA, SAFe are highly preferred. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.  

About the Company Join an innovative food manufacturer specializing in savory snacks and contribute to the development of the next generation of products. You'll become part of an international organization where innovation, collaboration, and continuous product development are at the heart of everything they do. Role Description As a Senior Product Developer, you will take the lead on innovation projects from concept through to successful product launch. You will translate consumer trends and new technologies into innovative food products while working closely with cross-functional teams and external partners. You will also ensure products meet quality standards, regulatory requirements, certifications, and cost objectives. Key Responsibilities Lead new product development projects from concept to commercial launch. Identify market trends and develop innovative product concepts. Create new recipes and improve existing products. Optimize production processes and manufacturing methods. Plan and support factory trials, analyzing results and implementing improvements. Collaborate closely with Production, Quality, Sales, Finance, and other internal teams. Build strong relationships with customers and suppliers throughout development projects. Prepare and maintain product specifications, recipes, and technical documentation. Ensure products comply with food safety regulations, quality standards, certifications (such as IFS and Halal), and cost targets. Requirements Bachelor's degree in Food Technology or a related field. At least 5 years of experience in Product Development within the food industry. Proven experience leading product development and innovation projects. Knowledge of cheese, poultry, meat, or meat alternatives is an advantage. Experience with structured product development methodologies, such as Stage-Gate. Strong project management and stakeholder management skills. Innovative, proactive, and results-driven mindset. Fluent Dutch is mandatory; good English communication skills are an advantage. Experience working in an international, cross-functional environment. Other Information Apply to our vacancy for more information. We look forward to hearing from you!

Company Overview Our client is a leading manufacturing organization focused on creating sustainable solutions that improve lives around the world. They prioritize safety and innovation, fostering a work environment that values continuous improvement and teamwork. Job Description We are seeking a dedicated Warehouse Operations Supervisor to oversee the storage and logistics processes at their Dordrecht location. This role involves leading a team responsible for managing materials, ensuring safety standards, and enhancing operational efficiency within the warehouse and support facilities. Responsibilities -Lead and support the team responsible for managing Maintenance, Repair, and Operations (MRO) goods, including inspection, storage, and issuing of materials in accordance with safety and operational standards. -Oversee the processes of kitting and staging materials, preparing shipments according to work orders. -Supervise safety equipment management, including inspection, repair, cleaning of safety apparel, filling air cylinders, and maintaining emergency mask sets. -Manage facility services such as handling internal and external mail, photocopying, and external printing services. -Ensure all activities adhere to safety procedures and company standards, conducting regular checks and audits. -Drive continuous process improvements to optimize team effectiveness and operational workflows. -coach and develop individual team members, managing performance, attendance, training, and behavior to foster growth. -Oversee HR-related tasks for the team, including absence management, scheduling, training, and performance reviews, supporting each member’s development. Requirements -Standard of HBO-level education or demonstrable ability to perform at this level. -Strong leadership skills with the ability to assess and improve individual and team performance. -Knowledge of continuous improvement methodologies, LEAN techniques, and data analysis using KPIs and graphs. -Excellent communication skills and a proactive, safety-oriented mindset. -Ability to work effectively under pressure and handle multiple priorities. 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 technology and innovation driven organization focused on advancing healthcare, digital solutions, and consumer products. The company operates across multiple international markets and brings together expertise in engineering, artificial intelligence, product development, and regulatory excellence to deliver impactful solutions. Role description The Senior Innovation Project Manager leads strategic and highly complex innovation programs from concept through market launch. This role drives the development of advanced medical devices, digital health platforms, AI enabled solutions, and consumer technologies while coordinating cross functional teams across multiple locations. The position combines strategic leadership with hands on program execution in a highly regulated environment. Responsibilities - Lead large scale innovation programs across multiple business units and functions - Drive end to end product realization from concept development through launch and lifecycle management - Define program scope, architecture, value creation strategies, timelines, budgets, and risk management plans - Coordinate teams across engineering, software, artificial intelligence, design, regulatory affairs, manufacturing, and supply chain - Ensure compliance with quality systems, product safety requirements, and global regulatory standards - Oversee program governance activities, executive reporting, and stakeholder alignment - Integrate AI and machine learning capabilities into products and development processes - Apply systems engineering principles across hardware, software, cloud, and connected technologies - Support cybersecurity, interoperability, and data governance requirements - Build relationships with external partners, universities, suppliers, and industry collaborators - Monitor market trends, emerging technologies, and competitive developments - Mentor multidisciplinary teams and contribute to organizational capability improvements Requirements - Master's degree in Engineering, Technology, Computer Science, Biomedical Engineering, Systems Engineering, or a related field - Minimum 10 years of experience managing complex multidisciplinary product development or innovation programs - Proven track record of bringing medical devices, digital health solutions, AI powered products, or consumer technologies to market - Experience working with development, supply chain, manufacturing, and regulatory teams - Strong understanding of medical device regulations and standards - Experience with AI and machine learning enabled products or AI driven project management practices - Expert project and program management skills - PMP, IPMA, SAFe, or equivalent certification - Strong stakeholder management and executive communication skills - Ability to lead global cross functional teams in complex environments Other Information Ready to lead breakthrough healthcare and AI innovations? Apply now and help shape the future of technology.