Data Governance & Risk Manager, amsterdam, Noord-Holland

Company A leading global biotechnology organization dedicated to discovering, developing, and delivering innovative medicines for patients with serious illnesses. Driven by science and powered by advanced technology, the organization focuses on areas such as oncology, cardiovascular disease, inflammation, and rare diseases. Its mission is centered on improving lives by turning cutting-edge science into meaningful therapies that address unmet medical needs. Role summary We are looking for a Product Lifecycle Manager to lead and coordinate end-to-end product launches, variations, and ongoing lifecycle activities at site level. The role combines project management, cross-functional stakeholder alignment, and operational discipline to ensure changes are implemented compliantly, on time, and with clear visibility across the organization. Key responsibilities •    Translate launch and lifecycle strategies into clear supply chain objectives, action plans, and timelines for assigned product groups. •    Own and maintain the end-to-end project plan, aligning inputs from regional and site stakeholders. •    Lead and manage the Change Control process to ensure launch and variation activities are delivered right first time and in line with internal procedures and guidance. •    Track milestones, manage dependencies, and drive adherence to agreed timelines; escalate risks and issues as needed. •    Facilitate Product Lifecycle Team meetings and lead project management meetings with relevant functions. •    Coordinate planning and implementation across key stakeholders including Quality, Regulatory, Production and Site Planning, Artwork, Warehouse, Customer Service, and Procurement. •    Provide status updates, reports, and metrics on launch execution, variation implementation, and site readiness. •    Identify opportunities lead improvement initiatives, embedding best practices across stakeholders. •    Support regional leads and senior stakeholders with project charters, workshops, and structured project delivery. Requirements •    Degree-level education (Bachelor’s or higher) or equivalent experience. •    Proven project management experience within supply chain, operations, or a related environment, in the biotech or pharma industry. •    Strong analytical and problem-solving skills with the ability to manage complex, cross-functional work. •    Strong stakeholder management and communication skills. •    Pharmaceutical industry experience preferred. Other information This is a hybrid position with one mandatory on-site day per week in Breda (Tuesdays). If you are interested and want to apply, please submit your application via the apply button and contact me.

Company  A global leader in animal health, committed to improving the wellbeing of animals, food safety, and sustainability. The organization develops and manufactures innovative medicines and vaccines for farm and companion animals, operating within a high-tech, biotechnological environment. Their site in Boxmeer forms part of an international network, producing essential veterinary products for the worldwide market, with a strong focus on quality, safety, and continuous improvement. Job Description: We are looking for a dedicated Bioprocess Technician to join our production team in Boxmeer. In this role, you will be a key contributor to the manufacturing of inactivated antigens for vaccines, working within a fast-paced, high-precision biotechnology environment. Your responsibilities will include supporting the production process, ensuring compliance with GMP and safety standards, and participating in process improvements to enhance efficiency and quality. Responsibilities: - Prepare and plan production activities for each manufacturing week, including media preparation. - Independently execute production tasks such as cell culture, virus propagation, inactivation, fermentation control, centrifugation, filtration, and handling of bioreactors and vessels. - Record all procedures accurately and complete batch documentation following strict protocols. - Identify, report, and document deviations or irregularities in the production process. - Evaluate the product quality and process methods, suggesting improvements where appropriate. - Support project teams in process optimization and participate in continuous improvement initiatives. - Maintain technical knowledge related to valve controls and replacement parts, and train colleagues when necessary. - Contribute to deviating process management by thoroughly documenting deviations and supporting root cause analysis. - Work primarily day shifts but may be required to participate in on-call, weekend, or shift work as needed in the future. Requirements: - Completed MBO-3 or MBO-4 level education, preferably in Biotechnology, Process Technology, or a related field. - Experience in a pharmaceutical or biotech production environment is preferred, but recent graduates are encouraged to apply. - Familiarity with aseptic techniques and working in controlled environments such as cleanrooms is advantageous. - Interest or affinity for virology, microbiology, and bioprocess technology, with willingness to undergo training. - Strong focus on quality and safety, with good communication skills in Dutch and English. - Ability to work under pressure, prioritize tasks, and collaborate in a team. 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 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 an experienced Senior Construction Project Manager you will oversee and coordinate CAPEX construction projects for the facilities in Bedum. The ideal candidate will be responsible for managing on-site activities, ensuring projects are completed safely, on time, and within budget, all while maintaining high standards of quality.   Responsibilities Leading the on-site execution of construction phases for CAPEX projects, ensuring alignment with project scope, schedule, and budget. Managing contractors, subcontractors, and vendors to guarantee compliance with safety, technical specifications, and quality standards. Collaborating with engineering, procurement, and operations teams to meet project milestones and resolve technical issues. Overseeing site logistics, permit processes, inspections, and quality assurance activities. Monitoring project progress, identifying risks, and providing regular updates to stakeholders. Supporting Mechanical Completion, commissioning, and handover procedures to operational teams. Ensuring all work complies with environmental, health, and safety regulations, as well as company policies. Managing stakeholder communication, work permits, and daily site meetings, operating independently and escalating issues when necessary.   Requirements Bachelor’s degree or equivalent experience in Civil Engineering, Mechanical Engineering, Construction Management, or related fields. 5 to 10 years of proven experience managing industrial CAPEX construction projects. Strong track record of safely delivering projects on schedule. Experience managing contractors and organizing construction sites. Knowledge of construction methods, materials, safety regulations, and project control processes. Excellent leadership, communication, and stakeholder management skills. Hands-on approach with the ability to work independently and manage complex project environments, including chemical and pharmaceutical sectors is a plus.   Other Information Apply to our vacancy for more information. Looking forward to getting in touch!  

Over het bedrijf Onze opdrachtgever is een wereldwijde organisatie binnen de diergezondheid die innovatieve vaccins voor dieren ontwikkelt en produceert. De locatie in Boxmeer is een hightech biotechnologische productieomgeving waar antigenen worden geproduceerd volgens strikte GMP- en EHS-standaarden. Functieomschrijving Als Bioprocess Technician voer je zelfstandig productieactiviteiten uit voor de productie van virale en bacteriële antigenen. Je werkt met bioreactoren, cel- en viruskweek, filtratie, centrifuges en single-use technologie en draagt bij aan continue verbetering en deviatiemanagement. Belangrijkste verantwoordelijkheden Voorbereiden van productieruns en mediabereidingen. Uitvoeren van cel- en viruskweek binnen een GMP-productieomgeving. Bedienen van bioreactoren, SUB's, centrifuges, filtratiesystemen en gerelateerde apparatuur. Uitvoeren van inactivatie en andere upstream- en downstream-processen. Correct invullen en afronden van batchdocumentatie en productieregistraties. Signaleren, documenteren en rapporteren van afwijkingen in het productieproces. Bijdragen aan procesverbeteringen en verbeterprojecten. Ondersteunen bij deviatiemanagement en root-cause onderzoeken. Kennis overdragen aan collega's via training-on-the-job. Werken volgens hoge kwaliteits-, veiligheids- en GMP-standaarden. Vereisten Afgeronde MBO-opleiding niveau 3 of 4, bij voorkeur in Biotechnologie, Procestechniek of een vergelijkbare richting. Affiniteit met biotechnologie, virologie, bacteriologie, microbiologie of procestechnologie. Ervaring binnen een GMP-, cleanroom- of gecontroleerde productieomgeving is een pré. Ervaring met aseptische werkzaamheden is een voordeel. Sterk kwaliteits- en veiligheidsbewustzijn. Hands-on en technisch ingesteld. Zelfstandig kunnen werken en tegelijkertijd een echte teamplayer zijn. Stressbestendig en in staat om prioriteiten te stellen. Goede mondelinge en schriftelijke communicatie in Nederlands en Engels. Bereidheid om te werken in een dynamische productieomgeving, inclusief incidenteel weekend- of consignatiewerk.

The Company Our client is a globally recognized family-owned company operating across the food, pet care, and confectionery industries, with well-known brands enjoyed by millions of consumers worldwide. With a strong focus on innovation, quality, and sustainable growth, the organization has a significant presence across international markets. Job Description As a Key Account Manager, you will drive profitable growth for a strategic retail customer by managing commercial strategy, negotiations, pricing, promotions, and trade investments. You will lead customer-facing execution across Joint Business Planning, shelf improvement, and key commercial projects while working closely with Marketing, Category, Supply Chain, and Finance teams. Key Responsibilities Drive profitable sales growth for a strategic retail customer, managing revenue, pricing, promotions, assortment and trade investments. Develop and execute Joint Business Plans and customer strategies in close collaboration with internal and external stakeholders. Lead key commercial projects related to customer strategy, shelf optimization, merchandising and execution. Build and maintain strong relationships with senior customer stakeholders through effective negotiation and fact-based presentations. Analyze customer and category performance, identify growth opportunities and translate insights into actionable commercial plans. Work closely with Marketing, Category Management, Supply Chain and Finance teams to ensure effective execution. Requirements Master's degree in Business Administration or a related field. 8+ years of experience in FMCG sales and/or Key Account Management. Strong experience managing strategic retail customers and commercial negotiations. Proven experience with Joint Business Planning, pricing, promotions and trade spend. Excellent analytical, influencing and negotiation skills with a strong commercial mindset. Fluent in both Dutch and English; comfortable working in a hybrid, project-driven environment. Other Information Apply to our vacancy for more information. We look forward to hearing from you!

About the Company Our client is a global healthcare organization supplying life-changing products to patients across more than 75 countries. You will join an international Supply Chain team responsible for ensuring reliable product supply while balancing capacity, inventory, cost, and business needs. Role Description As a Senior Product Planner, you will own the strategic and tactical supply planning for products and production lines. You will manage planning horizons from approximately 4–24 months, balancing supply, capacity, inventory, shelf life, and constraints while supporting product launches, phase-outs, and changing business requirements. Key Responsibilities Own strategic and tactical supply planning for assigned products and production lines. Manage supply plans across 4–24 month planning horizons in Rapid Response. Perform rough-cut capacity planning and optimise production capacity. Proactively manage inventory positions against strategic targets. Balance product availability, inventory, shelf life, cost, and scrap exposure. Identify supply constraints, risks, and deviations and develop corrective actions. Create scenario analyses to support complex supply chain decisions. Collaborate with supply sites, resource owners, procurement, and global Supply Chain teams. Contribute to planning meetings and provide input on strategic decisions. Support product launches, phase-outs, and other lifecycle changes. Requirements Bachelor’s or Master’s degree in Supply Chain, Business Administration, Engineering, or similar. Minimum 7 years of relevant Supply Chain Planning experience. Strong end-to-end Supply Chain Planning experience. Proven experience with strategic and tactical planning. Strong experience with product planning and production-line planning. Experience with rough-cut capacity planning and inventory optimisation. Strong analytical and data-driven decision-making skills. Experience with supply constraints, scenario planning, and supply plan deviations. Experience with Lean, Six Sigma, or other continuous improvement methodologies. Experience in pharma, medtech, food, beverages, ingredients, or another regulated environment is preferred. SAP and Rapid Response experience is a plus. Strong ownership, communication, and stakeholder management skills.

About the Company Our client is a global healthcare organization with a strong focus on research, pharmaceutical development, and innovative laboratory technologies. You will join an Analytical Development team supporting laboratory operations, equipment, automation, and data integrity. Role Description As an Automation & Equipment Lifecycle Specialist, you will support the introduction and lifecycle management of laboratory equipment while providing automation support for analytical systems. You will work with systems such as Empower and contribute to data integrity, system improvements, and technical solutions across the laboratory environment. Key Responsibilities Support the introduction, maintenance, and decommissioning of laboratory equipment. Manage equipment lifecycle documentation and related processes. Support automation of laboratory systems and applications. Work primarily with Waters Empower and also Chromeleon, Unifi, and ICE3. Translate user requirements into technical specifications. Ensure laboratory systems comply with data integrity standards. Support NPI projects and base business activities. Troubleshoot urgent technical and automation challenges. Identify opportunities to improve systems, processes, and data management. Collaborate with laboratory, technical, and other stakeholders across the organization. Requirements Bachelor’s degree in Life Sciences, Computer Science, or a related field. Experience or strong affinity with laboratory automation and analytical software. Strong experience with Waters Empower is strongly preferred. Knowledge of laboratory data acquisition and processing software. Experience with database systems; visual reporting is a plus. Knowledge of GMP quality systems. Strong analytical and technical problem-solving skills. Proactive, independent, and able to prioritize multiple activities. Strong communication and stakeholder management skills. Fluent in English; Dutch is a plus. Hands-on experience with HPLC, CE, cSDS, or similar analytical systems is an advantage.

Over het bedrijf Onze opdrachtgever is een toonaangevende productieorganisatie met een sterke focus op geavanceerde productieapparatuur, veiligheid, kwaliteit en continue verbetering. Je komt terecht in een Maintenance & Engineering team dat verantwoordelijk is voor de volledige levenscyclus van productieapparatuur en systemen. Functieomschrijving Als Senior Electrical Engineer ben je dé elektrotechnische specialist voor productieapparatuur en ondersteun je installaties gedurende de volledige levenscyclus. Je combineert hands-on troubleshooting met engineering, modificaties, elektrische veiligheid en de implementatie van nieuwe apparatuur. Belangrijkste verantwoordelijkheden Fungeren als elektrotechnisch expert voor productieapparatuur en engineeringprojecten. Optreden als Installation Responsible Person (IV) voor het toegewezen productiegebied. Ondersteunen van modificaties en introductie van nieuwe productieapparatuur. Bieden van tweedelijns ondersteuning bij complexe elektrische storingen. Beoordelen van elektrische aspecten van modificaties, onderhoud en kwalificaties. Zorgen voor naleving van NEN 3140, NEN-EN-IEC 60204-1, Arbobesluit en overige regelgeving. Coördineren van elektrische veiligheidsinspecties en opvolgen van bevindingen. Beoordelen van elektrische veiligheidsaanstellingen en relevante bevoegdheden. Opstellen van technische evaluaties, testprotocollen en assessmentrapporten. Samenwerken met Engineering, Automation, Validation, QA, Manufacturing, Supply Chain en externe leveranciers. Vereisten HBO- of WO-opleiding Elektrotechniek of een vergelijkbare technische richting. Minimaal 7 jaar relevante werkervaring, waarvan 5+ jaar binnen een productieomgeving. Aantoonbare ervaring als aangestelde Installation Responsible Person (IV) onder NEN 3140 — must-have. Sterke praktische kennis van NEN 3140, NEN-EN-IEC 60204-1 en Nederlandse elektrotechnische veiligheidsregelgeving. Sterke elektrotechnische kennis en ervaring met analytische troubleshooting. Ervaring met productieapparatuur en lifecycle management. Ervaring binnen een gereguleerde omgeving, zoals GMP, is een pré. Ervaring met CAPEX- of projectomgevingen is een pré. Bereid om incidenteel buiten reguliere werktijden te werken. Vloeiend Nederlands en Engels; native-level Nederlands heeft sterk de voorkeur.

Company   A leading asset management organization dedicated to responsible investing and strategic growth. The company focuses on managing data with integrity and ensuring compliance across all risk management processes, supporting its vision for sustainable and secure asset allocation. Role Description As a Senior Data Governance & Risk Lead, you are responsible for strengthening data governance, controls, and risk management across the organization. You will work closely with senior management, Risk, Compliance, IT, and international teams to identify data risks, develop effective controls, and ensure governance practices are embedded across business processes. Responsibilities - Advise on data governance policies, controls, and risk objectives. - Develop and implement data management controls. - Identify, assess, and monitor data-related risks. - Support data governance awareness and training initiatives. - Advise senior management and risk committees on data risks. - Monitor and report on the data risk profile. - Support continuous improvement of data governance and control frameworks. - Promote knowledge sharing across teams. Requirements - 5–10 years of experience in data management, governance, or risk within financial services. - Experience in banking, asset management, or another regulated environment. - Strong understanding of data controls and risk management. - Excellent communication and stakeholder management skills. - Strong analytical and organizational abilities. - Experience working with international teams and technical stakeholders. 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 leading organization in the financial services sector, specializing in mortgage underwriting and client support. Their team is known for its professionalism, continuous improvement, and commitment to delivering exceptional service in a dynamic industry. Role Description As a Senior Mortgage Process Coordinator, you are responsible for coordinating mortgage applications, supporting team performance, improving processes, and maintaining high service and quality standards. You will play a key role in guiding colleagues, developing training initiatives, analyzing processes, and driving continuous improvement within the Mid Office department. Responsibilities - Develop and implement training programs for team members and colleagues. - Create, analyze, and report on dashboards and performance metrics. - Handle administrative tasks such as scheduling, managing leave and sick leave records, and processing authorizations. - Monitor and coordinate security incidents, escalating complex issues as needed. - Conduct job interviews and manage onboarding, guiding colleagues through working procedures. - Participate in projects and working groups to improve internal processes. - Analyze current workflows and identify opportunities for efficiency and quality improvements. - Take ownership of specific focus areas, such as telephony coaching, quality control, internal audits, complaints, training, and risk management. Requirements - HBO (higher professional education) degree. - Minimum of 1 year experience as a Coordinator or Team Leader, ideally in financial services. - Strong analytical skills and excellent command of Excel. - Good advisory and communication skills. - Customer-oriented mindset with flexibility and a proactive approach. - Willingness to obtain WFT Basic and Mortgage Credit diplomas within the first year. - At least 3 years of experience as a Senior Underwriter with system knowledge of Hypocasso and Accelo. - Mortgage knowledge and experience in mortgage processing is essential. - Ability to explain complex matters patiently and clearly. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.