Commercial Contracts & Pricing Coordinator, Breda, Noord-Brabant

About our client   Our client is a global biopharmaceutical company with a major manufacturing site in Breda, the Netherlands. The site plays an important role in the production and supply of medicines and continues to invest in manufacturing capacity, technology, automation and digital innovation. As part of this ongoing development, the organization is working on projects that connect manufacturing, engineering, automation, IT/OT, digital systems and operational teams.   About the position We are looking for a Senior Project Manager to lead complex technology and digital manufacturing projects from initial concept through implementation and operational handover. You will work across Engineering, Manufacturing, Automation, IT/OT, Quality, Validation and external suppliers, making sure technology projects are delivered on time, within scope and in line with the requirements of a regulated manufacturing environment. The projects can cover areas such as manufacturing systems, automation, digital manufacturing, data solutions and technology infrastructure. This is a hands-on project leadership role for someone who is comfortable taking ownership, coordinating multiple stakeholders and driving projects from planning through to go-live.   Responsibilities Lead complex manufacturing technology and digital projects from initiation to completion. Establish project scope, planning, milestones, resources, risks and dependencies. Coordinate multidisciplinary teams across Engineering, Manufacturing, Automation, IT/OT, Quality and Validation. Drive technology implementation, system integration, testing, qualification and deployment. Manage external vendors, suppliers and system integrators. Lead project meetings, workshops, design reviews and decision-making sessions. Monitor progress, budget, risks, issues and changes and take corrective action when needed. Ensure projects meet relevant GMP, validation, cybersecurity and data integrity expectations. Prepare teams and systems for implementation, go-live and operational handover. Provide clear updates and recommendations to both technical and business stakeholders.   Requirements Bachelor's or Master's degree in Engineering, Automation, Manufacturing Systems, IT, Project Management or a related discipline. 10+ years of project management experience within manufacturing technology, automation, digital manufacturing, IT/OT or capital projects. Proven experience delivering projects through design, implementation, qualification/validation and handover. Experience working in a regulated manufacturing environment. Strong experience managing cross-functional and matrix teams. Confident stakeholder and vendor management skills. Strong project planning, risk management and problem-solving capabilities. Able to communicate complex technical topics clearly to different audiences. Professional fluency in English.   -Experience within pharmaceutical, biotech, medical device or another highly regulated industry is highly relevant. -Knowledge of MES, SCADA, automation, IT/OT integration, digital manufacturing, data platforms or Industry 4.0 technologies is a strong advantage. -PMP, PRINCE2, Agile or a similar project management certification is also beneficial.

Company: A leading pharmaceutical manufacturing facility based in Haarlem, dedicated to distributing over 2,500 different medicines and vaccines to more than 140 countries. The organisation operates through integrated process teams and centres of excellence, ensuring high standards of quality and compliance across its global supply network. Job Description: We are looking for a detail-oriented Quality Assurance Specialist to join our client’s team. The role involves supporting the quality release process for pharmaceutical products, ensuring all batches meet rigorous quality standards, and maintaining compliance with regulatory requirements. The position offers an opportunity to work within a dynamic team in a fast-paced manufacturing environment. Responsibilities: -Review and support investigations into deviations, complaints, and corrective and preventive actions (CAPAs). -Contribute to fostering a strong culture of quality awareness within the Haarlem production site. -Act as the quality representative in various projects, especially during the introduction of new products. -Assist different departments with GMP practices and implementing change controls. -Review and approve GMP documentation such as SOPs, validation/qualification reports, and change control records. -Collaborate closely with the vaccination packaging team, quality control laboratories, and Qualified  Persons to ensure batch release procedures are followed accurately. -Support ongoing quality assurance activities and participate in ongoing quality improvements. Requirements: -Bachelor’s or master’s degree in pharmacy, chemical engineering, life sciences, or a related field. -Several years of experience as a Quality Assurance or Quality Release Officer, or relevant internship experience during a master’s degree in pharmaceutical manufacturing. -Knowledge of GMP standards. -Experience with packaging technology and quality control is advantageous. -Familiarity with SAP is a plus. -Strong teamwork, communication, and interpersonal skills, with the ability to work independently. -Fluency in Dutch and English, both spoken and written. 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 global, innovation-driven organisation with a strong focus on consumer products and sustainability. From a modern R&D environment, multidisciplinary teams develop and improve packaging solutions that support both product quality and business continuity. The culture is hands-on, collaborative, and focused on delivering high-quality results in a practical way. Job Description We are looking for a Packaging Laboratory Specialist to support a busy R&D environment by running packaging tests and keeping the packaging laboratory operating smoothly. The Packaging Laboratory Specialist works closely with packaging developers, production sites, quality teams, and external partners to set up and execute tests on a wide range of packaging materials, ensuring accurate data and reliable reporting. Responsibilities - Manage day-to-day activities in the packaging laboratory to ensure smooth and efficient operations - Prepare, set up, and execute packaging material tests in line with agreed test plans - Align with packaging developers on what needs to be tested and confirm requirements before starting - Operate and maintain laboratory testing equipment and support basic troubleshooting when issues occur - Record results clearly and accurately, ensuring high-quality data and traceable documentation - Work according to quality procedures and contribute to continuous improvement of lab ways of working - Coordinate with internal stakeholders and external parties to keep testing timelines on track Requirements - Hands-on experience with laboratory testing methods and working with lab equipment - Affinity with packaging materials and an interest in packaging innovation - Ability to work accurately with data and documentation in a structured, quality-focused environment - Practical, proactive mindset and the ability to work in a dynamic setting - Bachelor’s or Master’s degree in Material Science, Technical Engineering, or a related field (or equivalent experience) - Good English communication skills (Dutch is an advantage) - Temporary Full-Time Contract Other Information The role is based on-site in Wageningen and involves working closely with an international R&D community. The team environment is collaborative and focused on delivering consistent, high-quality testing results that enable packaging development and improvement. 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 well-established food manufacturing organization supplying products to professional and consumer markets. The site operates in a dynamic, safety- and quality-driven environment, running a continuous production schedule and investing in operational improvement and technology upgrades. Job Description For a production site in Noordwijk, we are looking for an experienced Interim Production Site Manager (Food Manufacturing) to lead the factory through an important transformation phase. This role has full responsibility for day-to-day operations, performance improvement, and the further development of the site, with a strong focus on safety, food safety, quality, and operational excellence Responsibilities - Lead the site and ensure stable daily operations in a 24/7 production environment - Manage and develop the site leadership team across Production, Maintenance, - Technology/Operational Excellence, SHE, Quality, Planning & Logistics, and Finance - Drive improvements in safety performance, food safety standards, quality, and operational results - Strengthen processes, structure, and ways of working to improve performance and consistency - Lead change initiatives that build capability, ownership, and a continuous improvement culture on the shop floor - Support and guide technology upgrades and investment projects to prepare the site for future growth - Monitor key KPIs, translate insights into actions, and ensure follow-up and sustainable results Requirements - Extensive experience leading a manufacturing site as a Plant Manager / Site Leader / Factory Manager - Proven background in food manufacturing (required) - Experience managing operations in a 24/7 production environment - Strong change leadership skills, with experience in transformation and continuous improvement initiatives - Technical background, preferably in engineering or a comparable hands-on technical discipline - Experience with investment projects and technology/automation-related upgrades Other Information This is an on-site assignment in Noordwijk, where the Interim Production Site Manager (Food Manufacturing) will play a key role in stabilizing performance and leading the site through change. If you are interested and want to apply, please submit your application via the apply button below and contact me.

The Company A well established food manufacturing organization specializing in the production of butter and butter oil products for the professional market. The production facility operates continuously and is focused on operational excellence, food safety, process improvement, and future growth through technology and investment initiatives. About the Role We are seeking an experienced Manufacturing Plant Manager to lead a food production facility through a significant transformation phase. This interim leadership role will focus on stabilizing operational performance, strengthening team capabilities, driving continuous improvement, and preparing the site for future expansion and technology upgrades. The successful candidate will bring strong operational leadership together with a hands on technical background. Responsibilities - Lead the overall operations of a 24 hour manufacturing facility - Manage and develop the Site Management Team across Production, Maintenance, Technology, Operational Excellence, SHE, Quality, Planning and Logistics, and Finance - Drive operational performance improvements across safety, quality, productivity, and cost efficiency - Lead continuous improvement and transformation initiatives across the site - Build leadership capability and improve accountability throughout the organization - Support culture change and workforce development programs - Oversee technology upgrades, automation initiatives, and capital investment projects - Ensure compliance with food safety, quality, and regulatory standards - Manage plant performance through key operational metrics - Prepare the organization for future growth and organizational change Requirements - Extensive experience as a Manufacturing Plant Manager within a manufacturing environment - Proven track record leading change management and continuous improvement initiatives - Strong technical or engineering background - Experience within food manufacturing is essential - Experience managing 24 hour production operations - Knowledge of automation and manufacturing technology - Experience delivering investment and capital projects - Strong leadership and people development capabilities - Ability to drive operational excellence and performance improvements - Hands on manufacturing and engineering experience - Experience developing high performing production teams Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company Overview Our client is a leading organization specializing in the production of high-quality pharmaceutical products. Operating within a highly regulated environment, they focus on delivering excellence in manufacturing and packaging through strict adherence to GMP standards and quality protocols. Job Description We are seeking a dedicated Manufacturing Process operator to join the team in Breda. This role involves executing manual production and packaging activities within a controlled environment, ensuring consistent, accurate, and compliant operations in line with GMP standards. Responsibilities -Carry out manual production tasks according to Standard Operating Procedures (SOPs) -Perform packaging activities following established guidelines -Conduct in-process quality checks to ensure product standards -Maintain accurate and timely documentation, including batch records and logs, in compliance with GMP requirements -Identify, report, and support resolution of deviations or quality issues, participating in problem-solving -meetings with QA and Production teams -Set up and close down production lines as required -Perform routine cleaning activities on a daily, weekly, and monthly basis -Ensure the workspace remains safe, compliant, and organized -Execute repetitive manual tasks with precision and reliability -Collaborate effectively with team members to maintain smooth production flow Requirements -Minimum experience in a similar production or manufacturing role -Fluent in English -Comfortable working in a highly structured environment with strict adherence to procedures -Willing to commute to Breda -Open to working in a 2-shift OR 3 shifts system -Able to perform repetitive manual tasks with concentration and accuracy 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 leading global food and health organization with a strong portfolio of well-known brands. The company operates in a fast-paced, international environment focused on innovation, sustainability, and creating a healthier world. Role Description As a General Management Assistant, you will support a senior executive and the wider team with calendar management, meetings, travel arrangements, events, and administrative activities. You will act as a key contact for internal and external stakeholders while managing multiple priorities in a fast-paced international environment. Responsibilities - Manage complex international calendars, including internal and external meetings, workshops, conferences, and last-minute changes. - Coordinate business updates, management meetings, and team meetings, including agendas and logistics. - Manage travel arrangements and other calendar-related activities. - Handle Purchase Order and Vendor Management for the SN Adult team. - Support administrative activities, including expense declarations and documentation. - Coordinate annual holiday planning for the Leadership Team. - Organize team events, lunches, gifts, flowers, and other team-related activities. - Prepare and coordinate project materials and support ongoing team projects. - Act as a professional first point of contact for internal and external stakeholders. - Maintain confidentiality and act as a trusted gatekeeper and representative of the executive you support. - Build strong relationships across the organization and ensure smooth day-to-day coordination. Requirements - At least 4 years of relevant experience in an administrative or assistant role. - Strong organizational and time-management skills with the ability to manage multiple priorities simultaneously. - Excellent knowledge of Microsoft Office and Outlook. - Excellent command of English; Dutch is a plus. - Strong communication and interpersonal skills. - Proactive, self-driven, and solution-oriented approach. - High level of ownership, accountability, discretion, and confidentiality. - Comfortable working in a fast-paced, international, and constantly changing environment. - Professional attitude with a strong focus on providing high-quality support. 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 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 Senior Project Manager, you will lead complex manufacturing technology and digital innovation projects from planning and design through implementation, validation, and operational handover. You will coordinate cross-functional teams, vendors, and technology stakeholders to deliver automation, MES, IT/OT, digital manufacturing, and data-driven solutions within a regulated manufacturing environment. Key Responsibilities Lead construction and installation of manufacturing technology and digital projects from initial planning to operational launch. Define project scope, objectives, timelines, budgets, and resource needs. Develop detailed project plans, including milestones, dependencies, risks, and decision points. Manage project execution, monitor progress, and communicate with stakeholders to align expectations. Oversee the deployment of automation systems, data platforms, and digital manufacturing solutions. Coordinate requirements gathering, design reviews, testing, validation, and system qualification processes. Ensure technical solutions meet business needs and adhere to site standards and enterprise architecture. Manage external vendors, system integrators, and internal teams through workshops, reviews, and governance meetings. Provide clear status updates, escalate issues when necessary, and develop risk mitigation strategies. Requirements Bachelor’s or Master’s degree in Engineering, Automation, Manufacturing Systems, Information Technology, or a related field. Over 10 years of project management experience within manufacturing technology, automation, or digital solutions. Proven track record of delivering projects through design, implementation, validation, and operational handover. Experience working within regulated manufacturing environments. Strong leadership, stakeholder management, and communication skills. Ability to lead cross-functional and matrix teams effectively. Fluency in English. Other Information Apply to our vacancy for more information. We look forward to hearing from you!

The Company Our client is a global food and beverage company committed to bringing health through food to as many people as possible. With leading brands across Dairy, Plant-Based, Waters, and Specialized Nutrition, the company combines innovation, sustainability, and science to create healthier products for consumers worldwide. Job Description As an Executive Assistant, you will provide high-level administrative support to a VP and leadership team in a fast-paced international environment. You will manage complex calendars, travel arrangements, meetings, events, expenses, and vendor/PO activities while acting as a key point of contact for internal and external stakeholders. Key Responsibilities Provide high-level administrative support to senior leadership and the wider team in an international environment. Manage complex calendars, meeting schedules, travel arrangements, and related logistics. Organize business updates, leadership meetings, workshops, and team events. Handle purchase orders, vendor administration, expense reporting, and other operational tasks. Coordinate team communications, holiday planning, and maintain overall team calendars. Act as a key contact for internal and external stakeholders, ensuring smooth communication and efficient coordination. Requirements Minimum 4 years of experience as an Executive Assistant, Management Assistant, Personal Assistant, or similar role. Proven experience supporting senior leaders in a fast-paced international organization. Strong skills in Microsoft Office, Outlook, and calendar management. Experience with travel coordination, event organization, purchase orders, and expense administration. Excellent communication and organizational skills with a proactive and discreet working style. Fluent in English; Dutch language skills are an advantage. Other Information Apply to our vacancy for more information. We look forward to hearing from you!

Over het bedrijf Een internationale farmaceutische organisatie die vanuit de locatie in Haarlem duizenden geneesmiddelen- en vaccinverpakkingen naar meer dan 140 landen distribueert. De locatie werkt binnen een sterk gereguleerde GMP-omgeving met nauwe samenwerking tussen Productie, Quality Control en Quality Assurance. Functieomschrijving Als Quality Release Officer ondersteun je het vrijgeven van farmaceutische en vaccinbatches en zorg je ervoor dat aan alle kwaliteitseisen wordt voldaan tijdens productie en verpakking. Je werkt nauw samen met Quality Assurance, Quality Control, productie en Qualified Persons en ondersteunt onder andere deviatieonderzoeken, CAPA's, change controls en kwaliteitsprojecten. Belangrijkste verantwoordelijkheden Beoordelen en ondersteunen van deviatie-, CAPA- en marktklachtonderzoeken Ondersteunen van GMP-kwaliteitssystemen en kwaliteitsverbeteringen Vertegenwoordigen van Quality binnen projecten en nieuwe productintroducties Ondersteunen van afdelingen bij GMP-vereisten en wijzigingen in richtlijnen Beoordelen en autoriseren van GMP-documentatie, waaronder SOP's, kwalificatie/validatie en change controls Ondersteunen van batch release-activiteiten samen met Qualified Persons Beoordelen van kwalificatiedocumentatie zoals URS'en, protocollen en rapporten Verifiëren van kwalificatiedocumenten opgesteld door externe partijen Samenwerken met interne klanten en verschillende afdelingen Vereisten Ervaring met GMP Ervaring met farmaceutische verpakking en/of Quality Control is een pré Ervaring met kwalificatiedocumentatie en geautomatiseerde/laboratoriumsystemen SAP-ervaring is een pré Nauwkeurig, zelfstandig en resultaatgericht Sterke samenwerkings- en communicatieve vaardigheden Goede beheersing van Nederlands en Engels