Senior Engineering Project Manager, Boxmeer, Noord-Brabant

Technical Operator (Automated Lines) About the Role We are looking for experienced Technical Operators to operate, monitor, and optimize highly automated production lines in a GMP-regulated manufacturing environment. You will ensure efficient production, maintain equipment performance, troubleshoot technical issues, and contribute to continuous improvement initiatives. Key Responsibilities Operate automated production equipment following SOPs and GMP standards. Perform troubleshooting, root cause analysis, and optimize machine settings. Record production data using SAP/MES systems. Complete GMP documentation accurately. Participate in QA, Maintenance & Engineering, and Production triage meetings. Perform equipment setup, shutdown, and routine cleaning. Support Lean and Continuous Improvement initiatives. Ensure safe working practices and effective shift handovers. Requirements Minimum 3 years of experience in automated manufacturing. Experience in pharmaceutical, biotech, food, or FMCG manufacturing preferred. Knowledge of GMP, SOPs, SAP/MES, Lean, Six Sigma, RCA, 5 Why, TPM, SMED, Kaizen, and Poka-Yoke. Technical qualification (MBO, VAPRO B, or equivalent). Knowledge of mechatronics, pneumatics, and electronics. Fluent in English and willing to work shifts. Apply Now If you have a strong technical background and enjoy working with automated production systems, we encourage you to apply.  

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.

Company Overview: A leading pharmaceutical organization focused on the production of sterile medicines. They operate state-of-the-art facilities and are committed to maintaining the highest standards of quality and safety in their products. Job Description: We are seeking a skilled Validation Specialist to support the validation of sterilization processes. This is a project-based role based in Boxmeer, designed to ensure that filtration and sterilization methods meet strict industry standards. The successful candidate will play a vital part in investigating and optimizing filtration techniques to address current challenges with filter performance. Responsibilities: -investigate existing filtration processes used during sterilization. -Modify and improve filtration methods to ensure they meet sterilization  requirements. -Write validation protocols, reports, and statements to document findings and procedures. -Collaborate with cross-functional teams on-site to implement process modifications. -Ensure all activities comply with GMP guidelines and quality standards. -Support validation activities from initial assessment through to final implementation. Requirements: -Minimum of 5–6 years of experience in the pharmaceutical sector. -Proven experience in writing protocols, validation reports, and technical documentation. -Strong knowledge of GMP regulations, sterilization, and filtration processes. -Solid understanding of the chemistry of aqueous and oily solutions. -Excellent communication skills in English; familiarity with 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.

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.  

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.  

The Company A global leader in life sciences manufacturing that focuses on innovative engineering solutions and high quality production environments. The organization operates large scale capital investment projects and emphasizes safety, compliance, and continuous improvement across its global facilities. Role Description This is a senior level Project Manager position within a global engineering team, responsible for delivering large capital investment projects in a regulated manufacturing environment. You will independently lead complex engineering initiatives from concept through completion, ensuring projects are executed safely, on time, and within budget. The role requires strong leadership, stakeholder management, and hands on experience managing multi million euro projects across the full lifecycle. Responsibilities - Lead medium to high value capital projects from initiation to financial close out - Deliver projects in line with safety, quality, timeline, and budget expectations - Build and manage high performing cross functional project teams - Coordinate with internal stakeholders, contractors, suppliers, and engineering partners - Define project scope, timelines, budgets, and execution strategies - Manage governance, stage gate processes, and engineering standards - Oversee cost control, risk management, and change management - Monitor contractor performance and procurement processes - Ensure accurate project reporting, documentation, and financial tracking - Drive continuous improvement through lessons learned and project reviews - Promote strong safety culture across all project activities Requirements - Minimum 5 years of experience in engineering or capital project management - Proven experience delivering large scale projects valued at 15 to 25 million euros or higher - Strong understanding of full project lifecycle from feasibility to completion - Experience leading cross functional teams and managing multiple stakeholders - Hands on experience in cost control, scheduling, and risk management - Experience with contractor management and procurement processes - Strong knowledge of change management and project governance - Experience in regulated manufacturing environments is preferred - Strong English communication skills - Dutch language is an advantage but not required Other Information On site requirement: 4 days per week with 1 day remote flexibility Not open for freelancers

The Company : A leading player in the food industry in the Netherlands, this company boasts a portfolio of iconic brands focused on taste, convenience, health, and sustainability. Working closely with retail partners, they aim to foster sustainable growth for both their customers and the business, ensuring innovative and consumer-driven solutions in the FMCG sector. Role Description: We are seeking a Junior Business Development Coordinator for a temporary assignment from 1 August 2026 to 31 December 2026. In this role, you will support the company’s commercial objectives by assisting with customer account management, product innovations, promotional activities, and business analysis. Your contribution will help drive growth and strengthen relationships with retail partners across various categories within the Foods portfolio. Responsibilities: -Manage relationships with one or multiple customers, overseeing certain categories or product segments. -Prepare for and participate in customer meetings, visits, and negotiations. -Assist Key Account Managers with annual deals, quarterly reviews, and commercial negotiations. -Monitor sales figures, distribution, profitability, and achievement of targets. -Identify commercial opportunities and risks, providing proactive advice. -Collaborate with Marketing, Finance, Supply Chain, and other internal teams to ensure alignment on initiatives. -Coordinate the launch of new products and innovations with internal teams and customers. -Support assortment optimization and distribution expansion projects. -Analyze innovation and product performance, suggesting improvements. -Contribute to the development and evaluation of promotional plans and activities. -Monitor promotional budgets and results, maintaining consistency in promotional strategies across clients and categories. -Prepare sales analyses, forecasts, business reviews, and management reports. -Translate data and insights into actionable commercial plans. Requirements: -Bachelor’s or Master’s degree. -Passion for Sales, FMCG, and Retail. -Prior experience in FMCG, retail, or commercial roles is a plus. -Strong analytical, numerical, and data interpretation skills. -Excellent communication and negotiation abilities. -Proven stakeholder management skills. -Self-motivated, proactive, and entrepreneurial mindset. -Team-oriented with a winning attitude. -Fluent in Dutch and English. -Proficient in Excel and PowerPoint. Other Information: If you are interested and want to apply, please submit 

The Company A global organization operating in advanced biopharmaceutical manufacturing, focused on innovative therapies and strict quality and compliance standards. The company supports cutting-edge production processes in highly regulated environments to deliver life-changing treatments. Role Description This role focuses on supporting manufacturing operations within the Manufacturing Science and Technology function. The position plays a key role in ensuring smooth commercial production of cell-based therapies while maintaining compliance with regulatory requirements. You will be involved in process investigations, product release support, and continuous improvement initiatives while working closely with cross-functional teams. Responsibilities - Perform impact assessments to support product release activities - Lead and support deviation investigations using root cause analysis methodologies - Develop and manage corrective and preventive actions - Collaborate with manufacturing, quality, and technical teams to resolve issues - Author and review SOPs, batch records, and GMP documentation - Support change control processes and process improvements - Contribute to manufacturing projects and operational excellence - Ensure compliance with regulatory standards and internal quality systems Requirements - Bachelor’s degree in biochemical engineering, chemical engineering, biotechnology, or related field - Engineering background preferred - Experience with cell culture, cell therapy, or aseptic manufacturing - Strong knowledge of GMP and pharmaceutical manufacturing standards - Hands-on experience with deviation investigations, root cause analysis, CAPA, and change control - Experience in technical documentation and report writing - Strong understanding of biopharmaceutical manufacturing processes - Excellent communication and collaboration skills Other Information Department Manufacturing Science and Technology Function Manufacturing Operations and Compliance Support Work environment GMP regulated production setting

Company: Our client is a leading player in the food industry in the Netherlands, renowned for its strong brands and commitment to taste, convenience, health, and sustainability. They collaborate closely with retail partners to drive mutual growth and innovate within their category, positioning themselves as a key driver in the FMCG sector. Job Description: We are seeking a proactive and results-driven Business Development Coordinator to support the company's commercial growth initiatives. This temporary role involves assisting with customer account management, product innovations, promotional activities, and business analysis. The ideal candidate will work closely with various internal teams and external partners to help achieve ambitious sales and market expansion goals. Responsibilities: •    Manage relationships with one or multiple customers, overseeing part of the product portfolio. •    Prepare for and participate in customer meetings and visits to strengthen partnerships. •    Support senior account managers in negotiations, business reviews, and strategic discussions. •    Monitor sales figures, market share, distribution, and profitability targets, providing insights and recommendations. •    Identify new business opportunities and potential risks, advising accordingly. •    Coordinate the launch of new products and innovations with internal teams and clients. •    Support assortment optimization and distribution expansion initiatives. •    Evaluate the performance of product launches and provide improvement suggestions. •    Assist in developing promotional plans, analyze promotional activities, and ensure consistency across campaigns. •    Conduct data analysis on sales, volume, and market trends, supporting forecasting and planning processes. •    Prepare reports, presentations, and insights to support decision-making. Requirements: •    Bachelor's or Master's degree. •    Strong interest or experience in Sales, FMCG, or Retail sectors. •    Good analytical skills and numerical insight. •    Effective communication and negotiation abilities. •    Strong stakeholder management skills. •    Proactive, entrepreneurial mindset, and ability to work independently. •    Team-oriented with a winning attitude. •    Fluency in Dutch and English. •    Proficiency in Excel and PowerPoint. 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 leading global food & beverage company, focused on Essential Dairy & Plant-Based products, Waters, and Specialized Nutrition, with a mission to inspire healthier and more sustainable eating and drinking practices worldwide. Role Description: We’re looking for an experienced and strategic Regulatory Affairs Specialist to join the team on a temporary basis, covering maternity leave. This role is based in Rijswijk and involves supporting the regulatory framework across the Benelux region, working closely with colleagues in Brussels. The successful candidate will act as a key regulatory partner, ensuring product compliance, enabling innovation, and helping the company stay ahead in a competitive environment. Responsibilities: -Ensure all products comply with local regulations in the Netherlands, Belgium, and Luxembourg, including product composition and communication. -Review and assess all marketing, consumer, healthcare professional, and sales communication materials across various channels, ensuring regulatory adherence. -Contribute regulatory expertise to support innovation projects, working closely with development teams to provide guidance and solutions. -Validate labels, artworks, and packaging to meet legal and corporate standards. -Manage the notification process for product registrations and notifications in the Dutch, Belgian, and Luxembourg markets. Requirements: -Bachelor’s or master’s degree in Nutrition and Dietetics, Food Science, Law, or a related field. -Minimum of 4 years’ experience in a regulatory role within the industry or a law firm. -Native or fluent in Dutch; fluent in English; French language skills are a plus. Strong communication skills and proactive mindset, with the ability to work independently. -Excellent stakeholder management skills and the ability to translate complex regulations into clear business guidance. -Accurate, detail-oriented, and committed to regulatory processes and ethical standards. Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.