Manufacturing Process Technician, Breda, Noord-Brabant

Company Our client is a global, innovation-driven organisation in the life sciences sector. They operate in a highly regulated environment and support international clinical programs by ensuring products are prepared, labelled, and packaged accurately and safely for use worldwide. Quality, compliance, and teamwork are central to how the teams work every day. Job Description For our client in Breda, we are looking for a Packaging Operator (GMP) to support clinical labelling and packaging activities. In this role, the Clinical Packaging Operator (GMP) works in a day-shift team and carries out manual labelling, packaging, and assembly activities according to standard operating procedures. The work requires strong attention to detail, clear communication, and a quality-first mindset. Responsibilities - Execute clinical labelling and packaging activities according to standard operating procedures (SOPs) - Perform manual packaging, labelling, and assembly activities accurately and efficiently - Take ownership of tasks and results within the assigned area of responsibility - Escalate deviations, issues, or unexpected situations when necessary - Complete all required training according to the training plan and deadlines - Support batch-related logistics processes linked to packaging activities - Contribute to improvements in working processes, quality, and efficiency - Work in both room temperature areas and, when needed, in cold-room conditions (2–8°C) Requirements - Experience in a manual packaging environment (preferably within a regulated setting such as GMP/GDP) - Comfortable working according to procedures in a strongly regulated environment - Strong attention to detail; accurate and quality-focused way of working - Team player with clear communication skills and a flexible attitude - Willing and able to work on-site in Breda and adapt to changing priorities - Experience with SAP and/or MES is a plus Other Information The Clinical Packaging Operator (GMP) will join a dedicated team supporting important clinical activities in an international environment. If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company A leading provider of pharmaceutical manufacturing services, dedicated to high-quality production within a regulated environment. The company values precision, compliance, and continuous improvement to ensure the best outcomes for patients globally. Job Description We are seeking a skilled Production Operator - Semi-Automated Lines to join our client's team in Breda. This role involves operating and maintaining semi-automated production lines to ensure efficient, compliant, and high-quality manufacturing. The ideal candidate will support ongoing production activities, troubleshoot issues, and contribute to process improvements in a GMP-regulated setting. Responsibilities - Operate and oversee semi-automated production lines in line with SOPs and GMP standards. - Perform machine set-ups, changeovers, and line preparations. - Troubleshoot and resolve process disturbances to ensure smooth production flow. - Conduct minor mechanical and parameter adjustments to optimize equipment performance. - Record, verify, and document production data accurately in SAP/MES systems. - Ensure all GMP documentation, including batch records and logs, is completed correctly and on time. - Report deviations, participate in troubleshooting meetings, and support resolution efforts. - Execute daily, weekly, and monthly cleaning operations. - Support continuous improvement initiatives using Lean, Six Sigma, and other problem-solving methodologies. - Facilitate effective shift handovers and maintain clear communication within the team. - Uphold a safe, compliant, and well-organized working environment. Requirements - Minimum of 3 years’ experience in a production role, preferably in assembly and packaging. - Hands-on experience with automated and semi-automated production environments. - Fluent in English. - Comfortable working within structured procedures in a regulated GMP setting. - Willing to commute to Breda. - Able to work in shift systems. 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 a leading manufacturing organization where operational excellence, collaboration, and continuous improvement are key to delivering high-quality products. In this role, you will lead a production team, support employee development, and help drive a safe, efficient, and high-performing manufacturing environment. Role Description As an Operations Team Lead, you will be responsible for leading and developing a manufacturing operations team while ensuring daily production activities are executed safely, efficiently, and in line with quality standards. You will provide technical guidance, coach team members, and collaborate closely with cross-functional departments to optimize processes and build a culture of continuous improvement. Key Responsibilities Lead, coach, and develop production, maintenance, and support personnel Provide technical expertise and day-to-day operational leadership within the manufacturing environment Ensure safe, efficient, and compliant execution of production activities Support team development through coaching, training, and performance management Foster a culture of continuous improvement, collaboration, and open communication Maximize the potential of team members through ongoing development and constructive feedback Ensure employees have the appropriate tools, resources, and training to perform their roles successfully Collaborate with cross-functional teams to improve operational performance and resolve production challenges Support process improvements and contribute to operational excellence initiatives Monitor team performance and help achieve production, quality, and safety objectives Promote a positive working environment focused on accountability, engagement, and teamwork Requirements Bachelor's degree or equivalent working and thinking level is preferred Experience leading teams within a manufacturing or production environment Strong leadership and people development skills Experience coaching, mentoring, and training employees Excellent written and verbal communication skills Ability to work effectively with cross-functional teams and stakeholders Strong organizational and problem-solving skills Proactive mindset with a focus on continuous improvement Ability to motivate and develop high-performing teams Comfortable working in a dynamic manufacturing environment with changing priorities

The Company A leading organization in the pharmaceutical manufacturing industry, committed to maintaining the highest quality standards in its production processes. The company values precision, compliance, and continuous improvement to ensure the safety and efficacy of its products. Role Description We are seeking a proactive and detail-oriented Quality Assurance Officer to join the GMP manufacturing team. This role is vital in ensuring that the packaging, labeling, and production processes meet strict quality and regulatory standards. The successful candidate will play a key part in maintaining quality, supporting compliance, and resolving issues in a fast-paced production environment. Responsibilities -Conduct final quality verification for all packaging and labeling orders before release. -Review batch records and documentation to ensure data accuracy, compliance, and completeness. -Manage and resolve deviations or quality issues during production. Investigate, document, and follow up on deviations or non-compliance issues. -Collaborate closely with Production, Maintenance, QA colleagues, and other departments to ensure smooth operations. -Exercise escalation authority by stopping production if quality or compliance concerns arise. -Provide guidance and support to production staff on GMP standards and procedures. -Review and approve batch production records and deviation reports. Requirements -MBO or BSc degree in Pharmaceutical Sciences, Life Sciences, or a related field. At least 3 years of experience in Quality Assurance or manufacturing within the ---pharmaceutical or medical device sector, with a focus on batch record review and investigations. -Strong understanding of GMP, GDP, and GCP regulations, with the ability to interpret and apply them. -Proven attention to detail and a methodical approach to quality and compliance tasks. -Skilled team player with excellent communication skills and the confidence to challenge production when necessary. -Fluency in English. -Valid driver’s license is a plus. Other Information This role operates on a three-shift system, involving early, late, and night shifts, with no rotation. Shift hours are as follows:

Company A leading global consumer goods company specializing in Food, Home, and Personal Care products. With a presence in over 190 countries, the company reaches billions of consumers daily and boasts a portfolio of more than 400 well-known brands that are household names worldwide.   Job Description We are seeking a dedicated Financial Analyst to join the Benelux Finance team. In this role, you will support financial planning, analysis, and reporting processes, contributing to the company’s strategic performance management. The position involves collaborating across departments to ensure accurate financial forecasting, month-end closing activities, and project support.   Responsibilities Support the Sales & Operations Planning, Forecasting, and Month-End processes, including co-owning forecasts and results reporting. Assist in preparing monthly financial reviews, including insights and commentary for management presentations. Drive and support agile projects that add value to the finance function. Collaborate with cross-functional teams such as Sales and Marketing to identify risks and opportunities within the P&L. Contribute to continuous operational improvements and efficiency initiatives. Support ad-hoc analysis and reporting requests as needed.   Requirements Finance or related academic background, or equivalent practical experience. Proven experience in finance partnering, especially in a consumer goods environment. Strong analytical skills, with the ability to interpret data and provide actionable insights. Experience in financial forecasting, P&L management, and process support. Excellent communication skills in English, both spoken and written. Ability to work effectively with various stakeholders, including senior management. Flexibility, resilience, and the ability to adapt quickly to changing priorities. Proficiency in Excel, PowerPoint, and financial modelling.   Other Information If you are interested and want to apply, please submit your application via the apply button and contact me.

About the Company Join a global leader in healthcare technology, where innovation, safety, and user experience come together to improve patient outcomes. Within a highly regulated medical device environment, you will contribute to the development of safe, intuitive, and user-centered products used by healthcare professionals and patients worldwide. Role Description As a Usability Engineer & Validation Lead, you will be responsible for integrating human factors engineering and usability principles throughout the medical device development lifecycle. You will lead usability activities from early user research and requirements definition through design validation and post-market evaluation, ensuring products meet regulatory expectations, customer needs, and safety standards. Working closely with multidisciplinary global teams, you will influence product design decisions and ensure usability, quality, and patient safety are embedded into every stage of development. Key Responsibilities Lead usability engineering activities throughout the complete product development lifecycle Perform workflow analysis, user research, task analysis, and context-of-use evaluations to define user needs and usability requirements Develop usability engineering plans and coordinate activities with project managers, clinical marketing, engineering, and other stakeholders Lead usability risk management activities, including Usability FMEA Plan, execute, and document usability evaluations and ensure critical findings are incorporated into product improvements Analyze post-market data to identify usability issues and improvement opportunities Provide usability guidance to design teams regarding UI/UX solutions and design changes Ensure compliance with usability engineering standards, including IEC 62366-1, FDA Human Factors Guidance, and applicable global regulations Define product validation strategies, create validation plans and protocols, and execute design validation activities Develop high-quality technical documentation to support regulatory submissions and product releases Collaborate with multidisciplinary international teams across engineering, quality, regulatory, and product development Requirements Master's degree or PhD in Human Factors Engineering, Human-Computer Interaction (HCI), Cognitive Science, Product Design, Interaction Design, or a related field Minimum 2–3 years of experience in usability engineering within medical devices Proven experience across the full usability lifecycle, from user needs gathering through usability validation and post-market follow-up Experience performing task analysis, usability evaluations, and usability validation studies Experience supporting Design Validation, including validation strategies, protocols, execution, and reporting Strong understanding of medical device regulations and standards, including: IEC 62366-1, FDA Human Factors Guidance, EU MDR, ISO 13485, ISO 14971, FDA 21 CFR 820.30,NMPA guidelines Strong knowledge of human factors engineering, interaction design, cognitive ergonomics, and usability methodologies Experience collaborating within multidisciplinary and international teams Strong project management, communication, and stakeholder management skills Ability to advocate for user needs and challenge design decisions when required Excellent written and verbal English communication skills

Company: A leading global organization dedicated to delivering high-quality pharmaceutical products worldwide. The company values innovation, collaboration, and a commitment to excellence in healthcare supply chain management. Job Description: We are seeking a proactive and detail-oriented Supply Chain Operations Coordinator to join our team. The role involves managing the end-to-end coordination of pharmaceutical shipments, ensuring smooth import and export processes, and supporting global distribution activities. Responsibilities: - Coordinate and process supply orders daily to ensure timely distribution of pharmaceutical products globally. - Handle import/export documentation and ensure compliance with international shipping regulations. - Book shipments, monitor logistics status, and proactively address any potential issues. - Resolve service and transportation-related problems efficiently. - Manage return processes and collaborate with third-party logistics providers and internal teams. - Develop strong relationships with internal and external customers, including affiliates and distributors. - Participate in cross-functional project teams to improve supply chain processes. - Continuously review and suggest improvements to Order-to-Cash policies and procedures. - Maintain updated knowledge of GMP/GDP standards and ensure training requirements are met. - Support disaster recovery planning alongside corporate teams. - Perform other duties as necessary to support supply chain operations. Requirements: - Bachelor’s or Master’s degree with at least 2 years of supply chain experience in a GMP/GDP-regulated environment. - Ability to handle multiple tasks and work effectively within an international team. - Strong computer skills, including experience with ERP systems. - Excellent communication skills in English, both spoken and written. - Customer-focused attitude and attention to detail. - Problem-solving skills and ability to prioritize effectively. 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, research-driven pharmaceutical organization specializing in innovative medicines and vaccines. The Boxmeer site is one of the world's leading manufacturing and development locations for sterile veterinary vaccines, operating in a highly regulated GMP environment with a strong focus on quality, innovation, and continuous improvement. Role Overview We are looking for an experienced Sterilization Validation Engineer to support a critical sterilization validation project. You will investigate, validate, and optimize filtration processes used in sterile manufacturing, ensuring compliance with GMP and regulatory standards. Key Responsibilities Lead sterilization and filtration validation activities. Develop and execute validation protocols, reports, and technical documentation. Investigate and improve filtration processes. Ensure GMP compliance throughout validation activities. Collaborate with Engineering, Manufacturing, and Quality teams. Key Requirements Bachelor's or Master's degree in Engineering, Chemistry, Life Sciences, or a related field. Minimum 5–6 years of pharmaceutical validation experience. Strong knowledge of GMP and validation documentation. Experience with filtration and sterilization processes. Understanding of aqueous and oil-based solution chemistry. Fluent in English. If you're interested in this opportunity, click the application link below to apply. We look forward to reviewing your application.  

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.