Manufacturing Process Technician, Breda, Noord-Brabant

Job Vacancy — Senior Automation Engineer | Breda   About our client Our client is a global biotechnology company developing and manufacturing innovative medicines for patients worldwide. The Breda site is a large-scale manufacturing operation focused on the assembly, inspection, labeling and packaging of pharmaceutical products. The site operates in a highly regulated GMP environment, where reliable equipment, automation and data integrity are essential to maintaining safe, compliant and efficient production.   About the position We are looking for a Senior Automation Engineer to join the Equipment Engineering team in Breda. In this role, you will take ownership of the automation side of new and upgraded manufacturing equipment — from design and vendor testing through installation, qualification and operational handover. You will work closely with Engineering, Manufacturing, Maintenance, IT and external equipment suppliers to make sure automation systems are reliable, secure, compliant and ready for production. This is a hands-on role for someone who enjoys combining automation engineering, project execution and troubleshooting in a regulated manufacturing environment.   Responsibilities Lead the automation activities for new and upgraded manufacturing equipment. Review and develop automation design documentation, including URS, FDS, HDS and SDS. Support FAT, commissioning, testing and qualification activities. Work with PLC, HMI, SCADA, industrial PC and vision systems. Ensure equipment meets required automation, cybersecurity and data integrity standards. Support equipment integration with site systems, including the PI data historian. Develop and maintain backup/restore, parameter and audit-trail procedures. Support automation troubleshooting and provide on-floor hypercare during implementation. Assess preventive maintenance requirements and automation spare parts. Maintain equipment documentation and asset parameter lists. Train Maintenance, Engineering and relevant Operations teams. Report project progress and technical risks to project management. Support New Product Introduction (NPI) activities at the site.   Requirements Bachelor’s or Master’s degree in Automation Engineering, Industrial Automation, Industrial Information Systems or a related discipline. 5+ years of experience with automation/process control and information systems in pharmaceutical or biotechnology manufacturing. Proven experience with labeling and/or packaging equipment. Practical knowledge of PLC, HMI, SCADA, industrial PCs and vision systems such as Cognex. Experience working in a GMP/regulatory manufacturing environment. Experience delivering automation projects in cross-functional or international teams. Strong understanding of equipment implementation, testing and commissioning. Able to troubleshoot technical issues and translate them into practical solutions. Strong communication and stakeholder-management skills. Fluent English, written and spoken.

Company Our client is a global leader in the pharmaceutical industry, operating in a highly regulated GMP environment. They run complex manufacturing and packaging operations and invest continuously in engineering projects that strengthen compliance, reliability, and quality across the site. Job Description Our client is looking for a GMP Validation Engineer to support engineering projects focused on secondary packaging equipment. The role will drive commissioning, qualification, and validation (CQV) activities and ensure solutions are implemented in line with site standards, documentation expectations, and GMP compliance. Responsibilities - Lead and execute commissioning, qualification, and validation activities for packaging-related systems. - Develop, update, and maintain CQV documentation, such as: system criticality assessments, commissioning/qualification/validation plans, risk assessments, test protocols, requirements traceability matrices, CQV summary reports - Define and report test strategies that meet internal customer requirements and standard CQV procedures. - Provide technical guidance to project teams to ensure the implemented solution follows the validation approach and meets required standards. - Coordinate priorities, identify risks, and escalate where needed to keep project phases on track (design, implementation, testing, commissioning, validation). - Support additional tasks or engineering/validation projects as assigned by the supervisor. Requirements - Background in CQV (Commissioning, Qualification, Validation) within pharmaceutical manufacturing (at least 3 years hands-on experience). - Experience with secondary packaging systems, ideally including print & inspection systems (e.g., Systech, Cognex). - Experience with Computerized Systems Validation (CSV). - Strong technical documentation skills and good English technical writing. - Able to work independently with clear communication and strong stakeholder management. - Comfortable working in a GMP environment with strong attention to quality and compliance. Other Information The role is based on-site in Breda, Netherlands, within an engineering organization focused on delivering compliant technical solutions in a structured project environment. 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 leader in the pharmaceutical industry, operating in a highly regulated GMP environment. They run complex manufacturing and packaging operations and invest continuously in engineering projects that strengthen compliance, reliability, and quality across the site. Job Description Our client is looking for a GMP Validation Engineer to support engineering projects focused on secondary packaging equipment. The role will drive commissioning, qualification, and validation (CQV) activities and ensure solutions are implemented in line with site standards, documentation expectations, and GMP compliance. Responsibilities - Lead and execute commissioning, qualification, and validation activities for packaging-related systems. - Develop, update, and maintain CQV documentation, such as: system criticality assessments, commissioning/qualification/validation plans, risk assessments, test protocols, requirements traceability matrices, CQV summary reports - Define and report test strategies that meet internal customer requirements and standard CQV procedures. - Provide technical guidance to project teams to ensure the implemented solution follows the validation approach and meets required standards. - Coordinate priorities, identify risks, and escalate where needed to keep project phases on track (design, implementation, testing, commissioning, validation). - Support additional tasks or engineering/validation projects as assigned by the supervisor. Requirements - Background in CQV (Commissioning, Qualification, Validation) within pharmaceutical manufacturing (at least 3 years hands-on experience). - Experience with secondary packaging systems, ideally including print & inspection systems (e.g., Systech, Cognex). - Experience with Computerized Systems Validation (CSV). - Strong technical documentation skills and good English technical writing. - Able to work independently with clear communication and strong stakeholder management. - Comfortable working in a GMP environment with strong attention to quality and compliance. Other Information The role is based on-site in Breda, Netherlands, within an engineering organization focused on delivering compliant technical solutions in a structured project environment. If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company A leading global organization in the life sciences sector is expanding its manufacturing operations in the Netherlands. The site works in a highly regulated environment, with a strong focus on quality, compliance, and continuous improvement. The organization is investing in new and upgraded production and packaging equipment and is strengthening its engineering capabilities to support long-term operational readiness. Job Description For a production site in Breda, we are looking for an Equipment Automation Engineer to support the automation scope of new and upgraded manufacturing equipment. The Equipment Automation Engineer (Packaging & Inspection) will take ownership of automation deliverables across the full equipment lifecycle—design, installation, commissioning, and ongoing support—working closely with engineering, manufacturing, quality, and external equipment suppliers. Responsibilities - Leading automation activities for equipment projects in Device Assembly, Inspection, Labelling, and Packaging areas - Writing and/or reviewing key automation and engineering documentation (e.g., URS, FDS, HDS, SDS) - Supporting installation, testing, commissioning, and qualification activities (including vendor testing phases where needed) - Ensuring systems align with site and network security requirements (e.g., domain settings, firewall considerations) - Implementing internal automation standards for both hardware and software - Installing required monitoring tools and supporting data integrity assessments - Performing or supporting automation preventive maintenance assessments - Advising on automation spare parts and contributing to asset spare parts lists - Creating, testing, and maintaining backup/restore procedures and work instructions for configurable components - Creating parameter management and audit trail review work instructions - Creating and updating Asset Parameter Lists (APLs) - Supporting integration to a PI data historian (or similar data platform) - Training maintenance/engineering teams and relevant operators on automation-related topics - Providing “hypercare” support on the shop floor after implementation as required - Providing progress updates and reporting to (project) management and key stakeholders Requirements - Bachelor’s or Master’s degree in Industrial Automation Engineering, Industrial Information Systems, or similar - At least 5 years’ experience delivering automation / process control / information systems support in a regulated manufacturing environment (biotech, pharma, or similar) - Proven experience running workstreams independently within cross-functional project teams - Experience with labelling and packaging equipment is essential - Working knowledge of industrial automation technologies such as PLC, HMI, SCADA, industrial - PCs, and vision systems (e.g., Cognex) - Strong understanding of working in regulated environments (e.g., GMP) - Fluent in English (written and spoken) - Willingness to occasionally work outside office hours when project activities require it Other Information This position is based on-site in Breda, the Netherlands, and offers the opportunity to contribute to high-impact equipment projects within a modern, regulated production environment.

Company  A leading organization within the manufacturing sector dedicated to delivering high-quality, innovative solutions. The company values technical excellence, teamwork, and continuous improvement to ensure operational success and sustainability. Job Description We are seeking a proactive and experienced Senior Automation Engineer to join our dynamic team in Breda. This role focuses on overseeing automation systems involved in the installation, commissioning, and lifecycle management of advanced manufacturing equipment, particularly in device assembly, inspection, labeling, and packaging areas. The ideal candidate will ensure equipment reliability, security, and optimal performance through expert automation practices. Responsibilities Manage automation aspects of new equipment installations and upgrades, ensuring alignment with project timelines. Support New Product Introduction (NPI) and coordinate test phases at equipment vendors and on-site. Oversee automation design, including review and creation of technical documents such as URS, FDS, HDS, and SDS. Support equipment installation, testing, commissioning, and validation, considering network security settings. Ensure equipment security using Amgen standards and support the connection to data historians like PI. Participate in FAT, commissioning, and qualification activities. Conduct automation preventive maintenance and data integrity assessments. Advise on spare parts and develop asset spare parts lists for automation equipment. Create backup and restore procedures, parameter review protocols, and audit trail review procedures. Support automation training for Maintenance, Engineering, and Operators. Provide operational hypercare support and update documentation to maintain operational effectiveness. Requirements Bachelor’s or master’s degree in Industrial Automation Engineering or related fields. Minimum of 5 years’ experience in process control and information systems support within biopharmaceutical or pharmaceutical manufacturing environments. Proven ability to execute independent projects in cross-functional, global teams. Hands-on experience with labelling and packaging equipment, including PLC, HMI, SCADA, Cognex vision systems, and industrial PCs. Familiar with regulated environments (GMP, OSHA, EPA). Strong knowledge of automation standards, network security, and data management. Excellent communication skills in English, both written and spoken. Ability to work outside regular hours when necessary. 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 public organization dedicated to ensuring the safety, accessibility, and sustainability of national infrastructure. They are involved in large-scale projects that contribute to maintaining and improving key transport connections and public assets across the Netherlands. Job Description We are seeking an experienced Senior Project Controls Coordinator to support the management of maintenance and renewal projects for bridges in Zeeland. This role involves establishing and maintaining effective project control processes, providing vital oversight, and ensuring projects are delivered on time, within scope, and within budget. The successful candidate will be instrumental in building the project controls framework from the ground up, contributing to the safe and efficient operation of bridge infrastructure. Responsibilities -Develop, implement, and oversee project control systems across multiple bridge maintenance and renewal projects. -Ensure accurate tracking and reporting of project scope, schedule, finances, risks, quality, and documentation. -Provide clear insights and highlight potential issues or blind spots within project controls. -Collaborate with project teams to establish aligned processes for planning, budgeting, risk management, and quality assurance. -Translate findings into actionable recommendations for decision-making. -Liaise with colleagues to maintain high standards of project control quality and timeliness. -Lead and motivate a team of professionals, fostering a culture of accountability and continuous improvement. -Build the project controls framework in a relatively new environment, setting up processes and workflows from scratch. -Monitor project performance, anticipate challenges, and implement corrective measures where needed. -Ensure all project control activities comply with applicable frameworks and organizational standards. Requirements -Minimum of 5 years’ experience in project control or management. -Relevant higher education qualification (HBO level) in finance, economics, or business administration. -Solid understanding of the IPM model and the role of project controls within infrastructure projects. -Proven ability to establish project control processes independently from the ground up. -Strong leadership skills and experience in managing project control teams. -Excellent analytical skills, with the ability to identify and address control gaps. -Effective communicator, capable of working across disciplines and levels of the organization. -Flexibility to work on-site in Middelburg every Tuesday and adapt to project needs. -Proficiency in Dutch language. 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 Our client is a global pharmaceutical organization with a GMP manufacturing environment. The site Engineering organization supports technical projects that ensure reliable, compliant, and efficient manufacturing operations. Role Description As a CQV Engineer, you support technical projects from commissioning through qualification and validation. You develop and execute test strategies, prepare CQV documentation, and provide technical guidance to project teams to ensure systems meet customer requirements and GMP standards. Key Responsibilities Develop and maintain CQV documentation, including validation plans, risk assessments, protocols, and reports Lead commissioning, qualification, and validation activities Develop test strategies and execute qualification testing Support project teams with CQV and GMP guidance Ensure technical solutions align with validation requirements and procedures Track project activities, issues, and timelines Report progress and escalate issues when required Requirements Minimum 3 years of CQV experience within pharmaceutical manufacturing Hands-on commissioning and qualification experience in secondary packaging operations Experience with print and inspection systems, such as Systech or Cognex Experience with Computerized Systems Validation (CSV) Strong knowledge of GMP validation practices Experience developing validation and qualification documentation Good technical writing skills in English Strong communication and stakeholder management skills Able to work independently with limited supervision Strong analytical and problem-solving skills

The Company A global pharmaceutical manufacturing organization focused on delivering high quality healthcare products through advanced production technologies and strict regulatory compliance. The company operates in a highly regulated environment and emphasizes innovation, quality, operational excellence, and patient safety. Role description The Validation Engineer supports engineering and validation projects within a GMP regulated manufacturing environment. This role focuses on commissioning, qualification, and validation activities for secondary packaging systems and computerized systems. The position requires strong technical expertise, documentation skills, and the ability to work independently while ensuring compliance with established quality standards and procedures. Responsibilities - Develop and maintain validation documentation including criticality assessments, qualification plans, validation plans, risk assessments, test protocols, traceability matrices, and summary reports - Lead commissioning, qualification, and validation activities for manufacturing systems - Execute testing activities and document results according to GMP requirements - Support project teams to ensure technical solutions comply with validation plans and internal procedures - Provide technical guidance throughout project execution - Ensure documentation is complete, accurate, and inspection ready - Support project delivery through design, implementation, testing, commissioning, and validation phases - Complete additional assignments and projects as requested by management Requirements - Minimum 3 years of commissioning, qualification, and validation experience within pharmaceutical manufacturing - Experience with secondary packaging systems - Experience with print and inspection systems such as Systech and Cognex Knowledge of computerized systems validation - Hands on commissioning and qualification experience within secondary packaging operations - Strong understanding of validation lifecycle documentation - Experience working in a GMP regulated environment - Excellent technical writing skills in English - Strong communication and stakeholder management abilities - Critical thinking and problem solving skills - Ability to work independently with limited supervision - Strong project coordination and prioritization capability 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 international financial services organization where data, technology, and innovation drive business transformation. You will work within a technology-focused engineering environment, contributing to strategic data products that provide trusted insights and support enterprise-wide decision-making. Role Description We are looking for a Senior Data Engineer (Azure Synapse & Databricks) to support the development, optimization, and future evolution of enterprise data products. You will play a key role in enhancing existing solutions, building scalable data pipelines, and supporting the transition towards a modern Databricks-based platform. Responsibilities - Design, develop, and optimize data pipelines using Azure Synapse and Databricks. - Build scalable ELT/ETL frameworks and reusable data components. - Develop and maintain APIs and data products. - Improve data quality, reliability, performance, and maintainability. - Support platform modernization and migration initiatives. - Collaborate with Business Analysts, Architects, Product Owners, and engineering teams. - Contribute to CI/CD processes, testing, monitoring, and automation. - Drive knowledge transfer and reduce technical debt. Requirements - 5+ years of experience as a Data Engineer. - Strong experience with Azure Synapse Analytics and Azure Databricks. - Proficiency in Python, SQL, and PySpark. - Experience building and optimizing ELT/ETL pipelines and data warehousing solutions. - Hands-on experience with Azure Cloud, Azure Data Factory, Azure DevOps, Git, REST APIs, and CI/CD pipelines. - Knowledge of data modelling, distributed data processing, and Lakehouse architectures. - Experience with Medallion Architecture, Delta Lake, and Unity Catalog. - Experience delivering enterprise-scale data products and supporting platform migrations. - Strong stakeholder management, communication, and problem-solving skills. - Ability to work independently, take ownership, and drive initiatives forward. - Experience in banking/financial services and application landscape data is a plus. - Fluent in Dutch and English (mandatory). 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 public organization responsible for maintaining the safety, accessibility, and sustainability of national infrastructure, including roads, waterways, tunnels, bridges, and flood defenses across the Netherlands. They focus on delivering large-scale projects that support the country’s vital transportation and water management systems. Job Description: We are seeking a dedicated Project Coordinator to support the Dredging & Salvage cluster within a major waterway maintenance program. The ideal candidate will provide crucial organizational, coordination, and administrative support to ensure smooth project operations and facilitate effective communication within the team. Responsibilities: Organize and coordinate meetings, workshops, and work sessions, including preparing agendas and gathering input. Manage calendars and assist with scheduling for project leaders and team members. Draft, distribute, and archive meeting minutes, reports, and decision documents. Monitor and follow up on actions, decisions, and deadlines to ensure timely progress. Support project management with organizational tasks such as preparing reports, memos, and presentations. Maintain the accessibility and organization of project documents and information flows using platforms like SharePoint and Microsoft 365. Facilitate internal communication by structuring and maintaining project files and updates. Assist in preparing periodic progress reports for management and stakeholders. Identify opportunities to improve work processes and contribute to a well-organized project environment. Serve as a point of contact within the team for procedural and informational issues, ensuring smooth information exchange and decision-making support. Requirements: Higher professional education (HBO) in a relevant field such as Public Administration, Business Administration, or Management Support. Minimum of 5 years’ proven experience in project coordination, supporting project teams, or similar roles within complex, multi-stakeholder environments. At least 3 years’ experience organizing and supporting intricate meetings, including agenda setting, minute-taking, and action tracking. Fluency in Dutch, both spoken and written, with strong skills in reporting and document creation. Proficiency in Microsoft 365, SharePoint, and digital collaboration tools. Ability to work independently, prioritize tasks, and proactively address organizational needs. Available to work on-site in Rotterdam on Tuesdays and Thursdays. 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 global leader in animal health, committed to improving the well-being of animals and supporting the world’s food supply. They operate within a high-tech, innovative environment that develops and produces veterinary medicines. Their site in Boxmeer is part of an international network and specializes in the manufacturing and packaging of vaccines and medicines for a wide range of livestock and companion animals. Their production teams focus on vaccine development, viral and bacterial antigen production, working under strict GMP and EHS standards to ensure the highest quality and safety. Job Description: We are seeking an experienced Senior Bioprocess Technician to join their dynamic team in the Bioreactor Facility at the Boxmeer site. In this role, you will be responsible for supporting large-scale biotechnological production processes for animal vaccines, ensuring smooth operation, compliance, and continuous improvement within a high-tech environment. Responsibilities: Prepare production cultures and media meticulously for each production cycle Independently execute complex production tasks, including cell and virus culture management, fermenter control, centrifugation, filtration, and vessel handling Document all production activities precisely, ensuring batch records are complete and accurate Follow strict GMP and EHS guidelines and observe all safety and quality regulations Identify, report, and document deviations or issues in the production process Contribute to process improvement initiatives and participate in project teams Support deviation management through thorough documentation of any process variations Lead or participate in troubleshooting and technical tasks related to process control systems and mechanical aspects such as valves and fittings Train and mentor colleagues through knowledge transfer and on-the-job training Assist in organizational and logistical improvements to optimize production flow Support on-call and weekend shifts, with potential for future shift work or rotation Requirements: MBO level 3 or 4 in Biotechnology, Process Technology, or a related field Previous experience in bioprocessing, ideally within animal health or pharmaceutical manufacturing (entry-level candidates are encouraged to apply) Familiarity with aseptic techniques and working in controlled environments such as cleanrooms or biosafety cabinets (applicants with limited experience are encouraged to apply) Technical interest in virology, bacteriology, microbiology, and process technology, with willingness to undergo further training Strong understanding of process trending and change management High awareness of quality and safety standards Stress-resilient with good prioritization skills Excellent communication skills in Dutch and English Team-oriented with a proactive approach Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.