Senior Utility Systems Technician, Breda, Noord-Brabant

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 Utilities Maintenance Supervisor, you will oversee the maintenance and reliable operation of critical utility systems, including HVAC, refrigeration, chillers, compressed air, and boilers. You will coordinate and support a team of technicians, troubleshoot technical issues, and drive continuous improvements while ensuring safe and efficient operations in a regulated manufacturing environment. Key Responsibilities Planning, coordinating, and prioritizing maintenance activities for utility systems and building infrastructure. Providing technical guidance, coaching, and support to technicians and contractors. Troubleshooting complex issues related to utility systems and collaborating with engineering teams to find effective solutions. Working closely with contractors, vendors, and internal teams to resolve technical challenges and optimize system performance. Leading initiatives to improve system reliability and drive continuous improvement projects. Participating in an on-call rotation to support critical utility systems outside regular working hours. Requirements MBO+/HBO-level education or equivalent technical experience. Experience in utilities, facilities maintenance, or industrial installations. Strong troubleshooting skills with a hands-on approach. Proven ability to coordinate maintenance projects, manage contractors, and lead technical teams. Excellent communication skills in English and a collaborative attitude. Willingness to participate in an on-call support rotation. Previous experience in a GMP environment and familiarity with SAP PM or similar CMMS systems are advantageous. Other Information Apply to our vacancy for more information. We look forward to hearing from you!

Company: A leading biotechnology organization dedicated to serving patients worldwide. This company provides innovative medicines across a global network, focusing on maintaining a strong scientific foundation while fostering an entrepreneurial spirit. They promote fulfilling careers through challenging projects, professional development, and meaningful opportunities within a diverse and dynamic environment. Job Description: We are seeking a detail-oriented Senior Quality Assurance Specialist to oversee QA activities within the clinical supply chain. The role involves ensuring compliance with GMP and GDP standards for clinical trial products, supporting manufacturing and distribution processes, and maintaining high-quality standards across all supply chain operations. Responsibilities: •    Provide QA oversight for the clinical supply chain, including receipt, storage, and distribution of clinical trial products. •    Review and support batch certification processes to ensure compliance with EU and international regulations. •    Approve clinical label artwork and review deviations, ensuring procedural adherence. •    Assess and manage temperature excursions during transport and at clinical sites. •    Collaborate with stakeholders such as Global Clinical Supply Chain, Warehouse, Production, Quality, Clinical Research, and Regulatory Affairs to resolve compliance issues. •    Develop, review, and update SOPs and work instructions to align with corporate and regulatory standards. •    Prepare and analyze monthly quality metrics. •    Support on-site clinical packaging and labeling operations — including batch record review and issue resolution. •    Identify quality issues and work cross-functionally to implement corrective actions. Requirements: •    Master’s degree in Life Sciences or a related field. •    At least 3 years of QA or manufacturing experience within the pharmaceutical or medical device industry. •    Knowledge of GMP, GDP, and GCP regulations. •    Fluent in English, with strong communication skills. Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company A highly automated, fast-growing manufacturing site is expanding its operations and investing heavily in modern facilities, automation, and infrastructure. The environment is international, safety-driven, and strongly focused on quality and compliance. The site relies on critical utility systems to keep production, warehousing, and office operations running reliably every day. Job Description The Utilities Maintenance Team Lead supports the reliable operation of essential utility and facility systems in a complex industrial environment. This role combines strong hands-on technical knowledge with day-to-day coordination and coaching of technicians and external contractors. The Utilities Maintenance Team Lead helps ensure maintenance work is planned and executed safely, efficiently, and in line with compliance expectations, while also contributing to continuous improvement and reliability initiatives. Responsibilities - Coordinate, plan, and prioritize preventive and corrective maintenance across utility and facility systems. - Provide technical guidance, coaching, and practical support to technicians and contractors. - Troubleshoot and support resolution of complex issues related to utilities and building infrastructure. - Work closely with engineering, operations, and external vendors to align on technical solutions and execution plans. - Support reliability improvements and continuous improvement initiatives to reduce downtime and improve system performance. - Ensure maintenance activities are performed with a strong focus on safety, quality, and compliant documentation. - Participate in an on-call rotation to support critical systems when needed. Requirements - Relevant technical education or equivalent practical experience. - Experience with utilities, facilities, maintenance, or industrial installations. - Strong troubleshooting skills and a hands-on mindset. - Experience coordinating maintenance work, contractors, projects, or technical teams. - Strong communication skills and the ability to coach and support others. - Good English communication skills. - Experience in a regulated environment and familiarity with maintenance management systems (e.g., SAP PM or similar) is a plus. Other Information This is an opportunity for a professional who enjoys being close to the operation and wants to take ownership of critical infrastructure that directly supports site performance and growth. 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 globally operating biotechnology organization dedicated to developing and delivering high-quality medicines to patients worldwide. The site in Breda, the Netherlands, plays an important role in pharmaceutical manufacturing and packaging operations, maintaining high standards of quality, safety, and regulatory compliance. Job Description For our client in Breda, we are looking for a Manufacturing Technician to support pharmaceutical manufacturing activities. In this role, you will be responsible for running automated production equipment, maintaining efficient manufacturing processes, resolving technical issues, and ensuring all activities comply with Good Manufacturing Practices (GMP). Responsibilities - Run, control, and supervise automated production machinery and manufacturing lines. - Configure, set up, and adjust equipment according to production requirements. - Detect, diagnose, and resolve machine faults, process interruptions, and technical issues. - Enhance equipment performance and improve production efficiency. - Follow GMP regulations, Standard Operating Procedures (SOPs), work instructions, and safety guidelines. - Complete, update, and verify batch records, production logs, and manufacturing documentation. - Enter and validate production data using systems such as SAP and MES. - Report, document, and support investigations into deviations and abnormal process conditions. - Collaborate with Quality Assurance, Maintenance, Engineering, and Production teams to resolve operational problems. - Prepare, clean, and restore equipment during production changeovers and shutdowns. - Contribute to root cause analysis, Lean manufacturing, and continuous improvement initiatives. -Ensure the production area and equipment meet pharmaceutical quality and cleanliness standards. Requirements - Previous experience in manufacturing, machine operation, production, or process operations. - Experience working with automated machinery or industrial production lines is an advantage. - Technical knowledge of machine settings, equipment adjustments, and fault diagnosis. - Understanding of GMP, SOPs, batch records, and production documentation is desirable. - Experience with SAP, MES, or other manufacturing systems is a plus. - A background in mechanical engineering, mechatronics, electrical engineering, or a related technical field is beneficial. - Strong problem-solving skills, attention to detail, and a quality-focused mindset. - Ability to work collaboratively with cross-functional teams. - Willingness to work in a shift-based environment. Other Information The role is based on-site in Breda, the Netherlands, and offers the opportunity to work in a regulated pharmaceutical manufacturing environment with modern automated production equipment. If you are interested in this opportunity and would like to apply, please submit your application via the apply button below or contact me for more information.

The Company A global leader in biopharmaceutical manufacturing focused on producing high quality medicines that improve patient lives. The organization operates within a highly regulated environment and invests heavily in automation, operational excellence, and continuous improvement to ensure compliance and efficiency. About the Role As a Technical Operator, you will be responsible for operating, monitoring, and optimizing highly automated production lines within a GMP regulated manufacturing environment. You will play a key role in ensuring production targets, product quality, equipment reliability, and regulatory compliance are consistently achieved. This position combines technical troubleshooting, process optimization, documentation, and cross functional collaboration with Quality Assurance, Maintenance and Engineering, and Production teams. Responsibilities • Operate and monitor automated production equipment following SOPs and GMP requirements • Perform advanced troubleshooting and root cause analysis on equipment and processes • Adjust machine parameters and mechanical settings to optimize performance • Record and verify production data within SAP and MES systems • Analyze process performance and escalate deviations when necessary • Complete GMP documentation including batch records and production logs • Participate in triage meetings with QA, Maintenance and Engineering, and Production teams • Carry out equipment setup and shutdown activities • Execute daily, weekly, and monthly cleaning procedures • Monitor equipment performance and identify improvement opportunities • Support Lean and continuous improvement initiatives • Ensure effective shift handovers and team communication • Maintain a safe, compliant, and organized working environment Requirements • Minimum 3 years of experience in a production or manufacturing environment • Experience working with automated production systems • Experience within assembly, packaging, pharmaceutical, food, or similar manufacturing environments • Technical education such as MBO, VAPRO B, or equivalent • Knowledge of GMP standards and SOP driven environments • Experience with SAP and MES systems • Strong troubleshooting and root cause analysis skills • Familiarity with Lean Manufacturing, Six Sigma, and continuous improvement methodologies • Knowledge of mechatronics, pneumatics, and electronics • Ability to work effectively in structured and regulated environments • Strong communication and teamwork skills • Fluent English language skills Other Information Interested? Click Apply below

The Company A global biotechnology and pharmaceutical organization focused on developing and delivering innovative therapies that improve patient outcomes worldwide. Operating across multiple international markets, the company manages complex manufacturing and supply networks to ensure reliable product availability while maintaining high quality and regulatory standards. About the Role As a Supply Chain Manager you will be responsible for ensuring a stable and efficient supply of products across global markets. The role focuses on medium and long term supply planning, inventory optimization, production alignment, and stakeholder management. You will work closely with global supply chain teams, production sites, and business stakeholders to balance demand, capacity, inventory, and cost while supporting product launches and lifecycle management activities. Responsibilities - Own tactical and strategic supply planning activities - Manage medium and long term planning for assigned products and production lines - Maintain and optimize supply plans using Rapid Response planning tools - Participate in weekly and monthly planning meetings and governance reviews - Collaborate with global supply chain teams and manufacturing sites - Identify supply risks and opportunities and propose mitigation strategies - Drive inventory management aligned with strategic targets - Support product launches, phase outs, and lifecycle management activities - Conduct root cause analysis and implement corrective actions for supply deviations - Deliver scenario planning and business impact assessments - Monitor production capacity utilization and component availability - Ensure planning cycles are completed accurately and on time - Contribute to continuous improvement initiatives across the supply chain Requirements - Bachelor's or Master's degree in Supply Chain, Business Administration, Engineering, or a related field - Proven experience in end to end supply chain planning and operations - Experience within regulated industries such as pharmaceuticals, medical devices, food, beverages, or ingredients - Strong analytical and problem solving skills - Ability to influence stakeholders and build cross functional relationships - Experience with Lean, Six Sigma, or Continuous Improvement methodologies - Strong communication and collaboration skills - Leadership capabilities and ability to drive initiatives to completion - End to end supply chain perspective - Experience with SAP - Experience with Rapid Response planning systems is highly preferred 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 globally operating organization in the life sciences sector, focused on delivering high-quality medicines for patients worldwide. The site in the Netherlands plays a key role in labelling, packaging, storage, and distribution for both commercial and clinical supply chains, working in a fast-paced, international environment with high quality and compliance standards. Job Description For our client in Breda, we are looking for a Clinical Supply Chain Quality Assurance Specialist to provide QA oversight across the clinical supply chain and support production-related quality activities. The role ensures investigational medicinal products are handled in full compliance with GMP/GDP requirements, supporting smooth release, distribution, and packaging/labelling operations for clinical trials. Responsibilities - Provide quality guidance and oversight for investigational medicinal products to ensure GMP/GDP compliance - Review batch documentation to support batch certification activities - Review and approve clinical label artwork and support packaging/labelling quality checks - Assess and document temperature excursions during transport and at clinical sites/depots - Support investigation and resolution of quality/compliance issues related to manufacturing, packaging, and distribution - Review and approve minor deviations in line with internal procedures and regulatory expectations - Draft, update, and maintain operational SOPs and work instructions - Review SOPs to ensure alignment with corporate standards, site procedures, and regulatory requirements - Prepare and contribute to monthly quality metrics and reporting - Work cross-functionally with stakeholders across supply chain, warehouse/distribution, production, - quality, clinical operations, and regulatory teams - Perform QA-on-the-floor activities such as pack checks, batch record review, and compliance checks - ---during manufacturing activities Requirements - Master’s degree (preferably Life Sciences or a related field) - Several years of experience in Quality Assurance and/or manufacturing within pharma, biotech, or medical devices - Hands-on experience with documentation review (e.g., batch records) and deviation/investigation support - Solid knowledge of GMP and GDP (GCP is a plus) - Strong attention to detail, structured way of working, and a compliance-focused mindset - Good communication skills and ability to collaborate with multiple stakeholders - Fluent in English Other Information The role is based on-site in Breda and offers the opportunity to work in an international environment supporting clinical trial supply activities end-to-end. If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company A global manufacturing organization operating within a GMP-regulated environment, focused on delivering quality products that improve patients' lives. The company values innovation, teamwork, operational efficiency, and a strong culture of compliance and continuous improvement. Role Description As you are responsible for operating high-tech manufacturing equipment in a GMP-regulated environment, ensuring production runs smoothly, efficiently, and in full compliance with strict quality standards. As a Manufacturing Process Technician, you play a critical role in supporting the timely delivery of high-quality medicines, contributing directly to the organization’s commitment to patients and operational excellence. Responsibilities - Operate and monitor automated production and packaging equipment in line with GMP and SOP requirements. - Perform troubleshooting and root cause analysis (RCA) to resolve equipment and process issues. - Optimize machine settings and process parameters to improve efficiency and performance. - Maintain accurate GMP documentation, batch records, and production logs. - Record and verify production data using SAP, MES, or ERP systems. - Participate in cross-functional problem-solving and triage meetings with QA, Maintenance, and Production teams. - Carry out equipment setup, changeovers, line clearance, and shutdown activities. - Execute routine cleaning and basic maintenance activities. - Support Lean Manufacturing and Continuous Improvement initiatives. - Ensure effective shift handovers and maintain a safe, compliant, and organized workplace. Requirements - 3+ years of experience in automated production, manufacturing, assembly, or packaging environments. - Experience within Pharmaceutical, Biotechnology, Food, FMCG, or other regulated industries. - Knowledge of GMP regulations, SOPs, and quality standards. - Experience with SAP, MES, or other manufacturing systems. - Strong troubleshooting skills using RCA, 5 Why, Fishbone, Kaizen, TPM, or SMED methodologies. - Technical understanding of automation systems, mechatronics, pneumatics, sensors, and machine components. - Experience with Lean Manufacturing and Continuous Improvement programs. - Technical qualification such as MBO, VAPRO B, Engineering, Mechatronics, or equivalent. - Good communication skills and ability to work effectively with cross-functional teams. - Fluent in English and willing to work in a shift-based manufacturing environment. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.