Site Deployment Lead, Lochem, Gelderland

Over het bedrijf Sluit je aan bij een toonaangevende internationale farmaceutische producent waar geneesmiddelen worden geëtiketteerd, geassembleerd, opgeslagen en wereldwijd gedistribueerd. Je werkt in een GMP-gereguleerde productieomgeving en draagt bij aan betrouwbare productieprocessen, een hoge productkwaliteit en continue verbetering. Functieomschrijving Als Technical Operator – Semi-geautomatiseerde Productielijnen ben je verantwoordelijk voor het bedienen en bewaken van semi-geautomatiseerde productieapparatuur. Je zorgt ervoor dat het productieproces veilig, efficiënt en volgens de geldende kwaliteits- en GMP-richtlijnen verloopt. Daarnaast voer je machine-instellingen uit, los je technische en procesmatige storingen op, houd je productiegegevens nauwkeurig bij en draag je bij aan verbeterinitiatieven binnen een gestructureerde productieomgeving. Verantwoordelijkheden Bedienen en bewaken van semi-geautomatiseerde productie- en verpakkingslijnen. Uitvoeren van machine-instellingen, omstellingen, line clearance-werkzaamheden en reinigingsactiviteiten. Oplossen van storingen aan apparatuur en productieprocessen en uitvoeren van kleine machineafstellingen. Vastleggen van productieactiviteiten en batchgegevens in SAP- en MES-systemen. Ondersteunen bij afwijkingsonderzoeken (deviation investigations) en productiegerelateerde triageactiviteiten. Actief bijdragen aan Lean- en Continuous Improvement-initiatieven. Waarborgen van naleving van GMP-, veiligheids- en kwaliteitsrichtlijnen. Werken volgens SOP's (Standard Operating Procedures) en werkinstructies om een efficiënt productieproces te waarborgen. Bijdragen aan optimale prestaties van de apparatuur en een betrouwbare productie. Functie-eisen Afgeronde MBO-opleiding in een technische richting of een vergelijkbaar opleidingsniveau. Ervaring met het bedienen van productie-, assemblage-, etiketteer- of verpakkingsapparatuur. Technisch inzicht in productieprocessen en productieapparatuur. Sterke analytische vaardigheden en ervaring met het oplossen van technische storingen. Ervaring met Root Cause Analysis (RCA), 5 Why of vergelijkbare probleemoplossingsmethodieken is een pré. Ervaring binnen een GMP-omgeving of een andere gereguleerde productieomgeving. Ervaring met SAP en/of MES-systemen. Kennis van Lean Manufacturing of Continuous Improvement is een pré. Proactieve, nauwkeurige en kwaliteitsgerichte werkhouding. Goede beheersing van de Engelse taal. Bereidheid om te werken in een 3-ploegendienst, met de mogelijkheid om in de toekomst over te gaan naar een 5-ploegendienst. Arbeidsvoorwaarden Fulltime functie. Marktconform salaris met aantrekkelijke ploegentoeslagen. Ruime opleidings- en doorgroeimogelijkheden. Moderne GMP-productieomgeving met veel aandacht voor veiligheid, kwaliteit en het welzijn van medewerkers.

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. Role Description As a Production Operator, you will be responsible for operating and maintaining semi-automated production and packaging lines within a GMP-regulated manufacturing environment. You will ensure production processes run safely, efficiently, and in compliance with quality standards while supporting continuous improvement initiatives and minimizing production downtime. Responsibilities Run and oversee production machines to keep operations running smoothly. Prepare equipment for new production batches and switch products when needed. Spot and fix minor machine issues to reduce downtime. Enter and update production records using the company's systems. Help investigate production issues and support practical solutions. Suggest ideas to improve efficiency, quality, and daily operations. Follow safety, quality, and company procedures at all times. Work closely with your team to achieve daily production goals. Requirements A technical background or hands-on experience in a production or manufacturing environment. Previous experience working with production machinery or automated equipment. Comfortable troubleshooting basic machine or process issues. Experience in industries such as pharmaceuticals, biotechnology, food, medical devices, or other regulated environments is a plus. Familiarity with production systems such as SAP or similar software is an advantage. A proactive mindset with a willingness to learn and improve processes. Good communication skills in English. Willingness to work rotating 3-shift or 5-shift schedules. Other Information This is an excellent opportunity to join a global, high-tech manufacturing environment where you'll work with advanced automation technologies while developing your technical skills and career. A competitive salary, shift allowances, bonus, 13th-month salary, holiday allowance, and excellent development opportunities are offered. Apply to our vacancy for more information. We look forward to hearing from you!

The Company A global pharmaceutical manufacturing organization focused on innovation, quality, and operational excellence. The company operates highly automated production facilities within a GMP regulated environment and invests heavily in advanced manufacturing technologies and continuous improvement initiatives. Role Description As an Automation Operator, you will be responsible for operating, monitoring, and optimizing automated production lines to ensure safe, efficient, and compliant manufacturing processes. This role combines technical troubleshooting, equipment operation, and GMP documentation while supporting process improvements and production performance. Responsibilities - Operate and monitor automated production equipment according to SOPs and GMP standards - Perform troubleshooting and root cause analysis on automated systems - Adjust machine parameters and settings to improve operational performance - Record and verify production data within SAP and MES systems - Monitor process performance and report deviations when required - Complete batch records, production logs, and GMP documentation accurately - Participate in cross functional problem solving and triage meetings - Execute equipment startup and shutdown procedures - Perform routine cleaning activities according to production schedules - Identify and support continuous improvement opportunities - Contribute to Lean Manufacturing initiatives - Ensure smooth shift handovers and effective communication - Maintain a safe and compliant production environment Requirements - Minimum 3 years of experience in a similar manufacturing or production role - Experience working within automated production environments - Fluent English communication skills - Experience following SOPs and GMP procedures - Knowledge of assembly and packaging processes - Experience using SAP and MES systems - Strong troubleshooting and analytical skills - Experience with Lean Manufacturing and Six Sigma principles - Technical understanding of mechatronics, pneumatics, and electronics - Ability to understand and explain the function of sensors, valves, bearings, and automation components - Willingness to work in rotating 3-shift or 5-shift schedules. - Technical education such as MBO, VAPRO B, or equivalent Other Information - Shift based work environment - Pharmaceutical manufacturing environment - GMP regulated facility - Strong focus on automation, quality, and continuous improvement

About the Company Join a global leader in health technology where innovation is at the heart of everything. As part of a central Innovation Engineering organization, you will work across multiple business units to bring next-generation medical devices, AI-enabled healthcare solutions, and consumer health technologies from concept to market. This is an opportunity to lead high-impact, international innovation programs that shape the future of healthcare. Role Description As a Senior Innovation Project Manager, you will lead large-scale, multidisciplinary innovation programs spanning hardware, software, AI, digital health, and medical technologies. You will be responsible for driving projects from concept through development, validation, industrialization, and market launch while ensuring alignment with business strategy, regulatory requirements, and customer needs. Working with senior stakeholders across multiple global business units, you will combine strategic leadership with operational excellence to deliver innovative solutions that create enterprise-wide value. Key Responsibilities Lead complex cross-functional innovation programs from concept to commercial launch Define project scope, roadmap, timelines, budgets, and governance structures Translate customer, clinical, and business needs into innovative product development strategies Drive collaboration across R&D, Software, AI, Systems Engineering, Supply Chain, Manufacturing, Quality, Regulatory Affairs, and Commercial teams Ensure compliance with medical device regulations and quality standards, including FDA, MDR, ISO 13485, ISO 14971, and IEC 62304 Integrate AI and digital technologies into product development and innovation programs Manage program risks, dependencies, budgets, quality, and executive reporting Lead steering committees and executive governance meetings Build strong relationships with external partners, suppliers, research institutes, and technology partners Identify opportunities for platform reuse, process improvements, and enterprise-wide innovation Mentor multidisciplinary project teams and contribute to project management best practices Requirements 7+ years of experience leading complex multidisciplinary product development or innovation programs Proven experience delivering medical devices, digital health solutions, AI-enabled products, consumer health products, or consumer electronics from concept to launch Experience working within highly regulated environments Strong knowledge of FDA, MDR, ISO 13485, ISO 14971, IEC 62304, Quality Management Systems (QMS), and product development processes Experience managing large international and cross-functional stakeholder groups Demonstrated experience with AI/ML-enabled products or applying AI technologies within development programs Strong systems engineering mindset with experience across hardware, software, cloud, and digital technologies Excellent leadership, communication, stakeholder management, and decision-making skills PMP, IPMA, SAFe, or equivalent Project Management certification is required Fluent in English

The Company  A Global leading international dairy company with a cooperative heritage spanning over 150 years. The company processes milk into a diverse range of dairy products and ingredients, offering consumers high-quality options such as milk, yogurt, condensed milk, dairy-based beverages, cheese, butter, quark, and cream.. Role Description We are seeking a highly skilled Project Manager specializing in Commissioning & Start-Up (CSU) to oversee a major investment project at their Nuenen site. The role involves leading the CSU activities for new equipment installations, including a UHT system, homogeniser, and aseptic storage tank, ensuring the project meets quality, validation, and timeline standards for successful operational startup. Responsibilities -Develop and implement the overall CSU strategy and detailed plan. -Lead the CSU phase from mechanical completion through to first commercial production. -Act as the main point of contact for all CSU stakeholders, coordinating between project teams, site operations, suppliers, quality assurance, and the customer. -Support and oversee qualification and validation activities, ensuring compliance with project and customer specifications. -Incorporate product acceptance criteria and customer-specific requirements into the start-up process. -Identify potential risks, challenge assumptions, and establish practical timelines with clear milestones. -Maintain open communication with the customer regarding project progress, risks, and timeline adjustments. Review project planning and develop realistic, achievable schedules to meet critical deadlines. Requirements -Proven experience as a CSU Manager in large-scale food, dairy, beverage, pharmaceutical, or process industry projects. -Strong knowledge of commissioning, qualification, validation, and start-up methodologies. -Experience managing stakeholder relationships, including customer interface. -Ability to challenge plans constructively and offer practical solutions. -Excellent communication and leadership skills. -VCA certification (preferably VCA-vol), with fluency in both English and Dutch. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

Over het Bedrijf Sluit je aan bij een toonaangevende internationale producent in de voedingsmiddelenindustrie die investeert in de uitbreiding en modernisering van haar productiefaciliteiten. Binnen een groot investeringsproject speel je een cruciale rol in de succesvolle Commissioning & Start-Up van een nieuwe productielijn en zorg je voor een soepele overgang van de bouwfase naar commerciële productie. Rolomschrijving Als CSU Manager ben je verantwoordelijk voor het leiden van de volledige Commissioning & Start-Up-fase van een groot investeringsproject, waarbij een nieuwe UHT-installatie, homogenisator en aseptische opslagtank worden geïnstalleerd. Je ontwikkelt en implementeert de CSU-strategie, coördineert kwalificatie- en validatieactiviteiten en zorgt ervoor dat alle betrokken partijen gedurende het gehele traject optimaal samenwerken. Je combineert technische expertise met sterk stakeholdermanagement en een gestructureerde aanpak van documentatie en projectuitvoering. Belangrijkste Verantwoordelijkheden Ontwikkelen, beheren en uitvoeren van de volledige Commissioning & Start-Up-strategie Leiden van de CSU-fase vanaf mechanical completion tot en met commerciële productie Coördineren van kwalificatie- en validatieactiviteiten conform project- en klantvereisten Fungeren als belangrijkste aanspreekpunt voor projectteams, operations, quality, leveranciers en klanten Beoordelen en kritisch analyseren van de projectplanning en het identificeren van risico's en verbeterpunten Opstellen van een realistische planning, mijlpalen en CSU-roadmap Zorgen dat klantacceptatiecriteria worden geïntegreerd in de commissioningstrategie Onderhouden van communicatie met klanten over projectvoortgang, planning en oplevering Waarborgen van volledige en correcte projectdocumentatie gedurende commissioning en validatie Bijdragen aan een veilige, efficiënte en succesvolle projectuitvoering Vereisten HBO- of WO-opleiding in Werktuigbouwkunde, Procestechnologie, Food Technology, Engineering of een vergelijkbare technische richting Aantoonbare ervaring als Commissioning & Start-Up (CSU) Manager binnen grootschalige investeringsprojecten Grondige kennis van commissioning, kwalificatie, validatie en start-up processen Ervaring binnen de voedingsmiddelen-, zuivel-, farmaceutische-, dranken- of procesindustrie (ervaring binnen de zuivel is een sterke pré) Sterke stakeholdermanagementvaardigheden en ervaring met klantgerichte projecten Uitstekende plannings-, documentatie- en risicomanagementvaardigheden Ervaring met het aansturen en coördineren van multidisciplinaire projectteams In het bezit van een VCA-certificaat (VCA-VOL is een sterke pré) Goede beheersing van zowel de Nederlandse als Engelse taal Bereid om voornamelijk op locatie te werken en indien nodig incidenteel mee te draaien tijdens de opstartfase Opdrachtdetails Start: Zo snel mogelijk Eerste fase: 1–2 dagen per week (2026) Vanaf Q4 2026: 4–5 dagen per week tot en met Q2 2027 Standplaats: Nuenen (voornamelijk op locatie) ZZP'ers zijn welkom Opdrachtduur: Circa 9 maanden (voor ZZP in contracten van 6 maanden)

About The Company Our client is a leading global FMCG organization seeking a Response Planner to join its Integrated Planning team. This role is responsible for balancing short-term demand and supply, improving customer service, reducing business waste, and driving continuous planning improvements. Role Description As a Response Planner, you will manage the short-term (up to 6 weeks) demand and supply reconciliation process to ensure product availability while minimizing inventory waste. You will collaborate with cross-functional teams to manage service risks, optimize stock allocation through AATP Business Rules, and support continuous improvement initiatives with Genpact. Key Responsibilities Drive short-term demand and supply reconciliation. Manage service risks and customer order priorities. Own and maintain AATP Business Rules. Reduce excess, blocked, residual, and obsolete inventory. Support continuous improvement and root cause analysis. Collaborate with Sales, Customer Service, Market Supply Planning, and Genpact. Key Requirements Bachelor's degree in Supply Chain, Business, Engineering, or a related field. Experience in Response Planning, Supply Planning, or Integrated Planning. Knowledge of SAP S/4HANA, AATP, and planning tools (Kinaxis preferred). Strong analytical, stakeholder management, and communication skills. Interested? Click the application link below to submit your application and take the next step in your career.  

Company: A leading organization in the pharmaceutical industry dedicated to maintaining the highest standards of quality and safety in its research and production processes. Committed to innovation and compliance, the company provides a dynamic environment for professionals to contribute to impactful projects. Job Description: We are seeking a reliable and detail-oriented Quality Assurance Coordinator to support laboratory quality systems. The role involves ensuring regulatory compliance, managing quality data, and supporting GMP standards within the laboratory environment. Responsibilities: - Ensure the timely and accurate processing of regulatory changes within quality systems such as SAP, LIMS, and MS Office. - Maintain GMP compliance across all activities. - Collaborate closely with Qualified Persons and internal teams to facilitate quality assurance processes. - Support the implementation and documentation of quality procedures and updates. - Assist in audits and inspections related to quality standards. - Contribute to continuous improvement initiatives related to quality management. Requirements: - Minimum of 1 year of relevant work experience in a quality or laboratory environment. - Dutch language skills are essential; fluency in English is required. - Higher vocational education (HBO) in biochemistry, microbiology, or a related field. - Experience with SAP and knowledge of GMP/GDocP are preferred. 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 organization in the pharmaceutical and animal health sector, operating across multiple locations in the Netherlands. The company is known for its strong focus on safety, compliance, and innovation within engineering and production environments Role Description We are seeking a skilled QC Transfer Specialist to join our Animal Health division. In this role, you will ensure the successful transfer and validation of biological and analytical tests related to vaccines and pharmaceuticals. You will play a key part in transferring new tests from R&D or other sites into our quality control labs, ensuring compliance with GMP standards and meeting transfer timelines. Responsibilities -Lead and support the transfer of biological and analytical tests for vaccines and pharmaceutical products, ensuring reproducibility and quality. -Manage transfer projects, whether introducing new tests or transferring existing ones from R&D or other sites, within set timeframes. -Perform and validate transfer tests, support testing of post-transfer samples, and coordinate with the QC team for seamless integration. -Act as the primary contact for deviations, changes, audits, training, and documentation related to transfers, adhering to GMP procedures. -Collaborate with R&D and other sites to ensure smooth transfer processes and continuous improvement initiatives using Lean Six Sigma tools. -Monitor transfer progress, escalate issues when necessary, and drive towards timely completion of projects. Requirements -HBO education or higher in microbiology, analytical chemistry, or a related laboratory field. -Minimum of 5 years’ experience in a biological QC or similar lab environment, preferably within a GMP or GLP setting. -Proven experience with transfer processes, project management, and data analysis. Familiarity with SAP, LIMS, or similar electronic data systems. -Certification or experience with Lean Six Sigma, problem-solving, and root cause analysis is a plus. Accurate, solution-oriented, and able to work independently as well as part of a team. -Strong communication skills in English and Dutch, both written and spoken. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company: A global biotechnology company dedicated to improving patients' lives through innovative medicines. The Breda manufacturing site is a highly automated, GMP-regulated facility responsible for the production, labeling, assembly, and distribution of medicines to more than 75 countries worldwide. The company values innovation, operational excellence, continuous improvement, and collaboration while providing employees with excellent career development opportunities. Job Description: As a Technical Operator (GMP) – Automated Manufacturing, you'll play an important role in the day-to-day running of our manufacturing operation. Working within a GMP-regulated environment, you'll help ensure products are produced safely, efficiently, and to the highest quality standards. You'll work with advanced production equipment, support troubleshooting activities when issues arise, and help keep manufacturing processes running smoothly. Whether it's operating equipment, carrying out routine checks, recording production data, or identifying improvements, you'll be a key part of a team focused on delivering reliable results. This position is ideal for someone who enjoys a hands-on technical role, likes solving problems, and wants to contribute to a modern manufacturing environment where quality, safety, and continuous improvement are at the heart of everything we do. Responsibilities: Ensure production activities are completed according to GMP, quality, and safety standards. Operate automated equipment used for manufacturing, assembly, labeling, and packaging activities. Prepare production lines for new batches, including equipment set-up, changeovers, cleaning, and line clearance activities. Review and record manufacturing data using digital systems such as SAP and Manufacturing Execution Systems (MES). Investigate process deviations and support Root Cause Analysis (RCA / 5 Why) to prevent recurring issues. Identify opportunities to improve workflows, equipment performance, and operational efficiency through Lean Manufacturing and Continuous Improvement initiatives. Work closely with colleagues from Production, Engineering, Maintenance, and Quality teams to solve day-to-day operational challenges. Perform routine inspections, equipment adjustments, and basic first-line maintenance tasks. Monitor production performance and take appropriate action when abnormalities occur. Support a culture of teamwork, innovation, operational excellence, and continuous improvement. Requirements: This opportunity is ideal for someone who enjoys working in a technical environment, likes finding practical solutions, and takes pride in maintaining high standards of quality and compliance. We'd love to hear from you if you have: MBO-level technical qualification or equivalent experience. Experience working within manufacturing, production, processing, or other industrial operations. Experience operating or supporting automated machinery or technology-driven production environments. Strong problem-solving skills with a structured approach to troubleshooting. Previous experience within a GMP-regulated or other quality-controlled industry, such as pharmaceuticals, biotechnology, medical devices, food production, or chemicals. Knowledge of GMP requirements and quality-focused ways of working. Experience with production software or digital manufacturing systems such as SAP, MES, or similar platforms. A proactive attitude with a high level of ownership, accountability, and attention to detail. Good communication skills in English. Willingness to work a rotating 3-shift or 5-shift schedule. Other Information: This is an excellent opportunity to join a global biotechnology leader and work in a highly automated, GMP-regulated manufacturing environment. You'll benefit from competitive compensation, career development opportunities, and a collaborative, innovative workplace while contributing to the production of life-changing medicines for patients worldwide. If you are interested and would like to apply, please submit your application via the apply button below or contact me for more information