Pharmaceutical Packaging & Process Engineer, Oss, Noord-Brabant

The Company Our Company is a European food manufacturer specializing in frozen snacks and appetizers. The company operates multiple production locations across Europe. Role Overview We are looking for a Technical Administrative / Work Order Coordinator to support the Project Department (TD). The main focus of this role is processing data in a new work-order system and maintaining the related dashboard. Key Responsibilities Enter and process data accurately in the new work-order management system. Maintain and update the associated dashboard. Ensure work-order information is accurate and up to date. Support the Technical/Project Department with administrative and data-related tasks. Manage and organize information using Microsoft Excel. Work accurately with technical and administrative information. Requirements HBO-level education is preferred; candidates currently taking a gap year are particularly suitable. MBO-level candidates can also be considered with a strong affinity for technology. Excellent Excel skills are essential. Interest in or affinity with a technical environment. Strong attention to detail, accuracy, and organizational skills. Comfortable working with computer systems and able to work in a structured and independent manner. Other Information If you are interested in this opportunity and meet the requirements, please submit your application using the apply button below. For further information about this opportunity, feel free to get in touch.

Company Our client is a large industrial production environment where safety, compliance, and operational continuity are critical. The site delivers complex technical projects in a highly regulated setting and works closely with multidisciplinary teams and engineering contractors to ensure reliable, future-proof installations. Job Description We are looking for an Instrumentation & Electrical Engineer (Projects) to support and deliver electrical and instrumentation engineering activities across capital projects, maintenance improvements, and operational support. The Instrumentation & Electrical Engineer (Projects) will provide compliant designs, translate requirements into clear specifications, and help ensure projects are executed safely, efficiently, and to a high technical standard. Responsibilities - Deliver concept designs and translate them into clear, well-documented engineering solutions. - Prepare and review specifications and technical requirements, including quality and process safety considerations. - Coordinate and review engineering deliverables from external contractors to ensure completeness and compliance. - Ensure designs meet applicable standards and internal procedures for electrical and instrumentation work. - Manage and track engineering activities to support delivery against project schedules and budgets. - Act as a technical point of contact for internal stakeholders such as Maintenance, Operations, and Manufacturing/Process Technology. - Support site activities such as commissioning, start-up, troubleshooting, and technical handover where required. - Contribute to continuous improvement initiatives to strengthen project execution and engineering quality. Requirements - Bachelor’s or Master’s degree in Electrical Engineering, Industrial Automation, or a comparable discipline. - Practical engineering experience in an industrial environment (process industry preferred). - Strong working knowledge of relevant electrical/instrumentation standards and directives (e.g., ATEX/IEC 60079, EMC, Machinery Directive, IEC 60204, and common NEN standards). - Solid instrumentation knowledge; affinity with electrical engineering and design is required. - Understanding of process automation and safety-related systems (SIL/SIS knowledge is a plus). - Strong analytical skills, structured problem-solving approach, and clear communication. - Able to manage multiple priorities in a busy, project-driven environment. - Fluent in Dutch and English. - Willingness to complete an online assessment and screening as part of the process. - Temporary Full Time Contract (1 Year Duration) Other Information An online assessment and screening may be part of the recruitment process. 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 an international pharmaceutical organization focused on the development and production of high-quality medicines. Within a regulated production environment, the organization places strong emphasis on GMP compliance, quality assurance, continuous improvement and patient safety. Role Description As a QA Production Specialist, you will provide quality assurance support to pharmaceutical production, covering both bulk manufacturing and packaging activities. You will support production teams with deviations and quality issues, lead or contribute to root cause investigations and CAPAs, and assess the impact of deviations on production activities. You will also review GMP documentation, support audits and compliance investigations, contribute to improvement projects and provide quality-related training and knowledge transfer within the organization. Key Responsibilities Provide QA support to pharmaceutical production, including bulk manufacturing and packaging. Support production teams with deviations, quality issues and compliance questions. Assess deviations and advise whether production activities should be halted when required. Investigate and document deviations, complaints, root causes and CAPAs. Monitor production processes and identify deviations from established procedures. Review SOPs, validation protocols, BMRs and other GMP documentation. Participate in change controls, CAPAs, audits and compliance investigations. Develop and implement continuous improvement and quality improvement initiatives. Provide recommendations regarding product safety, occupational health and environmental matters. Deliver training and knowledge transfer and collaborate with Production, QA, QPs, Engineering and other stakeholders. Requirements Master's degree or equivalent academic working level, preferably in Pharmacy, Chemical Engineering or a related field. Experience within the pharmaceutical industry and production environment. Knowledge of (aseptic) pharmaceutical processes and production control systems. Strong knowledge of GMP and Quality Assurance systems. Experience with deviations, root cause investigations and CAPAs. Experience reviewing SOPs, BMRs, validation protocols and GMP documentation. Strong analytical, advisory, communication and reporting skills. Excellent command of spoken and written English. Ability to work effectively in a dynamic and demanding production environment. Strong quality-oriented, collaborative and results-driven mindset.

About the Company Our client is a global biopharmaceutical organization with a large manufacturing and supply chain operation in Breda. The site supports the production, packaging, storage and distribution of medicines to markets across Europe, Turkey, the Middle East and Africa, operating in a complex and highly regulated environment. Role Description As a Supply Chain – Detailed Scheduler, you will be responsible for managing short-term production planning for packaging lines and ensuring a stable and reliable supply of medicines. You will develop production plans, coordinate activities across departments and remove operational flow stoppers to support timely delivery. Working closely with manufacturing, quality, warehouse and supply chain teams, you will also contribute to continuous improvement, standardization and process automation within the supply planning organization. Key Responsibilities Manage short-term production planning for packaging lines. Create production plans, manage orders and support product launches and phase-in/phase-out activities. Monitor supply chain performance and proactively remove flow stoppers. Measure weekly and monthly KPIs, including MPS stability, and drive improvement actions. Facilitate daily operational meetings and coordinate actions across departments. Lead weekly capacity meetings with manufacturing, quality, warehouse and supply chain stakeholders. Drive standardization, simplification and automation of planning processes. Lead continuous improvement initiatives and root cause analyses. Collaborate cross-functionally to ensure realistic and achievable supply plans. Ensure stable operations and supply chain efficiency while working within GMP and GDP guidelines. Requirements Experience in supply chain planning within a GMP-regulated environment Strong analytical and problem-solving skills. Excellent interpersonal and collaborative skills. Ability to perform root cause analysis and work effectively in a team environment. Strong interest in standardization, process improvement and automation. Experience or interest in tools such as Tableau, Smartsheet, Databricks or RPA is preferred. Detail-oriented and able to coordinate multiple priorities. Willingness to work at least 3 days per week on-site in Breda.

About the Company Our client is an international food production organization specializing in frozen food products. Within a structured production and packaging environment, the organization focuses on delivering safe, high-quality products while maintaining efficient production processes and strong food safety standards. Role Description As an All-round Packing Operator, you will be responsible for operating, setting up, changing over and monitoring various packaging, box forming and palletizing systems. You will use your technical knowledge to resolve minor technical issues, monitor product quality and ensure a smooth production flow. Working closely with packing staff, assistant operators and supervisors, you will contribute to safe, efficient and high-quality production in a 3-shift environment. Key Responsibilities Set up, operate, change over and monitor packaging, box forming and palletizing systems. Perform quality and safety checks and accurately record results. Monitor product flow and make adjustments when deviations or malfunctions occur. Resolve minor technical breakdowns and involve the Technical Service when required. Coordinate daily activities with packing staff and assistant operators on assigned lines. Ensure correct processing, packaging and palletizing according to the production schedule. Follow applicable food safety, quality and hygiene procedures. Contribute to an orderly, clean and safe working environment. Participate actively in shift handovers and communicate relevant information clearly. Support smooth production and contribute to achieving planned production orders. Requirements At least 2 years of relevant experience in a production or packaging environment. Knowledge of HACCP and Food Defense. Experience or ability to provide and follow safety instructions. Experience with or willingness to participate in on-the-job training. Knowledge of allergens and food safety requirements. Technical understanding and a hands-on approach to resolving minor breakdowns. Able to work effectively with colleagues in a production and shift environment. Structured and quality-focused approach to working. Willingness to work in a 3-shift system: 07:15–15:15, 15:15–23:15 and 23:15–07:15.

Over het bedrijf Onze opdrachtgever is een internationale farmaceutische organisatie die actief is binnen een sterk gereguleerde omgeving, met een sterke focus op productkwaliteit, compliance en continue verbetering binnen productie- en kwaliteitsprocessen. Functieomschrijving Als QA Officer ondersteun je diverse Quality Assurance-activiteiten binnen een GMP-gereguleerde farmaceutische of biotechomgeving. Je draagt bij aan het behandelen van afwijkingen en CAPA's, root cause investigations, validatie- en kwalificatieactiviteiten en het beoordelen van kwaliteitsdocumentatie. Je werkt nauwkeurig volgens vastgestelde kwaliteitssystemen en schakelt effectief met verschillende interne en cross-functionele stakeholders. Belangrijkste verantwoordelijkheden Ondersteunen bij het behandelen en onderzoeken van GMP-afwijkingen. Bijdragen aan het opstellen, implementeren en opvolgen van CAPA's. Ondersteunen van root cause investigations met passende onderzoeksmethodieken. Deelnemen aan validatie- en kwalificatieactiviteiten. Beoordelen van GMP-documentatie op juistheid en compliance. Ondersteunen van Quality Assurance-activiteiten binnen farmaceutische of biotechproductie. Samenwerken met verschillende afdelingen rondom kwaliteits- en compliancevraagstukken. Zorgdragen voor een correcte en volledige documentatie van kwaliteitsactiviteiten. Functie-eisen Een relevante bacheloropleiding of gelijkwaardig niveau binnen een wetenschappelijke, farmaceutische of technische richting. Aantoonbare ervaring binnen een GMP-gereguleerde Sterke ervaring met deviations, CAPA's en root cause investigations. Ervaring met validatie en kwalificatie. Ervaring met het beoordelen van GMP-documentatie. Goede kennis van GMP-principes en kwaliteitssystemen. Vloeiende beheersing van Nederlands en Engels, zowel mondeling als schriftelijk.

About the Company Our client is an international technology organization providing advanced machinery and solutions for the food processing industry. Within a collaborative and multicultural production environment, the organization focuses on delivering high-quality, innovative and reliable equipment to customers worldwide. Role Description As an Assembly Mechanic, you will be responsible for the correct assembly of modules and complete machines according to customer specifications, technical drawings and quality standards. You will work closely with colleagues across the organization to ensure machines are assembled safely, efficiently and within agreed lead times. In addition to assembly activities, you will contribute to testing, troubleshooting and continuous improvement within your area of responsibility. Key Responsibilities Assemble mechanical and mechatronic modules and machines according to customer specifications. Work according to agreed lead times and standard production times. Follow assembly, disassembly, inspection, calibration and adjustment procedures. Perform test runs and verify the dynamic functions of machines. Read and work from technical drawings and assembly documentation. Operate industrial equipment safely and in accordance with applicable requirements. Ensure compliance with quality, health, safety and environmental standards. Identify technical issues, faults or deficiencies and communicate them to the Team Leader. Contribute to continuous improvement, including manufacturability and reproducibility improvements. Participate in work discussions and collaborate with other departments when required. Requirements Secondary education in a relevant technical field. Experience and/or affinity with mechanical or mechatronic assembly. Experience reading technical drawings. Technical problem-solving skills and a practical, hands-on approach. Strong teamworking and communication skills. Result-oriented and focused on quality and customer expectations. Able to work according to schedules, procedures and safety requirements. Experience in the food processing industry is a plus. Good command of English and Dutch or German, both written and spoken. Experience in a multicultural and multidisciplinary organization is an advantage.

Over het bedrijf Onze opdrachtgever is een internationale producent binnen de voedingsmiddelenindustrie waar kwaliteit, voedselveiligheid en continu verbeteren centraal staan. Je komt terecht in een dynamische productieomgeving waar samenwerking, ontwikkeling en eigenaarschap worden gestimuleerd. Functieomschrijving Als Voorman combineer je operationele werkzaamheden met het coördineren van de dagelijkse productie. Je bent het eerste aanspreekpunt voor medewerkers en teamleiders, bewaakt de voortgang van het productieproces en zorgt ervoor dat kwaliteit, voedselveiligheid en veiligheid altijd worden nageleefd. Daarnaast begeleid en coach je collega's en draag je actief bij aan een efficiënte en veilige werkomgeving. Belangrijkste verantwoordelijkheden Coördineren en ondersteunen van de dagelijkse productieactiviteiten. Operationeel aansturen, begeleiden en coachen van productiemedewerkers. Actief meewerken binnen productie, inpak of bereiding. Toezien op naleving van HACCP-, Food Defence-, allergenen-, kwaliteits- en veiligheidsvoorschriften. Geven van veiligheidsinstructies aan medewerkers. Bewaken van standaarden zoals 5S en SMED. Zelfstandig oplossen van kleine storingen en afstemmen met de Technische Dienst bij complexe storingen. Opstellen en beheren van werkinstructies en procedures. Begeleiden en inwerken van nieuwe medewerkers. Intensief samenwerken met Productie, Logistiek, QESH en de Technische Dienst. Functie-eisen MBO werk- en denkniveau met minimaal 2 jaar relevante ervaring. Ervaring binnen de voedingsmiddelenindustrie. Kennis van HACCP, Food Defence en allergenenbeheer. Ervaring met het geven van veiligheidsinstructies en het coachen van medewerkers. Praktische en hands-on instelling met een proactieve houding. Ervaring met het coördineren van productieprocessen. Goede communicatieve en leidinggevende vaardigheden. Goede beheersing van de Nederlandse taal.

The Company A leading international food and nutrition organization with a strong focus on governance, procurement excellence, and workforce compliance. The company operates in a highly regulated environment and works with a large network of suppliers, contractors, and service providers, ensuring all engagements comply with legal and internal policy requirements. About the Role We are seeking an experienced Contract Compliance Manager to support the review and assessment of Procurement Requests and Purchase Orders that contain labor related services. The role combines employment law expertise, procurement compliance, stakeholder management, and process improvement. You will play a key role in reducing compliance risks, clearing a significant backlog of assessments, and establishing a sustainable Way of Working for the future. Responsibilities Review Procurement Requests and Purchase Orders involving labor related services Assess whether engagements qualify as external workforce arrangements or genuine service based contracts Ensure compliance with employment legislation and internal procurement policies Redirect non compliant requests through the appropriate internal process Request, validate, challenge, and assess information provided by business stakeholders Provide objective and evidence based compliance decisions Prepare detailed assessments and recommendations for escalation cases Support and advise stakeholders on compliance requirements Design and implement a future Way of Working Develop templates, procedures, guidance documents, and communication materials Identify bottlenecks and improve process efficiency Reduce assessment lead times while maintaining quality standards Support onboarding and coaching of internal employees Ensure proper documentation and effective knowledge transfer Requirements Minimum 5 years of experience in contract compliance, procurement, employment law, workforce compliance, or contract management Strong understanding of employment legislation and external workforce regulations Knowledge of Dutch DBA legislation is essential Experience with procurement processes and contract governance Ability to assess service agreements and identify hidden labor arrangements Experience managing escalations and challenging senior stakeholders Knowledge of Statement of Work structures is highly desirable Strong analytical and investigative skills Excellent communication and stakeholder management skills HBO or WO educational level Ability to work independently in a fast paced environment Strong sense of integrity and objectivity Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company – General Description A dynamic organization supporting a project department in managing technical work orders and data systems. The company values technical understanding and efficient data management to ensure smooth project operations. Job Description We are looking for a diligent Data Coordinator to join our client's project team. This role involves processing and entering data into a new work order system and maintaining associated dashboards to ensure accurate project tracking and reporting. Responsibilities - Input and process data accurately within the new work order system. - Maintain and update dashboards related to project data. - Support the project department by ensuring timely and precise data entry. - Collaborate with technical and administrative teams to ensure data integrity. Requirements - A higher professional education (HBO) student with a technical affinity, or an MBO graduate with an interest in technology. - Excellent command of Excel is essential. - Availability for 30-40 hours per week, with a requirement to work daily. - Duration of the assignment is approximately 6 months, although this may vary. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.