Electronics UI Engineer, Best, Noord-Brabant

The Company Our client is an international organisation operating across multiple markets, with a strong focus on developing its people, strengthening organisational capabilities and building a future-ready workforce. Learning, development and talent transformation are key priorities within its HR strategy. About the Role We are looking for an experienced Interim Senior L&D Programme Manager to lead several high-priority Learning & Development initiatives. In this strategic role, you will take primary ownership of the Digital Learning Ecosystem and contribute to the organisation-wide Skills Programme. You will also lead the implementation of SHL development assessments and coordinate selected High Performing Team interventions across EMEA. Working closely with Digital HR, internal L&D teams, HR stakeholders, business leaders and external partners, you will provide strategic direction, drive project delivery and ensure that learning initiatives align with wider organisational capability priorities Responsibilities - Lead the L&D roadmap and programme delivery for the Digital Learning Ecosystem. - Provide direction to internal teams and coordinate project planning and execution with Digital HR and external vendors. - Drive improvements in digital learning technologies, learner experience, accessibility and adoption. - Represent Learning & Development within the organisation's Skills Programme. - Translate workforce skills requirements into learning, upskilling and reskilling initiatives. - Ensure L&D requirements are incorporated into skills governance, taxonomy, architecture and operating model decisions. - Lead the implementation, rollout and adoption of SHL development assessment solutions. - Support assessment-related policies, governance, stakeholder communication and the transition from existing assessment providers. - Coordinate High Performing Team interventions across EMEA, supporting stakeholders and facilitators throughout the process. - Monitor programme progress, evaluate outcomes and ensure follow-up actions are delivered. Requirements - Extensive experience in senior Learning & Development, Talent Development or HR transformation roles. - Proven track record of leading strategic, organisation-wide L&D programmes and complex projects. - Strong knowledge of digital learning ecosystems, LMS/LXP platforms and learning technologies. - Experience with skills-based organisations, skills frameworks, workforce capability development or skills transformation. - Experience implementing talent or development assessment solutions; SHL or comparable assessment platforms are an advantage. - Strong stakeholder management experience, working with senior business leaders, HR teams, Digital HR and external vendors. - Experience managing cross-functional and international programmes. - Excellent communication, leadership and influencing skills. - Strategic mindset combined with a hands-on approach to programme implementation and delivery. Other Information If you are interested in this opportunity, please submit your application via the apply button below and contact us for further information.  

The Company: An international organization operating within food production and nutritional ingredients, supplying products to both business and consumer markets worldwide. The production environment has a strong focus on quality, food safety, compliance and continuous improvement. About the Role We are looking for a Food Safety and Quality Specialist for a full time assignment in Beilen. You will take ownership of the validation management system and act as the Quality Assurance representative within validation, technical and packaging projects. You will collaborate closely with Production, Engineering, Technology, Maintenance and R&D to ensure that processes meet applicable quality and food safety requirements. Responsibilities: - Set up, integrate, maintain and continuously improve the validation management system and associated documentation - Prepare, execute and periodically review the Site Validation Master Plan - Represent Quality Assurance in validation, technical and packaging projects - Translate and implement quality policies and quality documentation - Advise employees and management on quality, food safety and quality management systems - Support and verify CAPA and change management activities - Conduct internal audits and support external audits - Deliver training related to quality and food safety - Act as Subject Matter Expert for assigned quality topics - Work closely with Production, Engineering, Technology, Maintenance, R&D and Continuous Improvement - Monitor relevant internal and external developments and translate them into improvements for the organization Requirements:  - HBO or academic working and thinking level - Several years of experience within the food or pharmaceutical industry - 3 to 5 years of validation experience preferred - Knowledge of HACCP, FSSC, GMP+ and relevant regulations - Experience with quality management systems and validation processes - Experience working in project based environments - Experience with SharePoint, SAP, KMS and MS Office - Strong analytical and problem solving capabilities - Proactive approach with the ability to work independently and take initiative - Strong communication and stakeholder management skills - Dutch language proficiency is important, combined with English - Experience within pharmaceutical, infant nutrition or food environments is preferred - Experience within a large organization is preferred 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 An international organization operating in a highly regulated medical technology environment, focused on developing safe and reliable products for users worldwide. Role Description As a Usability Engineer, you will ensure that products are safe and intuitive to use throughout the design and development process. You will lead usability engineering and risk management activities, working closely with multidisciplinary teams to identify potential use-related risks, implement mitigations and demonstrate product safety in line with relevant regulatory requirements. Key Responsibilities Lead usability engineering activities throughout the product design and development lifecycle. Conduct workflow analysis, user research and task analysis to identify user needs and define usability requirements. Lead Usability FMEA and collaborate with Risk Management to identify, assess and mitigate potential risks. Develop usability engineering plans and coordinate activities with project teams and relevant stakeholders. Plan, conduct and document usability evaluations, ensuring critical findings are addressed. Analyse post-market data and identify potential usability-related issues. Advise design teams on usability aspects of product and design changes. Support the development of user-centred interfaces and safe-to-use products. Define and execute design validation strategies, plans and protocols. Ensure compliance with relevant standards and regulations, including IEC 62366, FDA guidance and applicable medical device requirements. Requirements Master's degree or PhD in Human Factors Engineering, Human-Computer Interaction, Cognitive Science, Product or Interaction Design, or a related field. At least 2–3 years of usability engineering experience within the medical device industry, covering activities from user needs and requirements through usability validation and post-market follow-up. Practical experience with Usability FMEA, risk analysis and risk mitigation. Experience conducting and reporting usability evaluations. Experience with design validation, including strategy, plans, protocols and execution. Strong understanding of relevant medical device regulations and standards, such as IEC 62366-1, FDA Human Factors Guidance, FDA 21 CFR 820.30, EU MDR, ISO 13485 and ISO 14971. Knowledge of human factors, interaction design and cognitive and physical ergonomics. Strong project management, coordination and stakeholder management skills. Independent, proactive working style and the ability to collaborate across multidisciplinary teams. Excellent written and spoken English.

  Company Our client is a global pharmaceutical manufacturing organisation with a strong focus on quality, patient safety, and compliance. Their site operates in a highly regulated environment and is committed to continuous improvement, high standards of hygiene and safety, and reliable delivery of laboratory results that support product release. Job Description For our client, we are looking for a QC Microbiology Technician (Sterility & Endotoxin Testing) to perform routine and non-routine microbiological testing on a variety of samples in a regulated laboratory environment. The role is hands-on and includes testing, accurate documentation in digital systems, and supporting investigation and improvement activities to ensure quality standards and timelines are met. Responsibilities - Perform routine and non-routine microbiological analyses according to approved procedures and quality standards - Carry out bioburden testing using membrane filtration and plate-based methods - Test for specific microorganisms using selective/elective growth media - Perform endotoxin testing using gel-clot and kinetic chromogenic methods - Execute sterility testing on finished products - Support microorganism identification using methods such as Gram staining and/or MALDI-TOF - Perform growth media release testing where required - Work safely and accurately in safety cabinets and isolators - Record, review, and report results in a laboratory information system (LIMS) - Support inventory management for media and laboratory consumables - Maintain a clean and compliant working environment; clean and maintain equipment as required - Escalate deviations promptly and support deviation documentation and investigations - Contribute to validation/qualification activities for methods and equipment where applicable - Help improve documentation (SOPs, work instructions) and support audit readiness - Support training and knowledge sharing within the team Requirements - Laboratory education at MLO level 4 or higher, ideally with a microbiology specialisation - Experience working in a GMP/GLP regulated environment - Hands-on experience with core microbiology testing (bioburden, endotoxin, sterility) is strongly preferred - Experience working with LIMS or similar digital lab systems - Comfortable working in controlled environments using safety cabinets/isolators and following strict hygiene rules - Good written communication skills in Dutch and/or English (fluency in Dutch is preferred) - Accurate, quality-focused, and proactive working style with strong attention to detail - Willingness to follow strict PPE requirements (including use of a full-face mask when required) Other Information The role is based on-site in Haarlem and offers the opportunity to work in a structured QC environment where quality, safety, and documentation are key. 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 regulated, science-driven organisation operating in a GMP environment. The team supports product quality and patient safety through robust laboratory testing, strong documentation practices, and continuous improvement of quality processes. Job Description The Microbiology QC Analyst (GMP Laboratory) will perform routine and non-routine microbiological testing on a variety of samples in a controlled laboratory setting. The role combines hands-on analysis with accurate data recording in laboratory systems, while supporting deviations, investigations, and ongoing improvements to methods and documentation. Responsibilities - Perform routine and non-routine microbiological analyses according to approved procedures - Conduct key microbiology tests, including: Bioburden testing (e.g., membrane filtration, plate methods) Testing for specified microorganisms using selective/elective media Endotoxin testing (e.g., gel-clot and kinetic chromogenic techniques) Sterility testing on finished products Microorganism identification (e.g., Gram staining and/or MALDI-TOF) Media release testing - Work safely in controlled environments (e.g., safety cabinets/isolators) and follow aseptic practices - Record and report results accurately in laboratory systems (e.g., LIMS) - Maintain a clean, compliant work area; support equipment cleaning and basic upkeep - Identify, escalate, and help document deviations; support investigations and change controls - Contribute to validation/qualification activities for methods and equipment - Support documentation improvements (SOPs, work instructions) and readiness for audits - Assist with knowledge sharing and training of colleagues where needed Requirements - MLO Level 4 (or higher) with a specialisation in Microbiology (or equivalent education) - Experience working in a GMP/GLP laboratory environment - Hands-on experience with microbiological testing techniques and quality standards - Familiarity with LIMS or other digital laboratory systems - Strong attention to detail and data integrity mindset (accurate recording of raw data) - Proactive, responsible, and team-oriented communication style - Comfortable working with strict hygiene and safety requirements (including PPE use when required) - Good written communication skills in English (Dutch is a plus) Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

Start/End Dates: 09/11/2026 - 08/05/2027   Work Location: Beilen   Job Title: QC_QSHE - QA/QC Specialist HGRL 16   Job/Project Description: QA Specialist Validatie Locatie: Beilen | Fulltime Ben jij een kwaliteitsprofessional met ervaring in validatie, voedselveiligheid en kwaliteitsmanagementsystemen? Heb je een scherp analytisch vermogen en krijg je energie van het verbeteren van processen binnen een complexe productieomgeving? Dan zijn wij op zoek naar jou als QA Specialist Validatie. In deze rol draag je bij aan de kwaliteit en voedselveiligheid van onze producten en speel je een belangrijke rol in validatieprojecten binnen de fabriek. [Functiebes...validatie | Word] Wat ga je doen? Als QA Specialist Validatie ben je verantwoordelijk voor het opzetten, onderhouden en verder ontwikkelen van het validatiemanagementsysteem. Je bent hét aanspreekpunt voor validatievraagstukken en vertegenwoordigt Quality Assurance binnen technische en verpakkingsprojecten. Daarnaast werk je nauw samen met collega's van productie, technologie, engineering en R&D om te zorgen dat processen voldoen aan alle kwaliteits- en voedselveiligheidseisen. [Functiebes...validatie | Word] Je werkzaamheden bestaan onder andere uit: •       Opzetten, integreren, onderhouden en optimaliseren van het validatiemanagementsysteem en bijbehorende documentatie. •       Vertegenwoordigen van Quality Assurance binnen validatietrajecten, technische projecten en verpakkingsprojecten. •       Opstellen en uitvoeren van het Site Validation Master Plan en periodieke reviews. •       Vertalen, implementeren en optimaliseren van kwaliteitsbeleid en kwaliteitsdocumentatie. •       Adviseren van medewerkers en management over kwaliteit, voedselveiligheid en het kwaliteitsmanagementsysteem. •       Ondersteunen en verifiëren van CAPA's en change management processen. •       Uitvoeren van interne audits en ondersteunen bij externe audits. •       Verzorgen van trainingen op het gebied van kwaliteit en voedselveiligheid. •       Fungeren als Subject Matter Expert voor toegewezen kwaliteitsonderwerpen. •       Actief volgen van interne en externe ontwikkelingen binnen het vakgebied en deze vertalen naar de organisatie. [Functiebes...validatie | Word] Waar kom je terecht? Je werkt binnen het Local Quality Assurance team op de locatie in Beilen. Deze productielocatie produceert ingrediënten en kindervoeding voor zowel B2B- als B2C-klanten wereldwijd. Je hebt veel contact met productie, engineering, technologie, maintenance, R&D, continuous improvement en externe stakeholders zoals certificerende instanties, leveranciers en klanten. [Functiebes...validatie | Word] Wat breng je mee? Wij zoeken een kwaliteitsprofessional die zelfstandig kan werken en stevig in zijn of haar schoenen staat. Daarnaast beschik je over: •       HBO- of academisch werk- en denkniveau. •       Meerdere jaren ervaring binnen de levensmiddelen- of farmaceutische industrie. •       Kennis van en ervaring met HACCP, FSSC, GMP+ en relevante wet- en regelgeving. •       Ervaring met kwaliteitsmanagementsystemen en validatieprocessen. •       Ervaring met projectmatig werken. •       Ervaring met systemen zoals SharePoint, SAP, KMS en MS Office. •       Sterke analytische vaardigheden en een verbetergerichte mindset. •       Goede communicatieve vaardigheden en overtuigingskracht. [Functiebes...validatie | Word] Wie ben jij? Je bent een proactieve professional die kansen voor verbetering ziet en deze ook weet te realiseren. Je kunt goed schakelen tussen operationele en strategische vraagstukken, houdt overzicht in complexe situaties en werkt gemakkelijk samen met verschillende disciplines binnen de organisatie. [Functiebes...validatie | Word] Wat bieden wij? •       Een uitdagende functie binnen een internationale productieomgeving. •       Veel ruimte voor eigen initiatief en professionele ontwikkeling. •       De mogelijkheid om impact te maken op kwaliteit, voedselveiligheid en continue verbetering. •       Samenwerking met diverse specialisten binnen operations, technologie en kwaliteitszorg. •       Een dynamische werkomgeving waar kwaliteit centraal staat. Supplier Note: -       Vervanging van langdurige uitval. -       Startdatum z.s.m. tot 6 maanden na start. -       Functie is voor 38 uur, minder liever niet. -       Thuiswerken: ja, nadat de kandidaat goed is ingewerkt kan er 2 dagen in de week thuis gewerkt worden. -       Ervaring met validaties (3/5 jaar). -       Voorkeur voor kandidaten met een achtergrond in de frama/kindervoeding of anders voeding. -       Pre al een kandidaat ervaring heeft met het werken in een groot bedrijf. -       We zoeken iemand die pro-actief is, zelf initiatief neemt, iemand die aan de bel trekt wanneer nodig. -       Iemand met gevoel voor kwaliteit. -       Voornamelijk Nederlands maar ook Engels. Eventueel Fries is leuk. -       Er zullen 2 gesprekken plaatsvinden, 1 op locatie en 2e online. -       Geen ZZP -       Rate: 80 -       CV deadline is 6 november 13:00

Job Title: Equipment Engineer Down Stream Processing Location: Leiden, The Netherlands Essential: Experience with down steam processing equipment and processes The Role As an Downstream Equipment Engineer, You’ll ensure our production equipment meets the highest standards. You’ll be a key player in our team, performing project related tasks including but not limited to; new equipment and/or product introduction support, support test runs on software and/or equipment, perform operational documentation changes, write engineering/ technical memo’s, work closely together with related departments like Maintenance, Execution systems and Quality. Assist colleagues in routine tasks with and tackling more complex challenges with support. Your effective communication skills will shine as you interact with both internal and external customers. What impact will you also have: Your expertise and hands-op mentality will be crucial in implementing Operations unit objectives, such as supporting by introducing new equipment and maintaining existing systems. You’ll conduct analysis to identify root causes of equipment failures, downtime and inefficiencies and collaborate with cross-functional teams to develop strategies and implement improvements to minimize equipment downtime and associated losses. You’ll guide the management of routine data collection, analysis, and reporting to drive continuous process improvement, ensuring compliant documentation and timely completion of equipment records. You’ll initiate, drive, and lead equipment improvements in collaboration with stakeholders, and support formal escalation processes to highlight risks related to safety, product quality, and regulatory compliance. You’ll be the go-to expert for sophisticated Change Control designs, from initiation to completion. Qualifications We would love to hear from you if you have the following essential requirements: · Higher professional education (HBO) or university education (WO) education, in a relevant field (e.g. pharmaceutical sciences, biotechnology, biochemistry, life sciences, biological engineering, etc) · Knowledge and/or experience with pharmaceutical production process and equipment lifecycle management. · Affinity for production equipment (Chromatography systems, Virus Filtration Systems and UFDF and automation systems (e.g. MES, DeltaV). · Able to work in a high-quality environment (GMP) · A good balance of theoretical and practical insights. · A proactive approach with adaptable problem-solving skills, consistently assuming responsibility and taking a leadership role in your area of expertise. · A focus on excellence and a customer-centric approach. · Experience with lean methodologies and project management is a plus  

The Company Our client is a leading pharmaceutical organisation committed to producing high-quality medicines in a safe, compliant, and regulated manufacturing environment. About the Role We are looking for Manufacturing Operators to support pharmaceutical production activities at a manufacturing site in Haarlem, the Netherlands. In this role, you will execute production tasks, operate equipment, prepare materials, and maintain accurate documentation in accordance with approved procedures and Good Manufacturing Practices (GMP). You will work as part of a production team, ensuring safe, accurate, and reliable manufacturing operations. Responsibilities - Execute production activities according to approved procedures, GMP standards, and safety requirements. - Prepare materials, equipment, and work areas for production activities. - Operate manufacturing equipment following appropriate training and instructions. - Maintain accurate and timely production documentation. - Identify and report deviations, abnormalities, and safety concerns. - Follow established quality, hygiene, and safety procedures. - Communicate effectively with colleagues during shift handovers. - Participate in training and cross-functional learning activities. Requirements - MBO-level education, preferably in a technical, production, or life sciences discipline. - Minimum 1 year of pharmaceutical manufacturing experience. - Practical experience working in a GMP-regulated environment. - Dutch language proficiency at A2 level or higher. - Good command of English, both spoken and written. - Accurate, structured, and detail-oriented working style. - Ability to work effectively in a regulated production environment. - Must live in or around Haarlem and be able to commute by bicycle, walking, or own transport. - Willingness to work in a rotating shift schedule. Other Information If you are interested in this opportunity, please submit your application via the apply button below and contact us for further information.

Company Our client is a large, modern manufacturing site operating in a regulated environment where safety, quality, reliability, and continuous improvement are key. The organisation invests in technology, structured ways of working, and strong engineering standards to ensure stable operations and high performance. Job Description  We are looking for an Industrial Automation Systems Engineer to help ensure the reliability, security, and continuous improvement of an industrial automation environment. The role combines oversight of automation systems with hands-on technical problem-solving, supporting daily operations, and reviewing changes and projects to ensure they meet engineering and validation standards. Responsibilities - Ensure continuity, performance, quality, and cybersecurity of industrial automation systems. - Review and safeguard projects and changes impacting automation by checking requirements, engineering standards, and validation expectations. - Provide technical support for operational automation issues and contribute to improving procedures and best practices. - Lead and support root cause investigations to prevent repeat issues and reduce unplanned downtime, using structured continuous improvement methods. - Support maintenance, change management, and lifecycle management activities in collaboration with engineering, maintenance, automation, and improvement teams. - Coordinate external contractors and suppliers, ensuring work is delivered to internal engineering and automation standards. - Act as a subject matter expert for Level 2, Level 3, and Level 4 automation systems and related infrastructure. - Develop and deliver training to strengthen automation knowledge across internal teams and stakeholders. Requirements  - Experience in industrial automation within a production/manufacturing environment. - Strong troubleshooting skills and experience leading or contributing to root cause analysis. - Familiarity with engineering standards, structured change processes, and validation-driven ways of working. - Ability to work across multiple teams and manage external contractors/suppliers. - Comfortable taking ownership and acting as a technical subject matter expert in a complex automation landscape. - Clear communication skills, including the ability to share knowledge through coaching or training. -Temporary Full-Time 12 Months Contract Other Information The role is based on-site in Cuijk, Netherlands. If you are interested and want to apply, please submit your application via the apply button below and contact me.

The Company A global biotechnology and pharmaceutical organization focused on developing, manufacturing and delivering medicines to patients worldwide. The Breda site brings together more than 1000 professionals from 38 nationalities across manufacturing, supply chain, commercial operations and clinical research. About the Role The Pharmaceutical Packaging Engineer will strengthen packaging specifications and configurations for pharmaceutical products. The position works closely with international packaging specialists, Quality Assurance, artwork teams, manufacturing, supply chain and engineering functions. The role combines technical documentation, packaging component investigations, supplier collaboration and packaging improvement projects. Responsibilities - Create and maintain packaging component specifications and technical reports - Manage documentation changes in accordance with Change Control procedures - Create, review and approve packaging testing protocols and reports - Troubleshoot packaging component issues within production, warehouse and incoming inspection activities - Lead minor and major deviation investigations involving packaging components - Develop and maintain technical relationships with approved packaging suppliers - Lead and contribute to packaging component optimization projects - Support the introduction of new packaging solutions and components - Collaborate with Quality Assurance, Supply Chain, Manufacturing, Equipment Engineering and Validation Engineering - Ensure assigned project activities meet required quality standards and milestones Requirements - Degree in Packaging Design, Engineering or a related discipline, or relevant professional experience in pharmaceutical packaging engineering - Excellent understanding of Good Manufacturing Practices - Experience creating packaging material specifications and technical layout templates - Good knowledge of materials and equipment used in secondary and tertiary pharmaceutical packaging - Understanding of the relationship between packaging specifications, manufacturing, artwork, supplier and regulatory requirements - Strong technical troubleshooting and analytical skills - Strong organizational and project management capabilities - Excellent written and verbal English communication skills - Ability to manage multiple assignments and processes - Ability to independently determine the appropriate approach to projects Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.