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Head of Vattenfall Security Center Netherlands
Vacaturebeschrijving Where you will work Energy is our contribution to quality of life, day after day. With over 42.000 co-workers Vattenfall provides comprehensive electricity and heating offerings to several million customers in northern Europe. For the work ahead we need people who are fully dedicated to our customers and to a sustainable society, people like you. Main tasks and responsibilites Vattenfall Corporate Security is responsible for Information Security, Physical Security, Personnel Security, Event Security and National Security in all Vattenfall core countries. We are now looking for a Head of Security Center Netherlands. You will be responsible for the unit (including personnel) and to supply competence and resources to Corporate Security, Business Divisions (BD), Business Units (BU) and to Country Managers within your area of responsibility. You will report to the Vattenfall Chief Security Officer. You will act as a BD Security Officer (BSO) with focus on being a single point of contact for BD Asset Development and BD Asset Optimisation and Trading with an international responsibility. You will also act as Country Security Manager for Netherlands. The CSM supports the Country Manager to fulfil his/her duties, in particular to ensure country specific response to security threats and incidents in compliance with national legislation as well as to collaborate with national authorities regarding national security issues (including critical infrastructure protection). Requirements University degree in the respective field or equivalent. At least 5 year’s work experience as a Corporate Security Director with people responsibility or equivalent. Acts as a partner at BD level; works well with all levels of management and support staff in national as well international teams. Experienced in establishing and maintaining internal and external contacts. Experience from Security Management work in an international environment. Good competence within core Security areas and specialist within 1-2 areas. Fluent in English (spoken and written). The job requires travel, off-time work, and being a Duty Officer. A national security clearance might be necessary for the position. The working place is in Amsterdam. More information For more information regarding this vacancy, please contact Jasmijn van ‘t Hul, Recruiter, on the following number: 06-21 88 06 66 or apply directly through www.nuon.nl/werken.
Head of Vattenfall Security Center Netherlands
Vacaturebeschrijving Where you will work Energy is our contribution to quality of life, day after day. With over 42.000 co-workers Vattenfall provides comprehensive electricity and heating offerings to several million customers in northern Europe. For the work ahead we need people who are fully dedicated to our customers and to a sustainable society, people like you. Main tasks and responsibilites Vattenfall Corporate Security is responsible for Information Security, Physical Security, Personnel Security, Event Security and National Security in all Vattenfall core countries. We are now looking for a Head of Security Center Netherlands. You will be responsible for the unit (including personnel) and to supply competence and resources to Corporate Security, Business Divisions (BD), Business Units (BU) and to Country Managers within your area of responsibility. You will report to the Vattenfall Chief Security Officer. You will act as a BD Security Officer (BSO) with focus on being a single point of contact for BD Asset Development and BD Asset Optimisation and Trading with an international responsibility. You will also act as Country Security Manager for Netherlands. The CSM supports the Country Manager to fulfil his/her duties, in particular to ensure country specific response to security threats and incidents in compliance with national legislation as well as to collaborate with national authorities regarding national security issues (including critical infrastructure protection). Requirements University degree in the respective field or equivalent. At least 5 year’s work experience as a Corporate Security Director with people responsibility or equivalent. Acts as a partner at BD level; works well with all levels of management and support staff in national as well international teams. Experienced in establishing and maintaining internal and external contacts. Experience from Security Management work in an international environment. Good competence within core Security areas and specialist within 1-2 areas. Fluent in English (spoken and written). The job requires travel, off-time work, and being a Duty Officer. A national security clearance might be necessary for the position. The working place is in Amsterdam. More information For more information regarding this vacancy, please contact Jasmijn van ‘t Hul, Recruiter, on the following number: 06-21 88 06 66 or apply directly through www.nuon.nl/werken.
Head of Vattenfall Security Center Netherlands
Vacaturebeschrijving Where you will work Energy is our contribution to quality of life, day after day. With over 42.000 co-workers Vattenfall provides comprehensive electricity and heating offerings to several million customers in northern Europe. For the work ahead we need people who are fully dedicated to our customers and to a sustainable society, people like you. Main tasks and responsibilites Vattenfall Corporate Security is responsible for Information Security, Physical Security, Personnel Security, Event Security and National Security in all Vattenfall core countries. We are now looking for a Head of Security Center Netherlands. You will be responsible for the unit (including personnel) and to supply competence and resources to Corporate Security, Business Divisions (BD), Business Units (BU) and to Country Managers within your area of responsibility. You will report to the Vattenfall Chief Security Officer. You will act as a BD Security Officer (BSO) with focus on being a single point of contact for BD Asset Development and BD Asset Optimisation and Trading with an international responsibility. You will also act as Country Security Manager for Netherlands. The CSM supports the Country Manager to fulfil his/her duties, in particular to ensure country specific response to security threats and incidents in compliance with national legislation as well as to collaborate with national authorities regarding national security issues (including critical infrastructure protection). Requirements University degree in the respective field or equivalent. At least 5 year’s work experience as a Corporate Security Director with people responsibility or equivalent. Acts as a partner at BD level; works well with all levels of management and support staff in national as well international teams. Experienced in establishing and maintaining internal and external contacts. Experience from Security Management work in an international environment. Good competence within core Security areas and specialist within 1-2 areas. Fluent in English (spoken and written). The job requires travel, off-time work, and being a Duty Officer. A national security clearance might be necessary for the position. The working place is in Amsterdam. More information For more information regarding this vacancy, please contact Jasmijn van ‘t Hul, Recruiter, on the following number: 06-21 88 06 66 or apply directly through www.nuon.nl/werken.
SHE Engineer
(1,0 fte Nederland) Functie – rol en verantwoordelijkheden In de functie van SHE Engineer ben je verantwoordelijk voor het bewaken, uitvoeren en coördineren van activiteiten die betrekking hebben op veiligheid, gezondheid en milieu binnen de sales & after sales vestigingen en de processing plants. Een belangrijke taak is het coachen van managers en het medevormgeven en implementeren van het Benelux beleid ten aanzien van SHE. Daarnaast bewaak je de vastgestelde SHE doelstellingen binnen de organisatie. Je belangrijkste taken zijn: Ondersteunen en adviseren van de SHE Manager bij de ontwikkeling en uitvoering van het beleid ten aanzien van veiligheid, gezondheid, arbo en milieu. Ondersteunen van operationeel management bij de uitvoering van het SHE beleid en het aanleveren van management informatie. Preventiemedewerker binnen de diverse processing plants en vestigingen. Het onderhouden en verbeteren van het integraal SHE management-systeem. Opstellen van jaarplannen en uitvoeren van evaluaties en audits op het gebied van SHE Het initiëren en leiden van projecten inzake veiligheid, arbeidsomstandigheden en milieu. Onderhouden van contacten met externe instanties (o.a. klanten en bevoegd gezag) en begeleiding van externe audits, inspecties en controles. Jouw profiel: Technische of bedrijfskundige opleiding op Bachelor niveau. Een afgeronde MVK opleiding. Relevante werkervaring en kennis van bedrijfsprocessen in een vergelijkbare functie. Kennis van managementsystemen zoals OHSAS 18001, ISO-9001, ISO-14001, HACCP/ISO-22000. Je beschikt over doorzettingsvermogen en stressbestendigheid aangevuld met een enthousiaste en flexibele instelling. Een sterk analytisch, kritisch en probleemoplossend vermogen. Goede sociale en communicatieve vaardigheden en een uitstekende beheersing van de Nederlandse en Engelse taal in woord en geschrift
Sr Associate QA
Amgen discovers, develops, manufactures, and delivers innovative human therapeutics. A leader in biotechnology since 1980, Amgen was one of the first companies to realize the new science’s promise by bringing safe, effective medicines from lab, to manufacturing plant, to patient. Amgen therapeutics have changed the practice of medicine, helping millions of people around the world in the fight against cancer, kidney disease, rheumatoid arthritis, bone disease, and other serious illnesses. Amgen pioneered the development of novel products based on advances in recombinant DNA and molecular biology, and launched the biotechnology industry’s first blockbuster medicines. Today, as a Fortune 500 company serving millions of patients, Amgen continues to be an entrepreneurial, science-driven enterprise dedicated to helping people fight serious illness. Objective – To provide QA guidance and support in the production area at Amgen Breda – To perform batch record review of batches assembled, packaged and labeled and contract manufacturers. – To establish effective working relationships with Production, Warehouse, Maintenance and Engineering, QA Management and the Qualified Person Position Specific tasks: – Provide daily guidance and support to Production staff in regards to compliance with Standard Operating Procedures and Work Instructions. – Act as a first point of contact in case of production queries (quality related) during packaging and labeling operations. – Review and approve batch production record data entries before production activities take place – Perform finished product checks during (commercial) production runs – Compile and review batch records for lots assembled, packaged and labeled and contract manufacturers in preparation for disposition by Qualified Person. – Act as author for operational SOP’s and Work Instructions – Review of operational SOP’s and Work Instructions – Review and approve class I Non Conformances – Initiate and own QA Non Conformances as needed. In this job you work in 3 shifts (including night shifts) – MBO or Bachelor’s degree in Life Sciences or related field or the equivalent combination of education and/or experience. – Typically 3 years of related Quality Assurance or manufacturing experience in the pharmaceutical or medical device industry with experience in batch record review and investigations. – Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) and/ or Good Clinical Practice (GCP) knowledge with the ability to interpret and apply in mainly routine cases. – Manufacturing and/or Quality analytical processes and operations. – Fluent in English language. Amgen discovers, develops, manufactures, and delivers innovative human therapeutics. A leader in biotechnology since 1980, Amgen was one of the first companies to realize the new science’s promise by bringing safe, effective medicines from lab, to manufacturing plant, to patient. Amgen therapeutics have changed the practice of medicine, helping millions of people around the world in the fight against cancer, kidney disease, rheumatoid arthritis, bone disease, and other serious illnesses. Amgen pioneered the development of novel products based on advances in recombinant DNA and molecular biology, and launched the biotechnology industry’s first blockbuster medicines. Today, as a Fortune 500 company serving millions of patients, Amgen continues to be an entrepreneurial, science-driven enterprise dedicated to helping people fight serious illness. Objective – To provide QA guidance and support in the production area at Amgen Breda- To perform batch record review of batches assembled, packaged and labeled and contract manufacturers. – To establish effective working relationships with Production, Warehouse, Maintenance and Engineering, QA Management and the Qualified PersonPosition Specific tasks:- Provide daily guidance and support to Production staff in regards to compliance with Standard Operating Procedures and Work Instructions. – Act as a first point of contact in case of production queries (quality related) during packaging and labeling operations.- Review and approve batch production record data entries before production activities take place- Perform finished product checks during (commercial) production runs- Compile and review batch records for lots assembled, packaged and labeled and contract manufacturers in preparation for disposition by Qualified Person.- Act as author for operational SOP’s and Work Instructions- Review of operational SOP’s and Work Instructions- Review and approve class I Non Conformances- Initiate and own QA Non Conformances as needed.In this job you work in 3 shifts (including night shifts)- MBO or Bachelor’s degree in Life Sciences or related field or the equivalent combination of education and/or experience. – Typically 3 years of related Quality Assurance or manufacturing experience in the pharmaceutical or medical device industry with experience in batch record review and investigations.- Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) and/ or Good Clinical Practice (GCP) knowledge with the ability to interpret and apply in mainly routine cases.- Manufacturing and/or Quality analytical processes and operations.- Fluent in English language.
Sr Associate QA
Amgen discovers, develops, manufactures, and delivers innovative human therapeutics. A leader in biotechnology since 1980, Amgen was one of the first companies to realize the new science’s promise by bringing safe, effective medicines from lab, to manufacturing plant, to patient. Amgen therapeutics have changed the practice of medicine, helping millions of people around the world in the fight against cancer, kidney disease, rheumatoid arthritis, bone disease, and other serious illnesses. Amgen pioneered the development of novel products based on advances in recombinant DNA and molecular biology, and launched the biotechnology industry’s first blockbuster medicines. Today, as a Fortune 500 company serving millions of patients, Amgen continues to be an entrepreneurial, science-driven enterprise dedicated to helping people fight serious illness. Objective – To provide QA guidance and support in the production area at Amgen Breda – To perform batch record review of batches assembled, packaged and labeled and contract manufacturers. – To establish effective working relationships with Production, Warehouse, Maintenance and Engineering, QA Management and the Qualified Person Position Specific tasks: – Provide daily guidance and support to Production staff in regards to compliance with Standard Operating Procedures and Work Instructions. – Act as a first point of contact in case of production queries (quality related) during packaging and labeling operations. – Review and approve batch production record data entries before production activities take place – Perform finished product checks during (commercial) production runs – Compile and review batch records for lots assembled, packaged and labeled and contract manufacturers in preparation for disposition by Qualified Person. – Act as author for operational SOP’s and Work Instructions – Review of operational SOP’s and Work Instructions – Review and approve class I Non Conformances – Initiate and own QA Non Conformances as needed. In this job you work in 3 shifts (including night shifts) – MBO or Bachelor’s degree in Life Sciences or related field or the equivalent combination of education and/or experience. – Typically 3 years of related Quality Assurance or manufacturing experience in the pharmaceutical or medical device industry with experience in batch record review and investigations. – Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) and/ or Good Clinical Practice (GCP) knowledge with the ability to interpret and apply in mainly routine cases. – Manufacturing and/or Quality analytical processes and operations. – Fluent in English language. Amgen discovers, develops, manufactures, and delivers innovative human therapeutics. A leader in biotechnology since 1980, Amgen was one of the first companies to realize the new science’s promise by bringing safe, effective medicines from lab, to manufacturing plant, to patient. Amgen therapeutics have changed the practice of medicine, helping millions of people around the world in the fight against cancer, kidney disease, rheumatoid arthritis, bone disease, and other serious illnesses. Amgen pioneered the development of novel products based on advances in recombinant DNA and molecular biology, and launched the biotechnology industry’s first blockbuster medicines. Today, as a Fortune 500 company serving millions of patients, Amgen continues to be an entrepreneurial, science-driven enterprise dedicated to helping people fight serious illness. Objective – To provide QA guidance and support in the production area at Amgen Breda- To perform batch record review of batches assembled, packaged and labeled and contract manufacturers. – To establish effective working relationships with Production, Warehouse, Maintenance and Engineering, QA Management and the Qualified PersonPosition Specific tasks:- Provide daily guidance and support to Production staff in regards to compliance with Standard Operating Procedures and Work Instructions. – Act as a first point of contact in case of production queries (quality related) during packaging and labeling operations.- Review and approve batch production record data entries before production activities take place- Perform finished product checks during (commercial) production runs- Compile and review batch records for lots assembled, packaged and labeled and contract manufacturers in preparation for disposition by Qualified Person.- Act as author for operational SOP’s and Work Instructions- Review of operational SOP’s and Work Instructions- Review and approve class I Non Conformances- Initiate and own QA Non Conformances as needed.In this job you work in 3 shifts (including night shifts)- MBO or Bachelor’s degree in Life Sciences or related field or the equivalent combination of education and/or experience. – Typically 3 years of related Quality Assurance or manufacturing experience in the pharmaceutical or medical device industry with experience in batch record review and investigations.- Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) and/ or Good Clinical Practice (GCP) knowledge with the ability to interpret and apply in mainly routine cases.- Manufacturing and/or Quality analytical processes and operations.- Fluent in English language.
Integrator Environmental Control and Infrastructure
Education: Technical University Masters or Bachelor in Mechanical engineering, or related. Experience: • Experience in relevant industry and technology areas. • Experience with planning. Personal skills: • Candidate should be able to work independently in a dynamic explorative environment. • Robust personality is a must. • Strong pragmatic attitude with an analytical view. • Good communicational skills and good knowledge of English. Context of the position: The department of Environmental Control & Infrastructure (EC&I) is part of the hardware cluster within the development and engineering sector. The task of this department is to develop, deliver, integrate and qualify functional modules & parts of lithography tools related to temperature control and gas conditioning. Technology areas are: gas-, vacuum- and water-flow control, architecture and design, temperature control.
Integrator Environmental Control and Infrastructure
Education: Technical University Masters or Bachelor in Mechanical engineering, or related. Experience: • Experience in relevant industry and technology areas. • Experience with planning. Personal skills: • Candidate should be able to work independently in a dynamic explorative environment. • Robust personality is a must. • Strong pragmatic attitude with an analytical view. • Good communicational skills and good knowledge of English. Context of the position: The department of Environmental Control & Infrastructure (EC&I) is part of the hardware cluster within the development and engineering sector. The task of this department is to develop, deliver, integrate and qualify functional modules & parts of lithography tools related to temperature control and gas conditioning. Technology areas are: gas-, vacuum- and water-flow control, architecture and design, temperature control.
Safety Coördinator
Nutricia Advanced Medical Nutrition, onderdeel van de Medical Nutrition Division van het beursgenoteerde Danone, is Europees marktleider in medische voeding. Op het Supply Point Zoetermeer wordt zowel vloeibare medische voeding als vloeibare baby voeding ontwikkeld, geproduceerd en gedistribueerd naar 45 landen. Nutricia staat voor innovatie, vooruitstrevende techniek en kwaliteit vanwege de zeer hoge eisen die wij stellen aan de producten voor onze kwetsbare doelgroepen: baby’s, ouderen en zieken. Het Supply Point Zoetermeer heeft de afgelopen periode (5 jaar) een jaarlijkse groei gerealiseerd van 10-15%. Nutricia, Supply Point Zoetermeer, zoekt voor de afdeling Health Safety & Environment (HSE) een enthousiaste: Fulltime De Functie Als ‘Safety Coördinator’ ben je verantwoordelijk voor het inrichten en bewaken van veiligheid op zowel een operationele als tactische wijze binnen de productielocatie Zoetermeer. Hierbij kun je denken aan het adviseren van medewerkers op alle niveaus binnen de organisatie op het gebied van veiligheid en gezondheid, het vastleggen van processen, structuur aanbrengen binnen het HSE management systeem en het verder ontwikkelen hiervan. Je bent werkzaam in een dynamische omgeving die continu onderhevig is aan verbeteringen op het gebied van arbeidsomstandigheden, milieu aspecten en kwaliteit. Hierbij werk je nauw samen met je collega’s om uniformiteit en kwaliteit in de processen te waarborgen. Het functieprofiel: Het adviseren van de organisatie op het gebied van health & safety; Op de hoogte zijn van wet en regelgeving, normen, standaarden, best practices qua veiligheid en in staat zijn om deze om te zetten naar werkprocessen voor de gebruikers; Het verder ontwikkelen en onderhouden van het safety management systeem; Het plannen en (laten) uitvoeren van interne- en externe audits, werkplekinspecties en -onderzoeken, risico inventarisaties (RIE/TRA/HAZOP/FMEA); Het vervullen van de rol van preventiemedewerker conform de uitgangspunten van de Arbo-wet; Het opzetten, uitvoeren en/of beoordelen van HSE projectplannen (intern/extern); Het opzetten, voorbereiden en geven van veiligheidstrainingen; Het vervullen van administratieve taken zoals het periodiek verzamelen, analyseren en verwerken van veiligheidsgerelateerde gegevens, inclusief het archiveren ervan; Het assisteren bij calamiteiten en ongevalonderzoek, – rapportage en de communicatie hieromtrent; Het coördineren en begeleiden van externe specialisten/contractors op het gebied van veiligheid; Het HSE team bestaat uit drie medewerkers en je rapporteert in deze functie aan de HSE Officer. Het profiel Functie eisen: Je beschikt over HBO denk- en werkniveau met een technische achtergrond en je hebt tenminste de opleiding MVK met succes afgerond; Je hebt minimaal 3 tot 5 jaar werkervaring binnen een soortgelijke functie; Je hebt ervaring met MS Office- applicaties (o.a. Visio); Je beschikt over een uitstekende beheersing van de Nederlandse en Engelse taal in woord en geschrift. Persoonlijke kenmerken: Je bent energiek, flexibel, gedreven en je denkt procesmatig. Projecten en activiteiten wil je graag goed en volledig afronden op een systematische en nauwkeurige manier. Prioriteiten stellen is je tweede natuur en je kunt zodoende snel schakelen op verschillende niveaus binnen de organisatie. Stressbestendig, analytisch, communicatief en motiverend zijn tevens eigenschappen die jouw omschrijven. Herken jij jezelf in bovenstaand profiel? Reageer dan via onderstaande link of de HIRIS Self Service. Neem contact op met Folkert van den Beld, Senior Recruiter via telefoonnummer 06 1179 4893 voor meer informatie over de functie en/of procedure. NB: een assessment zal onderdeel uitmaken van deze procedure.
Teamleider Productie bij McCain Foods Holland
Aardappels zijn onze wereld, al vanaf het begin, toen de familie McCain op bescheiden schaal pootaardappelen verhandelde en exporteerde vanuit Florenceville in Canada. Het merk McCain heeft sinds 1956 een grote naamsbekendheid opgebouwd en McCain is uitgegroeid tot wereldwijd marktleider in diepvriesaardappelproducten. Tientallen productielijnen en vestigingen zijn sindsdien geopend en de verwachting is dat deze trend zich in de nabije toekomst zal voortzetten. Thuis en buiten de deur genieten miljoenen mensen van McCain: de lekkerste en beste aardappel- en snackproducten ter wereld. Door de invoering van de 5-ploegendienst zijn wij voor de vestiging Lelystad op zoek naar een: Teamleider Productie Functie omschrijving Teamleider Productie De Teamleider Productie draagt zorg voor het bewaken en aansturen van de productie afdeling op basis van de productieplanning, gericht op de realisatie van optimale resultaten conform de richtlijnen en specificaties op het gebied van veiligheid, kwaliteit, kwantiteit en dit tegen de laagste kosten ten einde de doelstellingen van zijn shift te behalen en zorgt voor een juiste ploegenoverdracht. De Teamleider Productie geeft direct en indirect leiding aan een team van medewerkers en draagt zorg voor een optimale bezetting in de shift zodat de doestellingen kunnen worden gerealiseerd. Dit houdt o.a. in: aansturen, coachen, corrigeren, motiveren en inspireren van de medewerkers. De Teamleider Productie is proactief in het initiëren van verbeteringsvoorstellen ten einde het productieproces zo veilig, efficiënt en betrouwbaar mogelijk te laten verlopen. De Teamleider Productie ziet er op toe dat tijdens de normale productie en tijdens lijnstilstanden door medewerkers en derden gewerkt wordt volgens bestaande procedures en wetgeving, ten einde ongevallen, lichamelijk letsel, foodsafety problemen, downtime evenals materiële en milieuschade te voorkomen. Is buiten kantooruren verantwoordelijk voor de gehele plant. McCain vraagt: – HBO-werk/denkniveau, bij voorkeur richting Levensmiddelen- of Procestechnologie – Meerdere jaren aantoonbare leidinggevende ervaring – Oog voor veiligheid – Een daadkrachtige, communicatieve en flexibele instelling – Een sterk analytisch vermogen – Een leidinggevende die kan aansturen, inspireren, coachen, en motiveren – Goede mondelinge en schriftelijke communicatieve vaardigheden in de Nederlandse en Engels taal Kijk voor meer informatie over ons op: http://www.mccain.nl. Solliciteren op de vacature Teamleider Productie Ben je toe aan een nieuwe uitdaging en herken je jezelf in bovengeschetst profiel? Dan nodigen wij je van harte uit om te reageren. Laat je CV met motivatie achter op onze sollicitatiepagina. Acquisitie naar aanleiding van deze vacature wordt niet op prijs gesteld