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Het overzicht van de statistiek van de lonen bij het beroep "QA in "

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Het overzicht van de statistiek van de lonen bij het beroep "QA in "

1 760 € Gemiddeld maandsalaris

Niveau van het gemiddelde loon tijdens de laatste 12 maanden: "QA in "

Valuta: EUR USD Jaar: 2021
Op de staafdiagram is de verandering van het gimiddelde loon van het beroep QA in getoond.

Vergelijking van het gemiddelde salaris voor de zoekopdracht "QA" in met de belangrijkste steden van het land

Valuta: EUR USD Jaar: 2021
Het staafdiagram vergelijkt het gemiddelde salaris voor de zoekopdracht "QA" met het gemiddelde salaris in de administratieve centra van de afgelopen maand.

Aanbevolen vacatures

Associate Director Quality Assurance (Live Vaccines
Merck Gruppe MSD Sharp & Dohme, Boxmeer, Noord-Brabant
Associate Director Quality Assurance (Live Vaccines) Location Boxmeer, Netherlands Job Type Full time This site is for Residents of Europe, Middle East, Africa, Latin America & Asia Pacific. Residents of the United States, Canada & Puerto Rico, please click here . Job Description We are looking for a coaching leader with a keen eye for individual and team potential. You are a skilled people manager and looking for an opportunity to develop a knowledgeable team in a complex and demanding organization and push them to the next level in terms of individual, team-, and quality development. We have an exciting new job opportunity at our location in Boxmeer and are looking to hire a Associate Director Quality Assurance (Live Vaccines) Welcome in our team Our Quality Assurance group consists of 9 teams (120 - 130 FTE) and ensures every single material inside our products is manufactured, processed, tested, packaged, stored and distributed aligned with our high-quality standards aligned to the regulatory requirements. Partnering across our internal manufacturing facilities, external contract manufacturers and suppliers we create an interdependent global manufacturing network committed to deliver a compliant, reliable supply to customers and patients on time, every time, across the globe. Purpose of the role Reporting into the Director Quality Assurance, you are responsible for managing and driving QA with responsibility for all (operational) quality assurance activities related to the production of live vaccines. Main tasks and responsibilities Managing and developing a team of 15 -20 QA specialists with the ambition to constantly improve People, Safety, Quality, Delivery and Cost; Define and implement departmental strategy and support the development of site Quality Operations strategy; Implement and further develop department procedures; Support the quality mindset development and pursue Zero Overdue Culture; Ensure quality guides are followed within the live vaccines department; Actively support and monitor all relevant training initiatives; Act as a Quality counterpart for the Director Quality Assurance on the development and execution of strategic initiatives; Creating and subsequently optimizing and improving QA processes; Develop and implement new initiatives to modernize QA processes, methodologies and technologies; Representing the Quality Team Live Vaccines during inspections and external visits; Where necessary, contribute to ad hoc situations and problems; Ensure good and constructive cooperation between relevant stakeholders for effective and efficient operation (amongst others Quality Control, Quality Assurance, Production, R&D, Regulatory Affairs) Your profile University degree (Masters or Ph.D.) in, (Bio)Chemistry, (Bio)Process Technology, or related scientific fields; At least 5 years of experience in a pharmaceutical manufacturing organization with demonstrated people management skills; Knowledge of cGMP regulations and expectations governing facilities, equipment and procedures for the manufacture of (bio)pharmaceutical products; You are an excellent people influencer, inspiring people with your drive, energy and enthusiasm; Excellent command of the Dutch and English language; Living at a reasonable distance from Boxmeer. What we offer We welcome you to a truly global, dynamic and challenging environment with great opportunities for personal development. Our benefits are very competitive, and the summary below will give you an idea of what you can expect. Competitive salary and a 3% year-end allowance; 35,5 days of leave; Attractive collective health care insurance package with considerable reduction rates; Solid Pension Plan; Annual bonus based on own and company performance Travel allowance for commuting Numerous training, coaching and e-learning modules for long term job opportunities and development Animal Health Our Animal Health Division is a trusted global leader in veterinary medicine, dedicated to preserving and improving health, well-being, and performance of animals and the people who care for them. We are a global team of professionals working together to make a positive difference in animal care and the world’s food supply and have a deep sense of responsibility towards our customers, consumers, animals, society, and our planet. Through our commitment to The Science of Healthier Animals®, we offer veterinarians, farmers, pet owners and governments one of the widest ranges of veterinary pharmaceuticals, vaccines and health management solutions and services as well as an extensive suite of digitally connected identification, traceability and monitoring products. We invest in dynamic and comprehensive R&D resources and a modern, global supply chain. We are present in more than 50 countries, while our products are available in some 150 markets. Who we are … We are known as Merck & Co., Inc., Kenilworth, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world. What we look for … In a world of rapid innovation, we seek brave Inventors who want to make an Impact in all aspects of our business, enabling breakthroughs that will affect generations to come. We encourage you to bring your disruptive thinking, collaborative spirit and diverse perspective to our organization. Together we will continue Inventing For Life, Impacting Lives while Inspiring Your Career Growth. INVENT. IMPACT. INSPIRE. We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace. For questions about this vacancy Please send an email including the vacancy number and job title to the following email address: RecruitmentNLMSD.com Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Kenilworth, NJ, USA, also known as Merck Sharp & Dohme Corp., Kenilworth, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: Domestic VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Shift: Valid Driving License: Hazardous Material(s): Number of Openings: 1 Requisition ID: R107980 Email this job to: Your name About Us We are one company, but we operate under two different corporate brand names. ​​​​​​​We are known as Merck & Co., Inc., Kenilworth, New Jersey, USA in the United States, Canada & Puerto Rico. We are known as MSD everywhere else. Not ready to apply? Join our Talent Community to stay connected and receive updates on the latest job opportunities. Sign up Now Get tailored job recommendations based on your interests. This careers website is intended for Residents of Europe, Middle East, Africa, Latin America & Asia Pacific. Residents in the United States, Canada & Puerto Rico, please visit this Careers website . Information on this site is for the purpose of presenting career opportunities at our organisation and give our audience a view of our culture, diversity and growth opportunities. Our Company is an equal opportunity employer, proudly embracing diversity in all of its manifestations. Reporting on our commitment to society, people and communities around the world An initiative to create a world where no woman has to die giving life The global animal health business unit of MSD
Associate Director Quality Assurance (Live Vaccines)
MSD animal health, Boxmeer, Noord-Brabant
Solliciteer direct Indien solliciteer direct u verwijst naar een ongeldig webadres, is de vacature waarschijnlijk inmiddels vervuld. Attendeer FMF hierop Associate Director Quality Assurance (Live Vaccines) Introductie We are looking for a coaching leader with a keen eye for individual and team potential. You are a skilled people manager and looking for an opportunity to develop a knowledgeable team in a complex and demanding organization and push them to the next level in terms of individual, team-, and quality development. Het bedrijf / The company Welcome in our team Our Quality Assurance group consists of 9 teams (120 - 130 FTE) and ensures every single material inside our products is manufactured, processed, tested, packaged, stored and distributed aligned with our high-quality standards aligned to the regulatory requirements. Partnering across our internal manufacturing facilities, external contract manufacturers and suppliers we create an interdependent global manufacturing network committed to deliver a compliant, reliable supply to customers and patients on time, every time, across the globe. Extra info Animal Health Our Animal Health Division is a trusted global leader in veterinary medicine, dedicated to preserving and improving health, well-being, and performance of animals and the people who care for them. We are a global team of professionals working together to make a positive difference in animal care and the world’s food supply and have a deep sense of responsibility towards our customers, consumers, animals, society, and our planet. Through our commitment to The Science of Healthier Animals®, we offer veterinarians, farmers, pet owners and governments one of the widest ranges of veterinary pharmaceuticals, vaccines and health management solutions and services as well as an extensive suite of digitally connected identification, traceability and monitoring products. We invest in dynamic and comprehensive R&D resources and a modern, global supply chain. We are present in more than 50 countries, while our products are available in some 150 markets. De functie / The role Purpose of the role Reporting into the Director Quality Assurance, you are responsible for managing and driving QA with responsibility for all (operational) quality assurance activities related to the production of live vaccines. Main tasks and responsibilities Managing and developing a team of 15 -20 QA specialists with the ambition to constantly improve People, Safety, Quality, Delivery and Cost; Define and implement departmental strategy and support the development of site Quality Operations strategy; Implement and further develop department procedures; Support the quality mindset development and pursue Zero Overdue Culture; Ensure quality guides are followed within the live vaccines department; Actively support and monitor all relevant training initiatives; Act as a Quality counterpart for the Director Quality Assurance on the development and execution of strategic initiatives; Creating and subsequently optimizing and improving QA processes; Develop and implement new initiatives to modernize QA processes, methodologies and technologies; Representing the Quality Team Live Vaccines during inspections and external visits; Where necessary, contribute to ad hoc situations and problems; Ensure good and constructive cooperation between relevant stakeholders for effective and efficient operation (amongst others Quality Control, Quality Assurance, Production, R&D, Regulatory Affairs) Het profiel / Your profile Your profile University degree (Masters or Ph.D.) in, (Bio)Chemistry, (Bio)Process Technology, or related scientific fields; At least 5 years of experience in a pharmaceutical manufacturing organization with demonstrated people management skills; Knowledge of cGMP regulations and expectations governing facilities, equipment and procedures for the manufacture of (bio)pharmaceutical products; You are an excellent people influencer, inspiring people with your drive, energy and enthusiasm; Excellent command of the Dutch and English language; Living at a reasonable distance from Boxmeer. Het aanbod / The offer What we offer We welcome you to a truly global, dynamic and challenging environment with great opportunities for personal development. Our benefits are very competitive, and the summary below will give you an idea of what you can expect. Competitive salary and a 3% year-end allowance; 35,5 days of leave; Attractive collective health care insurance package with considerable reduction rates; Solid Pension Plan; Annual bonus based on own and company performance Travel allowance for commuting Numerous training, coaching and e-learning modules for long term job opportunities and development Reactie / Reaction For questions about this vacancy Please send an email including the vacancy number and job title to the following email address: RecruitmentNLMSD.com Tenslotte / Finally Who we are … We are known as Merck & Co., Inc., Kenilworth, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world. What we look for … In a world of rapid innovation, we seek brave Inventors who want to make an Impact in all aspects of our business, enabling breakthroughs that will affect generations to come. We encourage you to bring your disruptive thinking, collaborative spirit and diverse perspective to our organization. Together we will continue Inventing For Life, Impacting Lives while Inspiring Your Career Growth. Solliciteer hier Indien solliciteer hier u verwijst naar een ongeldig webadres, is de vacature (hoogstwaarschijnlijk) inmiddels vervuld. Attendeer FMF hierop Uw referentie aan www.fmfvacatures.nl wordt gewaardeerd. Your referral to www.fmfvacatures.nl is appreciated. Gegevens Werkgever: MSD animal health Vacaturesteller: MSD animal health Standplaats: Boxmeer Geplaatst op FMF: 22 april 2021 Branche: Farma & Biotech Functie: QA / regulatory, Management Opleidingsniveau: WO/academisch / MSc Werkervaring: 5-10 jaar, > 10 jaar
Mangatwacht
Otter-Westelaken B.V., Boxmeer, NL
Heb jij veiligheid hoog in het vaandel staan en ben je alert op onveilige situaties? Dan kan je via ons kosteloos opgeleid worden tot mangatwacht!Als jij de stap wil maken naar een nieuwe baan als mangatwacht dan ben je:Je werkt samen met een team collega's aan de veiligheid op de locatie. Dit kan zijn tijdens werkzaamheden die uitgevoerd worden zoals bijvoorbeeld een verbouwing of reparatie. Als voorbeeld: er moet een reparatie uitgevoerd worden binnen een besloten ruimte. Jij bent dan degene die controleert of de monteur veilig zijn werk kan doen. Je houdt de omgeving in de gaten en zorgt ervoor dat niks de ingang van de ruimte afsluit. Daarnaast houd je contact met de monteur of alles goed gaat. Zie je iemand op de werkvloer die niet de juiste persoonlijke beschermingsmiddelen draagt dan spreek je diegene hierop aan. Voor jou staat veiligheid op nummer 1!Als mangatwacht ben je werkzaam op twee locaties, namelijk in Boxmeer en Oss. Dit kan per dag verschillen. Je werkt samen met een team van enthousiaste en gemotiveerde collega's aan hetzelfde doel: een veilige werksituatie creëren en houden. Hiervoor krijg je een door Otter-Westelaken verzorgde cursus bij een van onze opleiders. Heb je daarnaast nog geen VCA en BHV, of is deze verlopen, dan kan je ook deze via ons behalen. Hier zitten voor jou geen kosten aan verbonden.Mooie kans op een nieuwe baan met opleidingsmogelijkheden toch? Wees er snel bij en solliciteer direct!
Associate Director Quality Assurance (Live Vaccines)
Merck Sharp & Dohme Limited, Boxmeer, Noord-Brabant
Job DescriptionWe are looking for a coaching leader with a keen eye for individual and team potential. You are a skilled people manager and looking for an opportunity to develop a knowledgeable team in a complex and demanding organization and push them to the next level in terms of individual, team-, and quality development.We have an exciting new job opportunity at our location in Boxmeer and are looking to hire aAssociate Director Quality Assurance (Live Vaccines)Welcome in our teamOur Quality Assurance group consists of 9 teams (120 - 130 FTE) and ensures every single material inside our products is manufactured, processed, tested, packaged, stored and distributed aligned with our high-quality standards aligned to the regulatory requirements. Partnering across our internal manufacturing facilities, external contract manufacturers and suppliers we create an interdependent global manufacturing network committed to deliver a compliant, reliable supply to customers and patients on time, every time, across the globe.Purpose of the role Reporting into the Director Quality Assurance, you are responsible for managing and driving QA with responsibility for all (operational) quality assurance activities related to the production of live vaccines.Main tasks and responsibilitiesManaging and developing a team of 15 -20 QA specialists with the ambition to constantly improve People, Safety, Quality, Delivery and Cost;Define and implement departmental strategy and support the development of site Quality Operations strategy;Implement and further develop department procedures;Support the quality mindset development and pursue Zero Overdue Culture;Ensure quality guides are followed within the live vaccines department;Actively support and monitor all relevant training initiatives;Act as a Quality counterpart for the Director Quality Assurance on the development and execution of strategic initiatives;Creating and subsequently optimizing and improving QA processes;Develop and implement new initiatives to modernize QA processes, methodologies and technologies;Representing the Quality Team Live Vaccines during inspections and external visits;Where necessary, contribute to ad hoc situations and problems;Ensure good and constructive cooperation between relevant stakeholders for effective and efficient operation (amongst others Quality Control, Quality Assurance, Production, R&D, Regulatory Affairs)Your profileUniversity degree (Masters or Ph.D.) in, (Bio)Chemistry, (Bio)Process Technology, or related scientific fields;At least 5 years of experience in a pharmaceutical manufacturing organization with demonstrated people management skills;Knowledge of cGMP regulations and expectations governing facilities, equipment and procedures for the manufacture of (bio)pharmaceutical products;You are an excellent people influencer, inspiring people with your drive, energy and enthusiasm;Excellent command of the Dutch and English language;Living at a reasonable distance from Boxmeer.What we offerWe welcome you to a truly global, dynamic and challenging environment with great opportunities for personal development. Our benefits are very competitive, and the summary below will give you an idea of what you can expect.Competitive salary and a 3% year-end allowance;35,5 days of leave;Attractive collective health care insurance package with considerable reduction rates;Solid Pension Plan;Annual bonus based on own and company performanceTravel allowance for commutingNumerous training, coaching and e-learning modules for long term job opportunities and developmentAnimal HealthOur Animal Health Division is a trusted global leader in veterinary medicine, dedicated to preserving and improving health, well-being, and performance of animals and the people who care for them. We are a global team of professionals working together to make a positive difference in animal care and the world’s food supply and have a deep sense of responsibility towards our customers, consumers, animals, society, and our planet.Through our commitment to The Science of Healthier Animals®, we offer veterinarians, farmers, pet owners and governments one of the widest ranges of veterinary pharmaceuticals, vaccines and health management solutions and services as well as an extensive suite of digitally connected identification, traceability and monitoring products. We invest in dynamic and comprehensive R&D resources and a modern, global supply chain. We are present in more than 50 countries, while our products are available in some 150 markets.Who we are … We are known as Merck & Co., Inc., Kenilworth, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.What we look for … In a world of rapid innovation, we seek brave Inventors who want to make an Impact in all aspects of our business, enabling breakthroughs that will affect generations to come. We encourage you to bring your disruptive thinking, collaborative spirit and diverse perspective to our organization. Together we will continue Inventing For Life, Impacting Lives while Inspiring Your Career Growth.INVENT.IMPACT.INSPIRE. We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.For questions about this vacancyPlease send an email including the vacancy number and job title to the following email address: RecruitmentNLMSD.comCurrent Employees apply HERECurrent Contingent Workers apply HERESearch Firm Representatives Please Read Carefully Merck & Co., Inc., Kenilworth, NJ, USA, also known as Merck Sharp & Dohme Corp., Kenilworth, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: RegularRelocation:DomesticVISA Sponsorship:Travel Requirements:Flexible Work Arrangements:Shift:Valid Driving License:Hazardous Material(s):Number of Openings: 1Job InfoType: Full timeLocation: NLD - Boxmeer
Associate Director Commissioning & Qualification
Merck Sharp & Dohme Limited, Boxmeer, Noord-Brabant
Job DescriptionWe have an exciting new opportunity for anAssociate Director Commissioning & QualificationPurpose of the roleThe Associate Director functions under the guidance of the C&Q Leader within Global Engineering Solutions (GES) and works with our Engineering Partners to ensure individual projects have appropriate C&Q leadership during design and execution. This position will provide direct project support for projects as identified by the Technology Center and Area Delivery Directors including hyper-care support for strategic or at risk projects.The Associate Director exhibits strong leadership, interpersonal and communication skills, decision making and the ability to guide global work. The candidate should have a strong understanding of equipment and facility design, safety practices, standards, operations, maintenance and industry regulations. Flexibility with global travel as needed to support current project’s is also required.The Associate Director will contribute to the development and maintenance of core documents such as internal Practices, Procedures, Design Guides and Engineering Standards. In addition, they should participate in professional/technical organizations and in the development and delivery of subject matter training for GES.Primary responsibilitiesWork with Process Design Managers in the development of Regulatory Design Basis and C&Q Execution Strategy during Concept and Basis of Design phases of projects.Support project teams in assessing project level staffing needs to ensure that appropriate C&Q staffing, expertise and leadership (both with internal and external resources) exists to successfully execute projects.Facilitate GMP design reviews, design qualification and collaborate on the development of Project Validation Master Plans and execution of Product Quality Risk AssessmentsProvide direct project support for strategic and at risk projects to ensure successful execution of the C&Q strategy.Participate in project assessments for active projects to identify opportunities for improvement and confirm readiness for project to progress through the stagegate process.Acts as a subject matter expert on: regulatory compliance in facility and equipment design and qualification; C&Q execution planning; system boundary definition, system level and component criticality impact assessments, use of quality risk management, User Requirement Specs. and requirements traceability matrices, Construction QA/QC, Turnover Pack compilation, Document Mgt. Systems, FAT/SAT and C&Q protocol development.Support the implementation of GES standard work across all sites.Participate in the implementation of digital/paperless C&Q execution.Integration of Computer Systems Validation activities, in collaboration with Automation/IT partners, into the C&Q value stream.Facilitate C&Q peer reviews across projects to mitigate against unintended omissions/gaps in strategy and execution plans.Through use of leading indicator/KPI’s and regular assessments of critical to C&Q project deliverable progress, ensure right first time delivery for the C&Q phase.Ensure adherence to Quality Manual guidelines & GES Practices and Procedures.Your profileBachelor’s Degree in Chemical/Mechanical Engineering, Biotechnology or equivalent applied life sciences qualifications.Strong interpersonal and communication skills, decision making and the ability to guide work teams in the region.The candidate should have a strong understanding of equipment and facility design, safety practices, standards, operations, maintenance and industry regulations.Extensive C&Q experience, including a C&Q leadership role on a significant large capital project in the Pharmaceutical / Biotech IndustryExperience in Drug Substance, Drug Product and Labelling & Packaging as well as clean and black utility systemsExperience staffing and managing contract personnel on a project team basisDemonstrated knowledge of ISPE Baseline Guide 5; ASTM E-2500; FDA, EU regulatory requirementsExcellent analytical abilities and a solid base in engineering fundamentalsDemonstrated leadership, teamwork and interpersonal skillsProven written and verbal communication skills – English – as the platform language for communication in science and engineeringAbility to foster strong collaborative working relationships with internal colleagues and customers, and external partner resources in a culturally diverse environmentTeaching, training and coaching of internal colleagues and partner resourcesDynamic ability to work across a portfolio of projects;Change management - sponsor an end to end mindset – successful capital project delivery is a key enabler to a successful start-up in realizing on-time, reliable and compliant product supplyPassion for instilling a proactive safety, environmental and regulatory compliance cultureExperience in the following areas is preferred:Post-OQ/Tech Transfer phase – Clean Utility, HVAC/environmental and Process PQ’s; cleaning, thermal cycle development and validation; demonstration batch manufacture; operational readiness and maintenance readiness workstreams Familiar with our organizations Procedures and GuidelinesExperience with digital/paperless validationPrior project management knowledgeISPE GAMP 5 – Risk Based approach to compliant GxP Computer SystemsLean/Six sigma belt certification/experienceWhat we offerWe welcome you to a truly global, dynamic and challenging environment with great opportunities for personal development. Our benefits are very competitive, and the summary below will give you an idea of what you can expect.Competitive salary;Annual Incentive planAttractive collective health care insurance package with considerable reduction rates;Solid Pension Plan;Numerous training, coaching and e-learning modules for long term job opportunities and developmentCurrent Employees apply HERECurrent Contingent Workers apply HERESecondary Language(s) Job Description:Bachelor's Degree in Chemical EngineeringSearch Firm Representatives Please Read Carefully Merck & Co., Inc., Kenilworth, NJ, USA, also known as Merck Sharp & Dohme Corp., Kenilworth, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: RegularRelocation:No relocationVISA Sponsorship:Travel Requirements:50%Flexible Work Arrangements:Shift:Not IndicatedValid Driving License:Hazardous Material(s):Number of Openings: 1Job InfoType: Full timeLocation: NLD - Boxmeer, DEU - Unterschleissheim