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Het overzicht van de statistiek van de lonen bij het beroep "Automation Engineer in "

2 500 € Gemiddeld maandsalaris

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

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

Aanbevolen vacatures

Automation Engineer
Oxford Global Resources, Boxmeer, Noord-Brabant
Do you have experience in industrial automation engineer (PLC) and would you like to help with an improvement project at a large international customer? Then this is probably the role for you Job description As an Automation Engineer you will be working in a team with specialists on projects dealing with new construction, upgrades and improvement. In this role you coordinate projects with PLC / Scada systems. You make an inventory of the internal needs and create a project plan with specifications. You will then link with suppliers and ensure proper execution and documentation. . Responsibilities Coordinating projects with PLC / SCADA systems; Making an inventory of internal requirements; Writing specifications and (parts of) the project plan; Generate documentation so that implementation can be carried out. Profile Completed HBO or MSc degree with several years of work experience in industrial automation; Experience with PLC / SCADA systems (S7 / Tia, iFix / WinCC); You are eager to learn, motivated and think in solutions; You speak English and Dutch; Unlimited EU working permit. Terms of employment Employment: through Oxford Global Resources Solutions; Salary: €3700-€4800 depending on experience; Working hours: Full-time; Region: Den Bosch; Vacancy number: 17279. IMPORTANT NOTE: Unlimited EU working permit is required. Please do not apply if you do not have a working permit to live and work in the Netherlands. If you do not have an unlimited permit, y our application will not be processed . As a specialized recruitment company, we at Oxford Global Resources have a large offer of IT jobs in the area of Computer System Validation (CSV) and Programmable Logic Controller (PLC) within various sectors, including Pharmaceuticals, Biotechnology, Contract Manufacturing, Contract Research, Food Industry, Chemicals, Environment and Plants. Oxford is always looking for talent with expertise in Information engineering, IT, ICT, Biotechnology, Immunology, Biochemistry, Virology, Microbiology, Molecular Biology, Life Science, Analytical Chemistry, Physical Chemistry, Polymer Chemistry, Petrochemistry and Diagnostics. We would like to get in touch with candidates who have experience with one or more of the following technologies: PLC (Programmable Logic Controller), Computer System Validation (CSV), Citrix, Oracle, LIMS, Python, Vmware ESX, SQL, ITIL, SCRUM, Manufacturing execution system (MES), SCADA (Supervisory Control And Data Acquisition), Big data, Full stack development, Internet of things, Robotics, Data Science, Ethical Hacking, Security, Business Intelligence Do you find this vacancy interesting? Or are you looking for a position at MBO, HBO, BSc, WO, MSc or PhD and are you interested in the job Research Technician, IT Architect, Enterprise Architect, IT Project consultant, Infrastructure Specialist, CSV Specialist, PLC Engineer, Automation Engineer, Control System Engineer, Process Engineer, Automation Specialist, PLC software engineer, IT Consultant. Then contact us directly
Automation Engineer
Oxford Global Resources, Boxmeer, Noord-Brabant
Do you have experience in industrial automation engineer and would you like to help with an improvement project at a large international customer? Then this is probably the role for you Job description As an Automation Engineer you will be working in a team with specialists on projects dealing with new construction, upgrades and improvement. In this role you coordinate projects with PLC/Scada systems. You make an inventory of the internal needs and create a project plan with specifications. You will then link with suppliers and ensure proper execution and documentation. . Responsibilities Coordinating projects with Scada/PLC systems; Making an inventory of internal requirements; Writing specifications and (parts of) the project plan; Generate documentation so that implementation can be carried out. Profile Completed HBO or MSc degree with several years of work experience in industrial automation; Experience with Scada/PLC systems (S7 / Tia, iFix / WinCC); You are eager to learn, motivated and think in solutions; Have an EU working permit You speak English and Dutch. Terms of employment Employment: through Oxford Global Resources Solutions; Salary: €3700-€4800 depending on experience; Working hours: Full-time; Region: Den Bosch; Vacancy number: 17279. IMPORTANT NOTE: Unlimited EU working permit is required. Please do not apply if you do not have a working permit to live and work in the Netherlands. If you do not have an unlimited permit, y our application will not be processed As a specialized recruitment company, we at Oxford Global Resources have a large offer of IT jobs in the area of Computer System Validation (CSV) and Programmable Logic Controller (PLC) within various sectors, including Pharmaceuticals, Biotechnology, Contract Manufacturing, Contract Research, Food Industry, Chemicals, Environment and Plants. Oxford is always looking for talent with expertise in Information engineering, IT, ICT, Biotechnology, Immunology, Biochemistry, Virology, Microbiology, Molecular Biology, Life Science, Analytical Chemistry, Physical Chemistry, Polymer Chemistry, Petrochemistry and Diagnostics. We would like to get in touch with candidates who have experience with one or more of the following technologies: PLC (Programmable Logic Controller), Computer System Validation (CSV), Citrix, Oracle, LIMS, Python, Vmware ESX, SQL, ITIL, SCRUM, Manufacturing execution system (MES), SCADA (Supervisory Control And Data Acquisition), Big data, Full stack development, Internet of things, Robotics, Data Science, Ethical Hacking, Security, Business Intelligence Do you find this vacancy interesting? Or are you looking for a position at MBO, HBO, BSc, WO, MSc or PhD and are you interested in the job Research Technician, IT Architect, Enterprise Architect, IT Project consultant, Infrastructure Specialist, CSV Specialist, PLC Engineer, Automation Engineer, Control System Engineer, Process Engineer, Automation Specialist, PLC software engineer, IT Consultant. Then contact us directly
Analytical Transfer & Restructuring Senior Specialist (H/F)
Merck Sharp & Dohme Limited, Boxmeer, Noord-Brabant
Job DescriptionCe poste est en contrat CDD de 18 mois.Pharma Analytical Technology Solutions (PATS) soutient tous les sites de santé animale du monde entier dans la correction, l'amélioration et la validation des méthodes analytiques ainsi que dans tous les types d'investigations analytiques. Diriger et exécuter des activités de transfert analytique et introduire de nouvelles technologies analytiques complète le portefeuille de l'équipe.Nos ingénieurs soutiennent les opérations de fabrication internes et externes, restent opérationnels, s'améliorent et innovent en permanence. Grâce à notre vaste gamme d'installations et d'environnements, nos ingénieurs ont des opportunités dans de nombreux domaines variés, notamment la biologie, la chimie, l'automatisation, les projets d'investissement, la maintenance, la sécurité, le développement de processus, les services techniques, les services publics et la validation.Nous recherchons un(e) Senior Specialist Transfer & Restructuring Senior Specialist pour une période de 18 mois pour diriger et exécuter des activités de transfert analytique de site à site et de la partie Recherche et Développement à site pour les ingrédients pharmaceutiques actifs (APIs).Ce poste devrait idéalement être affilié à Igoville (France) mais peut également être affilié à Vienne (Autriche), Unterschleißheim (Allemagne) ou Friesoythe (Allemagne). Le poste nécessitera jusqu'à 10% de voyages internationaux.Vos principales responsabilités :• Prend en charge les transferts analytiques de Pharma Analytical Technology Solutions pour les ingrédients pharmaceutiques actifs (API)• Focalisation sur la conformité réglementaire et qualité de la méthode analytique par rapport aux directives actuelles des autorités pharmaceutiques, préparation à la soumission par une analyse détaillée des documents• Focus sur l'applicabilité des méthodes dans un environnement de contrôle qualité (CQ) de routine• Identifier les opportunités d'amélioration des méthodes en termes de modernisation et / ou de robustesse des méthodes• Soutient la préparation de la stratégie de transfert en termes de préparation à la soumission• Supporte le dépannage chez le fournisseur en cas d'investigations analytiques et de besoins critiques de développement de méthodes• Collabore avec les affaires réglementaires (RA), l'équipe de technologie API, la qualité externe, les fournisseurs externes et les équipes responsables des sites de division dans les activités de transfert• Prend en charge plusieurs activités de transfert analytique API simultanémentVotre profil :• Maîtrise, licence, diplôme d'ingénieur et une longue expérience dans une science pharmaceutique / chimique / analytique requise• Au moins 8 ans d'expérience dans la recherche et le développement, la fabrication et les tests d'ingrédients pharmaceutiques actifs (API) ou de produits pharmaceutiques requis• Une expérience dans les activités de transfert analytique et une large compréhension des plates-formes analytiques telles que les analyses pharmaceutiques (chimie humide, chromatographie et tests physico-chimiques) est un avantage• Une expérience du processus de soumission et d'examen des dossiers est un avantage• Solide expérience de travail dans des équipes de projet internationales• Capacité à travailler de manière indépendante et à prendre des décisions dans le cadre de lignes directrices et de politiques ayant un impact sur ses propres priorités pour respecter les délais• Maîtrise de la rédaction scientifique / technique et de l'utilisation courante de l'ordinateur (Word, Excel, PowerPoint, MS Project, etc.)Notre division de fabrication et d'approvisionnement s'est engagée à être le fournisseur de produits biopharmaceutiques le plus fiable au monde. Nos installations, ainsi que nos sous-traitants, fournisseurs et partenaires externes, créent un réseau de fabrication mondial interdépendant qui s'engage à fournir à chaque fois un approvisionnement fiable et de haute qualité aux clients et aux patients.Qui sommes-nous? Nous sommes connus sous le nom de Merck & Co., Inc., Kenilworth, New Jersey, USA aux États-Unis et au Canada et de MSD partout ailleurs. Depuis plus d’un siècle, nous inventons pour la vie, mettant au point des médicaments et des vaccins pour un grand nombre des maladies les plus éprouvantes au monde. Aujourd’hui, notre société continue d’être à l’avant-garde de la recherche afin d’offrir des solutions de santé novatrices et de faire progresser la prévention et le traitement des maladies qui menacent les gens et les animaux du monde entier.Que cherchons-nous? Dans un monde d’innovation rapide, nous cherchons des inventeurs courageux qui veulent avoir un impact dans tous les aspects de notre entreprise, permettant ainsi des percées qui auront une incidence sur les générations à venir. Nous vous encourageons à accroître la valeur de notre organisation en y apportant votre raisonnement perturbateur, votre esprit de collaboration et votre perspective diversifiée. Ensemble, nous continuerons à inventer pour la vie, à avoir une incidence sur la vie et à inspirer votre carrière.INVENT.IMPACT.INSPIRE. Current Employees apply HERECurrent Contingent Workers apply HERESecondary Language(s) Job Description:Pharma Analytical Technology Solutions (PATS) supports all Animal Health sites globally in analytical method remediation, improvement and validation as well as in all kind of analytical investigations. Leading and executing analytical transfer activities and introducing new analytical technologies completes the portfolio of the team.Our Engineers support internal and external manufacturing operations remain operational, continuously improve and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation.We are looking for a Senior Specialist (m/f/d) API Analytical Transfer & Restructuring for a period of 18 months to lead and execute analytical transfer activities for both, R&D to site as well as for site to site for active pharmaceutical ingredients (APIs).This position should be ideally be affiliated in Igoville (France) but can also be affiliated in Vienna (Austria), Unterschleißheim (Germany) or Friesoythe (Germany). The position will require up to 10% international travel.Your Key Responsibilities:Supports PATS API analytical transfers for active pharmaceutical ingredients (APIs)Focus on analytical method’s regulatory and quality compliance against current guidelines from pharmaceutical GMP authorities, readiness for submission by a detailed document analysisFocus on applicability of methods in routine Quality Control (QC) environmentIdentifying method improvement opportunities in terms of method modernization and/or robustnessSupports preparation of transfer strategy in terms of submission readinessSupports troubleshooting at the supplier in case of analytical investigations and critical method development needsCollaborates with Regulatory Affairs (RA), API technology team, external Quality, external suppliers and division site responsible teams in transfer activitiesSupports several API analytical transfer activities simultaneouslyYour Profile: Master, Bachelor, Engineer degree and long year experience in a Pharmaceutical/Chemical/Analytical Science requiredAt least 8 years’ experience in the research and development, manufacturing and testing of active pharmaceutical ingredients (APIs) or drug products requiredExperience in analytical transfer activities and broad understanding of analytical platforms like pharmaceutical analyses (wet chemistry, chromatography and physicochemical testing) is an advantageExperience in submission process and review of dossiers is an advantageSolid experience working in international project teamsAbility to work independently and make decisions within guidelines and policies that impact own priorities to meet deadlinesProficient in scientific/technical writing and current computer usage (Word, Excel, PowerPoint, MS Project etc.)Our Manufacturing & Supply Division is committed to be the most trusted supplier of biopharmaceuticals worldwide. Our facilities, along with our external contractors, suppliers, and partners, create an interdependent global manufacturing network that’s committed to delivering a high quality, reliable supply to customers and patients on time, every time.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.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: Project Temps (Fixed Term)Relocation:No relocationVISA Sponsorship:Travel Requirements:10%Flexible Work Arrangements:Flex Time, Remote WorkShift:Valid Driving License:Hazardous Material(s):Number of Openings: 1Job InfoType: Full timeLocation: FRA - Igoville, DEU - Friesoythe, NLD - Boxmeer, AUT - Vienna - Siemensstrasse, DEU - Unterschleissheim, ITA - Latina - Aprilia