Pharmaceutical Production Worker Stellenangebote


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14 Jobs für Pharmaceutical Production Worker


Stellenangebote Pharmaceutical Production Worker Jobs


Job vor 6 Tagen bei Jobleads gefunden

Stagiaire EHS Environnement, hygine et scurit (100)

• Neuenburg [. .. ] et mesure que vous dveloppez vos comptences et faites progresser votre carrire professionnelle. Rsum du projet Rattache au Responsable EHS, vous collaborerez et soutiendrez lquipe dans latteinte [...]
MEHR INFOS ZUM STELLENANGEBOT[...] des objectifs de production. Vous aurez pour mission les activits suivantes : Automatisation des performances EHS et reporting Cartographier et mesurer les indicateurs cls de performance EHS pour le site. Suivre et analyser diffrents indicateurs (production de dchets sur site, missions atmosphriques et bio dchets) . Grer le systme Enablon pour la gestion environnementale [. .. ] civil, ou toute autre caractristique de diversit. Pour plus dinformations sur notre engagement envers la diversit, lquit et linclusion, veuillez visiter https:/ / jobs. takeda. com/diversity Locations CHE-Neuchtel Worker Type Employee Worker Sub-Type Paid Intern (Fixed Term) (Trainee) Time Type Full time Seniority Level Not Applicable Employment Type Full-time Job Function Management and Manufacturing Industries Pharmaceutical Manufacturing #J-18808-Ljbffr 73145417 [. .. ]

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Job am 09.12.2025 bei Jobleads gefunden

Manager or Associate Principal, EMEA Life Science Strategy Supply Operations Consulting

• Berlin Beratungs-/ Consultingtätigkeiten [. .. ] accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. We are expanding our Life Sciences Supply Chain Operations [...]
MEHR INFOS ZUM STELLENANGEBOT[...] practice to support pharmaceutical and biotech clients across Europe. Both roles will be based in Germany or Switzerland with pan European responsibilities. Prior experience in consulting dedicated to pharmaceutical/ biotech supply chainparticularly commercial supply chains for marketed productsis strongly preferred. Key Responsibilities Project Management: Manage endtoend delivery of consulting projects in the supply chain/ [. .. ] strategy engagements by running scenarios on network redesign (e. g. consolidating vs. expanding sites, make vs. buy, etc. ) . Localization Outsourcing Strategies: Assist in projects where clients consider localizing production or outsourcing. Perform supplier/ Contract Manufacturing Organization (CMO) assessments and costbenefit analyses. Distribution Logistics Optimization: Map out clients distribution networks and logistics flows. Identify opportunities to reduce lead times or logistics costs. Advanced Therapy Supply Planning: Work on specialized projects for cell and gene therapies or other highvalue biologics. S [. .. ] management consulting environment. Strong communication, interpersonal, and teamworking skills, and strong written, numerical, and problemsolving skills. Able to adapt, learn quickly, and apply new knowledge. An effective and collaborative team worker. In Addition to the Skills and Experience Above a Manager/ Associate Principal Should Have Bachelors and masters degree or equivalent; graduate degree or MBA not required but a plus. A track record of leadership and people development. Fluency in English (spoken and written) . Willingness and ability to travel and [. .. ]

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Job am 05.12.2025 bei Jobleads gefunden Manager or Associate Principal, EMEA Life Science Strategy Supply Operations Consulting • München, Bayern Beratungs-/ Consultingtätigkeiten [. .. ] problem solvers, that do what we love to make a greater impact on human health. IQVIA EMEA Strategy Consulting is expanding its Life Sciences Supply Chain Operations [...]
MEHR INFOS ZUM STELLENANGEBOT[...] practice to support pharmaceutical and biotech clients in Europe. We are looking for talented individuals to lead and deliver projects that extend our clinical and commercial consulting offerings into supply chain and operations. Both roles will be based in Germany or Switzerland with pan European responsibilities. Prior experience in Consulting dedicated to pharmaceutical/ biotech [. .. ] expanding sites, make vs. buy, etc. ) . Evaluate the impact of changes on cost, capacity, resilience, and service levels. Localization Outsourcing Strategies: Assist in projects where clients consider localizing production or outsourcing. Perform supplier/ Contract Manufacturing Organization (CMO) assessments, costbenefit analyses of local vs. offshore manufacturing, and develop risk mitigation plans (dual sourcing, safety stock, etc. ) . Distribution Logistics Optimization: Map out clients distribution networks and logistics flows. Identify opportunities to reduce lead times or logistics costs (e. g. [. .. ] A good communicator with excellent interpersonal and teamworking skills and strong written, numerical, and problemsolving skills. Able to adapt, learn quickly, and apply new knowledge. An effective and collaborative team worker. Able to travel and work at clients site. Right to live and work in the recruiting country. Bachelors and masters degree or equivalent; graduate degree or MBA not required but a plus. A track record of leadership and people development. Fluency in English (spoken and written) . Whatever your career [. .. ]

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Job am 28.11.2025 bei Jobleads gefunden

Associate Director, API Process Engineering

• Oranienburg, Brandenburg Führungs-/ Leitungspositionen [. .. ] understanding, ensuring lessons learned are shared across products, sites, and functions. Collaborate closely with GMS functions (e. g. , Small Molecules Operations Units, network strategy) , site [...]
MEHR INFOS ZUM STELLENANGEBOT[...] leadership, Technical Services, Pharmaceutical Sciences, Global Quality, and Regulatory CMC. Provide technical support to marketing applications for global markets and lead preparation of responses to regulatory questions from health authorities. Utilize structured root cause analysis techniques to investigate process and equipment issues and deliver robust, sustainable corrective and preventive actions. Provide subject matter expertise [. .. ] disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law. Locations Zurich, Switzerland AUT-Wien-Industriestrasse 67, BEL-Lessines, CHE-Neuchatel, Hikari, Japan, IRL-Bray-Production, IRL-Dublin-Baggot Street, IRL-Grange Castle-Production, Lexington, MA, Linz, Austria, Oranienburg, Germany, SGP-Singapore-Woodlands, USA-CA-Thousand Oaks-Rancho Conejo, USA-MA-Cambridge, USA-MN-Brooklyn Park Worker Type Employee Worker Sub-Type Regular Time Type Full time #J-18808-Ljbffr 70790501 [. .. ]

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Job am 27.11.2025 bei Jobleads gefunden Associate Director, API Process Engineering • Oftringen, Aargau Führungs-/ Leitungspositionen [. .. ] understanding, ensuring lessons learned are shared across products, sites, and functions. Collaborate closely with GMS functions (e. g. , Small Molecules Operations Units, network strategy) , site [...]
MEHR INFOS ZUM STELLENANGEBOT[...] leadership, Technical Services, Pharmaceutical Sciences, Global Quality, and Regulatory CMC. Provide technical support to marketing applications for global markets and lead preparation of responses to regulatory questions from health authorities. Utilize structured root cause analysis techniques to investigate process and equipment issues and deliver robust, sustainable corrective and preventive actions. Provide subject matter expertise [. .. ] citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law. Locations Zurich, Switzerland AUT-Wien-Industriestrasse 67 BEL-Lessines CHE-Neuchatel, Hikari, Japan IRL-Bray-Production IRL-Dublin-Baggot Street IRL-Grange Castle-Production Lexington, MA Linz, Austria Oranienburg, Germany SGP-Singapore-Woodlands USA-CA-Thousand Oaks-Rancho Conejo USA-MA-Cambridge USA-MN-Brooklyn Park Worker Type Employee Worker Sub Type Regular Time Type Full time #J-18808-Ljbffr 70718194 [. .. ]

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Job am 27.11.2025 bei Jobleads gefunden Associate Director, API Process Engineering • Zürich Führungs-/ Leitungspositionen [. .. ] understanding, ensuring lessons learned are shared across products, sites, and functions. Collaborate closely with GMS functions (e. g. , Small Molecules Operations Units, network strategy) , site [...]
MEHR INFOS ZUM STELLENANGEBOT[...] leadership, Technical Services, Pharmaceutical Sciences, Global Quality, and Regulatory CMC. Provide technical support to marketing applications for global markets and lead preparation of responses to regulatory questions from health authorities. Utilize structured root cause analysis techniques to investigate process and equipment issues and deliver robust, sustainable corrective and preventive actions. Provide subject matter expertise [. .. ] disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law. Locations Zurich, Switzerland AUT-Wien-Industriestrasse 67, BEL-Lessines, CHE-Neuchatel, Hikari, Japan, IRL-Bray-Production, IRL-Dublin-Baggot Street, IRL-Grange Castle-Production, Lexington, MA, Linz, Austria, Oranienburg, Germany, SGP-Singapore-Woodlands, USA-CA-Thousand Oaks-Rancho Conejo, USA-MA-Cambridge, USA-MN-Brooklyn Park Worker Type Employee Worker Sub-Type Regular Time Type Full time #J-18808-Ljbffr 70719305 [. .. ]

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Job am 26.09.2025 bei Jobleads gefunden

Automation Engineer MES (f/m/d)

• Oranienburg, Brandenburg [. .. ] the local and global TAKEDA teams and our technology partners to drive the development of applications in a wide range of technologies: Scada systems, Historians, MES (Werum [...]
MEHR INFOS ZUM STELLENANGEBOT[...] PAS-X) and pharmaceutical production equipment Provide technical expertise, problem-solving skills and project management capabilities for automation projects Analyze and solve complex automation and-interface problems together with partners from IT. Lead and support development of requirement analysis and build End-to-End use cases Ensure technical availability of automation systems Work as automation [. .. ] living with disabilities, chronic illness, or neurodiversity, please feel free to let us know so that we can provide you with appropriate support during the application process. Locations Oranienburg, Germany Worker Type Employee Worker Sub-Type Regular Time Type Full time #J-18808-Ljbffr 63390654 [. .. ]

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Job am 15.09.2025 bei Jobleads gefunden

GRA CMC Director-Marketed Products Development Lead

• Zürich Führungs-/ Leitungspositionen [. .. ] colleagues, e. g. , colleagues within Takeda, Alliance Partners, and Health Authority representatives. What you bring to Takeda: BS/ BA Degree in a Scientific Discipline, Advanced Degree [...]
MEHR INFOS ZUM STELLENANGEBOT[...] preferred. 10+ years pharmaceutical Regulatory CMC experience including experience as an RA CMC product lead, or equivalent industry experience (e. g. , Pharmaceutical Development, Analytical Development, Production, Quality Assurance) . Experience with active pharmaceutical ingredient/ drug substances, drug products, biologics, analytical characterization, process scale-up or regulatory registration of products is required. Expert in developing alternate strategies based on guidance/ regulations. Expert in liaising with Regulatory Agencies having served as lead in successful Agency Interactions related to [. .. ] lifecycle, with a solid understanding of global submission complexities. Travel Requirements Willingness to travel to various meetings, including overnight trips. Requires approximately up to 10-30 travel. Locations Zurich, Switzerland Worker Type Employee Worker Sub-Type Regular Time Type Full time #J-18808-Ljbffr 62069505 [. .. ]

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Job am 14.09.2025 bei Jobleads gefunden GRA CMC Director-Marketed Products Development Lead • Zürich Führungs-/ Leitungspositionen [. .. ] colleagues, e. g. , colleagues within Takeda, Alliance Partners, and Health Authority representatives. What you bring to Takeda: BS/ BA Degree in a Scientific Discipline, Advanced Degree [...]
MEHR INFOS ZUM STELLENANGEBOT[...] preferred. 10+ years pharmaceutical Regulatory CMC experience including experience as an RA CMC product lead, or equivalent industry experience (e. g. , Pharmaceutical Development, Analytical Development, Production, Quality Assurance) . Experience with active pharmaceutical ingredient/ drug substances, drug products, biologics, analytical characterization, process scale-up or regulatory registration of products is required. Expert in developing alternate strategies based on guidance/ regulations. Expert in liaising with Regulatory Agencies having served as lead in successful Agency Interactions related to [. .. ] lifecycle, with a solid understanding of global submission complexities. Travel Requirements: Willingness to travel to various meetings, including overnight trips. Requires approximately up to 10-30 travel. Locations Zurich, Switzerland Worker Type Employee Worker Sub-Type Regular Time Type Full time #J-18808-Ljbffr 62009576 [. .. ]

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Job am 12.12.2025 bei Neuvoo gefunden Thermo Fisher Scientific

Student Worker (m/f/d) - Mass Spectrometry 20h/ week

• Bremen Werkstudenten [. .. ] manufacture of life-changing therapies, we are here to support them. Our global team of more than 100, 000 colleagues delivers an unrivaled combination of innovative technologies, purchasing [...]
MEHR INFOS ZUM STELLENANGEBOT[...] convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. Location/ Division Specific Information We are a research, development, and production site in Bremen currently, with about 500 employees, whose high-end measurement and analysis instruments (mass spectrometers) are used in research and science worldwide. Our innovative products in the fields of Life Sciences MS and Inorganic MS, as well as Trace Elemental Analysis, are among the top tier products globally in their respective markets. To strengthen our agile life science team, we are looking for a motivated student worker to collaborate with our research and development scientists. Your tasks and responsibilities will be diverse and exciting, with the opportunity to participate in product development projects in a highly motivated multi-disciplinary team: A day in the Life: Supporting our scientists to complete experiments in the laboratory Working in a [. .. ]

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Job am 06.12.2025 bei Neuvoo gefunden Takeda Automation Engineer MES (f/m/d) • Oranienburg, Brandenburg [. .. ] the local and global TAKEDA teams and our technology partners to drive the development of applications in a wide range of technologies: Scada systems, Historians, MES (Werum [...]
MEHR INFOS ZUM STELLENANGEBOT[...] PAS-X) and pharmaceutical production equipment Provide technical expertise, problem-solving skills and project managemen capabilities for automation projects Analyze and solve complex automation and-interface problems together with partners from IT. Lead and support development of requirement analysis and build End-to-End use cases Ensure technical availability of automation systems Work as automation [. .. ] living with disabilities, chronic illness, or neurodiversity, please feel free to let us know so that we can provide you with appropriate support during the application process. Locations Oranienburg, Germany Worker Type Employee Worker Sub-Type Regular Time Type Full time 71836093 [. .. ]

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Job am 03.12.2025 bei Neuvoo gefunden IQVIA Manager or Associate Principal, EMEA Life Science Strategy Supply Operations Consulting • Frankfurt, Hessen Beratungs-/ Consultingtätigkeiten [. .. ] problem solvers, that do what we love to make a greater impact on human health. IQVIA EMEA Strategy Consulting is expanding its Life Sciences Supply Chain Operations [...]
MEHR INFOS ZUM STELLENANGEBOT[...] practice to support pharmaceutical and biotech clients in Europe. We are looking for talented individuals to lead and deliver projects that extend our clinical and commercial consulting offerings into supply chain and operations. Both roles will be based in Germany or Switzerland with pan-European responsibilities. Prior experience in Consulting dedicated to pharmaceutical/ biotech [. .. ] expanding sites, make vs. buy, etc. ) . Evaluate the impact of changes on cost, capacity, resilience, and service levels. Localization Outsourcing Strategies: Assist in projects where clients consider localizing production or outsourcing. Perform supplier/ Contract Manufacturing Organization (CMO) assessments, cost-benefit analyses of local vs. offshore manufacturing, and develop risk mitigation plans (dual sourcing, safety stock, etc. ) . Distribution Logistics Optimization: Map out clients distribution networks and logistics flows. Identify opportunities to reduce lead times or logistics costs (e. [. .. ] communicator with excellent interpersonal and team-working skills and strong written, numerical, and problem-solving skills Able to adapt, learn quickly, and apply new knowledge An effective and collaborative team worker In addition to the skills and experience above a Manager/ Associate Principal should have: Bachelors and masters degree or equivalent, graduate degree or MBA not required but a plus A track record of leadership and people development Fluency in English (spoken and written) A willingness and ability to travel and [. .. ]

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Job am 03.12.2025 bei Neuvoo gefunden IQVIA Manager or Associate Principal, EMEA Life Science Strategy Supply Operations Consulting • Munich, Bavaria Beratungs-/ Consultingtätigkeiten [. .. ] problem solvers, that do what we love to make a greater impact on human health. IQVIA EMEA Strategy Consulting is expanding its Life Sciences Supply Chain Operations [...]
MEHR INFOS ZUM STELLENANGEBOT[...] practice to support pharmaceutical and biotech clients in Europe. We are looking for talented individuals to lead and deliver projects that extend our clinical and commercial consulting offerings into supply chain and operations. Both roles will be based in Germany or Switzerland with pan-European responsibilities. Prior experience in Consulting dedicated to pharmaceutical/ biotech [. .. ] expanding sites, make vs. buy, etc. ) . Evaluate the impact of changes on cost, capacity, resilience, and service levels. Localization Outsourcing Strategies: Assist in projects where clients consider localizing production or outsourcing. Perform supplier/ Contract Manufacturing Organization (CMO) assessments, cost-benefit analyses of local vs. offshore manufacturing, and develop risk mitigation plans (dual sourcing, safety stock, etc. ) . Distribution Logistics Optimization: Map out clients distribution networks and logistics flows. Identify opportunities to reduce lead times or logistics costs (e. [. .. ] communicator with excellent interpersonal and team-working skills and strong written, numerical, and problem-solving skills Able to adapt, learn quickly, and apply new knowledge An effective and collaborative team worker In addition to the skills and experience above a Manager/ Associate Principal should have: Bachelors and masters degree or equivalent, graduate degree or MBA not required but a plus A track record of leadership and people development Fluency in English (spoken and written) A willingness and ability to travel and [. .. ]

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Job am 03.12.2025 bei Neuvoo gefunden IQVIA Manager or Associate Principal, EMEA Life Science Strategy Supply Operations Consulting • Berlin Beratungs-/ Consultingtätigkeiten [. .. ] problem solvers, that do what we love to make a greater impact on human health. IQVIA EMEA Strategy Consulting is expanding its Life Sciences Supply Chain Operations [...]
MEHR INFOS ZUM STELLENANGEBOT[...] practice to support pharmaceutical and biotech clients in Europe. We are looking for talented individuals to lead and deliver projects that extend our clinical and commercial consulting offerings into supply chain and operations. Both roles will be based in Germany or Switzerland with pan-European responsibilities. Prior experience in Consulting dedicated to pharmaceutical/ biotech [. .. ] expanding sites, make vs. buy, etc. ) . Evaluate the impact of changes on cost, capacity, resilience, and service levels. Localization Outsourcing Strategies: Assist in projects where clients consider localizing production or outsourcing. Perform supplier/ Contract Manufacturing Organization (CMO) assessments, cost-benefit analyses of local vs. offshore manufacturing, and develop risk mitigation plans (dual sourcing, safety stock, etc. ) . Distribution Logistics Optimization: Map out clients distribution networks and logistics flows. Identify opportunities to reduce lead times or logistics costs (e. [. .. ] communicator with excellent interpersonal and team-working skills and strong written, numerical, and problem-solving skills Able to adapt, learn quickly, and apply new knowledge An effective and collaborative team worker In addition to the skills and experience above a Manager/ Associate Principal should have: Bachelors and masters degree or equivalent, graduate degree or MBA not required but a plus A track record of leadership and people development Fluency in English (spoken and written) A willingness and ability to travel and [. .. ]

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Häufig gestellte Fragen

Wieviel verdient man als Pharmaceutical Production Worker pro Jahr?

Als Pharmaceutical Production Worker verdient man zwischen EUR 28.000,- bis EUR 45.000,- im Jahr.


Wieviele offene Stellenangebote gibt es für Pharmaceutical Production Worker Jobs bei unserer Jobsuche?

Aktuell gibt es auf JobRobot 14 offene Stellenanzeigen für Pharmaceutical Production Worker Jobs.


In welchen Bundesländern werden die meisten Pharmaceutical Production Worker Jobs angeboten?

Die meisten Stellenanzeigen für Pharmaceutical Production Worker Jobs werden derzeit in Brandenburg (3 Jobs), Berlin (2 Jobs) und Sachsen-Anhalt (1 Jobs) angeboten.


Zu welchem Berufsfeld gehören Pharmaceutical Production Worker Jobs?

Pharmaceutical Production Worker Jobs gehören zum Berufsfeld Pharmazie.


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Dauer: 0.0566 s., Vers. V.2025-d-2007-Ind-141