444 active jobs
Explore 444 active Gmp job openings aggregated from hundreds of sources. Roles range from entry-level to executive, remote and on-site, refreshed hourly.
444 jobs · newest first
ATEM SD GmbH Deutschland, Nordrhein-Westfalen, Remscheid, West DE
System Administrator (m/w/d) Location: Remscheid, Germany (on-site preferred, remote possible) Languages: Fluent German (C1 level) and English Job Overview We are looking for an experienced and reliab...
Gi Life Sciences Stein Schweiz CH
General Information: 1. Start Date: immediately or agreement 2. Timeframe: temporary unlimited 3. Work Location: Schaffhausen 4. Workload: 100% 5. Shift work: 2 shift models Tasks: We manufacture inst...
CSL Plasma Schweiz CH
CSL Behring is a leading biotech company that has committed to saving lives. In Bern, we develop and market life-saving therapies for people with severe and rare diseases worldwide. Visit our career w...
team2work Österreich, Niederösterreich, Krems-Land, Senftenberg AT
For our long-standing customer, a globally successful manufacturing company in the pharmaceutical industry, which can showcase an extensive product range including vaccines and veterinary medications,...
Richter BioLogics GmbH Deutschland, Hamburg DE
Richter BioLogics is an innovative and leading biotechnology company. As a top-notch order developer and manufacturer, we contribute to the health of people worldwide with over 400 engaged employees a...
PlantaCorp GmbH Hamburg DE
We would like you to work in one of the most innovative companies in Hamburg? PlantaCorp is an ISO 22000- and GMP-certified German manufacturer of liposomal dietary supplements. Our unique, forward-th...
LKH-Univ. Klinikum Graz Österreich, Steiermark, Graz AT
Are you looking for new challenges? Are you at the beginning of your professional career or would you like to reorient yourself professionally? Do you enjoy working in highly professional, multidiscip...
team2work Österreich, Niederösterreich, Krems-Land, Senftenberg AT
For our long-standing customer, a manufacturing company in the pharmaceutical industry, we are looking to strengthen the existing team with Production Assistants for the area of sterile filling and vi...
IMAN GROUP España ES
From IMAN Temporing, a temporary work company, we are looking for a Quality Assurance Technician for one of our clients in the pharmaceutical sector. If you have experience in the quality area in the...
MARS Cosmetics India, Himachal Pradesh, Solan IN
Job Description: Plant Head (Manufacturing) — MARS Cosmetics Location: Baddi, Himachal Pradesh Function: Manufacturing / Supply Chain Role Summary Own end-to-end manufacturing at the Baddi plant—deliv...
Adecco Italia, Piemonte, Provincia di Torino, Torino IT
Adecco Italia Spa, is seeking a Chemical Analyst for a pharmaceutical company. The insertion is expected to replace maternity leave. The analyst will be required to perform analytical activities on ra...
Triga Consulting GmbH & Co KG Freiburg im Breisgau DE
In an established company in medical technology, which has developed high-quality systems for medical use for decades, you will take on a key role in validation management. You ensure that processes,...
Sii Sp. z o.o. Polska, kujawsko-pomorskie, Bydgoszcz PL
Manufacturing Batch Records Lead Place of work: Bydgoszcz Your scope of responsibilities Verification of global and local MBR regarding completeness, correctness, and compliance with GMP/GxP Ensuring...
Sii Sp. z o.o. Polska, pomorskie, Trójmiasto, Gdańsk PL
Manufacturing Batch Records Lead Place of work: Gdańsk Your scope of responsibilities Verification of global and local MBR regarding completeness, correctness, and compliance with GMP/GxP Ensuring con...
Sii Sp. z o.o. Polska, podkarpackie, Rzeszów PL
Manufacturing Batch Records Lead Place of work: Rzeszów Your scope of responsibilities Verification of global and local MBR regarding completeness, correctness, and compliance with GMP/GxP Ensuring co...
Sii Sp. z o.o. Polska, podlaskie, Białystok PL
Manufacturing Batch Records Lead Place of work: Białystok Your scope of responsibilities Verification of global and local MBR regarding completeness, correctness, and compliance with GMP/GxP Ensuring...
EXCO GmbH Plankstadt DE
You want to use your experience in quality control specifically and accompany exciting projects at a leading company in the Life-Science-Branche as part of our customer's project implementation in Pla...
Sii Sp. z o.o. Polska, podlaskie, Białystok PL
Validation Subject Matter Expert (f/m/x) Place of work: Białystok Technologies, which we use Required CSV MES GxP GMP EU Annex 11 compliance 21 CFR 11 Mile seen Industry 4.0 About the project Join an...
Sii Sp. z o.o. Polska, małopolskie, Kraków PL
Validation Subject Matter Expert (f/m/x) Place of work: Krakow Technologies used We require CSV MES GxP GMP EU Annex 11 compliance 21 CFR 11 Mile seen Industry 4.0 About the project Join an internatio...
Sii Sp. z o.o. Polska, łódzkie, Łódź PL
Validation Subject Matter Expert (f/m/x) Place of work: Łódź Technologies, which we use Required CSV MES GxP GMP EU Annex 11 compliance 21 CFR 11 Mile seen Industry 4.0 About the project Join an inter...
Sii Sp. z o.o. Polska, kujawsko-pomorskie, Toruń PL
Validation Subject Matter Expert (f/m/x) Place of work: Toruń Technologies, which we use Required CSV MES GxP GMP EU Annex 11 compliance 21 CFR 11 Mile seen Industry 4.0 About the project Join an inte...
Sii Sp. z o.o. Polska, lubelskie, Lublin PL
Validation Subject Matter Expert (f/m/x) Place of work: Lublin Technologies, which we use Required CSV MES GxP GMP EU Annex 11 compliance 21 CFR 11 Mile seen Industry 4.0 About the project Join an int...
Sii Sp. z o.o. Polska, kujawsko-pomorskie, Bydgoszcz PL
Validation Subject Matter Expert (f/m/x) Place of work: Bydgoszcz Technologies, which we use Required CSV MES GxP GMP EU Annex 11 compliance 21 CFR 11 Mile seen Industry 4.0 About the project Join an...
Sii Sp. z o.o. Polska, zachodniopomorskie, Szczecin PL
Validation Subject Matter Expert (f/m/x) Place of work: Szczecin Technologies, which we use Required CSV MES GxP GMP EU Annex 11 compliance 21 CFR 11 Mile seen Industry 4.0 About the project Join an i...
Sii Sp. z o.o. Polska, wielkopolskie, Poznań PL
Validation Subject Matter Expert (f/m/x) Place of work: Poznań Technologies, which we use Required CSV MES GxP GMP EU Annex 11 compliance 21 CFR 11 Mile seen Industry 4.0 About the project Join an int...
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