118 active jobs
Explore 118 active Lims job openings aggregated from hundreds of sources. Roles range from entry-level to executive, remote and on-site, refreshed hourly.
118 jobs · newest first
Link Group Polska, mazowieckie, Warszawa PL
Technical Program Manager (Pharma / SaaS Platforms) About the role We are looking for an experienced Technical Program Manager to join a global pharmaceutical organization and lead multiple strategic...
Company Name Ltd New Zealand, North Island, Greater Wellington, Wellington NZ
Te tūnga | The role We have an exciting opportunity for a 12-month fixed term (starting in September) full time Senior Technician role to join our Microbiology AMR team within the Health Security Grou...
Waters Corporation Singapore SG
Overview As Waters accelerates its cloud transformation and strengthens its industry leading informatics portfolio, a dedicated leader is needed to drive execution, revenue growth, and customer engage...
Cervel Group México, Hidalgo, Tulancingo de Bravo MX
Why join Chemicals Clean Lxry (CCL): We are a certified testing laboratory before EMA, specialized in industrial gas analysis and LP. Here you will work with international-class methodologies, with di...
Abbott New Zealand NZ
JOB DESCRIPTION: About Abbott Abbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future, anticipating changes in medical s...
BRÜGGEN ENGINEERING GmbH Ludwigshafen DE
Your career in pharmaceutical analytics. You will work with BRÜGGEN ENGINEERING in quantitative analysis of proteins and antibody determination in a regulated environment. You will support clinical an...
AXEPTA SA Schweiz, Kanton Waadt CH
To join one of our clients, a biopharmaceutical company in full growth based in the canton of Vaud. We are looking for an Expert QA for QC who will be responsible for supervising quality activities re...
Aenova Holding GmbH Prahova RO
Ideal Candidate Your Profile •Extensive expertise in the MES environment with deep knowledge of PAS X, particularly in Master Batch Record design, workflow configuration, and confident application of...
WuXi Biologics Singapore SG
WuXi Biologics is a premier provider of biologics services (from discovery to commercialization) with global customers in the biopharmaceutical and healthcare industries. We´re one of the world's top...
Tulip Interfaces Munich, Bavaria, Germany DE
This role is located in Munich, Germany - We are a hybrid work environment and are in the office 3+ days/per week. Tulip, the leader in AI-native frontline operations, is helping companies around the...
Sii Sp. z o.o. Polska, podlaskie, Białystok PL
Operation Master Data Lead (f/m/x) Miejsce pracy: Białystok Your responsibilities Define and implement the global Target Operating Model (TOM) for Manufacturing, QA/QC, and Supply Chain Develop and ma...
Sii Sp. z o.o. Polska, lubelskie, Lublin PL
Operation Master Data Lead (f/m/x) Miejsce pracy: Lublin Your responsibilities Define and implement the global Target Operating Model (TOM) for Manufacturing, QA/QC, and Supply Chain Develop and maint...
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, mazowieckie, Warszawa PL
Manufacturing Batch Records Lead Place of work: Warsaw 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, 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...
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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