Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Job Title: Systems Engineer Location: Madrid, Amsterdam, Luxembourg, or London Work schedule or timing: 8.30 AM to 5.30 PM CET Work Model: Hybrid Introduction to the role The Systems Engineer is a Tier 2 support role
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
The Opportunity: Manufacturing Operations Specialist Location: Hillegom, The Netherlands Employment Type: 1 year contract with permanent option after the first year, Full-time Do you enjoy bringing structure to complex manufacturing processes? Are you someone who naturally
Start Date: ASAP Contract Duration: 3 Months Salary: Grade 12 | €6,327 - €7,593 per month About the Role We are looking for an experienced Quality Assurance Specialist to support pharmaceutical production activities and ensure compliance
Role: Production Expert III/Senior Quality Assurance Specialist Location: Swensweg 5, Haarlem, NL, 2031 GA Duration: 3 Months from Start Fully onsite position. Required: Bachelor’s degree with several years of relevant work experience or Master’s degree in
Work ScheduleFirst Shift (Days) Environmental ConditionsOffice, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Warehouse Job Description As part of the Thermo Fisher Scientific team, you’ll discover
We are seeking a Senior Software Engineer to help us build Nebius Serverless AI — our GPU‑native platform for deploying inference endpoints, batch jobs, and AI workloads without managing infrastructure. Customers run production AI on it today;
Please note that preference will be given to candidates already residing in the Netherlands to ensure a smoother onboarding process. At this time, we are not able to provide relocation support. Maximaliseer uw kans op een
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Overview Overview Solliciteer nu, lees de vacaturedetails door naar beneden te scrollen. Controleer of u over de nodige vaardigheden beschikt voordat u een sollicitatie verstuurt. Associate Director Global CMC QU – Clinical GMP/GDP at Kyowa Kirin
A biotechnology company in Amsterdam is seeking a Quality Assurance Officer to manage QP batch releases and ensure compliance with GMP guidelines. Zorg ervoor dat u de informatie over deze vacature grondig leest voordat u een sollicitatie
Preparation of QP batch release for Products (Quality records, Batch record review, release documentation), overall QMS compliance relating to QA Operational tasks. You play a key role in executing structured simple Root Cause Analyses (RCA), tracking CAPA effectiveness, and supporting
Prothya Biosolutions is currently seeking a motivated and detail-oriented Senior QA Officer QMS to join our Quality Assurance team. In this role, you will play a key part in ensuring GMP compliance, supporting QP batch release activities,