JOB DESCRIPTION: Abbott is een wereldspeler op het gebied van gezondheid en streeft ernaar mensen niet alleen een langer, maar ook een beter leven te geven. Bij Abbott werken wereldwijd 100.000+ medewerkers in 150 landen aan
Job Title: Senior Systems Engineer Location: Amsterdam, Luxembourg, EMEA Work schedule or timing: 8.30 AM to 5.30 PM CET Work Model: Hybrid Introduction to the role The Senior Systems Engineer is a Tier 2 support role
This is Adyen Adyen provides payments, data, and financial products in a single solution for customers like Meta, Uber, H&M, and Microsoft - making us the financial technology platform of choice. At Adyen, everything we do
As the single point of ownership for end‑to‑end Supply Chain Management for the Benelux affiliate, you will oversee demand forecasting, supply planning, inventory control, logistics, and tender support. Acting as a key interface between the local
About the Role 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
Senior Quality Officer Preparation of QP batch release for Products (Quality records, Batch recordreview, 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,
Bioprocess Operator De Bilt | Dutch & English | GMP | Visual QC | Aseptic Tasks | Documentation Your new company Our client is a leading company in global biopharmaceuticals with a diverse portfolio of prescription
Job title: Qualified Person Company Description Good Health Cant Wait. Patients need solutions, and we find them. As a subsidiary of Dr. Reddys Laboratories, we are committed to improving quality of life. With innovative and cost-effective
Batch record review and support of the release process. Quality on the Shopfloor Approval of CAPAs & Deviations, you are responsible for managing minor deviations and resulting CAPAs, ensuring compliance with GMP standards, and supporting quality investigations. You