Do you enjoy coordinating complex processes, connecting stakeholders and ensuring a smooth manufacturing and release process? As we continue to expand our operations in Ghent, we are looking for a Batch Release Coordinator to join our Supply Chain team.
At Ardena, we’re helping shape the future of medicine. Our teams work on the development of innovative and complex therapies that can improve the lives of patients around the world. As a global Contract Development and
QC Laboratory Administrator Location: Verviers – laboratory‑based role We are looking for a QC Laboratory Administrator to support the quality release of raw materials, finished products and shelf‑life studies. In this role, you will play a key
At Legend Biotech we develop innovative cell therapies that bring new hope to patients with limited treatment options. Whether you are just starting out, looking for a fresh challenge or ready to apply your skills in
As a leading innovator of women’s health, we at Hologic are empowering people to live healthier lives everywhere, every day. Our Quality teams play a critical role in ensuring that our products meet the highest standards
Job Title: Quality Assurance Operations Specialist Location: Verviers Relocation assistance is provided for the successful candidate. The role: The Quality Assurance (QA) Operations Specialist is an experienced professional responsible for providing day‑to‑day support across all quality‑related
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description QC Project Leader (m/f/d) Job-ID: R-01350791 Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable
Locatie: Antwerpen Functieomschrijving Als Batch Release Analyst ben je verantwoordelijk voor de kwaliteitsbeoordeling en evaluatie van lokaal geproduceerde goederen. Je doet dit op basis van uitgevoerde controles, batchdocumentatie en procesgegevens. Je werkt nauw samen met de productieafdeling en
As a QA GMP Compliance Support , you will act as a Person‑in‑Plan (PIP) at a Contract Manufacturing Organization (CMO) in Germany. You will provide on‑site quality oversight of clinical drug product manufacturing activities and ensure