Job Description Pharmaceutical Packaging and Process Engineer Wij staan open voor junior, medior en senior profielen. Voor junior profielen de ambitie om zich verder te ontwikkelen richting verpakkings technologie. De functie De Pharmaceutical Packaging and Process Engineer levert technologische expertise
Career CategoryManufacturing Job Description At Amgen, were not just manufacturing medicines; were fueling a global mission to serve patients in over 100 countries. Our collaborative spirit and relentless pursuit of excellence have propelled us to the
We are seeking a highly experienced Primary Packaging Materials Scientist to act as a senior Subject Matter Expert (SME) supporting primary packaging activities for parenteral pharmaceutical products. Hoewel werkervaring en kwalificaties essentieel zijn voor deze functie, controleer dan of
Our client is a leading global biopharmaceutical company committed to developing innovative therapies and delivering high-quality products across the world. The organization emphasizes scientific excellence, operational innovation, and a collaborative culture to support patients and healthcare
Vacaturebeschrijving Wat je gaat doen In the position of productiemedewerker, you will play a key role in ensuring that medical nutrition products are packaged and labeled accurately. Working in a clean and well-organized environment, you will
Vacaturebeschrijving Wat je gaat doen You ensure medical nutrition products are packed, labeled and checked with precision. You follow clear procedures and help maintain a smooth production flow. Packaging and re‑packaging medical nutrition Printing and scanning labels using
Consultant | Partnering with Global Leaders in Pharma, Biotech, Food, Chemical & MedTech Industries | Driving Talent Solutions in Life Sciences… Klaar om te solliciteren? Voordat u dat doet, zorg ervoor dat u alle details met
Overview We are currently looking for a QA Specialist (GMP) for Amgen in Breda, the Netherlands to support a major pharmaceutical project focused on the introduction of new production lines and packaging equipment. In this role, you will
Orion Group Life Sciences are looking for a Senior Associate QA (GMP) (Validation / Packaging / PASX master data) for our Multinational Pharmaceutical/Biotechnology client based in Breda. Initial 12-month contract, with a high possibility of extension. This is
A pharmaceutical manufacturing company located in Breda is seeking a CQV Engineer to oversee commissioning, qualification, and validation activities in a GMP environment. Solliciteer snel! Er wordt een groot aantal sollicitanten verwacht voor de hieronder beschreven functie,
Job Title Vergroot uw kans op een sollicitatiegesprek door het volgende overzicht van deze functie te lezen voordat u solliciteert. CQV Engineer Sector Pharmaceutical / Medical Device Manufacturing Role The CQV Engineer is responsible for commissioning, qualification,
Overview Controleer hieronder of u heeft wat nodig is voor deze functie en, zo ja, solliciteer dan zo snel mogelijk. The technology department of FrieslandCampina in Veghel – the largest dairy processing site in the world
Commissioning Qualification Validation Engineer (GMP) Scroll naar beneden om alle bijbehorende functie-eisen en eventuele verantwoordelijkheden voor succesvolle kandidaten te zien. The CQV Engineer will support technical projects under minimal supervision and will report to Sr Manager
Vacaturebeschrijving Wat je gaat doen What You Will Do: Packaging: accurately package and check medical nutrition products according to established quality standards. Order handling: move and lift products weighing up to a maximum of 13 kilograms. For
Vacaturebeschrijving Wat je gaat doen You ensure medical nutrition products are packed, labeled and checked with precision. You follow clear procedures and help maintain a smooth production flow. Packaging and re‑packaging medical nutrition Printing and scanning labels using
Support role within the Maintenance & Engineering / Central Inventory Team , responsible for coordinating spare parts, materials, and inventory activities. The role ensures compliant material flow, accurate system administration, and operational readiness for maintenance, projects,