Sun Pharma is seeking a QA Officer to monitor and maintain product quality and compliance with EU GMP, national legislation, and client guidelines. Overweegt u te solliciteren op deze baan? Wacht niet langer, scroll naar beneden
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
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
Bring your Quality experience to Cell Therapy. Join our growing Cell Therapy team in Amsterdam in a hands-on Quality role. You will work with batch documentation, Quality systems and QPs, while helping us improve our processes as
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
Kwaliteit zit voor jou niet alleen in procedures en systemen, maar vooral in wat er dagelijks op de werkvloer gebeurt. Als QA Officer sta je dicht bij de productie en zorg je er samen met je
As a Senior LANSA Developer, you will: Design, develop, and maintain enterprise applications using Visual LANSA, RDML, and RDMLX. Build and enhance business logic, screen development, and reusable LANSA components. Develop and maintain applications within the
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
Adyen Geïnteresseerd in deze functie? U vindt alle relevante informatie in de omschrijving hieronder. Data Platform Engineers at Adyen build the foundational layer of tooling and processes for our on‑premise Big Data Platforms. These tools support
As our Qualified Person (QP)/ Responsible Person (RP) you are certifying the finished product and are responsible for ensuring that each finished medicinal product batch has been manufactured in accordance with GMP, the terms of the MIA
Sun Pharma is the world’s fifth largest specialty generic pharmaceutical company and India’s top pharmaceutical company. A vertically integrated business, economies of scale and an extremely skilled team enable us to deliver quality products in a
Drive meaningful change Als u overweegt een sollicitatie te sturen, zorg er dan voor dat u op de sollicitatieknop hieronder klikt na het lezen van de gehele omschrijving. Are you quality-driven, detail-oriented and eager to contribute
SUN Pharma is seeking a dynamic QA Specialist Biologics. As the QA Specialist Biologics, the selected candidate will play a pivotal role in ensuring the batch release and certification of our products for commercial use in Europe. Taking
Sciensus is seeking an experienced Qualified Person / Responsible Person (NL) to lead GMP and GDP compliance across our pharmaceutical operations in the Netherlands. Denkt u de juiste kandidaat te zijn voor de volgende functie? Solliciteer
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
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 indient.
Kyowa Kirin International plc. Ontdek hieronder precies welke vaardigheden, ervaring en kwalificaties u nodig heeft om te slagen in deze functie, voordat u solliciteert. in Hoofddorp is seeking an Associate Director Global CMC QU – Clinical
Job Title: Systems Engineer Hieronder staat alles wat u moet weten over wat deze vacature inhoudt, en wat er van sollicitanten wordt verwacht. Location: Madrid, Amsterdam, Luxembourg, or London Work schedule or timing: 8.30 AM to
The Senior Qualified Person (QP) will be responsible for certifying the release of IMPs for clinical trials in compliance with European and international GMP (Good Manufacturing Practice) standards. This role is critical to ensuring that Sun Pharma’s
MRC Holland is a biotechnology company located in Amsterdam, Netherlands, developing and manufacturing solutions for genetic inquiries, including MLPA®, digitalMLPA, and a Melt Assay for newborn screening. Scroll naar beneden voor een compleet overzicht van wat