Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative
WHO ARE WE? ROPU MIDI is a Regional Operating Unit that covers all local Human Pharma and Animal Health Operating Units across Belgium, Denmark, Norway, Finland, Greece, Portugal, Sweden, and The Netherlands. MIDI has a multicultural
Functional Consultant – OneStream XF Requirement ID: 10960805 Location: Amsterdam, Netherlands Work Arrangement: To be confirmed Start Date: 1 October 2026 Duration: 6 months Experience: 8–10 years Core Competency: Planning and Forecasting Essential Skill: OneStream XF
Company Overview Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases. We recognize the courage it takes
The Opportunity: We are “Avantor”, a Fortune 500 company, leading global provider of mission-critical products and services to customers in the BioPharma, healthcare, education & government, and advanced technologies & applied materials industries. Our portfolio is
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
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
Job Title: Systems Engineer Dien uw cv en eventuele aanvullende vereiste informatie in nadat u deze omschrijving heeft gelezen, door op de sollicitatieknop te klikken. Location: Madrid, Amsterdam, Luxembourg, or London Work schedule or timing: 8.30
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
As a OneStream XF Functional Consultant, you will: Provide hands-on application support and administration for OneStream XF. Support budgeting, forecasting, planning, financial reporting, and consolidation processes within OneStream. Manage and troubleshoot workflows, data loads, business rules,
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
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
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
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
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
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.
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