• Lead the design, configuration, and deployment of SAP EWM solutions tailored for the supply chain. Good to have pharma experience • Work closely with the MES team to design and implement robust EWM-MES integration for
About myTomorrows myTomorrows is a global health tech company dedicated to breaking down barriers for patients seeking treatment options. We strive to enable earlier and better treatment access by bridging the gap between those searching for
Company Description Santen is a specialized life sciences company with a proud over 130-year heritage focused exclusively on ophthalmology. As a Japan-originated, global company with a footprint in over 60 countries, we are dedicated to delivering
About the Company Prothya is dedicated to ensuring the registration (market authorization) of its medicinal products is obtained and maintained in compliance with regulatory standards. About the Role The purpose of the job is to compile
As our Validation Specialist IT (CSV/CSA), you will lead validation and compliance activities for GxP-regulated systems, digital transformation initiatives, equipment, infrastructure, and system integration projects across Prothya. Your role is responsible for defining validation strategies, ensuring regulatory
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
Role – Principal Consultant/SAP FICO S/4 Hana Consultant Technology – SAP FICO S/4 Hana Location – Netherlands Job Description: Today, the corporate landscape is dynamic, and the world ahead is full of possibilities! None of the
Werk met impact op levens. Wil jij als Process Operator B werken in een farmaceutische productieomgeving waar kwaliteit, veiligheid en precisie écht tellen? Voor Prothya zoekt procestechniek.nl een nauwkeurige operator die wil bijdragen aan de verwerking
As a QC Engineer Specialist you support the Quality Control Operations lab team with method validation, verification, transfer, troubleshooting and specification setting. Key responsibilities: Method verification/validation Perform and coordinate method development and validation/verification: Develop and implement
We are seeking an experienced Project Manager to lead the successful delivery of strategic business and IT initiatives across Prothya. In your role you are responsible for planning, executing, and governing cross-functional projects and programmes, ensuring
As our Senior Data Engineer / BI Specialist you will design, build, and maintain scalable data solutions using the Microsoft data platform. Your role will enable data-driven decision-making through modern data engineering, Microsoft Fabric, and Power
As our Validation Engineer IT you will support validation and compliance activities for GxP-regulated systems, digital transformation initiatives, equipment, infrastructure, and system integration projects across Prothya. Your role is responsible for executing validation activities throughout the project
About the Role Prothya is looking for an experienced and business-oriented Legal Counsel to join our organization. In this role, you will be responsible for leading and safeguarding corporate, commercial, governance, and compliance-related legal activities across
Bedrijfsomschrijving: Locatie: Amsterdam. Als u geïnteresseerd bent om op deze vacature te solliciteren, zorg er dan voor dat u voldoet aan de volgende, hieronder vermelde vereisten. Deze organisatie opereert binnen de procesindustrie en levert producten voor
Location: Leiden, Netherlands Company: Avantor At Avantor, we empower scientific breakthroughs that improve human health and quality of life. We are looking for a proactive and detail-oriented Laboratory Services Specialist to join our team in Leiden.
We are seeking an experienced and people-focused Supervisor, Laboratory Support Services to lead a team supporting critical laboratory operations within a highly regulated pharmaceutical environment. This role is ideal for a proven leader who thrives in
• Lead the design, configuration, and deployment of SAP EWM solutions tailored for the supply chain. Good to have pharma experience Als de volgende functie-eisen en ervaring overeenkomen met uw vaardigheden, zorg er dan voor dat
Overview Our client operates in the biopharmaceutical field and focuses on advanced cell‑based therapies for patients with severe and complex diseases. The organization combines cutting‑edge science with large‑scale operations in a highly regulated environment. To support
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
Details Working hours: 40 hours per week Contract duration: until 31 December 2026 (likely chance of extension) Responsibilities Creating, reviewing, and approving qualification protocols, executed protocol summary reports, and Requirements Traceability Matrices for equipment, utilities, facilities,