JLL empowers you to shape a brighter way. Our people at JLL are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients. We are
Job Description General/Position Summary The Senior Director, CGT Quality Systems, Personalized Medicine provides strategic Quality leadership for personalized medicine and advanced cell therapies across the patient journey. The role is accountable for advancing Quality oversight, governance,
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
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
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
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
We are a Pharma and Life Science IT service provider that has been successfully carrying out state-of-the-art projects for international customers for more than 30 years, now. Our consultants work in from home on our customers
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
Bedrijfsomschrijving: Locatie: Amsterdam. Deze organisatie opereert binnen de procesindustrie en levert producten voor de gezondheidszorg vanuit een streng gereguleerde omgeving. De werkzaamheden vinden plaats in een productieomgeving waar hygiëne, veiligheid en nauwkeurige documentatie centraal staan. Medewerkers
ProPharma provides consulting solutions across regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology to support biotech, medical device, and pharmaceutical organizations throughout the product lifecycle. Alle aanvullende informatie die u
Bristol Myers Squibb Netherlands is seeking a Senior Manager, OT Systems & Automation for the Leiden Cell Therapy Manufacturing facility. Heeft u de juiste kwalificaties en vaardigheden voor deze baan? Ontdek het hieronder en klik op
• 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,
ProPharma is seeking a Senior Compliance and Quality Assurance Qualified Person Consultant to support pharmaceutical and biotech clients across development and commercialization stages. You will act as SME in QA, lead projects on MIA/WDA and QP
Responsibilities 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 real-time
Job Details Job Location: Amsterdam - Amsterdam Voor de volgende functie kunnen diverse soft skills en ervaring vereist zijn. Zorg ervoor dat u het onderstaande overzicht zorgvuldig controleert. Position Summary The successful candidate is an experienced