MAT Research is a pioneering company in the field of pyrogen testing, committed to ushering in a new era of ethical and accurate diagnostics. Since 2016, we have been leading the development of the Monocyte Activation
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.
IQVIA is focused on using data and science to help healthcare clients find better solutions for their patients. Individuals joining us are assured of a rewarding career in Life Sciences Consulting, with opportunities to address diverse
At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered
ProQR Therapeutics is a NASDAQ-listed biotechnology company headquartered in Leiden, the Netherlands with an office in and Cambridge, Massachusetts, USA. At ProQR, we are on a mission to edit RNA, treat disease and change lives. A
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.
About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments
QbD Group offers knowledge & tailored solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, ATMP and Medical Devices/IVD. Currently we are looking for Project Managers (PM) in Qualification &
Newell Brands is a leading $8.3B consumer products company with a portfolio of iconic brands such as Graco®, Coleman®, Oster®, Rubbermaid® and Sharpie®, and 25,000 talented employees around the world. Our high-performance culture, unparalleled curiosity about
About the job Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam DAngelo, Larry Summers, and Jack Dorsey. Position: Regulatory
About the job Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam DAngelo, Larry Summers, and Jack Dorsey. Position: Regulatory
About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA‑approved treatments
ProQR Therapeutics in Leiden, NL is seeking a Clinical Operations Lead (full-time) to direct end-to-end management of outsourced clinical trials, ensuring data integrity and patient safety. Zorg ervoor dat u solliciteert met alle gevraagde informatie, zoals
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
Als Quality Director ben je verantwoordelijk voor het opzetten, beheren en verbeteren van onze kwaliteitsprocessen op locatie, waarbij je toezicht houdt op zowel de Quality Assurance (QA) als Quality Control (QC) activiteiten. Je rapporteert direct aan
Overview Direct message the job poster from Panda International Responsibilities Own global product registrations and support marketing teams with regulatory documentation Maintain and improve ISO 13485-certified QMS across outsourced production network Manage CE marking processes for
A fast-growing health company in Amsterdam is seeking a Regulatory & Quality Compliance Manager. Ontdek of deze vacature goed bij u past door alle informatie hieronder te lezen. This role involves ensuring compliance with EU MDR
Senior Quality Governance Lead (Operational) Heeft u wat nodig is om te slagen? De volgende informatie dient door alle kandidaten zorgvuldig gelezen te worden. Working mode: On-site Duration: 6 months Languages: English and Dutch The Senior
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,
The RMA Associate is responsible to receive, decontaminate, triage, and transact returned products; ensure compliant quarantine/recall handling; resolve missing-paperwork issues; and keep ERP inventory and financial touchpoints accurate while prioritizing high-volume weekly receipts in a regulated