If you are a current Jazz employee please apply via the Internal Career site Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Senior regulatory affairs CMC manager ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission
The Role: The Associate Director, CMC Regulatory Science-International will be based at the Harwell, UK site and as part of a team be responsible for preparing and overseeing CMC and Quality related agency correspondence and regulatory applications, as
Associate Director (Analytical Team Leader]), Early Chemical Development, Pharmaceutical Science Macclesfield UK - 3 days on site per week About AstraZeneca AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of
Your work will change lives. Including your own. The Impact You’ll Make Lead development and implementation of CMC regulatory strategy for small molecule investigational drugs in global Phase 1-3 clinical trials and marketing applications. Influence the regulatory strategy
The Role Moderna is looking for a Associate Director, CMC Regulatory Affairs-International, to join our team based in London, UK. This pivotal role will focus on preparing and overseeing CMC and Quality related agency correspondence and regulatory applications,
Job Opportunity: Business Development Manager - Licensing Location: Remote, United Kingdom Job Type: Full-time We are representing a fast-growing biotech company at the forefront of innovation, with broad cutting-edge technologies spanning a variety of therapeutic areas. This
About Relation Relation is a sector defining TechBio company developing transformational medicines, with technology at our core. Our ambition is to understand human biology in unprecedented ways, discovering therapies to treat some of life’s most devastating
Company Description AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives
Job purpose To manage a caseload of litigated and non-litigated personal injury claims with a value of up to £100,000.00, ensuring each case is progressed efficiently from initial instruction through to resolution. The role involves overseeing
Kenvue is currently recruiting for a:Senior Regulatory Affairs Specialist What we do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house
Company Description We are SGS – the worlds leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,500 employees operate a network of 2,500 offices and
Do you want to use your strong analytical, problem-solving skills to help find treatments for rare disease patients? About Healx Healx is an AI-powered tech bio company that is redesigning drug discovery. With 10,000 rare diseases
Introduction to role: Are you ready to define how cutting-edge peptide, oligonucleotide and other new modality medicines are measured, controlled and released from early development through commercial launch? In this role, you will set the analytical vision
The Vendor/Supplier QA Auditor role will support the quality oversight of external partners supporting R&D and regulated activities (e.g., CROs, CMOs, laboratories, technology vendors). Lead the end-to-end vendor lifecycle—due diligence, qualification, quality agreements, risk based monitoring,
The Vendor/Supplier QA Auditor role will own the quality oversight of external partners supporting R&D and regulated activities (e.g., CROs, CMOs, laboratories, technology vendors). Lead the end-to-end vendor lifecycle—due diligence, qualification, quality agreements, risk based monitoring,
Job Purpose As a Legal Advisor specialising in Low Velocity Impact (LVI) cases, you will be responsible for managing all aspects of non-litigated personal injury claims that involve allegations of fraud. Key Responsibilities Progressing claims in
Financial Accountant Location: Swindon, United Kingdom Role Summary: Onsite role, Monday – Friday 37.5 p/w. Our Swindon facility is home to our Zydis® fast-dissolving tablet development and manufacturing operation, alongside a CMC pharmaceutical analytical services unit offering ASAP
At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives