Regulatory Consultant - CMC (CMC with small molecule products) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum,
Regulatory CMC strategy manager ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are
CMC Leader (Director) Business Introduction We develop, manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of
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,
Since launching in 1989, CMC Markets (CMC) has become one of the worlds leading online financial trading businesses. CMC is listed on the London Stock Exchanges and serves retail and institutional clients through regulated offices and branches across the
Title: CMC Manager Location: United Kingdom Duration: 12-month contract (100% attendance) Company Overview Apsida Life Science is currently partnering with a clinical-stage biotechnology company that is developing a potent, selective, and orally bioavailable small-molecule. Responsibilities Support overall CMC program
The Role Scendea is seeking a highly motivated individual to join our global team as a full-time Senior Consultant (CMC). This is a hybrid position, affiliated to our either our Bishops Stortford (UK), Brisbane (AUS) or Washington,
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
Job title: Senior Project Manager Reporting to: Head of Operations Department: Project Management No of Direct reports: No direct reports (at appointment) Location: Bristol Summary: eXmoor Pharma is the only integrated cell and gene therapy CDMO
PE Global are currently recruiting for a Regulatory Affairs Specialist for an initial 6 month contract role with a leading multinational Consumer Health client based in Reading – hybrid (2/3 days per week in the office). Responsible
People Partner / HR Generalist (Interim Contract) St Albans | Office-Based (5 Days per Week) | Start ASAP A growing SME based in St Albans is entering an exciting period of change and is looking for an