Build our future together At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Temporary Quality Manager GCP - GVP, supporting our Global Development quality system in
Quality in a globalized drug safety network is a matter of operational resilience as much as regulatory mandate. This role serves as a GVP Auditor within our Research & Development Quality audit program, responsible for executing the
Temporary Quality Manager (GCP/GVP) Location: Uxbridge, London, UK – Hybrid/Remote Contract: Temporary Salary: £70,000 to £85,000 About the Opportunity We are seeking an experienced Temporary Quality Manager (GCP/GVP) to support a global development quality function within an innovative,
Zeta Global is looking for a Vice President, Impact Partners – UK to drive significant new revenue growth across our strategic existing customer base. This is a senior enterprise sales role. It is not a traditional
Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Director, Benefit/Risk Medical Adviser EU/UK to join our QPPV Office. Reporting
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
Company Description Medicine moves forward here. So will you. ADAMAS Consulting helps the worlds pharmaceutical and biotechnology companies uphold the highest standards of quality, compliance and patient safety. Since 2007 we have partnered with organizations across
DescriptionWho We Are BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions.Guided by our purpose to develop medicines that make a profound impact on people’s lives, our global teams have delivered a
A leading biotechnology company is looking for a GVP Compliance Lead to oversee compliance practices related to pharmacovigilance. The ideal candidate will have over 10 years of experience in regulated healthcare, knowledge of FDA and EMA regulations,
Overview BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. Since our founding in 1997, we have applied our scientific
Build our future together At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Temporary Quality Manager GCP - GVP, supporting our Global Development quality system in
BioMarin Pharmaceutical Inc. in London, UK is seeking an Associate Director, GVP Compliance to join our Global Quality organization. This role advises on Good Pharmacovigilance Practices (GVP), assesses compliance with global regulations, and supports readiness and execution of
At Gilead, were creating a healthier world for all people. For more than 35 years, weve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives
Moog is a performance culture that empowers people to achieve great things. Our people enjoy solving interesting technical challenges in a culture where everyone trusts each other to do the right thing. For you, working with
AstraZeneca in Luton, UK is seeking an Associate Director Audit & Assurance R&D QA to elevate GxP quality across R&D. You will lead risk-based GVP/GCP audits, strengthen inspection readiness, and translate complex regulations into practical guidance that
Medical Lead Consultant Remote | UK or Europe 6 Month Contract | Full Time BioTalent is exclusively supporting a global biopharmaceutical organisation that is seeking an experienced Medical Lead Consultant to provide medical oversight across both
Reporting to: VP Pharmacovigilance Location: London, UK / Hybrid Orchard Therapeutics is a global biotechnology gene therapy company dedicated to transforming the lives of people affected by rare diseases through the development of innovative, potentially curative
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
The Head of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs,
NIS P&D Study Delivery Lead, Associate Director - Oncology For candidates seeking to be located at our Stevenage site, this role will temporarily be based at Stevenage. However, the Company plans to relocate its offices to