Senior Regulatory Affairs Director, Life Sciences

Job SummaryWe are seeking a highly skilled Regulatory Affairs Director to lead our Global Therapeutic Area (TA) Regulatory Affairs team in Virology. As a key member of our team, you will be responsible for defining the regulatory strategy, plans, and objectives for assigned products or projects. You will also oversee the preparation and maintenance of...

**Job Description**Gilead Sciences, Inc. is a leading biopharmaceutical company that seeks an experienced Regulatory Affairs professional to join its team as an Associate Director, Global TA Regulatory Liaisons, Virology. This role will oversee the preparation and maintenance of regulatory submissions, labeling, and packaging for assigned products or...

Senior Regulatory Affairs Manager PositionWe are seeking a Senior Regulatory Affairs Manager/Consultant with 10+ years of experience in regulatory affairs, including CMC expertise. This challenging role offers the opportunity to work on diverse projects, manage client relationships, and contribute to regulatory strategies in a global pharmaceutical...

Gilead Sciences International, Ltd. is seeking a highly skilled Global Regulatory Affairs Director - Distributor Management to join our team. The successful candidate will be responsible for providing oversight and management of regulatory activities provided by Gilead's in-market partners in the Gilead Patient Solutions (GPS) region. This role requires...

Job SummaryGilead Sciences, Inc. is seeking a highly skilled Medical Affairs Director to lead the Cell Therapy team in the ACE region. The successful candidate will be responsible for developing and executing the Cell Therapy Medical Affairs Strategy across the ACE Region, collaborating with cross-functional teams, and contributing to the global strategy.Key...

Job SummaryThis is an exciting opportunity for an Associate Director to join the Gilead Global Regulatory Affiliates & Distributor team. The role requires effective stakeholder management and collaboration with cross-functional teams to oversee regulatory activities across the region.Key ResponsibilitiesManagement of regulatory capability for Gilead's...

Job SummaryWe are seeking a highly skilled and experienced Senior Medical Affairs Director to lead our Cell Therapy team in the ACE region. This role will be responsible for developing and executing the Cell Therapy Medical Affairs Strategy across the ACE Region.Key ResponsibilitiesDevelop and represent the Cell Therapy Medical Affairs Strategy across the...

**Job Summary**Gilead Sciences, Inc. is a biopharmaceutical company that develops life-changing scientific innovations. We are seeking an experienced Regulatory Affairs professional to join our team as an Associate Director, Global TA Regulatory Liaisons, Virology.This role requires a deep understanding of European Medicines Agency (EMA) regulations and...

Job Title: Medical Director for HIV Global AffairsGilead Sciences, Inc. is seeking a highly skilled Medical Director for HIV Global Affairs to join our team. As a key member of our Global Medical Affairs team, you will be responsible for developing and implementing the annual HIV Global Medical Affairs digital plan.Key Responsibilities:Develop and implement...

**About the Role**We are seeking a highly skilled Regulatory Affairs professional to fill the position of Associate Director, Global TA Regulatory Liaisons, Virology at Gilead Sciences, Inc.The successful candidate will have a deep understanding of European Medicines Agency (EMA) regulations and International Council for Harmonisation of Technical...

Gilead is seeking a highly experienced Senior Medical Affairs Director to lead the Cell Therapy team in the ACE region. This role will be accountable for developing and executing the Cell Therapy Medical Affairs Strategy across the ACE Region.Key ResponsibilitiesDevelop and represent the Cell Therapy Medical Affairs Strategy across the ACE Region.Collaborate...

Transforming Lives through Regulatory ExcellenceBristol Myers Squibb is a company that pushes the boundaries of what's possible in the world of pharmaceuticals. As an Associate Director, Global Regulatory Sciences, Precision Medicine, you'll be at the forefront of this innovation, driving regulatory strategies that bring life-changing treatments to patients...

Parexel is seeking a highly skilled Senior Regulatory Affairs Manager for biologics to join our team in the European region. This role can be performed from home or office locations.The ideal candidate will play a crucial role in worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological...

Regulatory Affairs Senior Associate RoleWe are seeking a highly skilled Regulatory Affairs Senior Associate to join our team at Regeneron Pharmaceuticals Inc.About the RoleThis is an exciting opportunity for a talented individual with a passion for regulatory affairs to support our CMC Regulatory submissions. As a key member of our team, you will play a...

When our values align, there's no limit to what we can achieve.   We are seeking a highly skilled and experienced Regulatory Affairs Director to join our team. As a Director, you will be responsible for the successful execution of multiple projects and ensuring client satisfaction. You will provide mentorship, leadership and direction to Managers and...

When our values align, there's no limit to what we can achieve.   We are seeking a highly skilled and experienced Regional Regulatory Affairs Director (EMEA) to join our team. As a Director, you will be responsible for the successful execution of multiple projects and ensuring client satisfaction. You will provide mentorship, leadership and...

Transforming Lives through Regulatory ExcellenceBristol Myers Squibb is a leader in the pharmaceutical industry, and we're seeking a talented Associate Director, Global Regulatory Sciences, Precision Medicine to join our team. In this role, you'll have the opportunity to work on cutting-edge projects that transform the lives of patients and drive innovation...

Senior Regulatory Affairs Associate / Regulatory Affairs Manager EU contract jobYour new company This global biopharmaceutical company is looking for an experienced Regulatory Affairs professional to join them on a contract basis, 12 month, hybrid contract job with scope for extensionYour new role As Senior Regulatory Affair Associate / Regulatory Affairs...

A global pharmaceutical company, based in Uxbridge is currently looking for a Senior Regulatory Affairs Manager to join their team. You will be a confident Regulatory Lead looking to work in an innovative therapy area, developing and defining regulatory plans across multiple products. This is a great opportunity to work with a team who take provide in...

We are seeking a talented Regulatory Affairs Specialist to join our dynamic team at BTA. As the CMC Regulatory Manager, you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological products.Key Responsibilities:Develop submission strategies and...