Global Regulatory Expert

About the RoleAs a Regulatory Affairs Manager, you will play a key role in planning and managing regulatory submissions (e.g., clinical trial and marketing applications) for products within our portfolio in compliance with global filing plans and local regulatory requirements.You will also be responsible for acting as a contact with relevant regulatory...

**PE Global is currently recruiting for a Regulatory Affairs Manager for a leading multi-national Biotech client based in Uxbridge with a hybrid work option.** **Role**: - Responsible for the generation of country specific regulatory strategies and providing feedback to internal teams regarding submission plans and execution of the strategy for one or more...

Austin Fraser is seeking an experienced Global Regulatory Compliance Manager to join their team in London on a full-time, 12-month temporary basis (35 hours per week). The estimated salary for this role is £70,000 - £90,000 per year.The successful candidate will be responsible for leading and managing the operational aspects of European regulatory filings,...

Job Summary:We are looking for a Senior Regulatory Affairs Manager to join our client's team in Uxbridge. The role involves developing and implementing regulatory strategies to ensure compliance with global regulatory requirements.The ideal candidate will have experience as a Regulatory Lead managing at least 1 product end to end lifecycle and be able to...

Job DescriptionA global pharmaceutical company in Uxbridge is seeking a Senior Regulatory Affairs Manager to join their team. The estimated salary for this role is around £70,000 - £100,000 per annum.The ideal candidate will be a confident Regulatory Lead with experience in developing and defining regulatory plans across multiple products. They will work...

Bristol-Myers Squibb is a world-renowned pharmaceutical company that offers a rewarding career opportunity as a Global Regulatory Compliance Officer.The estimated salary range for this role is $150,000 - $220,000 per annum, based on experience and qualifications.The ideal candidate will have at least 4+ years of US Medical Device Regulatory Affairs...

Key ResponsibilitiesAs a Regulatory Affairs Senior Manager, you will be responsible for operating as a Regulatory Lead, providing centralised regulatory strategy and guidance across the region.Your key responsibilities will include:Developing, contributing, and ensuring the accurate preparation of high-quality regulatory documents needed to support clinical...

Job Title: Regulatory Documentation ExpertLocation: United Kingdom - Uxbridge, United Kingdom - CambridgeAbout the Role:We are seeking a highly experienced Regulatory Documentation Expert to join our dynamic team at Gilead Sciences, Inc. As a key member of our Medical Writing department, you will play a crucial role in authoring and reviewing regulatory...

About the Role">As a Senior Regulatory Affairs Manager, you will be responsible for providing centralised regulatory strategy and guidance across the region.Your key responsibilities will include:">Developing and contributing to high-quality regulatory documents needed to support clinical trials and medical products.Providing regulatory guidance to enhance...

Bristol-Myers Squibb is a leading pharmaceutical company offering competitive salaries to skilled professionals.Our estimated salary range for this role is $120,000 - $180,000 per annum, depending on experience and qualifications.The ideal candidate will possess strong leadership skills and be able to develop global regulatory strategies to support the...

About UsCover-More Group is committed to providing reliable, fast, flexible, and bespoke services for our customers and partners. Our mission is to look after travellers at every step of their journey, and we strive to deliver exceptional customer experiences.The RoleThis is a unique opportunity to join a global group of professionals dedicated to making a...

Job DescriptionWe are looking for a highly experienced Compliance and Regulatory Expert to join our team in the UK. The successful candidate will be responsible for ensuring business continuity in RHD markets, including the UK, Ireland, Malta, and Cyprus, and will work closely with the European Product Compliance Department and Local Product Department to...

Our client, a global pharmaceutical company is currently looking for a EU Regulatory Strategist to join their team based on the outskirts of London on a full time, 12-month temporary basis (35 hours per week).In this role, you'll lead and manage the operational aspects of European regulatory filings, collaborating closely with European Regulatory groups...

Job DescriptionWe are seeking a highly skilled Mechanical Assembly Expert to join our team at Proactive Global. As a key member of our production team, you will be responsible for assembling and repairing mechanical components in a fast-paced manufacturing environment.Key Responsibilities:Assemble fabricated and pre-formed partsStrip, service, and rebuild...

Our client, a global pharmaceutical company is currently looking for a EU Regulatory Strategist to join their team based on the outskirts of London on a full time, 12-month temporary basis (35 hours per week). In this role, you'll lead and manage the operational aspects of European regulatory filings, collaborating closely with European Regulatory...

Our client, a global pharmaceutical company is currently looking for a EU Regulatory Strategist to join their team based on the outskirts of London on a full time, 12-month temporary basis (35 hours per week). In this role, you'll lead and manage the operational aspects of European regulatory filings, collaborating closely with European Regulatory...

Our client, a global pharmaceutical company is currently looking for a EU Regulatory Strategist to join their team based on the outskirts of London on a full time, 12-month temporary basis (35 hours per week). In this role, you'll lead and manage the operational aspects of European regulatory filings, collaborating closely with European Regulatory...

Our client, a global pharmaceutical company is currently looking for a EU Regulatory Strategist to join their team based on the outskirts of London on a full time, 12-month temporary basis (35 hours per week).In this role, you'll lead and manage the operational aspects of European regulatory filings, collaborating closely with European Regulatory groups and...

Job Summary:Clinical Professionals seeks a highly skilled Supply Chain Strategist for Clinical Trials to develop and implement supply chain strategies that meet the needs of our global clinical trials. This role requires a deep understanding of the global drug development process and ability to collaborate with cross-functional teams to drive supply chain...

Role OverviewPark Street People is currently looking for a Senior Regulatory Affairs Manager to join their team in Uxbridge. The ideal candidate will be a confident Regulatory Lead with experience in developing and defining regulatory plans across multiple products.The role involves working closely with the regulatory team and stakeholders to provide...