Regulatory Strategies Jobs in UK

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team thats revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases.As an employee youll be part of a continually growing organization working alongside e...

Job DescriptionThe Identification of Medicinal Products (IDMP) Business Analyst will play a key role in the management and leadership of the European implementation of the ISO Identification IDMPs standard in our Company. You will be part of a team progressing the strategic project and operational a...

Are you a driven and innovative Regulatory Affairs professional looking to make a meaningful impact on the global supply of medicinesJoin our Chemistry Manufacturing and Controls (CMC) Regulatory Affairs Group within Global Regulatory Affairs at GSK where we play an essential role in ensuring uninte...

Job Description Summary#LI-Hybrid (12 days per month on-site)Location: London (The Westworks) United Kingdom Internal Title: Team Lead Regulatory Translation SolutionsWe are seeking a strategic and experienced Regulatory Affairs professional to oversee the provision of timely high-quality regulatory...

Job Description SummaryOffice Location: London (The Westworks) United Kingdom #LI-Hybrid Hybrid (12 days per month on-site if living within 50 miles to our London office)#LI-Remote Remote (if living beyond 50 miles to our London office)Internal Title: Team Lead Regulatory Translation SolutionsWe are...

Job OverviewImplement regulatory strategies & deliverables for a portfolio of products early/late development or marketed products for the Europe Area Regulatory Affairs (ERA) including EU and non-EU countries such as CEE countries Israel Turkey Switzerland and the UK. Include fair representation of...

Job Description Summary#LI-Hybrid (12 days per month on-site)Location: London (The Westworks) United KingdomInternal Job Title: Global Program Regulatory ManagerWe are looking for an experienced and proactive Regulatory Affairs Manager to join our Global Regulatory Affairs team. This role is critica...

Job Description Summary#LI-Hybrid (12 days per month on-site)Location: London (The Westworks) United Kingdom or Dublin IrelandInternal Job Title: Global Program Regulatory Associate DirectorWe are looking for an experienced and proactive Senior Global Program Regulatory Manager to join our Global Re...

DescriptionAt a time when global technological developments and healthcare regulations are occurring and changing at an unprecedented rate the success of large complex global health companies requires regulatory leaders who are deeply steeped in the public and private levers that impact this industr...

Job Description Summary#LI-Hybrid (12 days per month on-site)Location: London (The Westworks) United KingdomInternal Job Title: Global Program Regulatory DirectorNovartis is seeking a Global Program Regulatory Director (GPRD) to lead global regulatory strategies for development and marketed products...

DescriptionAt a time when global technological developments and healthcare regulations are occurring and changing at an unprecedented rate the success of large complex global organizations that engage deeply in this space requires a legal/business leader who is deeply steeped in the levers both publ...

Job Description SummaryOffice Location: London (The Westworks) United Kingdom #LI-Hybrid Hybrid (12 days per month on-site if living within 50 miles to our London office)#LI-Remote Remote (if living beyond 50 miles to our London office)Internal Job Title: Global Program Regulatory DirectorNovartis i...

Job Description Summary#LI-Hybrid (12 days per month on-site)Location: London (The Westworks) United KingdomThe Associate Director Regulatory Affairs (Medical Devices) independently provides strategic and operational global medical device regulatory direction and documentation for projects/products...

Job Description SummaryOffice Location: London (The Westworks) United Kingdom #LI-Hybrid Hybrid (12 days per month on-site if living within 50 miles to our London office)#LI-Remote Remote (if living beyond 50 miles to our London office)The Associate Director Regulatory Affairs (Medical Devices) inde...

Job Description Summary#LI-Hybrid (12 days per month on-site)Location: London (The Westworks) United KingdomInternal Job Title: Global Program Regulatory ManagerWe are looking for an experienced and proactive Regulatory Affairs Manager to join our Global Regulatory Affairs team. This role is critica...

We are currently looking for a Regulatory CMC Manager Devices to join our team.As Regulatory CMC Manager Devices you will play a key role in driving the development and delivery of global device-related regulatory strategies and solutions that support GSKs mission to get ahead of disease together. Y...

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 and to ensure access to these therapies across the globe. We continue to fight aga...

Job Title Enforcement and Market Oversight Litigations LawyerDivision - Enforcement and Market OversightDepartment Wholesale and Unauthorised Business InvestigationsTeam Wholesale 2Salary National ranging from 79400 to 100000 and London from 87300 to 123500 (Salary offered will be based on skill...

CK Group are recruiting for a Regulatory Scientistto join a company in the pharmaceutical industry on a contract basis for 12 months.14.68-19.15 per hour PAYERegulatory ScientistRole:Provide region/country input and review of global strategic plans and global/regional submission plan and documents.P...

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team thats revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases.As an employee youll be part of a continually growing organization working alongside e...