Medical Writing Team Lead Immunology Regulatory Expert

Medical Writing Team LeadAt Johnson & Johnson Innovative Medicine, we're dedicated to helping people live full and healthy lives. Our team is responsible for discovering and developing innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases, and vaccines.We're seeking a Medical Writing...

Medical Writing Team LeadLifelancer is seeking a Medical Writing Team Lead to support our Oncology therapeutic area.The ideal candidate will have at least 8 years of relevant pharmaceutical/scientific experience and 6 years of medical writing experience. They will lead project-level/submission/indication writing teams, actively participate in medical writing...

Manager, Oncology Regulatory Medical WritingLifelancer is seeking a highly skilled Manager to join our Oncology Regulatory Medical Writing team. As a key member of our team, you will be responsible for leading projects and supporting the development of innovative medical solutions to address important unmet medical needs in oncology.The ideal candidate will...

Job Title: Medical Writing ManagerJob Summary:We are seeking a Medical Writing Manager to join our team at Johnson & Johnson Innovative Medicine. As a Medical Writing Manager, you will be responsible for leading medical writing projects and teams, ensuring high-quality content and compliance with regulatory guidelines.Key Responsibilities:Lead medical...

At CTI Clinical Trial and Consulting Services, we strive to deliver innovative medical solutions to address complex diseases. Our team is dedicated to helping people live full and healthy lives.The Regulatory Medical Writing team is seeking a skilled Medical Writing Manager to support our Oncology therapeutic area. This role may be located in the UK, other...

Lifelancer, a talent-hiring platform in Life Sciences, Pharma and IT, is seeking an experienced Regulatory Medical Writing Manager to support our Oncology therapeutic area. This role may be located in the UK, other European countries, or Canada.We value a colleague with at least 8 years of relevant pharmaceutical/scientific experience and at least 6 years of...

At Johnson & Johnson, we are committed to driving medical innovation and excellence in our Lifecycle Medicine portfolio.The role of Senior Medical Advisor offers a unique opportunity to leverage your expertise and contribute to the success of our business.This position is based at our High Wycombe office, where you will report directly to the UK LCM Medical...

Job SummaryThe Regulatory Affairs Specialist - Medical Devices will be responsible for preparing and submitting regulatory approval applications, ensuring compliance with medical device standards and regulations, and maintaining technical documentation for regulatory purposes. This role is ideal for recent graduates with backgrounds in engineering, science,...

As a Regulatory Affairs Specialist, you will play a vital role in ensuring the compliance of medical devices with regulatory standards and requirements. This position is ideal for recent graduates with backgrounds in engineering, science, or law who are eager to start a career in a stable and growing industry.About the RoleWe are seeking a highly motivated...

Job OverviewWe are seeking a highly skilled Regulatory Affairs Expert to lead our Consumer Health team. This role will be responsible for managing regulatory submissions and ensuring compliance with EU regulations.

**Key Responsibilities:**As an Automotive Customer Service Advisor, you will play a vital role in providing outstanding customer support and ensuring customer satisfaction.Your primary responsibilities will include:Leveraging your automotive industry experience or knowledge to provide expert advice to customers.Communicating clearly and professionally in...

Join Kenvue, a leader in the science-driven industry, and contribute to the growth and evolution of iconic brands.Job DescriptionSenior Manager Regulatory Affairs (m/f/d) UK & Ireland WJob SummaryKenvue is seeking a Senior Manager Regulatory Affairs to lead the Regulatory Affairs team in the UK and Ireland. The successful candidate will be responsible for...

Job Title: Automotive Project ManagerWe are seeking an experienced Automotive Project Manager to lead the development of Vehicle Test Systems from concept to user acceptance. As a key member of our team, you will be responsible for understanding automotive testing and industry regulatory requirements.Key Responsibilities:Lead development of Vehicle Test...

Kenvue Career OpportunityWe are seeking a highly skilled Regulatory Affairs Specialist to join our team in the UK. The successful candidate will be responsible for ensuring compliance with regulatory requirements for consumer healthcare products.About KenvueAt Kenvue, we believe that everyone deserves access to high-quality, innovative care solutions. Our...

Key Account Medical Writing LeadershipBarrington James is seeking a highly experienced Principal Medical Writer to lead scientific strategy and content development for key accounts. This role involves translating client objectives into compelling, multi-channel activities designed to drive behavior change.Responsibilities:Develop and execute scientific...

Unlock Your Potential in Medical EducationWe are seeking a dedicated and passionate individual to join our team as a Medical Education Specialist at the University of Buckingham Medical School. This is an exciting opportunity for someone looking to make a meaningful contribution to medical education while continuing their clinical work.This part-time role...

Project Manager - Automotive Vehicle TestingWe are seeking a skilled Project Manager to lead the development of Vehicle Test Systems from initial concept and specification through to the design and development of hardware, firmware, software, and mechanical components, culminating in user acceptance.The ideal candidate will have a strong understanding of...

Cpl Life Sciences is seeking an experienced Cosmetics Regulatory Affairs Expert to join their team on a 6-month contract basis.Salary: £65-£70 per hour.This role will be dedicated to cosmetics and a non-OTC portfolio. The successful candidate will be responsible for regulatory review and approval of product labelling, advertising copy, and key documents...

About the Role:As a Project Manager for Automotive Vehicle Test Development, you will be responsible for leading the development of Vehicle Test Systems from concept to user acceptance. This role requires a strong understanding of automotive testing and industry regulatory requirements.Key Skills:Project management experience in the automotive...

Regulatory Affairs SpecialistThe Regulatory Affairs Specialist is accountable for all regulatory activities associated with their assigned medicines, medical devices, cosmetics, and/or food supplement consumer products within their geographical and/or brand area of responsibility.This role involves compilation and submission of applications (post-approval...