OTC Medicines Regulatory Lead

ClinChoice, a global full-service CRO, is seeking an experienced Regulatory Affairs Manager for 3 months contract to work with one of our Consumer Health partners, focusing on over-the-counter (OTC) Pharmaceuticals.Key ResponsibilitiesManagement of products within the therapy area for OTC Medicines, Cosmetics, Medical Devices and/or Food...

Regulatory Affairs Manager for OTC ProductsClinChoice is seeking an experienced Regulatory Affairs Manager to join our team for a 3-month contract. As a key member of our Consumer Health department, you will be responsible for managing regulatory submissions and ensuring compliance with EU regulations and guidelines.Key Responsibilities:Develop and implement...

About the RoleWe are seeking an experienced Regulatory Affairs expert to join our team at Lifelancer, a leading talent-hiring platform in Life Sciences. As a key member of our team, you will be responsible for managing regulatory submissions and projects related to Over-the-Counter (OTC) products.

ClinChoice is seeking an experienced Regulatory Affairs Manager to join our team for a 3-month contract. As a key member of our Consumer Health department, you will be responsible for managing products within a therapy area for OTC Medicines, Cosmetics, Medical Devices, and/or Food Supplements.Key ResponsibilitiesDevelop and implement regulatory strategies...

Job Title: Regulatory Affairs SpecialistWe are seeking an experienced Regulatory Affairs Specialist to join our team at ClinChoice Inc. The ideal candidate will have a strong background in regulatory affairs, with a focus on over-the-counter (OTC) medicines.The salary for this role is estimated to be around $90,000 - $110,000 per annum, depending on...

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...

Cosmetic Regulatory Affairs Specialist OpportunityWe are seeking a highly experienced Regulatory Affairs Specialist to join our team on a 6-month contract basis. This role will be dedicated to cosmetics and a non-OTC portfolio.Key Responsibilities:Regulatory review and approval of product labelling for cosmetics and other non-OTC classes in the UK &...

Regulatory Affairs Specialist OpportunityWe are seeking an experienced Senior Regulatory Affairs Specialist to join our team at Cpl Life Sciences, specializing in cosmetics and non-OTC products.About the Role:Provide regulatory review and approval of product labeling and advertising materials for cosmetics and non-OTC classes in the UK and Ireland.Support...

Job SummaryKenvue is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our Regulatory Affairs department, you will be responsible for managing regulatory activities for a number of products within a therapy area for Cosmetics, OTC and/or Medical Devices in the UK, Ireland and Malta.Key ResponsibilitiesDevelop and...

Role OverviewWe are seeking a skilled Regulatory Affairs Manager to join our team at CK Group. The successful candidate will be responsible for managing post-approval activities for specified OTC products, including supporting the EMEA Regulatory Affairs team and coordinating worksharing procedures.Key Responsibilities• Develop regulatory strategies and...

CK Group is seeking a highly skilled Regulatory Affairs Manager to join a leading pharmaceutical company in High Wycombe. This contract role will involve managing post-approval activities for specified OTC products.Key Responsibilities:Support the EMEA Regulatory Affairs team with post-approval activities for MRP/DCP products across the EEA and coordinate...

Job Title: Regulatory Affairs Specialist/Consultant – CosmeticsJob Type: 6-month contract (Inside IR35)Location: Buckinghamshire, UK – 2x a week in officePay Rate: £65ph - £70phWe are seeking an experienced Regulatory Consultant to join our team on a 6-month contract basis. The successful candidate will be dedicated to cosmetics and a non-OTC...

Regulatory Affairs ManagerCK Group is seeking a highly skilled Regulatory Affairs Manager to join their team in the Pharmaceutical industry. This contract role is based in High Wycombe and will run until the end of March 2025.Key Responsibilities:Manage post-approval activities for specified OTC products, including supporting the EMEA Regulatory Affairs team...

Job Title: Regulatory Affairs ManagerCK Group is seeking a highly skilled Regulatory Affairs Manager to join their team. This is a contract role based in High Wycombe, requiring a strong understanding of post-approval activities for OTC products.Key Responsibilities:Support the EMEA Regulatory Affairs team with post-approval activities for MRP/DCP products...

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...

About the RoleWe are seeking a highly skilled Regulatory Affairs Executive to join our team in High Wycombe, UK. As a Senior Regulatory Affairs Executive, you will be responsible for managing regulatory strategies and activities for various products within the Cosmetics, OTC, and Medical Devices sectors in the UK, Ireland, and Malta.Key...

Job DescriptionRole: EMEA Regulatory Affairs ConsultantDuration: 5 monthsLocation: Remote - Hybrid workingKEY RESPONSIBILITIESManage post-approval activities for specified OTC products, supporting the EMEA Regulatory Affairs team for post-approval activities for MRP/DCP products across the EEA. Coordinate worksharing (WS) procedures for CMC and non-CMC...

Regulatory Affairs Manager Role:As a Regulatory Affairs Manager at CK Group, you will be responsible for managing post-approval activities for specified OTC products. This includes supporting the EMEA Regulatory Affairs team for post-approval activities for MRP/DCP products across EEA and coordinating worksharing (WS) procedures for CMC and non-CMC...

Job Title: Regulatory Affairs ManagerJob Type: ContractIndustry: PharmaceuticalLocation: High WycombeAbout the Role:The successful Regulatory Affairs Manager will be responsible for managing post-approval activities for specified OTC products, supporting the EMEA Regulatory Affairs team with post-approval activities for MRP/DCP products across the EEA, and...

Job Title: Senior Regulatory Affairs SpecialistCompany: World-Leading Consumer Healthcare CompanyJob Purpose:As a Senior Regulatory Affairs Specialist, you will leverage your extensive knowledge of the regulatory landscape to ensure compliance and successful product registrations, including new drug applications, cosmetics, and medical devices.Your strategic...