Regulatory Affairs Specialist Medical Devices

The OpportunityWe are seeking a highly skilled Regulatory Affairs Specialist to join our Global Regulatory Affairs – Innovative Medicines (Europe) team. As a key member of our team, you will be responsible for developing regulatory strategies during development, approval, and post-approval phases for submissions to EU Competent Authorities.A Day in the...

CK Group are recruiting for a Regulatory Affairs Manager, to join a global pharmaceutical company, based in Harlow, on a contract basis for 8 months (maternity leave cover). 18 per hour PAYE. Regulatory Affairs Manager Role: Responsibility/ownership of UK/IE assigned Marketing Authorisation Applications for New Chemical Entities, Generics/Hybrids,...

We are looking for a regulatory officer with knowledge of substance or mixture classification and SDS/label authoring experience. Role is in a large product stewardship department at a UK based global speciality chemicals business. The role will entail: Management of raw material data Validation of classifications, SDS and labels Liaison with suppliers...

We are seeking a skilled Regulatory Data Specialist to join our team at VRS Regulatory. As a key member of our Regulatory Affairs and Risk Assessment division, you will be responsible for managing raw material data, validating classifications, and liaising with suppliers to resolve discrepancies.The ideal candidate will have knowledge of CLP or GHS...

Regulatory Affairs Manager Role:Responsibility/ownership of UK/IE assigned Marketing Authorisation Applications for New Chemical Entities, Generics/Hybrids, devices, biosimilar and OTC products.Ensure that regulatory approvals are secured in a timely manner for on-time launches.Ensure that regulatory post approval regulatory obligations are fulfilled to...

Job Title: Regulatory Affairs ManagerLocation: UKContract Duration: 8 months (Inside IR35)Pay Rate: £32 - £37 per hourWork Structure: Monday to Friday, 7:30 AM – 3:30 PMOur client, a leading pharmaceutical company, is seeking an experienced Regulatory Affairs Manager to oversee regulatory activities for the UK and Ireland, focusing on Marketing...

We are seeking a skilled Regulatory Compliance Specialist to join our team at VRS Regulatory. As a key member of our Regulatory Affairs and Risk Assessment division, you will be responsible for managing raw material data, validating classifications, and liaising with suppliers to resolve discrepancies.The ideal candidate will have knowledge of CLP or GHS...

CK Group- Science, Clinical and Technical is seeking a highly skilled Regulatory Affairs Manager to join their team on a contract basis for 8 months. The successful candidate will be responsible for ensuring regulatory approvals are secured in a timely manner for on-time launches, and will provide regulatory strategies, guidance and support for product...

CK Group is seeking a Regulatory Affairs Manager to join a global pharmaceutical company in Harlow on a contract basis for 8 months. The successful candidate will be responsible for ensuring regulatory approvals are secured in a timely manner for on-time launches.Main Accountabilities:Responsibility/ownership of UK/IE assigned Marketing Authorisation...

We are recruiting a regulatory data management specialist to join our team at VRS Regulatory. As a leading specialist scientific recruiter, we focus on recruitment in Regulatory Affairs, Registrations, REACH, CLP, SDS Authoring, Product Safety, Compliance, Risk Assessment, Regulatory Toxicology, Regulatory Ecotoxicology, and Environmental Fate in the...

Regulatory Affairs Manager Role:As a Regulatory Affairs Manager at CK Group, you will be responsible for the ownership and management of UK and Ireland assigned Marketing Authorisation Applications for various products, including new chemical entities, generics, devices, and biosimilars. Your key objectives will include delivering new submission work plan...

CK Group are recruiting for a Regulatory Affairs Manager, to join a global pharmaceutical company, based in Harlow, on a contract basis for 8 months (maternity leave cover).   Salary: £30.18 per hour PAYE.   Regulatory Affairs Manager Role: Main Accountabilities: Responsibility/ownership of UK/IE assigned Marketing Authorisation Applications...

Regulatory Affairs Manager Role: As a Regulatory Affairs Manager at CK Group, you will be responsible for ensuring regulatory approvals are secured in a timely manner for on-time launches. This includes delivering new submission work plan commitments for all allocated products and ensuring regulatory post-approval regulatory obligations are fulfilled to...

CK Group are recruiting for a Regulatory Affairs Manager, to join a global pharmaceutical company, based in Harlow, on a contract basis for 8 months (maternity leave cover). Salary: £30.18 per hour PAYE. Regulatory Affairs Manager Role: Main Accountabilities: Responsibility/ownership of UK/IE assigned Marketing Authorisation Applications for New...

Regulatory Affairs Manager Role:Main Accountabilities:Responsibility/ownership of UK/IE assigned Marketing Authorisation Applications for New Chemical Entities, Generics/Hybrids, devices, biosimilar and OTC products.Deliver new submission work plan commitments for all allocated products.Ensure that regulatory approvals are secured in a timely manner for...

We are seeking a skilled Regulatory Data Coordinator to join our team at VRS Regulatory. The ideal candidate will have experience in managing raw material data and validating classifications, SDS and labels. The role will involve liaising with suppliers to resolve any discrepancies and classifying finished products.Main Responsibilities:Manage and validate...

Job DescriptionWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at VRS Regulatory. The successful candidate will have expertise in chemical regulatory compliance and a strong understanding of CLP and GHS classifications.The role will involve:Management of raw material data and validation of classifications, SDS, and...

Job DescriptionWe are looking for a regulatory officer with knowledge of substance or mixture classification and SDS/label authoring experience. Role is in a large product stewardship department at a UK based global speciality chemicals business.The role will entail:Management of raw material dataValidation of classifications, SDS and labelsLiaison with...

    We are looking for a regulatory expert with a strong understanding of substance and mixture classification, as well as experience in SDS and label authoring.The successful candidate will be responsible for:Management of Raw Material DataValidation of classifications, SDS, and labelsLiaison with suppliers to resolve discrepanciesClassification of...

We are recruiting for a highly experienced Regulatory Affairs expert to lead our team in Teva Pharmaceuticals’ Global Regulatory Affairs – Innovative Medicines (Europe) division. This is an exciting opportunity to work with key innovative products part of Teva’s Pivot to Growth strategy.The successful candidate will be based at our Harlow office, which...