Regulatory Medical Document Specialist

Job Title: Medical WriterJob Summary:We are seeking a skilled Medical Writer to join our team at Translate Plus. As a Medical Writer, you will be responsible for communicating complex scientific and medical information to various audiences, including healthcare professionals, regulatory agencies, and the public.Key Responsibilities:Clinical and Regulatory...

Role OverviewA Regulatory Affairs Specialist is sought to become an integral part of a prestigious healthcare organisation situated in the heart of London. As a Regulatory Affairs Specialist, you will play a pivotal role in steering the compliance and approval processes for innovative medical solutions that have a profound impact on patient care.Key Duties...

Regulatory Affairs Specialist OpportunityWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at VRS Regulatory. As a key member of our Regulatory Affairs and Risk Assessment division, you will play a crucial role in ensuring compliance with EU 1107/2009 regulations for plant protection products.Your primary responsibilities will...

Role OverviewA Regulatory Affairs Specialist is sought to become an integral part of a prestigious healthcare organisation. As a Regulatory Affairs Specialist, you will play a pivotal role in steering the compliance and approval processes for innovative medical solutions that have a profound impact on patient care.Key ResponsibilitiesDevelop and implement...

Regulatory Affairs Specialist - Chemical Compliance ExpertWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at VRS Regulatory. As a key member of our regulatory affairs team, you will be responsible for providing expert advice on chemical regulatory compliance and ensuring that our clients' products meet the necessary regulatory...

Regulatory Affairs Specialist OpportunityVRS Regulatory is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory affairs team, you will be responsible for providing regulatory advice to clients in the chemical regulatory science consultancy sector.Key Responsibilities:Providing clients with regulatory...

Regulatory Affairs Specialist - Chemistry/Analytical MethodsWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at VRS Regulatory. As a key member of our regulatory affairs team, you will be responsible for providing expert advice on substance and product registrations strategies, reviewing phys-chem data packages, and facilitating...

An exciting opportunity to lead regulatory strategy for plant protection products has become available within VRS Regulatory.As a Regulatory Affairs Specialist, you will be responsible for developing and implementing regulatory strategies for our product portfolio in specific geographical territories. This will involve managing a portfolio of plant...

Regulatory Affairs Career OpportunityVRS Regulatory is seeking a highly skilled Regulatory Affairs Specialist to join our team in delivering regulatory services related to chemistry and analytical methods for plant protection products.Key Responsibilities:Provide regulatory advice to clients on substance and product registrations strategies.Review phys-chem...

Key Responsibilities:Manage a portfolio of plant protection products in specific geographical territoriesDevelop regulatory strategy for the product portfolio in your territoryPrepare and review regulatory submissionsWork with the in-house regulatory science team to produce technical dossier sections and risk assessmentsSubmit regulatory applications and...

A leading pharmaceutical organisation is seeking a Medical Document Reviewer to join their medical affairs team.Key Responsibilities:Review and approve documents from various teams, including customer support, marketing, regulatory, clinical, scientific, and medical.Collaborate with the AQP for medical affairs teams to ensure seamless document approval...

A leading pharmaceutical organisation is seeking a Medical Document Reviewer to join their medical affairs team.Key Responsibilities:Review and approve documents from various teams, including customer support, marketing, regulatory, clinical, scientific, and medical.Collaborate with the AQP for medical affairs teams to ensure seamless document approval...

Job DescriptionAs a Regulatory Affairs Specialist at VRS Regulatory, you will have the opportunity to develop and implement regulatory strategies for plant protection products in specific geographical territories. Your key responsibilities will include managing a portfolio of plant protection products, developing regulatory submissions, and working with the...

We are seeking a highly skilled Senior Regulatory Affairs Specialist to join our team at the Medicines and Healthcare products Regulatory Agency. This is a full-time opportunity, on a permanent basis, and requires a minimum of 8 days per month working on site to enable collaboration and contact with partners and stakeholders.The Pharmacovigilance Policy Lead...

Key Role in Medical Device DevelopmentA growing medical devices company, Newton Colmore, is seeking an experienced regulatory engineer to assist with the management of regulatory affairs standards and quality management systems on their brand new IVD technology.This critical role will involve working closely with the quality assurance and design teams within...

Job Title: Medical Content SpecialistJob Summary:We are seeking a Medical Content Specialist to join our team at Translate Plus. As a Medical Content Specialist, you will be responsible for communicating complex scientific and medical information to various audiences, including healthcare professionals, regulatory agencies, and the public.Key...

Job Title: Regulatory & Policy AssessorDivision: Regulatory and Policy Section of the Medical Devices DepartmentThe Regulatory & Policy Assessor will work as part of the Policy and Stakeholder Engagement Team to contribute to the planning, coordination, and development of national and European policy for medical devices and in-vitro diagnostics. This...

Senior Regulatory Engineer - IVD Medical Devices SpecialistWe are seeking an experienced regulatory engineer to join our team at Newton Colmore Consulting. As a Senior Regulatory Engineer - IVD Medical Devices Specialist, you will be responsible for managing regulatory affairs standards and quality management systems on our brand new IVD technology.This is a...

Job Title: Medical Content SpecialistWe are seeking a Medical Content Specialist to join our team at Translate Plus. As a Medical Content Specialist, you will be responsible for communicating complex scientific and medical information to various audiences, including healthcare professionals, regulatory agencies, and the public.Key Responsibilities:Clinical...

Job Title: Medical Content SpecialistJob Summary:We are seeking a highly skilled Medical Content Specialist to join our team at Translate Plus. As a Medical Content Specialist, you will be responsible for creating high-quality medical content for our clients in the pharmaceutical and healthcare industries.Key Responsibilities:Develop and edit clinical study...