Regulatory Documentation Expert

Job OverviewWe are seeking a highly skilled Regulatory Document Specialist to join our team at VCLS. As a key member of the team, you will be responsible for creating high-quality medical documents for various client projects.The ideal candidate will have a strong background in regulatory affairs and excellent writing skills. You will work closely with...

We are seeking a highly experienced Regulatory Affairs Expert to join our growing team at VCLS. This role is ideal for someone with 4+ years of experience in regulatory affairs and a strong background in Clinical Trial Submissions.The successful candidate will play a key role in driving forward regulatory processes, ensuring compliance, and contributing to...

Gilead Sciences is a global biopharmaceutical company that is committed to making a difference in the lives of people with life-threatening diseases. We are seeking a highly skilled Senior Medical Writer to join our dynamic team. As a Senior Medical Writer, you will be responsible for authoring complex regulatory documents, including clinical study reports,...

Senior Medical Writing PositionWe are partnering with AL Solutions to find a highly skilled Senior Manager of Medical Writing. This key role involves creating high-quality regulatory documents and working closely with cross-functional teams to drive project success.About the OpportunityThe successful candidate will have extensive experience in medical...

Job OverviewWe are seeking a highly experienced Senior Director to lead our Regulatory Affairs team at Cpl Life Sciences. This role will provide strategic regulatory advice to clients, taking into account regulatory guidelines and available measures to facilitate regulatory input.Key Responsibilities:Lead client projects, providing expert regulatory guidance...

Regulatory Compliance ExpertAbout the Role:This is an exciting opportunity for a Regulatory Compliance Expert to join our team in Cambridge. As a key member of the product development team, you will play a critical role in ensuring that our products meet regulatory requirements and customer expectations.Responsibilities:- Develop and maintain knowledge of...

Regulatory Affairs Expert WantedWe are seeking a Regulatory Affairs Expert to join our team in Cambridge, UK. The successful candidate will have a strong background in pharma/biopharma and be able to work independently.About the Role:The ideal candidate will have at least 10 years' experience in regulatory affairs.Proven ability to manage projects and...

We offer an estimated salary of £60,000 - £80,000 per annum for this role, depending on experience. As a Regulatory Compliance Expert at Avenir Group, you will be responsible for ensuring that our operations comply with regulatory requirements and internal policies.The ideal candidate will have at least 5 years of compliance experience in the financial...

Award-Winning EmployerWe are seeking a seasoned Health and Safety Executive to lead our team in delivering exceptional health and safety outcomes. The successful candidate will have a proven track record in implementing effective risk controls and promoting a culture of safety within an organization.About the Opportunity:This role offers a competitive salary...

Job DescriptionWe are seeking a highly skilled Device Regulatory Expert to join our regulatory affairs team at Vectura Group. As a key member of our team, you will be responsible for ensuring compliance with global regulations and guidelines for medical devices and drug-device combination products.Key Responsibilities:Regulatory Leadership: Assume the role...

A competitive salary of £55,000 - £70,000 per annum is offered for this position.Eclectic Recruitment Ltd are working with a leading telecommunications company based in Cambridge to find an experienced Senior Regulatory Compliance Expert. This is a full-time permanent role with the option of hybrid working.Responsibilities include:Ensuring products meet...

The Regulatory Affairs Expert will be responsible for shaping IWF's policy positions and achieving real-world change through legislation, regulatory frameworks, and industry practice. This involves leading policy development, researching and gathering evidence, extracting information and communicating it effectively, engaging with stakeholders, and...

About the Role:We are looking for an accomplished Senior Director to join our team as a Regulatory Affairs Leader. You will oversee the Regulatory Affairs team, providing strategic regulatory advice to clients and driving global Regulatory Affairs Strategies.Responsibilities:Lead client projects, offering expert regulatory guidance.Prepare and review...

About the JobWe are seeking a Regulatory Compliance Expert to join our team at Russell Tobin in Cambridge. This is a 12-month contract with a maximum PAYE rate of £21.62 per hour and an umbrella rate of up to £24.23 per hour.The successful candidate will have a strong background in design control and risk management, with experience working in the...

Eclectic Recruitment Ltd is seeking a seasoned Regulatory Conformance Expert to join our team in Cambridge. As a Senior Conformance Engineer, you will be responsible for ensuring our clients' products meet stringent industry regulatory standards.The estimated salary for this role is £80,000 - £100,000 per annum, depending on experience.Responsibilities...

We are 52North, creators of Neutrocheck®, a med-tech company striving to transform patient experiences and set new industry standards through innovative technology.This exciting opportunity requires a Regulatory Compliance Expert to oversee our QMS, ensure adherence to regulations, and develop effective quality processes.ResponsibilitiesLeading the...

Ea First Compass House is a leading Cambridge-based software organisation offering hybrid working. We are currently seeking a Data Analysis and Documentation Expert to join our team and support the Group data and Oracle reporting teams.About the RoleTake ownership of analysis and documentation of finance reporting systems.Work collaboratively with Finance...

We are seeking a highly motivated and experienced Senior Manager of Regulatory Affairs to join our team at Sail Biomedicines. This role will be responsible for developing and executing our regulatory operations and planning, managing, and tracking regulatory submissions.Responsibilities:Develop regional regulatory operations that de-risk and accelerate the...

About the RoleuWorkin is seeking a skilled Documentation Quality Assurance Expert to support our document management process and ensure high-quality documentation.This is an excellent opportunity to work for a clean renewable company with a strong legacy.You will have the chance to contribute to continuous improvement efforts and develop your skills in...

About the RoleWe are looking for an experienced Language Data Documentation Expert to create guidelines for training annotators on improving and evaluating generative AI models. The successful candidate will also be responsible for making suggestions for updating or improving our content standards.Key responsibilities include producing high-quality...