Regulatory affairs specialist jobs in RichmondCreate job alerts

FULL TIME QA & RA SPECIALIST _IN-VITRO DIAGNOSTIC MANUFACTURING (GENETIC TESTING). SALARY NEG DEPENDANT UPON EXPERIENCE + BENEFITS THE ROLE Duties and responsibilities include but are not limited to: - Support the company Quality Management System (QMS) processes such as Complaints, Non...

Provide technical regulatory expertise on chemicals for product regulatory assessments. Monitor the regulatory horizon of regulatory impacts on chemicals, such as ATPs and the impact this may have on products. No experience in industry is required, but we still welcome your application if you're ...

Regulatory Affairs Specialist Location: Surrey 12 month contract £13. Update and maintain data on pure substances & raw materials within systems such as SAP Monitor the regulatory horizon of regulatory impacts on chemicals, such as ATPs and the impact this may have on products. No experience in

Provide technical regulatory expertise on chemicals for product regulatory assessments. Monitor the regulatory horizon of regulatory impacts on chemicals, such as ATPs and the impact this may have on produ.

The Regulatory Affairs Systems Specialist will support database maintenance for Regulatory Intelligence (RIR) and facilitate the Medical/Regulatory/Legal (MRL) and Claims review process. Reporting to Senior Manager – International Regulatory Affairs, additional direction from Global Regulatory Pr...

The Regulatory Affairs Specialist will be responsible for ensuring compliance with regulatory requirements for the development, approval, and marketing of the client’s products in the UK. We are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our consulting co...

The Regulatory Affairs Specialist reports directly to the Director of Global Regulatory Affairs. Demonstrable experience in regulatory affairs is preferred. Bachelor’s Degree in Regulatory Affairs, Food Science, Chemistry, Business Administration, or a related field is required.

Regulatory Analysis, Regulatory Mapping and Identifying Gaps between the FCA handbook and the business The ideal candidate will be a regulatory compliance specialist, ideally with a legal background. A leading Global Insurance company is recruiting for a Regulatory Affairs Specialist to join thei...

Supporting this work, we're looking for a Regulatory Affairs Specialist, where you'll play an important role in preparing and supporting both US and international regulatory submissions and strategies for our growing portfolio. This is ideal for an eager regulatory affairs professional who has Me...

Regulatory Affairs & Air System Safety Case Specialist (Associate or Experienced level) Regulatory Affairs & Air System Safety Case Specialist (Associate or Experienced level) Company: Boeing Defence United Kingdom Limited The Boeing Test and Evaluation UK Team is recruiting a Regulatory Affairs ...

We have an opportunity for a Regulatory Affairs Specialist, focusing on electrical safety and software development of industrial machines and electrical devices. Being the point of contact for our global sites regarding product-related regulatory affairs requirements. Further training on the topi...

EU Regulatory Affairs Specialist, London ASR Group, the world’s largest refiner and marketer of cane sugar, is seeking a Regulatory Affairs Specialist in London, UK. This role reports to the Director of Global Regulatory Affairs and involves managing regulatory compliance for products in the UK

A leading Global Insurance company is recruiting for a Regulatory Affairs Specialist to join their Compliance function. The ideal candidate will be a regulatory compliance specialist, ideally with a legal background. Have prior experience in regulatory affairs within financial services.

Supports both new product development and currently marketed product portfolio Review, interpret and communicate FDA/EU/international regulations and guidance documents to ensure complete and scientifically sound product submissions Support base business activities, such as Annual Reports, Supple...

Genuine interest and knowledge of the regulatory environment, with a desire to succeed in regulatory affairs in the pharmaceutical industry. Developing regulatory strategy and contributing to regulatory filing activities and documentation (including scientific advice and paediatric investigationa...

Regulatory Affairs Specialist (Sports Medicine) Regulatory Affairs Specialist (Sports Medicine) 1 month ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. London, England, United Kingdom 1 week ago London, England, United Kingdom 1 week ago Junior ...

As a Principal Specialist in Regulatory Affairs, with experience in EU MDR and MDD, you will work with the relevant global partners to develop and Implement regulatory strategies. Baxter is seeking a highly skilled and motivated individual to join our team as a Principal Specialist in Regulatory ...

Job Training Position Summary The Regulatory Affairs Specialist reports directly to the Director of Global Regulatory Affairs. Bachelor’s Degree in Regulatory Affairs, Food Science, Chemistry, Business Administration, or a related field is required. Work Experience Requirements Demonstrable exper...

EU Regulatory Affairs Specialist, London. This role reports to the Director of Global Regulatory Affairs and involves managing regulatory compliance for products in the UK and EU regions. Experience in regulatory affairs, preferably in Food & Beverage or CPG industries.

Genuine interest and knowledge of the regulatory environment, with a desire to succeed in regulatory affairs in the pharmaceutical industry. Join to apply for the Regulatory Affairs Specialist role at MSD in the UK Get AI-powered advice on this job and more exclusive features. Job Description Th

Regulatory Affairs Specialist - System Specialits. The primary responsibilities of the position are to ensure regulatory compliance of a defined group of Convatec products, drive regulatory processes and activities (such as regulatory strategy, product registration, change control, review of mark...

Join us! What the Regulatory Affairs Department does at Worldwide Regulatory Affairs navigates the complex regulatory landscape, ensuring the success of diverse clinical trials. Experience with the regulatory process in the UK and/or under EU-CTR (Poland, Denmark). As subject matter experts, the ...

Coming in as a Senior Regulatory Affairs Specialist, you will be liaising with internal colleagues and external clients and regulatory bodies, to ensure all company products meet regulatory and compliance standards. Do you have experience as a Regulatory Affairs Specialist?. At least 5 years expe...

As a Principal Specialist in Regulatory Affairs, with experience in EU MDR and MDD, you will work with the relevant global partners to develop and Implement regulatory strategies. What you'll bring: Degree in a relevant scientific field Experienced specialist in Regulatory affairs within the EU M...

Counsel and advise the BU in areas of product stewardship (including TSCA, FIFRA, CEPA, OSHA Hazard Communication, Hazardous Materials Transportation and HTSUS product classifications), product regulatory affairs, and product risk management as such areas may impact the research, development, man...

Job Title Regulatory Affairs Specialist Date April 2025 Location London, United Kingdom (Bedford St) Grade P2/15 Reports To Director of Global Regulatory Affairs FLSA Status N/A COMPANY DESCRIPTION ASR Group is the world’s largest refiner and marketer of cane sugar, with an annual production capa...

The Regulatory Affairs Specialist will be responsible for ensuring compliance with regulatory requirements for the development, approval, and marketing of the client’s products in the UK. We are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our consulting co...

Join us on our journey to #ForeverCaring The role: The Regulatory Affairs Systems Specialist will support database maintenance for Regulatory Intelligence (RIR) and facilitate the Medical/Regulatory/Legal (MRL) and Claims review process. Reporting to Senior Manager – International Regulatory Affa...

The R egulatory Affairs Specialist reports directly to the Director of Global Regulatory Affairs. Professional Experience – demonstrable experience in regulatory affairs is preferred. Bachelor’s Degree in Regulatory Affairs, Food Science, Chemistry, Business Administration or related field is re

With our headquarters in Boston, MA, we are growing and expanding our team which is located in 14 different countries! Regulatory Affairs Specialist Location: UK/ Europe (Remote) The Regulatory Affairs Specialist will be an integral part of Velsera's Regulatory team, focusing on ensuring complia

Regulatory Affairs navigates the complex regulatory landscape, ensuring the success of diverse clinical trials. What the Regulatory Affairs Department does at Worldwide. Serve as a subject matter expert and local point of contact for activities supporting regulatory submissions, site activation, ...

Counsel and advise the BU in areas of product stewardship (including TSCA, FIFRA, CEPA, OSHA Hazard Communication, Hazardous Materials Transportation and HTSUS product classifications), product regulatory affairs, and product risk management as such areas may impact the research, development, man...

Strong experience in scientific and/or regulatory compliance/affairs and/or a related technical area with food products or related product categories (such as food supplements, cosmetics, pharmaceuticals, and natural health products) with proficiency in food law, nutrition policy, and regulatory ...

Strong experience in scientific and/or regulatory compliance/affairs and/or a related technical area with food products or related product categories (such as food supplements, cosmetics, pharmaceuticals, and natural health products) with proficiency in food law, nutrition policy, and regulatory ...

The Regulatory Affairs Specialist will be an integral part of Velsera's Regulatory team, focusing on ensuring compliance with global medical device regulations and standards. Experience in preparing regulatory submissions and supporting regulatory strategy development. Bachelor's degree in Regula...

The Regulatory Affairs Specialist reports directly to the Director of Global Regulatory Affairs. Professional Experience - demonstrable experience in regulatory affairs is preferred. Actively support Global Regulatory Affairs department tasks according to workload and priorities, as required.

Regulatory Affairs & Air System Safety Case Specialist (Associate or Experienced level). Regulatory Affairs & Air System Safety Case Specialist (Associate or Experienced level). The Boeing Test and Evaluation UK Team is recruiting a Regulatory Affairs & Air System Safety Case Specialist to suppor...

Key Aspects of the Compliance Associate Role: Contribute to the firm’s approach on AML, sanctions, anti-bribery, and broader financial crime matters as a Compliance Associate Provide regulatory guidance on key frameworks including MiFID II, AIFMD, Market Abuse, and related UK/European regulat

EPR Support Specialist- Configuration Analyst- EPR Trainer- EPR Project Coordinator / Manager.

Duties and Responsibilities of a Senior Compliance Associate Managing and providing advice and guidance on AML and Financial Crime issues including CTF/ABC and Sanctions issues Providing regulatory advice on SM&CR, MiFID II, AIFMD, MAR and financial promotions issues Analysing the commercial

New: Medical Writer (Remote UK/Hybrid possible) Innovative growing healthcare consulting firm.An exciting opportunity to join a growing consulting firm with one of the best staff retention rates in the healthcare/pharma space.Be part of a fun, people focused culture where everyone looks out for e...

Key Aspects of the Compliance Associate Role: Contribute to the firm’s approach on AML, sanctions, anti-bribery, and broader financial crime matters as a Compliance Associate Provide regulatory guidance on key frameworks including MiFID II, AIFMD, Market Abuse, and related UK/European regulat

Role: Senior Marketing Data Analyst.Specialism(s): MMM (Marketing Mix Models), Experimentation, Geo-Testing, A/B Testing, SQL, Data Warehouse, Snowflake, Python/R, Statistical Analysis, Stakeholder Engagement, Communication, Presentation Skills.CPS Group UK are delighted to be working with a lead...

We provide tailored expertise in Medical Communications, Medical Education, Medical Affairs, and Medical Events for pharmaceutical and medical device companies across a huge variety of therapy areas. Strong understanding of medical terminology, clinical research/trial science and regulatory requi...

Senior Manager in Global Regulatory Affairs. Senior Manager, Global Regulatory Affairs. Global Regulatory Affairs (GRA) team.

We are partnering with one of the.UK and US to recruit a talented and experienced.This agency is widely recognised for its collaborative culture, exceptional training and development pathways, and strong reputation in both.As part of their continued growth, they are looking to hire a high-calibre...

We’re Hiring: Team Leader – Regulatory Affairs (IVD). A growing diagnostics innovator is building out its UK-based Regulatory Affairs team and looking for a. You’ll lead a small team (including RA officers and admin staff), take ownership of regulatory input into product changes and compliance

Ensure all deliverables meet internal and client quality standards, timelines, and regulatory requirements (e.