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Liaise with MHRA, EMA, and other authorities to ensure regulatory alignment. Advise internal stakeholders on regulatory risks and compliance. Represent the company in external regulatory forums and industry groups.

Provide critical support in developing global regulatory strategy, planning and execution of global investigational submissions and manages lifecycle regulatory activities in alignment with the Global Regulatory Lead (GRL). Research and apply regulatory intelligence and knowledge of strategic opt...

Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submis...

This is a fantastic opportunity for someone with a strong background in regulatory documentation—particularly SmPCs, PILs, and labelling compliance—to join a high-performing regulatory affairs team. Walker Cole are partnered with a leading pharmaceutical company in the UK that is looking to brin

Department Leader – Regulatory Affairs– IVDs. An exciting opportunity to join an established and growing IVD manufacturer and support a growing Regulatory Affairs Department. The Department Leader for Regulatory Affairs is also responsible for acting as an active participant in team meetings tha

Senior Regulatory Affairs Associate – Class III Devices | PMA Submissions | Remote + Monthly Onsite in Oxford | Equity + £100M Backed Start-up. Senior Regulatory Affairs Associate. Regulatory team and help take a breakthrough neuromodulation device through PMA submission and into the market.

The role will involve regulatory assessment, compliance review and documentation management to ensure cosmetic products meet the necessary legislation and safety standards in multiple territories, including the UK, EU, US and Canada. Conduct regulatory reviews of formulations, labelling, and pack...

Work from anywhere and shape powerful strategies that drive results! Enjoy the freedom of remote work while making a global impact.Proclinical is seeking a skilled CMC Writer to join our client's team, focusing on regulatory affairs within the oncology and biotechnology sectors.This role involves...

Senior Quality Assurance & Regulatory Affairs Specialist!. Senior Quality Assurance & Regulatory Affairs Specialist to.

Be among the first 25 applicants Direct message the job poster from Blackfield Associates Senior International Consultant - Regulatory Affairs and Executive Search Blackfield are supporting a specialty pharmaceutical distribution company, based in Greater Manchester, hiring for a Senior Regulator...

Winsford, England, United Kingdom 2 weeks ago Quality Assurance & Regulatory Affairs Specialist Manchester, England, United Kingdom 1 week ago Blackburn, England, United Kingdom 5 days ago Cheshire East, England, United Kingdom 2 weeks ago Certification Regulatory Affairs Associate Skelmersdale, ...

JOB TITLE : Head, Global Scientific and Regulatory Affairs (GSRA), EMEA Region LOCATION: UK. Manchester Head Office. REPORTS TO: Vice President, Global Scientific and Regulatory Affairs, located at the Ingredion Innovation Center, New Jersey, USA DIRECT REPORTS: Yes - three Company Background: In...

You Will Be Responsible For Data Analytics and Insights Identify and articulate problems that data analytics can address by assessing processes, determining requirements, and delivering insights and recommendations to executives and stakeholders. Job Function Data Analytics & Computational Scienc...

Other suitable skills and experience include Quality Assurance Manager, Regulatory Affairs Specialist, QA/RA Manager, Medical Device Auditor, Quality Systems Specialist, Compliance Officer, Risk Management Specialist #J-18808-Ljbffr. Key Responsibilities Lead and support continuous improvements w...

Social network you want to login/join with: Business Restructuring Senior Manager, Manchester col-narrow-left Client: BDO UK Location: Manchester, United Kingdom Job Category: Other - EU work permit required: Yes col-narrow-right Job Reference: 75352793cc13 Job Views: 4 Posted: 29.06.2025 Expiry ...

Job DescriptionJob Description JOB SUMMARY: The Quality Systems Manager will provide overall company leadership and direction for Quality Assurance and Regulatory Affairs Systems, encompassing both improvements and sustaining activities. Enhance company systems interface capabilities while optimi...

Regulatory Affairs Manager in the preparation and submission of documents for regulatory agencies. Previous experience in regulatory affairs in the medical device industry. Assisting with the preparation and submission of regulatory documents to regulatory agencies.

Job Title: Clinical Quality Assurance Manager - IVDs/Medical Devices Job Type: 12 months fixed-term contract, Maternity cover Location: Remote UK-based with occasional travel to the North West, England Remuneration: £50,000 + 10% Bonus Cpl Life Sciences is partnering with a leading organi...

I’m currently working with a leading biopharma company that is looking to expand its Medical Affairs team with the addition of a Senior Medical Affairs Manager. This is an excellent opportunity for someone with a few years of experience in Medical Affairs management who’s ready to step into a mo...

The Quality Assurance and Regulatory Affairs Manager will be responsible for developing, implementing, and maintaining quality and regulatory systems in compliance with FDA, ISO, and other global regulatory standards. Minimum of 8-10 years of experience in QA/RA roles within the medical device in...

Finance Business Partner – Advisory Base Location: Bristol, Manchester, Glasgow & Watford plus network of 20 offices nationally: www.kpmg88careers.co.uk/experienced-professional/#LeBlender.OfficeLocations The KPMG Business Services function is a cornerstone of our UK business. Operating f...

Resource Manager – Audit Base Location: Nationwide based from one of our 20 offices nationally (excluding London): www.kpmg88careers.co.uk/experienced-professional/#LeBlender.OfficeLocations The KPMG Business Services function is a cornerstone of our UK business. Operating from 20 UK loca...

The Quality Assurance and Regulatory Affairs Director will be responsible for developing, implementing, and maintaining quality and regulatory systems in compliance with FDA, ISO, and other global regulatory standards. Serve as the primary regulatory liaison with notified bodies, FDA and other gl...

Review marketing claims and ensure they meet legal and regulatory requirements. Support communication with regulatory authorities and assist in audits or inspections. Job Description Regulatory Officer £35,000+ dependent on experience Manchester Blush & Bloom are working on an exciting opportun

1 week ago Be among the first 25 applicants Direct message the job poster from Blackfield Associates Senior International Consultant - Regulatory Affairs and Executive Search Blackfield are supporting a specialty pharmaceutical distribution company, based in Greater Manchester, hiring for a Senio...

Social network you want to login/join with: Regulatory Affairs Manager - Pharmaceuticals As the Regulatory Affairs Manager for the UK and Ireland, you will provide expert regulatory guidance to our UK organization and manage all regulatory activities across the UK and Ireland. Liaise with regulat...

Job Description: Job Title: Department Leader – Regulatory Affairs– IVDs Job Type : Full-Time, permanent position Location: Outskirts of Edinburgh, Scotland, UK – (1 week per month on site) The role is a full-time, permanent position working 37. An exciting opportunity to join an establish

Social network you want to login/join with: Senior Vice President / Vice President of Regulatory Affairs., manchester col-narrow-left Client: Life Sciences Recruitment Location: manchester, United Kingdom Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 1 Posted: 31....

A world-renowned Chemical Manufacturer, celebrated for its cutting-edge product development and commitment to sustainability, is seeking an experienced Quality Manager to join its dynamic team at the Blackpool site. With a presence across multiple high-impact sectors - including aerospace, auto...

QUALITY & COMPLIANCE MANAGER - ARCHITECTURAL HARDWARE CRAWLEY – PERMANENT Job Overview: Working for an industry leader, Our client is a family run highly successful business who are seeing exceptional growth with their exceptionally highly quality products. Crawley is known for its diverse...

Disease Area Medical Lead – Ophthalmology Biopharma Company | United Kingdom Reporting to: UK Medical Affairs Leadership Location: United Kingdom Summary A leading global biopharmaceutical company focused on retinal disease is seeking a Disease Area Medical Lead to head its strategic ...

As an Innovation Strategy Consulting Manager, you will play a pivotal role in delivering high-impact projects from end-to-end, managing a team of consultants, and supercharging the growth of our Consultancy practice. Working directly with the Head of Consulting, you will take ownership of bu...

About The Role: We are partnered with a leading Pharmaceutical Company to recruit a skilled Data Management, subject matter expert to spearhead transformative, large-scale data projects with a global impact. We need someone who can begin within one month and possesses extensive expertise in...

Job Title: Wills and Probate Solicitor Location: Greater Manchester Salary: up to £65,000 DOE The Role My client is seeking a client-focused and dedicated Wills and Probate Solicitor to join their team. The role offers flexibility in location, provided the candidate is within a reasonab...

Job responsibilities (but not limited to): Coordinates, provides, and delivers methodological and statistical expertise and/or statistical analyses. In this matter supports both the Clinical Development portfolio as well as Strategic Medical Affairs in their support to Affiliates, thereby c...

An opportunity for a PhD Graduate with a thesis investigating endocrine disruption properties of chemicals, to join a well-regarded endocrine disruption risk assessment team. You will work on projects to evaluate the endocrine disrupting properties of chemical substances that are to be used in m...

Medical Information Specialist (Maternity Cover for 1 year- Starting Late September/ Early October 2025) Who are we? We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth op...

Job Summary: We are seeking an experienced and driven Senior PK/PD Modeller to join our Clinical Pharmacology team. In this role, you will be responsible for the design, development, and implementation of pharmacokinetic/pharmacodynamic (PK/PD) modeling strategies to support drug development ...

JOB DESCRIPTION Job Title: Commercial Manager Location: Newcastle Office with hybrid working Employment: Full-time Salary Range: A highly competitive package will be offered to the successful candidate with the ability to earn additional on target bonus. Department: Commercial Date: J...

Planet Pharma are currently partnered with a global pharma and we are actively seeking a Recruitment Operations Specialist to join on an initial contract basis. Key Responsibilities: - Support Strategic Hiring Plans: Translate strategic recruitment goals into actionable operational plan...

Are you an experienced QA/RA leader ready to shape the future of wound care? A pioneering MedTech start-up is seeking a Quality Assurance and Regulatory Affairs Manager to drive global regulatory strategy and quality systems for an innovative Advanced Tissue Repair Platform targeting chronic and...

Associate) Director, Clinical Affairs – Infectious Diseases | Global IVD Focus 📍 Remote – UK or France | Permanent Position A global diagnostics company is seeking an experienced Clinical Affairs leader to head their infectious disease clinical programme, supporting the development and global...

Certification and Conformance Regulatory Affairs Associate Location: Skelmersdale hybrid (3 days in office 2 home) Salary Range: £48,000 – £65,000 (depending on experience) Join a leading Industrial Manufacturing organisation and contribute to the advancement of safety and compliance in th...

About the role As a Satellite Regulatory Compliance Manager, you will focus on the management and meeting the regulatory compliance obligations across the EU. You will lead on the regulatory and licencing strategy for Europe, including ensuring that licenses are applied for and met in a timely ...

Percival is excited to be working with The ExtraCare Charitable Trust (ExtraCare) to source a new Chair for their Audit and Assurance Committee. The Committee provides independent oversight and critical challenge, enabling it to provide assurance to the Board. ExtraCare is a charity that re...

Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submis...

Job Title: Quality Control Analyst Location: Dartford, UK (On site role) FTE: Full-time Company: Pharmaceutical Company Contract Length: 6 Months with high chance of extension Role Summary Are you passionate about quality and science? Do you have hands-on experience in pharmaceutica...

Planet Pharma is partnering with a pharmaceutical client seeking to hire a Senior Project Manager to oversee the setup, execution, and management of Expanded Access Programs (EAP) and Post-Approval Named Patient Programs (PA-NPP). Key Responsibilities: - Manage the start-up, execution,...