Pharmaceutical regulatory affairs Work, Jobs in London, Eng (with Salaries)

Global Product Monitoring Vigilance Report Writer
Insulet Corporation —London
- Full-time
- Continuous improvement
- Communication skills
1d
Regulatory Technologist
Vitabiotics —London
- Full-time
- Hybrid work
- Writing skills
- Microsoft Office
- Databases
- Free parking
- Annual leave
Quick apply
8d
Medical Information Specialist - Afterhours
EVERSANA —London
- Weekend availability
- Remote
- Microsoft Word
- Computer literacy
- English
Quick apply
Regulatory Scientist
Orchard Therapeutics —London
- Full-time
- Hybrid work
- Writing skills
- Bachelor's degree
- Computer skills
Quick apply
Medical Information Specialist - US Hours
EVERSANA —London
- Full-time
- Remote
- Microsoft Word
- Computer literacy
- English
Quick apply
Director, Regulatory Affairs, EU Services
Bio Pharma Resourcing —London
- £60,000 a year
- Sales
- Customer service
- Public speaking
Global Regulatory Affairs Manager
GlaxoSmithKline —London
- Full-time
- Doctoral degree
- Writing skills
- Bachelor's degree
7h
Medical Affairs Coordinator
Servier —Slough
- Microsoft Office
- Databases
- Administrative experience
Associate Director, CMC Regulatory Affairs, International
Moderna, Inc. —London
- Full-time
- Engineering
- Master's degree
- Bachelor's degree
- Annual leave
Expert Consultant – Healthcare | Safety, Risk & Regulatory
Boston Consulting Group —London
- Full-time
- Doctoral degree
- Master's degree
- Business development
Head of/Director, International Regulatory Affairs
Hims & Hers —London
- £140,000 - £155,000 a year
- Full-time
- Hybrid work
- Master's degree
- Bachelor's degree
- AI
- Annual leave
Associate Director, IMACE Scientific Content, NS
Novartis —London
- £67,900 - £126,100 a year
- Full-time
- Hybrid work
- Doctoral degree
- English
- Continuous improvement
Director, Regulatory Affairs, Labelling
Ipsen Biopharm Ltd —London
- Full-time
- English
- Project management
- Continuous improvement
Global Change Facilitator – Regulatory CMC
BioPhorum —London
- Full-time
- Continuous improvement
- No degree
- Organisational skills
Quick apply
Manager, Oncology Regulatory Strategy
Pfizer —Walton-on-Thames
- Full-time
- Hybrid work
- Communication skills
- Negotiation
5d
Vice President, Regulatory Affairs – ELMAC
Amgen —Uxbridge
- Doctoral degree
- Master's degree
- Bachelor's degree
Content Writer - Pharmacovigilance
RxLogix Corporation —London
- Full-time
- Hybrid work
- Research
- Databases
- Bachelor's degree
Quick apply
Director, Government Affairs and Advocacy - Europe and International
GlaxoSmithKline —London
- Full-time
- Bachelor's degree
- Team management
- Travel
Global Medical Affairs Director, Immunology
Novartis —London
- £93,870 - £174,330 a year
- Full-time
- Hybrid work
- Doctoral degree
10d
Global Medical Affairs Director, Immunology, Rap-cel (CAR-T)
Novartis —London
- £93,870 - £174,330 a year
- Full-time
- Hybrid work
- Doctoral degree

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Global Product Monitoring Vigilance Report Writer

Insulet Corporation -
London

Apply Now

Job details

Full-time
1 day ago

Qualifications

Stakeholder engagement
Dashboard visualisation
Stakeholder collaboration
Stakeholder liaison
Complaint handling
Continuous improvement
Technical writing
Multidisciplinary collaboration
Cross-functional collaboration
Communication skills
ISO 13485
Cross-functional communication

Full job description

Job Summary

Are you an experienced Medical Device Vigilance or Pharmacovigilance professional looking to broaden your international exposure?



We are seeking a Post Market Surveillance & Vigilance Specialist to support global patient safety activities across multiple markets. This role offers the opportunity to work with cross-functional teams worldwide, contributing to complaint handling, adverse event reporting, post-market surveillance activities, trend analysis, regulatory compliance, and continuous improvement initiatives.

This is an excellent opportunity for someone who enjoys combining technical vigilance expertise with global stakeholder engagement in a growing, highly regulated environment.

What You'll Do

Manage and support complaint handling and post-market surveillance activities across international markets.
Review and investigate adverse events and product complaints.
Assess reportability and prepare vigilance submissions in accordance with applicable regulatory requirements.
Support Medical Device Reporting (MDR) and other global vigilance obligations.
Analyse complaint, reliability and product performance data to identify trends and potential safety signals.
Conduct device history record reviews and support investigations into product issues.
Partner with Quality, Regulatory Affairs, Customer Care, Manufacturing and Engineering teams globally.
Contribute to audit readiness and support inspections conducted by regulatory authorities and notified bodies.
Develop reports, dashboards and documentation to support compliance and decision-making.
Provide training and guidance to colleagues on complaint and vigilance processes.

What You'll Bring

Experience within medical device vigilance, post-market surveillance, complaint handling, product safety or pharmacovigilance .
Strong understanding of MDR vigilance requirements and adverse event reporting processes.
Experience assessing reportability and preparing regulatory submissions.
Ability to interpret and analyse safety, complaint or reliability data.
Strong written communication skills, including technical and regulatory writing.
Experience working within regulated healthcare, medical device, pharmaceutical or life sciences environments.
Ability to collaborate effectively with international stakeholders.

Particularly Attractive Experience

EU MDR, UK MDR or global vigilance reporting.
International market exposure.
Complaint investigation and trend analysis.
Medical device quality systems (ISO 13485) or equivalent.
FDA reporting or global post-market surveillance programmes.

Why Join Us?

Work with stakeholders across Europe, North America and other global markets.
Contribute directly to patient safety and product quality.
Expand your international regulatory and vigilance expertise.
Be part of a collaborative, mission-driven environment committed to improving lives.

Insulet Corporation (NASDAQ: PODD), headquartered in Massachusetts, is an innovative medical device company dedicated to simplifying life for people with diabetes and other conditions through its Omnipod product platform. The Omnipod Insulin Management System provides a unique alternative to traditional insulin delivery methods. With its simple, wearable design, the tubeless disposable Pod provides up to three days of non-stop insulin delivery, without the need to see or handle a needle. Insulet’s flagship innovation, the Omnipod 5 Automated Insulin Delivery System, integrates with a continuous glucose monitor to manage blood sugar with no multiple daily injections, zero fingersticks, and can be controlled by a compatible personal smartphone in the U.S. or by the Omnipod 5 Controller. Insulet also leverages the unique design of its Pod by tailoring its Omnipod technology platform for the delivery of non-insulin subcutaneous drugs across other therapeutic areas. For more information, please visit insulet.com and omnipod.com.

We are looking for highly motivated, performance-driven individuals to be a part of our expanding team. We do this by hiring amazing people guided by shared values who exceed customer expectations. Our continued success depends on it!

Please read our Privacy Notice to learn how Insulet handles your personal information when you apply .

Apply Now

Refine Your Search

pharmaceutical regulatory affairs jobs in london, eng

Global Product Monitoring Vigilance Report Writer

Regulatory Technologist

Medical Information Specialist - Afterhours

Regulatory Scientist

Medical Information Specialist - US Hours

Director, Regulatory Affairs, EU Services

Global Regulatory Affairs Manager

Medical Affairs Coordinator

Associate Director, CMC Regulatory Affairs, International

Expert Consultant – Healthcare | Safety, Risk & Regulatory

Head of/Director, International Regulatory Affairs

Associate Director, IMACE Scientific Content, NS

Director, Regulatory Affairs, Labelling

Global Change Facilitator – Regulatory CMC

Manager, Oncology Regulatory Strategy

Vice President, Regulatory Affairs – ELMAC

Content Writer - Pharmacovigilance

Director, Government Affairs and Advocacy - Europe and International

Global Medical Affairs Director, Immunology

Global Medical Affairs Director, Immunology, Rap-cel (CAR-T)

I want to receive the latest job alerts for pharmaceutical regulatory affairs in london, eng

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