Public affairs specialist Work, Jobs in Lightwater, Sry (with Salaries)

Senior Regulatory Affairs Specialist
Medicareplus International —Wembley
- £52,000 - £56,000 a year
- Employee assistance programme
- Employee discount
Quick apply
Science Estates Support Officer
Animal and Plant Health Agency —New Haw
- £33,350 - £34,435 a year
- Overtime
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
- Employee discount
Virology Quality Manager (ID4629)
Animal and Plant Health Agency —New Haw
- £38,795 - £41,375 a year
- Overtime
- Computer literacy
- Microsoft Office
- Presentation skills
- Annual leave
- Employee discount
Senior Counsel - Regulatory Law
Visa Europe Limited —London
- Doctoral degree
- English
- Financial services
Community Care & Welfare Solicitor or Legal Executive (4–8 years PQE)
Boyes Turner —Reading
- 8 hour shift
- Hybrid work
- Microsoft Office
- Supervising experience
- Mentoring

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public affairs specialist jobs near lightwater, sry

Senior Regulatory Affairs Specialist

Medicareplus International -
Wembley

Quick apply

Job details

£52,000 - £56,000 a year

Benefits

Employee assistance programme
Employee discount

Qualifications

Diagnostic evaluation

Full job description

At Medicareplus International, we pride ourselves on being a leading force in advanced wound care and infection prevention. Our mission focuses on creating innovative products that enhance patient care and support healthcare professionals. Join us in our commitment to excellence and become part of a culture that values collaboration and innovation.

We are now looking for a Senior RA Specialist to plan, prepare, and coordinate regulatory activities to ensure that the company’s medical devices comply with applicable global regulations, standards, and internal policies. The Senior RA Specialist will support product registrations, the compilation and upkeep of technical documentation, clinical evaluations, labelling compliance, and interactions with regulatory authorities and Notified Bodies.

Roles and Responsibilities

Technical Documentation

Develop and maintain Technical Documentation in line with ISO 13485, the Medical Device Regulation 2017/745 (EU MDR) and other applicable regulatory requirements.
Support the creation and review of labelling and marketing materials to ensure compliance with relevant regulations.
Participate in design and development projects to provide regulatory input on classification, intended use, and regulatory pathways.
Develop and maintain Clinical Evaluation Plans and reports in accordance with EU MDR
Coordinate the collection and analysis of clinical data, literature reviews, and post-market clinical follow-up activities.
Support the preparation of Periodic Safety Update Reports and Summary of Safety and Clinical Performance where applicable.
Collaborate with Clinical, Quality and Marketing teams to monitor and report on device performance and safety.

Regulatory Intelligence and Compliance

Monitor changes to applicable legislation, standards, and guidance, assess and communicate impact in line with the procedures.
Support implementation of regulatory updates into procedures, processes, and product documentation.

Quality System Support

Participate in internal and external audits, including Notified Body and Competent Authority inspections.
Support vigilance and post-market surveillance activities, including adverse event reporting, field safety corrective actions, and periodic safety update reports.
Assist in maintaining and improving the Quality Management System where it intersects with regulatory requirements.

Cross-Functional Collaboration

Liaise with Medicareplus SMEs, Quality Assurance, Clinical, Marketing and Operations, teams to ensure alignment of regulatory strategies with business objectives.
Provide regulatory and clinical support during product launches, changes, or discontinuations.

Experience

5+ years in the medical device industry in a similar Regulatory role.
Strong knowledge of EU MDR 2017/745, ISO 13485, and other relevant international regulatory frameworks and standards.
Proven ability to compile, maintain, and submit Technical Documentation, product registrations, and regulatory submissions to authorities and Notified Bodies.
Experienced in clinical evaluation activities, including Clinical Evaluation Plans/Reports, literature reviews, and post-market clinical follow-up.
Solid understanding of labelling compliance, product classification, intended use determination, and regulatory pathways during product development.
Skilled in post-market surveillance and vigilance activities, including adverse event reporting, PSURs, and field safety corrective actions.
Strong, pragmatic collaborator across Quality, Clinical, Marketing, R&D, and Operations, supporting product launches and ongoing compliance.

WHAT WE OFFER:

Competitive salary and bonus
25 days holiday + public/bank holiday
Mobile phone and laptop
Learning & Development - We encourage professional development and progression for all our team
Lifestyle Benefits: Our Employee Assistance Programme offers a range of services including financial, wellbeing and counselling via Wisdom Wellbeing. A range of discounts are offered via Bright Exchange
Online GP Services -Access to an online GP service via Livi
Team building events

Based in our Alperton office, this role is your chance to join a collaborative, supportive team of experts. If you want to work together to make a real difference, apply now!

Quick apply

Refine Your Search

public affairs specialist jobs in lightwater, sry

Senior Regulatory Affairs Specialist

Science Estates Support Officer

Virology Quality Manager (ID4629)

Senior Counsel - Regulatory Law

Community Care & Welfare Solicitor or Legal Executive (4–8 years PQE)

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