Regulatory affair Work, Jobs in Headington, Oxf (with Salaries)

Quality Assurance Regulatory Affairs Coordinator
Perspectum —Oxford
- £30,000 - £40,000 a year
- Full-time
- Microsoft Office
- IT
Quick apply
Senior Scientist, Analytical Development
Replimune —Abingdon
- Full-time
- Doctoral degree
- Computer literacy
- Master's degree
Quick apply
6d
Sr. Specialist, Regulatory Affairs
The Bountiful Company —Tring
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Senior Specialist Regulatory Affairs
Abbott Laboratories —Witney
- Full-time
- Maintenance
- Bachelor's degree
- Communication skills
Principal Scientist, Bioanalytical & Molecular Assays
Moderna, Inc. —Oxford
- Full-time
- Doctoral degree
- Master's degree
- Annual leave
Senior Regulatory Affairs Officer - Promotional & Non-Promotional Materials Review
Sanofi —Reading
- Hybrid work
- English
Local Study Associate Director
IQVIA —Reading
- Full-time
- Remote
- Patient monitoring
- English
- Project management
- Work from home
11d
Senior Commercial Officer - Infrastructure North & South
Department for Environment, Food and Rural Affairs —Reading
- £42,665 - £46,765 a year
- Part-time
- Presentation skills
- IT
- Leadership
2d
Director, Medical Affairs (Europe & International)
Immunocore —Oxford
- Doctoral degree
- Travel
- Patient care
Study Start Up Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
10d
Consents and Liaison Officer
Dalcour Maclaren —Bicester
- Military
- Driving
- Communication skills
- Free parking
- Annual leave
Quick apply
13d
Associate Director Global CMC QU – Clinical GMP/GDP
Kyowa Kirin International plc —Marlow
- £80,000 - £140,000 a year
- Full-time
- Bachelor's degree
- No degree
- Leadership
13d
PROJECT QUALITY MANAGER - SCIENCE & RESEARCH
Laing O'Rourke —Oxford
- Continuous improvement
- Construction experience
4d
Head of Spectrum & Regulatory Affairs
Open Cosmos —Didcot
- Hybrid work
- English
Senior Communications and Corporate Affairs Lead
LEO Pharma A/S —Maidenhead
- Marketing
- Project management
- AI
4d
Data Privacy Senior Executive
BDO —Reading
- Full-time
- Analysis skills
- Organisational skills
- AI
Data Privacy Assistant Manager
BDO —Reading
- Full-time
- Analysis skills
- Organisational skills
- AI
Regulation Manager
SSE —Reading
- £51,600 - £77,400 a year
- Full-time
- Computer networking
- Leadership
- Communication skills
- Employee discount
- Gym membership
12d
Senior Benefits Risk Management Lead
Bayer —Reading
- £110,000 - £130,000 a year
- Full-time
- Hybrid work
- English
- Leadership
- Communication skills
- Annual leave
- Employee discount
Associate Director Global CMC QU – Clinical GMP/GDP
Kyowa Kirin International —Marlow
- £66,814 - £134,641 a year
- Full-time
- Bachelor's degree
- No degree
- Leadership
Quick apply
13d

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regulatory affair jobs near headington, oxf

Quality Assurance Regulatory Affairs Coordinator

Perspectum -
Oxford

Quick apply

Job details

Full-time
£30,000 - £40,000 a year

Qualifications

Microsoft Office
IT

Full job description

We are looking for a highly organised and proactive Quality Assurance Regulatory Affairs (QARA) Coordinator to join our team at Perspectum. This is an exciting opportunity to play a key role in supporting the administration of quality and regulatory activities that ensure our continued compliance within a medical device environment.

About The Role

This role is ideal for someone who enjoys a hands-on, detail-oriented position, where maintaining documentation, coordinating timelines, and supporting cross-functional teams are essential to success. You will be instrumental in helping to ensure our Quality Management System (QMS) operates efficiently and that regulatory activities remain on track.

Duties include:

Develop and deliver QARA training and inductions on core QMS processes, procedures, and requirements
Create and maintain training materials, ensuring accurate and up-to-date training records across the business
Provide administrative support to ensure regulatory affairs (RA) activities and timelines are effectively managed
Support the development, implementation, and continuous improvement of QARA strategies and the QMS
Ensure compliance with local, national, and international regulations, monitoring regulatory changes and assessing their impact

About You:

You will be an excellent communicator with strong attention to detail and adopts a methodical approach. You’ll be collaborative, a team player and will help preserve team integrity. Your skills and experience will include:

Proactive and able to manage multiple priorities effectively
Comfortable working in a fast-paced, regulated environment
Excellent IT skills, ability to use MS Office and pick up bespoke systems with ease.

About Us

For details on all our benefits, please download our Benefits document under 'Information' on the right hand side of this screen.

At Perspectum, we are committed to fostering diversity, equity, and inclusion. We prioritise hiring based on merit, skills, and qualifications, valuing individuals for their unique contributions while ensuring a culture that respects and celebrates differences. If you require any reasonable adjustments as part of your application process, please let our Talent Team know.

Quick apply

Refine Your Search

regulatory affair jobs in headington, oxf

Quality Assurance Regulatory Affairs Coordinator

Senior Scientist, Analytical Development

Sr. Specialist, Regulatory Affairs

Senior Specialist Regulatory Affairs

Principal Scientist, Bioanalytical & Molecular Assays

Senior Regulatory Affairs Officer - Promotional & Non-Promotional Materials Review

Local Study Associate Director

Senior Commercial Officer - Infrastructure North & South

Director, Medical Affairs (Europe & International)

Study Start Up Associate

Consents and Liaison Officer

Associate Director Global CMC QU – Clinical GMP/GDP

PROJECT QUALITY MANAGER - SCIENCE & RESEARCH

Head of Spectrum & Regulatory Affairs

Senior Communications and Corporate Affairs Lead

Data Privacy Senior Executive

Data Privacy Assistant Manager

Regulation Manager

Senior Benefits Risk Management Lead

Associate Director Global CMC QU – Clinical GMP/GDP

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