nhs regulatory affairs Work, Jobs in england (with Salaries)

Quality Assurance & Regulatory Affairs Specialist
Pangaea Data —London
- Communication skills
- Flexible schedule
- Life insurance
Head of Medical Affairs, UK
Genmab —London
- Doctoral degree
- English
- Leadership
Regulatory / Compliance Manager
Sigma Consulting Group —London
- £50,000 a month
- Full-time
- Hybrid work
- AI
- Communication skills
Quick apply
Market Access and External Affairs Director (UK Pharma Commercial)
Roche —Welwyn
- IT
5d
Medical Affairs Lead - Lung
AstraZeneca —London
- Doctoral degree
- Master's degree
- No degree
6d
Medical Affairs Scientist
OGT —Cambridge
- Laboratory experience
- Bachelor's degree
- Organisational skills
- Employee discount
Quick apply
Director of Medical Affairs, Oncology
MSD —London
- Full-time
- Travel
- Leadership
12d
Regulatory Quality Assurance Manager
Alliance Medical Ltd —Guildford
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Associate Director, Resilience Strategic Partnerships – UK
Moderna, Inc. —London
- Full-time
- Master's degree
- Project management
- Agile
- Annual leave
Medical Director United Kingdom
GE HEALTHCARE —Chalfont Saint Giles
- Doctoral degree
- Leadership
Business Development Consultant, Life Sciences
Carnall Farrar —London
- Hybrid work
- CRM software
- Microsoft Office
- Business development
- Work from home
- Employee assistance programme
Quick apply
UK Market Access & Global Pricing Strategy Lead
Pharmanovia —London
- Hybrid work
- Analysis skills
- Negotiation
Senior Medical Director UK
BioNTech AG —London
- Full-time
- Doctoral degree
- English
- Master's degree
Commercial Lead - Uro-Oncology
Ferring Pharmaceuticals, Inc. —West Drayton
- Full-time
- Management
- Sales
- Master's degree
2d
Principal Electrical Building Services Engineer
Arup —Bristol
- Leadership
Marketing Executive
Zentiva Group, a.s. —Guildford
- Full-time
- Marketing
- Business development
- Project management
10h
Key Account Manager / Director – Pharma (UK)
CloserStill Media —London
- Hybrid work
- Sales
- Travel
- Communication skills
Quick apply
Radiology AI Solutions - Business Development Manager, North UK
DeepHealth —London
- £60,000 - £70,000 a year
- Full-time
- Hybrid work
- Up to 50% travel
- Sales
- English
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Senior Account Executive
Little Journey —Leeds
- £70,000 - £80,000 a year
- Full-time
- Remote
- Microsoft Powerpoint
- Sales
- IT
- Annual leave
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nhs regulatory affairs jobs near england

Quality Assurance & Regulatory Affairs Specialist

Pangaea Data
London

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Job details

Benefits

Private medical insurance
Flexible schedule
Life insurance

Qualifications

Quality assurance
Cybersecurity
Communication skills

Full job description

As the Quality Assurance & Regulatory Affairs Manager, you will be responsible for building and leading the company’s regulatory and quality foundation from the ground up.

LondonClinical & ScientificOperations

About Pangaea Data Limited

Pangaea Data (Pangaea) is a South San Francisco and London based business founded by Dr Vibhor Gupta and Prof Yike Guo (Director Data Science Institute at Imperial College London; Provost, Hong Kong University of Science and Technology). They have worked in medicine and computing for over 20 years and have raised over $300 million through their academic research, including a $110 million grant focused on development work on large language models in medicine. Pangaea’s AI platform is configured on clinical guidelines to find more untreated (undiagnosed, miscoded, at-risk) and under-treated patients with hard-to-diagnose conditions for screening and treatment at the point of care. Pangaea’s advisors include industry veterans from healthcare and the life sciences, including Lord David Prior (former chairman, NHS England) and Mr. Andy Palmer (former CIO, Novartis).

The Role

As the Quality Assurance & Regulatory Affairs Specialist you will be responsible for building and leading the company’s regulatory and quality foundation from the ground up. In this role, you will be expected to develop and implement a scalable QMS, prepare relevant projects for global regulatory submissions, and drive a culture of quality across the organization.

Key Responsibilities

Develop and Implement Regulatory & Quality Strategy:

Define, develop, and execute regulatory strategy for SaMD approval in key global regions.
Establish a fit-for-purpose Quality Management System (QMS) aligned with ISO 13485, 21 CFR Part 820, and other relevant standards.
Prepare, lead, and manage regulatory submissions and communications with authorities.
Ensure readiness for audits and facilitate inspections from regulatory authorities and certification bodies.

Training & Process Implementation:

Lead training initiatives to ensure all relevant teams understand and adhere to QMS and regulatory requirements.
Develop and maintain standard operating procedures, compliance documentation, and internal audit processes.
Serve as the internal authority on quality and regulatory matters, advising leadership and project teams.
Monitor relevant regulatory changes and update internal systems and policies accordingly.

Cross-Functional Collaboration:

Work closely with biomedical, clinical, engineering, and marketing teams to embed quality and regulatory considerations into every phase of development.
Ensure that project timelines and product goals are aligned with regulatory requirements.
Communicate regulatory risks and solutions to non-regulatory stakeholders.

Requirements

Personal Traits

Empathetic understanding of user and stakeholder needs, especially across varying stages of product maturity and regulatory environments.
Excellent communication and mediation skills, with the ability to convey complex regulatory and quality concepts to both technical and non-technical stakeholders.
Collaborative team player who thrives in cross-functional environments involving engineering, clinical, marketing, and executive stakeholders.

Must Haves:

Demonstrated experience in quality assurance and/or regulatory affairs in the medical device, diagnostics, or digital health industry.
Track record of hands-on experience with regulatory submissions and interactions with authorities in at least one major jurisdiction.
Strong working knowledge of ISO 13485, ISO 14971, IEC 62304, and other relevant SaMD standards.
Experience preparing for and supporting audits and inspections by regulatory bodies or notified bodies.
Demonstrated success in leading or implementing a QMS.

Nice to Have:

Direct experience with SaMD regulatory pathways
Experience working within a MedTech or health tech company, preferably in a fast-paced or startup environment
Experience navigating multi-region regulatory strategies
Familiarity with cybersecurity, privacy, and clinical evaluation requirements for digital health products
Experience working in or for a company that achieved first-time regulatory approval

Perks And Benefits

Flexible working hours.
Salary dependent on experience.
Benefits include private medical insurance, life insurance and travel cards.
You would join a small, dedicated and fast-growing team.
You will have the opportunity to learn about building a startup business from experienced professionals and serial entrepreneurs.
We are currently supported by serial entrepreneurs and angel investors. You will have the opportunity to experience an investment life cycle for a startup and meet leading venture capitalists.

Application Contact Information

Please submit your CV and coverletter outlining your relevant experience in Quality Assurance & Regulatory Affairs to [email protected].

General Information

Pangaea Data is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, colour, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances.

Apply Now

Refine Your Search

nhs regulatory affairs jobs in england

Quality Assurance & Regulatory Affairs Specialist

Head of Medical Affairs, UK

Regulatory / Compliance Manager

Market Access and External Affairs Director (UK Pharma Commercial)

Medical Affairs Lead - Lung

Medical Affairs Scientist

Director of Medical Affairs, Oncology

Regulatory Quality Assurance Manager

Associate Director, Resilience Strategic Partnerships – UK

Medical Director United Kingdom

Business Development Consultant, Life Sciences

UK Market Access & Global Pricing Strategy Lead

Senior Medical Director UK

Commercial Lead - Uro-Oncology

Principal Electrical Building Services Engineer

Marketing Executive

Key Account Manager / Director – Pharma (UK)

Radiology AI Solutions - Business Development Manager, North UK

Senior Account Executive