Science regulatory affairs Work, Jobs in London (with Salaries)

Quality Assurance & Regulatory Affairs Specialist
Pangaea Data —London
- Communication skills
- Flexible schedule
- Life insurance
Clinical Research Coordinator
SAVA —London
- Communication skills
Quick apply
2d
Scientific Editor
WebMD —London
- Full-time
- Microsoft Office
- Bachelor's degree
- Organisational skills
Quick apply
Sr. Regulatory Affairs Officer
Milpharm Ltd —Uxbridge
- £30,000 - £37,500 a year
- Full-time
- Maintenance
- Master's degree
- Bachelor's degree
- Life insurance
Quick apply
9d
Content Writer - Pharmacovigilance
RxLogix Corporation —London
- Full-time
- Hybrid work
- Bachelor's degree
- Medical terminology
Quick apply
Medical Information Specialist - US Hours
EVERSANA —London
- Full-time
- Remote
- Microsoft Word
- Spanish
- Microsoft Excel
Quick apply
Medical Science Liaison
Syneos Health Commercial Solutions —London
- Doctoral degree
- Travel
Regulatory Affairs Manager
Valorem Distribution —Greenhithe
- £45,000 - £65,000 a year
- Full-time
- Hybrid work
- English
- Organisational skills
- In-person
Quick apply
7d
Regulatory Affairs Scientist (Chemical Compliance)
Thermo Fisher Scientific —London
- £2,625.00 - £3,937.50 a month
- Full-time
- Hybrid work
- Master's degree
- Project management
- Bachelor's degree
Regulatory Affairs Associate/Manager
Transpire BIO Inc. —London
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Director, Regulatory Affairs, EU Services
Bio Pharma Resourcing —London
- £60,000 a year
- Management
- Public speaking
- Windows
Medical Science Liaison
サイネオス・ヘルス —London
- Doctoral degree
- Travel
Scientific Affairs Manager, UK - London
Rhythm Pharmaceuticals —London
- Full-time
- Doctoral degree
- Presentation skills
- Communication skills
Clinical Research Scientist - Medical Affairs
Skin Analytics Ltd —London
- Full-time
- Google Suite
- Doctoral degree
- Data analysis skills
- Annual leave
Quick apply
3d
Sr. Medical Writer (Regulatory)
サイネオス・ヘルス —London
- £80,600 - £145,000 a year
- Travel
- Contracts
- Employee stock purchase plan
- Annual leave
Regulatory Affairs Manager
pladis —Chiswick Park Station
- Full-time
Associate Director, CMC Regulatory Affairs, International
Moderna, Inc. —London
- Full-time
- Engineering
- Master's degree
- Bachelor's degree
- Annual leave
Medical Writer II - Publications
サイネオス・ヘルス —London
- £70,100 - £145,000 a year
- English
- Travel
- Contracts
- Employee stock purchase plan
- Annual leave
Regulatory Affairs Manager
Vodafone —London
- Full-time
- Analysis skills
- Leadership
- Communication skills
- Annual leave
Clinical Data & Device Specialist
SAVA —London
- Maths
Quick apply

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Quality Assurance & Regulatory Affairs Specialist

Pangaea Data
London

Apply Now

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

science regulatory affairs jobs in london

Quality Assurance & Regulatory Affairs Specialist

Clinical Research Coordinator

Scientific Editor

Sr. Regulatory Affairs Officer

Content Writer - Pharmacovigilance

Medical Information Specialist - US Hours

Medical Science Liaison

Regulatory Affairs Manager

Regulatory Affairs Scientist (Chemical Compliance)

Regulatory Affairs Associate/Manager

Director, Regulatory Affairs, EU Services

Medical Science Liaison

Scientific Affairs Manager, UK - London

Clinical Research Scientist - Medical Affairs

Sr. Medical Writer (Regulatory)

Regulatory Affairs Manager

Associate Director, CMC Regulatory Affairs, International

Medical Writer II - Publications

Regulatory Affairs Manager

Clinical Data & Device Specialist

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