Regulatory pharmaceutical Work, Jobs in United Kingdom (with Salaries)

Healthcare Compliance & Regulatory Advisor
Riddle Compliance —Remote
- £24,420.00 - £54,697.94 a year
- Part-time
- Remote
- English
- Analysis skills
- Bachelor's degree
Quick apply
1d
Clinical Trial Associate (Associate, Rater Services)
Cogstate —Remote
- £50,000 - £55,000 a year
- Remote
- Computer literacy
- English
- Project management
Quick apply
Regulatory Compliance Questionnaire Assistant
Starna Scientific Limited —Ilford
- £16,799 - £19,199 a year
- Part-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Free parking
Quick apply
1h
Country Approval Specialist - FSP
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- English
- Bachelor's degree
- Organisational skills
13d
Associate Scientist 1
Merck KGaA —Glasgow
- Computer literacy
- Bachelor's degree
- Organisational skills
9d
Associate Director, Regulatory Affairs - UK & Ireland
BeiGene —Remote
- £80,700 - £100,900 a year
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Office
- Bachelor's degree
3d
Audit Coordinator / Lead Auditor
Dechra Pharmaceuticals PLC —Remote
- Remote
- Data analysis skills
- Project management
- Bachelor's degree
- Employee assistance programme
6d
Production Operator - Pharmaceutical
Qmed Pharmaceuticals —London
- £26,436.80 a year
- Full-time
- Communication skills
- Mechanical knowledge
- Free parking
Quick apply
6d
Laboratory Analyst
GlaxoSmithKline —Ware
- Full-time
- Data analysis skills
- Laboratory experience
- Bachelor's degree
23h
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
R&D Assistant - Stability
Reckitt —Kingston upon Hull
- Laboratory experience
- Communication skills
- Employee assistance programme
- Life insurance
3d
Project Manager, Clinical Trials
Cogstate —Remote
- £55,000 - £60,000 a year
- Remote
- Computer Science
- Engineering
- Master's degree
- Annual leave
Quick apply
Scientific Associate, Chromatographic Bioanalysis
Charles River Laboratories —Tranent
- £27,951.22 a year
- Full-time
- Sales
- Bachelor's degree
- Free parking
- Employee discount
Medical Information Specialist - US Hours
EVERSANA —London
- Full-time
- Remote
- Microsoft Word
- Spanish
- Microsoft Excel
Quick apply
Medical Device Regulatory and Quality Consultant
PA Consulting —Melbourn
- Full-time
- Annual leave
Quick apply
Microbiologist
Thermo Fisher Scientific —Newport
- Full-time
- Oracle
- Microsoft Office
- Bachelor's degree
8d
Validation Officer
Target Healthcare Group —Belfast
- Full-time
- Computer literacy
- Microsoft Office
- Analysis skills
Quick apply
22h
QA Officer
Thermo Fisher Scientific —Cramlington
- Full-time
- Oracle
- Microsoft Outlook
- Microsoft Office
Senior Associate I, TMF Operations - UK - Remote
Worldwide Clinical Trials —England
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- Bachelor's degree

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regulatory pharmaceutical jobs near united kingdom

Healthcare Compliance & Regulatory Advisor

Riddle Compliance
Remote

Quick apply

Job details

Part-time
£24,420.00 - £54,697.94 a year
1 day ago

Qualifications

English
Analysis skills
Quality assurance
Bachelor's degree
Financial services
Communication skills

Full job description

About the Opportunity

We are seeking an experienced healthcare compliance, regulatory, legal, ethics, privacy, or risk management professional to support multinational organizations operating throughout Europe, the Middle East, and Africa.

This role offers the opportunity to work directly with executive leadership teams and senior advisors on complex compliance, governance, regulatory, privacy, anti-corruption, and risk management matters affecting multiple jurisdictions.

Particular emphasis will be placed on supporting organizations operating within the medical device, healthcare, pharmaceutical, life sciences, and other highly regulated industries.

The successful candidate will serve as a trusted advisor supporting the development, implementation, enhancement, and ongoing operation of sophisticated compliance programs, regulatory initiatives, investigations, governance activities, and operational compliance functions throughout the EMEA region.

Key Responsibilities

Compliance Program Leadership & Governance

Support the design, implementation, enhancement, and maintenance of enterprise compliance and ethics programs.
Assist organizations with developing scalable compliance infrastructures, governance frameworks, reporting mechanisms, and oversight processes.
Support compliance committee activities, executive reporting, risk management initiatives, and program effectiveness evaluations.
Provide strategic and practical compliance guidance to executive leadership teams.
Assist organizations in fostering a culture of ethics, compliance, accountability, and regulatory excellence.

Regulatory & Compliance Advisory

Conduct legal, regulatory, and compliance research across EMEA jurisdictions.
Monitor regulatory developments, enforcement trends, industry standards, and emerging compliance risks.
Prepare executive-level memoranda, reports, risk assessments, and compliance guidance.
Analyze regulatory obligations and provide recommendations regarding implementation priorities and risk mitigation strategies.

Healthcare, Commercial & Third-Party Compliance

Support reviews involving healthcare professional interactions, educational programs, sponsorships, grants, consultant engagements, speaker programs, and related activities.
Assist with anti-bribery, anti-corruption, ethics, and third-party risk management initiatives.
Support distributor, vendor, consultant, and business partner due diligence reviews.
Assist with commercialization governance, promotional activities, and operational compliance matters.
Provide guidance regarding MedTech Europe, EFPIA, ABPI, and other applicable industry expectations and best practices.

Policies, Procedures & Training

Draft, review, and maintain policies, procedures, codes of conduct, governance frameworks, standards, and guidance documents.
Develop compliance training materials, communications, awareness initiatives, and educational programs.
Support organization-wide compliance and ethics training initiatives involving anti-corruption, privacy, investigations, healthcare compliance, and related risk areas.
Assist with policy implementation and operationalization efforts across multiple jurisdictions.

Investigations, Monitoring & Risk Assessments

Conduct or support workplace investigations, compliance investigations, ethics matters, and issue management activities.
Assist with witness interviews, documentation reviews, findings reports, and remediation planning.
Conduct compliance risk assessments, monitoring activities, internal reviews, and gap analyses.
Support development of risk-based auditing and monitoring programs designed to evaluate compliance program effectiveness.

Privacy, Data Protection & Regulatory Affairs

Support privacy and data protection initiatives throughout the EMEA region.
Assist with GDPR compliance, international data transfers, vendor oversight, and privacy governance activities.
Support organizations in preparing for regulatory inquiries, audits, inspections, and examinations.
Interface with regulators, government agencies, notified bodies, accrediting organizations, and external stakeholders as needed.
Coordinate with local counsel and subject matter experts regarding jurisdiction-specific legal and regulatory matters.

Preferred Qualifications

Attorney, compliance professional, regulatory affairs professional, privacy professional, risk management professional, or related discipline.
Minimum five years of relevant experience.
Experience supporting multinational organizations operating across multiple EMEA jurisdictions.
Strong analytical, research, writing, communication, and problem-solving skills.
Excellent verbal and written English proficiency.
Demonstrated ability to work independently while effectively supporting executive leadership teams.
Experience within healthcare, medical device, pharmaceutical, life sciences, financial services, or other regulated industries strongly preferred.

Location

Candidates located in the United Kingdom, Ireland, Germany, France, Netherlands, Belgium, Switzerland, Spain, Italy, Sweden, Denmark, Poland, United Arab Emirates, Saudi Arabia, South Africa, or other EMEA jurisdictions are encouraged to apply.

Application Requirements

Please submit the following to [email protected]:

Resume / Curriculum Vitae
LinkedIn Profile, if available
Brief Summary of Relevant Experience
Desired Monthly Compensation
Weekly Availability
Earliest Available Start Date

Pay: £24,420.00-£54,697.94 per year

Work Location: Remote

Quick apply

Refine Your Search

regulatory pharmaceutical jobs in united kingdom

Healthcare Compliance & Regulatory Advisor

Clinical Trial Associate (Associate, Rater Services)

Regulatory Compliance Questionnaire Assistant

Country Approval Specialist - FSP

Associate Scientist 1

Associate Director, Regulatory Affairs - UK & Ireland

Audit Coordinator / Lead Auditor

Production Operator - Pharmaceutical

Laboratory Analyst

Sr. Regulatory Affairs Officer

Content Writer - Pharmacovigilance

R&D Assistant - Stability

Project Manager, Clinical Trials

Scientific Associate, Chromatographic Bioanalysis

Medical Information Specialist - US Hours

Medical Device Regulatory and Quality Consultant

Microbiologist

Validation Officer

QA Officer

Senior Associate I, TMF Operations - UK - Remote

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