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

Sr. Regulatory Affairs Officer
Milpharm Ltd —Uxbridge
- £30,000 - £38,000 a year
- Full-time
- Computer literacy
- Maintenance
- Master's degree
- Life insurance
Quick apply
Regulatory Scientist
Orchard Therapeutics —London
- Full-time
- Hybrid work
- Writing skills
- Bachelor's degree
- Computer skills
Quick apply
Regulatory Technologist
Vitabiotics —London
- Full-time
- Hybrid work
- Writing skills
- Microsoft Office
- Databases
- Free parking
- Annual leave
Quick apply
18h
Medical Information Specialist - Afterhours
EVERSANA —London
- Weekend availability
- Remote
- Microsoft Word
- Computer literacy
- English
Quick apply
Medical Information Specialist - US Hours
EVERSANA —London
- Full-time
- Remote
- Microsoft Word
- Computer literacy
- English
Quick apply
Specialist, Quality Audits - Biosimilars
Advanz Pharma —London
- Travel
- Employee assistance programme
Medical Affairs Coordinator
Servier —Slough
- Microsoft Office
- Databases
- Administrative experience
9d
Drug Safety Associate II
Corbus Pharmaceuticals Inc —London
- Remote
- Nursing
- Doctoral degree
- Master's degree
Quick apply
Regulatory Affairs Knowledge Management Capability Lead
Novartis —London
- £67,900 - £126,100 a year
- Full-time
- Hybrid work
- Leadership
14d
Scientific Affairs Manager, UK - London
Rhythm Pharmaceuticals —London
- Full-time
- Doctoral degree
- Presentation skills
- Communication skills
Medical Science Liaison - Neuroscience
Ipsen Ltd —London
- Full-time
- Doctoral degree
- English
- Master's degree
Clinical Science Liaison Specialist
Flen Health GmbH —London
- English
- Databases
- Presentation skills
1d
Expert Consultant – Healthcare | Safety, Risk & Regulatory
Boston Consulting Group —London
- Full-time
- Doctoral degree
- Master's degree
- Business development
12d
Vice President, Regulatory Affairs – ELMAC
Amgen —Uxbridge
- Doctoral degree
- Master's degree
- Bachelor's degree
Director, Regulatory Affairs, Labelling
Ipsen Biopharm Ltd —London
- Full-time
- English
- Project management
- Continuous improvement
Director, Regulatory Affairs, EU Services
Bio Pharma Resourcing —London
- £60,000 a year
- Sales
- Customer service
- Public speaking
Head of Quality UK
Vitabiotics —London
- Full-time
- Hybrid work
- Bachelor's degree
- Continuous improvement
- Quality control
- Free parking
- Annual leave
Quick apply
18h
Associate Director, CMC Regulatory Affairs, International
Moderna, Inc. —London
- Full-time
- Engineering
- Master's degree
- Bachelor's degree
- Annual leave
Associate Director, Global Medical Affairs (2-year contract)
BioNTech AG —London
- Full-time
- Doctoral degree
- Project management
- Travel
Content Writer - Pharmacovigilance
RxLogix Corporation —London
- Full-time
- Hybrid work
- Research
- Databases
- Bachelor's degree
Quick apply

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pharmaceutical regulatory affairs jobs near london

Sr. Regulatory Affairs Officer

Milpharm Ltd
Uxbridge

Quick apply

Job details

Full-time
£30,000 - £38,000 a year

Benefits

Company pension
Company events
Life insurance
On-site parking

Qualifications

Computer literacy
Regulatory reporting
Maintenance
Master's degree
Quality assurance
Records management
Bachelor's degree
Decision making
Data entry
Document management

Full job description

Participate in project teams and provide guidance in areas of expertise for both research and marketed products.
Follow up on technical-regulatory and scientific issues
Managing projects within regulatory department
Ensure appropriate standards and policies are maintained for all technical aspects of the company’s regulatory activities
Co-ordinate and prepare MA, variation applications for submission via National or European procedures.
Provide pharmaceutical, analytical, and other technical information to our affiliates, independent associated companies to assist with the registration and maintenance activities of existing MAs.
With appropriate support, plan responses to questions from Regulatory agencies during MA applications, MA renewals and variations.
Provide responses to regulatory questions relating to our group companies products registered or undergoing registration.
Assist with the maintenance of all MA’s with appropriate support.
Learn and be aware the current legislation, guidelines, and other relevant technical and scientific information appropriate for the role.
Maintain records of tasks and registered product information in the internal regulatory databases.
Take personal responsibility for representing the Department both internally and externally in own area of expertise.
Take responsibility for decision making within area of influence.

Must Have:

At least 5 years’ experience in Regulatory Affairs is preferable.
Preferable master's degree or equivalent qualification in Pharmaceutical sciences, Pharmaceutical analysis or Pharmaceutical formulation.
IT literate particularly in relation to using databases and document management system.

Job Type: Full-time

Pay: £30,000.00-£38,000.00 per year

Benefits:

Company events
Company pension
Life insurance
On-site parking

Ability to commute/relocate:

Uxbridge UB11 1AF: reliably commute or plan to relocate before starting work (required)

Experience:

Regulatory Affairs (Pharma) for UK Market: 5 years (required)

Work Location: In person

Quick apply

Refine Your Search

pharmaceutical regulatory affairs jobs in london

Sr. Regulatory Affairs Officer

Regulatory Scientist

Regulatory Technologist

Medical Information Specialist - Afterhours

Medical Information Specialist - US Hours

Specialist, Quality Audits - Biosimilars

Medical Affairs Coordinator

Drug Safety Associate II

Regulatory Affairs Knowledge Management Capability Lead

Scientific Affairs Manager, UK - London

Medical Science Liaison - Neuroscience

Clinical Science Liaison Specialist

Expert Consultant – Healthcare | Safety, Risk & Regulatory

Vice President, Regulatory Affairs – ELMAC

Director, Regulatory Affairs, Labelling

Director, Regulatory Affairs, EU Services

Head of Quality UK

Associate Director, CMC Regulatory Affairs, International

Associate Director, Global Medical Affairs (2-year contract)

Content Writer - Pharmacovigilance

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