Regulatory affairs specialist Work, Jobs in Amersham, Bkm (with Salaries)

Sr. Specialist, Regulatory Affairs
The Bountiful Company —Tring
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Outlook
Quick apply
Senior Regulatory Affairs Specialist
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
- Annual leave
Medical Device Regulatory Affairs Specialist
Clinica Engineering Medical Solutions Ltd —Reading
- £3,700 - £4,200 a month
- Full-time
- Engineering
- English
- Databases
Quick apply
Regulatory Affairs Specialist
Prinova Europe —London
- Full-time
- Hybrid work
- Microsoft Outlook
- ERP systems
- Continuous improvement
Quick apply
4d
ESG Compliance Manager
The Entertainer —Amersham
- £65,000 - £70,000 a year
- Full-time
- Project management
- No degree
Medical Information Specialist - Afterhours
EVERSANA —London
- Weekend availability
- Remote
- Microsoft Word
- Computer literacy
- English
Quick apply
Product Stewardship & Regulatory Specialist - EMEA
Axalta Coat. Sys. UK —Welwyn Garden City
- English
- Microsoft Office
- Bachelor's degree
- Annual leave
Quick apply
23h
Medical Information Specialist - US Hours
EVERSANA —London
- Full-time
- Remote
- Microsoft Word
- Computer literacy
- English
Quick apply
Global Product Monitoring Vigilance Report Writer
Insulet Corporation —London
- Full-time
- Continuous improvement
- Communication skills
2d
Sr. Compliance Specialist, EMEA
Insulet Corporation —London
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Spanish
Product Manager, Surgical Solutions - UK
BD —Winnersh
- £43,300 - £66,025 a year
- English
- Bachelor's degree
- Product management
10d
Regulatory Reporting Industrial Placement - September 2026
Buzzacott —London
- Microsoft Word
- Computer Science
- Organisational skills
Director, Government Affairs and Advocacy - Europe and International
GlaxoSmithKline —London
- Full-time
- Bachelor's degree
- Team management
- Travel
Study Start Up Manager
Fortrea —Maidenhead
- Full-time
- Remote
- English
- Bachelor's degree
9d
Clinical Data & Device Specialist
SAVA —London
Quick apply
South & EE Team Regulatory Affairs Lead
Shell Energy —London
- Full-time
- Management
- Engineering
- English
Medical Information Specialist - Spanish & English speaking
EVERSANA —London
- Full-time
- Remote
- Microsoft Word
- Spanish
- Computer literacy
Quick apply
Regulatory Engagement & Advocacy Manager – UK and France
Nadara —London
- Full-time
- Analysis skills
- Team management
- Communication skills
South & EE Team Regulatory Affairs Lead
Shell —London
- Full-time
- Management
- Engineering
- English
CMC Associate Director
Androlabs —London
- £85,000 - £108,000 a year
- Full-time
- Hybrid work
- Continuous improvement
- Budgeting
- Manufacturing
- Annual leave
Quick apply

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regulatory affairs specialist jobs near amersham, bkm

Sr. Specialist, Regulatory Affairs

The Bountiful Company -
Tring

Quick apply

Job details

Permanent

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Outlook
Labelling
Computer literacy
Writing skills
Microsoft Office Suite
Analysis skills
Compliance management
Bachelor's degree
Content management
Communication skills
Analytics

Full job description

Job Description

The Senior Regulatory Affairs Specialist plays a critical role ensuring in-market regulatory compliance of new and existing products, packaging and communications. An experienced regulatory or technical professional, the Senior Specialist will have, or quickly develop, a strong understanding of applicable regulations, guidance and industry best practice pertaining to the product portfolio they support.

The individual will work independently with a high level of responsibility. In addition to label content management and formula review they will take ownership of and deliver successfully smaller projects and specific regulatory elements within larger projects.

Review, maintain and create manuscript (label content) records for The Bountiful Company's product portfolio of Dietary Supplements, Foods, OTCs and Cosmetics, as applicable, by interpreting and applying applicable regulations and guidance.
Compiles and interprets substantiation documentation for accurate and compliant labeling.
As directed, take ownership of and deliver successfully smaller projects and specific regulatory elements within larger projects such as innovation, implementation of new regulations, portfolio assessment and change control.
Support review of product ideations, raw material assessment, formulation assessment, new claims, labels, advertising materials, third party products and related brand activities
Compile dossiers to support license or registration submissions or updates ensuring compliance with regulatory requirements, as applicable
US region: Draft FDA 30 Day Notification Letters
Performs various calculations and evaluations to substantiate compliant labeling: formula, percent daily values, vitamin & mineral conversions, nutritional claim support, structure/function claims.
Develop and maintain accurate and compliant label content for portfolio dietary supplements, foods, over the counter drug and cosmetic products, as applicable.
Demonstrates high level of understanding of applicable regulations and implements.
Follows Safety, Health, and Environmental policies and procedures.
Supervises and/or trains one or more regulatory associates, as relevant and when required
Performs other duties as assigned.

Qualifications

Ideal candidate would have previous exposure to and application of regulations pertaining to dietary supplements, foods, cosmetics or OTC pharmaceutical categories, label development or a scientific/ technical background
Functional experience: 3 to 5 years of relevant prior business experience preferred. 1 to 2 years of experience in a regulatory affairs, quality or equivalent technical role preferred.
Education: Bachelor degree required.

Skills

Strong written and verbal communication skills
A self-starter with willingness to learn and develop
Demonstrates strong team work, collaboration, attention to detail, analytical skills, and organization
Basic computer skills, including Microsoft Outlook, Excel, Word, and PowerPoint

Quick apply

Refine Your Search

regulatory affairs specialist jobs in amersham, bkm

Sr. Specialist, Regulatory Affairs

Senior Regulatory Affairs Specialist

Medical Device Regulatory Affairs Specialist

Regulatory Affairs Specialist

ESG Compliance Manager

Medical Information Specialist - Afterhours

Product Stewardship & Regulatory Specialist - EMEA

Medical Information Specialist - US Hours

Global Product Monitoring Vigilance Report Writer

Sr. Compliance Specialist, EMEA

Product Manager, Surgical Solutions - UK

Regulatory Reporting Industrial Placement - September 2026

Director, Government Affairs and Advocacy - Europe and International

Study Start Up Manager

Clinical Data & Device Specialist

South & EE Team Regulatory Affairs Lead

Medical Information Specialist - Spanish & English speaking

Regulatory Engagement & Advocacy Manager – UK and France

South & EE Team Regulatory Affairs Lead

CMC Associate Director

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