Regulatory affairs specialist Work, Jobs in Hertford (with Salaries)

Sr. Specialist, Regulatory Affairs
The Bountiful Company —Tring
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Outlook
Quick apply
Principal Regulatory Affairs Specialist (UK, IVDR) Remote UK
Cepheid —Amersham
- Full-time
- Remote
- Master's degree
- Databases
- Bachelor's degree
- Annual leave
Regulatory Affairs Specialist
Prinova Europe —London
- Full-time
- Hybrid work
- Microsoft Outlook
- ERP systems
- Continuous improvement
Quick apply
2d
Medical Information Specialist - Afterhours
EVERSANA —London
- Weekend availability
- Remote
- Microsoft Word
- Computer literacy
- English
Quick apply
Senior Manager – ESG and Sustainability Regulatory Legal
Pwc UK —London
- Full-time
- Hybrid work
- Business development
- Analysis skills
- Presentation skills
Medical Information Specialist - US Hours
EVERSANA —London
- Full-time
- Remote
- Microsoft Word
- Computer literacy
- English
Quick apply
Sr. Compliance Specialist, EMEA
Insulet Corporation —London
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Spanish
Global Product Monitoring Vigilance Report Writer
Insulet Corporation —London
- Full-time
- Continuous improvement
- Communication skills
21h
Regulatory Reporting Industrial Placement - September 2026
Buzzacott —London
- Microsoft Word
- Computer Science
- Organisational skills
Expert Consultant – Healthcare | Safety, Risk & Regulatory
Boston Consulting Group —London
- Full-time
- Doctoral degree
- Master's degree
- Business development
Director, Government Affairs and Advocacy - Europe and International
GlaxoSmithKline —London
- Full-time
- Bachelor's degree
- Team management
- Travel
Senior Professional - Regulatory Affairs Lifecycle Management - Biocides
Perrigo —London
- Hybrid work
- Continuous improvement
- Mentoring
- In-person
1d
Director - Regulatory Affairs Lifecycle Management Medicines
Perrigo —London
- Hybrid work
- Bachelor's degree
- Continuous improvement
- Team management
13d
Clinical Data & Device Specialist
SAVA —London
Quick apply
South & EE Team Regulatory Affairs Lead
Shell Energy —London
- Full-time
- Management
- Engineering
- English
Regulatory Engagement & Advocacy Manager – UK and France
Nadara —London
- Full-time
- Analysis skills
- Team management
- Communication skills
Medical Information Specialist - Spanish & English speaking
EVERSANA —London
- Full-time
- Remote
- Microsoft Word
- Spanish
- Computer literacy
Quick apply
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
Clinical Science Liaison Specialist
Flen Health GmbH —London
- English
- Databases
- Presentation skills
8d

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regulatory affairs specialist jobs near hertford

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

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Refine Your Search

regulatory affairs specialist jobs in hertford

Sr. Specialist, Regulatory Affairs

Principal Regulatory Affairs Specialist (UK, IVDR) Remote UK

Regulatory Affairs Specialist

Medical Information Specialist - Afterhours

Senior Manager – ESG and Sustainability Regulatory Legal

Medical Information Specialist - US Hours

Sr. Compliance Specialist, EMEA

Global Product Monitoring Vigilance Report Writer

Regulatory Reporting Industrial Placement - September 2026

Expert Consultant – Healthcare | Safety, Risk & Regulatory

Director, Government Affairs and Advocacy - Europe and International

Senior Professional - Regulatory Affairs Lifecycle Management - Biocides

Director - Regulatory Affairs Lifecycle Management Medicines

Clinical Data & Device Specialist

South & EE Team Regulatory Affairs Lead

Regulatory Engagement & Advocacy Manager – UK and France

Medical Information Specialist - Spanish & English speaking

South & EE Team Regulatory Affairs Lead

CMC Associate Director

Clinical Science Liaison Specialist

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