Regulatory affairs Work, Jobs in Milton Keynes, Bkm (with Salaries)

Sr. Specialist, Regulatory Affairs
The Bountiful Company —Tring
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Outlook
Quick apply
Global Medical Affairs Associate Director - Metabolic & Dermato-Oncology
Recordati —Hemel Hempstead
- Full-time
- Hybrid work
- English
- Quality control
- Travel
Vice President, Medical Affairs Rare Diseases
Recordati —Hemel Hempstead
- £245,552 - £368,358 a year
- Full-time
- Hybrid work
- Management
- Doctoral degree
- English
- Annual leave
Land and Property Programme Manager
East West Rail —Milton Keynes
- Hybrid work
- Team management
- Contracts
- Annual leave
- Employee assistance programme
Quick apply

Discover related jobs

Based on your search for regulatory affairs jobs.

Associate Regulatory Affairs Lifecycle Management - Medical Devices
Perrigo —London
Supports ongoing conformity and compliance of medical device products through defined lifecycle regulatory activities across assigned products and markets.
12d
Senior ESG Regulatory Operations Associate
Ralph Lauren —London
This role plays a key part in driving the implementation of ESG regulatory requirements across Ralph Lauren’s operations.

I want to receive the latest job alerts for regulatory affairs in milton keynes, bkm

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

regulatory affairs jobs near milton keynes, bkm

Medical Director jobs in Cambridge

Medical Director jobs in Widnes

Medical Information Associate jobs in London

Medical Device Sales Representative jobs in London

Medical Laboratory Assistant jobs in Manchester

Medical Director jobs in Birmingham

Vice President jobs in London

Vice President Real Estate Investment jobs in London

Vice President jobs in Manchester

Vice President jobs in Belfast

Vice President jobs in Canary Wharf

Program Manager jobs in Lyndhurst

Program Manager jobs in Huddersfield

Project Manager jobs in Plymouth

Event Manager jobs in Remote

Program Manager jobs in Stratford

Program Manager jobs in Saint Ives

Project Manager jobs in East Sussex

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 jobs in milton keynes, bkm

Sr. Specialist, Regulatory Affairs

Global Medical Affairs Associate Director - Metabolic & Dermato-Oncology

Vice President, Medical Affairs Rare Diseases

Land and Property Programme Manager

Discover related jobs

I want to receive the latest job alerts for regulatory affairs in milton keynes, bkm

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected