Affairs specialist Work, Jobs in Houghton Regis, Bdf (with Salaries)

Sr. Specialist, Regulatory Affairs
The Bountiful Company —Tring
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Training & Education Specialist, Urology - EMEA (Sacral Neuromodulation)
Boston Scientific —Welwyn
- Hybrid work
- English
- Analysis skills
- Project management
Principal Regulatory Affairs Specialist (UK, IVDR) Remote UK
Cepheid —Amersham
- Full-time
- Remote
- Master's degree
- Bachelor's degree
- Annual leave
5d
Senior Training and Development Specialist EMEA and APAC
Medtronic —Watford
- £53,600 - £80,400 a year
- Full-time
- Sales
- English
- In-person
6d
Sr. Drug Safety Specialist
GE HEALTHCARE —Chalfont Saint Giles
- Microsoft Word
- Microsoft Excel
- Microsoft Office
Regulatory Affairs Intern
GE HEALTHCARE —Chalfont Saint Giles
- Bachelor's degree
- Internship
6d
Associate Director
Edelman —London
- Full-time
- Communication skills
Vice President / Associate Director, Crisis & Risk
Edelman —London
- Full-time
- Project management
- IT
9d
Account Director - Corporate Reputation
Edelman —London
- Full-time
- Negotiation
Senior Account Manager - Corporate, Brand
Edelman —London
- Full-time
- Project management
- Organisational skills
- Communication skills
Experiential & Content Producer
Edelman —London
- Full-time
Senior Account Manager - Brand Marketing & Earned
Edelman —London
- Full-time
- Marketing

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Sr. Specialist, Regulatory Affairs

The Bountiful Company -
Tring

Quick apply

Job details

Permanent

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Microsoft Outlook
Analysis skills
Bachelor's degree
Computer skills
Communication skills

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

affairs specialist jobs in houghton regis, bdf

Sr. Specialist, Regulatory Affairs

Training & Education Specialist, Urology - EMEA (Sacral Neuromodulation)

Principal Regulatory Affairs Specialist (UK, IVDR) Remote UK

Senior Training and Development Specialist EMEA and APAC

Sr. Drug Safety Specialist

Regulatory Affairs Intern

Associate Director

Vice President / Associate Director, Crisis & Risk

Account Director - Corporate Reputation

Senior Account Manager - Corporate, Brand

Experiential & Content Producer

Senior Account Manager - Brand Marketing & Earned

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