Regulatory affairs Work, Jobs in Shillington, Bdf (with Salaries)

Sr. Specialist, Regulatory Affairs
The Bountiful Company —Tring
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Regulatory Affairs Manager UK&I
Medtronic —Watford
- £71,760 - £107,640 a year
- Full-time
- Analysis skills
- Project management
- Organisational skills
Principal Regulatory Affairs Specialist (UK, IVDR) Remote UK
Cepheid —Amersham
- Full-time
- Remote
- Master's degree
- Bachelor's degree
- Annual leave
6d
Senior Regulatory Affairs Director
AstraZeneca —Cambridge
- Presentation skills
- Organisational skills
- Leadership
12d
Regulatory Affairs Director
AstraZeneca —Cambridge
- Leadership
- Communication skills
5d
Medical Science Liaison
Merz Aesthetics GmbH —Hemel Hempstead
- Nursing
- Microsoft Office
- Driving
Quick apply
14d
Medical Director, Medical Safety
Jazz Pharmaceuticals —Cambridge
- £113,600 - £170,400 a year
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
Director Safety Surveillance & Risk Management (12 months fix term contract)
Viatris —Hatfield
- Full-time
- Hybrid work
- Bachelor's degree
- Time management
- Health & wellbeing programme
- Employee assistance programme
Corporate Public Affairs Lead
Roche —Welwyn
- Project management
- Communication skills
Marketing Communications Manager
Cycle Pharmaceuticals —Cambridge
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Gym membership
- Flexible schedule
1d

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regulatory affairs jobs near shillington, bdf

Sr. Specialist, Regulatory Affairs

The Bountiful Company -
Tring

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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

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regulatory affairs jobs in shillington, bdf

Sr. Specialist, Regulatory Affairs

Regulatory Affairs Manager UK&I

Principal Regulatory Affairs Specialist (UK, IVDR) Remote UK

Senior Regulatory Affairs Director

Regulatory Affairs Director

Medical Science Liaison

Medical Director, Medical Safety

Director Safety Surveillance & Risk Management (12 months fix term contract)

Corporate Public Affairs Lead

Marketing Communications Manager

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