Regulatory affairs specialist Work, Jobs in Barnet, Gtl (with Salaries)

Sr. Specialist, Regulatory Affairs
The Bountiful Company —Tring
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Nutrition Specialist (Global Regulatory & Corporate Affairs)
Oatly AB —London
- Part-time
- Hybrid work
- English
- Master's degree
- Travel
Quick apply
Principal Regulatory Affairs Specialist (UK, IVDR) Remote UK
Cepheid —Amersham
- Full-time
- Remote
- Master's degree
- Bachelor's degree
- Annual leave
7d
Medical Information Specialist - US Hours
EVERSANA —London
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- English
Quick apply
Quality and Regulatory Manager
Advanced Healthcare Technology Ltd —Waltham Cross
- £50,000 - £60,000 a year
- Full-time
- No degree
- Organisational skills
- In-person
- Free parking
Quick apply
Training & Education Specialist, Urology - EMEA (Sacral Neuromodulation)
Boston Scientific —Welwyn
- Hybrid work
- English
- Analysis skills
- Project management
Senior Regulatory Specialist
Androlabs —London
- £85,000 - £108,000 a year
- Full-time
- Hybrid work
- IT
- Annual leave
Quick apply
7d
Analyst - Regulatory Market Access and Compliance
Access Partnership —London
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Director - Regulatory Affairs Lifecycle Management Non-Medicines
Perrigo —London
- Hybrid work
- Bachelor's degree
- In-person
- Leadership
Regulatory Affairs Intern
GE HEALTHCARE —Chalfont Saint Giles
- Bachelor's degree
- Internship
8d
Communications Specialist, Improving Patient Information - £60,778 - £68,422 p.a. + benefits
Medicines and Healthcare Products Regulatory Agency —London
- From £60,778 a year
- Full-time
- Customer service
- Presentation skills
- Travel
- Annual leave
- Sick pay
6d
Quality Assessor
Medicines and Healthcare products Regulatory Agency —London
- Doctoral degree
- Marketing
- Presentation skills
8d
VodafoneThree - Senior Counsel – Customer Regulatory Implementation and Delivery
VodafoneThree —London
- Full-time
- Hybrid work
- Communication skills
- Employee discount
Quick apply
Quality Assessor - £60,778 - £68,422 p.a. + benefits
Medicines and Healthcare Products Regulatory Agency —London
- £60,778 - £68,422 a year
- Full-time
- Doctoral degree
- Marketing
- Presentation skills
- Annual leave
- Sick pay
8d
Sr. Drug Safety Specialist
GE HEALTHCARE —Chalfont Saint Giles
- Microsoft Word
- Microsoft Excel
- Microsoft Office
Regulatory and Scientific Affairs Senior Manager | Leatherhead Food Research
Sagentia Regulatory —Epsom
- Full-time
- Management
- Mentoring
- Organisational skills
Quick apply
Director - Regulatory Affairs Lifecycle Management Medicines
Perrigo —London
- Hybrid work
- Bachelor's degree
- In-person
- Leadership
Account Executive - Agricultural Regulatory Intelligence
FoodChain ID Group, Inc —London
- Full-time
- Remote
- Sales
- Salesforce
- English
1d
Medical Information Specialist - German & English speaking
EVERSANA —London
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- English
Quick apply
Specialist, Sustainability Regulatory Strategy & Execution
The Bank of New York Mellon Corporation —London
- Full-time
- Microsoft Powerpoint
- Presentation skills
- Bachelor's degree
8d

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regulatory affairs specialist jobs near barnet, gtl

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

regulatory affairs specialist jobs in barnet, gtl

Sr. Specialist, Regulatory Affairs

Nutrition Specialist (Global Regulatory & Corporate Affairs)

Principal Regulatory Affairs Specialist (UK, IVDR) Remote UK

Medical Information Specialist - US Hours

Quality and Regulatory Manager

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

Senior Regulatory Specialist

Analyst - Regulatory Market Access and Compliance

Director - Regulatory Affairs Lifecycle Management Non-Medicines

Regulatory Affairs Intern

Communications Specialist, Improving Patient Information - £60,778 - £68,422 p.a. + benefits

Quality Assessor

VodafoneThree - Senior Counsel – Customer Regulatory Implementation and Delivery

Quality Assessor - £60,778 - £68,422 p.a. + benefits

Sr. Drug Safety Specialist

Regulatory and Scientific Affairs Senior Manager | Leatherhead Food Research

Director - Regulatory Affairs Lifecycle Management Medicines

Account Executive - Agricultural Regulatory Intelligence

Medical Information Specialist - German & English speaking

Specialist, Sustainability Regulatory Strategy & Execution

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