Affairs & communications Work, Jobs in Thatcham, Brk (with Salaries)

Senior Regulatory Affairs Specialist
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
- Annual leave
MSL | Medical Science Liaison - UK (m/f/d)
PAION Pharma GmbH —Reading
- Travel
- Communication skills
Quick apply
Medical Device Regulatory Affairs Specialist
Clinica Engineering Medical Solutions Ltd —Reading
- £3,700 - £4,200 a month
- Full-time
- Engineering
- English
- Databases
Quick apply
Local Study Associate Director
IQVIA —Reading
- Full-time
- Remote
- English
- Bachelor's degree
- No degree
- Work from home
Head of Corporate Affairs
Oxford University Press —Oxford
- Hybrid work
- English
- Team management
- Leadership
- Employee discount
Researcher in Reproductive Demography
University of Oxford —Oxford
- £39,424 - £47,779 a year
- Full-time
- Doctoral degree
- Research
- Communication skills
Corporate Communications Apprentice
Sanofi —Reading
- Internship
Public Affairs & Communications Director
AALTO —Farnborough
- Leadership
- Employee assistance programme
- Employee discount
Quick apply
Senior Medical Writer (remote US-based)
Porterhouse Medical Group —Reading
- Remote
- Doctoral degree
- Research
- Master's degree
- Annual leave
Study Start Up Manager
Fortrea —Maidenhead
- Full-time
- Remote
- English
- Bachelor's degree
12d
Director, Medical Affairs (Europe & International)
Immunocore —Oxford
- Management
- Doctoral degree
- Travel
Incident Comms Specialist
Thames Water Utilites —Reading
- £49,000 - £55,000 a year
- Full-time
- Continuous improvement
- Leadership
- Annual leave
Sr Director, Drug Development Lead
IQVIA —Reading
- Full-time
- Remote
- Management
- Doctoral degree
- Master's degree
- Work from home
7d
Senior Technical Policy Executive
The Horticultural Trades Association —Didcot
- £35,000 - £40,000 a year
- Full-time
- Hybrid work
- CRM software
- Analysis skills
- Presentation skills
- Free parking
- Health & wellbeing programme
Quick apply
Creative Media Producer (temporary cover)
University of Oxford —Oxford
- £39,424 - £47,779 a year
- Part-time
- University
- Annual leave
13d
Practice Area Lead: Medical Affairs Communications
IQVIA —Reading
- Full-time
- Hybrid work
- Business development
- Training & development
- Leadership
Client Partner, Strategy Consulting Large Pharma Advisory, 1 year contract
IQVIA —Reading
- Full-time
- Hybrid work
- Organisational skills
- Communication skills
- Negotiation
6d
Head of Spectrum & Regulatory Affairs
Open Cosmos —Didcot
- Hybrid work
- Negotiation
Press Officer
Dynamic Planner —Reading
- Full-time
- Hybrid work
- Financial services
- AI
- Internship
11d
Director, Medical Affairs EMEA
Kenvue —Reading
- Hybrid work
- Management
- Continuous improvement
- Travel
- Annual leave

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Senior Regulatory Affairs Specialist

Kenvue -
Reading

Apply Now

Job details

Benefits

Annual leave

Qualifications

Stakeholder collaboration
Internal department liaison
English
Bachelor's degree
Organisational skills
Project schedule tracking
Multidisciplinary collaboration
Networking
Cross-functional collaboration
Communication skills
Project progress tracking
Time management

Full job description

Kenvue is currently recruiting for a:

Senior Regulatory Affairs Specialist

What we do

At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.

Who We Are

Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours.

Role reports to:

Senior CMC Manager

Location:

Europe/Middle East/Africa, United Kingdom, Reading, Berkshire

Work Location:

Hybrid

What you will do

The Senior Regulatory Affairs Specialist is accountable for all regulatory activities associated with EMEA medicinal products. Projects may include compilation and submission of applications (post approval and new submissions), resolution of Health Authority questions in cooperation with other functions, post-approval commitments and submission of variations/renewal applications where requested. This position reports into the Associate Director Regulatory Affairs and is based at Reading (hybrid).

What You Will Do

Prepares and submits regulatory submissions according to applicable EU regulatory requirements and guidelines for MRP or DCP to ensure maintenance and compliance of existing marketing authorisations.
Proven track record in EU regulatory procedures (MRP/DCP), with solid experience in non-CMC lifecycle management and safety updates.
Collects and evaluates information on regulatory requirements for quality, preclinical and clinical data to meet applicable regulations.
Monitors the progress of the regulatory authority review process through appropriate communication with the Health Authority, seeking opportunities to expedite regulatory approvals where possible.
Prioritizes, plans and monitors allocated projects against defined timelines
Develops and maintains a thorough understanding of the regulatory environment and supporting data requirements
Ensures that all assigned products comply with local regulatory and quality system requirements.
Assists in ensuring that the enterprise Regulatory systems are accurate and fully maintained
Identifies & initiates local process improvement opportunities and manage changes as required
Assists in the preparation for internal and external audits and inspections in collaboration with others
Partner with other critical functions to execute plans to address crises and other sensitive issues

Qualifications :

Required Qualifications
Relevant Bachelor's Degree or higher
6+yrs related regulatory experience, ideally on non-prescription EU procedures (MRP/DCP).
Proven track record in EU regulatory procedures (MRP/DCP), with solid experience in non-CMC lifecycle management and safety updates.
Good attention to details.
Excellent communication skills, with the ability to articulate and express concepts clearly both verbally and in writing, particularly when simplifying complex regulatory or technical issues.
Good interpersonal skills; able to build effective personal networks internally and externally.
Collaborative with a strong sense of ownership, willing to be held accountable and be rewarded for delivering results.
Strong organizational and time management skills with an ability to work under pressure.
Able to work effectively in a multi-cultural, highly matrixed organization
Proficiency in English

Desired Qualifications

Knowledge of consumer healthcare environment and product development
Understanding of processes and departments within a healthcare company
Effective time and organisation management

What’s In It For You

Competitive Benefit Package
Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More!
Learning & Development Opportunities
Employee Resource Groups

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.

Apply Now

Refine Your Search

affairs & communications jobs in thatcham, brk

Senior Regulatory Affairs Specialist

MSL | Medical Science Liaison - UK (m/f/d)

Medical Device Regulatory Affairs Specialist

Local Study Associate Director

Head of Corporate Affairs

Researcher in Reproductive Demography

Corporate Communications Apprentice

Public Affairs & Communications Director

Senior Medical Writer (remote US-based)

Study Start Up Manager

Director, Medical Affairs (Europe & International)

Incident Comms Specialist

Sr Director, Drug Development Lead

Senior Technical Policy Executive

Creative Media Producer (temporary cover)

Practice Area Lead: Medical Affairs Communications

Client Partner, Strategy Consulting Large Pharma Advisory, 1 year contract

Head of Spectrum & Regulatory Affairs

Press Officer

Director, Medical Affairs EMEA

I want to receive the latest job alerts for affairs & communications in thatcham, brk

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