Regulatory affairs lead Work, Jobs in Maidenhead, Eng (with Salaries)

PV Systems and Processes Lead x2
CSL Seqirus —Maidenhead
- Full-time
- No degree
- Leadership
- Communication skills
Head, PV and Regulatory QA
CSL Seqirus —Maidenhead
- Full-time
- Customer service
- Bachelor's degree
- Organisational skills
Regulatory Affairs Manager UK&I
Medtronic —Watford
- £71,760 - £107,640 a year
- Full-time
- Analysis skills
- Project management
- Organisational skills
Head of Global Regulatory Affairs
Karo Healthcare —Maidenhead
- Full-time
- Hybrid work
- Business
- Leadership
- Flexible schedule
Quick apply
Exec Director, Regulatory Affairs
Gilead Sciences —Uxbridge
- Full-time
- Hybrid work
- Management
- Doctoral degree
- English
Regional Ethics and Compliance Officer - International
CSL Seqirus —Maidenhead
- Full-time
- Bachelor's degree
- Travel
- Business
Director, Regulatory Affairs, Europe
GE HEALTHCARE —Chalfont Saint Giles
- Engineering
- Master's degree
- Bachelor's degree
Senior Benefits Risk Management Lead
Bayer —Reading
- £110,000 - £130,000 a year
- Full-time
- Hybrid work
- English
- Leadership
- Communication skills
- Annual leave
- Employee discount
Senior Regulatory Affairs Officer - Promotional & Non-Promotional Materials Review
Sanofi —Reading
- Hybrid work
- English
Associate Director Global CMC QU – Clinical GMP/GDP
Kyowa Kirin International plc —Marlow
- £80,000 - £140,000 a year
- Full-time
- Bachelor's degree
- No degree
- Leadership
9d
QA Senior Manager
Fortrea —Maidenhead
- Full-time
- Bachelor's degree
- Leadership
- Negotiation
Senior Pharmacovigilance Officer, Team Lead/ Case Processing Manager- Medical Device experience needed
PrimeVigilance —Guildford
- Full-time
- Remote
- Nursing
- English
- Microsoft Office
Quick apply
Regulatory Affairs Manager
Reckitt —Slough
- Management
- Communication skills
- Employee assistance programme
- Life insurance
Patient-Centered Outcomes Research (PCOR) Lead (UK)
UCB —Slough
- Doctoral degree
- Master's degree
- Leadership
2d
Associate Director Global CMC QU – Clinical GMP/GDP
Kyowa Kirin International —Marlow
- £66,814 - £134,641 a year
- Full-time
- Bachelor's degree
- No degree
- Leadership
Quick apply
8d
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 Manager
Elanco —Hook
- Full-time
- English
- Master's degree
- Leadership
Global Regulatory CMC Scientist (UK)
UCB —Slough
- Master's degree
- Bachelor's degree
- Leadership
Head of Global Labelling
CSL Seqirus —Maidenhead
- Full-time
- Leadership
Vice President, Regulatory Affairs – ELMAC
Amgen —Uxbridge
- Doctoral degree
- Master's degree
- Bachelor's degree

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regulatory affairs lead jobs near maidenhead, eng

PV Systems and Processes Lead x2

CSL Seqirus -
Maidenhead

Apply Now

Job details

Full-time

Qualifications

Quality assurance
Root cause analysis
Leadership
Communication skills

Full job description

Entity: CSL Seqirus

Job Category: Quality

Job Family: Quality Assurance

Job Type: Full Time

Location: Maidenhead, Berkshire, United Kingdom

Employer Reference: R-274200

Job Description

PV Systems & Process Lead

Patient safety depends on pharmacovigilance systems that work — and work well. In this role, you'll be at the centre of keeping CSL's global PV system compliant, continuously improving, and inspection-ready across Global Clinical Safety & Pharmacovigilance, Global Regulatory Affairs, Global Medical Affairs, affiliates, and commercial operations.

This is a role for someone who thrives at the intersection of regulatory expertise and practical problem-solving — someone who can spot a systemic compliance risk, build the relationships to address it, and drive the change that makes it stick.

What you'll do

You'll own the quality and compliance infrastructure that underpins CSL's PV system. Day-to-day, that means:

Providing expert GVP and PV legislation guidance across the organisation, and ensuring that regulatory changes translate into timely, concrete action
Leading investigation and resolution of deviations and non-compliances, including root cause analysis, CAPA development, and effectiveness tracking
Reviewing procedural documents across GCSP, GRA, and GMA for GVP compliance
Serving as the primary inspection coordinator for health authority and third-party PV audits in your region — from readiness planning through to CAPA close-out
Tracking quality and performance indicators, identifying trends, and escalating risks appropriately
Delivering PV quality training and sharing best practices across functions and affiliates

You'll also contribute to the broader audit programme and help shape the long-term PV audit strategy, in line with GVP Module IV.

What you'll bring

A science or life sciences degree (or equivalent through experience), plus significant experience in the pharmaceutical industry — mainly in PV or GxP Quality Assurance
Hands-on experience managing regulatory inspections and PV audits
Strong command of GVP regulations, ICH GCP, and relevant international requirements
Proven ability to lead deviation and CAPA management processes
The communication and leadership skills to influence across functions, regions, and seniority levels

About CSL Seqirus

CSL Seqirus is part of CSL. As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. With state-of-the-art production facilities in the U.S., the U.K. and Australia, CSL Seqirus utilizes egg, cell and adjuvant technologies to offer a broad portfolio of differentiated influenza vaccines in more than 20 countries around the world.

To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.

Our Benefits

For more information on CSL benefits visit How CSL Supports Your Well-being | CSL.

You Belong at CSL

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging

Equal Opportunity Employer

CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.

Apply Now

Refine Your Search

regulatory affairs lead jobs in maidenhead, eng

PV Systems and Processes Lead x2

Head, PV and Regulatory QA

Regulatory Affairs Manager UK&I

Head of Global Regulatory Affairs

Exec Director, Regulatory Affairs

Regional Ethics and Compliance Officer - International

Director, Regulatory Affairs, Europe

Senior Benefits Risk Management Lead

Senior Regulatory Affairs Officer - Promotional & Non-Promotional Materials Review

Associate Director Global CMC QU – Clinical GMP/GDP

QA Senior Manager

Senior Pharmacovigilance Officer, Team Lead/ Case Processing Manager- Medical Device experience needed

Regulatory Affairs Manager

Patient-Centered Outcomes Research (PCOR) Lead (UK)

Associate Director Global CMC QU – Clinical GMP/GDP

Principal Regulatory Affairs Specialist (UK, IVDR) Remote UK

Senior Regulatory Affairs Manager

Global Regulatory CMC Scientist (UK)

Head of Global Labelling

Vice President, Regulatory Affairs – ELMAC

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Job Description

About CSL Seqirus

Our Benefits

You Belong at CSL

Equal Opportunity Employer

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