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

PV Systems and Processes Lead x2
CSL Seqirus —Maidenhead
- Full-time
- Continuous improvement
- No degree
- Leadership
Patient-Centered Outcomes Research (PCOR) Lead (UK)
UCB —Slough
- Doctoral degree
- Master's degree
- Leadership
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
Regulatory Compliance Supervisor (m/f/x)
3M —Bracknell
- Full-time
- Engineering
- Research
- Master's degree
- Flexible schedule
Director of Public Affairs, UK
Abbott Laboratories —Maidenhead
- Full-time
- Bachelor's degree
- Budgeting
- Communication skills
Principal Regulatory Affairs Specialist (UK, IVDR) Remote UK
Cepheid —Amersham
- Full-time
- Remote
- Master's degree
- Databases
- Bachelor's degree
- Annual leave
Director - Regulatory Platforms
CSL Behring —Maidenhead
- Full-time
- Computer Science
- Bachelor's degree
- Travel
Head, PV and Regulatory QA
CSL Seqirus —Maidenhead
- Full-time
- Bachelor's degree
- Continuous improvement
- Quality control
Regulatory Affairs Manager
pladis —Chiswick Park Station
- Full-time
Northern Europe Regulatory Affairs Director
Kenvue —Reading
- Hybrid work
- Management
- English
- Analysis skills
Medical Affairs Coordinator
Servier —Slough
- Microsoft Office
- Databases
- Administrative experience
Senior Benefits Risk Management Lead
Bayer —Reading
- £110,000 - £130,000 a year
- Full-time
- Hybrid work
- English
- Databases
- Continuous improvement
- Annual leave
- Employee discount
Quality Assurance & Regulatory Affairs Executive - Maternity Cover
TensCare Ltd —Epsom
- £35,000 - £42,500 a year
- Temporary
- Hybrid work
- Bachelor's degree
- Continuous improvement
- Team management
- Profit sharing
- Work from home
Quick apply
Head of Global Labelling
CSL Seqirus —Maidenhead
- Full-time
- Management
- Continuous improvement
- Leadership
Sr Director, Drug Development Lead
IQVIA —Reading
- Full-time
- Remote
- Management
- Doctoral degree
- Master's degree
- Work from home
4d
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
Strategy & New Product Planning Associate
Biogen —Maidenhead
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Master's degree
- Analysis skills
1d
Vice President, Regulatory Affairs – ELMAC
Amgen —Uxbridge
- Doctoral degree
- Master's degree
- Bachelor's degree
RWE Strategy Lead, Developed Brands (UK)
UCB —Slough
- Hybrid work
- Doctoral degree
- Master's degree
- Travel
Regulatory Affairs Professional - Lifecycle Management - Non-Medicinal
Perrigo —London
- Hybrid work
- Continuous improvement
- In-person

I want to receive the latest job alerts for regulatory affairs lead in maidenhead, brk

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

regulatory affairs lead jobs near maidenhead, brk

PV Systems and Processes Lead x2

CSL Seqirus -
Maidenhead

Apply Now

Job details

Full-time

Qualifications

Quality control corrective actions
Non-conformance investigation
Defect resolution root cause analysis
Corrective and preventive actions (CAPA)
Compliance audits
Quality assurance
Continuous improvement
Continuous improvement cycles oversight
Clinical compliance monitoring
Good Clinical Practice (GCP)
Pharmaceutical industry setting experience
Root cause analysis
Leadership
Communication skills
Internal quality assurance
Good Clinical Practice (ICH-GCP) guidelines
Corporate regulatory compliance oversight

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, brk

PV Systems and Processes Lead x2

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

Associate Director Global CMC QU – Clinical GMP/GDP

Regulatory Compliance Supervisor (m/f/x)

Director of Public Affairs, UK

Principal Regulatory Affairs Specialist (UK, IVDR) Remote UK

Director - Regulatory Platforms

Head, PV and Regulatory QA

Regulatory Affairs Manager

Northern Europe Regulatory Affairs Director

Medical Affairs Coordinator

Senior Benefits Risk Management Lead

Quality Assurance & Regulatory Affairs Executive - Maternity Cover

Head of Global Labelling

Sr Director, Drug Development Lead

Associate Director Global CMC QU – Clinical GMP/GDP

Strategy & New Product Planning Associate

Vice President, Regulatory Affairs – ELMAC

RWE Strategy Lead, Developed Brands (UK)

Regulatory Affairs Professional - Lifecycle Management - Non-Medicinal

I want to receive the latest job alerts for regulatory affairs lead in maidenhead, brk

Related Searches

Explore jobs in more locations

Job Description

About CSL Seqirus

Our Benefits

You Belong at CSL

Equal Opportunity Employer

Jobseeker tools

Employer Tools

Browse

Stay Connected