Laboratory manager Work, Jobs in Esher, Sry (with Salaries)

GLP/GCLP Vendor Oversight and QA Lead (EU)
CSL Seqirus —Maidenhead
- Full-time
- Analysis skills
- Bachelor's degree
- Organisational skills
Associate Director – Laboratory Planning & Science Design
AECOM —London
- Full-time
- Hybrid work
- Business development
- Mentoring
- Leadership
Electronics Lab Lead
Everfox —London
- £39,600 - £54,000 a year
- Full-time
- Assembly
- Continuous improvement
- Scripting
- Annual leave
Senior Project Manager (Health and Life Sciences)
WSP —London
- Part-time
- Hybrid work
- Presentation skills
- Contracts
- Construction experience
- Flexitime
- Work from home
Technical Program Manager - Health AI Research
Microsoft —London
- £93,500 - £161,800 a year
- Full-time
- Machine learning
- AI
- Communication skills
Head of Life Sciences
London & Partners —London
- £82,000 - £86,000 a year
- Full-time
- Hybrid work
- CRM software
- Public speaking
- Microsoft Office
- Annual leave
Quick apply
Lecturer in Computing / VR Lab Lead
Regent College London —London
- £40,000 - £45,000 a year
- Weekend availability
- Doctoral degree
- Master's degree
- Communication skills
- Annual leave
- Employee assistance programme
Quick apply
Unified Endpoint Security Lab Lead
Lloyds Banking Group —London
- £146,591 - £172,460 a year
- Full-time
- Hybrid work
- Financial services
4d
Lead Scientist (OPM/MRX Specialist)
University College London —London
- Full-time
- Doctoral degree
- Engineering
- Organisational skills
- Annual leave
- Employee assistance programme
9d
Event Project Manager, Life Sciences (Europe - Remote)
SpotMe —London
- Travel
- In-person
Vulnerability Research Team Leader
Cellebrite —London
- Full-time
- English
- Team management
- Mentoring
Quick apply
Research Program Manager - Model Evals and Safety
Reflection —London
- Full-time
- Leadership
- Annual leave
Data Science Manager, Marketing
Google —London
- Master's degree
- Machine learning
- Team management
5d
Associate Director Life Sciences
Buro Happold —London
- Hybrid work
- Mentoring
- Leadership
- Employee assistance programme
- Employee discount
LAB People Strategy & Analytics Director - 12 month maternity cover
Boston Consulting Group —London
- Full-time
- Data analysis skills
- English
- Analysis skills
Director, Quality - GCP (Contract)
Compass Pathways —London
- Remote
- Bachelor's degree
- Continuous improvement
- No degree
- Annual leave
Quick apply
Manager, Lead Research Scientist, Training Data (Foundational Research)
Thomson Reuters —London
- Full-time
- Hybrid work
- Doctoral degree
- Research
- Master's degree
Senior Art Director, Brand Innovation Lab
Amazon Online UK Limited —London
- Full-time
- Presentation skills
- Time management
AI & Data Science Manager / Senior Manager
Capgemini Sogeti —London
- Hybrid work
- DevOps
- Business development
- Analysis skills
Research Program Manager - Research Infrastructure
Reflection —London
- Full-time
- Annual leave

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GLP/GCLP Vendor Oversight and QA Lead (EU)

CSL Seqirus -
Maidenhead

Apply Now

Job details

Full-time

Qualifications

GLP
Quality management change control procedures
Stakeholder liaison
Analysis skills
Quality assurance
Bachelor's degree
Risk management
Organisational skills
Supplier quality management
Supply chain quality assurance
Good Clinical Practice (GCP)
Quality management system (QMS) implementation
Communication skills
Internal quality assurance
Good Clinical Practice (ICH-GCP) guidelines
Analytics

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-275394

Job Description

GLP Vendor Oversight and QA Lead

The integrity of nonclinical data depends on more than what happens inside a company's walls. Much of the critical work in GLP-regulated research — safety studies, toxicology, analytical testing — is carried out by external laboratories and CROs. When that network of partners operates to the highest quality standards, the science is sound. When it doesn't, the consequences reach all the way to patients.

This role exists to make sure it works.

Why this role matters

GLP vendor oversight is often invisible when it's done well — and very visible when it isn't. As the internal authority on GLP and nonclinical vendor quality, you will be the person others turn to when the questions are difficult. If you take data integrity seriously, understand the regulatory landscape deeply, and want to shape how a global company manages its external nonclinical network, this is a role with real scope to make a difference.

About the role

Own quality oversight of external partners supporting nonclinical and GLP activities (CROs, laboratories, test facilities). Lead the vendor lifecycle: due diligence, qualification, quality agreements, risk-based monitoring, issue management and continuous improvement, ensuring adherence to GLP/GCP/GMP, data integrity and applicable regulations. Partner with Nonclinical Development, Procurement, Legal and IT.

Vendor Lifecycle and Governance: Run risk-based qualification and requalification, draft and maintain Quality Agreements, and set vendor KPIs and governance forums, ensuring actions and CAPAs are closed.
Inspections: Identify and prioritise vendors for audit on a risk basis; planning, conducting and grading sits with the audit function. Confirm vendor CAPAs are fit for purpose and run effectiveness checks. Coordinate inspection readiness and front- and back-room support.
Quality Systems and Compliance: Ensure vendor practices meet GLP/GCP/GMP, OECD GLP, 21 CFR Part 58, ICH, ISO and data integrity (ALCOA+). Provide input on third-party deviations, change control, CAPA, and the QMS.
Risk Management and Continuous Improvement: Lead vendor risk assessments (risk registers, FMEA) to set oversight frequency, improve vendor performance, and present trends at management reviews.
Cross-Functional Partnership: Embed quality requirements in scopes of work and contracts, guide technology transfers and data flows, and train internal stakeholders.
Maintain and share knowledge of Regulations and Requirements: Stay current with GLP and GxP regulations and translate changes into CSL requirements.

Position Qualifications and Experience Requirements:

Education: Bachelor's degree in a relevant scientific discipline.

Experience: 3+ years of GxP quality experience with direct vendor/CRO oversight and/or auditing (GLP/GCP/GMP), nonclinical/GLP preferred. Knowledge of OECD GLP, 21 CFR Part 58, Annex 11/Part 11 and data integrity (ALCOA+). Strong communication and negotiation skills.

Competencies: Works with limited supervision across multinational teams. Strong analytical, problem-solving, influencing and organisational skills. Knowledge of QMS implementation, regulatory frameworks and audit/inspection management.

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

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laboratory manager jobs in esher, sry

GLP/GCLP Vendor Oversight and QA Lead (EU)

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Job Description

About CSL Seqirus

Our Benefits

You Belong at CSL

Equal Opportunity Employer

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