Quality control manager Work, Jobs in Hazlemere, Bkm (with Salaries)

Head, PV and Regulatory QA
CSL Seqirus —Maidenhead
- Full-time
- Customer service
- Bachelor's degree
- Organisational skills
Quality Operations Lead
LINDAL Group —Leighton Buzzard
- Data analysis skills
- English
- Project management
- Annual leave
- Employee assistance programme
Quick apply
QA Operations Manager
Evotec —Abingdon
- Full-time
- Management
- Bachelor's degree
- Continuous improvement
3d
Deputy Quality Assurance Manager
Imperial College Healthcare NHS Trust —London
- £58,133 - £65,261 a year
- Full-time
3d
Associate Country Clinical Quality Manager
Fortrea —Maidenhead
- Full-time
- Analysis skills
- Bachelor's degree
Inbound Quality Shift Team Leader
Monica Vinader —London
- Analysis skills
- Quality control
- Travel
Quick apply
Project QA QC Manager
Kent —Woking
- Engineering
- Data analysis skills
- English
Lead Design Quality Assurance Engineer - 12m Inside IR35 Contractor
Safran Engineering Services UK Limited —Pitstone
- Engineering
- Analysis skills
- Bachelor's degree
Quick apply
Lead Customer Quality Assurance Engineer - 12m Inside IR35 Contractor
Safran Engineering Services UK Limited —Pitstone
- Engineering
- Analysis skills
- Bachelor's degree
Quick apply
6d
Clinical Quality Manager
TFS HealthScience —London
- Bachelor's degree
Quick apply

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Quality Operations Lead
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Head, PV and Regulatory QA

CSL Seqirus -
Maidenhead

Apply Now

Job details

Full-time

Qualifications

Clinical research
Customer service
Quality assurance
Bachelor's degree
Organisational skills
Leadership
Communication skills
Negotiation

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-274196

Job Description

The Head of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant with global regulations, ICH guidelines, and company standards. Your role bridges strategic oversight with hands on operational leadership: you design the audit strategy and governance framework that keeps the system fit for purpose, but you also own the day-to-day quality assurance of how PV actually works across the business.

You will direct both the strategic evolution of the PVRQA function and its operational delivery. This means setting the long term compliance roadmap while simultaneously managing inspections, deviation management, and the practical quality controls that keep the system sound. You partner with senior leadership on strategic direction, but you're equally engaged in the details that matter—ensuring SOPs are fit for purpose, CAPA workflows are rigorous, and systems are inspection-ready.

The Role

You will direct the strategic development of the Global PVRQA function, supporting both the global R&D business and regional affiliates. Your focus is on three core pillars: Strategic Governance, Operational Excellence, and Regulatory Intelligence.

Key Accountabilities:

Strategic Leadership: Harmonize processes within Global PVRQA and across other GxP areas. Contribute to the larger strategic vision of Global R&D Quality and interact with the Leadership Team to ensure continuous alignment.
Audit Strategy: Own the long-term, risk-based audit strategy aligned with GVP Module IV; deliver annual internal and external audit programs covering global systems, affiliates, and 3rd party vendors.
Inspection & Regulatory Management: Lead the preparation, conduct, and response phases for PV health authority inspections and 3rd party audits.
System Oversight: Monitor PV system health through oversight of deviation management, CAPA, change management, and performance reporting (KPIs).
Cross-Functional Expertise: Provide GVP consultancy and cross-GxP expertise (GCP, GDP, GCLP) to ensure coordination across functional areas, including Commercial and Clinical Development.
Operational Management: Oversight of PV IT systems, procedural quality assurance (SOPs), and third-party/vendor management.
Resource Stewardship: Direct budget development and resource allocation by strategically assessing workload and coordinating consultant activities.
Continuous Improvement: Monitor global regulatory trends and methodologies to implement improvement initiatives in response to the evolving landscape.

Your Profile

The successful candidate will be a high-calibre Quality Assurance professional with the executive presence to influence global cross-functional teams and the technical depth to safeguard our Pharmacovigilance system.

Qualifications & Experience:

Education: Undergraduate degree (BA/BS) in a Scientific or Life Sciences discipline; an advanced degree is preferred.
Industry Tenure: 10+ years of pharmaceutical industry experience specifically within Quality Assurance.
Leadership Track Record: Proven experience in a senior leadership capacity with deep knowledge of GVP/GCP regulations and international pharmacovigilance guidelines.
Technical Mastery: Extensive understanding of end-to-end pharmacovigilance processes, including Deviation/CAPA management and the conduct of clinical research.
Global Perspective: Experience working within global, cross-functional teams and managing complex regulatory interactions.

Leadership Attributes:

Strategic Acumen: The ability to quickly analyze complex circumstances and drive appropriate decisions and actions.
Communication & Influence: Excellent communication, negotiation, and influencing skills across all levels of the business.
Operational Rigor: Strong organizational skills with a focus on customer service and the ability to manage complex budgets and resourcing plans.

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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quality control manager jobs in hazlemere, bkm

Head, PV and Regulatory QA

Quality Operations Lead

QA Operations Manager

Deputy Quality Assurance Manager

Associate Country Clinical Quality Manager

Inbound Quality Shift Team Leader

Project QA QC Manager

Lead Design Quality Assurance Engineer - 12m Inside IR35 Contractor

Lead Customer Quality Assurance Engineer - 12m Inside IR35 Contractor

Clinical Quality Manager

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Job Description

About CSL Seqirus

Our Benefits

You Belong at CSL

Equal Opportunity Employer

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