At a Glance
- Tasks: Lead and maintain a robust Pharmacovigilance Quality Assurance programme ensuring compliance and patient safety.
- Company: Specialist pharmaceutical company dedicated to developing medicines for HIV treatment and prevention.
- Benefits: Hybrid working model, competitive salary, and opportunities for professional growth.
- Other info: Join a collaborative team focused on continuous improvement and quality management.
- Why this job: Make a real impact on patient safety while working with senior stakeholders in a dynamic environment.
- Qualifications: Extensive experience in Pharmacovigilance Quality Assurance and strong knowledge of global regulations.
The predicted salary is between 80000 - 100000 € per year.
We are a specialist pharmaceutical company 100% dedicated to developing medicines to treat and prevent HIV.
Position Summary
We are looking for an experienced Pharmacovigilance Quality Assurance Director to lead and maintain a robust PV Quality Assurance programme, ensuring that pharmacovigilance activities supporting our products remain fully compliant with global regulations and internal quality standards. In this senior role, you will act as a trusted quality and compliance partner, providing oversight, assurance and strategic guidance across the pharmacovigilance system. You will work closely with senior stakeholders, quality teams, and service providers to identify risk, drive continuous improvement and, most importantly, ensure patient safety.
Key Responsibilities
- Provide independent quality assurance and oversight of pharmacovigilance processes to ensure compliance with global PV legislation, company policies and regulatory expectations.
- Lead and manage the PV QA programme, including audit risk assessments, audit planning, execution oversight and follow-up.
- Oversee and track Corrective and Preventive Actions (CAPAs), verifying effectiveness and escalating risks or issues where required.
- Act as a key point of contact for PV inspection readiness and inspection management, ensuring teams are fully prepared and supported.
- Review and oversee audit outcomes that impact supported products, including those conducted by internal and external quality functions.
- Partner with senior leadership to identify quality, compliance and risk areas, agreeing and monitoring remediation plans.
- Maintain and develop Pharmacovigilance System Master File (PSMF) content related to audit and deviation management.
- Generate and present quality metrics, reports and insights to governance and oversight forums.
- Provide expert advice on PV compliance, quality improvement, risk assessment and regulatory interpretation.
- Support the ongoing development of the Quality Management System (QMS) underpinning pharmacovigilance activities.
- Build and maintain strong working relationships across internal quality and compliance teams and with external partners.
- Contribute to and deliver training programmes within your area of expertise.
About You
- Extensive experience in Pharmacovigilance Quality Assurance, PV compliance or regulatory quality within the pharmaceutical or biotechnology industry.
- Strong knowledge of global PV and GCP legislation, regulatory guidelines and inspection expectations.
- Proven experience managing PV audits, inspections and CAPAs.
- Confidence engaging with and influencing senior stakeholders on quality, risk and compliance matters.
- Excellent analytical, communication and stakeholder management skills.
- A proactive, collaborative mindset with a strong focus on patient safety and continuous improvement.
Location and Working Pattern
This role is based at our UK HQ in Central London, and operates on a hybrid working model. You will be expected to work on-site 2-3 days per week to collaborate with cross-functional teams and support critical activities.
Closing Date for Applications - CoP 22nd May 2026
Closing date for applications: 22nd May 2026. Please submit your application before this date.
ViiV is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities, please contact where you can also request a call.
Pharmacovigilance Quality Assurance Director in London employer: ENGINEERINGUK
ViiV is an exceptional employer, dedicated to fostering a collaborative and inclusive work environment in the heart of Central London. With a strong focus on employee growth, we offer extensive training programmes and opportunities for professional development within the specialised field of pharmacovigilance. Our hybrid working model promotes a healthy work-life balance while ensuring that our team remains engaged and connected, all while contributing to meaningful advancements in HIV treatment and prevention.
StudySmarter Expert Advice🤫
We think this is how you could land Pharmacovigilance Quality Assurance Director in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those in pharmacovigilance. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of global PV legislation and compliance standards. We want you to be the go-to expert in the room, so practice articulating your experience with audits and CAPAs.
✨Tip Number 3
Showcase your leadership skills! When discussing your past roles, highlight how you've influenced senior stakeholders and driven quality improvements. We love candidates who can demonstrate their impact.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets the attention it deserves. Plus, we’re always looking for passionate individuals who align with our mission.
We think you need these skills to ace Pharmacovigilance Quality Assurance Director in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Pharmacovigilance Quality Assurance Director role. Highlight your relevant experience in PV compliance and quality assurance, and don’t forget to showcase your knowledge of global regulations!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about patient safety and how your background makes you the perfect fit for our team. Keep it concise but impactful!
Showcase Your Achievements:When detailing your experience, focus on specific achievements that demonstrate your ability to manage audits, inspections, and CAPAs. Numbers and metrics can really make your application stand out!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, you’ll find all the details you need about the role there!
How to prepare for a job interview at ENGINEERINGUK
✨Know Your Stuff
Make sure you brush up on your knowledge of global pharmacovigilance regulations and guidelines. Familiarise yourself with the latest trends in PV compliance and be ready to discuss how they impact patient safety.
✨Showcase Your Experience
Prepare specific examples from your past roles where you've successfully managed audits, inspections, or CAPAs. Highlight your ability to influence senior stakeholders and drive continuous improvement in quality assurance processes.
✨Be a Team Player
Emphasise your collaborative mindset by discussing how you've built strong relationships with cross-functional teams. Share instances where your teamwork has led to successful outcomes in quality management or compliance.
✨Prepare for Questions
Anticipate questions about risk assessment and how you would handle potential compliance issues. Think about how you would present quality metrics and insights to governance forums, as this will likely come up during the interview.
