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- Tasks: Lead compliance and quality in pharmacovigilance systems to ensure patient safety.
- Company: Join CSL Seqirus, a global leader in influenza vaccine production.
- Benefits: Enjoy competitive benefits, including health support and a culture of inclusion.
- Other info: Dynamic role with opportunities for growth in a supportive environment.
- Why this job: Make a real impact on global health by ensuring drug safety and compliance.
- Qualifications: Science degree and experience in pharmaceutical PV or GxP Quality Assurance required.
The predicted salary is between 60000 - 80000 £ per year.
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
PV Systems and Processes Lead x2 in Charvil employer: CSL Seqirus
Contact Detail:
CSL Seqirus Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land PV Systems and Processes Lead x2 in Charvil
✨Tip Number 1
Network like a pro! Reach out to folks in the industry, especially those already at CSL or similar companies. A friendly chat can open doors and give you insider info that could make your application stand out.
✨Tip Number 2
Prepare for interviews by diving deep into CSL's values and recent projects. Show us you’re not just another candidate; demonstrate how your skills align with our mission and how you can contribute to our success.
✨Tip Number 3
Practice your STAR technique for answering behavioural questions. We want to hear about specific situations where you've tackled challenges, especially in compliance and quality assurance — it’s all about showing us your problem-solving prowess!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our team at CSL.
We think you need these skills to ace PV Systems and Processes Lead x2 in Charvil
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the role of PV Systems and Processes Lead. Highlight your experience in pharmacovigilance and regulatory compliance, and don’t forget to showcase any relevant achievements that demonstrate your problem-solving skills.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about pharmacovigilance and how your background makes you the perfect fit for CSL. Be sure to mention specific experiences that align with the job description.
Showcase Your Regulatory Knowledge: Since this role requires a strong command of GVP regulations and ICH GCP, make sure to highlight your knowledge in these areas. Use examples from your past work to illustrate how you've successfully navigated regulatory challenges.
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It’s the best way to ensure your application gets the attention it deserves, and you’ll find all the details you need right there!
How to prepare for a job interview at CSL Seqirus
✨Know Your Regulations
Make sure you brush up on GVP regulations, ICH GCP, and any relevant international requirements before your interview. Being able to discuss these confidently will show that you’re not just familiar with the rules but can also apply them practically.
✨Showcase Your Problem-Solving Skills
Prepare examples of how you've tackled compliance risks or led CAPA processes in the past. Use the STAR method (Situation, Task, Action, Result) to structure your answers, making it clear how your actions led to positive outcomes.
✨Build Relationships
Demonstrate your ability to influence across functions and seniority levels. Think of instances where you’ve successfully collaborated with different teams to drive change. This will highlight your interpersonal skills, which are crucial for this role.
✨Be Inspection Ready
Since you'll be coordinating inspections, it’s vital to convey your experience with regulatory audits. Discuss how you prepared for past inspections and what steps you took to ensure compliance. This will reassure the interviewers of your readiness for the role.