Director, GVP Audits & Compliance in Cambridge
Director, GVP Audits & Compliance

Director, GVP Audits & Compliance in Cambridge

Cambridge Full-Time 72000 - 108000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead audits and ensure compliance in R&D Quality for a top bio-pharmaceutical company.
  • Company: A leading bio-pharmaceutical organisation focused on improving patient lives.
  • Benefits: Competitive salary, health benefits, and opportunities to make a real impact.
  • Why this job: Join a mission-driven team and contribute to groundbreaking therapies.
  • Qualifications: Strong background in pharmacovigilance, quality management, and leadership skills.
  • Other info: Dynamic role with opportunities for professional growth and development.

The predicted salary is between 72000 - 108000 £ per year.

A leading bio-pharmaceutical organization in the UK is seeking a Director for GVP Audits to drive compliance and audit excellence within R&D Quality. The role involves overseeing audit processes, managing cross-functional teams, and developing robust audit procedures.

The ideal candidate will possess a significant background in pharmacovigilance and quality management, alongside strong leadership skills. Join a mission-driven team dedicated to improving patient lives and contributing to groundbreaking therapies.

Director, GVP Audits & Compliance in Cambridge employer: Gilead Sciences, Inc.

As a leading bio-pharmaceutical organisation in the UK, we pride ourselves on fostering a collaborative and innovative work culture that prioritises employee growth and development. Our commitment to improving patient lives is matched by our dedication to providing comprehensive benefits, including professional training opportunities and a supportive environment that encourages leadership and initiative. Join us to be part of a mission-driven team where your contributions directly impact the future of healthcare.
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Contact Detail:

Gilead Sciences, Inc. Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Director, GVP Audits & Compliance in Cambridge

✨Tip Number 1

Network like a pro! Reach out to professionals in the bio-pharmaceutical field, especially those involved in R&D Quality. A friendly chat can open doors and give you insights that might just land you that Director role.

✨Tip Number 2

Prepare for interviews by brushing up on your pharmacovigilance knowledge. We recommend creating a list of common interview questions related to audits and compliance, and practice your answers. Confidence is key!

✨Tip Number 3

Showcase your leadership skills! During interviews, share specific examples of how you've successfully managed cross-functional teams or improved audit processes. We want to see how you can drive compliance excellence.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.

We think you need these skills to ace Director, GVP Audits & Compliance in Cambridge

Pharmacovigilance
Quality Management
Audit Processes
Leadership Skills
Cross-Functional Team Management
Compliance
Audit Excellence
Robust Audit Procedures

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in pharmacovigilance and quality management. We want to see how your background aligns with the role, so don’t be shy about showcasing your relevant skills and achievements!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about compliance and audit excellence. We love seeing candidates who are genuinely excited about improving patient lives through their work.

Showcase Leadership Experience: Since this role involves managing cross-functional teams, make sure to highlight your leadership experience. We’re looking for someone who can inspire and guide others, so share examples of how you've successfully led teams in the past.

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity. Plus, it’s super easy!

How to prepare for a job interview at Gilead Sciences, Inc.

✨Know Your Stuff

Make sure you brush up on your pharmacovigilance and quality management knowledge. Understand the latest trends and regulations in the bio-pharmaceutical industry, as this will show your expertise and commitment to the field.

✨Showcase Leadership Skills

Prepare examples of how you've successfully led cross-functional teams in the past. Be ready to discuss specific challenges you faced and how you overcame them, as this will demonstrate your capability to manage and inspire others.

✨Understand the Company’s Mission

Familiarise yourself with the organisation's mission and values. Be prepared to articulate how your personal goals align with their mission to improve patient lives and contribute to groundbreaking therapies, as this will resonate well with the interviewers.

✨Ask Insightful Questions

Prepare thoughtful questions about the audit processes and compliance strategies they currently have in place. This not only shows your interest in the role but also gives you a chance to assess if the company is the right fit for you.

Director, GVP Audits & Compliance in Cambridge
Gilead Sciences, Inc.
Location: Cambridge
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  • Director, GVP Audits & Compliance in Cambridge

    Cambridge
    Full-Time
    72000 - 108000 £ / year (est.)
  • G

    Gilead Sciences, Inc.

    1001-5000
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