Associate Director - Quality Standards and Continuous Improvement in Uxbridge

Associate Director - Quality Standards and Continuous Improvement in Uxbridge

Uxbridge Full-Time 70000 - 90000 £ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Lead quality management and continuous improvement in a dynamic, science-driven environment.
  • Company: Join Regeneron, a leader in developing life-changing medicines.
  • Benefits: Comprehensive benefits including health programs, fitness centres, and equity awards.
  • Other info: Inclusive culture with opportunities for professional growth and development.
  • Why this job: Make a meaningful impact on patients' lives while advancing your career.
  • Qualifications: 10+ years in healthcare or pharma with expertise in quality management.

The predicted salary is between 70000 - 90000 £ per year.

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Quality Standards and Continuous Improvement to join our Global Development Quality team, supporting quality management system oversight, governance, quality events and continuous improvement across Global Development. In this role, you will help maintain effective quality standards and processes while collaborating with internal leaders, functional stakeholders and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organisation making a meaningful difference to patients worldwide.

Location: Uxbridge, Dublin, Warren or Armonk

Hybrid model

Discover your role:

  • Oversee the end-to-end Issue Management framework, ensuring standardized, compliant, and inspection-ready practices.
  • Define and evolve Issue Management and Quality Event strategies to support scalability, efficiency, and consistency.
  • Drive cross-functional alignment across Quality Event Leads (QEL) and functional teams to ensure consistent and right sized approach to issue management and quality decision-making.
  • Lead QEL forums and provide SME guidance on QMS governance, continuous improvement, and inspection readiness.
  • Ensure consistency in investigations, root cause analysis, CAPAs and documentation standards.
  • Lead and develop line reports whilst also supporting the broader QEL community through coaching, standard setting, and knowledge sharing.
  • Monitor Issue Management performance through metrics and trend analysis.

This role requires:

  • Bachelor’s degree with at least 10 years of relevant healthcare or pharmaceutical industry experience.
  • Experience in quality, compliance, quality management, quality assurance or clinical development.
  • Expertise or transferable skills related to Good Clinical Practice or Good Pharmacovigilance Practice.
  • Experience training, supervising, mentoring, developing staff and leading a small team.
  • Advanced knowledge of quality management system oversight, quality governance and continuous improvement.
  • Experience participating in, managing and leading regulatory agency inspections.

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, colour, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations.

Associate Director - Quality Standards and Continuous Improvement in Uxbridge employer: Regeneron Pharmaceuticals

At Regeneron, we pride ourselves on being an exceptional employer, offering a collaborative and inclusive work culture that empowers our employees to make a meaningful impact in the healthcare sector. With comprehensive benefits tailored to various locations, including health and wellness programmes, professional development opportunities, and a commitment to continuous improvement, we ensure our team members thrive both personally and professionally. Join us in Uxbridge, Dublin, Warren, or Armonk, where you can contribute to life-changing innovations while enjoying a supportive environment that values your growth and well-being.

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Contact Details:

Regeneron Pharmaceuticals Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Associate Director - Quality Standards and Continuous Improvement in Uxbridge

Tip Number 1

Network like a pro! Reach out to your connections in the healthcare and pharmaceutical sectors. We all know someone who knows someone, so don’t be shy about asking for introductions or insights into the company culture at Regeneron.

Tip Number 2

Prepare for the interview by diving deep into Regeneron's mission and values. We want to see how you align with our commitment to quality and continuous improvement. Think of specific examples from your experience that showcase your expertise in quality management and team leadership.

Tip Number 3

Showcase your problem-solving skills! Be ready to discuss how you've tackled quality issues in the past. We love candidates who can demonstrate their ability to drive cross-functional alignment and lead teams through challenges.

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, it shows us you’re genuinely interested in being part of our team at Regeneron.

We think you need these skills to ace Associate Director - Quality Standards and Continuous Improvement in Uxbridge

Quality Management System Oversight
Quality Governance
Continuous Improvement
Issue Management Framework
Root Cause Analysis
CAPA Documentation Standards
Regulatory Agency Inspections

Some tips for your application 🫡

Tailor Your Application:Make sure to customise your CV and cover letter to highlight your experience in quality management and continuous improvement. We want to see how your skills align with the role, so don’t hold back on showcasing your relevant achievements!

Showcase Your Leadership Skills:Since this role involves leading teams and mentoring others, be sure to include examples of your leadership experience. We love to see how you've developed staff and driven cross-functional collaboration in your previous roles.

Be Clear and Concise:When writing your application, keep it straightforward and to the point. Use clear language to describe your experiences and avoid jargon unless it's industry-specific. We appreciate clarity as much as you do!

Apply Through Our Website:We encourage you to apply directly through our website for a smoother process. It’s the best way to ensure your application gets into the right hands and shows us you’re serious about joining our team!

How to prepare for a job interview at Regeneron Pharmaceuticals

Know Your Quality Standards

Familiarise yourself with the latest quality management systems and standards relevant to the pharmaceutical industry. Be prepared to discuss how you’ve applied these in your previous roles, especially in relation to compliance and continuous improvement.

Showcase Your Leadership Skills

As an Associate Director, you'll be leading teams and driving cross-functional alignment. Prepare examples of how you've successfully mentored or developed staff in the past, and be ready to discuss your approach to fostering collaboration among diverse teams.

Prepare for Scenario-Based Questions

Expect questions that assess your problem-solving skills in real-world situations. Think of specific instances where you managed quality events or led investigations, and be ready to explain your thought process and the outcomes.

Understand Regeneron's Culture

Research Regeneron’s values and mission. Be ready to articulate how your personal values align with theirs, particularly regarding teamwork and making a meaningful difference in patients' lives. This will show your genuine interest in the role and the company.