At a Glance
- Tasks: Lead quality management and continuous improvement initiatives in a dynamic healthcare environment.
- Company: Join Regeneron, a science-driven company making a difference in patients' lives.
- Benefits: Comprehensive benefits including health programs, fitness centres, and equity awards.
- Other info: Hybrid work model with opportunities for professional growth and development.
- Why this job: Make a meaningful impact on global health while advancing your career.
- Qualifications: 10+ years in healthcare or pharma with expertise in quality management.
The predicted salary is between 60000 - 80000 £ 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.
Benefits:
We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels!
Equal Opportunity Employer: Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, 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 Improvement in Uxbridge employer: Regeneron
At Regeneron, we pride ourselves on being an exceptional employer, offering a collaborative and inclusive work culture that fosters innovation and personal growth. Our employees benefit from comprehensive health and wellness programs, competitive compensation packages, and opportunities for professional development within a fast-paced, science-driven environment. Join us in Uxbridge, Dublin, Warren, or Armonk, where you can make a meaningful impact on patients' lives while advancing your career in the healthcare and pharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Director, Quality Standards and 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 your experience aligns with their focus on quality standards and continuous improvement. Tailor your examples to show how you can contribute to their goals.
✨Tip Number 3
Showcase your leadership skills! If you've led teams or projects, make sure to highlight those experiences. Regeneron is looking for someone who can guide others and drive cross-functional alignment, so let’s make that clear.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we’re here to support you every step of the way, so take advantage of our resources to prepare yourself for success.
We think you need these skills to ace Associate Director, Quality Standards and Improvement in Uxbridge
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the role of Associate Director, Quality Standards and Improvement. Highlight your relevant experience in quality management and continuous improvement, and don’t forget to showcase any leadership roles you've had!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about quality standards in the healthcare industry and how your background aligns with Regeneron's mission. Keep it engaging and personal!
Showcase Your Achievements:When detailing your experience, focus on specific achievements that demonstrate your expertise in quality management systems and compliance. Use metrics where possible to show the impact of your work—numbers speak volumes!
Apply Through Our Website:We encourage you to apply through our website for the best chance of being noticed. It’s straightforward and ensures your application goes directly to the right team. Plus, we love seeing candidates who take the initiative!
How to prepare for a job interview at Regeneron
✨Know Your Quality Standards
Make sure you brush up on the latest quality management systems and standards relevant to the pharmaceutical industry. Familiarise yourself with Good Clinical Practice and Good Pharmacovigilance Practice, as these will likely come up during your interview.
✨Showcase Your Leadership Skills
As an Associate Director, you'll be expected to lead and develop teams. Prepare examples of how you've successfully mentored or supervised staff in the past. Highlight your experience in driving cross-functional alignment and how you’ve contributed to continuous improvement initiatives.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills, especially around issue management and quality events. Think of specific situations where you had to conduct root cause analysis or implement corrective actions, and be ready to discuss the outcomes.
✨Understand the Company Culture
Regeneron values inclusivity and innovation. Research their culture and think about how your personal values align with theirs. Be prepared to discuss how you can contribute to their mission of making a meaningful difference to patients worldwide.
