At a Glance
- Tasks: Lead quality management and continuous improvement initiatives in a dynamic healthcare environment.
- Company: Join Regeneron, a leader in life-changing medicine innovation.
- 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 real impact on quality standards in the pharmaceutical industry.
- Qualifications: 10+ years in healthcare with expertise in quality management and team leadership.
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.
Location & Work Model
Location: Uxbridge, Dublin, Warren or Armonk Hybrid model
Key Responsibilities
- 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 while also supporting the broader QEL community through coaching, standard setting, and knowledge sharing.
- Monitor Issue Management performance through metrics and trend analysis.
Requirements
- 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 offer comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (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 Statement
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 Continuous Improvement in Uxbridge employer: Initial Therapeutics, Inc.
At Regeneron, we pride ourselves on being an exceptional employer, offering a dynamic work environment that fosters innovation and collaboration in the healthcare and pharmaceutical sectors. Our commitment to employee growth is evident through comprehensive training programs and mentorship opportunities, while our hybrid work model in locations like Uxbridge and Dublin ensures a flexible balance between professional and personal life. With a strong focus on quality standards and continuous improvement, we empower our team members to make meaningful contributions to life-changing medicines, all within a culture that values diversity and inclusion.
Contact Details:
Initial Therapeutics, Inc. 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 those interviews by brushing up on your knowledge of quality management systems and continuous improvement strategies. We want you to showcase your expertise and how it aligns with Regeneron's mission to develop life-changing medicines.
✨Tip Number 3
Don’t forget to follow up after your interviews! A quick thank-you email can go a long way in showing your enthusiasm for the role. We believe that a little gratitude can make a big impression.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we’re always looking for passionate individuals who are ready to make an impact in quality standards and continuous improvement.
We think you need these skills to ace Associate Director - Quality Standards and Continuous Improvement in Uxbridge
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the skills and experiences that align with the Associate Director role. Highlight your expertise in quality management and continuous improvement, as these are key for us at Regeneron.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to tell us why you're passionate about quality standards and how your background makes you a perfect fit for our team. Be genuine and let your personality come through.
Showcase Relevant Experience:When detailing your experience, focus on specific achievements in quality management and compliance. We want to see how you've driven improvements and led teams in your previous roles—numbers and examples speak volumes!
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 the role. Plus, it’s super easy to do!
How to prepare for a job interview at Initial Therapeutics, Inc.
✨Know Your Quality Standards
Make sure you brush up on the latest quality management systems and practices 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
Be prepared to discuss your experience in leading teams and mentoring staff. Think of specific examples where you've driven cross-functional alignment or improved processes, as this aligns perfectly with the role's responsibilities.
✨Prepare for Scenario Questions
Expect questions that ask how you would handle specific quality events or compliance issues. Practise articulating your thought process and decision-making strategies, especially around root cause analysis and CAPAs.
✨Metrics Matter
Since monitoring performance through metrics is key in this role, be ready to talk about how you've used data to drive improvements in past positions. Bring examples of how you've analysed trends and implemented changes based on your findings.
