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)
R

At a Glance

  • Tasks: Lead quality management and continuous improvement in a dynamic healthcare environment.
  • Company: Join Regeneron, a science-driven company making a difference in patients' lives.
  • Benefits: Comprehensive health benefits, fitness programs, equity awards, and paid time off.
  • Other info: Inclusive culture with opportunities for career growth and mentorship.
  • Why this job: Make a real impact on global health while developing your leadership skills.
  • 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.

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!

Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.

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.

The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted.

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

At Regeneron, we pride ourselves on being a leading employer in the healthcare and pharmaceutical industry, offering a collaborative and inclusive work culture that fosters innovation and personal growth. Our comprehensive benefits package, including health and wellness programs, equity awards, and generous paid leave, reflects our commitment to supporting our employees' well-being. Join us in Uxbridge, Dublin, Warren, or Armonk, where you will have the opportunity to make a meaningful impact on patients' lives while advancing your career in a fast-growing, science-driven organisation.

R

Contact Details:

Regeneron Pharmaceuticals, 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 that sometimes it’s not just what you know, but who you know. Attend industry events or webinars to meet potential colleagues and leaders in the field.

Tip Number 2

Prepare for those interviews! Research Regeneron and understand their values and mission. We want to see how you can contribute to our quality standards and continuous improvement efforts. Practice common interview questions and be ready to discuss your relevant experience in detail.

Tip Number 3

Showcase your expertise! When you get the chance to speak with us, highlight your experience in quality management systems and compliance. We’re looking for someone who can lead and develop teams, so share examples of how you’ve done this in the past.

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 us you’re genuinely interested in joining our team at Regeneron. Let’s build the future together!

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
Root Cause Analysis
CAPA (Corrective and Preventive Actions)
Regulatory Agency Inspections

Some tips for your application 🫡

Tailor Your CV:Make sure your CV is tailored to the role of Associate Director. Highlight your experience in quality management and continuous improvement, and don’t forget to mention any relevant achievements that align with Regeneron's mission.

Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about quality standards and how your background makes you a perfect fit for the team. Keep it engaging and personal!

Showcase Your Leadership Skills:Since this role involves leading teams and mentoring others, be sure to highlight your leadership experience. Share specific examples of how you've developed staff or driven cross-functional collaboration in the past.

Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets the attention it deserves. Plus, you’ll find all the details you need about the role and our company culture there!

How to prepare for a job interview at Regeneron Pharmaceuticals, Inc

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

Prepare examples of how you've successfully led teams or projects in the past. Highlight your experience in mentoring and developing staff, as this role involves leading a small team and supporting the broader Quality Event Leads community.

Be Ready for Scenario Questions

Expect questions that assess your problem-solving skills, especially around issue management and quality events. Think of specific instances where you’ve handled investigations, root cause analysis, or CAPAs, and be ready to discuss your approach.

Understand Cross-Functional Collaboration

Since this role requires driving alignment across various teams, prepare to discuss how you've effectively collaborated with different stakeholders in previous roles. Be ready to share strategies you used to ensure consistent decision-making and communication.