Director, GPS Quality & Compliance in Cambridge

Director, GPS Quality & Compliance in Cambridge

Cambridge Full-Time No working from home possible
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At a Glance

  • Tasks: Lead quality event management and ensure inspection readiness in a dynamic pharmaceutical environment.
  • Company: Join Regeneron, a science-driven company making a real difference in patients' lives.
  • Benefits: Competitive salary, bonuses, health benefits, and a supportive work culture.
  • Other info: Inclusive workplace with excellent career growth opportunities.
  • Why this job: Make an impact in global patient safety while leading innovative quality initiatives.
  • Qualifications: 12+ years in pharma, deep knowledge of PV regulations, and strong leadership skills.

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Our Global Patient Safety (GPS) organization is seeking a Director, GPS Quality & Compliance to support our quality event management and inspection readiness programs. This role partners closely with the Senior Director, GPS leadership, Global Development Quality, and the QPPV Office, and operates as a functional leader who coordinates and delegates work across the team to ensure consistent, high-quality program delivery. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

  • Location: Warren, NJ (preferred), Armonk or Tarrytown, NY, or Cambridge, MA
  • Work model: 4 days/week on-site
  • Travel percentage: 20% with some fluctuation expected based on onsite audit/inspection support needs.

Discover your role:

  • Lead functional workstreams across quality event management and inspection programs, coordinating and delegating work across a team.
  • Serve as a trusted point of contact during GCP and GVP audits and inspections, guiding teams through preparation and real-time response.
  • Bring order to complexity by maintaining inspection readiness materials and translating regulatory frameworks into practical action.
  • Champion a culture of accountability and continuous improvement, acting as an escalation point when issues arise.
  • Turn data into direction, reviewing quality metrics and trend analyses to shape clear, actionable recommendations for senior leadership.
  • Communicate with confidence and clarity, presenting governance topics and quality insights to senior team members.
  • Lead through influence, coordinating across teams and functions regardless of formal reporting lines.

This role requires:

  • A Bachelor’s degree required; advanced degree preferred with a minimum of 12 years of pharmaceutical industry experience; Healthcare Professional background preferred.
  • Deep knowledge of global PV regulations, quality management systems, and inspection readiness frameworks (FDA CFR, GVP Modules).
  • Demonstrated experience facilitating FDA and EMA/MHRA inspections (GCP and GVP), including direct experience as an inspection point of contact.
  • Proven track record overseeing QMP governance, metrics programs, and cross-functional quality oversight.
  • Experience managing relationships across GDQ, QPPV Office, Regulatory Affairs, and vendors.
  • People management experience preferred.

We are committed to building a workplace with an inclusive culture. 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, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law.

Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience.

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

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

Director, GPS Quality & Compliance in Cambridge employer: Regeneron Pharmaceuticals

Regeneron is an exceptional employer, offering a dynamic work environment where innovation and collaboration thrive. As a Sales Specialist in Oncology, you will have the opportunity to engage with healthcare professionals and contribute to a growing oncology portfolio while benefiting from a comprehensive rewards package, including competitive bonuses and health programs. With a strong commitment to inclusivity and employee development, Regeneron fosters a culture that empowers you to excel in your career while making a meaningful impact in the healthcare sector.

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Contact Details:

Regeneron Pharmaceuticals Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Director, GPS Quality & Compliance in Cambridge

Unlock Networking Opportunities

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Tailor Your Approach

When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Regeneron Pharmaceuticals is looking for. A tailored application can really make you stand out!

We think you need these skills to ace Director, GPS Quality & Compliance in Cambridge

Quality Event Management
Inspection Readiness
GCP and GVP Audits
Regulatory Frameworks (FDA CFR, GVP Modules)
Data Analysis
Quality Metrics Review
Cross-Functional Coordination

Some tips for your application 🫡

Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Regeneron Pharmaceuticals!

Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Regeneron Pharmaceuticals that you're not just a fit for the job but also a safety-conscious candidate!

Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Regeneron Pharmaceuticals!

Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Regeneron Pharmaceuticals, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.

How to prepare for a job interview at Regeneron Pharmaceuticals

Understand the Science

Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Regeneron Pharmaceuticals that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.

Showcase Relevant Experience

If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.

Know Their Products

Take some time to familiarise yourself with Regeneron Pharmaceuticals’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.

Be Ready for Regulatory Scenarios

In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.