Temporary Quality Manager GCP - GVP

Build our future together At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Temporary Quality Manager GCP - GVP, supporting our Global Development quality system in a hybrid work model. In this role, you will support quality management system governance, quality event oversight, and continuous improvement activities while collaborating with Global Development functions and quality leaders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. When & where: UK, US, or Ireland Work model: Remote Discover your role: Engage Global Development stakeholders to drive process improvements, standardization, and regulatory compliance. Manage quality metrics and trend reporting to support continuous improvement. Oversee the Quality Event portfolio and provide subject matter expertise to functional teams. Lead quality data analysis, root cause investigations, and Corrective Action/Preventive Action development. Manage Quality System Metrics, including thresholds, reporting, actions, and effectiveness measures. Facilitate governance meetings and present data on Quality Management System health. Coordinate procedural document reviews and impact assessments across GDQGO. You promote quality culture and strengthen collaboration across Quality Management System elements. This role requires: Bachelor's degree and 6+ years of healthcare or pharmaceutical industry experience. Experience in Quality Management, Quality Assurance, or Clinical Development roles with Good Clinical Practice and/or Good Pharmacovigilance Practice expertise. Knowledge of Quality Management System oversight, governance, quality event management, and continuous improvement. Experience as a subject matter expert, process owner, or business process owner in a quality-related area. Experience delivering training and presenting quality and regulatory compliance information. Experience supporting or participating in regulatory agency inspections. Experience training, supervising, or mentoring staff. Strong project management, prioritization, organization, and time management skills. Strong communication, presentation, collaboration, and interpersonal relationship skills. Ability to identify process gaps, manage multiple priorities, and apply sound judgment with integrity and attention to detail. Does this sound like you? Apply now to take your first step towards living the Regeneron Way! 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, color, 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. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.  Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k)