Associate CMC Product Quality Compliance Specialist

Regeneron Pharmaceuticals, Inc.; United States; À distance; USD 110 000 - 150 000; Plein temps

Résumé du poste

Regeneron Pharmaceuticals, Inc. seeks a Quality representative to manage product and distribution compliance for commercial programs, guiding quality and regulatory elements across the life cycle strategy.

You will collaborate with CMC teams, alliance partners, CMOs and other stakeholders to ensure supply continuity and regulatory alignment. The role supports product quality reviews, regulatory submissions, and launch readiness, with oversight of change management, deviations, CAPAs, and ongoing

Qualifications

• Assoc Specialist requires BS/BA in Chemistry, Biology, or related field with relevant experience, preferably pharma or medical device, including some supervisory/leadership experience.
• Specialist requires BS/BA in Chemistry, Biology, or related field with 2+ years of relevant experience in pharmaceutical or medical device, including some supervisory/leadership experience.
• Sr Specialist requires BS/BA in Chemistry, Biology, or related field with 5+ years of relevant experience in pharmaceutical or medical device, including some supervisory/leadership experience.

Responsabilités

• Oversee the global change management implementation plan.
• Support evaluation of impact of proposed process changes, deviations and CAPAs on end-to-end supply chain.
• Oversee coordination and generation of annual PQRs and yearly biologic product reports (YBPR).
• Assess quality information to detect trends and determine actions needed.
• Ensure drug supply distribution compliance with global regulatory filings.
• Interact with global regulatory authorities during Agency inspections.
• Collaborate cross-functionally to support regulatory release and inventory review.
• Execute relationship management with Regulatory, Quality, Manufacturing, and Supply.
• Develop procedures and systems for tracking change controls and regulatory submissions/approvals.
• Support launch readiness and distribution compliance with GMP documentation and regulatory dossiers.
• Provide writing/strategy support in communications to regulatory agencies.
• Facilitate CARRs process in collaboration with CMC PM, CMC RA, IMT and SMEs.

Formation

Assoc Specialist: BS/BA in Chemistry or Biology, with relevant experience, supervisory/leadership

Specialist: BS/BA in Chemistry or Biology, 2+ years Pharmaceutical/Medical device experience, supervisory/leadership

Sr Specialist: BS/BA in Chemistry or Biology, 5+ years Pharmaceutical/Medical device experience, supervisory/leadership

Description du poste

Responsible for being a Quality representative for product and distribution compliance of Regeneron's commercial programs including support with the product quality reviews (PQR). This role supports the development, coordination and ownership of the quality and compliance elements of the life cycle strategy, including ownership of the global regulatory change management implementation plan, end-to-end optimization efforts and overseeing product management activities. Works collaboratively with CMC team members, alliance partners, collaborators and CMOs to ensure continuity of supply, consistency within and across programs, supply strategy alignment across functions, and compliance process efficiency.

Essential Duties and Responsibilities

• Oversees the global change management implementation plan
• Supports the evaluation of impact of proposed process changes, deviations and CAPAs on the end-to-end supply chain.
• Oversees the coordination and generation of the annual PQRs and yearly biologic product reports (YBPR).
• Assesses quality-related information to detect trends and works with subject matter experts to determine the need for actions required in response to those trends
• Ensures drug supply distribution compliance with all aspects of global regulatory filings to ensure stable supply positioning.
• Interacts with global regulatory authorities in support of the CMC activities during Agency inspections.
• Collaborates cross-functionally to support regulatory release process and inventory review.
• Executes relationship management with other areas of Regulatory, Quality, Manufacturing, and Supply organizations to support product distribution.
• Develops procedures and systems for enhanced tracking of change controls and global regulatory submissions/approvals.
• Support launch readiness and distribution compliance through ensuring appropriate GMP source documentation is in place to support regulatory activities and launch material is aligned with the applicable regulatory dossiers.
• Responsible for providing writing and strategy support in communications to regulatory agencies including product deviation reports (BPDR, QDR, PDR, etc.), clinical notice of events and agency inspection responses in collaboration with CMC RA, QA, and SMEs as applicable.
• Facilitates the commercial and registration requests (CARRs) process in collaboration with CMC PM, CMC RA, IMT and SMEs as applicable.

Education and Experience

• Assoc Specialist: Requires BS/BA in Chemistry, Biology, or related field, with relevant experience or equivalent combination of education and experience, preferably pharmaceutical or medical device, including some supervisory and/or leadership experience.
• Specialist: Requires BS/BA in Chemistry, Biology, or related field, with 2+ years of relevant experience in pharmaceutical or medical device, including some supervisory and/or leadership experience or equivalent combination of education and experience.
• Sr Specialist: Requires BS/BA in Chemistry, Biology, or related field, with 5+ years of relevant experience in pharmaceutical or medical device, including some supervisory and/or leadership experience or equivalent combination of education and experience.

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) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For a