Role Summary
Regeneron is hiring a Manager, QA (Process Validation Oversight) to lead a team dedicated to ensuring the integrity of our process validation processes. This role supports process validation activities, ensures global consistency, addresses recurring themes in process documentation, and plays a pivotal role in regulatory inspections and compliance.
Responsibilities
- Ensuring alignment between validation activities and Process Sciences initiatives to support successful transition of processes from development to manufacturing.
- Collaborate closely with internal Process Sciences team to provide technical expertise and ensure consistency in Process Validation strategies.
- Presenting/defending validation strategies, documentation, and processes to FDA and other regulatory agencies.
- Reviewing and approving process validation documents, procedures, and protocols, proposing modifications and corrections where necessary to meet regulatory requirements and expectations.
- Overseeing all aspects of QA Validation including review and approval of failure investigations, change controls, SOPs, Validation protocols and summary reports, and validation master plans.
- Conduct one-on-one discussions with team members to review their performance feedback and set development goals, fostering professional growth within the team.
Qualifications
- Required: Bachelorโs degree in Engineering, Chemistry, or Life Sciences.
- Required: 6+ years of experience for Associate Manager or 7+ years for Manager.
- Note: May substitute relevant experience in lieu of education requirement. Level is determined on qualifications relevant to the role.
Skills
- Hands-on validation experience in a GMP-regulated environment.
- Deep understanding and expertise in Process Validation.
- Ability to build strong, collaborative relationships across global internal teams.
- Continuous improvement mindset.
- Experienced leader who inspires and guides a multi-tiered team.
Education
- Bachelorโs degree in Engineering, Chemistry, or Life Sciences.