Compliance Specialist, Engineering & Automation

Role: Compliance Specialist supporting cGMP and procedural compliance within Regeneron's Technical Operations Engineering & Automation Department. Responsibilities: maintain knowledge of industry guidance, evaluate practices, support documentation (change controls, investigations, CAPAs, SOPs), serve as liaison between engineering and quality, identify continuous improvement opportunities, assist with audit/inspection coordination, and communicate effectively with stakeholders. Requirements: B.S. in life sciences, engineering, or related field; 0-2+ years (Associate), 2+ years (Specialist), or 5+ years (Senior) experience; strong understanding of cGMP biotech/pharma manufacturing and laboratory operations; proficiency in documentation and regulatory standards. HighValue: focus on biotech/pharma cGMP compliance, engineering and automation, audit/inspection support, and cross-functional collaboration. WorkSetup: Monday-Friday, Troy, NY; on-site; no travel specified.