Sr. Manager, Quality Systems and Compliance Technology

Role: Senior Manager, Quality Systems & Compliance Technology, responsible for leading and managing Avalo's electronic Quality Management System (eQMS) to ensure compliance with internal procedures and global regulations. Responsibilities include overseeing QMS governance, workflows, computer system validation, and vendor/system qualification; leading GxP compliance initiatives across GMP/GCP environments; supporting audit and inspection readiness; and driving digital transformation of quality systems. Requirements: Bachelor's in Life Sciences, Engineering, or related field; minimum 7 years in biotech/pharma QA; proven experience with enterprise QMS platforms (preferably Veeva), CSV activities for regulated GxP systems, and knowledge of FDA, EMA, ICH, and data integrity standards. Preferred: experience in a startup or small biotech setting, strong organizational and communication skills, and familiarity with remote collaboration tools. High-Value: focus on GxP compliance, QMS governance, SaaS validation, inspection support, and working in a fast-paced biotech environment. Work setup: hybrid in Chesterbrook, PA, with a minimum of 2 days/week in-office; some travel expected.