Associate Director Quality

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. The Associate Director Quality is responsible for ensuring that Quality performance, compliance, and operational excellence are embedded and maintained across all strategic initiatives, GMP operations, and support functions at the Rockville site.

Requirements

• Serve as a strong, accountable leader who motivates, mentors, and develops the Quality team
• Apply deep process knowledge and technical acumen to drive effective decision-making
• Represent Quality as an FDA-facing subject matter expert
• Ensure Quality deliverables for batch record review, lot disposition, and product release meet internal and external expectations
• Manage execution of on-the-floor Quality operations
• Provide technical expertise during investigations
• Monitor Quality support activities for client programs
• Act as a role model for effective problem-solving and triage

Benefits

• bonus/incentives based on performance
• 401K
• paid time off
• stock purchase program
• Health and wellness coverage
• employee and family wellbeing support programs
• work life balance flexibility