Supervisor Quality Compliance

📋 Description

• Lead and oversee the Quality Compliance team, managing daily activities, priorities, performance
• Build and maintain a strong culture of quality, compliance, candid communication, continuous
• Manage regulatory, internal, third-party, and customer audits and inspections, including
• Own and maintain the inspection readiness program, including training, readiness assessments
• Serve as a key representative during regulatory inspections, including front-room and back-room
• Lead internal audit planning and execution using risk- and budget-based approaches, ensuring

🎯 Requirements

• Bachelor’s degree in a scientific, engineering, or technical discipline.
• At least 8 years of experience in Quality and/or Compliance within the pharmaceutical industry.
• At least 5 years of experience managing inspections and audits, including regulatory and/or
• At least 3 years of experience leading or managing quality system elements, such as
• Strong knowledge of FDA and international regulatory requirements applicable to pharmaceutical
• Working knowledge of drug or device cGMP requirements and ISO 13485, along with familiarity with

🎁 Benefits

• Annual salary range of $100,000–$115,000, depending on experience and qualifications.
• Eligibility for a performance-based bonus.
• Comprehensive employee benefits package.
• Market-based compensation and commitment to equitable and fair pay practices.
• Primarily on-site work environment in Fort Collins, Colorado.
• Opportunities to lead a high-impact Quality Compliance function within a highly regulated