Quality Control Manager, Non-Sterile

Requirements

• Bachelor's degree in Chemistry, Biology, Pharmacy, Quality Management, Engineering, or related discipline
• 3+ years of experience in quality control or quality assurance, ideally in a non-sterile compounding or pharmaceutical manufacturing environment
• Strong working knowledge of USP <795> and applicable cGMP standards
• Experience in a regulated environment (FDA 21 CFR 210/211 experience a plus)
• Proven leadership skills with the ability to coach and develop quality and production personnel
• Exceptional interpersonal, verbal, and written communication skills
• Strong proficiency with Microsoft Office Suite (Word, Excel, PowerPoint, Outlook); MRP system experience preferred
• Ability to manage multiple priorities, work independently, and maintain high attention to detail
• Strong technical writing skills for SOPs, protocols, and reports
• Familiarity with quality metrics, root cause analysis, and statistical quality control methods
• Proven ability to build and maintain strong cross-functional partnerships, paired with clear, effective communication across all levels of the organization

Benefits

• Competitive salary & equity compensation for full-time roles
• Unlimited PTO and company holidays
• Comprehensive health benefits including medical, dental & vision, and parental leave
• Employee Stock Purchase Program (ESPP)
• 401k benefits with employer matching contribution