Sr. Director, Quality Operations

Our Work Matters

At Kindeva we make products that save lives, ensuring better health and well‑wellbeing for patients around the world.

Sr. Director of Quality Operations is responsible for leading all Quality Assurance (QA) functions in our St. Louis GMP manufacturing facility focused on sterile fill‑finish drug products and combination products. The role ensures full compliance with regulatory requirements while fostering a culture of quality, operational excellence, and inspection readiness.

• Provide overall leadership for the site Quality operations organization
• Act as a key member of the site leadership team, ensuring alignment of quality with manufacturing, engineering, supply chain, and regulatory functions
• Drive a culture of compliance, data integrity, and continuous improvement across the site
• Represent the site in global quality governance to ensure harmonization of systems and processes
• Ensure timely batch release decisions in alignment with cGMPs, regulatory standards, and client expectations
• Direct preparation for and manage regulatory inspections and client audits
• Provide oversight of deviations, CAPAs, change controls, and risk management
• Ensure compliance with combination product quality requirements (drug‑device interface)
• Ensure site operations comply with FDA, EMA, ICH, ISO 13485, and other global requirements
• Serve as the primary contact for regulatory inspections and audits
• Stay ahead of evolving regulations and implement proactive compliance strategies
• Lead, develop, and mentor QA teams to build a high‑performing organization
• Establish clear roles, career pathways, and succession planning for Quality leadership
• Promote collaboration, open communication, and accountability across all functions

• Bachelor’s degree in Life Sciences, Pharmacy, Engineering, or related field (advanced degree preferred)
• 15+ years of progressive GMP Quality experience, including at least 8 years in sterile drug product manufacturing
• Combination product experience required
• Demonstrated success in leading Quality organizations and hosting regulatory inspections

• Expert knowledge of cGMPs, Annex 1, ISO 13485, ICH guidelines, and combination product regulations
• Strong leadership, influencing, and organizational skills
• Proven ability to implement process improvements and lead through change
• Excellent problem‑solving and decision‑making capabilities
• High ethical standards and professional integrity

• Position requires vision acuity testing and onsite attendance—this position cannot be performed on a remote or telecommute basis
• The candidate must be able to complete aseptic gowning qualification and work in a Grade A/B classified area
• It is required to sit, stand, and occasionally lift items (up to ~25 pounds)
• Must have the ability to simultaneously multi‑task across multiple capabilities and functions and handle multiple competing priorities and requirements, including responding to frequent e‑mail and phone communications, and attending multiple meetings and conference calls

California residents should review our Notice for California Employees and Applicants before applying.

Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.