Sr Manager, Quality – BioAnalytical

Catalent Pharma Solutions • Kansas City, MO

4d • Onsite

About The Position

Sr. Manager, Quality – BioAnalytical Position Summary Shift: Monday – Friday 8am-5pm 100% on-site Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. The Sr Manager, Quality – BioAnalytical will lead key Quality functions within our Biologics Analytical Services (BAS) group in Kansas City, MO. This leader will oversee teams responsible for ensuring high-quality analytical testing, data integrity, and compliance across biologics programs. The role combines people leadership, quality oversight, customer interaction, and continuous improvement within a fast‑growing biologics environment.

Requirements

• Doctorate Degree in STEM discipline with minimum of 6 years related experience
• Master's Degree in STEM discipline with minimum of 10 years related experience
• Bachelor's Degree in STEM discipline with minimum of 12 years related experience
• Leadership experience minimum of 5 years.
• Experienced in most aspects of drug development and life cycle support, and able to develop useful strategies and tactics to meet regulatory milestones.

Nice To Haves

• Experience leading a manufacturing site operation (e.g. Quality Operations, QC Operations, Manufacturing) is strongly preferred.
• Able to lead difficult discussions with customers and subordinates and drive the conversation to an acceptable resolution.

Responsibilities

• Responsible for all activities within one or more functional areas.
• Responsible for management of department Capex.
• Identify and support implementation of new technologies within the BAS Quality Department.
• Ensure employee training is executed according to defined training plans and maintain current training plans.
• Identify, maintain, and report functional KPIs to site management.
• Monitor and report project milestone completion and timing.
• Drive continuous improvement through leading cross function teams to address process improvement, system improvement, new regulations/expectations, new business needs, training improvements, and KPI performance improvements.

Benefits

• Competitive medical benefits and 401K
• 152 hours PTO + 8 Paid Holidays
• Dynamic, fast-paced work environment
• Opportunity to work on Continuous Improvement Processes
• Catalent offers rewarding opportunities to further your career!
• Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world.
• Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
• Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us.
• Join us in making a difference. personal initiative. dynamic pace. meaningful work.

What This Job Offers

• Job Type: Full-time
• Career Level: Manager
• Education Level: Ph.D. or professional degree