Sr Manager, Quality – BioAnalytical

Catalent•Kansas City, MO

1d•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. The role: 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.

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.