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Catalent’s Kansas City facility seeks a Compliance Specialist II to support cGMP compliance across our manufacturing operations. The role focuses on reviewing and drafting batch records, SOPs, and ensuring documentation meets regulatory standards. It is an on-site position with a Monday–Friday schedule in Kansas City, MO.
The ideal candidate will have a High School Diploma and GMP experience is preferred. Physical ability to lift up to 50 pounds is also noted.
About Site Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses.
We have an opportunity for a Compliance Specialist II to join our team. In this role, you will support cGMP business units to ensure a high level of compliance. You will work under the direct guidance of a supervisor to ensure all documentation meets regulatory requirements, good manufacturing practices (cGMP), and standard operating procedures (SOPs). This position is key to maintaining quality and compliance across our operations.
Shift: Monday-Friday; 8:00am-5:00pm
Location: Kansas City, MO
100% Onsite
The Candidate
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.
Catalent is an Equal Opportunity Employer, including disability and veterans.