Science & ResearchOn site
Compliance Specialist III
CatalentKansas City, MO
Posted Oct 16, 2026
What you’d do
Support preparation, review, and approval of technical and regulatory documentation, ensuring cGMP compliance. Author and approve protocols, reports, SOPs, and batch records for pharmaceutical operations. Full time. Found on the employer's careers page on Oct 21, 2026. Apply through the link.
You’ll need
- Bachelor's Degree or HS diploma with equivalent regulated-industry experience
- cGMP compliance knowledge
- Experience authoring and reviewing technical documents
- Batch record and SOP drafting
- Attention to detail and ability to meet deadlines
Our summary of the listing. The full listing has the details.