Quality Compliance Professional - Production
Olon USAOhio, United States
Posted March 11, 2026
Full Time
About the Company
Olon USA is a US-based contract development and manufacturing organization (CDMO) that delivers end-to-end solutions for the pharmaceutical and biotech sectors. Leveraging more than 25 years of expertise in synthetic chemistry, analytical chemistry, and process engineering, the company specializes in the development, scale-up, and GMP-grade manufacturing of active pharmaceutical ingredients (APIs) and performance materials. Its integrated platform—supported by its recent acquisition of Ricerca Biosciences’ Chemical Division—offers first-time scale-ups, robust process optimization, and reliable, cost-effective production for both branded and generic drug substances. With a proven track record of on-time delivery and uncompromising quality, Olon USA provides comprehensive CRO services, GMP/GLP compliance, and end-to-end support from early development through commercial distribution.
Job Description
Ensure GMP compliance in API Production areas by reviewing batch records, communicating with facility maintenance team members, participating in deviation investigations and risk assessments, and collaborating in the drafting of SOP and MBR.
Requirements
- Must have direct experience with Quality Assurance within a regulated industry (USDA, FDA, ISO etc)
- Understands and applies comprehensive knowledge of quality and GMP principles and maintains current understanding of global GMP drug manufacturing regulations
- BA/BS degree in Science related field or manufacturing is highly preferred, however, strong experience in Quality Assurance in a regulated industry may be considered in absence of a 4 year degree
