Stability Coordinator
MedPharm LtdDurham, North Carolina, United States
Posted January 21, 2026
Full Time
About the Company
MedPharm Ltd is a leading CDMO specializing in the development and manufacturing of topical and transepithelial therapies. With over two decades of experience, they offer comprehensive services including formulation development, clinical trial supply manufacture, and high-potency capabilities. MedPharm stands out by combining cutting-edge research with deep regulatory expertise to deliver tailored solutions that ensure patient success worldwide.
Job Description
The Stability Coordinator will manage the Stability program for the QC/R&D laboratories, executing stability protocols, compiling stability reports, and trending data across the shelf-life of multiple products.
Requirements
- B.S with 4-6 years experience, or M.S with 2-3 years of experience
- 2-5 years ́ experience in a GMP laboratory setting in the pharmaceutical industry
- Experience managing a stability program
- Experience with Stability Software such as NovaTek, Scientek, SLIMS, etc.
- Good understanding of Ph. Eur/USP/NF, FDA Good Manufacturing Practices Regulations (GMP’s) and OSHA safety requirements.
Benefits
- Medical, dental, vision, and other benefits
