QC Chemist III, Raw Materials
MedPharmDurham, North Carolina, United States
Posted October 28, 2025
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 Quality Control Raw Materials Chemist III will ensure that testing, data review, and documentation are compliant with GMP regulations and internal procedures. This role operates within a GMP environment for a Quality Control CDMO, requiring strong communication and problem-solving skills. The position will also oversee the implementation of new instruments and the training of analysts.
Requirements
- Perform testing of raw materials, packaging components, and other samples.
- Author or act as author for lab investigations, analytical testing methods, deviations, protocols and SOPs for raw materials and raw material instrumentation.
- Provide technical support to the laboratory for method and instrument troubleshooting.
- Lead the Raw Materials laboratory implementation project.
- Train other analysts for raw materials testing.
- Schedule the QC laboratory Raw Materials workload.
- Monitor laboratory and data review activities.
- Oversee review of QC Raw Material data.
- Interact with third-party laboratories for microbial and analytical testing.
- Generate and/or review shipping paperwork.
- Create purchase requisitions for lab supplies.
- Perform weekly laboratory audit inspections.
- Perform sampling of raw materials.
- Review third party laboratory investigations and protocols.
