initiatives aligned with site objectives and MedPharm’s growth as a CDMO. Partner with higher ups to translate short- and long... requirements and adherence to MedPharm quality standards and client commitments. Collaborate closely with MS&T, Quality...
Position Summary – The Cleaning Validation Engineer oversees the development, maintenance, and governance of MedPharm..., ensuring compliance with cGMP, FDA, and global regulatory requirements. Supporting MedPharm’s growth into a late-stage...
in support of MedPharm US sites, including the GMP pharmaceutical manufacturing site and the Research and Development laboratory... site. This manager position represents MedPharm on all regulatory matters related to EH&S across both locations. The EHS...
for laboratory and facility equipment across MedPharm’s Durham sites, including the Stirrup Creek GMP manufacturing facility and the...
a critical role in leading and executing client programs across MedPharm’s end-to-end CDMO services. This client-facing position... and client programs. · Lead project team activities and ensure alignment between MedPharm and client expectations. · Provide...
to MedPharm’s Procedures. Contribute to the preparation and review of SOPs and Forms where applicable. Where applicable... studies that a study director would be leading are pre-clinical in vitro studies conducted at the MedPharm Research...
in leading and executing client programs across MedPharm’s end-to-end CDMO services. This client-facing position ensures seamless... project knowledge and fostering strong relationships. Lead project team activities and ensure alignment between MedPharm...
Job Summary The Sr. Process Engineer/Senior Scientist will lead late-stage development activities for topical and liquid oral pharmaceutical products, including process scale-up, technology transfer, commercial process validation, and manu...
Position Overview The Sr. Director, Quality Control and Analytical Development provides strategic, technical, and operational leadership to the site Quality Control and Analytical Development Laboratories. This role proactively leads impl...
Position Summary The Scientist III/ Sr. Scientist is responsible for developing and validating analytical methods to support drug formulation development in a GMP-compliant laboratory. This role involves performing validations, stability ...