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 ...
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...
Scientist II, Analytical R&D Position Summary The Scientist II, Analytical R&D, is responsible for developing and validating analytical methods to support drug formulation development in a GMP-compliant laboratory under supervision. Thi...
This position contributes to the company success by providing calibration and instrumentation oversight for lab equipment through executing scheduled calibrations and preventative / corrective maintenance in compliance with GMP regulations ...
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 ...
Job Purpose: The IT Operations Intern will support MedPharm’s Information Technology department during a 10–12 week... to MedPharm’s technology environment while developing practical skills in a regulated life-sciences setting. Summary of Key...
Position Summary The Manufacturing Operator is responsible for executing a wide range of operations in a cGMP-compliant biopharmaceutical manufacturing environment. This role involves operating, maintaining, and troubleshooting production...
initiatives aligned with site objectives and MedPharm’s growth as a CDMO. Partner with senior leadership to translate short... with regulatory requirements and adherence to MedPharm’s quality standards (SOPs), and client commitments. Collaborate closely...