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...
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...
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...
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 ...
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 ...
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...