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...
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...
Position Summary – The Chemist III/Sr. Chemist Raw Materials ensures that testing, data review, and documentation is compliant with GMP regulations, internal procedures, and applicable compendial requirements. The position will be operating...
Position Summary Responsible for performing regular predictive and preventive maintenance;responding to unplanned equipment failures;planning and carrying out all other repairs, projects and company initiatives;and addressing needed or...
Position Summary – The QC Chemist II position performs testing using a variety of analytical techniques. The successful candidate ensures that Testing and Documentation is compliant with GMP regulations and internal procedures. The position...
Position Summary – The Quality Control Raw Materials Chemist I performs testing using a variety of analytical techniques. The successful candidate ensures that Testing and Documentation is compliant with GMP regulations and internal procedu...
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...