Require young and skilled employees with experience in Parenteral/ Injectable formulations for our manufacturing facility. Equipment Qualification & Validation/ IPQA
Having IPQA experience in manufacturing & Packing of OSD. Proven experience in IPQA or a related field, with a strong understanding of pharmaceutical regulations and standards.
Develop and review Data Management procedures for clinical trials with sponsor companies and other departments; Establish/negotiate Data Management project timelines and ensure Data Management milestones are met