عمليات بحث ذات صلة

Cipla in Saudi Arabia is seeking an experienced Regulatory Affairs professional to review dossiers, coordinate with Cipla India RA, and manage submissions to the SFDA. The role involves ensuring complete applications, coordinating with authorities, and overseeing labeling, translations, and post-approval activities.The ideal candidate will have 9–10 years...

Review new/renewal dossiers and variations, identify gaps, and share observations with Cipla India RA. Ensure completeness of application, pricing forms, deficiency responses, and final eCTD sequences. Upload sequences on SDR portal with India RA and share back the submitted package. Continuously monitor SDR portal, update India RA on SFDA status changes,...

Cipla Saudi Site seeks an experienced Quality Control professional to oversee QC activities, instrument qualification, and regulatory readiness across cGMP-compliant operations.You will provide analytical troubleshooting for OOS/OOT, support technology transfer, and ensure ALCOA++ data integrity while preparing SOPs, protocols, and qualification reports for...

Support Quality Control for the Cipla Saudi Site and ensure timely execution of QC Laboratory Qualifications/Validation activities, Procurement of instruments and Equipment’s and area qualification. Provide strong scientific and analytical troubleshooting support for OOS/OOT, atypical results, laboratory deviations, impurity evaluations and regulatory...

Job Purpose: Ensuring Timely execution of Green field/ brown field projects to facilitate smooth and safe site operations without impacting Cost and Quality norms. Key Accountabilities: Project charter / Concept note Proven working experience as a lead Project Engineer in Pharmaceutical (API) Green field & brown field projects Assures technical accuracy...