About the Company:
766 million lives were moved by Novartis medications in 2021, and keeping in mind that we're pleased with this, we realize there is a lot more we could do to help improve and expand individuals' lives.
We accept new bits of knowledge, viewpoints and historic arrangements can be found at the crossing point of clinical science and advanced development. That a different, impartial and comprehensive climate moves better approaches for working.
We accept our true capacity can flourish and fill in an unbossed culture supported by uprightness, interest and adaptability. Furthermore, we can reexamine what's conceivable, when we team up with fortitude to forcefully and aggressively tackle the world's hardest clinical difficulties. Since the most serious endanger throughout everyday life, is the gamble of never trying!
Envision what you could do here at Novartis!
Join our Novartis Organization: On the off chance that this job isn't reasonable to your experience or vocation objectives however you wish to remain associated with hear more about Novartis and our profession open doors, join the Novartis.
About the Job:
Experience: M. Pharma or Equivalent degree with 4+ years of experience from a reputed pharma
Required to have experience in QA/Regulatory or in manufacturing/ Medical devices
Required experience with QA compliance management, MAH review, learning and documentation management and stability, release support services.
Job Roles and Responsibility:
• Perform and convey Quality Tasks administrations on the side of item quality consistence and administrative work processes. Hold accounts in work process applications (like SAP, Winged serpent, Metro, TEDI and so on) to guarantee suitable execution of administration expectations.
• Perform Quarterly consistent moving and revealing. Play out the job of QA approver for client grievances designated to QSC through appointed activity.
• Liable for the extraction and information gathering of scientific, producing (counting deviations, grumblings, and change demands) and administrative information (HA responsibilities, varieties) in a predefined design.
• Follow-up and following of objection test accessibility from Nation Association (CO) to CMO (Agreement Assembling Association). Send specialized objections to CMO for examination. Perform questions in AQWA/Trackwise according to the SOP.
• Heighten administration related GxP and non-GxP issues and guarantee opportune examination and consistence with nearby and worldwide working techniques. Support carrying out help quality and cycle improvement projects, CAPA the board inside Quality Assistance Centers.
• Liable for gathering security information and reports for item related assessments. (e. g. consistence Examinations, divestitures, item moves, approval. And so forth. Support upkeep of APR/PQR plan.
• Play out a job of progress control facilitator or change work chief in change control the executives frameworks like TrackWise and Nimble. Oversee different kind of progress control like item stewardship/Organization Stewardship/Resource Stewardship.
