Headline

Immediate Joiner | 3 Years PRC (Product Registration Cell) Experience at Cipla limited | SAP S4/HANA QM | PG Diploma in Drug Regulatory affairs.

About

Pharmaceutical professional with 3 years of QA/QC Documentation experience at Cipla, specializing in Change Control, Audit Support, Regulatory Documentation, PRC, and GMP compliance. Trained in SAP S/4HANA Quality Management (QM) with knowledge of inspection lot processing, quality notifications, results recording, and QM integration with MM & PP modules. Currently pursuing Diploma in Drug Regulatory Affairs from IPER Pune to strengthen expertise in regulatory submissions and compliance frameworks. Passionate about bridging pharmaceutical domain knowledge with SAP-driven digital transformation and regulatory excellence. Open to opportunities in SAP QM, Regulatory Affairs, Quality Assurance, and SAP-enabled pharma roles.

Location

India

Work experience

Senior Executive at Cipla, Oct 2022 - Sep 2025 · 3 yrs, Indore, Madhya Pradesh, India, Change Control ▪ QA/QC documentation lifecycle ▪ Regulatory submissions & responses ▪ Audit coordination (Internal, External, Regulatory) ▪ GMP, GDP & Data Integrity compliance

Education

D.D.R.A, I.P.E.R

Bachelor of Pharmacy, Sri Aurobindo Institute of Pharmacy