Job highlights

- Review batch manufacturing and packaging records (BMR / BPR)
- Proficient in analytical instrumentation and documentation practices
- We are looking for a skilled and proactive QA / QC skilled with 2 5 years of experience to join our quality team
- 2 5 years of hands-on experience in analytical techniques and instruments in a regulated environment

? : ? ? We are looking for a skilled and proactive QA/QC professional with 2 5 years of experience to join our quality team. The candidate will be responsible for executing and overseeing quality assurance and quality control activities in compliance with regulatory and company standards. ?

? Key Responsibilities: ?

? Quality Control?

- ? Perform analytical testing of raw materials, in-process samples, and finished products. ?
- ? Operate, calibrate, and troubleshoot instruments such as HPLC, UV-Vis, GC, FTIR, and KF. ?
- ? Prepare and review analytical documentation including test reports, COAs, and calibration records. ?
- ? Guide and Mentor QC Executives / Trainees for analytical testing

? Quality Assurance?

- ? Review batch manufacturing and packaging records (BMR/BPR). ?
- ? Investigate and document deviations, OOS, OOT, and implement CAPA with timely closure. ?




- ? Review and manage controlled documents (SOPs, protocols, forms) issuance, retrieval, and archival. ?
- ? Perform internal audits; support regulatory audits (e. g. , WHO, ISO, etc. ). ?
- ? Oversee GMP, GLP, hygiene training for production and QA/QC staff. ?
- ? Coordinate stability studies, analyze trends, and maintain stability protocols and logs. ?
- ? Ensure data integrity in documentation and electronic systems. ?
- ? Participate in risk assessment and mitigation for quality events. ?
- ? Support technology transfer, scale-up, and cross-functional quality activities. ?
- ? Evaluate and audit vendors and suppliers as part of QA oversight. ?

? Requirements: ?

- ? 2 5 years of hands-on experience in analytical techniques and instruments in a regulated environment. ?
- ? Strong understanding of cGMP, GLP, and ICH regulatory requirements. ?
- ? Proficient in analytical instrumentation and documentation practices. ?
- ? Ability to handle audits, deviations, and quality systems independently. ?
- ? Excellent communication, collaboration and organizational skills. ?
- ? Team player with attention to detail and accuracy. ?

📌 QA/QC Executive / Senior Executive Mana Pharma (Hyderabad)
🏢 Mana Pharma
📍 Hyderabad