Hetero is one of worlds leading producers of key Active Pharmaceutical Ingredients (APIs) and generic formulations with presence in 140 countries and backed by 30 years of experience in the pharma sector.
Polymed, we believe that innovation is the cornerstone of ensuring access to the best healthcare solutions for all. Prepare and maintain design and technical documentation in compliance with ISO 13485 and regulatory requirements; support audits and submissions
Zenotech Labs invites QA and QC professionals to manage IPQA activities for injectables, oversee packaging operations, and ensure BMR/BPR review with cGMP/GDP compliance.
To perform the calibration of QC instruments as per calibration schedule. Overall upkeep of respective working bench as well as of the section as per GLP.
The candidate must be capable of analyzing raw materials, finished products, and stability samples. Knowledge of AMV and QAMS will be given preference.
Support in sampling and testing of raw materials, finished products and stability analysis. Documentation: Maintaining accurate, real-time records of all analysis as per cGMP and GLP guidelines.