Job Description:

  • Analyzing RM/In-Process/FPs/PM
  • Analysis of Stability samples, preparing data for regulatory submissions
  • Maintaining Proper documentation like Instrument Logs of Analysis done in accordance with GLP, cGMP guideline, Raw Data, etc
  • Well versed with the Lims Software & Empower 3.
  • Exposure of Regulatory Audits like US FDA, MHRA, and WHO and many customer audits
  • Updating all equipment logs and registers

Location: Visakhapatnam

Qualification: B.Pharma, M.Pharma/MS/M.Sc – Chem/BioChem

Experience: 2-7 Yrs

Salary: Negotiable

Contact Details:

APPLY NOW

LEAVE A REPLY

Please enter your comment!
Please enter your name here