Quality Control (QC) Executive/Sr.
Executive (Pharma Formulations OSD)
Location: Visakhapatnam
Experience: 2-7 yrs
Qualification: M.Sc / B.Pharm /
M.Pharm
Job Description:
Responsible for the Analysis and
Review of Raw Material, In-Process, Finished products, packing.
Responsible for Stability Samples
Analysis and preparation of summary sheets and regulatory submission.
Proper Documentation like Raw data,
Instruments logs of the analysis carried out in compliance with GLP, cGMP
guidelines.
Well versed with the Lims
Software& Empower 3.
Participated in Regulatory Audits
like US FDA, MHRA,, and WHO and many customer audits
Updating all equipment logs and
registers
Required Candidate profile
Quality Control (QC) with minimum 2-7
years experience preferably Pharama Formulations (OSD)
Having experince of Analysis, RM,
Packing Material, Finished Products, and Stability
Documentation
Exposure to Regulatory Audits and
cGMP
JOIN WITH US - FOR REGULAR UPDATES
No comments:
Post a Comment