QA Officer-Reputed Pharma Industry-Hyderabad, Telangana, India-4LPA-Harshala
3 weeks ago
JOB DETAILS
1) Knowledge of GMP and QMS standards
2) Knowledge of regulatory affairs procedures
3) Knowledge of documentation
4) To Check the in process inspection of semi finished and finished product
5) To document all the reports.
6) Maintain discipline in controlled areas
7) To analyze the non conforming product & make the action plan for the same.
8) To audit the process parameters in Clean room & Controlled areas
9) Documentation as per ISO : 13485, WHO, GMP & CE Marking
10) Handling, maintaining the documents of market complaints
FUNCTIONAL AREA
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