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

11) To conduct and manage development of packaging material

12) To manage the testing of raw material, packing material and finished goods

13) Review of documents and records
FUNCTIONAL AREA
Quality Assurance, QC, QA, QA executive, Pharma QC, Pharma QA. Quality check, GMP, QMS, Inspection, Pharmaceutical QA, Medicine ...