3 - 10 Years
a. Develops and initiates standards and methods for
inspection, testing, and evaluationof the products
b. Establishes program to evaluate precision and accuracy
of production equipment and testing, measurement
and analytical equipment and facilities.
c. Develops and implements methods and procedures for disposition
of discrepant material and devises methods to assess cost and responsibility.
d. Maintain the Material Review Area to ensure that all products are distributed in a timely manner.
e. Suggests and implements changes in working conditions and
use of equipment to increase safety and efficiency of works,
department, or work crew.
f. Analyses and resolves work problems, or assists
workers in solving work problems.
g. Initiates or suggests plans to motivate workers to achieve work goals.
h. Maintains time and production records. Proper documentation
of Quality/QC, ISO, CE & FDA.
i. Training to all department regarding quality/SOP ®ulatory affairs
j. Maintaining of BMR records as per FDA regulations
|Salary||2 Lac 25 Thousand To 3 Lac 50 Thousand P.A.|
|Industry||Medical / Health Care / Hospitals|
|Work Experience||3 - 10 Years|
|Qualification||Diploma, B.Pharma, B.Sc, B.Tech/B.E, M.Pharma, M.Sc, M.Tech|
|Contact Person||Mr. G.K. Patel|