Job Role:
Quality control analysis of the Finished product, verify the quality of the product, carry out sampling, quality control analysis, prepare reagents, adjust SOP from main lab (india to Brazil lab), perform the validation analysis following ANVISA RDC 166, method transfers.
EXP : 2 to 3 years of experience in pharmaceutical laboratories and production, control and auditing of medicines, comprehensive knowledge of local regulations.
Responsibilities:
* Carrying out tests, measurements and quality control tests of the products, in accordance with the norms, designs and established standards
* apply Current Good Laboratory Practices and standard operating procedures designed by the company for your role
* Carry out the analysis of the finished product and other samples as appropriate
* Perform calibrations of all instruments in the quality control department
* Apply RDC#166 analytical methods and other requirements as appropriate
* Write validation protocols, reports and routine tests.
* Knowledge and management of test analysis, impurities, residual solvents, dissolution and other physical parameters as appropriate
* Knowledge and management of cGMP, cGLP, cGxP concepts of computerized systems
* Preparation of the Product Control Plan.
* Issuance of periodic, management or audit reports as required for both internal and external clients