Chemist (FDA Regulation)-HPS-784

Job Description:

1.Quality Control functions in Pharmaceutical manufacturing facility.

2.Testing and analysis of various raw materials and finished products.

3.Must be versatile with documentation as per GMP (Good Manufacturing Practice) including preparation of BMR, Analytical documents and other relevant statutory procedures.

4. Should have hands-on experience with statutory compliances, analytical instruments, with good knowledge of laboratory health and safety standard.

5.The person must have very sharp analytical acumen and must possess excellent knowledge of chemistry along with analytical techniques and research skills.

6.Needs to be capable in taking independent decisions relating to QC lab work.

• Preference

FDA approved chemist who is well versed with local FDA regulations.