1) To perform analysis of analytical method validation, method verification and technology transfer of Raw Materials, tablets and capsules formulation. 2) To operate sophisticated instruments like HPLC, GC, UV, FTIR, Dissolution etc. 3) To have knowledge on the current GMP with respect to pharmacopeial guidelines like ICH, USP & WHO. 4) Shall have knowledge of data integrity requirement, good laboratory practices and good documentation practices. 5) To complete analytical activities on time and right at first time. 6) To adhere with safety norms and policies defined by the organisation. 7) To have good communication skill and able to read, write and speak English. 8) To have ability of data analysis i.e. statistical measurement techniques used to evaluate and interpret data. 9) Preferably shall have exposure of audits like USFDA, WHO, MHRA etc. 10) Shall have knowledge of regulatory requirements of analytical techniques.
