SALIENT RESPONSIBILITES INCLUDES:

· Develop method for stability indicating assay, related compounds and drug product dissolution analysis

· Execute routine analytical work on a wide range of projects in product development.

· Support formulators in their formulation & process development, conducting stability, manufacturing support and regulatory filings.

· Conduct wet-chemical tests, titration and other common analytical methods such as utilizing HPLC.

· Generate and collate the data, perform required calculations, record experiments in a laboratory notebook following GMP / GLP practices.

· Calibrate and maintain analytical instruments and recommend improvements when necessary.

· Write and follow SOPs, methods of analysis, and potential validation plans.

· Read and understand suggested literature and correlate the data and preparation of the final report.

· Execute leadership qualities / skills to support an excellent pool of product development scientist

· Observe safe laboratory practices throughout the laboratory, and maintain good housekeeping in the office area

BASIC QUALIFICATIONS

· PhD in chemistry, pharmaceutical chemistry, pharmaceutics, biochemistry or related field with up to 5 years of experience (preferably in method development, stability evaluation, problem solving etc.,)

· Experience with HPLC, related spectroscopy and other common analytical methods.


ADDITIONAL QUALIFICATIONS

· Computer skills must include Microsoft Office Products Suite, e.g., Word, Excel. Computer database skills are desirable.

· Excellent written and oral communication skills

· Ability to pay attention to detail, including good documentation skills is required

· Understanding of cGMP and GLP