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Job Type

Full Time

Job Description

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Role & responsibilities

·       Independently design, plan and execute moderate to complex analytical method development experiments.

·       Analyse the data, communicate results to clients and write technical protocols and reports.

·       Prepare method protocols, & technical reports for characterization of analytical methods based on separation techniques (HPLC, UPLC, GC), Spectro-analytical technique (Ultraviolet-Visible Spectrophotometry) and dissolution testing.

·       Experience in developing pharmaceutical small molecules analytical chemistry methods for dissolution muti-media screening and analyzing data using compendial methods.

·       Exposure in stability testing as per ICH guidelines.


Preferred candidate profile

·       Experience in drug product analytical development within a commercial organization.

·       Good knowledge of three main pharmacopoeias (Japanese; JP, US; USP and European Ph. Eur,) and ICH guidelines related to method development and validation.

·       Excellent communication (oral and written), attention to detail, effective problem solving and decision-making skills.

·       Ability to work independently and as part of a team with internal and external clients, self-motivation, adaptability, and a positive attitude.

·       Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.


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