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Torrent Pharmaceuticals
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Walk in Interviews For Bioanalytical & ADL @ Gandhinagar, Gujarat

Walk in Interviews For Bioanalytical & ADL @ Gandhinagar, Gujarat

Torrent Pharmaceuticals

3 - 8 years

5 - 15 Lacs

gandhinagar

Posted:1 hour ago| Platform:

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Skills Required

routine analysis analytical method validation analytical method development osd nmr oncology alternative vendor development gc stability protocol hplc

Work Mode

Work from Office

Job Type

Full Time

Job Description

Analytical Development Laboratory

Position: Executive

Experience: 3-8 years

Qualification: M.Sc. / M.Pharm.

Job Responsibilities:

HPLC/GC/IC method development, feasibility, verification, equivalency, validation of API for complex OSD products, oncology products, topical products having exposure to regulated, Semi Regulated & India markets
Comparative evaluation of methods with alternative vendor methods versus existing primary vendor and regulatory impact analysis
Dissolution development, comparative dissolution, multimedia dissolution and statistical evaluation and report preparation
Good understanding and hands on experience of analytical instruments like HPLC, IC, GC etc.
NI/GI & NDSRI' with LCMS/GCMS expertise, Solid state characterization and API sameness study
Hands on experience on In-vitro Studies, E&L, Solid State characterization, IVPT/IVRT, Impurity characterization, sameness study
Well versed with USP/EP/BP/JP and various current regulatory guidelines (ICH/EMEA/FDA)
Perform maintenance and calibration of lab instruments / equipment.

Bioanalytical

Position: Executive

Experience: 3-8 years

Qualification: M.Sc. / M.Pharm.

Job Responsibilities:

To develop and validate sensetive and rugged bioanalytical methods by using different extraction (i.e. SPE, LLE etc.) and quantitation (i.e. LCMS, HPLC) techniques for analysis of drug substances
to conduct study sample analysis by following pre-defined procedures with required accuracy.
to operate, maintain and calibrate instruments adhering to written SOPs.
to follow defined procedures and keep proper documentation of the performed procedures to maintain GLP compliance in the laboratory.

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