1. Analysis of assigned samples
2. GMP, EHS and procedural compliance
3. Analytical data review
b. To coordinate for timely analysis of raw material, release and stability samples as per correct specification and accuracy of data
c. To coordinate with external lab for characterization study and Elemental impurities.
d. To use and maintain the equipment as per requirements for physical testing of stability samples.
e. Address plant queries in time of crisis
f. Provide extended Analytical support to global regions.
g. Maintaining laboratory notebooks as designated by supervisor
h. Preparation of technical documents such as analytical reports, protocols, Technical justifications etc.
i. Participate in handling and resolution of laboratory non-conformances with related documentation
j. Implement corrective actions as required.
b. Review of calibration records as required.
c. Participate in internal and external audits as required
d. Preparation of SOPs, test methods, etc.
e. Coordinate for instrument calibration as required
f. Participate in training sessions and inform supervisor of training requirements
k. Review of recommendation, technical feedback etc.
l. Preparation of technical documents such as analytical reports, test methods, etc.
Minimum Masters in Chemistry/Pharmaceutical sciences or similar technical discipline
Qualification : M.Sc, M.Pharm
Location : Maharashtra-Greater Mumbai
Industry Type : Pharma
Functional Area : R&D
End Date : 25th December, 2018
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