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Walk- In - Drive Method Validation/ FML AQA- MSN Laboratories, Formulation Unit - V, RK Puram, Hyderabad on Saturday
ASRD Responsibilities :
1) Execution of Analytical Method validations for drug products for various markets.
2) Execution of DPDM Method validations for drug products.
3) Analytical method transfers to the Quality control labs.
4) Performing the calibrations of the analytical instruments.
5) Preparation & review of Analytical Method validations protocols and reports.
6) Responsible for cGLP, documentation and implementation of departmental quality systems.
AQA Responsibilities :
1. Preparation and Review of AQA SOPs.
2. Review of validation protocols & reports.
3. Review of completed laboratory control records.
4. Making sure that effective systems are used for calibrating critical instruments.
5. Review of changes that potentially impact product quality.
6. Review of incidents / deviations and ensuring that they are resolved and closed with adequate CAPA.
7. Performing general system reviews.
8. Ensuring the implementation of continuous training program to departmental personnel as per established procedures.
9. Issue and Retrieval of Formats, Protocols, Reports and Relevant records.
10. Responsible for archival of GMP documents.
Interview Date :
Department : Formulation Analytical Research & Development(FAR&D)
Experience : 1 to 6 Years
Qualification : M. Pharmacy / M.Sc. / B Pharm
Position: Executive
Work Location : MSNF Unit -V, RK Puram, Hyderabad
Interview Venue Details : MSNF Unit -V, RK Puram, Hyderabad
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