Qc Chemist Fda Approved

2 weeks ago

Mumbai, India SV Placement Full time

5 - 8 years
- Vasai, Mumbai
- 6,00,000 - 9,00,000

Modify and validate analytical procedures to meet QC’s needs. Support design and development of experimental protocols, SOP’s, etc., consistent with cGMP/GLP. Participate in special projects and department meetings.

**Role & Responsibilities**:

- Responsible for overall incoming, in process/Finished goods inspection activities carried out at QC Inspect goods receipt cum inspection report for raw material
- Maintain master list of all inspection, measuring and test equipment
- Responsible for calibration of inspection, measuring and test equipment
- Responsible for prepare material rejection report in case of raw material /FG rejection on weekly/Monthly basis
- Maintain the records of incoming ,in process/final inspection
- Responsible for identifying the rejected lot in consultation with Manager(QC) Ensure the instruments used for inspection are duly calibrated and status is identified
- Responsible for in-house calibration of equipment according to the work instruction/Equipment manual
- Opening- 1- Employment Type- Full Time, Permanent- Industry Type- Pharmaceutical & Life Sciences- Functional Area- Quality Assurance- Education- B.Sc, B.Pharma, M.Pharma, M.Sc(Science)- Key Skills- FDA
- Quality Control
- QC
- Raw Material Inspection
- Method Validation
- GMP
- GC
- HPLC

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