i. Experienced in independent instrumental analysis of raw material, in process samples, finished product and stability samples of pharmaceutical products. ii. Well versed in analysis of Tablets, capsules, liquids samples, for common test as Assay, Related substances, Dissolution and preservative content analysis as per controlled specification and method of analysis. iii. Should able to operate, calibrate and maintain instruments like HPLC, GC, Dissolution apparatus, UV and FTIR etc. iv. Experience of Empower, Lab solution software shall be recommended. v. Exposure to perform AMV or development shall be preferred. vi. Aware about on line & good documentation practices. vii. Should have knowledge of Data integrity and QMS. viii. Should able to maintain cGMP, safety throughout the activities done in the laboratory. Calibrate and maintain instruments like HPLC, GC, Dissolution apparatus, UV and FTIR
i. Experienced in independent instrumental analysis of raw material, in process samples, finished product and stability samples of pharmaceutical products. ii. Well versed in analysis of Tablets, capsules, liquids samples, for common test as Assay, Related substances, Dissolution and preservative content analysis as per controlled specification and method of analysis. iii. Should able to operate, calibrate and maintain instruments like HPLC, GC, Dissolution apparatus, UV and FTIR etc. iv. Experience of Empower, Lab solution software shall be recommended. v. Exposure to perform AMV or development shall be preferred. vi. Aware about on line & good documentation practices. vii. Should have knowledge of Data integrity and QMS. viii. Should able to maintain cGMP, safety throughout the activities done in the laboratory. Calibrate and maintain instruments like HPLC, GC, Dissolution apparatus, UV and FTIR Location : - Mira Road,Kandivali
1. Should have performed instrumental analysis of stability samples, Intermediate and finished products by HPLC, UV Spectroscopy, Dissolution Test apparatus, LCMS, Particle Size Analyser and FTIR as per controlled specification and method of analysis. 2. Should able to calibrate and maintain instruments like HPLC, GC, LCMS, Dissolution apparatus UV and FTIR. 3. Should be able to performed method development and method validation on HPLC, GC and LCMS. 4. Should have well versed with ICH guideline of Stability and Method Validation. 5. Should have knowledge of Data integrity and QMS. 6. Should able to maintain cGMP throughout the activities done in the laboratory