Junior Officer-QC
Sun Pharmaceuticals, Inc
1. Sampling of raw material, Packaging material & distribution of samples.
2. Cleaning of Sampling Booth.
3. Receipt and verification of Lab Chemical and Glassware.
4. Calibration of balance as per current SOPs.
5. Proper destruction of samples after analysis as per respective SOPs.
6. To participate on internal and external Audits.
7. Ensure compliance to cGMP and safety standards in the QC laboratory.
8. To handle the documents of sampling of raw material.
9. Archival of all type of records related to Quality control department.
10. Recording Analytical data in SAP/LIMS & preparation of Certificate of analysis.
11. Handling of laboratory documents manual and software in QC and QA (retrieval/submission/receiving with QA and others departments).
12. Any other Assignment given by Lab in charge/ Manager Quality Control from time to time.
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
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