Job Summary
We are seeking an associate for the Quality team responsible for conducting sampling and analysis of packaging and raw material samples. The role involves ensuring accuracy in documentation, adherence to safety procedures, reporting discrepancies, and maintaining lab safety.
Responsibilities
- To conduct analysis of IP/FP/Stability/PV samples as allotted by the Group leader.
- Responsible for SAP activities and ROA preparation.
- Reviewing analytical records and raw data against Specification and STP.
- To ensure that the documentation done is online and error free.
- To ensure the correctness of the document before submitting it for the review of Group Leader.
- To ensure that only calibrated instruments/ equipment are used for analysis.
- To ensure that only valid reference standards are used for analysis.
- To ensure that the SOP / STP / reference standards are placed at their designated place after completion of the analysis.
- To ensure that the instruments / equipment are used with utmost care and as instructed in the relevant SOP.
- To ensure that the instruments / equipment are cleaned before & after analysis.
- To ensure that all Safety precautions and procedures are followed while conducting analysis.
- To report discrepancies in procedures / products to the group leader in time.
- To report Incidents / OOS / OOT in time to the Group leader.
- Any other responsibility assigned by Group Leader.
- Responsible for Lab Safety and follow the JSA.
- Ensure to use the proper PPE at workplace.
- To charge and withdrawal the stability sample as per interval.
- Stability study creation in SAP.
- Review the stability protocol.
- Ensuring timely completion of all the training assigned to self
Educational qualification: B. Pharma/B.Sc/M.Sc
Minimum work experience: 2 to 5 years of experience in a laboratory setting, preferably in the pharmaceutical or related industry