Executive
Actively Reviewing the ApplicationsLupin
India
Full-Time
On-site
Posted 3 weeks ago
•
Apply by July 30, 2026
Job Description
Job Description
Job Title_Executive _QA
Responsibilities
Minimum5 -8 years
Education
Graduation in Pharmacy
Masters in Chemistry
Competencies
Job Title_Executive _QA
Responsibilities
- To follow Good Laboratory Practices, Safety measures and good documentation practices and adherence to data integrity and data governance procedure while working.
- To follow Standard Operating Procedures and Standard Test Procedures while working with appropriate PPEs.
- To ensure user management and data security policy as laid down by the company
- Complete self-training on relevant SOPs and develop an understanding of the activities to be conducted prior to undertaking any task.
- To perform routine activities as per safety norms.
- Supervise compliance to all cGMP, cGxP, or any other regulatory requirements, including EH&S requirements.
- Complete self-training and monitor training of team members on the relevant SOPs.
- Report any quality concerns or suggestions for improvements to section heads, QC head and quality head.
- Execute and supervise all tasks and activities as per the applicable SOPs.
- Review and data processing of all QC analytical reports of all sections such as stability, finished products, raw materials, packaging materials, validation, and in-process as per specifications/STP, CTP, GTP etc. and with contemporaneous documentation.
- To ensure timely review of QC reports, standalone/server-based computer systems data and its audit trails. To ensure the integrity of data generated on these systems.
- To ensure proper investigation of OOS/OOT/OOC of samples/instruments/equipment results as per standard documents.
- To ensure cross verification of instrument calibration status label in laboratory.
- To conduct lab rounds to maintain good laboratory practices.
- To run query in Chromeleon software and ensure status of acquired samples.
- To review of single sequence prior to analysis.
- To ensure locking of sequences after review of data.
- To ensure lock of data pertaining to finished products, intermediate, raw material, working standards and calibration in SAP.
- To ensure the use of correct and current version of specification/TDS/protocol/CDS during analysis.
- To ensure validity of calibrators used during calibrations.
- To ensure preparation record of mobile phase, resolution solutions, volumetric solutions, reagent solutions, primary standards and analytical standards and usage within assigned validity periods.
- To ensure proper keeping of reference standards, working standards and test standards and calibration in SAP
- Regular participation in internal and external training programs.
- The above list is not exhaustive and may be assigned additional responsibilities from time to time.
- To ensure proper functioning and approval of IT-QA related activities
Minimum5 -8 years
Education
Graduation in Pharmacy
Masters in Chemistry
Competencies
Required Skills
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