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QC Professional
Lee Pharma
posted 21d ago
Job Role Insights
Fixed timing
Key skills for the job
Job Description
- Implementation of Laboratory requirement and enhancements to increase efficiency and ensure
- Responsible for compliance with respect to Quality compliance requirements for Laboratory application softwares and Data Integrity
- Lead Regulatory audits and its
- Supporting of verification of audit trail generated by the respective application softwares of Laboratory
- Supporting to Date and time verification of laboratory
- Handling of Quality Management system like Laboratory Incident, Out of Specification, Deviation, CAPA, and Change
- Involving in the laboratory investigation and find out root cause for error and implemented CAPA to eliminate those
- Coordination with QA/CQA & RA for QMS
- Ensuring that all the investigation completed within the
- Maintaining QMS tracker for the status of each QMS
- Ensuring effective functioning of the department
- Manpower planning for regular shift
- Assigning job responsibilities to overall Routine
- Providing technical expertise and leadership to meet specified
- Ensuring Quality of In-process, intermediates and finished
- Monitoring the Analytical method transfer activities whenever required and overall Supervision of quality control
- Maintaining 5S activity in laboratory
- Maintaining system as per GLP, GDP and cGMP
- Monitoring the all kinds of Investigation (Finished products and Raw materials), deviations, OOS, OOT, Customer complaints and incidents etc
- Monitoring of effective implementation of ISO 9001 &14001 standards
- Conducting of all trainings related to GLP, cGMP & on the job trainings for all personals.
- Maintenance of Annual Maintenance Contract (AMC).
- Reduce the consumption maximum, Recycle as possible as, Reuse optimum level for all natural resources
Employment Type: Full Time, Permanent
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Strict timing
Monday to Saturday
No travel
Day Shift
Lee Pharma Benefits
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