Sun Pharmaceuticals (EZ) Limited
Requirements
Education
- Master of Science (MSc) in Applied Chemistry
- Master of Pharmacy (M.Pharm) in Pharmaceutical Technology
Experience
- 7 to 9 years
- The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies
Additional Requirements
- Age 30 to 40 years
Responsibilities & Context
- Calibration Management:
- Prepare and maintain the calibration schedule for all Quality Control laboratory instruments.
- Perform calibration activities as per approved schedules, SOPs, and regulatory requirements.
- Ensure proper documentation and timely review of calibration records.
- Instrument Qualification & Maintenance:
- Maintain qualification status (IQ/OQ/PQ) of all QC instruments.
- Coordinate and ensure preventive maintenance of laboratory instruments as per schedule.
- Maintain complete and compliant documentation related to qualification and maintenance activities.
- Working Standard & Reference Standard Management:
- Prepare and maintain the Working Standard (WS) schedule.
- Prepare Working Standards as per approved SOPs and protocols.
- Maintain and control all documentation related to Working Standards, CRS, and Impurity CRS, including usage, storage, validity, and reconciliation records.
- Instrument Troubleshooting & Monitoring:
- Perform troubleshooting and calibration of HPLC systems.
- Monitor performance and ensure proper functioning of all QC laboratory instruments.
- Escalate instrument-related issues and support corrective actions.
- EDAMS / Data Management Activities:
- Perform EDAMS-related activities for the Quality Control laboratory.
- Ensure data accuracy, integrity, and compliance with applicable data integrity guidelines.
- Regulatory & Departmental Support:
- Carry out any other duties as assigned by superiors in support of departmental objectives, audit readiness, and regulatory compliance.
- To Support internal and external audits by providing required documentation and explanations.
- Compliance & Quality Responsibility:
- Ensure all activities are conducted in compliance with cGMP, GLP, SOPs, and regulatory guidelines by Maintaining a high level of data integrity, documentation accuracy, and laboratory discipline.
To apply for this job email your details to apply@chakricircular.com