About this role
Job Description
- In-process sampling and testing.
- Finished product sampling (Bulk finish and Packed samples).
- Hold time study execution and sampling at hold time stage, bulk finished and packed samples.
- Conducting the round of Quality Assurance to note down any deviations from the systems/ SOPs etc. and record the observations.
- Maintenance of instruments in the IPQC & routine calibration.
- Review log books and environmental monitoring files.
- Online review the different records such as equipment usage and cleaning records, area usage record, balance calibration records etc.
- Line clearances for different activities in the Production Department.
- Execution, Review and Release/Approval of documents like BRRs, ESPs in PAS-X System.
- Execution, review and approval of batch manufacturing records and batch packing records.
- Participate in equipment qualifications as per the requirements.
- Execution of cleaning validation & equipment qualification.
- Execution of Customer requirements (Samples and Documents).
- Review, preparation and revision of documents as per requirement.
15. To comply all EHS Rules, Procedures, Guidelines, Policy, Practices, Requirements & Applicable Legal Compliances.
Work Experience
1 to 3 Years
Education
Graduation Post Graduation in Pharmacy
## Competencies