Experience: 0-3 Years ONLY IN PHARMCEUTICAL INDUSTRY (Formulations)
Jobs Description:
- Authorization of all procedures and standard instructions of process, controls, etc.
- Investigation and closure of all deviations, OOS and complaints.
- Conducting self-inspections.
- Conducting vendor evaluation of raw materials.
- Should have sound knowledge of process validation. Should be familiar with preparation of process validation protocol and report.
- Should have knowledge of QMS System and Change Control, Deviation and CAPA Procedure.
- Review of Preventive maintenance & calibration of equipment and systems.
- Review of stability data to support retest or expiry dates and storage conditions and/or intermediates where appropriate.
- Risk analysis evaluation.
- Performing product quality reviews.
- Must understand standard operating procedure.
- Reviewing and Preparing Batch Release Documentation.