6 to 8 Years of experience in cGMP documentation of engineering in biopharma.
- Should be Well versed with cGMP and regulatory compliance for engineering documentation.
Responsible for Quality Management System documentation like Deviation, investigation, Change control, Corrective
- Action and Preventive Actions.
- Review and preparation of preventive maintenance Standard Operating Procedures with compliance for process and utilities Equipment’s.
- Responsible for Documentation related to Preventive maintenance, Breakdown maintenance, Logbook entries shall be carried out in line with Standard Operating Procedures.
- Responsible in Coordinating with team for Training and Development compliance.