Executive Projects and Engineering at Amneal India
Ahmedabad, gujarat, India -
Full Time


Start Date

Immediate

Expiry Date

28 Aug, 26

Salary

0.0

Posted On

30 May, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Plant Maintenance, PLC Troubleshooting, SCADA Programming, CSV Protocols, Equipment Qualification, cGMP, GEP, Validation Activity, Preventive Maintenance, URS Preparation, DQ, IQ, OQ, PQ, QRM, Inventory Management

Industry

Pharmaceutical Manufacturing

Description
Plant Maintenance: • Responsible for maintenance and breakdown activity related to plant equipment / machinery of injectable facility like eye drop filling machine, Autoclave, Isolator, PFS filling machine,ORABS/CRABS etc • To handle troubleshooting related to PLC and SCADA of process equipment.  • Preparation and review of CSV protocols.  • Handling of day-to-day data backup, time synchronization activities • Responsible for procuring & maintaining the critical spares inventory. • Responsible to carry out all work as per cGMP and GEP. • Responsible for updating and maintaining of all cGMP documents related to breakdown and preventive maintenance as per SOP. • Responsible to equipment qualification from initial documents /finalization of equipment to Qualification such as IQ, IOQ, OQ, PQ, PLC IOQ. • Responsible to Performed and monitor routine validation activity and PLC validation activity. • Responsible for Identifying areas of improvement and recommending process modifications and equipment calibrations to achieve operational efficiencies based on pre-set parameters. Other Duties: • Perform additional assignments or responsibilities as assigned by the Head of Department (HOD). • Contribute to continuous improvement initiatives within the department related to Operation and documentation.
Responsibilities
Responsible for the maintenance, troubleshooting, and validation of plant equipment and machinery in an injectable facility. This includes managing PLC/SCADA systems, executing CSV protocols, and ensuring all activities comply with cGMP and GEP standards.
Loading...