TM - Plant Engineer (Mechanical)
1 year ago Public Service Hyderabad 82 views Reference: 31302Job Details
"Required Knowledge Of Vial Filling Line , PFS , Autocalve , DHS , GMP Part washer Maintenance activity .
Having Knowledge of ISOLATOR base Filling Line maintenance line.
Responsible for the equipment availability at its full capacity for the production.
Responsible for the facility equipment operation and planned maintenance.
Responsible for the break down rectification in time and corrective action for the Non-Occurrence.
Support installation/modification, commissioning and qualification activities of new equipment and systems.
Should have Hands of ecperience to handle routine QMS element ( Incident , CAPA , Change control ).
Responsible for the equipment availability at its full capacity for the production by increasing overall equipment efficiency.
Responsible for planning and execution of preventive maintenance for facility equipment.
Responsible for the breakdown rectification in time and take corrective actions to avoid repetition of breakdown.
Responsible for maintaining and procurement of critical and regular spares as per equipment specification .
Responsible for support during installation and modifications of equipment and systems.
Responsible for support during qualification activities of new equipment and systems.
Responsible for the human and equipment safety in daily operations.
Ensure upkeep of emergency equipment, building awareness among colleagues and responding to emergencies in respective department / area.
All activity need to comply GMP and GEP requirement’s.
To ensure optimum utilization of utility and save energy.
To assist compliance of internal and external audits for Engineering department.
To prepare risk assessment / impact assessment investigation reports related to Engineering department.
Support for project related activity to uplift production requirement."
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Company Description
Dr. Reddy's began as a supplier to Indian drug manufacturers, but it soon started exporting to other less-regulated markets that had the advantage of not having to spend time and money on a manufacturing plant that would gain approval from a drug licensing body such as the U.S. Food and Drug Administration (FDA). By the early 1990s, the expanded scale and profitability from these unregulated markets enabled the company to begin focusing on getting approval from drug regulators for their formulations and bulk drug manufacturing plants in more-developed economies. This allowed their movement into regulated markets such as the US and Europe. In 2014, Dr. Reddy Laboratories was listed among 1200 of India's most trusted brands according to the Brand Trust Report 2014, a study conducted by Trust Research Advisory, a brand analytics company.[3]
By 2007, Dr. Reddy's had seven FDA plants producing active pharmaceutical ingredients in India and seven FDA-inspected and ISO 9001 (quality) and ISO 14001 (environmental management) certified plants making patient-ready medications five of them in India and two in the UK.[4]