Team member : HVAC & Utilities
1 year ago Public Service Hyderabad 83 views Reference: 30773Job Details
• Following the established procedures and policies of the department.
• Complying necessary legal requirements.
• Representing Engineering and QMS related audits as auditee.
• Handling internal and external audits related to Engineering and QMS and ensuring the closure of audit findings on time.
• Ensuring the compliance to non-conformances and implementation of corrective and preventive actions.
• Following good documentation, data control and cGMP regulations and ensuring the same from team members.
• Preparing/reviewing procedures and other documents related to Engineering.
• Motivating team members, skill development and encouraging for continual improvements.
• Following the delegated roles, responsibilities, objectives, and targets along with team members.
• Handling QMS documentation like change control, deviation, investigation and CAPA.
• Preparing qualification/validation protocols with reports and executing them.
• Performing risk assessment and impact assessments.
• Review of cross-functional department's documents.
• Ensuring minimum or no non-conformances and involving in investigations if occurred.
• Preparing schedules/planners for routine Engineering/maintenance activities
• Preparing facility drawings, utility PID and other drawings.
• Decision making on procedures.
• Ensuring completion of training by self and team members before initiating any activity. Conducting trainings.
• Ensuring activities as per preventive maintenance, calibration and other applicable schedules are performed on time.
• Preparing and presenting the departmental operations and maintenance status reports.
• Ensuring there are no data integrity related issues.
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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]