Site Engineering - Instrumentation and Automation
1 year ago Public Service Hyderabad 83 views Reference: 30239Job Details
- BE in Electronics and Instrumentation Engineering with about 7-10 years- experience in Pharma Formulations - Injectables
- • Responsible for equipment readiness for BMS/EMS (Honeywell and Siemens), Utilities (Clean and Black) and FMDs of Manufacturing and QC facilities.
• Responsible for all the planned maintenance and support for the facilities.
• Responsible for the Preventive Maintenance activities of BMS/EMS and Utilities (Instrumentation & Automation).
• Spares management as required.
• Responsible for Data Backup, Backup verification, Time synchronization and Audit trail review activities of BMS/EMS systems
• Responsible for the break down rectification on time and corrective action for the non-occurrence.
• Accountable for breakdown notifications closures on time.
• Accountable for the monthly alarm verifications of the GMP and non-GMP critical equipment’s.
• Responsible for QMS compliance like Change Controls, Incidents, SIR, and CAPA.
• Periodic revisions of SOPs and new SOPs preparations.
• Responsible for Building Management Systems (BMS) & Environmental Monitoring Systems (EMS) troubleshooting, maintenance and system qualification activities.
• Accountable for equipment/system/instruments qualifications and requalification’s.
• Accountable for small projects / modifications in-house in all the areas.
• Accountable for quality and safety standard targets are met as per the procedures.
• Responsible for the human and equipment safety in daily operations.
• Accountable for the contract people employed during general shift on the safety training & work activities.
• Audit SME for the BMS/EMS systems. - 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
- Knowledge of calibration & maintenance practices for DCS/PLC/SCADA & SIS., SMART, FF & pneumatic field instruments.
- Knowledge of Instrumentation engineering functions related to plant process and operations.
- Performing the DQ, IQ, OQ and PQ for all instrumentation equipment in order to ensure complete validation in adherence to cGMP and 21 CFR 11 requirements.
- Calibration, commissioning & trouble shooting of various field instruments such as Temperature, pressure transmitters, Level transmitters, Flow transmitters, temperature controllers.
- Mapping of critical Instrumentation v/s spares.
- Compliance to preventive maintenance & calibration,
- Preparation of SOP for quick revival & trouble shooting of DCS/PLC/SCADA system.
- Standardization of Identified field instruments.
- Responsible for raising purchase indent for various spares parts required by their department for maintenance work.
- To maintain all records.
- Responsible for adherence to EHS policy.
- Training and development of team members.
- Awareness about responsible care (Environment, Health, Safety and Security)
- 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
Company Description
Dr. Reddy's Laboratories is an Indian multinational pharmaceutical company based in Hyderabad. The company was founded by Kallam Anji Reddy, who previously worked in the mentor institute Indian Drugs and Pharmaceuticals Limited.[2] Dr. Reddy's manufactures and markets a wide range of pharmaceuticals in India and overseas. The company has over 190 medications, 60 active pharmaceutical ingredients (APIs) for drug manufacture, diagnostic kits, critical care, and biotechnology.
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]
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]
