Average salary: Rs246,856 /yearly
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- ...control proposals. Assess quality and regulatory impact of proposed changes. Monitor implementation and closure timelines. Documentation & Compliance Review SOPs, protocols, reports, and quality documents. Ensure compliance with GDP (Good Documentation...SuggestedFull time
Rs 3 - 15 lakhs p.a.
...process manufacturing, and final product inspection. The role involves working directly on the shop floor to inspect, measure, approve, document, and improve product quality. You will also contribute to strengthening the plant's quality systems by developing inspection formats,...SuggestedFull timeRelocationWeekday workRs 3 - 3.84 lakhs p.a.
...of tasks 6. Conduct online research and data gathering 7. Maintain and update databases, records, and spreadsheets 8. Handle documentation and other administrative tasks 9. Follow up on pending tasks and ensure deadlines are met 10. Provide general virtual/...SuggestedImmediate startUS shiftNight shiftRs 12 - 15 lakhs p.a.
...standards, regulations, and guidelines, and support processes that maintain compliance across the organisation. Reporting and Documentation: Maintain detailed records of interactions with external parties, regulatory authorities, and stakeholders. Prepare regular reports...SuggestedFull timeRs 15 - 17 lakhs p.a.
...activities comply with company policies and applicable regulations. Maintain accurate purchase orders, invoices, contracts, and related documentation, and coordinate with finance on budgets and cost approvals. Coordinate with production, sales, warehouse, and finance teams to...SuggestedFull timeContract work- ...discipline Key Responsibilities: Ensure compliance with USFDA, GMP, and ISO 13485 requirements. Maintain and review quality documentation and records. Support CAPA, deviation, change control, and non-conformance management. Assist in internal audits, regulatory...SuggestedPermanent employment
- ...survival/time-to-event methods and trend analysis. Ensure statistical methods, assumptions and thresholds are scientifically justified and documented in the CEP/CER. · Assess whether observed adverse-event and complication rates remain within predefined acceptance criteria and...SuggestedFull time
- ...and performance testing of finished products. o Approve batch release only after meeting defined quality specifications. 5. Documentation & Reporting o Maintain accurate records of quality inspections, audits, and test results. o Prepare monthly quality reports...SuggestedFull time
- ...adherence to applicable industry standards, regulations, and guidelines, and implement processes to maintain compliance. Reporting and documentation: Maintain records of interactions with external parties, regulatory authorities, and stakeholders. Prepare regular reports and...SuggestedFull time
- ...manufacturing, maintenance, or quality-related activities. Read and understand mechanical drawings, specifications, and technical documents. Monitor machines, equipment, and production processes. Support installation, inspection, troubleshooting, and maintenance of...SuggestedPermanent employment
- ...signals, and analogue I/O . Follow plant safety procedures, permit-to-work systems, and maintenance standards . Maintain documentation such as inspection reports, calibration records, and maintenance history. Requirements # Instrumentation fundamentals # PLC...SuggestedFull time
- ...Ensure compliance with applicable statutory, regulatory, and legal EHS requirements , including maintaining relevant records and documentation. Conduct routine workplace safety inspections and audits, identify non-compliances, and follow up on corrective actions....SuggestedFull timeFor contractors
- ...Target Achievement ~ Daily Output Monitoring & Reporting ~ Basic Knowledge of GMP/CGMP ~ SOP Compliance & Production Documentation ~ Quality Control & Rejection Monitoring ~ Machine Troubleshooting & Downtime Monitoring ~5S, Housekeeping & Safety...SuggestedFull timeShift work
- .... Job Responsibility - Monitoring of qualification and validation activities. - Preparation of technical files and related documentation. - Preparation and review of qualification & validation protocols and reports. - Review of raw data, including analytical reports...SuggestedFull time
- ...and Breakdown Maintenance Equipment & Instrument Calibration RO Water Plant Operation Basic Troubleshooting Maintenance Documentation & Reporting Basic Knowledge of GMP/CGMP and SOPs Safety Compliance & 5S Basic Computer Knowledge Willingness to Work...SuggestedFull timeShift work
- ...Execute day-to-day manufacturing of urology medical devices. Prepare and maintain Batch Manufacturing Records (BMR) and production documentation. Ensure compliance with ISO 13485, GMP, and company Quality Management System. Coordinate with QA, QC, R&D, Engineering, and...Full time