Average salary: Rs625,000 /yearly
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- Deviation & CAPA Management Identify, report, and investigate production deviations. Coordinate with cross-functional teams to implement Corrective and Preventive Actions (CAPA). Track the effectiveness and timely closure of CAPAs. Change Control Management Participate...QMS
- ...troubleshooting of computer systems & equipment Ensure compliance with pharma guidelines (GMP, cGMP, ALCOA+, Data Integrity) Handle QMS activities: Change Control, CAPA, Deviation & Incident management Support computerized system validation activities Work with...QMSImmediate start
- ...including HEPA filter integrity testing (PAO/DOP) Particle Counting Air Visualization (Smoke Studies) and Recovery Tests. Compliance & QMS: Manage HVAC-related Change Controls and Deviations . Investigate any Out of Specification (OOS) environmental conditions (...QMSFull time
- ...technical review of Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) to ensure 100% compliance with ALCOA principles. QMS Ownership: Lead the investigation and documentation of Deviations Change Controls and CAPAs .Ensure all Out of Specification (OOS)...QMSFull time
- ...preventive actions (CAPA) related to cleaning validation activities. Close validation-related tasks in systems like Track Wise or other QMS platforms. Training & Technical Support Impart training on cleaning validation principles, protocols, sampling techniques, and...QMS
- ...To ensure compliance with cGMP, USFDA, and other regulatory requirements by implementing and maintaining Quality Management System (QMS) practices within the Production department. Responsible for documentation, deviation handling, and continuous improvement initiatives...QMS
- ...machines in the shop. Encourage people to follow the directives, procedures and systems. Implement the procedural requirements of QMS. Ensure discipline is maintained in the shop. Ensure systematic feedback to all operators & technologists. Maintain sufficient...QMSFor contractorsShift work
- ...Responsibilities ~1. Quality Systems & Compliance ~ Ensure effective implementation and sustenance of Quality Management Systems (QMS) across the site. ~ Drive compliance with cGMP, regulatory guidelines (USFDA, MHRA, EU-GMP, WHO, CDSCO). ~ Ensure site readiness for...QMS
- ...actions to eliminate potential future complications and take corrective measures when necessary. Quality Assurance & Quality Control / QMS: Accountable for the plant's quality performance and fostering a culture of quality awareness among team members. Educate the team...QMSFull timeLocal area
- ...regulations and internal policies. Job Responsibilities.. . Develop, implement, and maintain robust Quality Management Systems (QMS) in accordance with company policies and regulatory requirements. . Conduct regular quality audits, inspections, and assessments of...QMS
- ...statistical and financial records. Creation, development and amendment of the requisites SOPs and other documents.Maintain and update QMS records. Preparation and implementation of technical training programs for workmen and staff. Updating critical spares list time to...QMSLong term contractFull time

