via Career pages·2d ago
Senior Executive Quality Assurance
Abbott Laboratories
Full-timeOn-sitevalidation documentationprocess validationcalibration managementsop preparationchange controlregulatory complianceiso 9001qrm (quality records management)dariusisotrainsoltraqplant layout reviewequipment decommissioninghvac validationtraining module developmentstakeholder coordination
Location:Baddi, Himāchal Pradesh, IndiaType:Full-timePosted:2d ago
Followings will be the responsibilities of the position holder:
- Preparation and review of qualification and Validation documents (URS, DQ, IQ, OQ, PQ, etc.) for ODF Facility.
- Preparation and updation of Validation Master Plan, CVMP, SMF, Quality Manual and planner for ODF facility.
- Execution of qualification and requalification activities for ODF facility.
- To review plant layouts and drawings for ODF facility.
- To perform decommissioning study of equipment’s for ODF facility.
- To perform activity in software Darius, ISOtrain, and SolTRAQ for ODF facility.
- Co-ordination with other departments for streamlining qualification activities for ODF facility.
- Execution of process validation protocols for ODF facility.
- Monitoring of calibration activities and review of related documents.
- Preparation of SOP, training modules on validation and execution of training sessions for ODF facility.
- Review of Calibration and Preventive maintenance related documents.
- Execution of Qualification/Validation activity for critical utilities e.g., compressed air, nitrogen, HVAC/area validation, Purified Water.
- Preparation, execution of documents related to computer system validation for ODF facility.
- Perform QRM for qualification activities for ODF facility.
- To initiate and review the change control activity for ODF facility.
- Implementation of new regulatory and Abbott guidance / EQDs related to qualification.
- To ensure compliance of qualification activities as per Abbott, EQD and AQ requirement
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