Senior Executive (Calibration )

Sahajanand Medical Technologies; Hyderabad; On-site; INR 600,000 - 900,000; Full time

Job summary

Sahajanand Medical Technologies located in Hyderabad seeks a Calibration and Validation Specialist to manage calibration activities for measuring, monitoring, and test equipment. You will prepare validation protocols and documents, coordinate internal and external calibration, and maintain calibration records for equipment across manufacturing, lab, and utility areas.

The role involves IQ/OQ/PQ qualification, URS and risk assessments, and validation reports, with opportunities to support clean

Responsibilities

• Plan, coordinate, and execute calibration activities for measuring, monitoring, and test equipment as per approved procedures and calibration schedules.
• Prepare and execute validation protocols, reports, and related documentation.
• Coordinate internal and external calibration activities and ensure calibration is performed within the defined due dates.
• Maintain and update instrument master lists, calibration records, equipment history cards, and calibration status.
• Perform equipment qualification (IQ/OQ/PQ) and validation activities for manufacturing, laboratory, and utility equipment.
• Prepare and review URS, risk assessments, qualification protocols, validation protocols, and validation reports.
• Prepare & support clean room validation, packaging/sealing validation, and revalidation activities, as applicable.
• Develop and execute validation plans, test cases, acceptance criteria, and sampling plans based on applicable requirements.

Job description

Job description

Roles & Responsibilities

• Plan, coordinate, and execute calibration activities for measuring, monitoring, and test equipment as per approved procedures and calibration schedules.
• Prepare and execute validation protocols, reports, and related documentation.
• Coordinate internal and external calibration activities and ensure calibration is performed within the defined due dates.
• Maintain and update instrument master lists, calibration records, equipment history cards, and calibration status.
• Perform equipment qualification (IQ/OQ/PQ) and validation activities for manufacturing, laboratory, and utility equipment.
• Prepare and review URS, risk assessments, qualification protocols, validation protocols, and validation reports.
• Prepare & support clean room validation, packaging/sealing validation, and revalidation activities, as applicable.
• Develop and execute validation plans, test cases, acceptance criteria, and sampling plans based on applicable requirements.