Qa Executive

Selective Global Search; Poriebhat; On-site; INR 600,000 - 900,000; Full time

Job summary

Selective Global Search in India seeks a Validation Specialist to execute and monitor qualification activities in line with approved procedures and regulatory requirements. The role involves reviewing qualification and validation protocols, reports, and documentation, and planning cleaning validation and process validation to ensure timely completion.

You will maintain the Validation Master Plan (VMP), coordinate with cross-functional teams, review schedules, and provide training to personnel on

Responsibilities

• Execute and monitor qualification activities in compliance with approved procedures and regulatory requirements.
• Review qualification and validation protocols, reports, and associated documentation.
• Plan, coordinate, and execute cleaning validation activities.
• Plan and monitor process validation activities to ensure timely and effective completion.
• Prepare, review, and maintain the Validation Master Plan (VMP).
• Coordinate with cross-functional departments for the planning, execution, and completion of qualification and validation activities.
• Review and approve qualification and calibration schedules.
• Provide training to personnel on qualification, validation, and relevant GMP requirements

Job description

Role & responsibilities

• Execute and monitor qualification activities in compliance with approved procedures and regulatory requirements.
• Review qualification and validation protocols, reports, and associated documentation.
• Plan, coordinate, and execute cleaning validation activities.
• Plan and monitor process validation activities to ensure timely and effective completion.
• Prepare, review, and maintain the Validation Master Plan (VMP).
• Coordinate with cross-functional departments for the planning, execution, and completion of qualification and validation activities.
• Review and approve qualification and calibration schedules.

Provide training to personnel on qualification, validation, and relevant GMP requirements