Qa Executive

Selective Global Search; South Goa District; On-site; INR 540,000 - 660,000; Full time

Job summary

Selective Global Search in Goa plant is seeking an Executive (QA) Qualification & Validation with 4-5 years of relevant experience. Location: Goa Plant; candidates from Maharashtra or nearby Goa preferred.

You will execute and monitor qualification activities, review protocols and reports, plan cleaning and process validation, maintain the Validation Master Plan (VMP), and coordinate cross-functional teams. Training personnel on GMP requirements will be part of the role.

Qualifications

• 4–5 years experience in qualification & validation.
• Experience with GMP/regulatory requirements.
• Candidates from Maharashtra or nearby Goa preferred.

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.

Skills

QA

Validation

Education

B.Pharma / M.Pharma

Job description

Executive (QA) Qualification & Validation

Location: Goa Plant

Experience: 4 to 5 years (Candidates should be from Maharashtra or nearby Goa Location only)

Salary: Up to 6 LPA

Educational Qualification: B.Pharma / M.Pharma

JD

• 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.