QA Validation Professional

Farbe Firma Pvt. Ltd.; Ankleshwar; On-site; INR 600,000 - 900,000; Full time

Job summary

Farbe Firma Pvt. Ltd. in Ankleshwar, Gujarat, India, is seeking a QA/Validation professional to develop and execute validation protocols for equipment, processes, and systems.

The role focuses on ensuring product quality and regulatory compliance within a fast-paced pharmaceutical manufacturing environment. You will review validation documents, participate in IQ/OQ/PQ cycles, and coordinate with engineering, quality, and production teams to maintain compliant operations under WHO-GMP, FDA, and

Qualifications

• QA/Validation experience in pharmaceutical industry.
• Knowledge of IQ, OQ, PQ validation.
• Familiarity with regulatory guidelines (WHO-GMP, FDA, MHRA)

Responsibilities

• Develop and execute validation protocols for equipment, processes, and systems
• Review and approve validation documentation and reports
• Ensure compliance with WHO-GMP, FDA, and MHRA guidelines
• Conduct validation of manufacturing equipment, utilities, and computer systems
• Coordinate with cross-functional teams for validation activities

Skills

Validation protocols (IQ/OQ/PQ)

Regulatory compliance

Cross-functional coordination

Education

Bachelor's degree in Pharmacy, Chemistry, or Life Sciences

Job description

• Develop and execute validation protocols for equipment, processes, and systems
• Review and approve validation documentation and reports
• Ensure compliance with WHO-GMP, FDA, and MHRA guidelines
• Conduct validation of manufacturing equipment, utilities, and computer systems
• Coordinate with cross-functional teams for validation activities

Requirements

• Bachelors degree in Pharmacy, Chemistry, or Life Sciences
• Minimum 3-4 years experience in QA/Validation in pharmaceutical industry
• Knowledge of validation protocols (IQ, OQ, PQ) and regulatory requirements
• Experience with equipment, process, cleaning, and computer system validation