Description:
• Prepare and review qualification protocols and reports for equipment, utilities, and systems (DQ, IQ, OQ, PQ, as applicable).
• Coordinate and monitor qualification activities with Engineering, Production, and Validation teams.
• Ensure qualification documentation complies with GMP and regulatory requirements. Maintain qualification schedules and ensure periodic requalification is completed on time.
• Conduct quality risk assessments using tools such as FMEA, HACCP, or risk matrices.
• Identify potential quality risks and recommend appropriate mitigation strategies.
• Ensure risk management documentation is maintained and periodically reviewed.
• Draft, review, revise, and maintain Standard Operating Procedures (SOPs), work instructions, protocols, and quality documents.
• Ensure document control procedures are followed throughout the document lifecycle.
• Coordinate periodic review of controlled documents.
• Provide training on new or revised SOPs and maintain training records.
• Identify opportunities for process improvement and quality enhancement.




• Support implementation of quality metrics and trend analysis.
• Participate in cross-functional quality improvement projects.
• Develop and review process validation protocols, reports, and validation master plans.
• Coordinate execution of process validation activities with cross-functional teams.
• Evaluate validation data and ensure processes consistently meet predefined acceptance criteria.
• Support cleaning validation, analytical method validation, and computerized system validation where applicable. Additional

Skills:
• Knowledge of GAMP 5 and 21 CFR Part 11.
• Strong Understanding of ALCOA+ principles.
• Performing risk assessments using tools like FMEA, HACCP, and risk matrices.
• Hands-on experience with IQ, OQ, PQ, and requalification of manufacturing and laboratory equipment.
• Solid Project Management Skills Qualifications

Education:
• B. Pharm B. Pharm
- Required
• M. Pharm M. Pharm
- Preferred

Experience:
• 2 years or more in 2
- 5 Years Specialized Knowledge: Licenses:

📌 Executive, QA Validation (Ahmedabad)
🏢 Amneal India
📍 Ahmedabad