- Design and execute validation protocols for process and cleaning validation activities, including IQ (Installation Qualification), OQ (Operational Qualification), PQ (Performance Qualification), and CV (Cleaning Validation).
- Develop and maintain a validation master plan (VMP) that aligns with regulatory requirements and organizational goals.
- Conduct process validation studies to ensure manufacturing processes consistently produce products that meet predefined quality attributes.
- Analyze process performance and critical parameters during validation runs and document results.
- Ensure adherence to Positive Manufacturing Practices (GMP) during all validation activities.
- Develop and execute cleaning validation protocols to confirm the effectiveness of cleaning procedures in removing residues, contaminants, and microorganisms.
- Establish acceptable residue limits and cleaning verification procedures based on product toxicology and batch size.
- Monitor cleaning practices and perform periodic revalidation as required.

📌 Executive - Process and cleaning validation expert (Vadodara)
🏢 Alembic Pharmaceuticals
📍 Vadodara