We are looking for a Sr. Executive QA Equipment Validation to manage and review equipment qualification and validation activities in compliance with cGMP, regulatory requirements, SOPs, and quality standards.

Key Responsibilities
Execute/review DQ, IQ, OQ and PQ activities for pharmaceutical manufacturing and laboratory equipment.
Prepare and review URS, validation protocols, qualification reports, risk assessments and related documents.
Ensure equipment qualification activities are performed as per approved protocols and timelines.
Review equipment specifications, drawings, manuals, calibration and maintenance records.
Coordinate with Engineering, Production, QC, QA and vendors for qualification activities.
Review and manage deviations, discrepancies, CAPA and change controls related to validation.
Ensure proper documentation and compliance with GMP, data integrity and validation requirements.




Support periodic review, requalification and validation lifecycle management.
Participate in internal, customer and regulatory audits/inspections and provide validation-related documentation.
Maintain validation trackers and ensure timely closure of qualification activities.

Required Skills
Positive knowledge of equipment qualification, validation lifecycle and GMP requirements.
Hands-on experience with IQ/OQ/PQ, risk assessment, deviation, CAPA and change control.
Solid documentation and report-writing skills.
Valuable coordination and communication skills with cross-functional teams.
Experience in a pharmaceutical manufacturing environment is preferred.

📌 Qa Equipment Validation Baddi
🏢 Maya Biotech
📍 Baddi