Job Description: Junior Executive – Quality Assurance (USFDA – MYVAL) Experience: 1–3 years in the Medical Device/Pharmaceutical industry Qualification: B.Pharm / M.Pharm / B.Sc. / M.Sc. in a relevant discipline Key Responsibilities: • Ensure compliance with USFDA, GMP, and ISO 13485 requirements. • Maintain and review quality documentation and records. • Support CAPA, deviation, change control, and non-conformance management. • Assist in internal audits, regulatory inspections, and quality system activities. • Ensure adherence to SOPs and quality standards. Requirements Key Skills: • Knowledge of USFDA regulations and Quality Management Systems (QMS). • Documentation and record management. • CAPA, deviation handling, and root cause analysis. • Audit readiness and regulatory compliance. • Attention to detail and effective communication.