Junior Executive QA
Summary
Quality assurance role at Meril Life Sciences (USFDA – MYVAL): the person maintains and reviews quality documentation, handles CAPA, deviations, change control and non-conformances, and supports internal audits and regulatory inspections, ensuring compliance with USFDA, GMP and ISO 13485. Requires 1–3 years in the medical device/pharma industry and a B.Pharm/M.Pharm/B.Sc./M.Sc.
Job Description: Junior Executive – Quality Assurance (USFDA – MYVAL)
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.