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Role overview
Job description
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.
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About this listing
- Source: Meril Life Sciences's official careers site · still listed there on 9 Nov 2026
- Posted 14 Oct 2026
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What they are looking for
Skills & requirements
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
Hiring company
Meril Life Sciences
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