Alencure Biotech is looking for a detail-oriented QMS Executive to manage and maintain the Quality Management System in compliance with pharmaceutical industry standards, GMP guidelines, and regulatory requirements.

Experience: 3-4years
Department: Quality Assurance (QA)
Job Type: Full time | On-site

Key Responsibilities

- Maintain and update QMS documentation, including SOPs, policies, and quality records.
- Manage document control, issuance, revision, and archival.
- Coordinate CAPA, deviations, change controls, and non-conformance reports.
- Support internal audits, external audits, and regulatory inspections.
- Ensure compliance with GMP and applicable pharmaceutical quality standards.
- Track training records and coordinate employee training on SOPs.
- Monitor QMS activities and ensure timely closure of quality-related actions.
- Coordinate with QA,



QC, Production, and other departments to maintain compliance.

Required Qualifications & Skills

- B.Pharm, M.Pharm, B.Sc., M.Sc., or a relevant qualification.
- Knowledge of GMP, GDP, SOPs, and pharmaceutical quality systems.
- Good documentation, communication, and coordination skills.
- Attention to detail and the ability to maintain accurate records.
- Basic knowledge of CAPA, deviation management, change control, and audit processes.

Interested candidates can apply on [email protected] or +91-XXXXXXXXXX.

Benefits:

- Commuter assistance
- Paid sick time
- Provident Fund

Work Location: In person

📌 QMS Engineer (Amb)
🏢 Alencure Biotech Pvt.LTD
📍 Amb