ARNI MEDICA PVT LTD
Jr QA Executive
Patancheru, INOn-sitePermanentFull-time
Posted Sep 26, 2026
Arni Medica is a leading medical device manufacturer specializing in contract manufacturing, new product development, and high-quality production of nephrology and healthcare products. We are seeking enthusiastic and detail-oriented fresh graduates to join our Quality Assurance (QA) team. This role provides exposure to quality systems, documentation, and regulatory compliance in a medical device manufacturing environment.
Requirements
- Assist in implementation and maintenance of Quality Management System (QMS).
- Support preparation, review, and control of SOPs, formats, and QA documents.
- Ensure Good Documentation Practices (GDP) across departments.
- Review Batch Manufacturing Records (BMR) and Device History Records (DHR).
- Assist in in-process quality assurance activities and line clearances.
- Support validation activities (IQ/OQ/PQ) and equipment qualification documentation.
- Participate in internal audits and assist during external audits (ISO 13485, GMP).
- Help in handling deviations, CAPA, and change control documentation.
- Ensure compliance with ISO 13485, GMP, and regulatory requirements.
- Maintain training records and assist in QA-related training programs.
- Basic knowledge of QA concepts and documentation practices
- Understanding of ISO 13485, GMP (basic level) is an advantage
- Strong attention to detail and willingness to learn
- Good documentation, analytical, and communication skills
- Ability to work in a regulated cleanroom and manufacturing environment
Role snapshot
Job type
Full-time
Required skills
Quality Management System (QMS) implementation and maintenanceSOP preparation and document controlGood Documentation Practices (GDP)Review of Batch Manufacturing Records (BMR) and Device History Records (DHR)In-process quality assurance and line clearance proceduresValidation and equipment qualification documentation (IQ/OQ/PQ)Internal auditing and audit support for ISO 13485/GMPDeviation, CAPA, and change control managementRegulatory compliance with ISO 13485 and GMPTraining records management and QA training supportQA concepts and documentation practicesAttention to detailAnalytical skillsAbility to work in a regulated cleanroom and manufacturing environment
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