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ARNI MEDICA PVT LTD

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.
Skills Requried:

  • 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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