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 Valuable 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:

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• 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

📌 Jr QA Executive (Hyderabad)
🏢 Arni Medica
📍 Hyderabad