Job Description
-

Job Description
• Support departmental activities related to QC Testing, compliance and operational excellence.
• Perform incoming, in-process, and final inspection of medical devices as per approved specifications.
• Verify product conformity against drawings, technical specifications, approved standards, acceptance criteria, and quality plans.
• Prepare, review and maintain technical documents, records, reports and related documentation.
• Identify non-conforming products, prepare Non-Conformance Reports (NCR), participate in investigations, and support implementation of Corrective and Preventive Actions (CAPA).
• Coordinate with Production, QA, Regulatory Affairs, R&D;, Purchase, and Suppliers for quality-related issues and timely resolution of non-conformities.
• Ensure measuring and test equipment are properly identified, calibrated, maintained, and used according to approved procedures.
• Ensure compliance with applicable regulatory requirements, company policies, quality management systems and standard operating procedures.
• Support qualification, validation, method verification, new product introduction , and process improvement activities.
• Support internal and external audits, inspection, and compliance-related activities.




• Monitor assigned tasks, identify potential issues and ensure timely resolution through cross-functional coordination.
• Follow laboratory safety practices, maintain housekeeping of the QC area, and ensure proper handling and storage of inspection equipment and samples.
• Perform any other duties assigned by the reporting manager to support organizational objectives. Key

Skills:
• Good communication and interpersonal skills.
• Strong analytical and problem-solving abilities.
• Proficiency in MS Office (Excel, Word, PowerPoint).
• Good organizational and time management skills.
• Ability to work independently as well as in a team.
• Willingness to learn and adapt to changing business requirements. Desired Candidate Profile:
• Bachelor's degree in Engineering, Pharmacy, Life Sciences, Biomedical Engineering, Biotechnology or a related discipline.
• Relevant experience in the medical device, pharmaceutical, or healthcare industry will be preferred.
• Valuable understanding of documentation practices, regulatory/compliance requirements, and quality systems. Note :
- Urgent Requirement Years of

Experience:
- 1-5 years

📌 Quality Control (Vapi)
🏢 Meril
📍 Vapi