Join a team focused on dependable orthopaedic care.
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Open Positions
Regulatory Affairs Executive
Regulatory Affairs · Ahmedabad · Full-time
Responsible for regulatory documentation, product registrations, license applications, renewals, regulatory submissions, and maintaining compliance with applicable medical device regulations and requirements.
Requirements
• Prepare and maintain regulatory documents and records.
• Handle product registrations, licenses, renewals, and regulatory submissions.
• Ensure compliance with applicable medical device regulations and requirements.
• Coordinate with CDSCO and other regulatory authorities as required.
• Maintain regulatory certificates, approvals, and product documentation.
• Track regulatory timelines, renewals, and submission status.
• Support audits and inspections by providing required regulatory documents.
• Coordinate with QA, QC, Production, and other departments for regulatory requirements.
Apply by 31 October 2026
Quality Check Executive
QC Department · Ahmedbad · Full-time
Responsible for conducting incoming, in-process, and final quality inspections of orthopedic products, verifying dimensions and specifications, maintaining QC records, identifying non-conformities, and ensuring compliance with company quality procedures and ISO 13485 requirements.
Requirements
• Conduct incoming, in-process, and final inspection of products.
• Check dimensions, specifications, surface finish, and product quality as per approved drawings.
• Use and maintain measuring instruments and ensure calibration validity.
• Identify, segregate, and report non-conforming products.
• Maintain inspection reports, QC records, and batch traceability.
• Verify packaging, labeling, quantity, and product identification before dispatch.
• Coordinate with Production and QA/QC for quality issues and corrective actions.
• Ensure compliance with SOPs, ISO 13485 requirements, and company quality procedures.
Apply by 31 October 2026
YOUR APPLICATION
Apply to SA Orthocure
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