Lars Medicare Pvt. Ltd.
Website:
larsmedicare.com
Job details:
Company Description
Lars Medicare Pvt. Ltd. is a distinguished manufacturer of high-quality IV Catheters and single-use medical devices, headquartered in New Delhi, India. Founded in 2007, the company operates a state-of-the-art, CE and ISO 13485 certified production facility in a pollution-free zone near New Delhi. As a 100% Export Oriented Unit (EOU), Lars Medicare serves customers in over 100 countries, including regions such as Asia Pacific and Latin America. With branches in Dubai, UAE, and Toronto, Canada, the company is committed to delivering world-class medical devices that prioritize quality, innovation, and cost-effectiveness. Customers trust Lars Medicare for its dedication to continuous development and breakthrough engineering.
Job Title: QA MR Executive (Quality Assurance – Management Representative Executive)
Company: Lars Medicare Pvt. Ltd.
Location: Sonipat, Haryana
Reporting To: QA Manager / GM – QA / MR
Experience: 2–5 years
Responsibilities
- Maintain the Quality Management System (QMS) in strict accordance with ISO 13485 and ISO 9001 standards.
- Ensure all departments consistently follow approved SOPs, quality policies, and operational procedures.
- Manage the document control system, overseeing the issuance, revision, and archiving of SOPs, manuals, and records.
- Verify that only the most recent and approved versions of QMS documentation are accessible for operational use.
- Plan and coordinate internal quality audits across various departments and prepare detailed audit reports.
- Execute follow-up actions to ensure the timely closure of Corrective and Preventive Actions (CAPA) resulting from audits.
- Prepare comprehensive data, reports, and minutes for Management Review Meetings (MRM).
- Track and monitor the status of all action items decided during management reviews.
- Manage non-conformities and deviations, ensuring root-cause analysis and proper documentation are completed.
- Coordinate and maintain accurate employee training records regarding SOPs and quality procedures.
- Support the organization in preparing for external certification audits and regulatory inspections.
- Ensure full traceability and record retention of all quality documents as per company and regulatory policy.
- Monitor quality objectives and performance indicators to support continuous improvement initiatives.
- Assist in maintaining compliance with global regulatory standards and quality certifications.
- Facilitate training programs related to quality systems and regulatory requirements for all relevant staff.
Requirements
- B.Pharm / M.Pharm / B.Sc / M.Sc in Quality, Microbiology, Biotechnology, or a related field.
- 2–5 years of professional experience in QA or QMS documentation.
- Solid understanding of ISO 13485 standards and medical device quality requirements.
- Proven experience in coordinating internal audits and managing CAPA systems.
- Proficiency in technical writing and maintaining complex document control systems.
- Strong organizational skills with a focus on traceability and record retention.
- Share CV on - operation@larsmedicare.com
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