Quality Control Manager

Company Description

Lars Medicare Pvt. Ltd. is a renowned manufacturer of high-quality IV Catheters and other single-use medical devices. With CE and ISO 13485 certified production facilities, the company exports its products to over 100 countries across Asia Pacific, Latin America, and beyond. Headquartered in New Delhi, India, Lars Medicare serves global markets through branches in Dubai, UAE, and Toronto, Canada. Established in 2007 as a 100% Export Oriented Unit (EOU), the company focuses on designing, developing, and manufacturing world-class medical devices. Known for breakthrough engineering, top-notch quality, and cost-effective solutions, Lars Medicare is a trusted partner for its international clientele.

Job Title: Manager Quality Control (QC)

Company: Lars Medicare Pvt. Ltd.

Location: Sonipat, Haryana

Reporting To: GM QC / QA / RA or Head Quality

Experience: 610 years

Responsibilities

• Manage and supervise all Quality Control laboratory operations to ensure seamless daily functioning.
• Oversee the testing of raw materials, packaging materials, in-process samples, and finished products against approved specifications.
• Guarantee the timely release of materials and finished goods following successful testing and validation.
• Review and approve all laboratory test reports and Certificates of Analysis (COA).
• Monitor chemical, physical, and microbiological testing to ensure total adherence to established methods.
• Ensure the calibration, qualification, and preventive maintenance of all laboratory equipment and instruments.
• Maintain rigorous records of instrument usage logs and calibration schedules to prevent operational lapses.
• Enforce strict compliance with Good Laboratory Practices (GLP), GMP, and ISO quality standards.
• Maintain comprehensive laboratory records and quality documentation to ensure 100% traceability of testing data.
• Lead investigations into Out-of-Specification (OOS) results and quality deviations to identify root causes.
• Coordinate with the QA department to implement effective Corrective and Preventive Actions (CAPA).
• Review and approve validation protocols and reports for all laboratory test methods and verification processes.
• Prepare the QC department for internal audits, certification audits, and regulatory inspections.
• Assign testing responsibilities, monitor staff performance, and provide technical training to QC analysts.
• Implement best practices and continuous improvement initiatives to enhance laboratory testing accuracy and efficiency.

Requirements

• M.Sc / B.Pharm / M.Pharm in Chemistry, Microbiology, Biotechnology, or a related field.
• 610 years of professional experience in Quality Control within pharmaceutical or medical device manufacturing.
• Proven expertise in handling OOS investigations and root-cause analysis in a regulated environment.
• Solid understanding of GLP, ISO 13485, and GMP documentation requirements.
• Strong technical knowledge of laboratory instrument calibration and method validation.
• Demonstrated leadership skills with the ability to manage a team of analysts and laboratory technicians.