AddressAbout us
MERIL
DELIVERING WORLD-CLASS HEALTHCARE SOLUTIONS
Founded in 2006, Meril is an India-based, global medical device company that is dedicated to the innovation, design and development of novel, clinically relevant and state-of-the-art devices. Our fundamental aim is to champion the alleviation of human suffering and improve quality of life. To enable this, we are committed to R&D, innovation in manufacturing medical technology, scientific communication, and contemporary distribution avenues.
Meril was born with the aim of improving the quality of human life through innovative and advanced healthcare solutions. As a medical device manufacturer, we exist to improve the inventiveness in healthcare so that people’s lives are enriched. We continually seek excellence in providing answers to some of medicine’s toughest questions.
Meril manufactures medical solutions in the form of vascular intervention devices, orthopaedic supplements, in-vitro diagnostics, endo-surgery and ENT products. It is our core commitment to ensure the delivery of advance healthcare solutions. Our inclination towards research and development is reflected in our diverse offerings. We ensure that we adhere to the best quality of standards in manufacturing, scientific communication and distribution to deliver path-breaking healthcare products to the world.
We collaborate with physicians and global innovators to identify unmet clinical needs and develop revolutionary therapies. We encourage research and academic collaborations and remain available to interact on exciting opportunities.
Headquartered in India with a manpower of more than 4000, Meril currently conducts business in more than 100 countries. We have 100% subsidiaries in India, USA, Germany, Brazil, Russia, South Africa, Bangladesh and Turkey. We have set up operations in China and Japan too.
- Ensure that all quality control processes and procedures align with relevant regulatory requirements, such as ISO 13485, FDA (U.S. Food and Drug Administration) regulations, and other international standards specific to medical devices
- Establish and maintain a robust QMS that covers all aspects of quality control, including documentation, training, and audits.
- Establish and maintain a robust QMS that covers all aspects of quality control, including documentation, training, and audits.
- Oversee the inspection and testing of medical devices to ensure they meet specified quality standards. This includes setting up testing protocols
- Develop procedures for handling nonconforming products and implementing corrective and preventive actions (CAPA) to address and prevent recurring issues.
- Collaborate with the supply chain and procurement teams to evaluate and ensure the quality of materials and components supplied by external vendors.
- Maintain accurate and up-to-date records related to quality control, including specifications, test results, and compliance documentation
- Provide training to quality control personnel to ensure they have the necessary skills and knowledge to perform their roles effectively.
- Investigate the root causes of quality issues and implement corrective actions to prevent their recurrence.
- Develop and execute risk management strategies to identify and mitigate potential risks in the production and use of medical devices.
- Prepare for and participate in regulatory audits and inspections, ensuring that the organization is compliant with all applicable standards and regulations
- Drive continuous improvement initiatives within the quality control department, using data and feedback to enhance processes and reduce defects.
- Provide regular reports to senior management on the performance of the quality control department, including metrics, key findings, and areas of improvement
- Manage the process of changes to products or processes, ensuring that these changes are well-documented, reviewed, and approved while maintaining quality standards.
- Ensure that products are only released to the market after they have passed all quality control checks and meet the necessary regulatory requirements
- Supervise and lead a team of quality control professionals, providing guidance, training, and support to achieve department goals.
Requirements
Orthopedic Quality Control experience is must.
Benefits
All benefits as per the company norms
Salary
5 to 9 Lakhs (PA)
Work Experience
5+ years
Industry
Medical Device
City
Pardi
State/Province
Gujarat
Country
India
Zip/Postal Code
396191
