G3 MEDICAL SYSTEMS PRIVATE LIMITED
Location
Chennai | India
Job description
Company Description G3 Medical Systems Private Limited is a proud manufacturer of Make in India – Energi CO2 Lasers, and is the exclusive distributor of the world's leading medical aesthetics systems to empower practices.
Role Description This is a full-time on-site role located in Chennai, as a Quality and Regulatory professional. The Quality and Regulatory professional will be responsible for ensuring that our products meet regulatory requirements and industry standards, as well as maintaining quality control procedures to ensure customer satisfaction. Also will be responsible guiding the maintenance QMS systems across the organization by coordinating and guiding the production team and other allied teams. Qualifications Should be ready to work for 5 years minimum. People looking for intern or short term exposure do not apply Bachelor's degree in Engineering, Life Sciences, or related fields Minimum 2-3 years of experience in Quality and Regulatory Compliance Experience in regulatory compliance specifically for medical devices is a must Working knowledge of ISO 13485, GMP, and other applicable regulatory requirements Excellent written and verbal communication skills Ability to work independently and as part of a team Attention to detail and strong organization skills Familiarity with CDSCO, FDA, CE, and other country-specific requirements is preferredJob tags
Salary
