Work Flexibility: Hybrid What you will do:
• Review, assess, and process customer complaints in accordance with established procedures and regulatory requirements.
• Conduct complaint investigations to determine failure modes, root causes, and product performance concerns.
• Collaborate with manufacturing, engineering, R&D;, regulatory, and service teams to support complaint resolution.
• Ensure complaint records are complete, accurate, and closed within established timelines.
• Support adverse event and vigilance assessments where applicable.
• Act as a quality representative for complaint-related projects and initiatives.
• Provide guidance and training on complaint handling requirements and best practices.
• Partner with Post Market Surveillance, Regulatory Affairs, and Manufacturing teams to address quality concerns and drive product improvements. What you Need: Required
skills:
• Experience
- 2 years
- 4 years
• Experience on Quality Management (ISO 13485 or 21 CFR 820); TrackWise tool; Root Cause Analysis (RCA), CAPA, and risk management.
• Understanding on Medical Device Risk Management; Current Product Development (NPD) Cycle
• Problem solving and decision making and project management experience and experience to lead & achieve global process improvement efforts.
• Basic knowledge of BI Tools and Automation tools. (e.g. Power BI, Ui Path, etc.) Preferred
skills:
• BE/BTech/ME/MTech in Bio Medical / Mechanical Engineering / Electrical Engineering or related field from premier institutes
• At least 1+ years of experience in complaint handling or customer quality and 1 to 4 years of experience in Medical Device/Automotive/Manufacturing domain. Travel Percentage: 10%