Key Responsibilities:
- Manufacturing Operations:
- Oversee and participate in the manufacturing processes for dental chairs ensuring adherence to design specifications and production schedules.
- Develop implement and optimize manufacturing procedures to improve efficiency and reduce costs.
- Collaborate with crossfunctional teams to address production challenges and improve product quality.
- Testing and Quality Assurance:
- Perform functional and safety testing of dental chairs to ensure compliance with industry standards and regulatory requirements.
- Conduct root cause analysis and implement corrective actions for product defects or failures.
- Maintain accurate records of testing procedures results and improvements.
- Regulatory Compliance:
- Ensure that manufacturing and testing processes meet relevant medical device regulations (e.g. ISO 13485 FDA standards).
- Prepare and maintain documentation required for audits and regulatory submissions.
- Product Development Support:
- Provide technical input during product design and development to ensure manufacturability and testability.
- Assist in prototyping validation and verification activities for new dental chair models.
- Equipment and Tools Management:
- Maintain and calibrate manufacturing and testing equipment to ensure accurate performance.
- Recommend and implement improvements in tools and equipment to enhance production and testing capabilities.
Requirements
Qualifications and Skills:
- Bachelor s degree in Biomedical Engineering Mechanical Engineering or a related field.
- Minimum 2 years of experience in manufacturing and testing of medical devices.
- Knowledge of medical device standards and regulations (e.g. ISO 13485 FDA CE Marking).
- Handson experience with manufacturing tools equipment and quality assurance techniques.
- Strong problemsolving skills and attention to detail.
- Proficiency in CAD software and data analysis tools is a plus.
- Excellent communication and teamwork abilities.
Qualifications and Skills: Bachelor s degree in Biomedical Engineering, Mechanical Engineering, or a related field. Minimum 2 years of experience in manufacturing and testing of medical devices. Knowledge of medical device standards and regulations (e.g., ISO 13485, FDA, CE Marking). Hands-on experience with manufacturing tools, equipment, and quality assurance techniques. Strong problem-solving skills and attention to detail. Proficiency in CAD software and data analysis tools is a plus. Excellent communication and teamwork abilities.
Education
B.Tech / BE in Biomedical or Mechanical Engineering