Position Summary:

The Cutera Quality Assurance department is devoted to assuring safe, reliable and effective products that exceed patient, physician and clinic expectations. The department plays a vital role in product and process quality supporting design, development, manufacturing, and distribution of all Cutera products including systems, hand pieces and accessories. The Quality Technician plays a crucial role in ensuring that Cutera products and services meet established quality standards and comply with relevant regulations by working with a team of dedicated individuals within and across departments to verify conformity of Cutera products and supporting manufacturing, testing and quality procedures and processes.

This is a temporary 6-month contract with potential to convert full-time. The working shift is Monday-Friday, 8:00am - 4:30pm PT.

Duties & Responsibilities:

• Develop and maintain expert knowledge of Cutera quality control procedures, processes, and test methods.
• Conduct thorough inspections of products or services to ensure they meet established quality standards including, but not limited to, Cutera laser systems, handpieces, and accessories.
• Perform various testing and analysis procedures, such as dimensional checks, material testing, laser power measurements and laser system and handpiece functional testing.
• Collect and analyze quality data to identify trends, patterns, and areas for improvement.
• Prepare and maintain detailed records of quality inspection results.
• Collaborate with production and engineering teams to identify and implement process improvements that enhance product quality.
• Provide recommendations for adjustments to manufacturing processes or procedures.
• Create and update quality documentation, including inspection procedures, checklists, and reports.
• Ensure that all quality-related documentation complies with regulatory standards.
• Investigate and determine the root causes of quality issues or defects.
• Develop and implement corrective and preventive actions to address identified issues.
• Communicate issues and defects to peers in manufacturing and engineering.
• Escalate issues to management as appropriate.
• Provide training to production and quality control staff on quality standards, procedures, and best practices.
• Ensure compliance with industry regulations, quality standards, and company policies.
• Stay informed about changes in regulations and standards affecting the industry.
• Verify quality control processes are performed per procedure and communicate discrepancies in procedures and processes to quality engineering and quality management.
• Other duties as needed or required.

Minimum Requirements & Qualifications:

• High school diploma or equivalent
• 5+ years of experience in medical device quality control, manufacturing, or related field.
• Working knowledge of quality management systems and methodologies.
• Proficiency in using various quality measurement tools and equipment.
• Excellent analytical and problem-solving skills.
• Effective communication and interpersonal skills.
• Attention to detail and a commitment to maintaining high-quality standards.
• Familiarity with industry-specific regulations and standards.
• Computer proficiency required in Word, Excel, and FileMaker Pro.