Offer summary
Qualifications:
Bachelor's degree in Science or Engineering with at least 7 years of relevant industry experience, Experience in medical devices or a regulated industry, knowledge of FDA and ISO standards, management experience, and technical writing skills.
Key responsabilities:
- Develop and maintain technical quality assurance and control systems
- Supervise team and lead quality engineering processes such as FMEA and Six Sigma techniques
- Resolve complex quality issues, drive continuous improvement, and ensure compliance with regulations
- Review data on product defects, recommend improvements, and be proactive in problem-solving