Quality Engineer
Are you ready to take your career in Quality Engineering to the next level? A prestigious opportunity has arisen for a dedicated Quality Engineer in Charlotte, NC. This permanent position is ideal for someone with a solid background in a heavily regulated industry, preferably within medical devices where there has been exposure to regulations like ISO 13485. Join a team where your skills in CAPA, risk management, and PPAP will play a crucial role in maintaining and enhancing product quality.
Key Responsibilities:
- Implementing and managing Corrective and Preventive Action (CAPA) systems.
- Conducting detailed risk management activities to ensure product safety and efficacy.
- Applying Production Part Approval Process (PPAP) methodologies to support manufacturing processes.
Skills Required:
- CAPA Experience: Proven track record in developing and maintaining corrective and preventive action systems.
- Risk Management: Ability to identify, evaluate, and mitigate risks associated with product design and manufacturing.
- Experience in Heavily Regulated Industry: Knowledge of stringent regulatory standards, with a preference for those experienced in the medical device sector.
- PPAP Experience: Familiarity with Production Part Approval Process protocols to ensure all manufactured parts meet required specifications and quality standards.
This role offers a unique challenge to further your expertise in quality assurance within the critical field of medical devices. If you are committed to excellence and ready to make a significant impact, we encourage you to apply for this exciting opportunity as a Quality Engineer.
