Quality Engineer in Staunton

Cadence VA is looking for a dedicated Quality Engineer to ensure the highest standards of quality and compliance throughout our manufacturing processes. As a Quality Engineer for a Contract Medical Device Manufacturing Organization, you will be responsible for ensuring that all products are manufactured and delivered according to the strictest quality standards. You will work closely with manufacturing, engineering, and regulatory teams to ensure compliance with ISO 13485, FDA, and other applicable medical device regulations. Your role will involve maintaining the quality management system (QMS), leading validation efforts, and driving continuous improvements in quality processes.

Why should you choose Cadence?

• Shape the Future of Healthcare : Join a team dedicated to producing cutting-edge medical devices that advance patient outcomes and revolutionize healthcare delivery worldwide.
• Challenge Yourself : Take on exciting challenges and solve complex problems as you navigate the dynamic regulatory landscape and continuously improve quality practices in a fast-paced manufacturing environment.
• Be a Leader in Quality Excellence : Lead the charge in furthering our reputation for excellence by implementing best-in-class quality systems and driving continuous improvement initiatives across our manufacturing operations.
• Be Part of Something Meaningful : Join a company that is committed to making a positive impact on people's lives, where your contributions as a Quality Engineer play a vital role in ensuring the safety and efficacy of medical devices that save lives every day.

Key Responsibilities

Ensure compliance with ISO 13485, FDA 21 CFR Part 820, and other relevant standards.

Support continuous improvement projects to enhance manufacturing processes, reduce defects, and improve overall product quality.

Lead and prepare protocols and reports for validation work.

Qualify and manage suppliers, ensuring that raw materials and components meet required specifications for medical device manufacturing.

Prepare and review technical documentation, including protocols, validation plans, work instructions, and Standard Operating Procedures (SOPs).

Provide quality training to staff on cleanroom operations, regulatory compliance, and quality standards.

Qualifications

If you are interested in applying for this job please press the Apply Button and follow the application process. Energy Jobline wishes you the very best of luck in your next career move.

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