Description

You will own design quality engineering and compliance activities within the medical device industry.

This role is on-site.

Responsibilities

• Execute design control processes and maintain design files.
• Conduct process verifications and validations.
• Perform Design and/or Process Failure Modes Effects and Analysis (DFMEA/PFMEA).
• Apply strong problem-solving and decision-making skills to technical challenges.
• Lead project responsibilities and balance multiple priorities effectively.

Required Skills

• Bachelor's degree in a Technical or Scientific discipline.
• 5+ years of work experience in the medical device industry.
• Hands-on experience with Design Quality Engineering.
• Deep understanding of Design Control regulations and practices.
• Proven experience conducting Process Verifications and Validations.
• Proficiency in conducting DFMEA and PFMEA.
• Strong initiative and follow-through in executing project goals.

Key Skills

Education

Bachelor's degree