Engineer will be working in a team environment with others to resolve daily issues on a Medical Device Manufacturing Line.
• Responsibilities include investigating non-conforming product, scrap, yields and determining root cause and contributing factors.
• Other areas include equipment work order reviews after repairs from technicians to determine product impact and release equipment back to production use.
• Exercise knowledge of technical skills and understanding of the business objectives, manufacturing operations and dynamics of the company's environment to take an effective and proactive leadership role in a specific technical manufacturing discipline.
• Set direction for, lead, and take ownership of complex manufacturing engineering technical tasks that may have multiple inter-coordinating elements.
• Expectation that the individual will be able both to anticipate and identify key issues and make recommendations for resolution where precedent may not exist and creative thinking is required.
• Resolution may involve the application of new methods and approaches and may require the consideration of impact with other system components.
• Interaction with peers and mentors on the individual's projects is generally in the context of peer review to confirm the rationale for task approach direction as well as peer review of verification/validation activities.
Required:
• BS/MS degree in engineering or science.
• 0-3 years of related experience.
• Preferred experience with CAPA, DMAIC & Root Cause Analysis.
• Preferred Medical Device/Pharma/FDA or other regulated background.
As an equal opportunity employer, ICONMA prides itself on creating an employment environment
that supports and encourages the abilities of all persons regardless of race, color, gender, age, sexual
orientation, citizenship, or disability.