Process Engineer II

Role: Process Engineer II responsible for optimizing and sustaining manufacturing processes in a medical device environment. Primary objectives include improving process efficiency, quality, and lifecycle management using lean and Six Sigma methodologies. Responsibilities encompass cross-functional collaboration with EHS, product development, quality, and regulatory teams; executing validation studies; conducting statistical process control and technical investigations; implementing process improvements; and developing training programs. Qualifications: Bachelor's degree in Chemical or Mechanical Engineering; minimum of 3 years industry experience, preferably in medical devices; lean Six Sigma experience and cleanroom manufacturing exposure are advantageous. High-Value: Medical device manufacturing, GMP compliance, process validation (IQ/OQ/PQ), lifecycle management, continuous improvement with lean Six Sigma, and cross-functional project participation. Work setup and travel details are not specified.