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Engineer, Manufacturing
Ref No.: 18-18310
Location: Westford, Massachusetts
Evaluation of production equipment Production support and process validation Troubleshoot manufacturing process and equipment Protocol and report writing Generate and modify manufacturing process documentation Work with cross functional teams as required Develop and implement process improvements

• 2-5 Years hands on validation experience
• Must have worked in the medical device manufacturing industry
• Must have excellent verbal and written communication skills
• Must be adept at statistical analysis (Minitab experience preferred)
• Experience in test method development and validation
• Fiber optic experience is a plus
• IQ/OQ/PQ experience required
• Catheter experience preferred