A Day In The Life Of Our Senior Manufacturing Engineer
- Be a leader in process validation (IQ/OQ/PQ/PPQ) for the team, developing the protocols and test processes
- Provide daily support to troubleshoot and resolve manufacturing production issues including material, method, while following GMP and the company Quality Management System.
- Create and revise manufacturing-related risk documents including pFMEA’s and Manufacturing Line Specifications
- Identify root cause(s) of operational failures and support Corrective and Preventive Action plans by providing solutions using problem-solving skills including Fishbone, 5 Whys, Pareto Charts etc..
- Generate production metrics including yields, scrap rates, capacity/bottlenecks and cycle times and routinely present to management.
- Define and implement continuous process improvements to existing manufacturing operations including process verification, MFG documentation updates and process validation.
- Perform routine equipment preventative maintenance and/or repair and serve as manufacturing liaison for external calibration activities.
- Design, document, assemble, qualify and release custom and off the shelf manufacturing and testing tooling, fixtures and equipment. Create and release associated maintenance and calibration procedures.
- Author and execute manufacturing documentation, including protocols, reports, manufacturing process instructions, work instructions and equipment/fixture specifications.
- Other manufacturing engineering duties or support as assigned or requested.
- This role requires the use of varying levels of personal protective equipment (including, gowns, masks/face shields, gloves, and safety glasses).
About You
- Degree in Manufacturing/Industrial, Mechanical, or Electrical Engineering
- Minimum 5 years experience in the medical device industry in a manufacturing engineering capacity working with complex hardware/software devices
- Catheter experience is a plus!
- Experience in working with CM, especially an OUS CM
- Working knowledge of ISO 13485 and 21 CFR 820.
- Understanding of statistical methods
- SolidWorks or equivalent experience
- Proficient with standard business software (MS Office, Excel, Outlook etc.)
- Excellent written and oral communication skills are required
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