Manufacturing validation engineer

Job duties:

1. Process and equipment qualification (IQ/OQ/PQ).
2. Development of test methods for Design V&V, Process Validation, and Production
3. Validation of test methods
4. Execution of Engineering Builds, Gauge R&R Studies, Attribute Analysis Studies, and other validation work
5. Authoring/releasing of new test methods and editing/redlining of old test methods

The education/experience I am looking for is as follows:

• This position requires a Bachelor of Science in Engineering or combination of relevant education and experience as well as 5 years relevant experience in medical device manufacturing.
• Expertise in medical device manufacturing and with strong working knowledge of cGMPs.
• Clean room environment experience
• Manufacturing Engineering and automation experience.
• Experience with Test Method Validation and/or Measurement System Analysis is preferred.
• Knowledge of computer software for the analysis of data, specifically Microsoft Excel and statistical packages (Minitab preferred), is a plus.
• Demonstrated understanding of FDA Quality System Regulation (21 CFR 820) and ISO 13485.
• Strong organizational skills, detail oriented.
• Ability to collaborate within an organization across all functional departments (e.g. Legal, Regulatory, Operations, Procurement, Clinical Affairs, Operations, Marketing, Quality, etc.)
• Ability to work to a deadline and to handle multiple tasks simultaneously.
• Experience with Microsoft Office including Microsoft Word, Excel, PowerPoint, and Project.