DEKA Research & Development Quality Assurance Inspector in Manchester, New Hampshire

DEKA R&D has an immediate opening for a Quality Assurance Inspector to work in a manufacturing environment in a dynamic Medical Device Research, Development and manufacturing company. This position reports to the Manufacturing QA Manager and is a high visibility role that has significant and direct impact on the manufacturing process and success of projects. The hours for this role will be 10:00 AM - 6:00 PM.

Responsibilities:

  • Perform inspection of purchased components / material and manufactured product according to specifications

  • Participate in the development and/or revision of Operation and Inspection Procedures

  • Review Device History Records, Work Orders and other documentation for compliance to established procedures and Good Documentation Practices

  • Participate in Material Review Board meetings for disposition of rejected material

  • Review proposed process changes that apply to the inspection function

  • Assist in performing calibration of equipment

  • Conduct process audits against written procedures

Qualifications:

  • 3 years experience in an inspection role in a medical device environment

  • Measurement skills utilizing mechanical measuring equipment

  • Micrometers, calipers, drop indicators

  • Blueprint interpretation

  • Basic computer skills and knowledge

  • Familiarity with standard sampling plans

  • Proper handling of Electro-static discharge (ESD) sensitive components

  • Printed circuit board assembly / solder quality inspection experience