Responsibilities: The incumbent may be required to perform all or a combination of the following essential functions as determined by business necessity.

Assist in the design and development of new products by contributing to risk analysis, verification, and validation test plans, etc.

Good understanding of statistical techniques, risk analysis, Gage R&R, Cpk, ANOVA and DOE.

Good problem-solving experience with Cause & Effect diagrams, Failure Mode Effect Analysis, Root- Cause, -Why, D.

Approve Engineering Change Orders, review prints and be familiar with Geometric Tolerancing.

Maintain Quality Records.

Perform Corrective Actions and Non-conformance assessments.

Assist in investigating customer complaints.

Perform internal audits as well as supplier audits.

Support Incoming Inspection.

Review Work Instructions, Quality Plans, FMEAs, specifications, drawings, quality systems and analysis trends.

Participate in and lead continual improvement projects.

Support environmental and sterilization monitoring.

Some travel is required for supplier support. Requirements: Bachelor's Degree in Mechanical or Biomedical engineering or equivalent experience.

Very good written and verbal communication skills.

At least years of engineering experience; preferably in the medical device industry.

CQE/CQA certification helpful but not required.

Certified biomedical auditor is preferred.

Familiar with FDA CFR, ISO.

Experience with aseptic production and/or sterilization is preferred.

Accuracy, thoroughness, attention to detail, legibility in completing records is essential.

Lean and Sigma knowledge a plus.