Bachelor’s, or higher, degree in engineering or applicable science/technology program
3+ years of experience in a cGMP Quality Assurance/Compliant environment (medical devices preferred)
Effective communication, coaching/mentoring, and presenting skills
Ability to manage change
Independent and sound decision making capabilities
Project management to deliver on time results
Leadership skills / Emotional Intelligence
Ability to utilize statistics at a moderate level for trending and interpretation of statistical data
Competencies:
Proficient with Microsoft Office tools, especially Excel
Technical writing
Statistical analysis – Minitab or other software equivalent, preferred
Bachelor's degree