Engineer Principal Jobs in Utah

Leadership experience: proven ability to lead and manage cross-functional teams, effectively communicate with all levels of management, and drive effective change.

Proven Project Management skills, with ability to produce results.

Serves as a mentor and advisor for the Quality team to assist in developing Quality Engineering skills and capabilities.

Leads promotion of Quality and Regulatory requirements.

Applies the requirements of the Quality System to processes, products or services.

Minimum of 8 years related experience, preferably in the medical device industry related to process/quality engineering.

At least five (5) years of successful teaching experience

At least three (3) years of successful experience as an administrator or supervisor

Knowledge of New Jersey Core Curriculum Content Standards

Knowledge of budgeting and budget implementation

Leadership Requirements under the ISSLC Standards:

Ability to analyze data and to make evidence-based decisions.

In-depth-knowledge of SNT-TC-1A regarding training personnel including testing and certification.

Lead & co-ordinate NDT related requirements, including training.

Minimum of Eight years of applicable experience required; manufacturing experience, with previous NDE testing and supervision experience preferred.

Identification and resolution of significant product, process, hardware and software quality issues pertaining to NDE inspections on in-process and final materials.

Drive continuous improvement projects pertinent to the implementation, deployment and maintenance of the NDE program.

Understanding of ultrasonic testing using immersion technique.

Masters degree with 7+ years’ relevant experience OR PhD degree with 3+ years relevant experience

Experience with development of drug-device combination (DDC) products and primary packaging

Experience of using CAD and Simulation software

Working experience of managing multiple projects of varying complexity simultaneously.

Liaise with our internal and external manufacturing partners to assess early technology device Design for Manufacturability and Assembly (DFMA).

Identify opportunities and propose potential mitigations during participation in design reviews at critical stages of device and product development.