R&D Sustaining Engineer Jr

**SUMMARY**:
**ESSENTIAL DUTIES AND RESPONSIBILITIES**:

- Execute test protocols, summarize data, analyze
- Investigate design history files, design specifications, test reports and manufacturing documentation to provide accurate and timely technical information for Regulatory submissions.
- Prepare product drawings and illustrations for Regulatory submission.
- Attend appropriate meetings - technical and core team, providing updates as required.
**REQUIREMENTS**:

- Ability to read, analyze, interpret, create, and meet product specifications, technical procedures, and worldwide governmental regulations.
- Ability to execute testing, statistically analyze data
- Excellent interpersonal skills works well within a team, able to collaborate with and influence others.
- Excellent oral and written communication skills.
**Job Requirements**:
**EDUCATION and/or EXPERIENCE**:

- Bachelor's in Engineering required.
BS in Mechanical or Materials Engineering preferred.
- 1 year engineering experience in medical device product development and/or manufacturing environment preferred.
- Experience with mechanical characterization methods such as tensile, compression or modulus testing preferred.
- FDA Quality System Regulation Part 820 and ISO 13485 experience preferred.
- Microsoft Office skills(Excel, Word, Power Point & Outlook)

**Operating Company**:
Ormco