Ensure suppliers comply with CVI QMS requirements.
Responsibilities- Create and update Supplier Quality documentation.
- Maintain a robust supplier quality program.
- Engage with suppliers to create or update qualifications.
- Train to CVI's Quality Management System
- Update Supplier Files starting with High Risk Critical Suppliers and working down through the supplier risk categories.
- Assist supplier quality investigations; Draw from supplier expertise
- Work with Supplier Quality Enginner in resolution of incoming quality inspection supplier discrepancies
- Attend Purchased product nonconformance meeting (MRB)
- Provide engineering support to the incoming inspection function
-Currently pursuing a Bachelor's or Master's degree in a technical discipline.
- Some knowledge of medical device regulations, pertinent standards and
-Proficient in Microsoft Word/Excel/Outlook,
-Excellent oral and written communication skills.
-Ability to work independently and in a team.
- Works under general office environment conditions.
- Utilizes close visual acuity for working with computers and equipment.
-Frequently required to sit, stand, walk, and communicate.