Position : Quality Document Specialist
Location : San Diego CA
Duration : 12 Months Contract
Total Hours/week :40.00
1st shift
Description:
- Responsible for the efficient and effective performance of testing in conformance with regulations and standards.
- Responsibilities include inspection analysis of results determining final disposition of some product and detecting nonconforming conditions.
- Works within clearly defined SOPs and/or scientific methods.
- Adheres to quality guidelines.
- Complies with regulations and standards.
- Identifies basic noncompliance within regulations and standards.
- Maintains appropriate licenses / training / certifications as needed.
Experience & Skills:
- Two to three years experience.
- Proven ability to correctly interpret drawings and geometric dimensions and tolerances.
- Able to use standard measuring equipment including calipers RandomAccess memory (RAM) optic micrometers pin gauges gage blocks etc.
- Previous experience participating in continuous improvement activities.
- Demonstrated understanding in the use of calibrated equipment and ability to follow equipment maintenance repair procedures.
- Documentation review
- Electronic and hard copy review as it relates to product release
- History of med device background
- Pharmaceuticals scientific
- Proficient at writing
- Looking for someone who has a degree scientific would be preferred
- Computer work
- SAP would be nice to have
- Product releases
Required Experience:
Unclear Seniority