Location: Lake Forest, CA
Duration: 6 months
Major Accountabilities:
- Performs manufacturing documentation review to ensure GxP compliance to internal and external regulations
- Executes product release from **** Global Technical Service Repair Center
- Effectively communicates quality needs to Operations and Supply Chain Teams
- Collaborates across functions to ensure seamless operational execution in the Repair Center
- Trains other on and communicates Good Documentation Practices and other Quality principles
- Meets individual and team performance goals as defined in annual objectives.
Key Requirements/Minimum Qualifications:
- High School Diploma
- The ability to fluently read, write, understand, and communicate in English.
- Work hours: M-F, 40 hours/week, Daytime shift. Option to work 9/80 shift
Top 3 Must Haves:
Prior experience working in Quality in Medical Device or other Regulated Industry
Solid Understanding of Good Documentation Practices
Ability to communicate effectively to peers and supervisors
Job Type: Contract
Pay: $40.00 - $42.00 per hour
Schedule:
Experience:
- Medical device troubleshooting: 2 years (Required)
- Complaint handling: 1 year (Required)
- MDR: 1 year (Required)
- Returned device repair: 1 year (Required)
Work Location: In person