Data Quality Engineer
Data Quality Engineer
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
Design Quality Engineer
Irving TX
Long Term
Mandatory Skills:
1. Design & clinical risk management DFMEA production risk management PFMEA and overall risk summary reporting
2. Review and approve design documentation including Verification & Validation rationales risk documents (design and process) standards evaluations mechanical test protocols and reports.
3. Ability to work in a team setting within Design Quality and cross-functionally
4. Provide leadership in all areas of the Quality System including but not limited to corrective and preventive actions product complaints post market surveillance nonconforming materials risk management and audit support functions
Job Details:-
1. Provide support for review of existing documents assessing gaps revising documents creating design
engineering rationales to meet EU MDR requirements Sustaining engineering quality support
2. Review and approve design documentation including Verification & Validation rationales risk documents
(design and process) standards evaluations mechanical test protocols and reports.
3. Support risk management activities including planning design & clinical risk management DFMEA production risk management PFMEA and overall risk summary reporting
4. Revise review and approve verification and validation activities as required
5. Review and approve any required drawing updates including design impact assessments Review and approve any labeling updates including design impact assessments
6. Deliverables to be quarterly based on assigned files. Apply statistical methods and design/process excellence tools to support design engineering rationales/memos as required
7. Provide leadership in all areas of the Quality System including but not limited to corrective and preventive actions product complaints post market surveillance nonconforming materials risk management and audit support functions
8. Provide leadership in the understanding of medical device regulations to other disciplines.
9. Ability to work in a team setting within Design Quality and cross-functionally is required
10. Communicate effectively at all levels within Quality as well as cross functionally with departments such as Product Development Regulatory Medical Affairs Manufacturing and Marketing
11. Know and follow all laws and policies that apply to ones job and maintain the highest levels of
professionalism ethics and compliance at all times.
Employment Type
Full-time
