Quality Assurance Engineer H/M
at Safran
Industrial, Qro., Mexico -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 26 Dec, 2024 | Not Specified | 01 Oct, 2024 | N/A | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
DESCRIPTION DU POSTE
Quality Assurance Engineer is responsible for surveillance all the compliance, effectiveness and quality of the shop processes with the applicable aeronautical authorities, OEM, customers, Quality Management System, and company procedures requirements.
DESCRIPTION COMPLÏ¿½MENTAIRE
- Verify that SAESA’s Quality System is followed and updated as required
- Works with other areas in the review and preparation of internal procedures, assure its compliance with Company’s Policies and the Authority requirements
- Participate in Quality Investigations & establish root causes of non-conformities & customer complains. (Problem-solving and risk management knowledge (8Ds, bow-tie, FMEA)
- Performs internal audits of different areas
- Reports & request action plans for non-conformances and improvement opportunities detected
- Validates the Capability Self Evaluation form for each new process implemented in the Company
- Participates in the creation, analysis and updating of quality indicators as required in order to establish action plans
- Verifies and validate the first article (FAI) for new processes
- Validates qualification file for special processes
- Performs returns of experience (RETEX) and briefings for her/his assigned gate
- Performs training on Quality Fundamentals in the On Boarding plan
- Preforms the Spot Audits and the calibration for personnel participating in the spot audit program as auditors and verifies completion of the action plan for the spot audits and On Job Monitoring of her/his specific gates
- Quarantine and scrap management
- Follow up of the RPP
- Revision and validation of Request For Change
- Evaluate the technicians and inspector capability and knowledge in order to validate their new scopes in roster
- Calibration Program
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Production / Maintenance / Quality
Software Testing, Clinical Pharmacy
Graduate
Proficient
1
Industrial, Qro., Mexico