
Supplier Process Engineer
- Mexicali, B.C.
- Permanente
- Tiempo completo
- Work with suppliers to execute cost reductions, capacity improvements, and risk mitigation.
- Select the right process and supplier for the part, considering long term fit and total cost of ownership.
- Work with product development, test engineering, and supplier to design, develop, qualify, and implement functional test processes at supplier.
- Manage supplier changes including manufacturing process changes, production optimization, facility changes, new equipment qualification, and new line validations
- Collaborate with suppliers and internal stakeholders to determine deliverables and define timelines.
- Complete project deliverables including: Supplier pFMEA, Component Qualification (FAIR), Process Validations (IQ/OQ/PQ), Inspection Reports, Gage R&R, and Process Capability Analysis.
- Lead the team in overcoming difficult process issues.
- Develop suppliers to excel in all KPIs including Supplier owned quality, capacity, and sub-tier management.
- Drive changes to ISI requirements as necessary by initiating and managing changes to specifications and drawings through the engineering change order process.
- Own and drive to closure supplier variances from symptom through root cause analysis to corrective action, including careful CAPA/SCAR documentation.
- Provide technical support for failure analysis of discrepant production components, assemblies, and field returns. Lead investigations where appropriate.
- Effectively prioritize and advance multiple concurrent projects and tasks.
- Clearly communicate project status to key stakeholders internally and in our supply chain.
- Experience in engineering and manufacturing of medical devices and the aviation industry.
- 5 years of experience in Supplier Development, Supplier Engineering, Supplier Process, or related field preferred.
- Excellent written and verbal communication skills in English (Full Bilingual), a natural team builder/leader.
- Excellent analytical and problem-solving skills along with good judgment.
- Demonstrable knowledge in evaluating and challenging supplier technical, quality, and business capabilities.
- Experience in a high-volume medical device company is a plus.
- Ability to read and interpret detailed mechanical drawings (GD&T) and communicate technical information.
- Ability to travel to suppliers on an as-needed basis - domestic and international.
- BS degree in Electrical Engineering, Mechanical Engineering or equivalent.
- Knowledge of Six Sigma and Lean Manufacturing techniques, certification preferred.
- Knowledge of 21 CFR part 820 and ISO 13485 is a plus.
- Proficient in MS Office and ERP Information Systems, preferably SAP.
- Available for international travel (20% of the year) and have a valid visa
- Ability to travel to suppliers on an as-needed basis - domestic and international.
- Experience in a high-volume medical device company is a plus.
- Knowledge of 21 CFR part 820 and ISO 13485 is a plus.