What are the responsibilities and job description for the Supplier Quality Engineer - #W2role position at TekOne IT Services Pvt. Ltd.?
Role: Supplier Quality Engineer
Location: Irving, TX - 75038
Duration: 12 Months on W2
Shift Timings: 8 am to 5 pm
Location: Irving, TX - 75038
Duration: 12 Months on W2
Shift Timings: 8 am to 5 pm
- 100% Onsite role.
- The role involves managing nonconforming materials from suppliers and collaborating with cross-functional teams on the Material Review Board (MRB) process.
- Responsibilities include investigating supplier-related quality issues, identifying corrective actions, monitoring supplier performance, and contributing to continuous improvement projects aimed at enhancing part quality, yields, and cost efficiency.
- Supplier Quality Engineer with 2 to 5 years of experience.
- Proficiency in quality tools such as corrective actions, CAPA, Material Review Board (MRB), and quality hold processes.
- Experience in manufacturing environments, ideally with exposure to supplier quality roles.
- Knowledge of ISO 13485, FDA, and GMP standards preferred, though ISO 9001 is acceptable.
- Ability to interpret engineering drawings and specifications, particularly in areas like printed circuit boards, pumps, motors, and other mechanical parts.
- Strong computer skills, including experience with ERP systems like ADMS, Oracle, or SAP, and proficiency in Microsoft Office for data analysis.
- ERP systems knowledge, preferably ADMS (Oracle-based) or SAP.
- Proficiency in Microsoft Office, particularly Excel, for data analysis and reporting.
- Day-to-day Responsibilities: Manage nonconforming material processes and MRB activities; Work closely with suppliers to resolve quality issues and implement corrective actions; Monitor supplier performance, including calculating supplier scorecards and managing audit schedules; Support continuous improvement initiatives with suppliers to improve product quality and reduce costs; Collaborate with cross-functional teams on quality investigations and material disposition.
- Bachelor's degree (Mechanical, Biomedical, Industrial Engineering) with 3 to 5 years of experience.
- Experience with ISO 13485, FDA, and GMP regulations.
- Familiarity with various mechanical components, including circuit boards, pumps, motors, and injection-molded parts.
- Strong engineering skills, particularly in interpreting technical drawings and specifications.
- Quality tools and processes (CAPA, MRB).
- Manufacturing experience.
- Engineering drawing interpretation.
- ERP systems experience.
