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Supplier Quality Engineer Jobs
Company | SCIEX |
Address | Guelph, Ontario, Canada |
Employment type | FULL_TIME |
Salary | |
Category | Biotechnology Research |
Expires | 2023-08-18 |
Posted at | 10 months ago |
For over 50 years, SCIEX has been developing groundbreaking technologies and solutions in mass spectrometry and capillary electrophoresis. Our products enable our customers to quickly respond to environmental hazards, better understand biomarkers relevant to disease, improve patient care in the clinic, bring relevant drugs to market faster and keep food healthier and safer. At SCIEX, you’ll find a rewarding role that amplifies your impact on the world and helps you realize life’s potential.
- Monitor supplier performances according to Sciex KPI and supplier Scorecard measurement, and work with supplier for quality improvements.
- Ensure suppliers related NCMR (vendor fault yes) is dispositioned in timely manner.
- Work closely with cross-functional SMEs such as Product Manager, Project Buyer, Design Authority, Manufacturing Engineers, etc., to ensure the materials, components that provided by suppliers are met.
- Support all Continual Improvement initiatives/ activities to improve KPIs.
- Conduct supplier qualification activities not limited to new suppliers on boarding qualification.
- Other duties / ad hoc tasks as assigned
- Provide necessary guidance to supplier, to ensure SCAR is closed appropriately.
- Conduct supplier audits to ensure new or existing suppliers’ QMS and processes meet applicable requirements includes Sciex requirements, suppliers’ ISO standards, or FDA QSR (GMP) where applicable.
- Support factory customer complaint investigation and NPI project where needed, to help reduce/eliminate Field Installation and Warranty defectives.
- Bachelor's degree in a scientific or engineering discipline (mechanical, electrical, software/computer engineering expertise preferable) and/or training or equivalent combination of education and experience.
- 30-50% travel may be required travel regionally and internationally.
- Experience working in manufacturing environment in quality assurance / supplier quality or regulated industry such as medical devices manufacturing is preferred.
- Knowledge in 6 sigma, CPK and SPC will be an added advantage.
- Minimum 2 years’ experience of working in a regulated environment - ISO 13485:2016 and ISO 9001:2015.
- Frequent travel at regional and internationally.
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