What are the responsibilities and job description for the Supplier Quality Engineer position at Laborie?
We believe that great healthcare is an essential safeguard of human dignity. At Laborie, we know the work we do matters – it’s what fuels our motivation and contributes to our success. If you’re ready to make a positive impact in the lives of patients across the globe, we’d like to meet you. We support and empower our employees to grow their careers in an environment that encourages a sense of belonging and a connection to doing good. We’re not afraid to roll up our sleeves to make our goals a reality and work together to solve for our customers. We reward and recognize our employees based on our values of Aspire to Greatness, Respect All, Own It, Working Together, Persist with Passion. Who We’re Looking For: The primary emphasis of the Supplier Quality Engineer is to assist with managing product quality through the implementation of supplier/contract manufacturer evaluation procedures, use of risk management tools, and auditing of current and prospective vendors. About the Role:
- Identify and manage the risks associated with supplied materials and maintain and implementing quality system procedures for supplier evaluation.
- Use risk management tools to identify and mitigate supplier risks and participate in the supplier selection and monitoring process.
- Audit current or future suppliers to ensure their compliance to quality system requirements & material specifications and assist with the evaluation and disposition of nonconforming materials.
- Issue and provide technical direction to supplier corrective action requests and monitor and compile reports for Supplier KPI’s, Scorecards.
- Assist with quality assurance processes such as internal auditing, complaint handling, and CAPA fulfillment.
- Participate in product design and development projects as needed and provide engineering support to products including risk management activities.
- Bachelors' degree in an engineering or related scientific field and a minimum of 5 years of experience in quality assurance.
- Knowledge of ISO 13485 and 21CFR compliant quality systems.
- Experience with internal and external auditing.
- Experience applying statistical methods to quality assurance.
- Required to read and understand the following documents:
- Refer to the current version of the Training Matrix Q620-FRM-03 or equivalent
- Paid time off and paid volunteer time
- Medical, Dental, Vision and Flexible Spending Account
- Health Savings Account with Company Funded Contributions
- 401k Retirement Plan with Company Match
- Parental Leave and Adoption Services
- Health and Wellness Programs and Events