Title: Manufacturing Engineer
Location: Ontario, Canada & United States
Rate: $40-45/Hr on W2
Job Summary:
- 5+ years of Medical device Manufacturing experience
- Support in Manufacturing process remediation and readiness activities for new product launch.
- Support Design Transfer deliverables, including tracking and scheduling.
- Support/Initiate Change Order for manufacturing documentation such as but not limited to, manufacturing procedures, shop floor paperwork, and inspection procedures.
- Risk Management updates – PFMEA.
- Part creation in Windchill. BOM and configuration management.
- Work with cross functional teams as required, especially with R&D, Quality, and Regulatory teams.
- Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
Preferred
- Knowledge of ISO and/or FDA quality system regulations as it pertains to design transfer and process control.
- Previous medical device experience
Benefits:
This a contract position does not include employer-provided benefits.
Equal Opportunity Employer:
We are an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to
race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
Background Check:
Background checks may be conducted in accordance with applicable law.
Work Authorization:
Applicants must be authorized to work in the United States.
