Duties: Review our manufacturing specifications to identify materials needed for production. Research, source, and assess the best vendors to supply the necessary materials. Create Annual Supplier Audit Schedule and execute Audits as planned. Manage completion of correction and corrective actions at Supplier sites. Review and approve quality document changes. Participate in Management review meetings to present Supplier performance trends. Participate in the Material Review Board meetings to determine root cause failure and serve as liaison with Suppliers. Manage the Supplier Corrective action program SCAR. Maintain accuracy and completeness of all Supplier Files. Work with Quality Operations to implement quality improvements (e.g., complaint investigations, defect analysis, control charts, data analysis, lead quality and CIP teams, CAPA). Develop quality inspection criteria for incoming inspection and final inspection. Serves as an Internal Auditor and performs internal and supplier audits. Requires a Bachelor's degree in Bioengineering, Biomedical Engineering, or related field plus 2 years of experience in quality assurance in the medical device industry. This position requires 2 years of experience with the following: • Medical Device Single Audit Program; • Medical Device Quality Assurance; • Supplier Audits; • Analytical skills; • ISO 13485; and • Quality control standards and regulations. 40 hours/week, $68,949- $100,000 per year. Applicants who are interested in this position may apply at www.jobpostingtoday.com Ref# 82753
Learn MoreJob Summary: Responsible for developing Lean solutions for production and manufacturing engineering. Support programs by optimizing processes and developing tooling and equipment.
Learn MoreThe Sr. Product Development Engineer (PDE) is actively engaged in executing the main elements of New Product Realization to introduce to market novel surgery-ready surgical instruments. As a team member in this role, you will participate with the following activities: Concept Development, Design & Development, Performance Evaluation, Design Verification & Validation, and Design Transfer. You will serve as Core Team Member from Product Development, partnering with cross-functional SME on projects. This role includes both hands-on activities and planning, with a focus on innovation, execution, and efficiency.
Learn MoreEffectively assemble cleanroom devices per specific work instructions and or all required documentation within work order package.
Learn More