Senior Supplier Quality Engineer

Summary of Duties

Executes supplier development engineering for the Company’s supplier base. Works with manufacturers and service suppliers to ensure product / services provided meet company requirements. Interfaces with other departments as well as with suppliers and other external parties on issues related to product manufacturability and product changes.

• Plans, organizes, directs and reports on all engineering supplier development activities such as raw materials changes, contracted designed and manufactured items, packaging materials, service providers, and laboratories to assure procurements meet or exceed the requirements.
• Works directly with the Company manufacturing plants and the contract manufacturer to integrate the incoming performance of raw material and component supplier to collaboratively resolve issues.
• Assures that customer technical requirements are adhered to by supplier and that a quality system is maintained.
• Develops procedures for supplier management to establish world class supplier processes.
• Conducts programs designed to improve supplier performance, productivity, and process validation.
• Supports quality issues through Supplier Corrective Action Reports as needed and provides assistance to develop corrective actions in an effort to reduce and eliminate defects.
• Manages cost savings initiatives with suppliers through integration into Merit manufacturing facilities.
• Manages supply chain resiliency programs which include but are not limited to supplier consolidation, dual sourcing, acquisition integrations.
• Responsible for ensuring that the cost savings initiatives and supply chain resiliency programs are communicated effectively to senior leadership.
• Develops reports on supplier performance for company management.
• Liaises between corporate and manufacturing sites for the deployment and communication of needs and new or improved requirements.
• Performs a variety of other tasks and related work, as required.

• Lifting — Not to exceed 50 lbs. – local practice may apply.
• Writing
• Sitting
• Standing
• Bending
• Vision
• Color perception
• Depth perception
• Reading
• Field of vision/peripheral
• Fine motor skills

Education and/or experience equivalent to bachelor's degree in engineering or a related field. A minimum of eight (8) years of experience in engineering in the medical device industry. Working knowledge of the Quality System Regulation and ISO 13485 quality system standards. Familiarity with process development and process change. Demonstrated computer skills preferably spreadsheets, word processing, database and other applicable software programs.

• Six Sigma/Lean certification.

• Verbal and Written Communication
• Interpersonal skills

The risk category explains whether or not employees are likely to come into contact with blood or body fluids while performing their jobs. Risk category III states employment and procedures that do not require exposure.

• Multiple shifts and hours to choose from:
  Days, Swing (Eve), and Nights
• Medical/Dental & Other Insurances (eligible the first of month after 30 days)
• Low Cost Onsite Medical Clinic
• Two (2) Onsite Cafeterias
• Employee Garden | Gardening Classes
• 3 Weeks' Vacation | 1 Week Sick-Time | Paid Holidays
• 401K | Health Savings Account

Military veterans are encouraged to apply.