Quality Engineer Supervisor

SUMMARY:

Direct the development and administration of the company’s quality assurance (QA) system throughout the organization, in accordance with customer and company requirements. Responsible for developing, training establishing a strong Quality Engineering team. Ensure the quality assurance policies and procedures are followed as they relate to ISO, QS and other related registrations. Lead an internal audit team to support registrations

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KEY ACCOUNTABILITIE

1. S:Actively promote and drive a culture of safet
2. y.Develop and manage SPG, MN’s quality system and quality engineers to achieve SPG, MN’s On-Time Delivery, Complaint Rate and Cost of Poor-Quality objective
3. s.Daily supervision of Quality Engineers & engagement with the metrology lab to ensure product realization commitments are me
4. t.Develop a cross functional Engineers team and coordinate training to ensure that their skills levels and performance meet organizational need
5. s.Manage Quality Engineering team and indirect functions to achieve SPG, MN’s business and quality objective

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KEY RESPONSIBILITI

1. ES:Promote a safe work environme
2. nt.Lead by example in support of SPG core values: We are passionate about: The lives our products touch, Safety, Quality & Compliance, Customers, and delivering resul
3. ts.Foster a culture of mutual respect, honesty, communication, and teamwo
4. rk.Provide continuous feedback to subordinates and co-worke
5. rs.Participate in Management Review meeti
6. ng.Manage the Quality Engineers involvement from purchase order receipt to shipment of produ
7. ct.Mentor the Quality Engineering function including defining activities, providing continuous feedback, and providing input for goal setti
8. ng.Support Sales during the quotation process by reviewing quality requirements and estimating SPG, MN’s cost to comp
9. ly.Complete customer Certificate of Compliance for REACH, RoHS, Prop65 e
10. tc.Support SPG, MN’s improvement process by providing training in problem solving and improvement methodology (5S, Root cause Analysis, Process FME
11. A).Plans, develops, and coordinates work activities for Quality Technicians team for production support and final product relea

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Job Qualificat

• ions
  An advanced degree with a minimum of 3 years of relevant experience or 8 years of Quality Engineering experience in the Medical or defense indu
• stry.Ability to read, analyze, and interpret common scientific and technical journals, blueprints, financial reports, and legal docum
• ents.Ability to respond to common inquiries or complaints from customers, regulatory agencies including Food and Drug Administration (FDA) and Federal Acquisition Regulation (FAR) representatives/agencies, members of the business commu
• nity.Ability to effectively present information to top manage
• ment.Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutat
• ions.Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory and factor anal
• ysis.Ability to define problems, collect data, investigate to establish facts, Root Cause, corrective actions and draw valid conclusions based on evaluation of effectiveness
• data.Ability to interpret an extensive variety of technical instructions in mathematical or diagram form such as Geometric dimensioning and tolerancing facilitating abstract and concrete varia