Quality Control Positions Needed

One of the most profitable divisions of a multibillion-dollar corporation with an very healthy backlog and more contracts on the way.
As a Member of the Management team this Quality Director will have:
  • Drive Lean Six Sigma/continuous improvement methodologies plant-wide
  • Develop and support strategic initiatives and collaborate with management continuously increase efficiencies and optimize cost
  • Responsibility for effective root cause analysis, CAPA
  • Direct communication with the customer
  • Accountability for QMS system and KPI metrics
  • maintenance of ISO9001 compliance
  • Complete audit responsibility
  • Manage 3 departments inspection, compliance, QMS (25 indirect, 3 direct)
Key requirements:
  • BS degree
  • Recent 5+ years of experience managing an ISO certified defense/aerospace manufacturing quality department
  • Experience with Lean manufacturing / Six Sigma
  • Demonstrated ability to improve quality, cost, and delivery goals
  • In-depth Problem Solving/Root Cause Analysis and risk analysis (FMEA/FTA)
  • Prior ERP system experience
Location:  Newington NH area
Compensation:  100-130 base plus bonus potential 

Director of Quality
This is an opportunity to join an established company that is experiencing exponential growth.  They have introduced the “first ever” consumer medical device and projections are a 50% increase in sales in 2018.  
They have been using a ISO13485 certified contractor.  Now this corporation wants to implement an internal 13485 compliant quality management system. As the resident expert on all things quality, this Manager will:
  • Take a hands-on role in obtaining and maintaining ISO13485 certification 
  • Write procedures and establish a documentation system
  • Ensure processes for ISO COMPLIANT QMS are established, implemented, documented and maintained
  • Build the quality department; train and direct quality personnel; manage budget
  • Coordinate, review, investigate and resolve complaints 
  • Oversee site audits; audit documentation; findings reporting
  • Suggest and implement corrective actions
  • Participate as a Member of Senior Staff
Key qualifications required:
  • BS degree
  • At least 10 years of experience in quality
  • Track record of direct involvement/hands-on experience obtaining ISO 13485 certification
  • Prior quality management experience
  • Adept at writing procedures
  • Experience setting up 13485 quality documentation system
  • Complete understanding of manufacturing from receiving the material to shipping product
  • 5-10%  international travel
Location: Webster/Worcester, MA area
Compensation:  115-130 base + bonus
Leslie Gabriele
Gabriele & Company
Recruiters for Materials and Manufacturing
781 276 7999
Gabriele & Company specializes in the placement of:
2 Emery Road, Bedford, MA 01730-1061

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