Quality Control Positions Needed

NEAG

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DIRECTOR of QUALITY

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