Job Description
The Director of Quality Systems will be responsible for maintaining the Jabil Global Quality Systems and implementing improvements to drive Quality as a competitive advantage.
Essential Duties & Responsibilities
Will drive Global Quality System compliance to ISO 9001, ISO 13485, AS 9100, TS 16949 and ESD 20.20 standards
Coordinates global quality initiatives and facilitates the sharing of best practices.
Propose, facilitate and execute new quality systems process to establish Quality as a competitive advantage
Defines, develops, and implements Corporate Quality System development strategies that contribute to business development and strategic directions - quality integration of new manufacturing sites including new site quality integration activity, especially those related to M&A opportunities.
Defines and implements the most efficient quality processes and tools, which support Jabil’s business.
Coordinates plant input to tool set requirements.
Prioritizes initiatives and creates implementation plans in conjunction with corporate IT.
Develops supporting metrics for business processes.
Develops functional Assessment checklists.
Develops and documents cookbook and reference material.
Creates, delivers, and evaluates educational material in conjunction with Jabil U to Functional Managers
Will function as the primary interface to our global registrar
Comply and follow all procedures within the company security policy.
May perform other duties and responsibilities as assigned.
Knowledge Requirements
Experienced quality systems leader with proven history designing and implementing global quality processes
Quality experience leading ISO 9000, ISO 13485, ISO 14000, TS 16949, AS 9100 systems
Ability to translate customer and business needs into value added quality process in operations, engineering and business services
Must have successfully registered manufacturing operations to ISO and / or TS quality systems standards in a $2B+ business
Proven experience leading management review, customer audits, registrar audits and business gap closure teams
Experienced systems auditor with a track record of both identifying system gaps and then closing them
Must have an outstanding history of successful system audits and product registrations.
Successful history working with the FDA on compliance audits and 510K registrations
Successful history leading change management (i.e. AQP, APQP, IP/PQ/OQ)
Experienced working with FDA CFR 820 standards with no FDA warnings or major findings
Successful background in operations in addition to quality management
Education & Experience Requirements
Bachelor's Degree required. Masters Degree preferred.
Degree in Engineering required and Master Degree in Business Administration preferred.
Minimum of 10 years work-related experience required in Quality Management in a High Tech industry
Operations management experience
Six Sigma Black Belt
Foreign language (especially Mandarin) expertise preferred.
Or an equivalent combination of education, training or experience.
Sunday, September 27, 2015
Posts
