Required Education and Experience:

• 3 - 4 years' experience overseeing ISO/IATF 169419 Quality Management System
• Post Secondary Education in Business Administration or QMS
• Ability to communicate effectively to all levels of plant personnel with ease
• Ability to collaborate successfully with cross functional teams.
• Good organizational, interpersonal, and problem-solving skills, strong attention to detail
• Ability to work to meet deadlines and multiple demands
• Ability to train team members at all levels of the organization
• Ability to uphold confidentiality
• Demonstrates the ability to work effectively in a team environment
• Quality System experience (IATF16949 and/or ISO 9001)
• IATF16949 Lead Auditor Certificate
• Core Tools experience (FMEA, Control Plan, APQP, SPC, MSA)
• Ability to work independently and knowledge of best practices.
• Previous Quality Engineering experience strongly recommended.
• Previous Experience with CMM Programming / Operation or Laser Scanning recommended.

Job Functions:

Quality Management System (QMS)

• Implementing the QMS in support of the company business operations in order to improve cost effectiveness, service quality, and business development
• Creating, auditing/evaluating, revising, reporting, and maintenance of the division ISO/IATF16949; Martinrea Protocols management system, including the procedures, policies and forms
• Monitoring the KPIs of the division and report to the management team
• Performing and managing the QMS/MMS audit with in-house internal quality auditors to very that all activities are performed against the established or documented standard procedures
• Monitoring all identified non-compliances in the QMS and evaluating effectiveness of the preventative and corrective actions
• Maintaining relationships with outside organizations and auditors to ensure our compliance and ability to take care of our customers
• Coordinates with all levels of the organization in developing ISO/TS 16949 compliant processes and documentation, champions the document control system
• Co-ordinates the training of internal auditors, ensures ISO/TS 16949 internal audits are scheduled, executed and closed with all related corrective actions, reports on the status of internal audits to management
• Navigates designated web pages, for customers & Martinrea, to ensure customer specific requirements are understood and incorporated in the systems used at Rollstar; conducts training as necessary
• Manages and leads corrective action events pertaining to internal and external issues up to and including verification, implementation, and closure.
• Ability to comprehend and evaluate the value add/cost implications involved in implementing actions to the company and its overall operations.
• Coordinates external audits, auditors and accompany external audits through the process.
• Maintenance of Quality Management System
• Participates in plant wide continuous improvement projects
• Work on Advanced Product Quality Planning as required to support product launches
• Abide by all Company polices including, but not limited to the following: Health and Safety, Quality and Environmental Systems, Human Resources policies, and the Martinrea Employee Handbook

Environmental Management System (EMS)

• Responsible for all elements of the Environmental Management program, including but not limited to policy creation/ maintenance, program role out, training and communications.
• Environmental Management Representative, responsible for reporting performance indicators and concerns to Sr. Management.
• Management Advisor regarding Environmental legislation in relation to the workplace.
• Perform hazard assessments of workplace and provide feedback to Management
• Co-ordinates the training of internal auditors, ensures ISO 14001 internal audits are scheduled, executed and closed with all related corrective actions, reports on the status of internal audits to management
• Lead and conduct internal audits for EMS
• Document Control for Environmental Management System

Layer Process Audits/ Process Walks

• Implement/ monitor and schedule Layer Process Audits
• Create, evaluate, revise, report, and maintain the audit results, procedures and forms
• Monitoring the KPIs of the LPA /Process walks and report to the management team

Document Control

• Document control Administrator
• Create, evaluate, revise, report, and maintain the QMS documentation (procedures and forms)

Quality Engineering - per business needs

• Participates Advanced Product Quality Planning (APQP) with cross-functional teams on the development of new and existing components to meet critical customer deadlines.
• Implements new procedures and processes in prototype stages of product launches to comply with the customer specifications.
• Responsible for development of CP/PFD/ assist in development of PFMEA
• Develops appropriate key dimensional control points on the new programs in conjunction with the program manager and customer.
• Dimensionally verify products using laser scan or CMM
• Develops and maintains the Control Plan documentation and procedures
• Plans and prepares the PPAP submissions for new products and engineering changes to meet customer deadlines and specific customer requirements (MRD's and Run @ Rate)
• Lead problem solving efforts relating to launch quality issues and production products
• Conduct capability studies and gauge R & R analysis
• To review and make recommendations for the disposition of non-conforming/suspect products in a timely manner and ensure formal corrective actions are answered within customers guidelines
• To notify internal and external customers of potential problems and make recommendations for resolutions
• Tracking customer satisfaction measurable and communicating to appropriate personnel and/or management