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ISO / TS16949 Automotive Quality Management System

What is TS 16949?

The result of the IATF's effort is the TS 16949 specification. TS 16949 form the requirements or the application of ISO 9001 for automotive production and relevant service part organizations.

Who are the IATF?

The IATF is an ad hoc group of OEM's and automotive trade associations whose common goal is to improve the quality of products to automotive customers worldwide. IATF members include the Big 3, along with Fiat, Citroen, VW, Renault and national automotive trade associations from the US, Germany, UK, Italy and France. Additionally, the Japanese vehicle association, JAMA, has been involved with the IATF's efforts to develop TS 16949.

TS 16949 Internal Auditor Training

Auditing is critical to ensure compliance and find out the gaps. It maximizes the benefits of implementing TS 16949. Effective auditing is a highly specialized skill and IQMS trains key personnel from your organization to be successful internal auditors.


 
 

 

Training Topics

  • The requirements of TS 16949
  • Auditing techniques compatible with TS 16949
  • How to plan, perform and report on an audit
  • How to take corrective action
  • Architecture of the TS 16949 Documentation
  • Preparation of Checklists
  • Nonconformities – Major and Minor
  • Seeking Objective Evidence Through Documentation

Learning Outcomes

  • Better understanding of the TS 16949 Requirements
  • Learn how to Conduct Internal Audits
  • Audit Process and Cycle
  • Tips for Effective Auditing
  • Preparing and Using Checklist
  • How to Seek Objective Evidence
  • Hands-on/Practical Experience
  • Internal Auditor Certificate (upon successful completion)

Benefits to Your Business

  • Identify opportunities for improvement
  • High quality auditing will ensure that your organization is always compliant with the necessary requirements of TS 16949.
  • Each participant will receive a seminar manual and a team breakout workbook that includes case studies.
  • A guide on "how to" audit TS 16949 elements and the objective evidence required will be taught and provided for participants.

TS 16949 Pre- Assessments / Gap Analysis

We will conduct a third party assessment/audit (gap analysis) of your existing Quality Assurance (Control) Systems which will determine the level of compliance of your facility to quality standards such as TS 16949, ISO 9000 and HAACCP.

We will conduct an assessment on the current quality system and general condition of the company. This will include interviewing key personnel in each department or area. For example, this may include the management team, team leaders, supervisors, office staff, operators, etc…
The assessment will entail the investigation and assessment of existing quality system elements as they apply to the applicable standard.

It is a comprehensive review of a company's quality systems and procedures. Non-compliance's to the standard are noted, and a report issued.

It will also include some general questions to determine the overall condition of the company. For example, questions to determine some of the strengths and weaknesses (opportunities for improvement) of the organization. This will help us identify any barriers that may prevent you from obtaining your goal of Registration.

The responses will be summarized and reports will be issued (including recommendations) and reviewed with the management team.

TS 16949 Implementation Process

  • Management Commitment and Support
  • TS 16949 Audit/Assessment (Gap Analysis)
  • Development of an Implementation Plan
  • Provide Awareness Training to all employees
  • Allocate Resources that will be necessary to develop and implement the system
  • Prepare Quality System Documentation - Tier 1, 2, 3 documents (Quality Manual, Quality System Procedures, Work Instructions and Quality Records/Forms)
  • Determine Training Needs of Employees - Job and Employee Skill Matrix (ie. overview of new system, internal auditing, problem solving, teamwork, etc...)
  • Implement the New System
  • Conduct Internal Audits
  • Take Corrective Actions, if necessary
  • Re-Audit/Follow-up, if necessary
  • Registrar Audit Preparation/Training
  • Registration Application
  • Registration Audit
  • Registration Certificate Issued
  • Maintain, Improve and Innovate the System

TS 19949 Documentation

Documentation plays an important part of a Quality Management System.
We can help you with every level of documentation:

  • We can write the documents for you.
  • We can provide templates so you can write them on your own.
  • We can review your current documentation for compliance.
  • We can review your current documentation for improvement of opportunities.

TS 16949 Consulting
IQMS
is a management-consulting firm designed to create value for manufacturers and product developers. Our clients include organizations from the industrial and consumer products, service and medical device sectors. Providing training and hands-on consulting services in the areas of TS 16949, lean manufacturing, six sigma, and world class manufacturing and design; we can help you achieve lower costs, improved productivity, and improved time-to-market.

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IQMS is the largest quality management consulting organizations which offers a wide range of consulting services like ISO 9001, ISO 27001, ISO 14001, OHSAS 18001, SA 8000 & ISO 22000 HACCP Certification, CMMI, Six Sigma, Lean Manufacturing, Kaizen, 5S Implementation, Toyota Production System.
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