QTEC Consulting Corporation

• Quality System Implementation and Auditing

• ISO 9001:2001

• TS16949

• ISO 13485 Model Year

• Manual, Procedure, and Work Instruction Writing
• Chrysler Process Sign-Off (PSO)
• Process Flow, Control Plan, and FMEA Development
• Business System Implementation

• Product Development Systems

• Engineering Change Systems

• Risk Management Implementation - ISO 14971

On-Site Training is available in all the subjects noted above.  Our most popular training is in Quality System Implementation and Auditing

Quality System Implementation and Auditing

Our most popular repeat service. If you do not have time to consider internal ISO9001:2000 or TS16949 audits, or you need a fresh pair of eyes to prepare for your surveillance audit, call QTEC!

Key Benefits

• A fresh pair of eyes. QTEC personnel will view your processes and procedures from a new perspective.
• Resources. A good internal audit can be severely time intensive and may get neglected. Or maybe you need professional talent to make your presentation "just right."
• Experience. QTEC personnel have been involved in more than 30 successful surveillance audits.

Production Part Approval Process (PPAP) and Process Sign Off (PSO) Preparation

Are you in the automotive industry? A QTEC representative can ensure you meet all the customer specific approval requirements of DaimlerChrysler, Ford, and General Motors. 

Manual and Procedure Writing

Are you seeking ISO or QS Certification, but overwhelmed by the paperwork? Allow QTEC to write concise, compliant documents for YOUR company, without creating a paperwork nightmare.

If you are setting up a new process, or you are just beginning to document your operator instructions, a QTEC quality engineer can create all the instructions and visual aids your company needs.

Let QTEC write the Operation Descriptions and create full display boards with OD’s, visual aids, digital photos, shadow boards and your company or customer logos. The QTEC representative will also verify the Operation Descriptions match the process flow, control plan, and FMEA, and will make improvements accordingly.

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Process Flow, Control Plan, and FMEA Development

Do you need help documenting your process controls?  Let a QTEC quality engineer write your process flow, control plan, and PFMEA.

Are you sure all your documents are current and match each other? QTEC can review and update your process control documents.  Using an outsider allows a “fresh pair of eyes” to evaluate your system, so errors you may be overlooking can be spotted.

Specific Quality Engineering Service Examples

Automotive Industry (Multiple Plants), Tier 1 Suppliers, Fortune 150 Companies

Developing and maintaining: control plan, FMEA, customer PPAP’s, customer corrective actions, plant corrective action system, operation descriptions, management operating systems (MOS), DaimlerChrysler on-line PRISM corrective action system. Converting all process documentation to industry-required software package.

Porcelain Enameling Industry - Metal Fabricating and Job Shop Enameling Plant

Developing and maintaining all process work instructions, all level 1, 2, and 3 ISO 9000 documentation, meeting customer quality reporting requirements, developing new quality reporting systems for customers.