ISO 9001:2015

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Let our proven track record in effectively assisting companies to identify and implement improvement opportunities and to facilitate the transformation process.

sijrawticertification.co.in understand that each organization or person is unique. Our Solutions are comprehensive and will be customized to meet your specific needs.

For example, our consultants can take your company through ISO 9000/9001 from start to finish, and in most cases you have ready for registration in 1 to 3 months.

This comprehensive implementation program is tailored to your individual plans and may include a benchmark visit, an overview of the standards, writing and revising documentation, on-site or off-site training of personnel, assistance with implementation, liaison with the registrar, reassessments and follow-up evaluations, and consulting during the registration process.

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

  • 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 opportunities for improvement.

Typical Documentation Structure
Documentation requirements are usually divided in four Tiers:

  • Quality Policy and Quality Manual
  • Quality System Procedures
  • Work/Job Instructions
  • Quality Records

What is a Quality Manual?
A Quality Manual is the statement of the organization’s quality policy and describing the quality system of an organization. It is usually written by managers from top-level management and the quality department.

What is a Procedure?
Procedures define activities at the departmental level and written by department supervisors. They are usually referred to in a quality system, as a “written” procedure or a “documented” procedure. Procedures should ideally be organized into the ISO 9001 outline structure, indicating the ISO 9001 clause (4.1 – 4.20) under which they fall, though is not an ISO 9001 requirement.

What is a Work Instruction?
Work instructions describe how work is accomplished, it is 100% of how to complete a specific task or operation, and are usually written by the operators and trainers.

What are Records?
Quality records provide the backbone of the quality system.

Quality records consist of all forms, or controlled documents and quality records (hard copy and electronic) necessary for the quality system to operate. Quality records usually consist of all completed forms and charts.

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 ISO 9000, TS 16949, ISO 14001 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.

The information gathered here will be used to develop your implementation and action plans. Again, our auditors will provide you with a detailed written report and recommendations for improvements.

A needs assessment is an ideal way to start a quality system implementation program or to ensure your company is in the position to successfully pass a registration audit.

Auditing is critical to ensure compliance and find out the gaps. It maximizes the benefits of implementing ISO9001 . 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 ISO 9000
  • Auditing techniques compatible with ISO 9000.
  • How to plan, perform and report on an audit
  • How to take corrective action.
  • Architecture of ISO 9000 Documentation.
  • Preparation of Checklists
  • Nonconformities – Major and Minor
  • Seeking Objective Evidence Through Documentation

Learning Outcomes:

  • Better understanding of ISO 9000 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 most exacting requirements of ISO 9000.


Training Options

Please contact us at your earliest to jump start your Quality Drive. All of our training programs can be customized to meet your organization’s needs. Our programs can be scheduled for a half-day seminar, full-day seminar, or multiple-day seminars

How Can We Help ?

Sijrawticertification consists of full-time trainers and consultants with industry-diverse experience. While we do use industry proven approaches and methodologies, we tailor these to fit your organization’s specific needs.

A unique combination of manufacturing experience, business and financial expertise, and a “hands-on” approach creates a recipe for our clients’ success. We not only identify and prioritize opportunities to add significantly to your bottom line; we develop and help our clients implement a plan for exploiting those opportunities to achieve financially measurable success.

” The mission of ISO is to promote development of standardization and related activities in the world with a view to facilitate the international exchange of goods and services, and to develop cooperation in the spheres of intellectual, scientific, technological and economic activity.”

The scope of ISO is not limited to any particular industry; it covers all standardization fields. It may specify the tasks that a certain range of equipment must be able to perform, or describe in detail an apparatus and its safety features. ISO 9000 and Iso14000 are two of the most recognized standards series. The standards embody comprehensive quality management concepts and guidance, together with several models for external quality assurance requirements. ISO 9000:2000 and ISO 9004:2000 are guidance standards. They describe what is necessary to accomplish the requirements outlined in the measured standard 9001:2000 (Which replaced 9002 & 9003 effective December 15, 2000) Increasing public concern over the world’s environment led to a new set of standards in 1996.

What is ISO 9000?

sijrawti certification is a premiere source for ISO 9000/9001 Training and Consulting Services.

ISO 9000 is an International Quality System Standard. It started out as a European Standard but has become a global quality standard that applies to any business or country in the world.

ISO 9000 is rapidly becoming the most popular quality standard in the world. Thousands of organizations have already adopted this important standard, and many more are in the process of doing so.

ISO 9000 applies to all types of organizations. It doesn’t matter what size they are or what they do. It can help both product and service oriented organizations achieve standards of quality that are recognized and respected throughout the world.

When you purchase a product or service from an organization that is registered to the appropriate ISO 9000 standard, you have important assurances that the quality of what you receive will be as you expect. In addition, with the year 2000 revision of the standard, quality objectives, continual improvement, and monitoring of customer satisfaction provide the customer with increased assurances that their needs and expectations will be met.

Here’s how it works. You decide that you need to develop a quality system that meets the ISO 9000 standards. You choose to follow this path because you feel the need to control the quality of your products and services, to reduce the costs associated with poor quality, or to become more competitive. Or, you choose this path simply because your customers expect you to do so or because a regulatory body has made it mandatory.

You then develop a quality system that meets the ISO 9001 quality system requirements. In the course of doing so, you also consider ISO’s many guidelines.
Once your quality system has been developed and implemented, you carry out an internal audit to make sure your system is working properly.

Then you invite an accredited external auditor (registrar) to evaluate the effectiveness of your quality system. If your auditors like what they see, they will certify that your quality system has met all of ISO’s requirements. They will then issue an official certificate to you and they will record your achievement in their registry. You can then announce to the world that the quality of your products and services is managed, controlled, and assured by a registered ISO 9000 quality system.