Importance of OHSAS Lead Auditor Courses Training

OHSAS 18001 is an international standard for occupation, health and safety that provide a systematic approach to occupational health and safety system which assess the work place hazards and implement protective measure to day to day operation. OHSAS 18001 is published by ISO in July 2007 was developed in extensive demand for an acknowledged standard against to certify and review the OHSA system. OHSAS 18001 is one of the important standards of 18000 families which demonstrate the prerequisite of all areas of business system of the organization and the compliance of the employees, excellent business morals with appropriate business accomplish and government rules.   Implementing work safety environment and working relations convey a successful working process which perks ups of financial condition in organization. This standards is generally applicable to business organization having heavy work duty and high hazard environment, it will covers all the aspects resembling planning and hazard identification, hazard assessments, communication, guidance and operational observations. 

OHSAS 18001 lead auditor training 

OHSAS certification noticeably reveals occupational health and safety management system awareness, OHSAS training, emergency attentiveness, compliance to legal obligations, performance measuring and upgrading in addition to efficient safety constraints. The OHSAS 18001 certification demonstrate the requirements of occupational health and safety management system that facilitates an business organization to develop and implement health & safety legislation within the organization it will also helps in improving the occupational health and safety  performances. By implementing OHSAS 18001 system, organization get benefited with higher productivity, reduce the consequence of government against health & safety in organization, the main benefit to the organization is reduction in accidents, improve performance and reduce the insurance cost.  It is essential to maintain, manage occupational health & safety issues are involved within a business organization day to day activities. If any unawareness of the significance of any aspects then it will leads to hazard, health issues, valuable employee’s loss, some time it will lead to loss in contracts, production & services. It will be mandatory to circumspectly identification of the hazards, hazard assessments and determined controls up-to-date. OHSAS 18001 certification training guiding principle endows with a complete model for occupational, health, safety management systems.

IRCA approved lead auditor courses training provides employees with comprehension and skills concerning to the OHSAS 18001 auditing program. OHSAS lead auditor courses training help you to learn OHSAS 18001 standards, ways to maintain safety within the organization, avoid hazard in probably dangerous equipment. By learning OHSAS lead auditor courses one can establish correct OH & S management system that will accumulate all from being injured on the duty.

OHSAS 18001 Safety Procedures

A major part of the OHSAS 18001 standards will be the preparation and implementation of SAFETY PROCEDURES for successful OHSAS control. These process should cover up all functions, activities and processes that have, or could have (if unrestrained), an important direct or indirect effect on the OHSAS.

The type and range of the safety procedures should be suitable to the nature, involves and OHSAS significance of the function, bustle or process that they address. In all cases, conversely, the objectives should be to control the action in question in accord with particular requirements.

OHSAS 18001 Occupational Health & Safety procedures need to be written down, made accessible to relevant employees, monitors, documented and updated. The safety methods should not be issued in isolation; they should be a elementary part of the enterprise's OHSAS Policy and management system as a whole. Their purpose is to define clearly the organizational structure and management controls. In order for procedures to be efficient, employees at all levels of the organization will need to be given training to take advantage of and control.

The organization OHSAS policies, purposes and programmes need to be interpreted into specific safety procedures, which set out:

* Actions obligatory to support the OHSAS 18001 Policy and to transmit out tasks without damage to the OHSAS performance of the organization.
* Consistency of understanding and action.
* Permanence and uniformity of performance when personnel and transforms occurs and
* A basis for control of the OHSAS management system and its efficiency.

OHSAS 18001 Occupational Health and Safety management system process are expected to be required for the areas given below. Conversely this is not the comprehensive list. Depending on the requirement of the projected OHSAS many more methods may need to be developed.

* Work instructions covering day-to day actions and arrangements, irregular working and emergency situations.
* Monitoring and manage arrangements and activities.
* Contractor, supplier and other procurement activities and understandings.
* Product, process and other alter procedures; and
* other requirements compulsory to achieve the OHSAS policy and programme; these may perhaps relate to:
* achieving compliance with particular programme requirements.
* Research compliance with particular programme requirements.
* Assortment and use of raw materials, purchasing, product take back, energy utilize, life cycle analysis.

Development Structure of OHSAS 18001 Safety Procedure:

The OHSAS 18001 safety procedures may be developed in the format given below.

1. Purpose: The objectives of the procedure are clarified.

2. Scope: Define the area/dept./activities to which the procedure is appropriate.

3. Responsibility: Find out the person who is responsible for carrying out of the purpose.

Write the designation of that person.

4. Activities: Here steps of the actions should be mentioned i.e. the progression of the acts

required for achieving the purpose.

5. Verification and Monitoring: Here the answer to the following question should be given.

* Who will verify that the set procedure is being followed?

* How will the procedure be verified?

6. Records: Every procedure may produce some document e.g. procedure Deviation Report,

Action Taken Report etc. At this time all records should be compiled in a table.

OHSAS lead auditor course in India helps to train the employees and staff for the OHSAS 18001 certification audit which implements best OHSMS in the organization. One of the important benefits of OHSAS lead auditor courses training is to implements such verified OHSAS system that helps to gain confidence and faith of employees and stakeholders as well as gains market credibility of the organization. 

ISO 9001: 2008 Quality Management System

About ISO 9000 Family

The ISO 9000 family of standards compacts mainly with the use of quality management systems to ensure that the customers and clients of an organization encompass their needs met. More than one million organizations are ISO 9000 certified world-wide, making it one of the most used standards created by the International Organization of Standardization. When organizations are ISO 9000 certified, they are telling their customers that they want to bring quality products and services to them, in addition to communicating that they have plans in place to make sure that quality is always managed and is one of the organization's greatest concerns.

ISO 9001: Quality Management Systems and its Requirements

The biggest part of the ISO 9001 standard is the creation and implementation of a quality management system. These systems are used to deliver quality products to customers and guarantee that quality remains reliable.

Quality Management System Process

In order to rally the requirements for the ISO 9001, an organization ought to create a booklet or document that illustrates every aspect of their quality management system. A quality management system is in fact anything that the company or organization does to develop the quality of its products or services. Quality management systems generally necessitate enhancement as time goes on.

The document must include the scope of the system and what it relates to, as well as defining numerous terms so that every level of the organization can identify with it. The document must also have a section that includes the layout of the system and a portion that is designated to management liability. A portion must also be included that outlines resource management in reference to the quality management system, and it must also comprise the approaches that the system is measured and enhanced over time. The ISO 9001 also requires a quality manual or quality policy, both of which can be integrated in the document.

Internal Audits

Often time’s businesses need to audit themselves in order to ensure they are following their quality management system so their certification does not get stripped. Internal audits can be approved by any level of the organization and obligation follow the quality manual and document that were created. In some organizations, teams of internal auditors are trained to mark and correct certain violations of the ISO 9001 so that they are fixed ahead of external audits are done.

Certification

There are several authorization bodies located in several countries around the world that are able to provide certification for the ISO 9001, as well as numerous other ISO standards. These Certification Boards (CBs) are not technically authorized entities, but they are frequently supported by local governments.

Benefits of Implementing QMS

There are several benefits concerned with creating a QMS. Not only has ISO 9001 compliance revealed to increase customer constancy and trust, but it has also been shown to increase competence and operational excellent in organizations. The ISO actually forces organizations to become more operationally well-organized because they want to get certification. Organizations that are looking to raise their efficiency and are having hitch with retaining clients or customers should reflect on implementing a QMS and acquiring ISO 9001 certification.

Proper and regular audit checks will only heighten the business. Lead auditor courses will give an auditor who is efficient, proficient and knows the work properly. While selection of lead auditor training courses, try to enroll with organizations which are accredited with IRCA. As irca approved lead auditor courses are recognized at global level and enhance your chances to become lead auditor in ISO Certification Company.

5 Days QMS lead auditor training Mumbai

Objectives of Course –

Our QMS Lead Auditor course designed for professionals who involved in auditing or responsibility to manage establishes, implement and maintain quality management system. This course is also beneficial for those who want to pursue there career in auditing, Quality Managers, Quality Assurance & Quality Control Engineer.

QMS Lead Auditor Training Mumbai

Course Content -

QMS Auditor/Lead Auditor Training - IRCA approved (A17552).

The course is outlined to provide delegates with the knowledge and skills needed to audit and quality management system. QMS lead auditor training comprises of lectures and workshops including role play and case studies which develop full understanding of quality audit process and the practical sessions focus on audit process for QMS Documentation (Stage 1) as per ISO 19011 and ISO 17021

Course Introduction –

Eight Major Quality Principles
ISO 9001:2008 Standard Overview
Requirement of ISO 9001:2008
Workshop Conformity Assessment
Introduction to audit-Process Approach Audit
Audit plans & preparation
Auditor skills and techniques for process auditing
Onsite Simulated Certification Audit (Stage 2) as per ISO 19011 and ISO 17021
Certification and Accreditation process
IRCA registration Process
Written Examination

Course Fee -

IRCA approved lead auditor training Course fee is just 18600 which also includes certifications & exam fee.

Course Duration -

IRCA approved lead auditor courses runs for five days running from 8.30 am until 7.00 pm for the first four days and from 8.30 am until 4.00 pm on the final day. QMS lead auditor courses training course may be run in-house for organizations wishing to train a team of auditors. Our courses are held at various locations in India, including Kolkata, Delhi, Chennai, Bangalore & Kochi.

For further information contacts us

Mr. S. K Roy

Call:  9874389139
Email: mbm@tr-cbl.com    Website: http://tcbkf.com/                                                                                                                   

5 Days QMS lead auditor programme in Delhi

5 Days Interactive QMS lead auditor programme in Delhi

Objectives of Course –

Our QMS Lead Auditor course designed for professionals who involved in auditing or responsibility to manage establishes, implement and maintain quality management system. This course is also beneficial for those who want to pursue there career in auditing, Quality Managers, Quality Assurance & Quality Control Engineer.

IRCA approved lead auditor courses

         IRCA approved lead auditor courses

Course Content -

QMS Auditor/Lead Auditor Training - IRCA approved (A17552).

The course is outlined to provide delegates with the knowledge and skills needed to audit and quality management system. QMS lead auditor training comprises of lectures and workshops including role play and case studies which develop full understanding of quality audit process and the practical sessions focus on audit process for QMS Documentation (Stage 1) as per ISO 19011 and ISO 17021

Course Introduction –

Eight Major Quality Principles
ISO 9001:2008 Standard Overview
Requirement of ISO 9001:2008
Workshop Conformity Assessment
Introduction to audit-Process Approach Audit
Audit plans & preparation
Auditor skills and techniques for process auditing
Onsite Simulated Certification Audit (Stage 2) as per ISO 19011 and ISO 17021
Certification and Accreditation process
IRCA registration Process
Written Examination

Course Fee - Just 18000 + Taxes

Course Duration -

IRCA approved lead auditor courses runs for five days running from 8.30 am until 7.00 pm for the first four days and from 8.30 am until 4.00 pm on the final day. QMS lead auditor courses training course may be run in-house for organizations wishing to train a team of auditors. Our courses are held at various locations in India, including Kolkata, Delhi, Chennai Bangalore & Kochi.

For further information contacts us

Mr. S. K Roy
L.22/11, Lower Ground Floor, DLF Phase II, Near Private Hospital, Gurgaon 122001, Haryana, India.
Phone: +91 98743 89139
Email: mbm@tr-cbl.com

Website: http://tcbkf.com/

ISO 9001 Auditor Job Responsibilities

An ISO auditor key role is to performing audits and they have does their work on regular basis. To be able to understand the work of an ISO lead auditor better, it’s essential to learn and take professional ISO lead auditor courses training to carry out task being done during an ISO audit. Let’s suppose there’s a company that wants to become ISO certified. In order to verify if this company can be legitimately based on ISO standards, an audit will be conducted. And in continuation with the process audit is divided into several different phases.

audit cycle

Detailed steps required to conduct an audit 

Planning phase (preliminary review)

·         Exposure of the audit needed will be identified

·         Identification of people from the auditees who are directly liable based on the coverage of the audit

·         All the necessary documents will be identified

·         Detailed elements of the company to facilitate the need to be audited will be identified

·         Time frame required completing the audit

·         Task of team members who will carry out the audit

·         Instructions will be prearranged to the members of the team as to each member’s role and scope of dependability in the audit

·         Development of checklist

Audit phase

During the audit phase there is an open meeting in between the auditor and the auditees, auditor notify the auditees with brief discussion about the scope and objectives of the audit led by the auditor and they also provides an overview of the process involved in conducting of audit, particularly when it comes to non-compliance.  Date and the time of the ultimate meeting are also set in addition to arrangements for the departure of the auditors.

The definite audit is at this instant conducted. This is administered using the checklist to facilitate which is previously developed and will be revised and expanded as needed. It will be resolute during this phase as to whether the implemented system is well thought-out compliant or non-compliant. This will be based on objective data that has been collected, examined and documented. Any non-compliant procedures will be noticeable and precised with explanation included. For every movement being audited, the auditor will signify whether it is acceptable, not acceptable and/or not applicable. Remarks will also be made as obligatory. The auditees should sign and recognize every non-compliant activity that is found.

Results of the audit are now appraised. One time the audit is finished; the audit team will meet and talk about their judgments. Non-compliant activities and their legality will be reviewed. These findings are finally documented as ‘Corrective Action Request’ and only the character of the non-compliant activity is point out.

The auditors and the auditees meet just the once more for the closing meeting. The ISO lead auditor will now talk about a summary of the pronouncement and will ensure that the Corrective action request is noticeably understood by the auditees. The auditees is subsequently asked to take action to the findings and is probable to administer action plans to make sure that the non-compliant activities will be compliant. This meeting can also be exploits for the auditees to reveal that the substantiation provided is not enough for the corrective action recommended. If the lead auditors have the same opinion to this, then the Corrective action request (CAR) for the particular non-compliance will be closed out and this is documented. The auditees also have the option not to acknowledge non-compliance. This, in addition, is documented.

Audit Report

This is organized under the assistance of the lead auditor. Significant information concerning the audit is integrated in this report, such as:

·         The name/company name of the auditees

·         The coverage of the audit

·         Time frame needed to complete the audit.

·         Identification of people from the auditees who are directly liable based on the reporting of the audit, with company legislature/member of staff and the audit criterion (e.g. quality system standard)

·         Credentials of non-compliant actions

·         Audit results

If a summarize audit is supposed necessary, it is to be stated here. Follow ups are typically for purposes of guarantee that CAR is put into serviced for non-compliance and closed out once accomplished. A deadline is generally given to correct non-compliance.

Out-of-the-way from ISO audits, auditors are also requested to guarantee that they are constantly updated with existing ISO standards, other requirements including legal prerequisites and about general trends (e.g. quality) in the management systems that they specialize on.

In conclusion, ISO auditors have a set of tasks that need to be accomplished. Because of the fact that each organization has a different need, every audit is diverse and consequently consents to more experience to be gained. ISO auditors also work together a lot with people similar to supervisors such as the ISO lead auditor, member auditors, and the personnel of the auditees. It is not abnormal for divergences to take place and for that reason it is an anticipation of auditors to be able to handle such circumstances as professionally as probable.

It is just as exciting as it is tough to be an ISO auditor. The job of auditor is very demanding and one should take into concern all that has been mentioned in order to decide whether he/she beyond doubt wants to pursue auditor career. Find out more about courses or programs related to IRCA approved lead auditor courses | QMS lead auditor courses training | ISO lead auditor courses .

If you are fascinated in becoming an ISO auditor, then visit us at IRCA approved courses or Lead auditor training in India. Act today and start your career in ISO!!!