Root Cause Analysis

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Course Description

The Root Cause Analysis 1-day course will focus on a problem-solving model examining situations leading to continuous improvement and preventing future incidents.  The course will focus on the root cause with systematic investigation to prevent future occurrences.  During the class students will apply what they have learned.

Who should attend?

This course is intended for individuals responsible for quality, risk, safety, managers, technicians, engineers and supervisors tasked to correct and prevent unwanted situations at work.

Certification:
Upon completion of the course, the participants will receive a certificate.

Location and Dates

October 11, 2018

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Course Materials

Course material (i.e. slides, exercises, etc.) will be provided.

Cost

$495 per person




Certification

Upon completion of the course, participants will receive a certificate to recognize the time and topics covered during this course.

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2-Day Internal Auditor Training

Training

ISO 9001:2015 Internal Auditor Training

 Course Description

The ISO 9001:2015 Internal Auditor 2-Day Course will focus on the general understanding of the concepts of the standard and the principles and practices of effective internal audits in accordance with ISO 19011 (an international standard that sets guidelines for management systems auditing).  Each clause of the standard is explored.  Students will learn what requirements mean, how to apply them, and how to audit the requirements.

Learning Objectives

  • Understanding quality management definitions, the 7 Quality management Principles of ISO 9001, concepts and guidelines
  • Understanding the roles and responsibilities of the Internal Auditor, how to develop an audit plan, and how to conduct opening and closing meetings
  • Learn how to verify that your organization’s current practices are conforming to requirements by gathering objective evidence through observation, interviewing, and document sampling
  • Conducting all phases of an internal audit
  • Preparing and presenting effective reports

Who Should Attend?

This course is intended for individuals responsible for conducting, managing, or participating in Quality Management System internal audits or supplier audits, including Quality Directors, QA/QC Managers or Supervisors, Manufacturing, Process or Supply Chain Engineers, ISO Coordinators, and Individuals interested in conducting, managing, or participating in first-party (internal) audits.

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Location and Dates

June 18th – June 19th of 2018

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Course Materials

Course material (i.e. slides, exercises, etc.) will be provided.

Cost

$495 per person




Certification

Upon completion of the course, participants will receive a certificate to recognize the time and topics covered during this course.

[contact-form to=”training@exolytic.com”][contact-field label=”Name” type=”name” required=”1″ /][contact-field label=”Email” type=”email” required=”1″ /][contact-field label=”Comment” type=”textarea” required=”1″ /][/contact-form]

 

2-Day Internal Auditor Training

Training

ISO 9001:2015 Internal Auditor Training

 Course Description

The ISO 9001:2015 Internal Auditor 2-Day Course will focus on the general understanding of the concepts of the standard and the principles and practices of effective internal audits in accordance with ISO 19011 (an international standard that sets guidelines for management systems auditing).  Each clause of the standard is explored.  Students will learn what requirements mean, how to apply them, and how to audit the requirements.

Learning Objectives

  • Understanding quality management definitions, the 7 Quality management Principles of ISO 9001, concepts and guidelines
  • Understanding the roles and responsibilities of the Internal Auditor, how to develop an audit plan, and how to conduct opening and closing meetings
  • Learn how to verify that your organization’s current practices are conforming to requirements by gathering objective evidence through observation, interviewing, and document sampling
  • Conducting all phases of an internal audit
  • Preparing and presenting effective reports

Who Should Attend?

This course is intended for individuals responsible for conducting, managing, or participating in Quality Management System internal audits or supplier audits, including Quality Directors, QA/QC Managers or Supervisors, Manufacturing, Process or Supply Chain Engineers, ISO Coordinators, and Individuals interested in conducting, managing, or participating in first-party (internal) audits.

people-woman-coffee-meeting.jpg

Location and Dates

June 18th – June 19th of 2018

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Course Materials

Course material (i.e. slides, exercises, etc.) will be provided.

Cost

$495 per person




Certification

Upon completion of the course, participants will receive a certificate to recognize the time and topics covered during this course.

[contact-form to=”training@exolytic.com”][contact-field label=”Name” type=”name” required=”1″ /][contact-field label=”Email” type=”email” required=”1″ /][contact-field label=”Comment” type=”textarea” required=”1″ /][/contact-form]

 

Lead Auditor Course ISO 9001:2015

Quality Management Systems Lead Auditor Course ISO 9001:2015
(IRCA Accredited) Course Reference No. A17952

This 5-day Quality Management Systems Lead Auditor Course ISO 9001:2015 is designed to provide participants with the knowledge and skills required to perform first, second and third party audits of management systems that meet the criteria of ISO 9001 according to ISO 17021 and ISO 19011.

Over 5 days, you’ll develop auditing skills through a balance of formal classroom tutorials, practical role-playing, group workshops, open forum discussions with a written examination on your final day.

This course is certificated by the IRCA Governing Board and satisfies the formal training requirements for individuals seeking registration under IRCA Auditor Certification Scheme.


 

 

Prior to attending you will be expected to have prior knowledge on:

  • Management system
    • PDCA Cycle
    • Core elements of a management system and the interrelationship between top management, responsibility, policy, objectives, planning, implementation, measurement, review and continuous improvement.
  • Quality management
    • The Seven Principles of Quality Management as in ISO 9000
    • Relationship between Quality Management and Customer Satisfaction
    • The process approach used in quality management.
    • The model of a process-based Quality Management System, the structure and content of ISO 9001.
  • ISO 9001:2015
    • Requirements of ISO 9001:2015
    • Commonly used Terms and Definitions of Quality Management as in ISO 9000:2015

It is advisable that participants have prior experience in auditing activities.

Upon successful completion of this course students will be capable of:

  • 
Performing effective value added audits of quality management systems and reporting the outcomes
  • Leading an audit of a company’s quality management system and determine whether or not it meets the requirements of ISO 9001
  • Understand key elements of ISO 19011 and ISO/IEC 17021 standards
  • Plan an audit against a set of audit criteria
  • Successfully execute a quality management systems audit
  • Creating relevant audit reports
  • Examining Quality Management System
  • Understanding and auditing ”Context of the Organization”
  • Auditing “Leadership”
  • Auditing ”Planning for QMS”
  • Auditing “support”.
  • Auditing “Operation”.
  • Auditing “Performance evaluation & Improvement”.

Who Should Attend:

  • Quality professionals interested in leading and conducting ISO9001 audits
  • Management representatives
  • Quality managers and directors
  • Consultants

Additionally

  • Your business will have in-house knowledge and skills to undertake and lead a quality management systems audit at a supplier/subcontractor
  • Your organization will benefit having the ability to conduct regular ISO9001 audits to improve quality standards

Cost (Per Person):

$1,735.00

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Pricing discounts are available for early enrollment and additional discounts are available for multiple attendees from the same company or group.

For additional information, please feel free to submit the following.

A representative will be in contact to answer any additional questions.

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Public Course Dates and Locations:


Sponsored by ExoLytic, Inc.

August 22, 2016, to August 26, 2016 – Wakefield, MA

Certificate:


Delegates will be assessed on the basis of their progress throughout the exercises.

You will gain 40 CPD points on completing the course

Those who successfully complete the course assessment and written examination will fulfill the training requirements for certification as an IRCA QMS Lead Auditor.

There is a final examination for this course.

Delegates who successfully complete both the examination and the continuous assessment will be awarded a certificate of Successful Completion and will satisfy the formal training requirements for IRCA QMS Auditor Certification scheme.

Global PCS in collaboration with ExoLytic, Inc. is offering a series of training sessions to reach out to a wide market share of individuals seeking accredited lead auditor training.  Global PCS with the assistance of ExoLytic, Inc. has partnered with professional associations tp offer the training to their members and clients while maintaining an open enrollment to others interested in joining any of the offered classes.

ISO 9001:2015 Full Day Session

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One Day ISO 9001:2015 Introduction


 

ISO 9001:2015 is released. Due to overwhelming demand, Exolytic is offering a one-day class explaining this new revision.

In this full-day session, you will learn:

  • Why the standard changes
  • What the key changes are and how they will impact your quality system
  • How to approach implementation of ISO 9001:2015
  • How to prepare for transition to ISO 9001:2015 from existing QMS
  • Process Approach and Plan, Do, Check, and Act Model
  • Review of updated quality management principles
  • How to effectively manage Risk Based Thinking
  • Documented information requirements

This class is important for anyone, regardless of whether considering or already registered to ISO.

 

Dates:

Location: