This course will help you:

• • Gain the confidence to lead and manage a team of auditors
  • Be prepared for a successful second party ISO 45001assessment
  • Be able to audit according to internationally recognized best practice (ISO 19011)
  • Develop professionally and gain a recognized qualification
  • Network with likeminded peers

This is the course for you if:

• • You already have a thorough knowledge of the requirements of ISO 45001 Occupational Health and Safety Management
  • You need to lead a second party audit in your organization
  • You are a manager who is responsible for a team of internal auditors

Day 1

• • Course aims, objectives and structure
  • First, second and third party audits
  • Typical audit activities
  • Audit objectives, scopes and criteria
  • Audit resources
  • Roles, responsibilities and confidentiality
  • Audit methods
  • Stage 1 audit
  • Stage 2 audit
  • Audit plan
  • Work documents
  • Opening meeting
  • Audit evidence
  • Effective communication
  • Audit findings
  • Audit meetings
  • Closing meeting
  • Audit reports
  • Audit follow-up

Day 2

• • Purpose and benefits of an OH&S Management System
  • Terminology
  • ISO 45001 model and plan-do-check-act
  • OH&S processes
  • Identifying legal and other requirements
  • The role of the OH&S auditor
  • OH&S documentation
  • Initiating the audit
  • Document review
  • Audit plan
  • Work documents
  • Opening meeting
  • Observations
  • Interviewing ‘top management’

Day 3

• • Specimen Exam: Sections 1and 2 review and process audit preparation
  • Calibration against any documented information (e.g. context, planning, MR) i.e. confirm line-of-sight for the OH&S MS
  • Video – Workers’ representative interview
  • Auditing processes: Design, technical sales and procurement ( +WRULD, stress)
  • Auditing processes: Printed Circuit Board (PCB) population and wave solder (electrical + safety)
  • Audit trails
  • Auditing processes: Frame construction and assembly (+WRULD and stress)

 Day 4

• • Specimen Exam: Section 3 review
  • Auditing Processes: Cabinet testing (Test Lab) and loading onto lorries (+electrical safety, stress and WRULD)
  • Nonconformities
  • Closing meeting
  • Audit report
  • Audit follow-up
  • Specimen exam: Section 44

Day 5

• • Hand in homework – audit report
  • The certification and accreditation process, the role of CQI IRCA, the CQI IRCA OHS auditor certification requirements and code of conduct
  • Final questions/final revision
  • Evaluation
  • Introduction/readiness to the exam
  • Exam
  • End of course

Upon successful completion of the course, you will receive a CQI and IRCA certified training course certificate.