ISO upgrade 9001:2008 to ISO9001:2015
Details
Introduction
This course is developed to train QMS committee members /key personnel to understanding the QMS requirements, especially new standards. It is designed as an In-house training course to suit the specific needs of each organization.
Objectives
- To understand the changes in ISO 9001:2015
- To develop strategies for the organization to effectively implement the changes
- To prepare for documentation upgrading
- To prepare for external audit on ISO 9001:2015
Who should attend
ISO Steering Committee Members, Management Representatives, Department Managers, Internal Auditors, Executives and all others involved in the QMS system.
Methodology
This course is equipped with various workshop and case studies to enhance participants understanding
Program Duration
2 days
Class size
A maximum of 25 per session for impactful participationOutline
Consultation Programs
1. ISO 9001:2015 Awareness For Competent Application Training. (including hands-on practical workshops to):- Determine external & internal issues, interested parties requirements, context statement, scope
- Discuss quality policy & objectives planning
- SWOT analysis
- Risks & Opportunities register
2. Review & finalise the current documentation to comply with ISO 9001:2015 requirements: Context statement, SWOT analysis, Risk and Opportunity Register, Quality Policy, Organizational Process Management Plan and Quality Objectives Plan.
3. Off-site Consultancy support for:
a) Reviewing the QMS documentation Manual, procedures, WI and other supporting documents.
b) System implementation includes guidance on internal audit and management review.
4. ISO 9001:2015 Internal Auditor Training (process approach, risk & opportunity).
5. Briefing on Top Management Commitment & be prepared for Management Review Meeting.
6. Mock Audit.
7. Off-site Consultancy Support on the closure of the Corrective Action issued during Mock Audit.
Speaker/s
· IRCA QMS ISO 9000 Series Lead Auditor (UK)
· Lead Auditor, ISO 13485 with Directive 93/42/EEC and 98/79/EC, QMS for Medical Devices
· Lead Auditor, OHSAS 18001
· ISO 9001 Auditor Training
· ISO 14001 Auditor Training
· Registered Trainer under Human Resource Development Fund (HRDF)
· Registered Trainer under Ministry of Finance (Cert. No. 284180)