This is an interactive 5-day workshop designed to give you knowledge of becoming a Lead Auditor. This training is registered with International Registrar of Certified Auditors (IRCA) and it fulfils the requirements for applying for an Audito
DurationThis is an interactive 5-day workshop designed to give you knowledge of becoming a Lead Auditor. This training is registered with International Registrar of Certified Auditors (IRCA) and it fulfils the requirements for applying for an Auditor/Lead Auditor to the IRCA Scheme.
By the end of this training, you will be able to perform first, second and third party audits of QMS against ISO 9001:2015 as per the guidelines of ISO 19011 and ISO 17021 as applicable.
Learning Outcomes:
- Describe the purpose of a quality management system (QMS)
- Explain the purpose, content and interrelationship of ISO 9000:2015, ISO 19011:2011, and ISO 17021:2011
- Explain the high level structure and risk based approach
- Describe the roles and responsibilities of auditors and lead auditors
- Interpret the requirements of ISO 9001:2015 within the context of audit
- Plan and conduct an audit in accordance with ISO 19011 and ISO 17021 and demonstrate the ability to:
- Gather objective evidence, through effective interviewing, observation, sampling and note taking
- Plan and prepare effectively
- Analyze and interpret information in order to determine conformance with requirements
- Undertake audit follow-up activities, including evaluating the effectiveness of corrective action
- Report the audit, including writing valid, factual and value-adding non-conformity report
TUV Rheinland Middle East provides a wide range of occupational training solutions. It is an approved training provider of CQI-IRCA(UK).
The TUV Rheinland Group is a leading independent testing, training, certification and inspection services provider. The group currently employees around 19,700 employees worldwide since its humble beginning in 1872 with a headquarter in Cologne (Germany).
This course will teach you about management system, structure and aim of OHSAS:18001-2007, requirements of OHSAS:18001 (based on PDCA cycle), overview of ISO standards/series, document requirements for Audit and so much more.
A course participation certificate is provided of 31 CPD (Continuing Professional Development) upon completion. This 5-day training course will teach you about implementing and managing a Quality Management System (QMS) as per ISO 9001:2015.
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This training will give you comprehensive knowledge of the tools and techniques used for Root Cause Analysis and Correct Action-Preventive Action (CAPA). The knowledge acquired here will help you to facilitate an effective problem-solving an
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