Become an ISO 22716 Lead Auditor and ensure GMP
ISO 22716 is a globally applied standard that presents the main principles of Good Manufacturing Practices (GMP) for the cosmetics industry. It is all about the control of quality during the entire process of developing cosmetic products which includes production, storage, and distribution. ISO 22716 Certified Lead Auditors in Liberec are ultimately in charge of ensuring the implementation of standards. These auditors obtain specific training in order to build profound knowledge of ISO 22716 requirements and auditing principles at a high level. With this information, they carry out audits, which involve planning, conducting, and reporting on audits representing a comparison between the cosmetic manufacturing activities of a company and ISO 22716 standards. They unbiasedly gauge these areas, which indicate areas for improvement and strength thereby resulting in the production of good cosmetic profucts.
ISO 22716 Lead Auditor Training: Master GMP Audits for the Cosmetics Industry
ISO 22716 Lead Auditor Training in Liberec takes an individual to a level that they become right person with the right expertise to carry out the external identification of GMP standards compliance for cosmetics manufacturing. Training includes lectures, workshops and simulative auditory tasks. With all this participants can be said to know by heart the ISO 22716 requirements, the audit methodologies, and the report-writing and corrective action procedures. The training program dives into four major topics, quality management systems (QMS), production risk management, and documentation control. Through this training program, participants will gain knowledge to do the audits, prepare, conduct, and lead the activities that will help them be responsible for the products quality and safety.
ISO 22716 Lead Auditor Certification Exam: Ensuring Candidate Competency
After attending the training session, knowledge of candidates will be evaluated in ISO 22716 Lead Auditor Exam in Liberec. The exam will be a multiple choice test of 30 questions that is needed to be completed in 60 minutes which covers core competency of ISO 22716 standard. ISO standard that sets quality management systems to good manufacturing practices for cosmetics, risk management, documentation control, auditing methodologies and related topics will be covered. The candidates are eligible to earn the certification if they attain a passing score of 70% or more.
Corporate Group Training
- Customized Training
- Live Instructor-led
- Onsite/Online
- Flexible Dates
| ISO 22716 Lead Auditor Exam Details in Liberec | |
| Exam Name | ISO 22716 Lead Auditor Certification |
| Exam Format | Multiple choice, subjective |
| Total Questions | 20 Questions |
| Passing Score | 70% |
| Exam Duration | 2 Hours |
Key Features of ISO 22716 Lead Auditor Good Manufacturing Practices Certification Training in Liberec Czechia
ISO 22716 Lead Auditor Training course offered by Unichrone in Liberec makes professionals acquainted with the capacity to thrive in the cosmetic industry. Our comprehensive training program, led by qualified instructors, is not limited to basic academic knowledge only but equips participants with practical real-world scenarios. The hands-on workshops and simulated audits build up the relevant competency in participants for design, pre-consolation, and reporting on audits. The curriculum is tailored to cover such areas as quality management systems for cosmetics, risk management strategies, and documentation control best practices which are based on ISO 22716 standard. Candidates acquiring the certification will have the advantage over the others since they can effectively pass through the assessment of whether organizations adhere to Good Manufacturing Practices (GMP). They will be capable of producing quality cosmetic products. ISO 22716 Lead Auditor Certification in Liberec provides graduates with an opportunity to reach executive professionals in the realm of cosmetics such as lead auditor, quality control manager, and regulatory consultant among others, and a network of professionals.
- 4 Day Interactive Instructor –led Online Classroom or Group Training in Liberec Czechia
- Course study materials designed by subject matter experts
- Mock Tests to prepare in a best way
- Highly qualified, expert trainers with vast industrial experience
- Enrich with Industry best practices and case studies and present trends
- ISO 22716 Lead Auditor Training Course adhered with International Standards
- End-to-end support via phone, mail, and chat
- Convenient Weekday/Weekend ISO 22716 Lead Auditor Training Course schedule in Liberec Czechia
ISO 22716 Lead Auditor Certification Benefits
Higher Salary
With this renowned credential, aspirants earn higher salary packages when compared to non-certified professionals in the field
Individual accomplishments
Aspirants can look for higher career prospects at an early stage in their life with the most esteemed certification
Gain credibility
Owning the certification makes it easier to earn the trust and respect of professionals working in the same field
Rigorous study plan
The course content is prescribed as per the exam requirements, covering the necessary topics to ace the exam in the first attempt
Diverse job roles
Attaining the certification enhances the spirit of individuals to pursue diverse job roles in the organization
Sophisticated skillset
With this certification, individuals acquire refined skills and techniques required to play their part in an organization
ISO 22716 Lead Auditor Training Course Curriculum
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Module 1: Introduction to ISO 22716
Topics
- · Introduction
- · Scope
- · Terms and Definitions
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Module 2: Good Manufacturing Practices (GMP)
Topics
- · What is GMP?
- · Components of GMP
- · GMP Principles
- · Regulations and Standards
- · How to Comply with Guidelines?
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Module 3: Personnel
Topics
- · Principle
- · Organisation
- · Key Responsibilities
- · Training
- · Personnel Hygiene and Health
- · Visitors and Untrained Personnel
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Module 4: Premises
Topics
- · Principle
- · Types of Area
- · Space
- · Flow
- · Floors, Walls, Ceilings, Windows
- · Washing and Toilet Facilities
- · Lighting
- · Ventilation
- · Pipework, Drains, and Ducts
- · Cleaning and Sanitisation
- · Maintenance
- · Consumables
- · Pest Control
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Module 5: Equipment
Topics
- · Principle
- · Equipment Design
- · Installation
- · Calibration
- · Cleaning and Sanitisation
- · Maintenance
- · Consumables
- · Authorisations
- · Back-Up Systems
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Module 6: Raw Materials and Packaging Materials
Topics
- · Principle
- · Purchasing
- · Receipt
- · Identification and Status
- · Release
- · Storage
- · Re-Evaluation
- · Quality of Water Used in Production
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Module 7: Production
Topics
- · Principle
- · Manufacturing Operations
- · Packaging Operations
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Module 8: Finished Products
Topics
- · Principle
- · Release
- · Storage
- · Shipment
- · Returns
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Module 9: Introduction to Internal Auditor
Topics
- · Who is Internal Auditor?
- · Duties of Internal Auditor
- · Soft and Hard Skills for Internal Auditor
- · Internal Vs External Auditor
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Module 10: Internal audit
Topics
- · Principle
- · Approach
- · Follow-Up
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Module 11: GMP Audit
Topics
- · What is GMP Audit?
- · What is Involved in the GMP Audit Process?
- · How to Prepare for a Typical GMP Audit?
- · Hosting GMP Audit
- · Common Mistakes Made During GMP Audits
- · GMP Auditing Best Practices
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Module 12: GMP Supplier Audit
Topics
- · Conducting a GMP Supplier Audit
- · Supplier Audit Checklist
- · Quality Policy
- · Training and Accountability
- · General Organisation
- · Supply Access
- · Steps to Successfully Perform the GMP Supplier Audit
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Module 13: Quality Control Laboratory
Topics
- · Principle
- · Test Methods
- · Acceptance Criteria
- · Results
- · Out-of-Specification Results
- · Reagents, Solutions, Reference Standards, Culture Media
- · Sampling
- · Retain Sample
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Module 14: Treatment of Product
Topics
- · Rejected Finished Products, Bulk Products, Raw Materials, and Packaging Materials
- · Reprocessed Finished Products and Bulk Products
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Module 15: Wastes
Topics
- · Principle
- · Types of Waste
- · Flow
- · Containers
- · Disposal
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Module 16: Subcontracting
Topics
- · Principle
- · Types of Subcontracting
- · Contract Giver
- · Contract Acceptor
- · Contract
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Module 17: Implementing GMP
Topics
- · Quality Management
- · Sanitation and Hygiene
- · Building and Facilitation
- · Equipment
- · Raw Materials
- · Personnel
- · Validation and Qualification
- · Complaints
- · Documentation and Recordkeeping
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Module 18: Lead Auditor
Topics
- · Who is Lead Auditor?
- · Roles and responsibilities of Lead Auditor
- · Audit Report
- · Types of Audit Process
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Module 19: Deviations
Topics
- · Deviations Overview
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Module 20: Complaints and Recalls
Topics
- · Principle
- · Product Complaints
- · Product Recalls
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Module 21: Change Control
Topics
- · Change Control Overview
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Module 22: Structured GMP Audit
Topics
- · Customer Communication
- · Auditor Selection
- · Auditor Planning
- · Audit Preparation
- · Audit Execution
- · Audit Report
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Module 23: Documentation
Topics
- · Principle
- · Type of Document
- · Writing, Approval, and Distribution
- · Revision
- · Archiving
