Dilate your competence with ISO 22716 Certification
ISO 22716 Lead Auditor Certification familiarizes an individual with conventions, rules and regulations of good manufacturing processes, with the cosmetic industry complying with the ISO 22716 standard. It frames the requirements relating to equipment, personnel, premises, quality maintenance, manufacturing processes, raw materials, labeling and distribution. In addition, this certification for Good Manufacturing Practices mandates professionals to conduct GMP audits. Furthermore, this certification encourages continuous monitoring and review of cosmetic production processes to expand opportunities for improvement. ISO 22716 Certification demonstrates compliance with the standard, and reinforces an organization's authenticity with stakeholders in terms of quality, safety and adequacy. Therefore, ISO 22716 GMP Certification helps professionals to have a great time in the job market with cosmic growth opportunities.
Implementation of Good Manufacturing Practices in an organization
ISO 22716 is an international standard that balms cosmetic businesses, providing a comprehensive framework for ensuring excellence in quality, security and efficacy of their products through implementation of good manufacturing practices bespoke to the ISO 22716 standard. By adhering to Good Manufacturing Principles, organizations can reduce variations in product quality and maintain efficiency in storage and shipment. Furthermore, it enables organizations to flourish with enhanced brand reputation. ISO 22716 implementation aids in conducting audits, eliminates risk of commodity recalls, erases detrimental events, and waive legal liabilities due to the production of unsafe products. Therefore, ISO 22716 GMP Certification in Saint Lucia upswings organizations' potency to adopt cost-effectiveness and accomplish economic stability strategically, and sustainably.
Acknowledge Good Manufacturing Practices with ISO 22716 Lead Auditor Training in Saint Lucia
ISO 22716 Lead Auditor Course increases their abundance in planning and executing audits of cosmetic production processes to evaluate compliance with ISO 22716 standard requirements. ISO 22716 Good Manufacturing Practices Training calibrates in recognizing deviations in operations, infrastructures, or documentation and to implement corrective actions.The course covers all topics in GMP including components, internal auditing, structure of GMP audit and implementation process. ISO 22716 Lead Auditor Training in Saint Lucia deeply focuses on treatment of a product and types of subcontracting. Participants are instructed to take an ISO 22716 Lead Auditor Exam after consummating training. This exam is articulated uniquely based on training topics and course materials so that it adds fickleness for candidates. Attending the exam enables individuals to evaluate their understanding of GMP ISO 22716 standard and their competence to audit, from a lead Auditor perspective.
Corporate Group Training

- Customized Training
- Live Instructor-led
- Onsite/Online
- Flexible Dates
ISO 22716 Lead Auditor Exam Details | |
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 Certification Training in Saint Lucia
ISO 22716 Lead Auditor Training in Saint Lucia is aimed at providing detailed knowledge into a structured approach of good manufacturing practices in the cosmetic industry. This training course offered by Unichrone is well-crafted, providing abounding information on all ISO 22716 requisites. Furthermore, it enables cosmetic production firms to elevate their operational efficiency by identifying non conformities, categorizing corrective measurements, monitoring progress, and icing continuous improvement. This Good Manufacturing Practice Training in Saint Lucia is consolidated to acquire tactical consciousness in regulatory requirements that are relevant to cosmetic product manufacturing. We provide an eminent package of course materials with case studies and hands on projects. Furthermore, we offer continuous back till course completion. Candidates can opt for live instructor-led online or in-classroom training according to their availability. Organizations seek professionals with good manufacturing practice certificates and a sound understanding of the principles, practices, and necessities of ISO 22716 standard to propagate in the dynamic industry. Therefore, aspirants aspiring to become lead auditors in cosmetic businesses can anticipate a level headed ascent in their career graph with this ISO 22716 Lead Auditor Course.
- 4 Day Interactive Instructor –led Online Classroom or Group Training in Saint Lucia
- Course study materials designed by subject matter experts
- Mock Tests to prepare in a best way
- Highly qualified, expert & accredited trainers with vast 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 Saint Lucia
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