Quality Management 101: Optimizing Enterprise Maintenance with ISO Standards
Transform Maintenance With ISO 9001 Insights for Proactive, Quality-Driven Results!
Instructor :
John E Lincoln
Webinar ID:
12553
Date: DEC 05, 2024 (THU)
Start Time: 10 AM PT - 11 AM PT
Duration: 1 Hr.
Buy This Course in a Pack of 3 courses at 35% Discount HERE:
🔍 Quality & Safety Assurance Master Pack (Pack of 3)
“Strengthen Quality and Risk Management for Safe Pharmaceutical Products”
3 Courses Included:
-
- Quality Risk Management: An In-Depth Guide to ICH Q9 (R1) for Safe and Effective Pharmaceutical Products, duration 90 Mins., find out more details here
- Fast-Track FDA Approvals: Mastering NDAs, INDs, and Drug Manufacturing Standards, duration 60 Mins., find out more details here
- Quality Management 101: Optimizing Enterprise Maintenance with ISO Standards, duration 60 Mins., find out more details here
Why This Pack?
This bundle equips professionals with critical knowledge in quality assurance and risk management, from new drug applications to overarching quality management systems (QMS). It’s ideal for professionals dedicated to maintaining high standards in product safety and regulatory alignment.
Target Audience: Quality Assurance Managers, Regulatory Affairs Specialists, Pharmaceutical Production Managers
Why Buy the Pack?
-
- End-to-End Quality Management: Gain in-depth expertise from drug applications to quality systems management.
Buy This Course in a Pack of 3 courses at 35% Discount HERE:
🔍 Quality & Safety Assurance Master Pack (Pack of 3)
“Strengthen Quality and Risk Management for Safe Pharmaceutical Products”
3 Courses Included:
-
- Quality Risk Management: An In-Depth Guide to ICH Q9 (R1) for Safe and Effective Pharmaceutical Products, duration 90 Mins., find out more details here
- Fast-Track FDA Approvals: Mastering NDAs, INDs, and Drug Manufacturing Standards, duration 60 Mins., find out more details here
- Quality Management 101: Optimizing Enterprise Maintenance with ISO Standards, duration 60 Mins., find out more details here
Why This Pack?
This bundle equips professionals with critical knowledge in quality assurance and risk management, from new drug applications to overarching quality management systems (QMS). It’s ideal for professionals dedicated to maintaining high standards in product safety and regulatory alignment.
Target Audience: Quality Assurance Managers, Regulatory Affairs Specialists, Pharmaceutical Production Managers
Why Buy the Pack?
-
- End-to-End Quality Management: Gain in-depth expertise from drug applications to quality systems management.
- Safety First: Prioritize product safety and compliance with robust quality frameworks.
- Optimal Value: Comprehensive quality assurance guidance at a lower cost than individual purchases.
Note: Do you want to custom design your pack and choose courses of your choice? Just drop us an email at support@compliancemeet.com or call at Toll Free: +1 (888) 959-4972. We’ll be happy to help you!
                                 Buy All 3 Courses at a 35% discount HERE
What will you learn
-
- Overview Of Quality Management Systems For Enhanced Maintenance Practices.
- Managing Systems, Personnel, And Physical Plant Under QMS Standards.
- Importance Of Documentation: “If It Isn’t Documented, It Didn’t Happen.”
- Control Of Materials, Products, And Manufacturing For Quality Outcomes.
- Preventive And Predictive Maintenance To Minimize Downtime And Failures.
- Validation Processes To Ensure Compliance With ….
-
- Overview Of Quality Management Systems For Enhanced Maintenance Practices.
- Managing Systems, Personnel, And Physical Plant Under QMS Standards.
- Importance Of Documentation: “If It Isn’t Documented, It Didn’t Happen.”
- Control Of Materials, Products, And Manufacturing For Quality Outcomes.
- Preventive And Predictive Maintenance To Minimize Downtime And Failures.
- Validation Processes To Ensure Compliance With Required Specifications.
- Handling Complaints And Post-Production Issues For Continuous Quality Control.
Course Description
Unlock the essentials of an enterprise-focused Quality Management System (QMS) tailored for maintenance professionals.
This 60-minute webinar dives into the framework of ISO 9001, the internationally recognized standard for Quality Management Systems, equipping you with tools and strategies to elevate maintenance performance and efficiency across your organization.
In this session, you will:
-
- Understand Core QMS Requirements: Explore the foundational elements of a Quality Management System and how they specifically support maintenance operations.
- Apply CAPA for Proactive Maintenance: Learn about Corrective and Preventative Actions (CAPA) to address and prevent recurring maintenance challenges.
- Adopt Preventive and Predictive Techniques: Shift from reactive to proactive maintenance with strategies that keep equipment reliable and minimize downtime.
- Manage Routine and Urgent Repairs: Discover best practices for handling both scheduled and emergency repairs under the QMS framework.
- Leverage Continuous Improvement Tools: Gain insights into Statistical Process Control (SPC) and Six Sigma methodologies to drive ongoing improvements in maintenance processes.
This webinar emphasizes the alignment of maintenance activities under the QMS “umbrella,” ensuring every action—whether an inspection, repair, or improvement—is consistent with ISO 9001 standards.
Ideal for professionals aiming to integrate quality management with maintenance, this course provides actionable insights to help you build a resilient, quality-driven maintenance strategy that supports organizational goals.
Equip yourself with practical tools and a proven approach to enhance maintenance operations with confidence and clarity.
Join Now!
Unlock the essentials of an enterprise-focused Quality Management System (QMS) tailored for maintenance professionals.
This 60-minute webinar dives into the framework of ISO 9001, the internationally recognized standard for Quality Management Systems, equipping you with tools and strategies to elevate maintenance performance and efficiency across your organization.
In this session, you will:
-
- Understand Core QMS Requirements: Explore the foundational elements of a Quality Management System and how they specifically support maintenance operations.
- Apply CAPA for Proactive Maintenance: Learn about Corrective and Preventative Actions (CAPA) to address and prevent recurring maintenance challenges.
- Adopt Preventive and Predictive Techniques: Shift from reactive to proactive maintenance with strategies that keep equipment reliable and minimize downtime.
- Manage Routine and Urgent Repairs: Discover best practices for handling both scheduled and emergency repairs under the QMS framework.
- Leverage Continuous Improvement Tools: Gain insights into Statistical Process Control (SPC) and Six Sigma methodologies to drive ongoing improvements in maintenance processes.
This webinar emphasizes the alignment of maintenance activities under the QMS “umbrella,” ensuring every action—whether an inspection, repair, or improvement—is consistent with ISO 9001 standards.
Ideal for professionals aiming to integrate quality management with maintenance, this course provides actionable insights to help you build a resilient, quality-driven maintenance strategy that supports organizational goals.
Equip yourself with practical tools and a proven approach to enhance maintenance operations with confidence and clarity.
Join Now!
Why you should attend
Integrating Quality Management with enterprise maintenance practices is no longer optional—it’s essential for maintaining operational efficiency, reducing costs, and ensuring compliance.
This webinar equips you with the insights and skills needed to build a QMS-aligned maintenance strategy that can drive measurable results across your organization.
By attending, you will:
-
- Enhance Preventive and Predictive Maintenance: Learn how ISO 9001 principles can optimize your preventive and predictive maintenance programs, helping you move from a reactive approach to a proactive maintenance model.
- Streamline Processes and Improve Consistency: Discover the QMS requirements for systems, personnel, buildings, and equipment, ensuring your processes are well-documented and consistently applied.
- Optimize Documentation and Records Management: Understand best practices for maintaining accurate documentation and records to ensure traceability, compliance, and streamlined audits.
- Elevate Materials Management and Resource Allocation: Gain insights into materials management to minimize waste, improve inventory control, and boost resource efficiency.
- Master Post-Production Analytics: Learn how to apply descriptive, diagnostic, predictive, and prescriptive analytics to continuously monitor and improve maintenance performance.
Whether you’re a maintenance professional, quality manager, or operations leader, this webinar provides actionable strategies that directly address industry challenges.
Attending will help you enhance your skills, improve your team’s productivity, and advance your career by aligning your maintenance activities with ISO 9001 standards for quality and reliability.
Take this step toward a more resilient, quality-driven maintenance approach and secure your spot today!
Enroll Now!
Integrating Quality Management with enterprise maintenance practices is no longer optional—it’s essential for maintaining operational efficiency, reducing costs, and ensuring compliance.
This webinar equips you with the insights and skills needed to build a QMS-aligned maintenance strategy that can drive measurable results across your organization.
By attending, you will:
-
- Enhance Preventive and Predictive Maintenance: Learn how ISO 9001 principles can optimize your preventive and predictive maintenance programs, helping you move from a reactive approach to a proactive maintenance model.
- Streamline Processes and Improve Consistency: Discover the QMS requirements for systems, personnel, buildings, and equipment, ensuring your processes are well-documented and consistently applied.
- Optimize Documentation and Records Management: Understand best practices for maintaining accurate documentation and records to ensure traceability, compliance, and streamlined audits.
- Elevate Materials Management and Resource Allocation: Gain insights into materials management to minimize waste, improve inventory control, and boost resource efficiency.
- Master Post-Production Analytics: Learn how to apply descriptive, diagnostic, predictive, and prescriptive analytics to continuously monitor and improve maintenance performance.
Whether you’re a maintenance professional, quality manager, or operations leader, this webinar provides actionable strategies that directly address industry challenges.
Attending will help you enhance your skills, improve your team’s productivity, and advance your career by aligning your maintenance activities with ISO 9001 standards for quality and reliability.
Take this step toward a more resilient, quality-driven maintenance approach and secure your spot today!
Enroll Now!
Areas Covered
-
- QMS Overview: Gain a foundational understanding of Quality Management Systems and how they support robust, reliable maintenance practices across the organization.
- Systems, Personnel, and Physical Plant Management: Learn best practices for managing personnel, systems, and the physical plant to ensure alignment with QMS standards.
- Documentation Essentials: Discover the critical role of documentation—because if it isn’t documented, it didn’t happen. Ensure all procedures, actions, and maintenance records meet compliance and quality requirements.
- Material and Product Control: Understand how to effectively control materials, products, and manufacturing processes to reduce variability and improve quality outcomes.
- Preventive and Predictive Maintenance: Explore preventive and predictive maintenance strategies designed to anticipate and mitigate issues before they arise, reducing downtime and enhancing equipment longevity.
- Validations: Learn about validation processes to verify that maintenance practices and products meet required specifications and quality benchmarks.
- Material and Product Rejection: Address issues related to material/product rejection, fall-off, and scrap, implementing strategies to minimize waste and optimize resource use.
- Complaint Handling and Post-Production Management: Gain insights into handling customer complaints and other post-production issues, ensuring that quality and compliance standards are upheld beyond initial production.
BONUS:
-
- PDF copy of the presentation handout for your future reference.
- Soft copy of the certificate of completion on request.
- Q&A Session with the Presenter: Get your pressing questions answered verbally, via chat or email.
-
- QMS Overview: Gain a foundational understanding of Quality Management Systems and how they support robust, reliable maintenance practices across the organization.
- Systems, Personnel, and Physical Plant Management: Learn best practices for managing personnel, systems, and the physical plant to ensure alignment with QMS standards.
- Documentation Essentials: Discover the critical role of documentation—because if it isn’t documented, it didn’t happen. Ensure all procedures, actions, and maintenance records meet compliance and quality requirements.
- Material and Product Control: Understand how to effectively control materials, products, and manufacturing processes to reduce variability and improve quality outcomes.
- Preventive and Predictive Maintenance: Explore preventive and predictive maintenance strategies designed to anticipate and mitigate issues before they arise, reducing downtime and enhancing equipment longevity.
- Validations: Learn about validation processes to verify that maintenance practices and products meet required specifications and quality benchmarks.
- Material and Product Rejection: Address issues related to material/product rejection, fall-off, and scrap, implementing strategies to minimize waste and optimize resource use.
- Complaint Handling and Post-Production Management: Gain insights into handling customer complaints and other post-production issues, ensuring that quality and compliance standards are upheld beyond initial production.
BONUS:
-
- PDF copy of the presentation handout for your future reference.
- Soft copy of the certificate of completion on request.
- Q&A Session with the Presenter: Get your pressing questions answered verbally, via chat or email.
Who is this course for
Everybody benefits from watching this. Even better when done as a group!
-
- Maintenance Leaders Seeking Reliable, Quality-Driven Processes
- Operations Managers Focused on Reducing Downtime
- Quality Control Professionals Aiming for Consistency
- Facilities Managers Committed to Proactive Asset Management
- Training Managers Designing Competency Development Paths
- HR Leaders Looking to Boost Compliance and Standards
- Production Supervisors Managing Material and Product Quality
- Continuous Improvement Specialists Focused on Optimization
- Compliance Officers Ensuring Standards Are Met Across Departments
Everybody benefits from watching this. Even better when done as a group!
-
- Maintenance Leaders Seeking Reliable, Quality-Driven Processes
- Operations Managers Focused on Reducing Downtime
- Quality Control Professionals Aiming for Consistency
- Facilities Managers Committed to Proactive Asset Management
- Training Managers Designing Competency Development Paths
- HR Leaders Looking to Boost Compliance and Standards
- Production Supervisors Managing Material and Product Quality
- Continuous Improvement Specialists Focused on Optimization
- Compliance Officers Ensuring Standards Are Met Across Departments
Instructor Profile
John E. Lincoln is a medical device and regulatory affairs consultant. He has helped companies to implement or modify their GMP systems and procedures, product risk management, U.S. FDA responses. In addition, he has successfully designed, written and run all types of process, equipment and software qualifications/validations, which have passed FDA audit or submission scrutiny, and described in peer-reviewed technical articles, and workshops, world wide.
John has also managed pilot production, regulatory affairs, product development/design control, 510(k) submissions, risk management per ISO 14971, and projects; with over 28 years of experience in the FDA-regulated medical products industry – working with start-ups to Fortune 100 companies, including Abbott Laboratories, Hospira, Tyco/Mallinckrodt. He is a graduate of UCLA.
