Enhance supplier management skills with this comprehensive course. Learn to manage relationships, perform risk assessments, and develop quality agreements. Engage in practical exercises, create customized scorecards, and gain strategies for supplier performance monitoring and nonconformance management.
Dublin, Oct. 31, 2025 (GLOBE NEWSWIRE) -- The "Supplier And Contract Manufacturer Management Course (Dec 3rd - Dec 4th, 2025)" training has been added to ResearchAndMarkets.com's offering.
This comprehensive supplier management course is designed to enhance your skills in effectively managing supplier relationships throughout their lifecycle.
From supplier identification and qualification to building strong relationships, risk management, continuous assessment, and exit planning, this course covers it all. Learn how to leverage risk assessment techniques to rank suppliers and minimize the need for extensive audits. Gain valuable insights into determining whether a supplier is suitable for sole sourcing.
Engage in practical exercises to create your own customized supplier scorecard tailored to your company's requirements and develop quality agreements that promote clear communication. Walk away equipped with strategies for ongoing supplier process performance monitoring and efficient management of nonconforming incidents and changes.
Learning Objective
This live training seminar includes the following for each registered attendee:
Who Should Attend:
This course is ideal for professionals involved in supply chain management, quality assurance, regulatory compliance, and manufacturing. Specifically, the following individuals will benefit:
This course is a must for anyone looking to strengthen supplier relationships, enhance contract manufacturer oversight, and ensure regulatory and quality compliance throughout the manufacturing process.
Key Topics Covered:
DAY 1
Session 1: Objectives
Understanding Regulatory Requirements and Standards for Supplier and Contract Manufacturer (CM) Management:
European Union (EU) directives and guidelines
*Includes break
Session 2: The Cost of Poor Quality from Suppliers and CMs:
Strategic Management of Suppliers:
*Includes break
Session 3: Risk Management - A Lifecycle Approach:
Supplier qualification:
*Daily Wrap-up and Discussion
DAY 2
Session 4: Supplier qualification:
Making your Supplier Quality Agreement a Great Resource:
*Includes break
Session 5: Monitoring Your Supplier's Performance to Reduce Risks and Costs:
Partnering with a Supplier or CM for Improvement:
Session 6: Supplier Assessments:
Speakers:
Kelly Thomas
Vice President
Stallergenes Greer
Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations. Her experience covers all Quality Systems ; as well as, all areas of validation; including, process/product validation, facilities validation, CSV and 21 CFR Part 11, test method validation, equipment/automated processes and cleaning validation.
Utilizing strategic thinking, risk based approaches, and Lean principles, she has demonstrated success in steering and managing complex projects within the pharmaceutical and medical device industries.
For more information about this training visit https://www.researchandmarkets.com/r/oplgmm
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