In this on-demand webinar, MMT’s Crew Feighery delves into the intricacies of implementing automation in the medical device manufacturing sector. Attendees will gain a comprehensive understanding of the common pitfalls that often arise during the automation scoping process and how to navigate them effectively.
Crew Feighery, Sr. Vice President of Commercial Sales & Marketing
Whether you’re a manufacturing engineer, quality assurance professional, or operations manager, this session will provide valuable insights and practical solutions for automation processes, including:
- The significance of the 80/20 rule and its application to medical device manufacturing.
- Critical considerations for process integration and the importance of individual process evaluation.
- Strategies for reviewing manufacturing drawings in conjunction with quality assurance knowledge to ensure compliance with current work instructions and specifications.
- The role of inspection practices and the necessity of incorporating thorough quality checks despite operator fatigue.
- Challenges related to changeover times between part numbers and product families, focusing on processes that are feasible for automation.
- Emphasizing adherence to environmental, health, and safety regulations throughout the automation journey.
- Collaborating with suppliers on user requirement specifications (URS) and factory acceptance testing (FAT).
- Recognizing the risk of scope creep and the importance of buffer time within project timelines.
Furthermore, we explore the keys to successful long-term automation, from the critical nature of FAT and site acceptance testing (SAT) to the importance of operator training and cross-training practices. We will discuss how to maintain optimal machine performance, monitor input material consistency, and ensure proper maintenance routines, all while securing turn-key documentation for implemented solutions.
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