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From Concept to Culture: Elevating GMP Compliance in Life Sciences
This event is now available on demand.
Event Overview:
In the rapidly evolving landscape of the Life Sciences industry, achieving and maintaining GMP compliance while embracing digitalization has become more essential than ever before. Join us for an insightful webinar where we delve into the intricate balance between regulatory compliance and digital transformation, featuring real-world insights from Corium Innovations, a leading commercial-stage biopharmaceutical company.
In the past year, Corium Innovations has utilized Blue Mountain RAM to boost compliance and forge a new culture around maintenance management. Their approach involves fostering a culture of compliance at the technician level, which has significantly enhanced their operational efficiency and regulatory adherence. In this webinar, we explore Corium Innovations' journey, showcasing practical strategies for leveraging Blue Mountain RAM's compliance features to enhance operational efficiency, foster a culture of compliance, and navigate the evolving landscape of the Life Sciences industry.
Key Learning Objectives:
Corium Innovations’ strategy for integrating compliance features into their maintenance management culture.
The role of Blue Mountain RAM in streamlining compliance processes and enhancing visibility.
Best practices for leveraging compliance dashboards to ensure timely completion of work records.
Who Should Attend:
Heads of Quality
Quality Assurance Managers
Quality Control Managers
Directors of Quality
Quality Managers
Facility Managers
Directors of Facilities
Directors of Engineering
Engineering Managers
Directors of IT
IT Managers
IT specialists
Directors of Operations
Operations Managers
Featured Speakers
Shane McGrath
is a highly experienced professional in the Pharmaceutical Industry, with a decade of experience in various roles such as Quality Lab Technician, Metrologist, Quality Engineer, and Validation Engineer. He holds a BS and an MBA with a focus on Managing Technology, both from Grand Valley State University. Currently, he manages the Validation at Corium Innovations, where he is responsible for Equipment, Facilities, Utilities, and Computerized Systems. Shane has led the implementation and validation of multiple enterprise-level validated systems, including the successful deployment of Blue Mountain RAM R4 for his site.
Speaker's LinkedIn:
https://www.linkedin.com/in/shmcgrath/
Jennifer Chang
QA Intelligence Specialist
Blue Mountain
Jennifer Chang
is a seasoned quality professional with over a decade of experience in pharmaceutical manufacturing, bringing specialized expertise in quality systems, regulatory compliance, software quality assurance, and risk management. Through her role as QA Intelligence Specialist, Jennifer leverages profound industry knowledge to promote ongoing compliance and continuous improvement at Blue Mountain. Jennifer employs a practical approach to decrypt intricate regulatory guidance and assists customers in navigating a complex and evolving compliance landscape.
Speaker's Email:
jlchang@coolblue.com
Speaker's LinkedIn:
https://www.linkedin.com/in/jennifer-c-5231a2163/
Ginny Lee
Executive Director of Global Services
Blue Mountain
Ginny Lee
, the Executive Director of Global Services at Blue Mountain, possesses over 20 years of experience in the Life Science industry. She is responsible for developing strategies and operations to deliver best-in-class services in implementation, project management, and educational services, focusing on GMP compliance and customer satisfaction. Ginny's diverse background in the pharmaceutical industry, including roles at companies such as MPI Research, Merck, and Amgen, brings a unique perspective and skill set to her leadership at Blue Mountain.
Speaker's Email:
gdlee@coolblue.com
Speaker's LinkedIn:
https://www.linkedin.com/in/ginny-d-lee/
For any technical questions please contact David Ambrose:
dambrose@mjhlifesciences.com
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