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Automated Active Microbial Collection in Aseptic Filling Lines

Duration: 1h
When? September 17, 2025
Time options:

Recent regulatory revisions have included the expectation that automation and other advanced solutions be utilized as key tools going forward for implementing and improving contamination control strategies (CCS) and, specifically, environmental monitoring programs.  As part of this presentation, AST’s Principal Commissioning, Qualification and Validation Engineer Jason Rossi will be presenting on best practices for implementing automated environmental monitoring solutions, including automatic active microbial collection, in an aseptic filling line.

What you'll learn:
  • How automated solutions decrease risk and strengthen a CCS
  • Critical zone placement, operation, and qualification of automated active viable monitoring solutions for aseptic filling lines
  • Intervention planning for environmental monitoring in a fully automated filling setting

 

Can’t attend live? Don’t worry!

Register for one of the sessions and we’ll send you the recording afterwards.

 

Who should attend:
  • QA Managers/Directors
  • QC Microbiologists/Analysts
  • Environmental Monitoring Specialists
  • Compliance Officers
  • Auditors
  • Production Managers
  • Process Engineers
  • Automation Engineers
  • Manufacturing Technicians working in sterile environments
  • Validation Engineers
  • Commissioning Engineers
Duration: 1h
When? September 17, 2025
Time options:
Webinar Presented By:
Marc Machauer
Marc Machauer
Global OEM Coordinator

Marc is a recognized expert in aseptic fill-finish line design, engineering, and environmental monitoring for GMP-regulated pharmaceutical and biotechnology manufacturing. With hands-on experience in complex systems, Marc brings deep technical insight to contamination control and cleanroom integrity. His background includes implementing advanced aseptic processing technologies such as isolators, restricted access barrier systems (RABS), and cleanroom curtain enclosures. Having collaborated with leading pharmaceutical manufacturers across Europe and the United States, Marc offers practical expertise in meeting regulatory requirements while optimizing production in sterile environments. He currently serves as the Global OEM Coordinator at Particle Measuring Systems, a worldwide leader in cleanroom contamination monitoring solutions for the life sciences and microelectronics industries.

Jason Rossi
Jason Rossi
Principal Commissioning, Qualification and Validation Engineer at AST

Jason Rossi has over 29 years of operational expertise and leadership in various capacities throughout the pharmaceutical manufacturing industry. His experience includes project management, GMP facility and equipment design and installation, technology transfer, targeted drug manufacturing, and onsite CQV program development.

At AST, Jason leads team efforts to ensure that AST’s products, systems, and processes meet the highest standards of quality and compliance, and spearheads on-site CGMP strategies in line with the latest regulations, technological advancements, and best practices for documentation, quality risk management, and validation.

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