How can a scalable, flexible biopharma facility be designed with the right plant layout, cleanroom configuration, and manufacturing technologies?
Biopharmaceutical manufacturers are making significant capital investments in greenfield facilities, facility expansion, and modernization projects. Decisions on plant capacity, clean room design, automation, and future-ready technologies can affect operations over time. From facility concept design and URS development through implementation, manufacturing operations must be engineered for flexibility and scalability to support future products, processes, and capacity demands.
We combine the bioprocessing expertise, manufacturing technologies, and global infrastructure needed to facilitate plant construction. From process and facility design through equipment selection, implementation, and qualification, our teams support pharmaceutical manufacturers and accelerate all phases of their investment projects. These services include:
- Full support from our process development scientists, bioprocessing engineers, investment project teams, and system engineers
- M Lab™ Collaboration Centers where customers can test, assess, and work directly with bioprocess equipment while receiving MSAT specialist support on technology selection, process scale-up, tech transfer, and implementation
- A scalable, connected downstream suite of single-use systems and consumables, and equipment installation & qualification services - backed by data analytics, automation, and control software
- Global supply network of regionalized and redundant facilities to enhance supply resilience
Successful investment projects, large and small, require multidisciplinary expertise across process development, engineering, manufacturing, and project execution. Our technical resources help organizations evaluate options, address technical challenges, and make informed decisions.
Download our Bioprocessing Ecosystem brochure to learn more about our integrated approach to drug manufacturing plants.
How we support you from facility design to implementation
This series of articles from our bioprocessing experts and systems engineers examines key considerations in facility design, technology selection, and qualification for biopharmaceutical manufacturing projects.
No one-size-fits-all solution exists for process and plant layout. Evaluate the different options for future-ready manufacturing.
Learn how to create compliant, fit-for-purpose URS that addresses the complexity and interdependence of modern manufacturing.
Review CSV requirements and redefine computer validation in biopharma, from documentation effort to risk and intended use approach.
Learn how we’re expanding our single-use manufacturing network to ensure reliable, high-quality regional production.
The experts behind your bioprocess development and manufacturing projects
More than 140 process development scientists and bioprocessing engineers, with an average of 20 years of experience, provide technical resources for bioprocess development and manufacturing programs, at your production site or at our M Lab™ Collaboration Centers. Their scientific, engineering, and manufacturing experience helps organizations navigate technical challenges and advance manufacturing projects.
Our Investment Projects Team supports facility projects with expertise in plant design, execution, and startup. They leverage single-use and integrated platform solutions to enable flexible manufacturing through scalable, configurable production environments.
As production lines are built and run, our global network of systems engineers supports manufacturing systems throughout their operational life cycle, from installation and qualification to training and ongoing maintenance, ensuring equipment runs smoothly and efficiently.
Planning a manufacturing investment project? Connect with our team.
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Our systems are supported by Bio4C ProcessPad™ data analytics software and Common Control Platform® (CCP) control software for process monitoring, data analysis, systems automation, and control.



