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Industrial Operations and Product Supply (IOPS)

Grounded in excellence. Driven by innovation.

What we do

Industrial Operations and Product Supply (IOPS) turns cutting-edge science into innovative biologic medicines to improve the lives of patients worldwide. Our commitment to operational excellence and patient safety ensures we consistently produce the highest-quality medicines, including approved therapeutic proteins as well as those involved in clinical studies.

LEARN ABOUT US AND OUR FEATURED TEAMS.

Global Manufacturing

Global Manufacturing produces quality drug substance and formulated drug substance in a timely manner using robust, science-based processes that patients can trust. This includes producing therapeutic proteins and biologic drug products for clinical and commercial use.

Drug Product Manufacturing

Drug Product Manufacturing supports and delivers internal fill and finish manufacturing capabilities within IOPS’ new state-of-the-art facility. Additionally, the External Manufacturing team schedules, plans and manages the global manufacturing of products that occur at Contract Manufacturing Organizations (CMO).

Quality Assurance & Compliance

Quality Assurance & Compliance ensures that established procedures and guidelines are in place so that IOPS can operate efficiently and processes are consistently followed every step of the way. They play a role in nearly all aspects of Regeneron's business. Additionally, the Compliance team manages proactive evaluation of IOPS Good Manufacturing Practices (GMP) compliance against regulatory trends and builds strong inspection readiness capabilities across the organization.

Support Functions

There are a number of support functions that help ensure IOPS has the tools, resources and information it needs to consistently produce products for patients as efficiently as possible. These include Information Technology (IT), Human Resources (HR), Law, Continuous Improvement (CI), Diversity, Equity and Inclusion (DEI), Technical Training, Finance and Accounting.

CMC Regulatory Sciences

CMC Regulatory Sciences manages and authors product Chemistry Manufacturing and Control (CMC)-related information for our global clinical and commercial regulatory submission documents, such as Investigational New Drug (IND) applications and Biologic License Applications (BLA).

Quality Control

Quality Control conducts analysis of materials to ensure that quality specifications and standards are met throughout the production process. They also establish the analytical methods to test raw materials, in-process materials, bulk drug substances, finished drug products and packaging components.

Process Sciences

Process Sciences supports drug substance, drug product and combination product manufacturing operations through process characterization, device design, validation, technology transfer, investigations and process data oversight. They investigate all production events and trends.

Technical Operations

Several technical functions help ensure IOPS has the infrastructure, tools and resources it needs to consistently produce products in a safe and comfortable environment. Some functions include Facilities Maintenance, Engineering, Automation, Warehouse and Logistics.

Day in the Life

Grant Anicete

Biotech Production Specialist I / IOPS Rensselaer

Mary Makenna

Lead Quality Control Analyst / IOPS Raheen

Ashley Lebby

Lead Senior Biotech Production Specialist / IOPS Rensselaer

CREATING A CULTURE OF INNOVATION

One of our most important values is our commitment to scientific excellence. We also emphasize collaboration and teamwork, recognizing that no single individual can solve all the challenges facing the biotech industry.

More about our Culture
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Join our talent community

Tell us a bit about who you are and what you’re looking for, and we’ll keep in touch when opportunities open up.

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