ATS Life Sciences provides high-quality, high-value automation solutions to manufacturers of medical technology and pharmaceutical products where regulatory compliance is critical. We are dedicated to assisting our customers in improving quality of life for people around the world. When there is no room for error, and product failure is not an option, leading life sciences companies trust us to resolve their production challenges.

ATS Life Sciences is a division of ATS Corporation, an industry-leading automation solutions provider to many of the world’s most successful companies.

Quick Facts

Icon of a globe
5 sites around the world
Icon of three
1,000 employees
40+ years of life sciences experience
icon representing square meters
44,130 square meters floor space

There Is an Automation Solution for Your Unique Product

You design your products to improve the human condition. Oftentimes you are employing new processes and technologies. The result is a unique product with distinct advantages over other products. Standard manufacturing solutions aren’t sufficient. Don’t compromise. ATS Life Sciences has a long history of successfully solving novel production problems with clever automation. We will find the appropriate solution that moves your business forward.

Supporting Your Product Lifecycle

It doesn’t matter where you are in your automation journey—we are here to support you. We are staffed to understand what makes your market, product, process, and operation unique. From research and development to product retirement, we deliver solutions and services that will help you achieve your goals.

Our Focus on Quality and Compliance

Quality is more than customer satisfaction. It is also a commitment to deliver automation solutions that are compliant with customer and regulatory requirements. This belief is the basis for our quality policy. We demonstrate our commitment to our quality policy every day through the following activities and more.

  • ISO 9001 certifications of our facilities
  • ISO 13485 certifications of specific facilities
  • Adoption of GMP and GDP practices
  • Processes and templates implemented for design reviews, change control, non-compliance issues, requirements traceability, and commissioning and qualification
  • Supplier Management and auditing
  • Internal auditing regimen
  • Preventive and corrective actions
  • In-process and final product inspections

Thinking Globally. Acting Locally.
Always Within Your Reach.

With manufacturing sites in North America and Europe, we have a highly flexible supply base. You will experience the same quality of service regardless of the site of execution. 

Contact Us