Career Opportunities

Curiosity + Expertise = Innovation.

At Gateway Analytical, we’re more than just an FDA-registered cGMP analytical laboratory; we’re your partners in safety and innovation. Our expertise in parenteral testing services cover a broad range of services such as process and formulation development, product-package validation, clinical and commercial manufacturing, visual inspection, quality control, release testing, and beyond.

We’re FDA-inspected, cGMP-certified, and DEA-licensed. We follow several ISO standards, too.

Here’s what you can expect from us when we work together. Read it, reach out, and let’s get started.

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When your career is your passion, it shouldn’t be called work.

Gateway Analytical is always interested in growing our team of problem solvers. If you want to be our next expert, then take a look at our current job listings below and submit your information as directed.

You should never let expertise go to waste. That’s why our team also devotes time to building and supporting a healthy ecosystem for the entire industry to thrive.

When carefully building our team of expert scientists, we may have underestimated their ambition. In addition to working with you on unique projects, they’re hard at work pioneering new techniques to better understand and interpret the happenings of the microscopic world. You can read our latest publications, view posters and presentations from technical conferences, and even watch videos we’ve created.

Early-Phase Development

Comprehensive packages designed to navigate clinical & regulatory complexities of parenteral product-package and container-closure development, from concept to market readiness.

Container Closure
Integrity Testing

Quantitative, non-destructive, deterministic leak detection technologies for products stored in vials, syringes, cartridges, flexible containers, and bottles.

Particulate
Analysis

Multi-analytical methods to count, size, and characterize visible and subvisible particulate matter in pharmaceuticals, disposable containers, single-use systems, raw materials, and medical devices.

Medical Device
Analysis

Rigorous studies focused on enumerating particulate matter and identifying potential chemical compounds that could migrate from medical devices into the environment or directly impact patient health.

Extractables
& Leachables

Studies aimed at identifying potentially harmful compounds in manufacturing components and final containers to ensure the safety and efficacy of pharmaceutical products.

Empowering Your Journey Toward Enhanced Patient Care

Covering every stage of the drug development journey with our state-of-the-art, FDA-inspected, cGMP-compliant facilities designed to minimize bottlenecks and maximize success.