Who We Are

At Pioneer GMP Consulting, we aim to be the most trusted partner for building future-ready operations in the life sciences industry. 

We understand you have choices when selecting a GMP consulting and delivery partner. What sets us apart is over 30 years of hands-on experience, blending proven industry practices with modern, forward-looking solutions that work in the real world. Our team of seasoned consultants doesn’t just follow industry trends — we anticipate them, continually adapting to deliver effective, efficient, and future-ready results.

Whether providing Fractional Leadership, Organizational Transformation, GMP Readiness and Roadmapping, or Facility Startup support, we approach every engagement with a focus on long-term success. Our mission goes beyond helping you meet today’s compliance requirements but positioning your organization to thrive in an evolving regulatory environment. With Pioneer GMP, you’re not just keeping pace — you’re leading the way.

Vision

To turn every aspect of GMP—from compliance to execution—into a driver of business success.

Mission

We apply critical thinking and modern tools to transform traditional GMP practices—empowering our clients to meet today’s requirements while preparing for tomorrow’s demands.

Meet Our Principals

  • Chris brings over 30 years of Life Sciences experience, with expertise spanning engineering, automation, equipment qualification, computerized systems validation, process validation, and quality assurance. After nearly 20 years in industry roles at Pfizer, Genentech, and Shire HGT, Chris joined Azzur Group in 2013 to establish their New England Consulting office. Over the next five years, he successfully expanded the office to over 70 consultants while co-developing a new business unit offering GMP cleanroom hoteling services. Chris later transitioned to lead Azzur Group’s Consulting business unit, where he oversaw a nationwide expansion, opening 10 offices and driving significant revenue growth. During this time, he also provided consulting services to clients, acting as the Lead CQV Project Manager for six new facility startups, implementing phase-appropriate GMPs for clinical stage companies, conducting master planning, and supporting regulatory activities.

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  • Dr. Thomas Page brings over 35 years of Life Sciences experience, having worked at clinical development and CDMO companies in roles supporting operations, engineering, process development, and business development. His expertise spans a range of products, including blood-based therapies, vaccines, recombinant proteins, monoclonal antibodies (mAbs), and advanced therapy medicinal products. Over the course of his career, Dr. Page has led the design, construction, validation, and operation of assets valued at over $1 billion in both the public and private sectors. He holds numerous patents and publications and is passionate about advancing faster, better, and more cost-effective responses to pandemics and emerging health threats. Additionally, he is committed to supporting the next generation of biotechnologists and developing biotechnology hubs.

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