Global Leaders in Commissioning, Qualification & Validation

Helping biotech and pharmaceutical organisations build and validate compliant GMP facilities—on time, on budget, and inspection-ready from day one.
About

Who are Zyme Biotech?

Zyme Biotech is a global leader in Commissioning, Qualification & Validation (CQV), backed by a team of  specialists and more than a decade of hands-on experience.
Our strength lies in translating strategy into execution, delivering inspection-ready facilities, optimizing validated processes, and ensuring seamless regulatory compliance.This approach enables our partners to achieve measurable performance, operational excellence, and sustained GMP readiness.
Augmenting Expertise

Specialized CQV Knowledge

Our team combines deep expertise across Commissioning, Qualification & Validation (CQV), GMP compliance, and biotech project delivery. From facility design through performance qualification, we provide the technical insight needed at every stage of your project lifecycle.

Global Delivery Experience

With on-the-ground experience across Europe, the GCC, and the US, our experts apply global GMP standards and local regulatory knowledge to every engagement, delivering inspection-ready outcomes for leading biotech and pharmaceutical companies.

Adaptive Project Integration

We scale our capabilities to match your project’s demands, seamlessly integrating additional expertise into our core CQV teams. This flexible, collaborative model ensures you always have access to the right specialists, exactly when and where you need them.
Our partners
AI solution provider and integrator specialising in the biotech sector. Leveraging advanced AI technologies to enhance pharmaceutical manufacturing. Dedicated to innovation, AI-driven tools streamline complex processes, enhance decision-making, and automate knowledge work, ensuring operational excellence.
BioEra works in cooperation with global strategic partners in the fields of project management, engineering work for pharmaceutical factories, scientific and operational consulting for biopharmaceutical industries, business development, artificial intelligence applications, e-marketing and application design. in Riyadh, Kingdom of Saudi Arabia.
ServBlock specializes in applying blockchain technology to secure and streamline pharmaceutical  supply chain processes, ensuring transparency and efficiency. ServBlock’s secure and transparent platform is designed to address the unique challenges faced by the pharmaceutical industry, enabling end-to-end traceability.
Setting the electronic validation standard for 20 years, ValGenesis Validation Lifecycle Management System (VLMS) provides unparalleled power, capability, and flexibility to enable 100% paperless, risk-based validation.

Connect design, qualification and production with the unified digital platform for life sciences.

Our Collaborative Partnerships

BioEra Project Management Company is a Saudi company headquartered in Riyadh, Kingdom of Saudi Arabia.
BioEra Project Management Company is a Saudi company headquartered in Riyadh, Kingdom of Saudi Arabia.
ServBlock specializes in applying blockchain technology to secure and streamline pharmaceutical  supply chain processes, ensuring transparency and efficiency.
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Zyme helped us successfully pass all regulatory inspections on the first attempt.
Client in Large-Scale Biotech Facility
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Team

Senior Leadership

CEO

John Ward

For over a decade, John has been at the forefront of the highly regulated pharmaceutical manufacturing industry, working alongside many of the world's leading biotech companies in his role as principal consultant within the validation space. Most recently as a product owner in Pfizer's global Smart Factory team.

As a seasoned project manager, John excels in overseeing large-scale greenfield projects, demonstrating exceptional strategic planning and execution capabilities. From concept to completion, his holistic approach ensures successful outcomes, solidifying his reputation as a preeminent figure in biotech manufacturing.
COO

Kevin Ward

Extensive sales leadership experience and a track record of driving company growth towards successful exits. His expertise in strategic sales, team building, and market expansion plays a pivotal role in propelling Zyme People's mission in the biotech regulatory consultancy space.

Kevin's visionary approach and commitment to operational excellence continue to shape the company's success and innovation in the industry.
CTO

Thomas Ward

A profound background in technology, with significant stints at Microsoft and Oracle. His expertise in software development, cloud solutions, and enterprise architecture has been instrumental in driving technological innovation at Zyme People.

Thomas's leadership in integrating cutting-edge tech solutions enhances the company's regulatory consultancy services, positioning Zyme People as a leader in biotech efficiency and compliance.

Senior Management

Process Engineering

Mick Cummins

Chartered Engineer with over nine years of experience, has become a pivotal figure in the biopharmaceutical industry, delivering technical and consulting services. Possessing expertise in bio pharmaceutical manufacturing, specifically in equipment design, qualification, and handover.
Lead auditor

Robert Kowalski

A seasoned engineer and an ISO13485 QMS Internal Auditor with a rich background spanning the biopharmaceutical, pharmaceutical, polymer, and FMCG industries. His experience encompasses high-value process and utility equipment, specializing in QMS.
Regulatory affars

Bozena Pawlowska

A distinguished Regulatory Affairs professional, with a prolific
background in the pharmaceutical industry. With over a decade of experience, Bozena has cultivated a deep expertise in regulatory compliance, good manufacturing practices, and the execution of complex validation protocols.
Project Management

Kieran Duffy

24 Years Experience in thePharmaceutical Industry. Strong background in Project Management of Pharmaceutical Projects complimented by technical expertise in the areas of Drug Substance Manufacture and Formulation Fill Finish.

Let’s discuss
your next project

Connect with us today to discuss how our CQV expertise can help you deliver inspection-ready, compliant, and high-performing biotech facilities right the first time.
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