Bridging Technology and Compliance in Life Sciences Manufacturing
QY Innovation was founded with a clear purpose: to help pharmaceutical and biotech companies navigate the complex intersection of manufacturing technology, operational efficiency, and regulatory compliance.
We understand that in Life Sciences, technology decisions carry regulatory implications. Every system must be validated, every process must be documented, and every change must be controlled. Our team brings the technical depth and regulatory awareness to get it right — the first time.
What Drives Us
These principles guide every engagement, every recommendation, and every line of code we deliver.
Quality & Compliance
We build solutions that meet the highest quality standards and regulatory requirements from day one.
Technical Excellence
We stay at the forefront of manufacturing technology, bringing best-in-class solutions to our clients.
Partnership
We invest in long-term relationships, becoming trusted advisors to our clients' organisations.
Integrity
We provide honest, vendor-independent advice focused on what's best for your business and patients.
Results-Driven
We measure success by the tangible outcomes we deliver — on time, on budget, and audit-ready.
Continuous Learning
We constantly expand our knowledge to stay ahead of evolving regulations and technologies.
Our Core Competencies
A multidisciplinary team with deep specialisation across manufacturing technology and compliance.
Manufacturing Technology
MES/MOM platforms, historian systems, EBR, LIMS integration, and real-time production analytics. We architect and implement the technology backbone of modern pharmaceutical manufacturing.
Automation & Control
PLC/DCS programming, SCADA systems, batch control (ISA-88), and process analytical technology (PAT). From design to commissioning and qualification.
IT/OT Convergence
Network architecture, cybersecurity (IEC 62443), virtualisation, and cloud strategies for manufacturing environments. Bridging the gap between enterprise IT and plant floor OT.
Regulatory Compliance
Computer System Validation, GAMP 5, 21 CFR Part 11, EU Annex 11, data integrity, and quality management systems. Ensuring every system is audit-ready.