System Services
System Initialization & Testing
Ensure a seamless startup and robust performance through structured commissioning, testing, and qualification protocols.
Discuss system startup
We design, optimize, and qualify pharmaceutical and biotechnological systems — fully GMP-compliant, risk-based, and driven by deep process understanding.
QEngineering delivers end-to-end engineering expertise for pharmaceutical, biotech, and high-potent production environments. From concept to commissioning, we ensure technical integrity, regulatory compliance, and long-term operational excellence.
Our multidisciplinary team combines process engineering, automation, facility design, and validation expertise. We work closely with your stakeholders to deliver solutions that are technically robust, inspection-ready, and optimized for operational efficiency—whether you're building a new facility, upgrading existing systems, or preparing for regulatory audits.
Send us a brief request about your project. We respond with a first assessment and next steps within 1–2 business days.
From system initialization to lifecycle documentation — QEngineering supports you across the entire project lifecycle with robust, GMP-aligned engineering services.
Ensure a seamless startup and robust performance through structured commissioning, testing, and qualification protocols.
Discuss system startup
Identify optimization potential, improve long-term reliability, and increase efficiency through engineering-driven assessments.
Improve process reliability
Strengthen your project execution with reliable engineering oversight, aligned to timelines, costs, and regulatory expectations.
Get project support
GAMP 5–aligned validation strategies to qualify systems and processes in accordance with global GMP standards.
Plan validation strategy
Inspection-ready documentation and audit support to maintain lifecycle compliance and regulatory transparency.
Secure documentation support
Solutions for sterile, high-potent, OSD, BFS, and contained manufacturing environments — integrated, safe, and scalable.
Explore pharma solutionsWe support your projects across the entire lifecycle: from feasibility and concept studies to detailed design, execution, commissioning, and qualification. Our approach combines technical depth, GMP integration, and structured risk management.
Compliance is embedded into every engineering decision — not added at the end.
We identify technical and regulatory risks early and align mitigation plans with your stakeholders.
Quality management and documentation standards you can rely on in audits and inspections.
Lessons learned and best practices continuously feed back into your next project phase.
Share a few details about your system, facility, or project. Our QEngineering experts will contact you with a structured response and proposed next steps.
