No deviation Tech Stack

CQV and regulatory compliance services for pharma manufacturing in Asia-Pacific

Pharmaceutical Manufacturing Singapore 51–200 employees Founded 2007 Privately Held

No deviation delivers engineering consultancy, commissioning & qualification (CQV), and regulatory compliance support to pharmaceutical and biotech manufacturers across Asia and Europe. The tech stack reveals a manufacturing operations footprint: LIMS, MES, SCADA, DCS, and EAM platforms (SAP, Oracle, IBM Maximo, Infor) sit alongside lab instrumentation (HPLC, LC-MS, UPLC). Active hiring is concentrated in engineering (23 roles) and manufacturing (12 roles), with a mid-to-senior seniority mix — matching their core workload of equipment qualification, process validation, and MES migration projects.

Tech Stack 29 technologies

Core StackSAP Oracle Primavera P6 Siemens Word Excel PowerPoint HPLC UPLC GCP LC-MS LIMS DeltaV MES SAP PM IBM Maximo Infor EAM BMS SCADA Microsoft Project Ignition Outlook PLC DCS WinCC Rockwell Automation Emerson DeltaV Siemens Opcenter Windows

What No deviation Is Building

◆Challenges

Ensuring compliance with gmp/gxp
Compliance with gmp standards
Accurate migration of production data
Managing deviations and capas
Process sustainment
System migration compliance
Commissioning and qualification of specialized chemical synthesis facility
Transition from legacy systems to new mes platform
Process deviations
Process robustness and efficiency

▲Active Projects

Mes system implementation
Commissioning and qualification of analytical laboratories
Smart manufacturing initiative for media and buffer preparation
Process validation for upstream harvest
Equipment qualification and validation
Cleaning validation activities
Process deviation investigations
Qc equipment qualification (group b and c)
Controlled experiments
Cqv activities for isolators, filling lines, lyophilizers, packaging and capping machines, compounding systems, and cleanrooms

Hiring Activity

Accelerating45 roles · 20 in 30d

Department

Engineering

Manufacturing

Quality

Ops

Finance

Operations

Seniority

Mid

Senior

Junior

Manager

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About No deviation

No deviation, founded in 2007, operates as a privately held consultancy serving pharmaceutical and biotech companies with compliance and operational support. The firm offers three core service lines: CQV execution (commissioning, qualification, and validation) aligned with GAMP 5 and Annex 15 standards; quality and regulatory audit readiness, including QMS remediation and documentation; and digital enablement (paperless validation tools, data integrity, process digitalization). The company is headquartered in Singapore and operates primarily across Asia-Pacific and Europe. Current project work spans process validation, equipment qualification, cleaning validation, system migration compliance, and deviation investigations — all grounded in their Understand-Observe-Define-Implement framework.

HeadquartersSingapore

Company Size51–200 employees

Founded2007

Hiring MarketsSingapore

Frequently Asked Questions

What is No deviation's main business?

No deviation provides CQV (Commissioning, Qualification & Validation) engineering, regulatory compliance consulting, and digital enablement services to pharmaceutical and biotech manufacturers. They support projects from equipment qualification through process validation to QMS remediation and paperless validation implementation.

What technologies does No deviation use?

No deviation operates with LIMS, MES (including DeltaV), SCADA, and EAM platforms (SAP, Oracle, IBM Maximo). Lab-side, they work with HPLC, LC-MS, and UPLC instrumentation. They also deploy paperless validation tools and process digitalization platforms.