PQE Group Tech Stack

GMP compliance and quality consulting for pharma, biotech, and medical devices

Business Consulting and Services Reggello, FI 1,001–5,000 employees Founded 1998 Privately Held

PQE Group is a 25-year-old life-sciences compliance consultancy spanning 45+ offices and 2,000+ employees across 25+ languages, executing turnkey quality projects in GCP, GLP, GMP, GVP, and GDP. The tech stack reveals a manufacturing-operations focus (AVEVA PI, Rockwell, FactoryTalk, SAP QM, LIMS) rather than software product development, and hiring is concentrated in engineering and manufacturing roles—matching active projects in computer-system validation, pharma 4.0, and aseptic-filling qualification.

Tech Stack 44 technologies

Core StackSiemens SAP Power BI Tableau Python SAP S/4HANA LIMS Rockwell Automation AVEVA PI FactoryTalk WinCC MES HPLC GCP SAP HANA Qlik SQL R Microsoft Office Chromeleon Word Excel PowerPoint Outlook Visio CRM PLC SCADA SAP QM SAP SD+14 more

AdoptingLIMS

What PQE Group Is Building

◆Challenges

Ensuring gmp compliance
Increasing demand for quality services
System validation
Reducing cost and risk
Managing deviations
Complex it/ot architectures
Compliance with gxp regulations
Meeting high market demand
Validating aseptic filling operations
Timely and compliant qualification of manufacturing systems

▲Active Projects

Computer system validation
Pharma 4.0 projects
Annual product quality reviews
Regulatory strategy for eu/uk/switzerland markets
Maa submissions via centralized and decentralized procedures
Next generation manufacturing
Csv and data integrity projects
Qualification plan development
Long-term production support at client in bari
Policy harmonization

Hiring Activity

Accelerating100 roles · 55 in 30d

Department

Engineering

Manufacturing

Quality

Ops

Sales

Legal

Healthcare

Seniority

Senior

Mid

Junior

Intern

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About PQE Group

PQE Group delivers compliance consulting and quality solutions for regulated life-sciences companies—pharmaceutical, biotech, medical device, and SaMD firms of all sizes. The firm has completed over 25,000 projects for 1,400+ clients since 1998, with a multidisciplinary workforce (40% women, 50+ nationalities) distributed across 16+ countries. Core services center on regulatory strategy, manufacturing-system qualification, and data-integrity projects that help clients maintain GMP compliance and submit MAA applications through centralized and decentralized EU/UK procedures. Operations span both long-term client support and discrete project delivery.

HeadquartersReggello, FI

Company Size1,001–5,000 employees

Founded1998

Hiring MarketsItaly, France, Germany, Spain, Mexico, Belgium, Argentina, India

Frequently Asked Questions

What does PQE Group do?

PQE Group provides GMP compliance consulting and quality solutions for the pharmaceutical, biotech, and medical-device industries. The firm executes computer-system validation, manufacturing qualification, regulatory-strategy work, and data-integrity projects across 45+ global offices for clients ranging from small enterprises to large corporations.

Where is PQE Group located?

PQE Group is headquartered in Reggello, Italy, with 45+ offices across 16+ countries including France, Germany, Spain, Mexico, Belgium, India, Poland, Australia, Ireland, and others. The workforce operates in 25+ languages.