Automation that Drives Compliance, Speed & Scalability

E Tech Group delivers secure, integrated, and automated manufacturing environments for life sciences facilities worldwide, boosting compliance, efficiency, and performance across every stage of production.

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70+

Life Sciences Clients

200+

Validated projects annually

30+

Office Locations Across the Globe

60+

Consecutive quality audits passed

24/7

Support with global engineering capability

200+

Life Sciences Engineers

Overview

Life sciences manufacturers must not only innovate quickly and extend product lifecycles, they must do so while staying compliant with rigorous global regulatory standards. We transform regulated manufacturing ecosystems.

With more than 30 years supporting leading biotech, pharmaceutical, and medical device organizations, E Tech Group delivers vendor‑agnostic automation solutions in drug development, commercial drug manufacturing to fill & finish, packaging, and warehousing. Our comprehensive services portfolio helps clients modernize operations, enhance compliance and optimize throughput at every stage of their journey.

Where We Work

We support clients across diverse segments of the life sciences industry, including key sectors such as:

Life Sciences Sectors We Support:

Automation and Digitalization Services:

Biotech and Biologics

API Manufacturing

Medical Device and Diagnostics

Cell and Gene Therapy

Laboratories (R&D, QC, high-throughput labs)

Distributed Control Systems (DCS)

SCADA Systems

Manufacturing Execution Systems (MES)

Electronic Batch Records (EBR)

LIMS and Laboratory Informatics

Robotics and High-Throughput Automation

Fill and Finish Automation

Packaging and Serialization Systems

Environmental Monitoring Systems (EMS)

Building Management Systems (BMS)

Process Control and Utilities Automation

Remote Monitoring and Industrial IoT

Data Integration and Historian Platforms

Validated Controls System Design Implementation

Key Challenges We Solve

Regulatory Compliance: Validated systems with full GAMP documentation and audit readiness.

Integration Complexity: Unified Namespace, MES/SCADA/BMS/serialization ecosystems.

Downtime Risks: 24/7 support and validation services.

Project Complexity: Full‑service consulting, design, build, and startup.

Scalability: Modular platforms that grow from clinical to commercial.

Data Integrity: Real-time data, audit trails, ALCOA+ compliance.

Modernization & Obsolescence: Upgrades that reduce risk and future‑proof operations.

Innovative Solutions: AI readiness, Lab automation and industrial robotics that enhance throughput, precision, and flexibility.

Our Capabilities

Automation & Control Systems
- PLC and DCS programming
- SCADA and HMI development
- Control panel design and build
- OEM skid integration
- Batch automation following ISA-88
Engineering & Consulting
- FEED studies
- System design and architecture
- Procurement and build support
- Startup and commissioning
Compliance & Validation
- GAMP 5 documentation
- 21 CFR Part 11 compliance
- DQ, IQ, OQ, PQ support
- Audit readiness
Manufacturing Systems Integration
- MES and EBR integration
- QA/QC workflow digitization
- Serialization and tracking systems
- BMS and EMS integration
IT/OT & Cybersecurity
- IT/OT assessments
- Network architecture
- ISA/IEC 62443 security
Service & Support
- 24/7 support for operations
- Maintenance and system upgrades
- Embedded engineering teams

Data & Digital Infrastructure
- Historian systems
- Centralized data layers
- Role-based data governance
- Data visualization
- Business intelligence
Next-Generation Automation
- Digital twins
- AI and machine learning analytics
- IIoT integration
- Real-time OEE dashboards
Modern Integration Technologies
- MQTT architectures
- OPC UA connectivity
- Unified Namespace
- REST API communication
Specialized Life Sciences Systems
- Lyophilizer automation
- Lab automation & Industrial Robotics
- LIMS integration
Scalable Production & Modernization
- Obsolescence upgrades
- Modular, expandable platforms
- Automation for emerging therapies

Expertise in Action

Upgrading a QBMS while Enhancing Existing Functionality

E Tech Group developed and integrated a creative solution delivering the desired functionality between previously incompatible software and hardware components.

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Implementing a Hybrid SCADA Solution Using PlantPAx 5.0 and 4.10

We developed a hybrid SCADA solution for a BMS in a biopharma co-packing facility

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Using the OSI PI System for a Large Pharmaceutical Customer

A Pharmaceutical customer chose the OSI PI Software Suite because it provides various architecture and licensing options to accommodate customers’ needs.

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Understanding the S88 Standard: A Comprehensive Guide for Beginners

The S88 standard offers a structured approach to designing, implementing, and maintaining batch processes. In this article we will cover the basics of what S88 is, how it can be used, advantages of it and more.

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Building an Automation Infrastructure

The better you know what you already have in place, the easier it is to plan for a successful future.

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Biotech Manufacturing Scale-up Rockwell FT View and OSI Historian 21CFR Part 11 Compliant

E Tech Group designed, installed, configured, and tested a new OSI PI Historian system compliant with FDA’s 21 CFR Part 11 regulation and EU GMP Annex 11 on electronic signatures and records for a biotech start-up.

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Customized Validated Critical Monitoring System

E Tech Group supported a biopharmaceutical’s expansion with a new validated control system. The company focuses on serious, debilitating, and genetic diseases.

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BioTech Manufacturing Scale-Up

A promising biotech startup with drug candidates progressing from stage 2 to stage 3 clinical had limited automation staffing. The startup turned to E Tech Group to transition their processes to full-scale manufacturing.

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Increased Flexibility & Better Quality for Pharmaceutical Manufacturer

E Tech Group’s engineers implemented a low-cost Rockwell Automation PlantPAx process automation system to upgrade a single-product semiwork facility.

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Why E Tech Group

E Tech Group delivers the technical depth, speed, and compliance‑focused responsiveness that life sciences manufacturers rely on, supporting operations across multiple sites and global regions.

We provide:

Maximum uptime through validated, compliant, and risk‑mitigating automation strategies, applied consistently across global production environments
Higher throughput with systems designed for biotech, pharma, and medical device production, from pilot facilities to multi‑site commercial manufacturing
Consistent product quality and full regulatory confidence across GMP environments, regardless of location or region
Scalable modernization that supports growth from clinical to commercial without disruption, including global rollouts and site expansions
End‑to‑end project execution from early consulting through long‑term support and validation, coordinated across regions and time zones
Embedded engineering and staff augmentation to expand client teams efficiently, both locally and globally
Vendor‑agnostic integration across leading life sciences automation and data platforms, enabling standardized solutions deployed worldwide

With over 30 years of experience and 24/7 global support, E Tech Group is uniquely structured to deliver fast, compliant, and high‑quality execution across life sciences operations, supporting organizations with international footprints where accuracy, traceability, and audit readiness are essential.

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