our solutions.

Focus on Patients.

We'll perfect your Operations.

In today’s bio-pharmaceutical landscape, internal teams are under pressure to cut OPEX while holding the line on quality, safety and compliance. Ventritech acts as your third-party GMP operations and engineering partner — combining operational excellence consulting, digital transformation and automation, and cGMP-trained manpower, EPF projects — so your people can stay focused on product, patients and innovation.

We plug into your existing organisation to stabilise equipment, clear engineering backlogs and keep every shift inspection-ready.

Expert Guidance, Real-World Solutions

Operational Excellence & Engineering Consultancy

Ventritech combines hands-on E&I engineering experience with Lean / TPS methods to solve chronic plant issues, not just write reports. We work alongside your engineers and supervisors to troubleshoot control and instrumentation problems, remove bottlenecks and build a practical, KPI-driven OPEX roadmap.

What we deliver:

1. Electrical & Instrumentation (E&I) Engineering Consultancy

• Deep troubleshooting of control systems, instrumentation and automation networks

• Structured root cause analysis and corrective actions for recurring failures

• Vendor liaison and technical procurement support

• Upgrade strategies to improve reliability, safety and compliance

2. Operational Excellence (OE) & Organization Production System

• Lean manufacturing principles tailored to cGMP environments

• Plant performance diagnostics to identify losses and bottlenecks

• Design and implementation of site-specific Production Systems (OPS)

• Coaching and training to embed continuous improvement culture

3. Process & Productivity Improvement

• KPI-driven reviews to improve OEE and line throughput

• Data-driven solutions for yield, changeover and labour efficiency

• Implementation support for automation, digital workflows and predictive maintenance

4. vtrac - AI powered assistant for the Bio-Pharmaceutical Manufacturing industry.

• For teams starting their digital transformation, we can extend this work with vtrac, our AI-powered assistant to help with troubleshooting, deviation drafting and SOP gap analysis.

Need a dedicated support on-site? Schedule an OE & Engineering Consulting Call

GMP Staff Augmentation & Outsourced Operations

Ensure uninterrupted GMP compliance and smooth day-to-day operations, with Ventritech’s specialised staff augmentation services. We provide pre-qualified, cGMP-trained personnel to absorb non-core but GMP-critical work during audits, shutdowns, expansions and high-load periods — without increasing your permanent headcount.

Where our teams plug in:

• Specialised cleaning & sensitive equipment handling

  • Cleaning and care for process equipment and utilities that general FM cleaners cannot touch

  • Support for shutdowns, changeovers and high-risk cleaning activities

• GMP logistics & packaging support

  • Re-labelling, re-packing and kitting of finished goods and components

  • Line-side material handling, sampling logistics and documentation support

• Production & maintenance support

  • Extra hands for shutdowns, commissioning and validation campaigns

  • Short- to mid-term cover for leave, vacancies and expansion phases

All personnel are trained to work within your site procedures and quality systems, giving you flexible capacity without long-term headcount commitments.

EPF - Engineer, Procure, Fabricate

Ventritech provides full-scope Engineering, Procurement and Fabrication (EPF) services tailored for bio-pharmaceutical facilities. By consolidating project execution under a single GMP-experienced partner, we help you compress timelines, control costs and maintain alignment with FDA, EMA, PIC/S and ISO expectations from concept through commissioning.

We apply proven project execution methodologies, standardised design templates and vendor-agnostic procurement to deliver compliant, fully integrated systems and components. Our approach routinely delivers up to 30–40% total lifecycle cost savings compared to traditional multi-vendor models — while giving you clearer ownership and control over critical systems.

Our Services:

Engineering / Fabrication

• Preventive maintenance and upgrade packages

• Custom equipment fabrication (SS316 / SS316L)

• Cleanroom-grade fabrication (ISO 14644-1 Class 7/8)

• Proprietary alloy fabrication (e.g. Hastelloy, Titanium)

• Hybrid stainless / single-use assemblies

• Non-standard port and connection configurations

• ASME BPE-compliant orbital welding

Procurement

• Vendor-agnostic equipment and parts sourcing

• Inventory review and optimisation for critical spares

• Consumables and MRO procurement with GMP documentation

• Support for CAPEX planning and OPEX reduction

Planning a utility upgrade, capacity expansion, modifications or procurement? Contact us to explore EPF delivery models suitable for your site.

Pharmaceutical Digital Transformation and Automation

Automation & Data Integration: Powering Precision in Bio-Pharma Manufacturing

In an environment where small deviations can compromise patient safety, VentriTech designs and implements end-to-end automation and data integration that turns fragmented systems into a single, compliant source of truth. We help you reduce manual interventions, shorten batch release times and strengthen data integrity across utilities, process equipment and quality systems.

Our Expertise includes:

1. Process Automation

• DeltaV DCS systems

• PLC / SCADA systems

• CIP / SIP automation

• MES / SCADA / LIMS integration

• Electronic Batch Record (eBR) design & implementation

• Data integrity risk assessment aligned to ALCOA+

2. Commissioning and Validation

• User Requirement Specifications (URS)

• Functional Specifications (FS)

• Design Specifications (DS)

• Factory Acceptance Test (FAT)

• Site Acceptance Test (SAT)

3. Technical Expertise Support

• Project commissioning support for new lines and upgrades

• Long-term embedded automation engineers to stabilise operations

Ready to modernise your automation stack without disrupting production? Book a call to discuss your current systems and roadmap.

Ready to streamline your pharma operations?

Share a few details about your facility, current challenges and timelines.

Our technical leadership will review your situation and propose one or more engagement options — from a 30-minute executive briefing to a focused pilot project or staffed support package.

Let's work together!