EFU Validation Engineer

About No deviation

At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation.

We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development – empowering our team members to grow personally and professionally.

Position Overview

The EFU Engineer (Equipment Facilities Utilities) provides engineering support for facilities and utilities systems directly associated with manufacturing and laboratory equipment within a GMP-regulated pharmaceutical environment. This role ensures that equipment-related utilities are reliable, compliant, and fit for purpose to support routine operations, commissioning and qualification activities, and regulatory inspections. The EFU Engineer works closely with operations, validation, QA, facilities, and project teams to maintain equipment readiness and production continuity.

Key Responsibilities

• Provide engineering support for equipment-associated facilities and utilities systems supporting manufacturing and laboratory operations in a GMP environment
• Support clean utilities, HVAC interfaces, and equipment-related electrical and mechanical services
• Act as facilities focal point for equipment installation, relocation, and upgrades
• Support commissioning and qualification (IQ/OQ/PQ) of equipment-related utilities, including utilities verification and functional testing
• Prepare, review, and support GMP documentation such as protocols, reports, change controls, deviations, and CAPAs
• Provide day-to-day operational support and troubleshoot utilities-related equipment issues impacting production
• Support deviation investigations and implement corrective actions with maintenance teams, vendors, and contractors
• Support capital projects, new equipment introduction, and facility or utility system upgrades
• Coordinate with equipment engineering, facilities, validation, QA, and production teams
• Manage vendor activities and ensure safe, compliant execution of on-site works
  

Required Qualifications

• Diploma or Bachelors degree in Mechanical Engineering, Electrical Engineering, Facilities/Building Services Engineering, or related technical discipline
• 2–8 years of experience in pharmaceutical, biotech, or GMP-regulated manufacturing environments
• Hands-on experience with equipment-associated utilities and facilities engineering systems
• Experience supporting commissioning, qualification, or validation activities
• Working knowledge of GMP facilities, utilities systems, and equipment–utilities interfaces
• Ability to read and interpret P&IDs, layouts, equipment utility requirements, and technical drawings
• Familiarity with engineering change control, safety systems, permit-to-work, and contractor management
• Strong troubleshooting, communication, and structured documentation skills

Why join us?

• Generous Leave Policy.
• Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs.
• Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company.
• Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated.
• Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career.

How to apply

Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you're passionate about making an impact, we want you on our team!

Please submit your resume, outlining your qualifications and experience relevant to the role, here.