Project CQV 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 Project CQV Engineer is responsible for planning, executing, and delivering commissioning and qualification activities for GMP manufacturing and laboratory equipment within a project environment. The role supports the full equipment lifecycle from design review through qualification and handover to operations, ensuring systems are fit for intended use, compliant with regulatory requirements, and delivered in alignment with project schedules and milestones.

Key Responsibilities

• Execute IQ, OQ, and PQ activities for manufacturing, packaging, process, support, and applicable QC laboratory equipment
• Support equipment walkdowns, readiness checks, punch-list management, and closure activities
• Coordinate with equipment vendors during installation, FAT, SAT, and qualification execution
• Participate in design reviews, equipment URS reviews, and risk assessments (e.g. FMEA)
• Support project schedules and ensure timely delivery of equipment CQV milestones
• Prepare, execute, and review validation documentation including protocols, reports, and traceability matrices
• Manage deviations, change controls, and CAPAs in compliance with GMP requirements
• Support transition from project execution to operational handover
• Collaborate cross-functionally with Project Engineering, Manufacturing, MSAT, QA, and external vendors
• Provide on-site support during critical project phases and support regulatory inspections and audits as an equipment CQV SME

Required Qualifications

• Diploma or Bachelors degree in Engineering (Chemical, Mechanical, Electrical, Automation), Pharmaceutical Sciences, or a related discipline
• 2–8 years of experience in equipment CQV / validation within pharmaceutical or biotechnology projects
• Hands-on experience executing equipment IQ, OQ, and PQ activities
• Experience coordinating with vendors during equipment installation and project delivery
• Exposure to greenfield, brownfield, or facility expansion projects is an advantage

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.