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 This role is responsible for supporting commissioning and start-up activities across upstream, downstream, utilities, and process equipment systems within a GMP-regulated environment. The engineer will work closely with cross-functional teams including QA, Validation, Engineering, EHS, and Operations to ensure systems are safely and compliantly brought into service. The role involves reviewing engineering documentation, executing commissioning activities, and ensuring smooth handover to operations through structured verification and testing processes. Key Responsibilities • Execute commissioning activities for upstream, downstream, utilities, and process equipment systems • Review P&IDs, process flow diagrams, design specifications, and vendor documentation • Lead system walkdowns, punch listing, and mechanical completion verification • Coordinate SAT, IOQ support, loop checks, functional testing, and start-up activities • Collaborate with QA, Validation, Engineering, EHS, and Operations to ensure GMP compliance • Support troubleshooting, deviation resolution, and handover to operations Required Qualifications • Degree/Diploma in Engineering (Chemical, Mechanical, Electrical or related discipline) • Experience in pharmaceutical, biotech, or regulated manufacturing environment preferred • Understanding of commissioning, qualification, and validation activities (SAT, IOQ, etc.) • Ability to interpret engineering documents (P&IDs, process flow diagrams, specifications) • Strong cross-functional coordination and communication skills • Familiarity with GMP requirements and controlled manufacturing environments 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.