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 Engineer is responsible for supporting and managing end-to-end execution of capital and improvement projects within a GMP-regulated environment. This role involves coordinating facility modifications, overseeing process equipment installation, and ensuring projects are delivered on time, within budget, and in compliance with quality and safety standards. The Project Engineer works closely with cross-functional teams and external partners to drive successful project outcomes from design through commissioning and handover. The position requires strong technical, organizational, and stakeholder management capabilities.
Key Responsibilities
- Support and manage full project lifecycle from concept through commissioning and qualification
- Coordinate facility modification works across architectural and mechanical scopes
- Lead or support process equipment installation, integration, and startup activities
- Develop and review project documentation (URS, design specs, layouts, schedules, risk assessments, cost estimates)
- Collaborate with internal stakeholders (Quality, Operations, Maintenance, EHS) and external vendors/contractors
- Ensure compliance with GMP, safety, and engineering standards
- Support or lead commissioning, qualification, and handover activities (IQ/OQ/PQ)
- Track project timelines, monitor progress, and mitigate risks
- Participate in change controls, deviations, and technical discussions with Quality/Regulatory teams
- Ensure proper documentation, reporting, and project close-out
Required Qualifications
- Degree in Engineering (Mechanical, Chemical, Process, or related discipline)
- 2–5 years of experience in pharmaceutical, biotech, or GMP-regulated industries
- Experience in project execution, equipment installation, and/or CQV activities
- Familiarity with GMP requirements and regulatory standards
- Knowledge of documentation such as URS, risk assessments, and validation protocols
- Strong coordination and stakeholder management skills
- Ability to manage multiple tasks and meet project deadlines
- Good communication and problem-solving 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.
