Senior Process Engineer

Overview
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. We foster a culture of collaboration, inclusion, and continuous development empowering our team members to grow personally and professionally.
Position Overview
We are seeking an experienced Senior Process Engineer to join the project team on-site role in Singapore. This role involves installation, energization, commissioning (SAT), and qualification of multiple superskids as part of an upstream drug substance production train. The engineer will oversee key systems within an integrated production environment, including fermentation, extraction, and the preparation and storage of media, buffers, and antigens.
Key Responsibilities
Ensure correct construction and commissioning of fermentation, extraction, and media/buffer packages in compliance with internal and regulatory requirements
Troubleshoot process equipment and provide technical resolutions
Act as the representative for all process-related activities and installations
Track engineering progress and ensure alignment with project specifications
Review technical documentation and detailed design studies (e.g., P&IDs, datasheets, functional specifications, 3D models)
Oversee construction, testing, and change management processes
Supervise contractors and perform on-site inspections (e.g., P&ID walkdowns, SAT execution)
Provide technical support across commissioning, testing, and qualification phases
Required Qualifications
Bachelors degree in Chemical or Process Engineering
Minimum of 10 years of experience in Process Engineering, especially in capital investment projects from design to facility start-up
Extensive experience in commissioning and qualification of integrated production systems
Strong knowledge in functional and technical process requirements, control systems, and regulatory compliance
Proficient in Microsoft Office Suite, Visio, and Project; experience with SchedulePro/SuperPro or similar tools is preferred
Fluent in English; proficiency in French, German, or Mandarin is a plus
Demonstrated ability to work autonomously and manage contractors in a high-demand cGMP and EHS environment
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.
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Management and Manufacturing
Industries
Pharmaceutical Manufacturing
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