MES Engineer

1 week ago

Singapore NO DEVIATION PTE. LTD. Full time $80,000 - $120,000 per year

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

We are seeking a detail-oriented and proactive professional responsible for the design, development, and validation of Master Batch Records (MBRs) and associated systems. This role requires close collaboration with cross-functional teams to ensure compliant, efficient, and effective batch record solutions that integrate seamlessly with manufacturing operations and equipment.

Key Responsibilities

  • Develop, configure, and test Master Batch Records (MBRs) and Parameter Value Lists (PVLs) from initial design through to final approval.
  • Conduct MBR design reviews in collaboration with Operations, Process Development, and Quality teams.
  • Draft, execute, and review Application Lifecycle Management (ALM) test scripts and test sets to validate MBR design.
  • Design, configure, and test equipment integration to enable MBR interaction with shop floor systems (e.g., OSI PI, Recipe Managers, DeltaV).

Required Qualifications

  • Bachelors degree in Chemical Engineering, Biotechnology, Life Sciences, or related field.
  • Strong hands-on experience with downstream processing operations, including understanding of process steps, critical parameters, and typical plant operations.
  • Prior involvement in MES implementation or system validation projects (e.g., PAS-X, Siemens Opcenter) is highly preferred.
  • Ability to independently assess MES design documents and provide process-aligned feedback.

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.

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