PCS Software Engineer

NO DEVIATION PTE. LTD.; Singapore; On-site; SGD 80,000 - 100,000; Full time

Job summary

A leading pharmaceutical consultancy in Singapore is seeking an experienced engineer to focus on PCS configuration and commissioning. The role involves collaborating on software development, reviewing design documents, and supporting qualification activities. Ideal candidates will have a degree in engineering and significant experience in GMP environments. Generous leave policies and comprehensive health coverage are part of what makes this role attractive. Join a team where innovation and collaboration are key to success.

Benefits

Generous Leave Policy

Comprehensive Health & Wellness Coverage

Professional Development Opportunities

Inclusive Culture

Qualifications

• 5–10 years of experience in GMP pharmaceutical environments.
• Hands-on experience with process automation systems.
• Familiarity with FAT/SAT activities.

Responsibilities

• Support the design and development of PCS software.
• Review PCS-related design documentation.
• Conduct Factory Acceptance Testing.

Skills

GMP manufacturing

Process automation

Troubleshooting

Commissioning

Collaboration

Education

Diploma or Bachelor's degree in Chemical Engineering or related field

Tools

Emerson DeltaV

Job description

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 role focuses on translating manufacturing process requirements into PCS configuration, working closely with PCS vendor and client workflow, and supporting end‑to‑end commissioning, qualification, and process validation activities associated with the PCS.

Key Responsibilities

• Collaborate with various workstreams to support the design and development of the PCS software in collaboration with Emerson.
• Develop Functional Specifications (FS) and Design Specifications (DS) in collaboration with Emerson and in alignment with GSK project requirements.
• Attend technical and project management meetings and contribute to the overall execution and progress of the project.
• Review PCS‑related design documentation and provide feedback to ensure compliance with user requirements and approved standards.
• Witness Factory Acceptance Testing (FAT) conducted by Emerson to ensure that the PCS software conforms to the approved user requirements and design documentation.
• Track project deliverables, maintain documentation, and ensure adherence to the agreed schedule.
• Support and track change management processes throughout the project lifecycle.
• Support Engineering and Performance Process Qualification (PPQ) batches as required.
• Provide support to Commissioning and Qualification (C&Q) activities, including:
  • Cold and Hot Loop Checks
  • PCS network interface testing and troubleshooting
  • Batch software commissioning and functional testing
  • Qualification testing, including Installation Qualification (IQ) and Operational Qualification (OQ)

Required Qualifications

• Diploma or Bachelors degree in Chemical Engineering, Biochemical Engineering, Pharmaceutical Engineering, Automation, Electrical, Instrumentation, or a related engineering discipline.
• Minimum 5–10 years of experience supporting GMP manufacturing environments in the pharmaceutical or biopharmaceutical industry.
• Hands‑on experience supporting process automation or PCS systems (e.g. Emerson DeltaV) in a process execution, commissioning, or operational support capacity.
• Demonstrated experience working with manufacturing processes, batch operations, and process control strategies in upstream, downstream, or fill/finish operations.
• Experience supporting commissioning and qualification activities (e.g. loop checks, functional testing, IQ/OQ support) in collaboration with CQV teams.
• Exposure to FAT/SAT activities, including review or witnessing of test execution and issue follow‑up.
• Experience supporting PPQ or engineering batches, including on‑floor PCS or process execution support.
• Working knowledge of PCS/automation systems (e.g. DeltaV) sufficient to support testing, commissioning, and troubleshooting activities.
• Ability to review and support development of FS and DS documentation from a process and operational perspective.
• Basic troubleshooting capability across PCS interfaces, batch execution, and process instrumentation.

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.