Senior Manufacturing Science and Technology (MSAT) Engineer
Date Posted: January 22, 2026
Job Description
The Senior MSAT Engineer drives the technical success of a major brownfield project in Singapore as it transitions from SAT into active Commissioning and Qualification (C&Q). Operating within the Operational Readiness function, you ensure that all systems, equipment, and processes meet the rigorous technical standards required for start-up and manufacturing handover. You act as a technical leader on the floor, bridging the gap between engineering design and operational reality to ensure a seamless transition into production.
Key Responsibilities
- Drive SAT and Commissioning Activities by leading system testing, functional verification, and trial runs to ensure operational excellence.
- Execute Qualification Protocols, providing hands-on support for IQ, OQ, and PQ phases within a high-stakes brownfield environment.
- Master Technical Troubleshooting during start-up and trial operations to resolve complex process or equipment-related issues immediately.
- Lead System Readiness by ensuring all equipment operates as intended before the final handover to the Manufacturing team.
- Partner with Cross-Functional Teams, including Operations, CQV, Engineering, and Quality, to maintain total alignment during project execution.
- Provide Expert Technical Input for the development and review of commissioning, qualification, and readiness documentation.
- Optimize Process Equipment, specifically focusing on the performance and reliability of ultrafiltration and centrifuge systems.
- Facilitate Seamless Handovers to Operations by verifying that all technical and compliance requirements are met following successful qualification.
Required Qualifications and Skills
- Bachelor’s degree in Chemical Engineering, Biochemical Engineering, Biotechnology, or a related discipline.
- 5–10+ years of experience in MSAT, process engineering, or manufacturing support within the pharmaceutical sector.
- Demonstrate extensive experience supporting Commissioning and Qualification (C&Q) workflows in a strict GMP environment.
- Hands-on expertise with ultrafiltration and centrifuge systems, including their specific operational and validation challenges.
- Offer strong troubleshooting capabilities specifically tailored for the high-pressure environment of plant start-ups and trial runs.
- Solid understanding of GMP manufacturing requirements and operational readiness standards.
- Excel at working in cross-functional teams and translating technical data into actionable operational strategies.
If you are keen to grow your career with this job, apply with us and send us your resume now. All shortlisted candidates will be contacted shortly.
Reference no.: 122-4948-2918-NW
Registration no.: 968446516E