- Islandwide (Singapore) Singapore
Working Location
Job Description
Responsibilities
We are seeking an experienced Senior Process Technician to provide core process engineering support, oversee key equipment systems, drive continuous improvement, and act as a critical bridge between Manufacturing Science & Technology (MS&T) and Automation teams.
1. Engineering & Design
Develop and maintain process engineering documentation, including P&IDs, URS, SRA, and FRA.
Participate in design reviews, qualification activities, and HAZOP studies.
2. Validation & Quality Systems
Support full life-cycle qualification and validation activities, including IQ/OQ/PQ, FAT, and SAT.
Lead and manage change controls, deviations, and CAPAs related to process engineering.
3. Equipment Ownership & Operations
Maintain primary ownership and technical oversight of SIP, CIP, Washers, and Autoclaves.
Provide independent, expert process engineering support to ensure smooth, reliable site operations.
Provide on-call/24/7 support for advanced troubleshooting, technical optimization, and risk mitigation.
4. Cross-Functional Collaboration & Automation
Serve as the bridge between MS&T and Automation, translating process requirements into automation EMs, recipes, and parameters.
Support recipe testing and collaborate with automation teams to implement system changes.
5. Continuous Improvement & Leadership
Lead engineering-driven improvements focused on yield enhancement, cycle time reduction, and equipment modification.
Step into leadership roles, represent the team in meetings, or provide limited resource accountability when required.
Handle other ad-hoc engineering and operational duties as assigned.
Education
Diploma or Bachelor’s Degree in Chemical Engineering, Mechanical Engineering, Bioprocess Engineering, Biotechnology, or a related technical discipline. (Relevant technical experience may be considered in lieu of a degree).
Industry Experience
Preferred Industry: Pharmaceutical, Biopharmaceutical, Biotechnology, or Fine Chemicals operating under strict cGMP environments.
Experience in regulated manufacturing environments with hands-on exposure to clean utility/sterilization systems (CIP/SIP/Autoclaves) and automated control systems (DeltaV/PLC/SCADA).
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