Lead Process Engineer – CIP/SIP & GMP Automation
No-Deviation-Pte.-Ltd
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Benefits offered by this job
Job summary
No deviation in Singapore is seeking an experienced Process Lead Engineer to provide technical leadership for CIP, SIP, washers and autoclaves in pharmaceutical manufacturing. You will collaborate with MS&T, Engineering, Automation and Operations to ensure compliant, reliable operations.
The role involves qualification & validation activities (IQ/OQ/PQ, FAT/SAT), process design support, optimization, and risk assessments, with emphasis on change control, deviations, CAPAs, and practical
Qualifications
- Degree in Chemical/Mechanical/Pharmaceutical Engineering or related field.
- Experience in pharmaceutical GMP manufacturing environment.
- Heads-on CIP and SIP systems experience preferred.
- Familiar with P&IDs, URS, risk assessments (SRA/FRA) and HAZOP.
- Experience with IQ/OQ/PQ, FAT/SAT, commissioning and validation.
- Strong change control, deviation investigations and CAPA experience.
Responsibilities
- Provide technical ownership for CIP, SIP and related process systems.
- Develop and maintain process engineering documentation throughout lifecycle.
- Support design reviews, URS, SRA, FRA, FAT/SAT, and validation.
- Lead continuous improvement for process reliability and efficiency.
- Interface between MS&T and Automation to translate requirements.
- Support change controls, deviations, CAPAs, and investigations.
Skills
Education
Tools
Job description
No deviation in Singapore is seeking an experienced Process Lead Engineer to provide technical leadership for CIP, SIP, washers and autoclaves in pharmaceutical manufacturing. You will collaborate with MS&T, Engineering, Automation and Operations to ensure compliant, reliable operations.
The role involves qualification & validation activities (IQ/OQ/PQ, FAT/SAT), process design support, optimization, and risk assessments, with emphasis on change control, deviations, CAPAs, and practical
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