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Company
MATRIX PROCESS AUTOMATION PTE. LTD.
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Job Description
Roles & Responsibilities - Support C&Q execution for process equipment, utilities, and manufacturing systems.
- Review and execute qualification protocols (IQ, OQ, PQ) and support FAT/SAT activities.
- Provide process and operational inputduring commissioning and troubleshooting.
- Support DeltaV-related activities (recipes, phases, batch execution understanding).
- Develop/review C&Q documentation (URS, risk assessments, protocols, reports).
- Ensure adherence to GMP, regulatory, and data integrity requirements.
- Collaborate with operations, QA, and automation teams to meet project deliverables
- Bachelor's degree in chemical / Biochemical / Process / Mechanical Engineering or related field.
- 4–6 years' experience in pharmaceutical/biotech manufacturing or operations, with exposure to C&Q.
- Strong process knowledge of pharmaceutical manufacturing.
- Working knowledge of DeltaV – recipes, batch execution, troubleshooting.
- Hands-on experience with C&Q documentation and execution (IQ, OQ, PQ).
- Good knowledge of cGMP, FDA/EMA guidelines, and industry practices.
Tell employers what skills you have Recipes
Factory
Troubleshooting
Microsoft Office
Construction
GMP
Electrical
PLC
FPSO
Project Management
Instrumentation
Power Systems
Manufacturing
Chemical Engineering
Commissioning
Mechanical Engineering
About MATRIX PROCESS AUTOMATION PTE. LTD.
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