for process equipment, utilities, and manufacturing systems.
Review and execute qualification protocols (IQ, OQ, PQ) and support FAT/SAT activities.
Provide
process and operational input
during 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.
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