Process Engineer-C&Q (Pharmaceutical Manufacturing Operations)

·        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 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.

Requirements

·        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.