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.

Responsibilities

. Good 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.