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.