Job Description

Role Overview:
We are looking for Process Engineers (4-6 years) with strong manufacturing operations and process knowledge to support Commissioning & Qualification (C&Q) activities. Candidates with working knowledge of DeltaV -- including recipes, phases, and batch execution -- will be preferred. The role involves collaborating with manufacturing, QA, and automation teams to ensure equipment and process systems are qualified and ready for GMP production.
Key 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 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
Qualifications and 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.

Skills Required