Quality Assurance Engineer

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.

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.