Job Description

The candidate is responsible for Equipment Package Ownership (full lifecycle \xe2\x80\x93 Engineering Design, Build, Testing (FAT), Installation and Commissioning), including experience in commissioning and qualification of process equipment.

Responsibilities:

• Experience in upstream / downstream / Central services process operation, (experience in equipment design for process equipment will be an advantage).

• Responsible for basic and detailed design, commissioning and qualification activities, including URS development, FAT, SAT, DQ, IQ, OQ and PQ.

• Review industry practices for best-in-class approach.

• Ensure that the appropriate Quality standards are applied consistent with best practice and internal Quality Standards and expectations.

• Engage with project teams to deliver the project from conceptual through implementation phase, encompassing support for a wide range of engineering and construction requirements.

• Coordinates with different functions like manufacturing, project engineering team, validation and quality for implementation of changes associated with the project.

• Work independently and/or with the project manager to complete the engineering projects within schedule, budget and quality constraints.

• Any other task as assigned by Supervisor/Manager.
  

• Diploma/Degree in Chemical Engineering, Chemistry or equivalent with at least 5 years\' experience in a process engineering role or similar role with a biologics manufacturing plan

• Process Engineer with 2-5 years of experience

• In Biologics industry with understanding of cGMP requirement

• Should have Design experience at various stages of project (Base, Detailed design)

• Preferably handling the Autoclave, Glove box, CIP Skid during project phase

• Able to support Installation, Commissioning & Qualification activity at site.

• Any other task given related to Process.