The Life Sciences Senior system engineer is an integral member of the Life Sciences COE team, who reports to LE/PE and undertakes the Design, Implementation, Internal testing and Factory acceptance test of respective Process/Function area for Process Systems and Solutions (PSS) projects.
The senior system engineer in Life Sciences COE:
Supports Lead engineer as Area/Sub lead for the Medium to Large size projects.
Has good knowledge of the DeltaV system and exposure to S88 architecture .
Has hands on experience on Batch process Applications e.g- in Biotech, Pharma, F&B, Terminal automation etc.
Has Design and configuration experience of Medium to Complex Equiment modules/sequences .
Understands and has aptitude to follow strict procedural guide lines and adherence to standards .
Has penchant for details and documentation .
Reviews and guides System engineers’s work.
Independently lead small size projects.
Coordination with overseas offices and customers –
To understand and document the Scope, Schedule and Budget of work to be done.
Channelling the TQ’s.
Weekly meetings.
Progress reporting.
Project Execution –
Interpret PFD and other project documentation to develop Process Functional requirement.
Interpret Functional requirement documents and developing Detail Designs Documents
Develop Configuration and Test guidelines.
Develop Test Specifications and supervise/execute Test protocols
Design, implementation and testing of User interface system including Dynamo/FP/DT/Batch.
Conducting or participation in FAT/SAT/Commissioning.
Have strict Vigil on Scope creeps and Scope changes
Escalate project issues/risk proactively to lead engineer/PM, if possible with mitigation plan.
Take full ownership of the allocated work and direct sub-ordinates.
Coach and develop system engineer skills.
Willingness to travel to Customer site or Emerson overseas offices for short/long term
Quality Control & Assurance
Implementation of EEEC IMS processes/documentation as & when required throughout the project.
Adopts to WA quality requirements and Cutomer’s regulatory guidelines
Already Certified or gets certified on GAMP5 and GDP requirement of Pharma projects
Practices and promotes First time right approach
Strictly follows GDP (Good Documenattion Practices)
Other Duties – Perform other additional specific duties, when requested by the business. These will, typically, be strategic in nature but could potentially be anything that the post holder is suitably qualified and experienced to undertake. These duties may be assigned to the person under guidance of a supervisor.
Requisition ID : 23010408
Emerson is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, marital status, political affiliation, sexual orientation, gender identity, genetic information, disability or protected veteran status. We are committed to providing a workplace free of any discrimination or harassment.
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