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PURPOSE:
. Design, develop and maintain process automation systems to support manufacturing processes.
. Ensure good performance of the automation systems.
. Ensure compliance with Standard Operating Procedures (SOPs), Health, Safety and Environment (HSE) regulations and Current Good Manufacturing Practices (CGMPs) within his/her purview.
RESPONSIBILITIES:
Project Support
. Support the automation team on site projects, i.e new product introductions or new technology introductions by performing automation assessments, implementation and qualification activities.
Operation Support
. Provide technical support to automation systems related issues in manufacturing operations.
. Maintain the GMP compliant state of the assigned automation systems.
. Perform periodic alarm managements/audit trails reviews.
. Perform periodic preventive maintenance and review for automation systems.
. Support 24/7 on call operational support.
Develop, revise and review SOP's as needed.
Audit Support
. Participate in non-conformance investigations and implementation of corrective actions.
. Participate in external/internal compliance audits.
REQUIREMENTS:
. Degree or Master's in Engineering (Chemical / Electrical & Electronics / Instrumentation / Pharmaceutical)
. 4+ years of relevant work experience in Biotechnology / Pharmaceutical is highly preferred Chemical / Oil & Gas industries is considered
. Proficiency in programming/troubleshooting of Control Systems applications especially DeltaV, Siemens etc. preferably in pharmaceutical industry.
. Experience in OT Communication protocol i.e Device net, Ethernet/IP, Modbus TCP etc
. Knowledge of GAMP/GMP and familiarity with documentation in regulated environment.
. An ideal candidate must be a self-driven team player and communicate technical solutions to stakeholders.
Date Posted: 20/08/2025
Job ID: 124256467