Antaes
Job Description:
Contribute to Life Science projects for Antaes Asia clients
Perform routine preventive, corrective, and predictive maintenance on manufacturing and utility equipment (e.g. bioreactors, chromatography skids, ultrafiltration systems, mixers, autoclaves, CIP/SIP systems).
Troubleshoot mechanical/electrical issues to minimize equipment downtime and support uninterrupted production.
Assist in equipment installation, commissioning, and qualification (IQ/OQ/PQ) in compliance with regulatory expectations.
Create and update Bill of Materials (BOMs), spare parts lists, and maintenance documentation in CMMS/ERP systems.
Execute maintenance activities according to SOPs, GMP, safety, and EHS standards.
Support root cause investigation and implement corrective/preventive actions (CAPA) for equipment-related deviations.
Collaborate with cross-functional teams including Manufacturing, Engineering, Validation, and Quality.
Participate in continuous improvement initiatives to enhance equipment reliability and lifecycle management.
Participate in design reviews, HAZOPs, FATs/SATs as needed for utility and equipment systems.
Contribute to the promotion of Antaes services on top of assistance provided to clients
Job Requirements:
Diploma / Technical Certificate in Mechanical, Electrical, Mechatronics, Engineering, or related field.
2–5 years of hands-on maintenance experience in pharmaceutical, biologics, or regulated manufacturing is preferred.
Experience working with GMP-regulated equipment and CMMS systems (e.g. SAP, Maximo).
Familiarity with BOM structuring, spare parts management, and equipment documentation.
Strong mechanical/electrical troubleshooting skills
Understanding of GMP and cleanroom practices
Ability to interpret P&IDs, schematics, and equipment manuals
Strong analytical, troubleshooting, and documentation skills.
Candidate must be highly motivated, be able to work independently as well as in a team and have good organizational and oral and written communication skills
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Contribute to Life Science projects for Antaes Asia clients
Perform routine preventive, corrective, and predictive maintenance on manufacturing and utility equipment (e.g. bioreactors, chromatography skids, ultrafiltration systems, mixers, autoclaves, CIP/SIP systems).
Troubleshoot mechanical/electrical issues to minimize equipment downtime and support uninterrupted production.
Assist in equipment installation, commissioning, and qualification (IQ/OQ/PQ) in compliance with regulatory expectations.
Create and update Bill of Materials (BOMs), spare parts lists, and maintenance documentation in CMMS/ERP systems.
Execute maintenance activities according to SOPs, GMP, safety, and EHS standards.
Support root cause investigation and implement corrective/preventive actions (CAPA) for equipment-related deviations.
Collaborate with cross-functional teams including Manufacturing, Engineering, Validation, and Quality.
Participate in continuous improvement initiatives to enhance equipment reliability and lifecycle management.
Participate in design reviews, HAZOPs, FATs/SATs as needed for utility and equipment systems.
Contribute to the promotion of Antaes services on top of assistance provided to clients
Job Requirements:
Diploma / Technical Certificate in Mechanical, Electrical, Mechatronics, Engineering, or related field.
2–5 years of hands-on maintenance experience in pharmaceutical, biologics, or regulated manufacturing is preferred.
Experience working with GMP-regulated equipment and CMMS systems (e.g. SAP, Maximo).
Familiarity with BOM structuring, spare parts management, and equipment documentation.
Strong mechanical/electrical troubleshooting skills
Understanding of GMP and cleanroom practices
Ability to interpret P&IDs, schematics, and equipment manuals
Strong analytical, troubleshooting, and documentation skills.
Candidate must be highly motivated, be able to work independently as well as in a team and have good organizational and oral and written communication skills
#J-18808-Ljbffr