Responsibilities to include hands-on involvement with design, installation and commissioning (including FAT/ SAT) for facility and building systems (HVAC, Clean Rooms, Cold Rooms, BMS, EMS, etc.) and utilities (Chiller, Compressed Air, WFI, Purified Water, Clean Steam, Sanitary Piping Systems, etc.). Individual will be responsible for providing the design services of equipment and facility automation systems for our customers, and planning and coordinating all the engineering related activities in our projects.
Responsibilities will include:
? Design and design review for our customers.
? Prepare FAT/SAT and commissioning protocols for our projects.
? Execute and supervise the system installation and commissioning on site.
? Provide as-built drawings, operation & maintenance manuals, and all the handover related documentation for our projects.
? Provide trouble-shooting, total solutions and technical proposals for our customers.
The successful candidate will possess a BS degree or higher in chemical/ mechanical/ electrical engineering and must have a minimum of 5 years of hands-on facility engineering experience in the pharmaceutical industry (preferably parenteral manufacturing).
Technical knowledge regarding the design and operation of facility equipment is required.
Candidate must have demonstrated ability to solve technical problems and ability to work independently. Experience in equipment commissioning, qualification, validation and maintenance programs is required. Solid experience with pharmaceutical manufacturing and support equipment is essential; working knowledge of process control systems (expertise with DDC/PLC hardware and SCADA computer systems) is required.

Candidate must have excellent organizational, communication and personal work management and writing skills.