Based in either RTP-North Carolina/ San 
Francisco (Bay Area)/ Eastern US (NJ/PA), the 
successful candidate will work with a group of 
talented process engineers involved in the 
design, automation, commissioning and start up 
of various processes and facilities. A 
combination of strong technical aptitude, 
project engineering skills and dedication to 
excellence, make up the ideal skill set required 
for this position. 

Responsibilities include generation of 
engineering specifications and drawings, review 
of engineering documents, field-testing of 
equipment/systems such (fermentors, 
chromatography systems, high purity water and 
steam systems, control systems (SCADA, DCS, BMS, 
PLCs), vial and syringe filling equipment as 
well as Isolators). Responsibilities also 
include generation and execution of 
commissioning & qualification technical test 
plans (FAT, SAT, IQ/OQ, PQ) and final reports 
summarizing testing activities and deviations 
across a wide variety of equipment, utilities 
and automation systems used in the bio-
pharmaceutical industry. Project engineering 
responsibilities include client-management, 
project scheduling/budgeting, and coordination 
of client and ADVENT resources for effective 
project delivery. 


Requirements:
 
The position requires a minimum B.S. degree in 
Chemical Engineering or related discipline and 
prior work experience of 5 years in the 
pharmaceutical or biotechnology industries. An 
advanced degree is a plus. 

The candidate must have direct experience in the 
design or commissioning/qualification of the 
following systems: Strong Upstream/Downstream 
bulk process equipment, Lyophillization, Aseptic 
Filling of vial and syringe forms, 
Sterilization, Pasteurization, Clean-In-Place, 
Clean Utilities (WFI/PW, Pure Steam, Clean 
Gases). SCADA, ABB or Delta V DCS experience is 
a plus.
 

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