×
Register Here to Apply for Jobs or Post Jobs. X

Project Process Engineer

Job in Salina, Saline County, Kansas, 67401, USA
Listing for: Hydrogen UK Ltd
Full Time position
Listed on 2026-07-24
Job specializations:
  • Engineering
    Validation Engineer, Process Engineer, Pharma Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 151536 - 158424 USD Yearly USD 151536.00 158424.00 YEAR
Job Description & How to Apply Below

Project Process Engineer

Wilson, NC (100% on-site) with travel to Shanghai, China

W2

Contract:

August 2026 – December 2027

Pay: $110‑115 /hr

We are seeking an experienced Project Process Engineer to support the startup, commissioning, troubleshooting, and qualification of large-scale bioprocess manufacturing equipment. This role will play a key part in bringing new production systems online at a biopharmaceutical manufacturing facility.

The position requires on‑site support in Wilson, NC, along with international travel to Shanghai, China for equipment design reviews and Factory Acceptance Testing (FAT).

Responsibilities
  • Lead startup, SAT, commissioning, and troubleshooting of large-scale stainless steel bioprocess equipment, including bioreactors, CIP skids, and transfer systems.
  • Support Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), equipment verification, and commissioning activities.
  • Perform dry and wet testing of automated batch recipes and support initial production runs.
  • Verify equipment installation against design drawings, P&IDs, component lists, and perform I/O validation.
  • Troubleshoot process equipment and perform minor mechanical repairs, including valve diaphragms, tri-clamps, and position switches.
  • Partner with Process Controls Engineers to debug and optimize control loops and update functional specifications.
  • Coordinate major equipment repairs, piping modifications, and mechanical maintenance activities.
  • Develop startup, commissioning, operational, and preventive maintenance documentation and SOPs.
  • Document commissioning activities to support equipment qualification and validation efforts.
  • Assist with qualification execution and support manufacturing readiness activities.
  • Coordinate daily startup activities with production personnel and engineering teams.
Qualifications
  • Experience with startup, commissioning, and troubleshooting of bioprocess manufacturing equipment.
  • Hands‑on experience with stainless steel bioreactors, CIP systems, transfer lines, or similar pharmaceutical process equipment.
  • Knowledge of FAT, SAT, commissioning, qualification, and validation processes.
  • Ability to interpret engineering drawings, P&IDs, and equipment documentation.
  • Experience working in GMP or regulated pharmaceutical/biotechnology manufacturing environments.
  • Strong troubleshooting and cross‑functional communication skills.
  • Willingness to travel internationally for equipment reviews and FAT activities.
Schedule
  • August 2026 – February 2027: Part‑time support
  • March 2027 – December 2027: Full‑time support

Beginning in April 2027
, candidates must be available to work one of the following shifts:

  • Sunday – Wednesday | 6:00 AM – 4:30 PM
  • Sunday – Wednesday | 3:30 PM – 2:00 AM
  • Wednesday – Saturday | 6:00 AM – 4:30 PM
  • Wednesday – Saturday | 3:30 PM – 2:00 AM
#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary