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

Equipment Engineer

Job in Aurora, Kane County, Illinois, 60505, USA
Listing for: i-Pharm GxP
Full Time, Contract position
Listed on 2026-06-14
Job specializations:
  • Engineering
    Validation Engineer, Pharma Engineer
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Contract: 12-month Contract (4-5 year scope, likely renewals)

Onsite Requirement: Full-Time, 5x days a week onsite

Overview

We are supporting a large-scale GMP manufacturing expansion programme and are seeking experienced Equipment Engineers to take full lifecycle ownership of critical Fill Finish equipment within a highly regulated pharmaceutical environment.

This is a hands‑on role covering the complete equipment lifecycle - from concept, design and procurement through commissioning, qualification, startup and operational handover. You will work closely with Engineering, CQV, Automation, Manufacturing, Quality, Validation and Vendors throughout.

Key Responsibilities
  • Own equipment lifecycle activities from concept and procurement through to operational handover.
  • Develop URS, Purchase Specifications and Design Specifications; participate in RFQ processes and vendor selection.
  • Lead and participate in design reviews, P&, FAT, SAT and vendor oversight activities.
  • Oversee installation, commissioning, startup, cycle development and operational readiness.
  • Support CQV Leads with qualification strategy, risk‑based approaches and IQ/OQ/PQ execution.
  • Support Validation Leads with Media Fills, Cleaning Validation, PPQ and protocol development.
  • Support Automation and Control System requirements including ISA-88, alarm categorisation and interlock assessments.
  • Develop SOPs, training materials and operational documentation; deliver handover to Manufacturing and Operations.
Required Experience
  • 5–7+ years in GMP pharmaceutical or biotech manufacturing, with proven experience in aseptic Fill Finish environments.
  • Strong end‑to‑end experience across URS development, design reviews, FAT/SAT, commissioning, qualification and validation.
  • Solid understanding of GMP lifecycle management, CQV principles, risk‑based qualification and current Annex 1 requirements.
  • Strong troubleshooting capability, vendor management experience and a genuine equipment ownership mindset.
Preferred Experience
  • Hands‑on experience with one or more:
    Filling Equipment, Lyophilizers, Isolators, Autoclaves, Washers, Inspection Equipment, CCIT, Stopper Processing Equipment, Tanks and Process Piping.
  • Experience supporting automation integration, recipe setup and operational configuration.
  • Comfortable taking ownership in a fast‑paced, large‑scale capital project environment.
#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