More jobs:
Equipment Engineer
Job in
Aurora, Kane County, Illinois, 60505, USA
Listed on 2026-06-14
Listing for:
i-Pharm GxP
Full Time, Contract
position Listed on 2026-06-14
Job specializations:
-
Engineering
Validation Engineer, Pharma Engineer
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
OverviewWe 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.
- 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.
- 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.
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