Project Engineer

Company: Cpl Healthcare
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Job Description:

Project Engineer (Capital / Automation Projects)

FMCG Manufacturing | Hampshire | 12-month contract | Outside IR35 | Rate to be discussed

We’re supporting a large FMCG manufacturing site in Hampshire who are looking to appoint an experienced Project Engineer to support a major automation and capital investment programme.

This is a hands‑on delivery role within a highly regulated manufacturing environment, focused on delivering equipment upgrades, automation projects and production improvements across the site.

Key Responsibilities

  • Deliver capital and automation projects from concept through to installation, commissioning and handover
  • Manage multiple concurrent engineering projects, ensuring delivery to time, cost and quality targets
  • Produce and manage User Requirement Specifications (URS) in collaboration with production, engineering and quality teams
  • Coordinate equipment suppliers, contractors and internal stakeholders through design, build and installation phases
  • Lead Factory Acceptance Tests (FAT) and support Site Acceptance Testing (SAT) activities
  • Support equipment installation and commissioning in a GMP‑regulated manufacturing environment
  • Ensure compliance with validation requirements (DQ, IQ, OQ, PQ) where applicable
  • Manage project planning, scheduling, risk management and reporting activities
  • Support procurement, tendering and supplier selection for capital equipment
  • Ensure all project work is delivered safely, in line with regulatory, quality and H&S requirements
  • Engage with cross‑functional teams to ensure smooth integration of new equipment into production
  • Drive continuous improvement and support wider engineering and automation initiatives

Requirements

  • Proven experience as a Project Engineer within FMCG, pharmaceutical, food & beverage, cosmetics or other regulated manufacturing environments
  • Strong experience delivering capital projects, automation upgrades or production line improvements
  • Hands‑on involvement in FAT/SAT, commissioning and equipment installation
  • Experience working in GMP or similarly regulated environments
  • Understanding of validation processes (DQ, IQ, OQ, PQ) advantageous
  • Strong stakeholder management across engineering, production, quality and suppliers
  • Ability to manage multiple projects simultaneously in a fast‑paced manufacturing environment

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Posted: June 27th, 2026