JobConnect

Process Engineer - Utilities

  • PSC Biotech
  • Melbourne, Australia
  • A$100,000 – A$130,000

We are looking for a

Process Engineer - Utilities to join our team on a 12-month contract.

Work alongside a talented PSC Biotech Team in an exciting, developing, and diverse biotechnology landscape.

The role is also responsible and accountable for supporting the PSC mission: “to maintain the integrity and professionalism of our products and services while enabling steady growth and development.”

Key Duties and Responsibilities

  • Support process engineering activities for new, modified, and existing utility and manufacturing systems across the project lifecycle.

  • Support the design, installation, startup, commissioning, qualification, and optimisation of utility systems and associated process equipment.

  • Prepare, review, revise, and complete controlled engineering and CQV documentation, including specifications, drawings, risk assessments, test protocols, reports, procedures, and turnover records.

  • Execute and document DQ, FAT, SAT, IQ, OQ, PQ, and other commissioning or validation activities, as applicable to the assigned systems and project scope.

  • Perform field verification, system walkdowns, inspections, testing, troubleshooting, and readiness checks for utilities, equipment, instruments, controls, and interfaces.

  • Assess utility capacity, performance, reliability, and compliance against process requirements, user requirements, design intent, and operational needs.

  • Support process startup and the introduction of new or modified equipment and systems into GMP operations.

  • Provide process engineering input into technical specifications, equipment selection, P&IDs, layouts, control strategies, operating parameters, and system boundaries.

  • Assist with technology transfer, process scale-up, equipment readiness, and the development or revision of SOPs and operating documentation.

  • Troubleshoot process and utility issues, identify root causes, and recommend practical improvements that strengthen safety, compliance, reliability, and performance.

  • Collaborate with client teams, quality, operations, maintenance, automation, vendors, and contractors to deliver project milestones and resolve technical issues.

  • Provide clear progress updates, escalate risks or constraints promptly, and complete assigned deliverables within agreed timelines.

  • Work safely and comply with PSC and client policies, procedures, permit requirements, and site safety expectations.

  • Additional duties and responsibilities may be assigned from time to time.

Utilities Experience

  • Experience supporting one or more of the following is desirable, depending on the project scope:

  • Clean and process utilities

    , such as purified water

    , water for injection, clean steam

    , process gases, compressed air

    , and clean-in-place systems.

  • Plant utilities,

    such as HVAC

    , chilled water, cooling water, glycol, steam, condensate, electrical interfaces, and waste systems.

  • Process equipment, including vessels, pumps, valves, heat exchangers, piping, instrumentation, automated skids, and associated control systems.

  • Aseptic, controlled, or highly automated manufacturing environments.

Requirements

  • Bachelor Degree in Engineering, Science, or

    a related

    discipline.

  • At least 2 years of relevant engineering experience within pharmaceutical, biotechnology, medical device, or another regulated GMP environment.

  • Practical experience supporting process development, utilities, equipment startup, commissioning, qualification, validation, or manufacturing operations.

  • Experience preparing, reviewing, or executing engineering and CQV documentation, such as specifications, risk assessments, FAT, SAT, IQ, OQ, PQ, protocols, and reports.

  • Working knowledge of GMP, GDP, data integrity, quality systems, and regulated project delivery expectations.

  • Ability to read and interpret technical drawings, P&IDs, specifications, manuals, and vendor documentation.

  • Strong analytical, troubleshooting, organisation, and written communication skills.

  • Ability to work collaboratively across disciplines and manage competing priorities in a project environment.

Skills

  • Process Engineering
  • Commissioning and Qualification (CQV)
  • GMP Compliance
  • Utility Systems
  • Validation Protocols (IQ/OQ/PQ)
  • Risk assessment
  • Technical Documentation

Related jobs

PSC BiotechApply for this job