C

CAI

Operational readiness consulting for pharma

Pharmaceutical Commissioning Qualification Validation Engineer

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeMelbourne VIC, AustraliaA$73.2k - A$115k /yr

About the Job

Requirements

  • A BS or MS in a relevant science or engineering field, or equivalent years of hands-on experience.
  • Two to seven years of experience performing commissioning and/or qualification activities in an FDA-regulated industry.
  • Experience with facilities and equipment startup, walkdowns and troubleshooting, utilities such as WFI, RO, and HVAC, building automation or pharmaceutical manufacturing processes and equipment, FAT/SAT, URS, design review, P&IDs, IQ/OQ/PQs, and generation and execution activities is ideally preferred.
  • Strong technical problem-solving and troubleshooting skills, with knowledge of typical project technical issues.
  • High attention to detail.
  • Ability to multitask and take initiative to complete assigned tasks accurately by established deadlines.
  • Ability to work independently and quickly build and nurture a project team.
  • Experience planning or directing C&Q activities.
  • Proficiency in life science manufacturing processes such as biotech, aseptic processing, aseptic fill/finish, OSD, or gene therapy, or equivalent experience.
  • Expertise in Microsoft Word and Excel.
  • Excellent oral and written English.
  • Ability to work in Australia without sponsorship.

Responsibilities

  • Develop documentation to support commissioning, qualification, and validation.
  • Support documentation for the commissioning, qualification, and validation of pharmaceutical facilities, utilities, and equipment.
  • Write and execute protocols, perform field verification, and develop summary reports at client sites.
  • Provide cGMP leadership and guidance for integrating and delivering CQV services for life sciences clients.
  • Manage the C&Q documentation and execution lifecycle from SLIA generation through OQ completion.
  • Support onsite and offsite activities, including FATs, SATs, IOQ and PQ executions, and system walkdowns.
  • Travel domestically if required.

Desired Qualifications

  • Familiarity with Baseline Guide 5 (Second Edition).

About the Company

CAI

Operational readiness consulting for pharma

CAI Technical Consulting Malaysia SDN (brand cagents.com) provides operational readiness consulting for pharmaceutical, biotech, and healthcare firms. It helps clients prepare for full-scale production through quick operational readiness assessments, gap-tailored plans, and hands-on implementation support in areas like project planning, production operations, asset management, reliability, and sustainability, plus Digital Pathology Validation for Leica Biosystems to meet regulatory standards. The firm differentiates itself by combining rapid assessments with practical, cost-effective strategies, ongoing industry collaboration, and global delivery that informs tailored solutions. Its goal is to help clients accelerate their path to compliant, scalable operations and successful production scale-up.

Company size
1,001-5,000
Company stage
Pre-seed
Total funding
$3.4M
Headquarters
Indianapolis, IN
Founded
1996

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