C

CAI

Operational readiness consulting for pharma

Computer Systems Validation Engineer

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeBrisbane QLD, Australia

About the Job

Requirements

  • BS in a Computer Science or Engineering field or equivalent experience
  • Minimum 2-7 years’ experience with Computer systems validation
  • Minimum 2-7 years' experience working in a GMP environment
  • Experience in Data Integrity with GAMP and 483, compliance, deep 21CFR Part 11 experience highly desired
  • Experience in biotech and pharma is preferred over medical device
  • Experience with MES, Delta V, PI is a plus. We use all major systems as we serve a multitude of clients. Rockwell, GE, Emerson, ABB, Werum, Siemens, Honeywell and their associated platforms, PAS-X, Syncade, FactoryTalk, PharmaSuite, Control Logix, PLM, Simatic, iFix, Wonderware, Siemens, etc.

Responsibilities

  • Prepares/reviews validation documentation related to projects/change controls.
  • Manages change controls and other compliance related tasks e.g., non-conformances.
  • Participates in the review of current and future CSV procedures and polices
  • Analyses the results of testing and determines the acceptability of results against predetermined criteria.
  • Investigates and troubleshoots problems which occur and determines solutions or recommendations for changes and/or improvements.
  • Identifies current and anticipated requirements for compliant computerized operations and suggests methods for the identification, implementation, and maintenance of the procedures, actions, and documentation necessary to ensure compliance within the operation.
  • Coordinates with other departments or outside contractors/vendors to complete validation tasks.
  • Participates in regulatory audits and communicates company’s computer validation policies.
  • Assesses company’s computer systems and identifies any potential Part 11 or Annex 11 gaps.
  • Manages projects and prepares status reports using Microsoft project and other communication tools.
  • May supervise, lead, or manage lower-level personnel.

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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