Full-Time

CSV Engineer

CAI

CAI

501-1,000 employees

Operational readiness consulting for pharma

No salary listed

Brisbane QLD, Australia

In Person

Category
Biology & Biotech (2)
,
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
  • Excellent oral and written communication skills in English; Fluent in English
  • Able to travel domestically and internationally as required
  • Excellent technical problem-solving and troubleshooting skills, with solid knowledge of typical project technical issues
  • High attention to detail
  • Ability to multi-task and take initiative to accomplish assigned tasks accurately by established deadlines
  • Independent individual and yet a strong team player
Responsibilities
  • Develop and execute protocols and test scripts for computer systems validation in line with GxP requirements; identify gaps and consult on and direct plans for resolution
  • Write GxP computer validation and 21 CFR Part 11 related documentation such as assessments, plans, User Requirements Specifications, Functional Requirements Specifications, Requirements Traceability Matrix, and summary reports
  • Prepares/reviews validation documentation related to projects/change controls
  • Manage change controls and other compliance related tasks e.g., non-conformances
  • Participate in the review of current and future CSV procedures and polices
  • Analyze testing results and determine acceptability against predetermined criteria
  • Investigate and troubleshoot problems and determine solutions or recommendations for changes and/or improvements
  • Identify current and anticipated requirements for compliant computerized operations and suggest methods for the identification, implementation, and maintenance of the procedures, actions, and documentation necessary to ensure compliance within the operation
  • Coordinate with other departments or outside contractors/vendors to complete validation tasks
  • Participate in regulatory audits and communicate company’s computer validation policies
  • Assess company’s computer systems and identify any potential Part 11 or Annex 11 gaps
  • Manage projects and prepare status reports using Microsoft Project and other communication tools
  • May supervise, lead, or manage lower-level personnel
Desired Qualifications
  • 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
  • Experience with major systems and platforms such as Rockwell, GE, Emerson, ABB, Werum, Siemens, Honeywell and their associated platforms (PAS-X, Syncade, FactoryTalk, PharmaSuite, Control Logix, PLM, Simatic, iFix, Wonderware)

CAI Technical Consulting Malaysia SDN (cagents.com) delivers operational readiness consulting for pharmaceutical, biotechnology, and healthcare clients to prepare for full-scale production. It works by conducting operational readiness assessments and then providing tailored implementation plans that cover project planning, production operations, asset management, reliability, and sustainability, plus specialized services like Digital Pathology Validation for Leica Biosystems. The firm differentiates itself through active industry collaboration, ongoing professional development, and a global, hands-on approach that pairs quick assessments with practical, cost-effective solutions. Its goal is to help clients achieve operational excellence and successful scale-up by delivering ready-to-deploy strategies and compliant processes.

Company Size

501-1,000

Company Stage

Pre-seed

Total Funding

$3.4M

Headquarters

Indianapolis, Indiana

Founded

1996

Simplify Jobs

Simplify's Take

What believers are saying

  • JLL Partners investment expands CAI globally across four continents for 700 professionals.
  • Fedegari partnership integrates turnkey sterilization, cutting biotech lifecycle costs.
  • CAI's CQV services marked 30 years in 2026, accelerating facility compliance worldwide.

What critics are saying

  • Oracle Life Sciences automates CQV with cloud platforms, eroding CAI's share in 12 months.
  • Fedegari sells sterilization systems directly, capturing pharma clients in 18 months.
  • JLL-mandated expansion dilutes CAI expertise, causing CQV failures in 24 months.

What makes CAI unique

  • CAI specializes in commissioning, qualification, and validation for life sciences facilities.
  • CAI delivers operational readiness assessments for biotech and pharma full-scale production.
  • CAI pioneered neurodiversity hiring in enterprise consulting services.

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Benefits

100% Employee Owned

24 Days PTO/5 Sick days per year + Additional Holidays depending on Country

Medical / Dental / Vision (In accordance with each countries’ applicable regulations)

Professional Development (Approximately $5,000 paid career-related, continuing education)

ESOP/401k – 15% Company Contribution

Company Paid Long-Term Disability

Company Paid Life Insurance

Company Paid Parental Leave (In accordance with each countries’ applicable regulations)

Other Benefits Depending on Country