C

CAI

Operational readiness consulting for pharma

Computer System Validation Engineer

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeMilan, Metropolitan City of Milan, Italy€34.4k - €45.8k /yr

About the Job

Requirements

  • A Bachelor of Science degree in Computer Science or an Engineering field, or equivalent experience.
  • Two to seven years of experience with computer systems validation.
  • Two years of experience working in a Good Manufacturing Practice environment.
  • Knowledge of aseptic processes.
  • Experience with filling-line computer systems validation and automation.
  • Fluent in English, with excellent oral and written communication skills.
  • Able to travel domestically and internationally as required.
  • Must be a European citizen or hold a valid residence permit for Europe.

Responsibilities

  • Develop and execute protocols and test scripts for computer systems validation.
  • Identify gaps and consult on and direct plans for resolution.
  • Write Good Practice (GxP) computer validation and 21 CFR Part 11 documentation, including assessments, plans, user requirements specifications, functional requirements specifications, requirements traceability matrices, and summary reports.
  • Create strategies to balance short-term requirements with long-range business plans.
  • Pursue initiatives to capitalize on strengths and market opportunities and counter competitive threats.
  • Align area priorities with the broader organization's direction and strategic priorities.
  • Apply financial and economic insights to improve short- and long-term business results.
  • Promote risk awareness and review risk management performance.
  • Use financial reports and analyses to identify and evaluate strategic priorities and investments.
  • Foster a customer-focused environment and anticipate customer requirements, expectations, and needs.
  • Create systems and processes that make it easier for customers to do business with CAI.
  • Maintain accountability, encourage managed risk taking, delegate assignments appropriately, and keep people focused.
  • Monitor progress and redirect efforts when goals change or are not met.
  • Ensure people have the resources, information, authority, empowerment, and support needed to achieve objectives.
  • Identify others' agendas, concerns, and motivations; negotiate persuasive, mutually beneficial solutions; and cultivate organizational networks.
  • Inspire and coach others, provide feedback and guidance, shape roles and assignments to develop capabilities, and develop successors and talent pools.
  • Promote recruitment, advancement, and success of people from diverse backgrounds.
  • Foster ownership and commitment, encourage challenging goals and high performance standards, and support ongoing learning and development.
  • Develop and drive a safe and inclusive work culture, take well-reasoned stands with integrity, make people and business decisions, and develop safe working processes and initiatives.

Desired Qualifications

  • Experience with data integrity, GAMP, 483 compliance, consent decree work, and 21 CFR Part 11 is highly desired.
  • Biotechnology and pharmaceutical experience is preferred over medical device experience.
  • Experience with MES, DeltaV, PI, Rockwell, GE, Emerson, ABB, Werum, Siemens, Honeywell, PAS-X, Syncade, FactoryTalk, PharmaSuite, ControlLogix, PLM, Simatic, iFix, or Wonderware is a plus.

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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