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Zifo

Specialist scientific informatics services for science

CSV Validation Analyst

Regulatory & Quality (Life Sciences)Updated on Nov 7
Full-timeMexico City, CDMX, MexicoHybrid

About the Job

Requirements

  • Execute and comply with software development life cycle, change, access, inventory, and operational management procedures for business-critical applications and platforms.
  • Support evaluation, pilot testing, selection, and ongoing management of information technology vendors and partners aligned with business and compliance requirements.
  • Lead or support validation of computerized systems and laboratory instruments, including installation, configuration, troubleshooting, and documentation such as standard operating procedures and installation, operational, and performance qualification.
  • Ensure ongoing data integrity, backup, and regulatory compliance for good manufacturing practice laboratory and manufacturing systems.
  • Provide technical input and support for investigations, change controls, corrective and preventive actions, decommissioning, and audit readiness activities.
  • Participate in or lead periodic reviews, user access reviews, and audit trail reviews for good manufacturing practice systems.
  • Execute and support user acceptance testing, collaborating with information technology and business teams on issue resolution.
  • Deliver hands-on operational support for quality control and manufacturing instrument systems, including break/fix support and reliability issues in validated and production environments.
  • Manage user account provisioning and deactivation in compliance with access control standard operating procedures.
  • Bachelor's degree in Information Technology, Computer Science, Life Sciences, or a related field and at least 3 years of relevant experience in a laboratory environment or biotech/pharma setting; alternatively, a Master's degree and 3–5 or more years of relevant experience.
  • Strong operational knowledge of laboratory information technology environments, including instrument connectivity and client/server architectures.
  • Proficiency in Windows operating system administration, including registry, system files, security, local accounts, and policies.
  • Working knowledge of network technologies, including virtual local area networks, firewalls, security protocols, and instrument local area networks.
  • Experience supporting validated systems in a regulated GxP environment.
  • Knowledge of 21 CFR Part 11, Annex 11, data integrity, and computer system validation processes.
  • Familiarity with laboratory instrumentation and enterprise information technology solutions used in biopharma, including liquid chromatography systems such as Waters and Agilent, AKTA, SoftMaxPro, Geneious, electronic laboratory notebooks and laboratory information management systems such as Sapio, imaging systems, bioreactors, plate readers, and sequencers.

Responsibilities

  • Support laboratory equipment and applications, both good manufacturing practice and non-good manufacturing practice.
  • Troubleshoot hardware and software issues.
  • Perform computer system validation activities, including change controls, validation execution, non-conformance reports, audit information requests, and corrective and preventive actions.
  • Maintain data integrity and compliance.
  • Administer system configuration, access management, security patching, and data backup processes.
  • Work collaboratively within cross-functional teams including colleagues, consultants, vendors, and managed service providers, and independently to support day-to-day operations and project-based initiatives.

About the Company

Zifo

Specialist scientific informatics services for science

Zifo provides tailored scientific informatics services across Laboratory/R&D, Manufacturing, and Trial operations to help science-driven organizations discover, develop, manufacture, and test products for global health. It partners with clients to assess needs, design and implement data-driven solutions, and manage ongoing operations using consulting, development, and managed services, leveraging cloud, HPC, data modeling, and instrument data. It differentiates itself with end-to-end informatics capabilities and deep domain knowledge, from transformation coaching to validation and custom integrations, all aimed at supporting research, development, manufacturing, and trials. Its goal is to empower customers to push the boundaries of science and technology while advancing global health and wellbeing.

Company size
1,001-5,000
Company stage
Growth Equity (Non-Venture Capital)
Total funding
$250M
Headquarters
New York, NY
Founded
2008

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