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argenx

Develops antibody-based therapies for autoimmune diseases

Digital Technology Computer System Assurance Expert

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeRemote in USANo salary listedRemote

About the Job

Requirements

  • Knowledge of the system development lifecycle and project management principles.
  • Ability to collaborate effectively within cross-functional teams and networks.
  • Demonstrated communication skills in a multicultural and multilingual global environment.
  • Demonstrable experience with project management, proactive planning, priority setting, and securing alignment.
  • Bachelor’s or Master’s degree preferred in Life Sciences, Engineering, Computer Science, Information Systems, or related fields.
  • Five or more years of experience in a validation role with responsibility for managing validation of GxP computer systems in a biopharmaceutical or medical device company.
  • Five or more years of experience authoring and executing validation deliverables, including Validation Plans, IQ/OQ/PQ protocols, and Traceability Matrices, for complex systems.

Responsibilities

  • Develop and execute risk-based validation plans for assigned computer system projects, aligned with enterprise Computer System Assurance methodology and regulatory expectations.
  • Manage creation and review of project validation lifecycle documentation, including Validation Plans, Test Plans, and Traceability Matrices, in accordance with procedure.
  • Lead and manage day-to-day validation testing, coordinating with project teams, business users, and Digital Quality to ensure protocols are followed correctly and on schedule.
  • Maintain systems’ validated state by managing validation activities related to change controls and contributing to periodic reviews.
  • Serve as the primary validation point of contact for assigned projects, providing expert guidance and resolving execution-level challenges.
  • Co-create with project teams to complete validation deliverables on time and to the required quality standard.
  • Provide project-execution feedback to the validation capability lead to support continuous improvement of the risk-based Computer System Assurance process.
  • Provide project teams with direction and support on validation and qualification tasks and activities.
  • Develop project-level validation plans and execute the full range of validation documentation and testing, including CT, FT, and UAT.
  • Translate validation strategy into clear, executable tasks for project teams and stakeholders.

Desired Qualifications

  • Experience leading project teams or managing the work of other validation specialists or contractors is a plus.

About the Company

argenx

Develops antibody-based therapies for autoimmune diseases

Argenx develops and markets antibody-based therapies for severe autoimmune diseases, turning immunology research into medicines. Its lead drug, efgartigimod (VYVGART), and the subcutaneous VYVGART Hytrulo treat conditions like generalized myasthenia gravis and CIDP by modulating the immune system through FcRn pathways. The company differentiates itself with antibody engineering and a co-creation model with academic and industry partners, plus a pipeline targeting FcRn-, complement-, and other autoimmune pathways and a global development footprint. Its goal is to provide effective antibody medicines for autoimmune diseases and broaden global patient access.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Amsterdam, Netherlands
Founded
2008

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