Computer System Validation Engineer

Technoviz LLC

Computer System Validation Engineer

madison, WI
Full Time
Paid
  • Responsibilities

    Benefits:

    Competitive salary

    Opportunity for advancement

    Training & development

    Job Summary

    We are seeking a skilled System Validation Engineer to join our team! As a System Validation Engineer, you will be responsible for validating documentation Authoring (validation plans, user requirements specifications, risk assessment, IQ-OQ-PQ protocols, trace matrix and summary reports) and responsible for assuring a system/application meets its requirements as outlined in system specification (URS/FRS) per process defined in the Validation Plan for the project.

    Responsibilities

    Validate GMP Lab systems and Equipment

    Identify and escalate, as necessary project risks and issues to the CSVC Manager

    Engage in multiple CSVC projects through the assimilation of data, establishing facts and drawing valid conclusions to deliver results in accordance with resources, constraints and business needs

    Be able to prepare reports on defects and problems that arise during system testing

    Have solid oral and written communication skills and teamwork skills

    Work with business representatives to ensure the test cases reflect business rules and processes

    Fulfills the role of a subject matter expert role for critical quality and compliance GxP end-use applications supporting Animal Health business processes

    Work with business representatives to ensure the test cases reflect business rules and processes

    Fulfills a subject matter expert role(s) for critical quality and compliance GxP end-use applications supporting Animal Health business processes.

    Qualifications

    Be a good team player, able to meet deadlines and handle changing priorities

    Have strong judgment capabilities to clarify requirements when necessary

    Have the ability to work with cross functional teams

    Have solid experience working with validated systems

    GMP/Regulated lab, more than 5 years of CSV experience required

    Technical writing Experience

    Highly skilled in Computerized System testing and validation in the healthcare industry

    Knowledge of GxP regulations (e.g. 21 CFR Part 11, Annex 11)

    Solid project organizational skills and ability to multi-task with strong analytical problem-solving skills

    Excellent communication including written, verbal, and listening skills

    Self-motivated, detail oriented, takes initiative and ability to work independently without close supervision

    BS in Science or Technical Writing Degree