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Contract Position - Sr. Computer system Validation Engineer in St.Joseph, MO @ 35640407 - Pay: $80 per hour

InnoCom
Saint Joseph, MO Full Time
POSTED ON 3/15/2025 CLOSED ON 4/10/2025

What are the responsibilities and job description for the Contract Position - Sr. Computer system Validation Engineer in St.Joseph, MO @ 35640407 - Pay: $80 per hour position at InnoCom?

Position : Computer System Validation Engineer

Location : St.Joseph, MO

Duration : 12 months

Pay Rate : $80 / hr on w2 without benefits

Duties :

  • Validation documentation Authoring (validation plans, user requirements specifications, risk assessment, IQ-OQ-PQ protocols, trace matrix and summary reports)
  • Experience in validating GMP Lab systems and Equipment 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.
  • 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.
  • 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.
  • 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.

Skills :

  • Required Experience 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.
  • Ability to multi-task. Must have 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.
  • Education : BS in Science or Technical Writing Degree

    Required Skills : GMP,

    Salary : $80

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