image
  • Snapboard
  • Activity
  • Reports
  • Campaign
Welcome ,
loadingbar
Loading, Please wait..!!

Sr Computer System Validation Engineer

  • ... Posted on: Jan 09, 2025
  • ... Cortex consultants LLC
  • ... Saint Joseph, Missouri
  • ... Salary: Not Available
  • ... Full-time

Sr Computer System Validation Engineer   

Job Title :

Sr Computer System Validation Engineer

Job Type :

Full-time

Job Location :

Saint Joseph Missouri United States

Remote :

No

Jobcon Logo Job Description :

Sr. Computer System Validation Engineer

St. Joseph, MO

Contract position

Job Description:

  • 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.

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.

Keywords:

Education: BS in Science or Technical Writing Degree

Required Skills:

GMP

Jobcon Logo Position Details

Posted:

Jan 09, 2025

Employment:

Full-time

Salary:

Not Available

Snaprecruit ID:

SD-CIE-5bca18c758eb98d9bd67c9298a28dd1a3f890a69026090d198d5581c486deb46

City:

Saint Joseph

Job Origin:

CIEPAL_ORGANIC_FEED

Share this job:

  • linkedin

Jobcon Logo
A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

Sr Computer System Validation Engineer    Apply

Click on the below icons to share this job to Linkedin, Twitter!

Sr. Computer System Validation Engineer

St. Joseph, MO

Contract position

Job Description:

  • 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.

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.

Keywords:

Education: BS in Science or Technical Writing Degree

Required Skills:

GMP

Loading
Please wait..!!