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

Contract Position Sr Computer System Validation

  • ... Posted on: Jan 09, 2025
  • ... InnoCom
  • ... St. Joseph, Missouri
  • ... Salary: Not Available
  • ... Full-time

Contract Position Sr Computer System Validation   

Job Title :

Contract Position Sr Computer System Validation

Job Type :

Full-time

Job Location :

St. Joseph Missouri United States

Remote :

No

Jobcon Logo Job Description :

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,

Jobcon Logo Position Details

Posted:

Jan 09, 2025

Employment:

Full-time

Salary:

Not Available

Snaprecruit ID:

SD-CIE-17d38524265959af69b65f9359e075a874af53c392277365b93f8ef94f4e5c61

City:

St. 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!

Contract Position Sr Computer System Validation    Apply

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

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,

Loading
Please wait..!!