Fort Washington, PA · On-site
$107K - $127K/yr
Execute Computer System validation (CSV) protocols. Write and resolve protocol deviations. Write test summary reports. Prior Wonderware, Allen Bradley, field wiring experience is a plus. Candidate ...
Fort Washington, PA · On-site
$107K - $127K/yr
Execute Computer System validation (CSV) protocols. Write and resolve protocol deviations. Write test summary reports. Prior Wonderware, Allen Bradley, field wiring experience is a plus. Candidate ...
Marlborough, MA · On-site
$40/hr
Create and/or review computer system validation test scripts, validation schedules, risk assessments, requirement specifications, protocols and reports, traceability matrices, and validation summary ...
Marlborough, MA · On-site
$40/hr
Create and/or review computer system validation test scripts, validation schedules, risk assessments, requirement specifications, protocols and reports, traceability matrices, and validation summary ...
Marlborough, MA · On-site
$45/hr
Bachelors or Masters in Computer Science, Computer Information Systems, Information Technology or ... Understands lifecycle approach as well as risk based approach to validation * Generally familiar ...
Marlborough, MA · On-site
$45/hr
Bachelors or Masters in Computer Science, Computer Information Systems, Information Technology or ... Understands lifecycle approach as well as risk based approach to validation * Generally familiar ...
Caguas, PR · On-site
Computer Validation Lifecycle among others * Leader with great interpersonal skills Fully Bilingual
Caguas, PR · On-site
Computer Validation Lifecycle among others * Leader with great interpersonal skills Fully Bilingual
Title: Computer Validation Specialist-PQM Location: Fort Worth, TX Company: PharmEng Technology Inc. PharmEng Technology is a full service consulting firm that serves the pharmaceutical, medical ...
Title: Computer Validation Specialist-PQM Location: Fort Worth, TX Company: PharmEng Technology Inc. PharmEng Technology is a full service consulting firm that serves the pharmaceutical, medical ...
Statiscal data Analyst and Six Sigma Green Belt Certified - Prefered Knolwlwdge in Validations Strategies Development and Implementations Product Tranfers Computer Validation Lifecycle among others ...
Statiscal data Analyst and Six Sigma Green Belt Certified - Prefered Knolwlwdge in Validations Strategies Development and Implementations Product Tranfers Computer Validation Lifecycle among others ...
$75K - $106K/yr
... computer validation documentation (e.g., URS, FRS, RTM, summary reports) Generate and execute test protocols and scripts Ensure adherence to 21 CFR Part 11 and data integrity principles Review and ...
$75K - $106K/yr
... computer validation documentation (e.g., URS, FRS, RTM, summary reports) Generate and execute test protocols and scripts Ensure adherence to 21 CFR Part 11 and data integrity principles Review and ...
Indianapolis, IN · On-site
$75K - $106K/yr
... computer validation documentation (e.g., URS, FRS, RTM, summary reports) Generate and execute test protocols and scripts Ensure adherence to 21 CFR Part 11 and data integrity principles Review and ...
Indianapolis, IN · On-site
$75K - $106K/yr
... computer validation documentation (e.g., URS, FRS, RTM, summary reports) Generate and execute test protocols and scripts Ensure adherence to 21 CFR Part 11 and data integrity principles Review and ...
Rockville, MD · On-site
$75K - $106K/yr
... computer validation documentation (e.g., URS, FRS, RTM, summary reports) Generate and execute test protocols and scripts Ensure adherence to 21 CFR Part 11 and data integrity principles Review and ...
Quick apply
Rockville, MD · On-site
$75K - $106K/yr
... computer validation documentation (e.g., URS, FRS, RTM, summary reports) Generate and execute test protocols and scripts Ensure adherence to 21 CFR Part 11 and data integrity principles Review and ...
Rockville, MD · On-site
$75K - $106K/yr
... computer validation documentation (e.g., URS, FRS, RTM, summary reports) Generate and execute test protocols and scripts Ensure adherence to 21 CFR Part 11 and data integrity principles Review and ...
Rockville, MD · On-site
$75K - $106K/yr
... computer validation documentation (e.g., URS, FRS, RTM, summary reports) Generate and execute test protocols and scripts Ensure adherence to 21 CFR Part 11 and data integrity principles Review and ...
Indianapolis, IN · On-site
$75K - $106K/yr
... computer validation documentation (e.g., URS, FRS, RTM, summary reports) Generate and execute test protocols and scripts Ensure adherence to 21 CFR Part 11 and data integrity principles Review and ...
Indianapolis, IN · On-site
$75K - $106K/yr
... computer validation documentation (e.g., URS, FRS, RTM, summary reports) Generate and execute test protocols and scripts Ensure adherence to 21 CFR Part 11 and data integrity principles Review and ...
Indianapolis, IN · On-site
$75K - $106K/yr
... computer validation documentation (e.g., URS, FRS, RTM, summary reports) Generate and execute test protocols and scripts Ensure adherence to 21 CFR Part 11 and data integrity principles Review and ...
Quick apply
Indianapolis, IN · On-site
$75K - $106K/yr
... computer validation documentation (e.g., URS, FRS, RTM, summary reports) Generate and execute test protocols and scripts Ensure adherence to 21 CFR Part 11 and data integrity principles Review and ...
Rockville, MD · On-site
$75K - $106K/yr
... computer validation documentation (e.g., URS, FRS, RTM, summary reports) Generate and execute test protocols and scripts Ensure adherence to 21 CFR Part 11 and data integrity principles Review and ...
Rockville, MD · On-site
$75K - $106K/yr
... computer validation documentation (e.g., URS, FRS, RTM, summary reports) Generate and execute test protocols and scripts Ensure adherence to 21 CFR Part 11 and data integrity principles Review and ...
At least 2-4 years of Computer System Validation experience in a laboratory environment. Past experience writing, reviewing and executing computer validation documentation (Validation Plan, IQ, OQ ...
At least 2-4 years of Computer System Validation experience in a laboratory environment. Past experience writing, reviewing and executing computer validation documentation (Validation Plan, IQ, OQ ...
Brooklyn Park, MN · On-site +1
Represent Client during FDA or other regulatory agency inspections involving computer validation, electronic record/electronic signature, and data integrity. Initiate process improvements to reduce ...
Brooklyn Park, MN · On-site +1
Represent Client during FDA or other regulatory agency inspections involving computer validation, electronic record/electronic signature, and data integrity. Initiate process improvements to reduce ...
King Of Prussia, PA · On-site +1
This role will be responsible for equipment/facility/computer validation projects in a hands-on role including writing validation protocols, scheduling, and executing testing, gathering, and ...
King Of Prussia, PA · On-site +1
This role will be responsible for equipment/facility/computer validation projects in a hands-on role including writing validation protocols, scheduling, and executing testing, gathering, and ...
Review Equipment, Process, Computer Validation, and Bioanalytical Method Development Validation executed documentation to ensure compliance with approved protocols, quality standards, and applicable ...
Review Equipment, Process, Computer Validation, and Bioanalytical Method Development Validation executed documentation to ensure compliance with approved protocols, quality standards, and applicable ...
The Impact You Will Make The Computer System Validation (CSV) Specialist is responsible for ensuring that all GxP computer systems used in pharmaceutical manufacturing environments are validated ...
The Impact You Will Make The Computer System Validation (CSV) Specialist is responsible for ensuring that all GxP computer systems used in pharmaceutical manufacturing environments are validated ...
Performs and leads computer system validation projects related to authoring and executing validation documentation for laboratory instruments/equipment and systems according to the ISPE GAMP 5 ...
Quick apply
Performs and leads computer system validation projects related to authoring and executing validation documentation for laboratory instruments/equipment and systems according to the ISPE GAMP 5 ...
The Impact You Will Make The Computer System Validation (CSV) Specialist is responsible for ensuring that all GxP computer systems used in pharmaceutical manufacturing environments are validated ...
The Impact You Will Make The Computer System Validation (CSV) Specialist is responsible for ensuring that all GxP computer systems used in pharmaceutical manufacturing environments are validated ...
$10.58 - $17.44
2% of jobs
$17.44 - $24.30
9% of jobs
$24.30 - $31.16
1% of jobs
$31.16 - $38.02
4% of jobs
$42.19 is the 25th percentile. Wages below this are outliers.
$38.02 - $44.89
15% of jobs
$44.89 - $51.75
9% of jobs
The median wage is $57.47 / hr.
$51.75 - $58.61
13% of jobs
$64.07 is the 75th percentile. Wages above this are outliers.
$58.61 - $65.47
29% of jobs
$65.47 - $72.33
12% of jobs
$72.33 - $79.20
2% of jobs
$79.20 - $86.06
5% of jobs
$10
$54
$86
| Aspect | Computer Validation | Quality Assurance Specialist |
|---|---|---|
| Required Credentials | GxP, 21 CFR Part 11, validation certifications | ISO standards, QA certifications, GxP knowledge |
| Work Environment | Pharmaceutical, biotech, regulated industries | Manufacturing, healthcare, regulated industries |
| Employer & Industry Usage | Regulated industries requiring validated systems | Ensuring quality compliance across processes |
Computer Validation focuses on verifying that computer systems meet regulatory requirements and function correctly, primarily in regulated industries. Quality Assurance Specialists oversee overall quality processes, ensuring compliance and standards across various operations. While both roles require knowledge of GxP and industry regulations, Computer Validation is more technical and system-specific, whereas QA Specialists have a broader scope in quality management.
$107K - $127K/yr
Contractor
Re-posted 25 days ago
A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
This project is to perform engineering modifications and CSV validation to an automated control system utilizing Wonderware InTouch, InBatch and ArchestrA and Allen Bradley Control Logix PLCs.
Candidate will take direction from Lead Automation Engineer/Project Manager.
Execute Computer System validation (CSV) protocols. Write and resolve protocol deviations.
Write test summary reports. Prior Wonderware, Allen Bradley, field wiring experience is a plus.
Candidate must have at least 5 years of experience performing Computer System Validation in a regulated industry.
Warm Regards
Sweta Verma
732-549-5907
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Recruiting and staffing services
51 - 200 Employees
Edison, NJ, US
1996
