Create and/or review computer system validation test scripts, validation schedules, risk assessments, requirement specifications, protocols and reports, traceability matrices, and validation summary ...
Create and/or review computer system validation test scripts, validation schedules, risk assessments, requirement specifications, protocols and reports, traceability matrices, and validation summary ...
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 ...
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 ...
Front End Developer
$109.40K - $127.20K/yr
GAMP5); computer validation practices (e.g. CSV) is a plus. Experience working with an Agile methodology IntelliJ IDE Required Skills: React, HTML, Javascript. Additional Skills: Web Developer ...
Front End Developer
$109.40K - $127.20K/yr
GAMP5); computer validation practices (e.g. CSV) is a plus. Experience working with an Agile methodology IntelliJ IDE Required Skills: React, HTML, Javascript. Additional Skills: Web Developer ...
GAMP5); computer validation practices (e.g. CSV) is a plus. Experience working with an Agile methodology IntelliJ IDE You are autonomous, you can work in agile project mode and in direct ...
GAMP5); computer validation practices (e.g. CSV) is a plus. Experience working with an Agile methodology IntelliJ IDE You are autonomous, you can work in agile project mode and in direct ...
GAMP5); computer validation practices (e.g. CSV) is a plus. Experience working with an Agile methodology. You are autonomous, you can work in agile project mode and in direct collaboration with ...
GAMP5); computer validation practices (e.g. CSV) is a plus. Experience working with an Agile methodology. You are autonomous, you can work in agile project mode and in direct collaboration with ...
... computer system validation, 21 CFR Parts 210 and 211, and Part 11, Electronic Records and Electronic Signatures. Candidate requires strong interpersonal, oral and written communication skills as ...
... computer system validation, 21 CFR Parts 210 and 211, and Part 11, Electronic Records and Electronic Signatures. Candidate requires strong interpersonal, oral and written communication skills as ...
Director, Validation
Bedford, NH · On-site
The scope of responsibility encompasses all planning and implementation of drug and medical device overall validation activities, including computer systems, in a CMO aseptic fill finish environment ...
Director, Validation
Bedford, NH · On-site
The scope of responsibility encompasses all planning and implementation of drug and medical device overall validation activities, including computer systems, in a CMO aseptic fill finish environment ...
Director, Validation
Bedford, NH · On-site
The scope of responsibility encompasses all planning and implementation of drug and medical device overall validation activities, including computer systems, in a CMO aseptic fill finish environment ...
Director, Validation
Bedford, NH · On-site
The scope of responsibility encompasses all planning and implementation of drug and medical device overall validation activities, including computer systems, in a CMO aseptic fill finish environment ...
Validation Coordinator
Billerica, MA · On-site
Seeking a self-motivated Project Coordinator to coordinate validation testing on Biopharmaceutical ... computer/data skills Additional Information Thanks Warm Regards Ricky Bansal 732-429-1925
Validation Coordinator
Billerica, MA · On-site
Seeking a self-motivated Project Coordinator to coordinate validation testing on Biopharmaceutical ... computer/data skills Additional Information Thanks Warm Regards Ricky Bansal 732-429-1925
Validation Engineer
Waltham, MA · On-site
Syner-G is seeking a Validation Engineer with 5-10 years of experience supporting and leading ... While performing the duties of this job, the employee is regularly required to use a computer ...
Validation Engineer
Waltham, MA · On-site
Syner-G is seeking a Validation Engineer with 5-10 years of experience supporting and leading ... While performing the duties of this job, the employee is regularly required to use a computer ...
Automation Validation Lead
Andover, MA · On-site +1
Automation Validation Lead Location : Andover, MA Duration - 6 months (possible extension ... Ethernet Profibus OPC The ideal candidate should be familiar with the following computer system ...
Automation Validation Lead
Andover, MA · On-site +1
Automation Validation Lead Location : Andover, MA Duration - 6 months (possible extension ... Ethernet Profibus OPC The ideal candidate should be familiar with the following computer system ...
Quality Validation Engineer
Devens, MA · Hybrid
Bachelor's degree in Engineering, Computer Science/Information Systems, Life Sciences, or related ... Experience: 3-7+ years of validation experience in a regulated manufacturing environment with ...
Quality Validation Engineer
Devens, MA · Hybrid
Bachelor's degree in Engineering, Computer Science/Information Systems, Life Sciences, or related ... Experience: 3-7+ years of validation experience in a regulated manufacturing environment with ...
Quality Validation Engineer
Devens, MA · Hybrid
Bachelor's degree in Engineering, Computer Science/Information Systems, Life Sciences, or related ... Experience: 3-7+ years of validation experience in a regulated manufacturing environment with ...
Quality Validation Engineer
Devens, MA · Hybrid
Bachelor's degree in Engineering, Computer Science/Information Systems, Life Sciences, or related ... Experience: 3-7+ years of validation experience in a regulated manufacturing environment with ...
Quality Validation Engineer
Devens, MA · On-site
Bachelor's degree in Engineering, Computer Science/Information Systems, Life Sciences, or related ... Experience: 3-7+ years of validation experience in a regulated manufacturing environment with ...
Quality Validation Engineer
Devens, MA · On-site
Bachelor's degree in Engineering, Computer Science/Information Systems, Life Sciences, or related ... Experience: 3-7+ years of validation experience in a regulated manufacturing environment with ...
Quality Validation Engineer
Devens, MA · Hybrid
Bachelor's degree in Engineering, Computer Science/Information Systems, Life Sciences, or related ... Experience: 3-7+ years of validation experience in a regulated manufacturing environment with ...
Quality Validation Engineer
Devens, MA · Hybrid
Bachelor's degree in Engineering, Computer Science/Information Systems, Life Sciences, or related ... Experience: 3-7+ years of validation experience in a regulated manufacturing environment with ...
Software Validation Engineer
Northborough, MA · On-site
Participate in system implementations, enhancements, and integrations as the computer system validation representative. * Review supplier documentation, perform supplier assessments, and evaluate ...
Software Validation Engineer
Northborough, MA · On-site
Participate in system implementations, enhancements, and integrations as the computer system validation representative. * Review supplier documentation, perform supplier assessments, and evaluate ...
Participate in system implementations, enhancements, and integrations as the computer system validation representative. * Review supplier documentation, perform supplier assessments, and evaluate ...
Participate in system implementations, enhancements, and integrations as the computer system validation representative. * Review supplier documentation, perform supplier assessments, and evaluate ...
Software Validation Engineer
Northborough, MA · On-site
$95K - $105K/yr
Participate in system implementations, enhancements, and integrations as the computer system validation representative. * Review supplier documentation, perform supplier assessments, and evaluate ...
Software Validation Engineer
Northborough, MA · On-site
$95K - $105K/yr
Participate in system implementations, enhancements, and integrations as the computer system validation representative. * Review supplier documentation, perform supplier assessments, and evaluate ...
Validation Engineer II
$104K - $115.50K/yr
Job Summary Validation Engineer II is expected to execute validation and qualification activities ... Operate computer/office machines, autoclave, depyrogenation oven, vial filler, freeze dryer, steam ...
Validation Engineer II
$104K - $115.50K/yr
Job Summary Validation Engineer II is expected to execute validation and qualification activities ... Operate computer/office machines, autoclave, depyrogenation oven, vial filler, freeze dryer, steam ...
Validation Engineer II
Billerica, MA · On-site
$104K - $115.50K/yr
Job Summary Validation Engineer II is expected to execute validation and qualification activities ... Operate computer/office machines, autoclave, depyrogenation oven, vial filler, freeze dryer, steam ...
Validation Engineer II
Billerica, MA · On-site
$104K - $115.50K/yr
Job Summary Validation Engineer II is expected to execute validation and qualification activities ... Operate computer/office machines, autoclave, depyrogenation oven, vial filler, freeze dryer, steam ...
Computer Validation information
See Devens, MA salary details
$11.77 - $19.40
2% of jobs
$19.40 - $27.04
9% of jobs
$27.04 - $34.68
1% of jobs
$34.68 - $42.31
4% of jobs
$46.95 is the 25th percentile. Wages below this are outliers.
$42.31 - $49.95
15% of jobs
$49.95 - $57.58
9% of jobs
The median wage is $63.94 / hr.
$57.58 - $65.22
13% of jobs
$71.30 is the 75th percentile. Wages above this are outliers.
$65.22 - $72.85
29% of jobs
$72.85 - $80.49
12% of jobs
$80.49 - $88.12
2% of jobs
$88.12 - $95.76
5% of jobs
$11
$60
$95
How much do computer validation jobs pay per hour?
What is the difference between Computer Validation vs Quality Assurance Specialist?
| 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.

$40/hr
Contractor
Posted 24 days ago
Job description
Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job.Â
Hands on position responsible for authoring test scripts and other
CSV documents required for the validation of GAMP 5 Category 4
(configurable off the shelf) computer systems. Candidates should be
familiar with COTS systems used for clinical development and quality
activities in a pharmaceutical environment. Work with business users
and Information Technology to ensure the systems remain in a validated
state through appropriate change control procedures. May require
participation in early morning and/or evening teleconferences with
global project teams.
- Create
and/or review computer system validation test scripts, validation
schedules, risk assessments, requirement specifications, protocols and
reports, traceability matrices, and validation summary reports according
to the timelines in the project plan. Review applicable procedures and
system training manuals as applicable. Participate in project team
meeting. (85%) - Document
requirements for business requirements, system security, user roles,
workflows, data flows, GxP requirements and how these systems fit into
the larger IT infrastructure. (10%) - Work
with IT and User Groups to: (a) evaluate change control requests, (b)
assess regulatory risk associated with such requests and (c) determine
the corresponding validation requirements for such changes. (5%)
- 2 - 3 years experience writing CSV test scripts, protocols and summary reports in global environments
- Bachelors or Masters in Computer Science, Computer Information Systems, Information Technology or related discipline.Â
Knowledge and skills (general and technical):
- Sufficiently
knowledgeable of FDA/EU/MHLW Regulatory Requirements and industry best
practices for computerized system validation to complete tasks - Experience working with global teams particularly with team members from Japan
- Understands lifecycle approach as well as risk based approach to validation
- Generally familiar with GXP regulations particularly in the GCP and Quality areas
- Able to work both independently and as a member of a cross-functional project team
- Good written and oral communication skills
- Good problem solving skills
- Microsoft products such as Word, Excel, Project, and Visio.
- Familiar
with Information Technology principles, functionalities and
capabilities of computer systems; and how computer systems relate to and
integrate with larger corporate IT infrastructures
$40/hr
6 MONTHS +
About Global Channel Management
Sourced by ZipRecruiter
Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Global Channel Management understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at the same time requiring the best talent for the job. GCM's Ownership and Management teams have extensive Staffing, Recruiting, HR and Executive Leadership knowledge, Experience and Expertise. Our Understanding and Commitment to our Client's Satisfaction are key reasons GCM has been successful in establishing long term relationships.
Industry
Recruiting and staffing services
Company size
11 - 50 Employees
Headquarters location
Austell, GA, US
Year founded
2009