GAMP 5 Risk-Based validation / ICH Q9 hands-on implementation knowledge * Manufacturing, Distribution process and procedure * Experience in managing large implementations/upgrade project * Strong ...
GAMP 5 Risk-Based validation / ICH Q9 hands-on implementation knowledge * Manufacturing, Distribution process and procedure * Experience in managing large implementations/upgrade project * Strong ...
GAMP 5 Risk-Based validation / ICH Q9 hands-on implementation knowledge * Manufacturing, Distribution process and procedure * Experience in managing large implementations/upgrade project * Strong ...
GAMP 5 Risk-Based validation / ICH Q9 hands-on implementation knowledge * Manufacturing, Distribution process and procedure * Experience in managing large implementations/upgrade project * Strong ...
Partner with system owners, QA, and IT to maintain systems in a validated state through change control and periodic review * Execute risk assessments and data integrity assessments aligned with ALCOA ...
Partner with system owners, QA, and IT to maintain systems in a validated state through change control and periodic review * Execute risk assessments and data integrity assessments aligned with ALCOA ...
Partner with system owners, QA, and IT to maintain systems in a validated state through change control and periodic review * Execute risk assessments and data integrity assessments aligned with ALCOA ...
Partner with system owners, QA, and IT to maintain systems in a validated state through change control and periodic review * Execute risk assessments and data integrity assessments aligned with ALCOA ...
Computer Systems Validation (CSV) Specialist/Validation Specialist
Totowa, NJ · On-site
$95K - $105K/yr
Supporting the development and maintenance of procedures related to Computer System Validation, Data Integrity, and 21 CFR Part 11 and EudraLex Volume 4 Annex 11 compliance. Assisting with ...
Computer Systems Validation (CSV) Specialist/Validation Specialist
Totowa, NJ · On-site
$95K - $105K/yr
Supporting the development and maintenance of procedures related to Computer System Validation, Data Integrity, and 21 CFR Part 11 and EudraLex Volume 4 Annex 11 compliance. Assisting with ...
Computer Systems Validation (CSV) Specialist/Validation Specialist
Totowa, NJ · On-site
$95K - $105K/yr
... Computer System Validation, Data Integrity, and 21 CFR Part 11 and EudraLex Volume 4 Annex 11 compliance. • Assisting with qualification of computerized systems impacting cGMP operations using a ...
Computer Systems Validation (CSV) Specialist/Validation Specialist
Totowa, NJ · On-site
$95K - $105K/yr
... Computer System Validation, Data Integrity, and 21 CFR Part 11 and EudraLex Volume 4 Annex 11 compliance. • Assisting with qualification of computerized systems impacting cGMP operations using a ...
... Computer System Validation- Life Sciences We are looking for smart, self-driven, high-energy people with intellectual curiosity and passion for excellence; specifically, we are looking for candidates ...
... Computer System Validation- Life Sciences We are looking for smart, self-driven, high-energy people with intellectual curiosity and passion for excellence; specifically, we are looking for candidates ...
Associate Director - Computer Systems Validation
Somerville, NJ · On-site
$135K - $180K/yr
The leader of Computer System Validation and Computer Software Assurance (CSV/CSA) is responsible for leading and governing all site-wide CSV and CSA activities to ensure that computerized systems ...
Quick apply
Associate Director - Computer Systems Validation
Somerville, NJ · On-site
$135K - $180K/yr
The leader of Computer System Validation and Computer Software Assurance (CSV/CSA) is responsible for leading and governing all site-wide CSV and CSA activities to ensure that computerized systems ...
Sr. Manager Quality Assurance Validation Computerization Systems The incumbent will be responsible ... Generate or review/update computer system related policies, procedures, templates, forms, etc.
Quick apply
Sr. Manager Quality Assurance Validation Computerization Systems The incumbent will be responsible ... Generate or review/update computer system related policies, procedures, templates, forms, etc.
... and computer system validation (CSV). * Familiarity with upstream and downstream biopharmaceutical processes. * Proficiency in tools such as Studio 5000 Logix Designer, FTView SE & ME. Thanks ...
Quick apply
... and computer system validation (CSV). * Familiarity with upstream and downstream biopharmaceutical processes. * Proficiency in tools such as Studio 5000 Logix Designer, FTView SE & ME. Thanks ...
... and computer system validation (CSV). * Familiarity with upstream and downstream biopharmaceutical processes. * Proficiency in tools such as Studio 5000 Logix Designer, FTView SE & ME. Thanks ...
Quick apply
... and computer system validation (CSV). * Familiarity with upstream and downstream biopharmaceutical processes. * Proficiency in tools such as Studio 5000 Logix Designer, FTView SE & ME. Thanks ...
Validation Engineer II
East Windsor, NJ · On-site
Manages the full lifecycle of Computer System Validation, qualifying facilities, equipment, and processes, and developing key validation documentation, including Factory Acceptance Testing, Site ...
Validation Engineer II
East Windsor, NJ · On-site
Manages the full lifecycle of Computer System Validation, qualifying facilities, equipment, and processes, and developing key validation documentation, including Factory Acceptance Testing, Site ...
Validation Engineer II
Hightstown, NJ · On-site
Manages the full lifecycle of Computer System Validation, qualifying facilities, equipment, and processes, and developing key validation documentation, including Factory Acceptance Testing, Site ...
Quick apply
Validation Engineer II
Hightstown, NJ · On-site
Manages the full lifecycle of Computer System Validation, qualifying facilities, equipment, and processes, and developing key validation documentation, including Factory Acceptance Testing, Site ...
Generate or review/update computer system related policies, procedures, templates, forms, etc ... Comprehensive knowledge in Software Validation and Data Integrity Principles. * Demonstrated ...
Quick apply
Generate or review/update computer system related policies, procedures, templates, forms, etc ... Comprehensive knowledge in Software Validation and Data Integrity Principles. * Demonstrated ...
Generate or review/update computer system related policies, procedures, templates, forms, etc ... Comprehensive knowledge in Software Validation and Data Integrity Principles. * Demonstrated ...
Quick apply
Generate or review/update computer system related policies, procedures, templates, forms, etc ... Comprehensive knowledge in Software Validation and Data Integrity Principles. * Demonstrated ...
Generate or review/update computer system related policies, procedures, templates, forms, etc ... Comprehensive knowledge in Software Validation and Data Integrity Principles. * Demonstrated ...
Quick apply
Generate or review/update computer system related policies, procedures, templates, forms, etc ... Comprehensive knowledge in Software Validation and Data Integrity Principles. * Demonstrated ...
Global Quality System Developer and Validation Analyst
Piscataway, NJ · On-site
$86K/yr
You will also be responsible to conduct computer system validation activities to ensure the system is validated and maintains its validation status.You will architect global rollouts, ensure systems ...
Global Quality System Developer and Validation Analyst
Piscataway, NJ · On-site
$86K/yr
You will also be responsible to conduct computer system validation activities to ensure the system is validated and maintains its validation status.You will architect global rollouts, ensure systems ...
Global Quality System Developer and Validation Analyst
Piscataway, NJ · On-site
$86K/yr
You will also be responsible to conduct computer system validation activities to ensure the system is validated and maintains its validation status.You will architect global rollouts, ensure systems ...
Global Quality System Developer and Validation Analyst
Piscataway, NJ · On-site
$86K/yr
You will also be responsible to conduct computer system validation activities to ensure the system is validated and maintains its validation status.You will architect global rollouts, ensure systems ...
NAVA Software solutions is looking for a Sr. System Test / Validation Engineer Details: Sr. System ... Bachelor's Degree in Computer Science, Computer Engineering or related discipline * Experience ...
NAVA Software solutions is looking for a Sr. System Test / Validation Engineer Details: Sr. System ... Bachelor's Degree in Computer Science, Computer Engineering or related discipline * Experience ...
(Sr.) Validation Engineer
$80K - $120K/yr
Support facility, utility, equipment, process, cleaning, and computer system validation (CSV) activities. * Support technology transfer and startup activities for new client manufacturing programs.
(Sr.) Validation Engineer
$80K - $120K/yr
Support facility, utility, equipment, process, cleaning, and computer system validation (CSV) activities. * Support technology transfer and startup activities for new client manufacturing programs.
Computer System Validation information
See New Jersey salary details
$10.74 - $17.70
2% of jobs
$17.70 - $24.67
9% of jobs
$24.67 - $31.64
1% of jobs
$31.64 - $38.60
4% of jobs
$42.83 is the 25th percentile. Wages below this are outliers.
$38.60 - $45.57
15% of jobs
$45.57 - $52.54
9% of jobs
The median wage is $58.34 / hr.
$52.54 - $59.50
13% of jobs
$65.05 is the 75th percentile. Wages above this are outliers.
$59.50 - $66.47
29% of jobs
$66.47 - $73.44
12% of jobs
$73.44 - $80.40
2% of jobs
$80.40 - $87.37
5% of jobs
$10
$55
$87
How much do computer system validation jobs pay per hour?
What are some typical challenges faced in Computer System Validation roles?
Professionals in Computer System Validation often encounter challenges such as keeping up with evolving regulatory requirements, ensuring complete and accurate documentation, and coordinating with cross-functional teams to implement validation protocols. Balancing thoroughness with project deadlines can also be demanding, as every validation step must stand up to external audits. However, these challenges provide valuable experience, strengthen project management abilities, and emphasize teamwork—key attributes that support career advancement into validation leadership or quality assurance roles.
What is a Computer System Validation job?
A Computer System Validation (CSV) job involves ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, meet compliance and regulatory requirements. CSV professionals develop and execute validation protocols to confirm that software, hardware, and processes function as intended and maintain data integrity. They work with quality assurance, IT, and regulatory teams to document compliance with standards like FDA 21 CFR Part 11 and GxP. This role is critical in maintaining system reliability, product quality, and patient safety.
What are the key skills and qualifications needed to thrive in the Computer System Validation position, and why are they important?
To excel in Computer System Validation, candidates typically need a background in computer science, engineering, or life sciences, with expertise in validating software and systems in regulated environments such as pharmaceuticals or medical devices. Familiarity with tools like validation documentation software, GAMP 5 guidelines, FDA 21 CFR Part 11 regulations, and potentially certifications like CSV Professional or Six Sigma is highly valued. Strong attention to detail, analytical thinking, and effective communication skills help professionals work collaboratively and document findings precisely. These abilities ensure compliance, data integrity, and the reliability of computerized systems critical to safety and quality.
What is the work of computer system validation?
What degree is best for cis jobs?
What is the salary of SoC validation engineer?

Contractor
Re-posted 14 days ago
Job description
iTvorks provides answers to enterprises in a wide range of business sectors such as medical, real estate, and finance among others. We have reliably helped many organizations see their visions come to life by entirely managing the lifecycles of their products, infrastructure and applications.
Job Description
Candidate needs to work from our Client site Based in Foster City CA.
- 21 CFR Part 210 / 211
- GAMP 5 Risk-Based validation / ICH Q9 hands-on implementation knowledge
- Manufacturing, Distribution process and procedure
- Experience in managing large implementations/upgrade project
- Strong knowledge on change management procedure & process; Should have handled more than 20+ change requests
- Hands-on knowledge of Deviation and CAPA Management
- Leading and managing testing and validation activities in synchronization with project scope, schedule, and objective
- Must possess formal training/certification on Testing & Validation
- Excellent communication skills
- Excellent technical writing skills
- Should be able to work independently with minimum supervision
Should have worked in cross-functional environments and comfortable to liaison with business
Qualifications
Below applications Experience Must.
- SAP
- Oracle EBS
- LIMS
- VEEVA or Salesforce
Additional Information
All your information will be kept confidential according to EEO guidelines.