Computer Systems Validation (Analytical) Supervisor Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed. As the Computer Computer ...
Computer Systems Validation (Analytical) Supervisor Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed. As the Computer Computer ...
Position Summary The Computer System Validation (CSV) role is responsible for developing, executing, and maintaining validation documentation to ensure IT systems comply with local and global ...
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Position Summary The Computer System Validation (CSV) role is responsible for developing, executing, and maintaining validation documentation to ensure IT systems comply with local and global ...
Computer Systems Validation (Analytical) Supervisor Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed. As the Computer Computer ...
Computer Systems Validation (Analytical) Supervisor Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed. As the Computer Computer ...
Computer Systems Validation Specialist III Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed. The Computer Systems Validation (CSV ...
Computer Systems Validation Specialist III Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed. The Computer Systems Validation (CSV ...
Senior Specialist, Computer System Validation
Syracuse, NY · On-site
$60K - $88K/yr
Position Summary The Computer System Validation (CSV) role is responsible for developing, executing, and maintaining validation documentation to ensure IT systems comply with local and global ...
Senior Specialist, Computer System Validation
Syracuse, NY · On-site
$60K - $88K/yr
Position Summary The Computer System Validation (CSV) role is responsible for developing, executing, and maintaining validation documentation to ensure IT systems comply with local and global ...
Travel to site is required. and Qualification: * 3 to 5+ years of Computer systems validation (CSV) experience in computerized equipment, QC lab and manufacturing systems is required * Author, review ...
Travel to site is required. and Qualification: * 3 to 5+ years of Computer systems validation (CSV) experience in computerized equipment, QC lab and manufacturing systems is required * Author, review ...
The Computer Systems Validation Engineer supports validation lifecycle activities for automation and control systems within a regulated pharmaceutical manufacturing environment. This role works ...
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The Computer Systems Validation Engineer supports validation lifecycle activities for automation and control systems within a regulated pharmaceutical manufacturing environment. This role works ...
Computer System Validation Engineer
Tustin, CA · On-site
$82K - $104.40K/yr
The Computer System Validation Engineer is responsible for providing technical validation support for manufacturing equipment, laboratory instruments, computer systems, networks, and software that ...
Computer System Validation Engineer
Tustin, CA · On-site
$82K - $104.40K/yr
The Computer System Validation Engineer is responsible for providing technical validation support for manufacturing equipment, laboratory instruments, computer systems, networks, and software that ...
... validation exceptions/deviations for Computer and IT systems. b. Expertise in MES/Delta-V/LIMS/Lab Equipment and Manufacturing CSV systems. Schedules and executes validations per ASTM, GAMP V ...
... validation exceptions/deviations for Computer and IT systems. b. Expertise in MES/Delta-V/LIMS/Lab Equipment and Manufacturing CSV systems. Schedules and executes validations per ASTM, GAMP V ...
The Computer Systems Validation Engineer supports validation lifecycle activities for automation and control systems within a regulated pharmaceutical manufacturing environment. This role works ...
The Computer Systems Validation Engineer supports validation lifecycle activities for automation and control systems within a regulated pharmaceutical manufacturing environment. This role works ...
Draft Requirements and computer systems validation documents using GAMP 5 * Execute test protocols for the software validation. * Initiate and execute change management for existing qualified systems.
Draft Requirements and computer systems validation documents using GAMP 5 * Execute test protocols for the software validation. * Initiate and execute change management for existing qualified systems.
We are seeking a Validation Engineer with strong experience in Computer Systems Validation (CSV), equipment qualification, and GMP-regulated environments. The ideal candidate will support validation ...
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We are seeking a Validation Engineer with strong experience in Computer Systems Validation (CSV), equipment qualification, and GMP-regulated environments. The ideal candidate will support validation ...
Computer Systems Validation Engineer
Cleveland, OH · On-site
$80K - $100K/yr
Join us as a Computer Systems Validation Engineer! Join Abeona Therapeutics Inc. as a Computer Systems Validation Engineer and be part of a mission-driven organization devoted to putting patients ...
Computer Systems Validation Engineer
Cleveland, OH · On-site
$80K - $100K/yr
Join us as a Computer Systems Validation Engineer! Join Abeona Therapeutics Inc. as a Computer Systems Validation Engineer and be part of a mission-driven organization devoted to putting patients ...
Our Computer Systems Validation Leads work directly with our clients to support activities that include, but are not limited to, documentation review and approval, including change controls ...
Our Computer Systems Validation Leads work directly with our clients to support activities that include, but are not limited to, documentation review and approval, including change controls ...
Author documents related to GxP Systems Draft Requirements and computer systems validation documents using GAMP 5 Execute test protocols for the software validation. Initiate and execute change ...
Author documents related to GxP Systems Draft Requirements and computer systems validation documents using GAMP 5 Execute test protocols for the software validation. Initiate and execute change ...
Our Computer Systems Validation Leads work directly with our clients to support activities that include, but are not limited to, documentation review and approval, including change controls ...
Our Computer Systems Validation Leads work directly with our clients to support activities that include, but are not limited to, documentation review and approval, including change controls ...
Computer Systems Validation Engineer
Cleveland, OH · On-site
$80K - $100K/yr
Join us as a Computer Systems Validation Engineer! Join Abeona Therapeutics Inc. as a Computer Systems Validation Engineer and be part of a mission-driven organization devoted to putting patients ...
Quick apply
Computer Systems Validation Engineer
Cleveland, OH · On-site
$80K - $100K/yr
Join us as a Computer Systems Validation Engineer! Join Abeona Therapeutics Inc. as a Computer Systems Validation Engineer and be part of a mission-driven organization devoted to putting patients ...
Our Computer Systems Validation Leads work directly with our clients to support activities that include, but are not limited to, documentation review and approval, including change controls ...
Quick apply
Our Computer Systems Validation Leads work directly with our clients to support activities that include, but are not limited to, documentation review and approval, including change controls ...
Tata Consultancy Services is seeking a Computer System Validation Lead to oversee CSV activities in regulated environments. The role involves ensuring compliance with regulations, authoring ...
Tata Consultancy Services is seeking a Computer System Validation Lead to oversee CSV activities in regulated environments. The role involves ensuring compliance with regulations, authoring ...
Computer systems integrations and validation experience in regulated operations (preferably GMP operations). * Strong experience authoring and executing validation documentation (test scripts ...
Computer systems integrations and validation experience in regulated operations (preferably GMP operations). * Strong experience authoring and executing validation documentation (test scripts ...
Computer Validation information
See salary details
$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
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.
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Full-time
Posted 16 days ago
Lonza rating
8.1
Based on 39 frontline employees who took The Breakroom Quiz
33rd of 71 rated pharmaceutical
Job description
Computer Systems Validation (Analytical) Supervisor
Location:Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.
As the Computer Computer Systems Validation (CSV) Supervisor youwill lead a team of professionals to deliver validation projects on schedule while ensuring strict adherence to Quality and Data Integrity standards. You will collaborate with Operations Technology (OT), Engineering, and Quality Assurance to support site goals, enhance compliance, and drive on-time, right-first-time performance.
What you will get:
Competitive salary and comprehensive benefits package.
Opportunities for career development and advancement.
Supportive and collaborative team environment.
Access to cutting-edge technology and tools.
Commitment to employee well-being and safety.
Inclusive workplace culture.
Recognition and reward for your contributions.
Access to our full list of global benefits:https://www.lonza.com/careers/benefits
What you will do:
Provide technical support for the design, operation, and troubleshooting of analytical equipment across departments.
Lead the planning and execution of equipment-related IQ/OQ/PQ validation plans and process improvements.
Manage Quality Management System (TW) records, review EDMS documents, and lead risk assessments and change controls.
Identify quality concerns, engage stakeholders, and drive issues to final resolution.
Coach and develop staff through performance reviews, career planning, and consistent 1:1 meetings.
Handle administrative duties, including daily meetings, task assignment, and hiring/onboarding activities.
Partner with CSV, OT, and other validation teams to ensure site-wide consistency and compliance.
What we are looking for:
Bachelor's degree of Science/Engineering is required.
5-10 years' of Computer Systems Validation experience - Manufacturing and QC systems.
Advanced knowledge of manufacturing operations, Validation principles (process, equipment, systems), and Data Integrity.
Hands-on experience managing deviations, change controls, and CAPAs within systems like TrackWise.
Proven ability to lead medium-to-large projects, drive planning/controlling, and utilize tools like RCA, FMEA, and VSM.
Strong verbal/written communication skills and effective leadership in fostering cross-functional, customer-focused collaboration.
Expert knowledge of GMP/Safety standards and proficiency in MS Office (Project, Excel, Word, PowerPoint).
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
About Lonza
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