... system validation documentation Additional Job Standards * Experience in IT/Computer validation (to leverage important inputs on how to handle the workflow, howto avoiddata integrity problems ...
... system validation documentation Additional Job Standards * Experience in IT/Computer validation (to leverage important inputs on how to handle the workflow, howto avoiddata integrity problems ...
Associate Director Data and Systems QA
$123K - $180.40K/yr
Provide direct quality oversight to LP1 computer system validation (CSQA) and assist others in interpretation of regulatory and corporate requirements as it relates to CSQA and data integrity ...
Associate Director Data and Systems QA
$123K - $180.40K/yr
Provide direct quality oversight to LP1 computer system validation (CSQA) and assist others in interpretation of regulatory and corporate requirements as it relates to CSQA and data integrity ...
The Senior Computer Systems Validation Specialist focused on Building Management Systems to support a regulated pharmaceutical manufacturing environment. The specialist will support a Site Automation ...
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The Senior Computer Systems Validation Specialist focused on Building Management Systems to support a regulated pharmaceutical manufacturing environment. The specialist will support a Site Automation ...
Senior Automation Engineer
Indianapolis, IN · On-site
$99.40K - $130.50K/yr
Support Computer System Validation activities, including Installation Qualification, Operational Qualification, and Performance Qualification. * Execute and review system verification and validation ...
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Senior Automation Engineer
Indianapolis, IN · On-site
$99.40K - $130.50K/yr
Support Computer System Validation activities, including Installation Qualification, Operational Qualification, and Performance Qualification. * Execute and review system verification and validation ...
Senior Automation Engineer
Indianapolis, IN · On-site
$99.40K - $130.50K/yr
Support Computer System Validation activities, including Installation Qualification, Operational Qualification, and Performance Qualification. * Execute and review system verification and validation ...
Senior Automation Engineer
Indianapolis, IN · On-site
$99.40K - $130.50K/yr
Support Computer System Validation activities, including Installation Qualification, Operational Qualification, and Performance Qualification. * Execute and review system verification and validation ...
Validation & Compliance * Produce and maintain Computer System Validation (CSV) documentation, standard operating procedures (SOPs), and validation plans in alignment with applicable regulatory ...
Validation & Compliance * Produce and maintain Computer System Validation (CSV) documentation, standard operating procedures (SOPs), and validation plans in alignment with applicable regulatory ...
Validation & Compliance * Produce and maintain Computer System Validation (CSV) documentation, standard operating procedures (SOPs), and validation plans in alignment with applicable regulatory ...
Validation & Compliance * Produce and maintain Computer System Validation (CSV) documentation, standard operating procedures (SOPs), and validation plans in alignment with applicable regulatory ...
Validation & Compliance * Produce and maintain Computer System Validation (CSV) documentation, standard operating procedures (SOPs), and validation plans in alignment with applicable regulatory ...
Validation & Compliance * Produce and maintain Computer System Validation (CSV) documentation, standard operating procedures (SOPs), and validation plans in alignment with applicable regulatory ...
Validation & Compliance * Produce and maintain Computer System Validation (CSV) documentation, standard operating procedures (SOPs), and validation plans in alignment with applicable regulatory ...
Validation & Compliance * Produce and maintain Computer System Validation (CSV) documentation, standard operating procedures (SOPs), and validation plans in alignment with applicable regulatory ...
Validation & Compliance * Produce and maintain Computer System Validation (CSV) documentation, standard operating procedures (SOPs), and validation plans in alignment with applicable regulatory ...
Validation & Compliance * Produce and maintain Computer System Validation (CSV) documentation, standard operating procedures (SOPs), and validation plans in alignment with applicable regulatory ...
Strong knowledge of GMP's, regulatory requirements and computer system validation principles
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Strong knowledge of GMP's, regulatory requirements and computer system validation principles
Advise on validation strategy for future automation system upgrades and expansions. * Demonstrated experience in computer systems validation (CSV) for automation and control systems in a ...
Advise on validation strategy for future automation system upgrades and expansions. * Demonstrated experience in computer systems validation (CSV) for automation and control systems in a ...
Strong knowledge of GMPs, regulatory requirements, and computer system validation * (CSV) principles * Excellent verbal and written communication skills for both technical and non-technical ...
Quick apply
Strong knowledge of GMPs, regulatory requirements, and computer system validation * (CSV) principles * Excellent verbal and written communication skills for both technical and non-technical ...
Automation Project Lead
$90.80K - $119K/yr
... and computer system validation principles Strong knowledge of GMP's, regulatory requirements and computer system validation principles Excellent written and verbal communication skills for both ...
Automation Project Lead
$90.80K - $119K/yr
... and computer system validation principles Strong knowledge of GMP's, regulatory requirements and computer system validation principles Excellent written and verbal communication skills for both ...
Automation PLC Lead
Indianapolis, IN · Hybrid
... computer system validation deliverables (alarm rationalization, system overview, source code reviews, testing, etc.) Secure vendor documents for skidded equipment to integrate with validation ...
Automation PLC Lead
Indianapolis, IN · Hybrid
... computer system validation deliverables (alarm rationalization, system overview, source code reviews, testing, etc.) Secure vendor documents for skidded equipment to integrate with validation ...
Automation Project Lead
Indianapolis, IN · On-site
$90.80K - $119K/yr
... computer system validation principles • Strong knowledge of GMP's, regulatory requirements and computer system validation principles • Excellent written and verbal communication skills for both ...
Automation Project Lead
Indianapolis, IN · On-site
$90.80K - $119K/yr
... computer system validation principles • Strong knowledge of GMP's, regulatory requirements and computer system validation principles • Excellent written and verbal communication skills for both ...
Automation PLC Lead
Indianapolis, IN · On-site
... computer system validation deliverables (alarm rationalization, system overview, source code reviews, testing, etc.). • Secure vendor documents for skidded equipment to integrate with validation ...
Automation PLC Lead
Indianapolis, IN · On-site
... computer system validation deliverables (alarm rationalization, system overview, source code reviews, testing, etc.). • Secure vendor documents for skidded equipment to integrate with validation ...
Senior MES Engineer
$97.80K - $134.30K/yr
Provide technical support to Computer System Validation (CSV) activities, including MES qualification and data integrity assessments. Work closely with IT to implement OT solutions in an integrated ...
Senior MES Engineer
$97.80K - $134.30K/yr
Provide technical support to Computer System Validation (CSV) activities, including MES qualification and data integrity assessments. Work closely with IT to implement OT solutions in an integrated ...
GMP Engineer
Indianapolis, IN · On-site
Support internal and external audits related to system validation and regulatory compliance ... Prolonged periods of sitting while working at a desk or computer. * Ability to occasionally lift up ...
GMP Engineer
Indianapolis, IN · On-site
Support internal and external audits related to system validation and regulatory compliance ... Prolonged periods of sitting while working at a desk or computer. * Ability to occasionally lift up ...
Senior MES Engineer
$94.10K - $129.20K/yr
... to Computer System Validation (CSV) activities, including MES qualification and data integrity assessments. · Work closely with IT to implement OT solutions in an integrated and secure network.
Senior MES Engineer
$94.10K - $129.20K/yr
... to Computer System Validation (CSV) activities, including MES qualification and data integrity assessments. · Work closely with IT to implement OT solutions in an integrated and secure network.
Computer System Validation information
See Indiana salary details
$10.06 - $16.59
2% of jobs
$16.59 - $23.12
9% of jobs
$23.12 - $29.65
1% of jobs
$29.65 - $36.18
4% of jobs
$40.15 is the 25th percentile. Wages below this are outliers.
$36.18 - $42.71
15% of jobs
$42.71 - $49.24
9% of jobs
The median wage is $54.68 / hr.
$49.24 - $55.77
13% of jobs
$60.97 is the 75th percentile. Wages above this are outliers.
$55.77 - $62.30
29% of jobs
$62.30 - $68.83
12% of jobs
$68.83 - $75.36
2% of jobs
$75.36 - $81.89
5% of jobs
$10
$51
$81
How much do computer system validation jobs pay per hour?
What is a Computer System Validation job?
What are the key skills and qualifications needed to thrive in the Computer System Validation position, and why are they important?
What are some typical challenges faced in Computer System Validation roles?
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 21 days ago
Labcorp rating
6.6
Based on 1,081 frontline employees who took The Breakroom Quiz
78th of 103 rated laboratories
Job description
Labcorp is seeking a Laboratory Systems Validation Specialist to join our team at Scicor Drive in Indianapolis, Indiana.
Work Schedule
Monday through Friday, day shift
Job Responsibilities
Technical & Operational Support
- Operate and support laboratory instruments, interfaces, LIS/LIMS, and middleware platforms (e.g., Data Innovations Instrument Manager, Siemens CentraLink).
- Lead and provide guidance during system validations for instruments, middleware, and other lab systems.
- Support change control processes for laboratory systems.
- Collaborate with SMEs to define expected system behaviors and translate them into clear technical requirements, including data workflow considerations across systems.
- Provide technical consultation to internal and external clients.
Leadership & Project Management
- Gather and document system requirements using established methodologies.
- Create and maintain validation documentation; experience in GxP and CAP/CLIA environments preferred. Knowledge of SDLC/GAMP is a plus.
- Lead testing activities for laboratory workflows, physical automation, and instrument middleware platforms.
- Oversee requirements gathering for middleware interface development.
- Coordinate with project managers and resource owners to support system testing.
- Ensure timely delivery of services and maintain strong client relationships.
- Drive client satisfaction and identify opportunities for additional business.
Performance Monitoring & Quality
- Monitor system testing progress and performance metrics; identify and escalate issues when needed.
- Review and prepare test results for QA to ensure complete, compliant test packages.
- Balance operational support duties with ongoing project responsibilities.
- Ensure adequate resource allocation to meet performance and quality standards.
- Maintain regulatory compliance.
- Collaborate with other sites and cross-functional teams.
General Responsibilities
- Perform qualification specialist duties as needed.
- Coordinate review, approval, and archiving of validation documentation.
- Provide written and verbal updates to project managers and leadership.
- Complete all HR- and training-related requirements; maintain an up-to-date training file.
- Submit monthly status reports.
- Support a culture of continuous improvement, quality, and productivity.
Minimum Qualifications
- 3 or more years' experience in a Laboratory System Analyst or Laboratory System Validations role.
- Bachelor of Science (BS) in Clinical Laboratory Science, Biology, Chemistry, Public Health, Microbiology, Computer, Technology, Animal Science, and/or Medical Technology
Preferred Qualifications
- 1 or more years experience of knowledge of lab workflow and processes
- 1 or more years experience in laboratory software testing such as Navify, FCS Express, Infinicyte
- 1 or more years of experience or supporting client audits by providing an overview of the system validation documentation
Additional Job Standards
- Experience in IT/Computer validation (to leverage important inputs on how to handle the workflow, howto avoiddata integrity problems,evaluate upfront solutions with less validation effort and capture any event possibility required bya system when setting complex rules)
- Experience in requirements gathering, documentation in a regulatory environment
- Strong knowledge of 21 CFR Part 11 requirements and CAP/CLIA regulations
- Background in information systems, data analysis, workflow analysis
- Ability to effectively communicate with our clients at all levels of the organizations and primarily within the laboratory
About Labcorp
At Labcorp, we are a global leader of innovative and comprehensive laboratory services that helps doctors, hospitals, pharmaceutical companies, researchers and patients make clear and confident decisions.
Through our unparalleled diagnostics and drug development laboratory capabilities, our nearly 70,000 employees combine cutting-edge innovation, science and technology to solve some of today's biggest health challenges, accelerate life-changing healthcare breakthroughs and impact lives around the world.
Here, you are empowered to own your career journey and create a personalized development plan with the support of your team.
Benefits:Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible toparticipatein the 401(k) Plan only. For more detailed information, pleaseclick here.
Labcorp is proud to be an Equal Opportunity Employer:
Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.
We encourage all to apply
If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit ouraccessibility siteor contact us atLabcorp Accessibility. Formore information about how we collect and store your personal data, please see ourPrivacy Statement.
About Labcorp
Sourced by ZipRecruiter
Industry
Scientific research and development services
Company size
10,000+ Employees
Headquarters location
Burlington, NC, US
Year founded
1978