The ideal candidate will have strong hands-on experience with Veeva LIMS, Computer System Validation (CSV)/Computer Software Assurance (CSA), and pharmaceutical/biotechnology validation practices
New
The ideal candidate will have strong hands-on experience with Veeva LIMS, Computer System Validation (CSV)/Computer Software Assurance (CSA), and pharmaceutical/biotechnology validation practices
New
Experience managing quality records (EN/SICAR, Change Controls, Deviations, CAPAs, CAPA-EV) using TrackWise or Veeva System * Demonstrated proficiency in managing change controls in alignment with ...
Experience managing quality records (EN/SICAR, Change Controls, Deviations, CAPAs, CAPA-EV) using TrackWise or Veeva System * Demonstrated proficiency in managing change controls in alignment with ...
Serve as the subject matter expert for the document management system, including eQMS/Veeva Vault functionality, document authoring, revision workflows, and controlled document lifecycle processes.
Quick apply
Serve as the subject matter expert for the document management system, including eQMS/Veeva Vault functionality, document authoring, revision workflows, and controlled document lifecycle processes.
Serve as the subject matter expert for the document management system, including eQMS/Veeva Vault functionality, document authoring, revision workflows, and controlled document lifecycle processes.
Serve as the subject matter expert for the document management system, including eQMS/Veeva Vault functionality, document authoring, revision workflows, and controlled document lifecycle processes.
Serve as the subject matter expert for the document management system, including eQMS/Veeva Vault functionality, document authoring, revision workflows, and controlled document lifecycle processes.
Serve as the subject matter expert for the document management system, including eQMS/Veeva Vault functionality, document authoring, revision workflows, and controlled document lifecycle processes.
Manager, Document Control (QA Operations)
Columbus, OH · On-site
$95 - $125/hr
Serve as the subject matter expert for the document management system, including eQMS /Veeva Vault functionality, document authoring, revision workflows, and controlled document lifecycle processes.
Manager, Document Control (QA Operations)
Columbus, OH · On-site
$95 - $125/hr
Serve as the subject matter expert for the document management system, including eQMS /Veeva Vault functionality, document authoring, revision workflows, and controlled document lifecycle processes.
System Test and Validation Lead
Columbus, OH · On-site +1
Experience supporting periodic review programs for validated systems and associated CAPA triggers * Experience validating cloud or software as a service platforms, including Veeva, ServiceNow, or ...
System Test and Validation Lead
Columbus, OH · On-site +1
Experience supporting periodic review programs for validated systems and associated CAPA triggers * Experience validating cloud or software as a service platforms, including Veeva, ServiceNow, or ...
System Test and Validation Lead
Columbus, OH · On-site +1
Experience supporting periodic review programs for validated systems and associated CAPA triggers * Experience validating cloud or software as a service platforms, including Veeva, ServiceNow, or ...
System Test and Validation Lead
Columbus, OH · On-site +1
Experience supporting periodic review programs for validated systems and associated CAPA triggers * Experience validating cloud or software as a service platforms, including Veeva, ServiceNow, or ...
System Test and Validation Lead
Columbus, OH · On-site +1
Experience supporting periodic review programs for validated systems and associated CAPA triggers * Experience validating cloud or software as a service platforms, including Veeva, ServiceNow, or ...
System Test and Validation Lead
Columbus, OH · On-site +1
Experience supporting periodic review programs for validated systems and associated CAPA triggers * Experience validating cloud or software as a service platforms, including Veeva, ServiceNow, or ...
Specialist Technical Writing
New Albany, OH · On-site
$70 - $100/hr
B.S. 2+ YOE would be ideal, previous Veeva experience, and prior deviation and CAPA experience ... Generate, own, and provide subject matter expertise to Quality System records as minor deviations ...
Specialist Technical Writing
New Albany, OH · On-site
$70 - $100/hr
B.S. 2+ YOE would be ideal, previous Veeva experience, and prior deviation and CAPA experience ... Generate, own, and provide subject matter expertise to Quality System records as minor deviations ...
Experience supporting periodic review programs for validated systems and associated CAPA triggers * Experience validating cloud or software as a service platforms, including Veeva, ServiceNow, or ...
Experience supporting periodic review programs for validated systems and associated CAPA triggers * Experience validating cloud or software as a service platforms, including Veeva, ServiceNow, or ...
Utilize manufacturing and quality systems as required, including eBR, Veeva, SAP, and Microsoft Office applications, to manage records and track timelines Training Support: Support training ...
Utilize manufacturing and quality systems as required, including eBR, Veeva, SAP, and Microsoft Office applications, to manage records and track timelines Training Support: Support training ...
System Utilization: Utilize manufacturing and quality systems as required, including eBR, Veeva, SAP, and Microsoft Office applications, to manage records and track timelines * Training Support:
System Utilization: Utilize manufacturing and quality systems as required, including eBR, Veeva, SAP, and Microsoft Office applications, to manage records and track timelines * Training Support:
Utilize manufacturing and quality systems as required, including eBR, Veeva, SAP, and Microsoft Office applications, to manage records and track timelines Training Support: Support training ...
Utilize manufacturing and quality systems as required, including eBR, Veeva, SAP, and Microsoft Office applications, to manage records and track timelines Training Support: Support training ...
System Utilization: Utilize manufacturing and quality systems as required, including eBR, Veeva, SAP, and Microsoft Office applications, to manage records and track timelines * Training Support:
System Utilization: Utilize manufacturing and quality systems as required, including eBR, Veeva, SAP, and Microsoft Office applications, to manage records and track timelines * Training Support:
System Utilization: Utilize manufacturing and quality systems as required, including eBR, Veeva, SAP, and Microsoft Office applications, to manage records and track timelines * Training Support:
System Utilization: Utilize manufacturing and quality systems as required, including eBR, Veeva, SAP, and Microsoft Office applications, to manage records and track timelines * Training Support:
Senior CQV Validation Engineer - Combination Products & Packaging Manufacturing - (JP15567)
New Albany, OH · On-site
$55 - $63/hr
Hands-on experience using electronic quality and document management systems, including KNEAT, Veeva, TrackWise, or equivalent platforms for managing validation documentation, change controls ...
Quick apply
Senior CQV Validation Engineer - Combination Products & Packaging Manufacturing - (JP15567)
New Albany, OH · On-site
$55 - $63/hr
Hands-on experience using electronic quality and document management systems, including KNEAT, Veeva, TrackWise, or equivalent platforms for managing validation documentation, change controls ...
Maintain and optimize systems supporting scientific communications, field education, and medical ... Experience with platforms such as Salesforce, SAP, Veeva, or KOL management tools is a plus
Maintain and optimize systems supporting scientific communications, field education, and medical ... Experience with platforms such as Salesforce, SAP, Veeva, or KOL management tools is a plus
Sr. Clinical Research Associate
Delaware, OH · On-site +1
Systems & Collaboration * Utilize and maintain accurate study data in clinical systems, including Veeva Vault CTMS and CDMS. * Work crossfunctionally with internal teams and CROs to ensure ...
Sr. Clinical Research Associate
Delaware, OH · On-site +1
Systems & Collaboration * Utilize and maintain accurate study data in clinical systems, including Veeva Vault CTMS and CDMS. * Work crossfunctionally with internal teams and CROs to ensure ...
Experience with Quality IT systems (eQMS, Veeva, Trackwise, etc.).Knowledgeable in business processes in quality roles, manufacturing, or lab operations.Key experience: (e.g., process engineering ...
Experience with Quality IT systems (eQMS, Veeva, Trackwise, etc.).Knowledgeable in business processes in quality roles, manufacturing, or lab operations.Key experience: (e.g., process engineering ...
Veeva Systems information
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$36K - $43.3K
23% of jobs
$44.3K is the 25th percentile. Wages below this are outliers.
$43.3K - $50.5K
15% of jobs
$50.5K - $57.8K
6% of jobs
The median wage is $64.1K / yr.
$57.8K - $65.1K
7% of jobs
$65.1K - $72.4K
11% of jobs
$72.4K - $79.6K
7% of jobs
$82.9K is the 75th percentile. Wages above this are outliers.
$79.6K - $86.9K
11% of jobs
$86.9K - $94.2K
5% of jobs
$94.2K - $101.5K
8% of jobs
$101.5K - $108.7K
3% of jobs
$108.7K - $116K
2% of jobs
$36K
$68.4K
$116K
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Posted 2 days ago
New
Job description
Title : Veeva LIMS SME Consultant / Senior Validation Engineer
Location: Columbus, OH – Onsite
Job Description:We are seeking an experienced Veeva LIMS SME Consultant / Senior Validation Engineer to support a Veeva LIMS implementation and validation activities within a GxP-regulated environment.
The ideal candidate will have strong hands-on experience with Veeva LIMS, Computer System Validation (CSV)/Computer Software Assurance (CSA), and pharmaceutical/biotechnology validation practices.
Responsibilities:-
Lead/support Veeva LIMS implementation and validation activities throughout the system lifecycle, from requirements and design through testing, deployment, and validation closeout.
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Develop and/or review validation deliverables including URS, risk assessments, validation plans, test scripts, traceability matrices, validation summary reports, and SOPs.
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Partner with Quality, Laboratory, IT, Business Process Owners, and system stakeholders to define requirements and ensure compliance with business and regulatory needs.
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Support Veeva LIMS configuration, functional testing, integration testing, UAT, and defect resolution.
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Apply risk-based CSV/CSA principles and applicable GxP requirements to maintain the validated state of the system.
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Support data migration, interfaces, integrations, and related systems as part of the LIMS implementation.
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Participate in change control, deviations, CAPAs, periodic reviews, and other system lifecycle activities.
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Provide technical and validation expertise during implementation meetings, workshops, testing activities, and issue resolution.
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Ensure compliance with GAMP 5, 21 CFR Part 11, EU Annex 11, and data integrity principles.
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Support inspection and audit readiness by ensuring complete, accurate, and traceable validation documentation.
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Bachelor's degree in Engineering, Computer Science, Life Sciences, or a related technical discipline.
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5+ years of experience in CSV, CSA, quality, or validation engineering within pharmaceutical, biotechnology, or other GxP-regulated environments.
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Hands-on Veeva LIMS implementation, validation, or lifecycle management experience is required.
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Strong understanding of CSV/CSA methodologies, GxP requirements, risk-based validation, and data integrity.
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Experience developing and executing validation/testing documentation.
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Strong knowledge of 21 CFR Part 11, EU Annex 11, and GAMP 5.
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Strong project management, organizational, communication, and problem-solving skills.
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Must be willing to work onsite in Columbus, OH.