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Qualification Lead - IT/OT

  • Qualification Lead - IT/OT job type Posted on: Nov 03, 2026
  • Qualification Lead - IT/OT experience level Avacone
  • Qualification Lead - IT/OT employment type Indianapolis, Iowa
  • Qualification Lead - IT/OT employment type Onsite
  • Qualification Lead - IT/OT salary Full-time

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Job Title :

Qualification Lead - IT/OT

Job Type :

Full-Time

Job Location :

Indianapolis Iowa United States

Remote :

No

Jobcon Logo Job Description :

Job Description

Job Description

Qualification Lead Role:

·       Primary focus is to ensure that the qualification of the OT system, quality management for IT and OT systems, ensuring that the required validation / qualification deliverables are implemented according to the Customer Quality Manual and the relevant regulatory requirements

·       According to the Customer procedures, author, review and/or approve various validation / qualification deliverables

·       Review / approve validation / qualification deliverables as provided by the supplier of the relevant system(s), ensure that such deliverables are compliant to the Customer requirements

·       Lead the project test resources in relation to the validation / qualifications related activities of the project

·       Act as the project’s quality representative in relation to testing activities, engaging with local site QA and/or QA eCPL

·       Report on the status of the various quality-related activities for key stakeholders

·       Engagement with the suppliers to advise the suppliers on the suitable completion of supplier provisioned validation / qualification deliverables.

Required Validation Activities

  • Qualify IT/OT systems per Customer Quality Manual.
  • Author, execute and review URS, FS, IQ, OQ and test protocols in Kneat.
  • Perform test execution, troubleshooting and defect resolution.
  • Review supplier deliverables and verify compliance.
  • Coordinate with QA, PCM, ITOT teams and suppliers.
  • Participate in FAT, SAT, commissioning and startup activities.

Desired Experience Profile

The candidate profiles proposed for this RFP emphasize:

  • Strong CSV/CQV experience.
  • GMP-regulated pharmaceutical manufacturing background.
  • GAMP 5, EU GMP Annex 11, 21 CFR Part 11 knowledge.
  • Experience with PLC, SCADA, DCS, MES, Historian, and IT/OT systems.
  • Hands-on IQ/OQ/PQ execution and FAT/SAT support.
  • Experience using Kneat, ValGenesis, Veeva Vault, TrackWise, ServiceNow or similar validation platforms.

Jobcon Logo Position Details

Posted:

Nov 03, 2026

Reference Number:

0a3c2f28

Employment:

Full-time

City:

Indianapolis

Job Origin:

ziprecruiter

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Job Description

Job Description

Qualification Lead Role:

·       Primary focus is to ensure that the qualification of the OT system, quality management for IT and OT systems, ensuring that the required validation / qualification deliverables are implemented according to the Customer Quality Manual and the relevant regulatory requirements

·       According to the Customer procedures, author, review and/or approve various validation / qualification deliverables

·       Review / approve validation / qualification deliverables as provided by the supplier of the relevant system(s), ensure that such deliverables are compliant to the Customer requirements

·       Lead the project test resources in relation to the validation / qualifications related activities of the project

·       Act as the project’s quality representative in relation to testing activities, engaging with local site QA and/or QA eCPL

·       Report on the status of the various quality-related activities for key stakeholders

·       Engagement with the suppliers to advise the suppliers on the suitable completion of supplier provisioned validation / qualification deliverables.

Required Validation Activities

  • Qualify IT/OT systems per Customer Quality Manual.
  • Author, execute and review URS, FS, IQ, OQ and test protocols in Kneat.
  • Perform test execution, troubleshooting and defect resolution.
  • Review supplier deliverables and verify compliance.
  • Coordinate with QA, PCM, ITOT teams and suppliers.
  • Participate in FAT, SAT, commissioning and startup activities.

Desired Experience Profile

The candidate profiles proposed for this RFP emphasize:

  • Strong CSV/CQV experience.
  • GMP-regulated pharmaceutical manufacturing background.
  • GAMP 5, EU GMP Annex 11, 21 CFR Part 11 knowledge.
  • Experience with PLC, SCADA, DCS, MES, Historian, and IT/OT systems.
  • Hands-on IQ/OQ/PQ execution and FAT/SAT support.
  • Experience using Kneat, ValGenesis, Veeva Vault, TrackWise, ServiceNow or similar validation platforms.

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