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CSV Engineer

  • CSV Engineer job type Posted on: Nov 03, 2026
  • CSV Engineer experience level i-Pharm GxP
  • CSV Engineer employment type Lebanon, Indiana
  • CSV Engineer employment type Onsite
  • CSV Engineer salary Full-time

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Job Title :

CSV Engineer

Job Type :

Full-Time

Job Location :

Lebanon Indiana United States

Remote :

No

Jobcon Logo Job Description :

C&Q Automation / CSV Engineer | Lebanon, IndianaWe’re looking for an experienced C&Q Automation / CSV Engineer to join a major pharmaceutical capital program in Lebanon, Indiana. You’ll qualify the control and building systems that run a new GMP manufacturing facility.Contract details:12-month contract, with extensions anticipatedFully onsite in Lebanon, IndianaCompetitive W2 hourly rateUpcoming start datesWhat you’ll be doing:Commissioning and qualifying automated process control systems (DeltaV, Rockwell or Siemens)Qualifying building and environmental monitoring systems (BMS/EMS), such as Johnson Controls or Siemens DesigoWriting and executing CSV and IOQ protocols, including traceability and data integrity checksWorking with Automation, Engineering and QA to bring systems to GMP standardsWhat we’re looking for:5+ years of C&Q or CSV experience in pharmaceutical or biotech GMP facilitiesHands-on experience with DCS/PLC or BMS/EMS platformsA good understanding of GAMP 5, data integrity and risk-based validationGreenfield experience and Kneat experience are a strong plus

Jobcon Logo Position Details

Posted:

Nov 03, 2026

Reference Number:

10440_4485738013

Employment:

Full-time

City:

Lebanon

Job Origin:

APPCAST_CPC

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C&Q Automation / CSV Engineer | Lebanon, IndianaWe’re looking for an experienced C&Q Automation / CSV Engineer to join a major pharmaceutical capital program in Lebanon, Indiana. You’ll qualify the control and building systems that run a new GMP manufacturing facility.Contract details:12-month contract, with extensions anticipatedFully onsite in Lebanon, IndianaCompetitive W2 hourly rateUpcoming start datesWhat you’ll be doing:Commissioning and qualifying automated process control systems (DeltaV, Rockwell or Siemens)Qualifying building and environmental monitoring systems (BMS/EMS), such as Johnson Controls or Siemens DesigoWriting and executing CSV and IOQ protocols, including traceability and data integrity checksWorking with Automation, Engineering and QA to bring systems to GMP standardsWhat we’re looking for:5+ years of C&Q or CSV experience in pharmaceutical or biotech GMP facilitiesHands-on experience with DCS/PLC or BMS/EMS platformsA good understanding of GAMP 5, data integrity and risk-based validationGreenfield experience and Kneat experience are a strong plus

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