CSV Engineer

i-Pharm GxP; Lebanon (IN); On-site; USD 55,000 - 110,000; Full time

Job summary

i-Pharm GxP in Lebanon, Indiana is seeking an experienced C&Q Automation/CSV Engineer to qualify control and building systems for a new GMP manufacturing facility. The role is a 12-month contract, fully onsite in Lebanon, Indiana, with a competitive W2 hourly rate.

You will commission and qualify automated process control systems (DeltaV, Rockwell or Siemens), qualify BMS/EMS environments, and write CSV and IOQ protocols while ensuring traceability and data integrity.

Qualifications

• 5+ years of C&Q or CSV experience in pharmaceutical or biotech GMP facilities.
• Hands-on experience with DCS/PLC or BMS/EMS platforms.
• A good understanding of GAMP 5, data integrity and risk-based validation.
• Greenfield experience and Kneat experience are a strong plus.

Responsibilities

• 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 Desigo.
• Writing and executing CSV and IOQ protocols, including traceability and data integrity checks.
• Working with Automation, Engineering and QA to bring systems to GMP standards.

Skills

CSV experience

C&Q experience

DCS/PLC platforms

BMS/EMS platforms

GAMP 5 knowledge

Data integrity

Risk-based validation

Greenfield experience

Kneat experience

Tools

DeltaV

Rockwell

Siemens

Johnson Controls

Desigo

Job description

We’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.

• 12-month contract, with extensions anticipated
• Fully onsite in Lebanon, Indiana
• Competitive W2 hourly rate

What 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 Desigo
• Writing and executing CSV and IOQ protocols, including traceability and data integrity checks
• Working with Automation, Engineering and QA to bring systems to GMP standards

What we’re looking for:

• 5+ years of C&Q or CSV experience in pharmaceutical or biotech GMP facilities
• Hands-on experience with DCS/PLC or BMS/EMS platforms
• A good understanding of GAMP 5, data integrity and risk-based validation
• Greenfield experience and Kneat experience are a strong plus