Process Engineer - CIP

Staftonic LLC; New York (NY); On-site; USD 83,000 - 116,000; Full time

Job summary

A leading company in pharmaceutical manufacturing seeks a Process Engineer – CIP to enhance and validate Clean-in-Place systems. The successful candidate will lead CIP-related activities and work with cross-functional teams, ensuring compliance with GMP standards. This mid-senior level role requires over 12 years of experience and a solid educational background in Chemical Engineering, along with strong expertise in automation and CIP systems.

Qualifications

• 12+ years of experience in pharmaceutical/GMP manufacturing.
• Willingness to work onsite and support shift-based operations.

Responsibilities

• Lead development and troubleshooting of CIP cycles.
• Perform hydraulic calculations (e.g., flow rate, pump sizing, pressure drop).
• Support commissioning and integration of automated CIP systems.

Skills

Strong communication

Coordination skills

Expertise in CIP systems

Education

Bachelor’s degree in Chemical Engineering

Tools

SCADA

DeltaV

PLC

Job description

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Process Engineer - CIP

Job Description:

We are hiring a Process Engineer – CIP to support the development, optimization, and validation of Clean-in-Place (CIP) systems within a pharmaceutical fill/finish facility. This role will serve as the technical lead for all CIP-related activities, working closely with cross-functional teams including automation, validation, and operations.

Key Responsibilities:

• Lead development and troubleshooting of CIP cycles
• Perform hydraulic calculations (e.g., flow rate, pump sizing, pressure drop)
• Support commissioning and integration of automated CIP systems (SCADA, DeltaV, PLC)
• Review batch records and ensure cleaning processes meet GMP standards
• Collaborate with QA and validation on cleaning verification and documentation
• Serve as liaison with vendors for CIP equipment and support

Requirements:

• Bachelor’s degree in Chemical Engineering or related field
• 12+ years of experience in pharmaceutical/GMP manufacturing
• Strong expertise in CIP systems and cleaning validation
• Experience with automation systems (e.g., SCADA, DeltaV, PLC)
• Strong communication and coordination skills
• Willingness to work onsite and support shift-based operations

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

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