CIP – Automation Engineer (DeltaV)

Intellectt Inc; North Carolina; On-site; USD 85,000 - 110,000; Full time

Job summary

A leading biopharmaceutical manufacturer seeks a CIP – Automation Engineer to provide automation support for utilities and Clean-in-Place systems. The role involves hands-on troubleshooting and compliance assurance, requiring a bachelor's degree and several years of experience in a GMP-regulated environment. This is a mid-senior level contract position based in North Carolina, offering competitive compensation.

Qualifications

• 5+ years of automation engineering experience in a GMP-regulated environment.
• Hands-on experience with DeltaV DCS platforms.
• Knowledge of CIP systems and related utility operations.

Responsibilities

• Lead automation support for Utilities and CIP systems.
• Troubleshoot process automation systems built on DeltaV.
• Ensure compliance with GMP and data integrity standards.

Skills

Troubleshooting

Problem-Solving

Communication

Education

Bachelor’s degree in Engineering

Tools

DeltaV DCS

CIP systems

Job description

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Direct message the job poster from Intellectt Inc

Unicorn Recruiter | Tech & Business Talent Specialist | People-First Hiring Partner | Empowering Careers, Enabling Growth @ Intellectt Inc |…

Hello,

One of my clients is currently seeking a CIP – Automation Engineer (DeltaV). If this role aligns with your experience or interests, I’d love to connect with you. Please share your updated resume with me at [e-mail], or feel free to call me directly at [phone] to discuss further.

Location: Onsite – North Carolina

Duration: 6 Months

Industry: Biopharmaceutical Manufacturing / Life Sciences

Job Overview:

Our client is seeking a highly skilled and detail-oriented Automation Engineer with expertise in DeltaV, CIP (Clean-in-Place) systems, and utilities automation to support the Drug Substance Manufacturing (DSM) area of a major biopharmaceutical facility. This is an onsite role requiring hands-on support of process automation systems to ensure smooth and compliant manufacturing operations.

Key Responsibilities:

• Serve as the automation support lead for Utilities and CIP systems within the DSM suite.
• Provide daily operational support and troubleshooting for process automation systems built on the Emerson DeltaV DCS platform.
• Support the automation lifecycle including design review, software development, hardware integration, system commissioning, qualification (IQ/OQ/PQ), and validation activities.
• Monitor and resolve system alarms, failures, or process anomalies in a timely manner to minimize manufacturing downtime.
• Perform configuration updates, logic changes, and scripting for DeltaV control strategies related to utilities and CIP.
• Work closely with Manufacturing, Quality, Engineering, and Validation teams to maintain compliance with GMP, 21 CFR Part 11, and data integrity standards.
• Support change control, deviation investigations, and continuous improvement initiatives for automation systems.
• Participate in cross-functional meetings and project teams to support new process introduction, system upgrades, and technical troubleshooting.

Qualifications:

• Bachelor’s degree in Engineering, Automation, Computer Science, or a related technical field.
• 5+ years of automation engineering experience in a GMP-regulated, biopharmaceutical, or life sciences manufacturing environment.
• Hands-on experience with DeltaV DCS platforms, including CIP/Utilities system configuration and support.
• Strong understanding of CIP systems, WFI, Clean Steam, RO, HVAC, and other clean utility operations.
• Knowledge of ISA S88, batch process control, and GAMP5 methodologies.
• Familiarity with validation and qualification documentation, including URS, FRS, IOQ protocols.
• Strong troubleshooting, problem-solving, and communication skills.
• Experience with automation change management, CAPA, and deviation support is highly preferred.

Nice to Have:

• Previous experience supporting Drug Substance Manufacturing (DSM) or biologics operations.
• Knowledge of KNEAT, TrackWise, or similar quality systems.
• Ability to collaborate in cross-functional, fast-paced teams and manage competing priorities.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Industries

  Biotechnology Research, Pharmaceutical Manufacturing, and Medical Equipment Manufacturing

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