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Entry-Level Automation Engineer

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Onsite

Entry-Level Automation Engineer

Virtue America

Entry-Level Automation Engineer

Skills

Testing & QACompliance

5 days ago

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Important information


Contract type:

Freelance / Contract

Location:

New York, NY, USA

Work mode:

Onsite

Published on:

21 October 2026

What they need


Job Title: Entry-Level Automation Engineer

Location: New York

Employment Type: Contract

Experience: 0–2 Years

Job Summary

We are seeking an Entry-Level Automation Engineer to support automation systems and manufacturing equipment in a GMP-regulated pharmaceutical or life sciences environment. This role is ideal for recent graduates looking to build a career in industrial automation, process control, and manufacturing technologies.

Key Responsibilities

  • Support PLC, HMI, SCADA, and DCS systems used in manufacturing operations
  • Assist with automation system configuration, testing, and troubleshooting
  • Support equipment commissioning, qualification, and validation ( IQ/OQ/PQ )
  • Monitor automated production systems and resolve technical issues
  • Prepare and maintain automation documentation, SOPs, and validation reports
  • Support change controls, deviations, and CAPA activities
  • Ensure compliance with GMP/cGMP , FDA regulations, and 21 CFR Part 11
  • Collaborate with Manufacturing, QA, QC, Validation, and Engineering teams
  • Assist with automation upgrades and continuous improvement projects

Required Qualifications

  • Bachelor's degree in Electrical Engineering, Automation Engineering, Mechanical Engineering, Mechatronics, Computer Engineering , or a related field
  • 0–2 years of automation or manufacturing experience (internships/co-ops accepted)
  • Basic knowledge of PLC, HMI, SCADA, or DCS systems
  • Understanding of GMP/cGMP and industrial automation concepts
  • Strong analytical, troubleshooting, and communication skills

Preferred Skills

  • Exposure to Allen-Bradley, Siemens, DeltaV, Ignition, or Wonderware
  • Basic knowledge of sensors, actuators, instrumentation, and control systems
  • Familiarity with Good Documentation Practices (GDP) and 21 CFR Part 11
  • Internship or academic project experience in pharmaceutical, biotechnology, or life sciences manufacturing

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