Automation Engineer

This role focuses on commissioning, validating, and troubleshooting advanced automation and control systems within a GMP pharmaceutical manufacturing environment. You will work on a high-profile, long-term project at a state-of-the-art facility, collaborating closely with a team of engineers to deliver reliable, efficient, and compliant process control solutions.

Responsibilities

• Execute automation commissioning and validation protocols for process control systems in a GMP/pharmaceutical environment.
• Troubleshoot and remediate commissioning and validation non-conformances to ensure systems operate safely, reliably, and in compliance with applicable standards.
• Collaborate in a team environment with internal engineers and client stakeholders to design and deliver state-of-the-art control systems that improve manufacturing efficiency, product quality, and overall profitability.
• Define, configure, and implement programmable logic controller (PLC) solutions, with a focus on Rockwell/Allen-Bradley platforms.
• Perform testing, on-site commissioning, and qualification of control systems to verify performance and adherence to functional and regulatory requirements.
• Work with minimal supervision, taking ownership of assigned tasks and driving them to completion within project timelines.
• Document commissioning activities, test results, and remediation actions in a clear and compliant manner.

• Bachelor of Science degree in Electrical Engineering, Computer Engineering, Chemical Engineering, or Electrical Technology.
• 2–8 years of experience in automation or a closely related field.
• Hands-on experience configuring, troubleshooting, and supporting Rockwell/Allen-Bradley PLCs.
• Proficiency with Allen-Bradley and Rockwell automation platforms.
• Demonstrated troubleshooting skills for control systems and automation equipment.
• Previous work experience in a GMP/pharmaceutical manufacturing environment.
• Proven ability to execute assignments with little supervision and to work effectively in a team setting.
• Experience with commissioning and validation of automation and control systems.

• Experience executing structured commissioning and validation protocols for process automation systems.
• Familiarity with control system qualification in highly regulated industries.
• Strong communication skills to interface with engineering teams and client representatives.
• Ability to adapt to changing project needs and to support long-term project assignments.
• Interest in long-term career growth on large, complex automation projects, with potential to move between projects as needed.

You will work on-site at a modern, large-scale, state-of-the-art pharmaceutical manufacturing facility composed of multiple interlinked buildings and designed for high quality, high efficiency, and highly reliable production. The environment centers on delivering robust control systems, primarily using Rockwell/Allen-Bradley technologies, in a GMP-regulated setting. You will collaborate closely with a team of approximately five other engineers on the same site, supporting a high-profile project with strong long-term potential. The schedule is expected to follow a 4x10-hour format, with shifts highly likely to be on weekends. Typical schedules may include a weekend shift from Thursday to Sunday, approximately 10:00 a.m. to 9:00 p.m., or an evening shift from Wednesday night to Saturday night, typically around 8:00 p.m. to 7:00 a.m., with Sunday morning off. The role is fully on-site in a production and facilities environment, where you will spend significant time around operational manufacturing equipment and automation systems.

Job Type & Location

This is a Contract to Hire position based out of Concord, NC.

The pay range for this position is $60.00 - $65.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in Concord,NC.

This position is anticipated to close on Apr 30, 2026.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people

Actalent is an equal opportunity employer.

About Actalent

Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000 extraordinary employees who connect their passion with purpose every day.

Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Salary : $60 - $65