Automation Engineering Technician

NCBiotech; Zebulon, Northern (NC, KY); Hybrid; USD 95,000 - 130,000; Full time

Benefits offered by this job

Onsite cafeteria

Onsite gym

Health & Wellness clinic

Job summary

GSK is seeking an on-site Automation and Controls Engineer at the Zebulon, NC facility to support value stream production equipment and projects. You will assist with installation, commissioning, and validation, drive continuous improvement, and mentor maintenance staff.

The role requires 5+ years in industrial automation, strong instrumentation/controls knowledge, and experience with ERP/SAP and industrial IT tools. On-site presence is expected at a GMP site with opportunities for growth.

Qualifications

• Associate’s degree in relevant technical field or equivalent experience.
• 5+ years in industrial automation/engineering with instrumentation, controls, PLCs, HMIs, and electrical/mechanical systems.
• Experience in cGMP/FDA-regulated environments preferred.

Responsibilities

• Provide daily floor production support for automation and instrumentation issues.
• Develop and implement equipment improvements focusing on OEE, reliability, safety, and quality.
• Contribute to maintenance strategy improvements and participate in continuous improvement projects.
• Create technical documentation such as Change Control Requests and training materials.

Skills

Industrial automation

Troubleshooting

Documentation

On-site collaboration

Education

Associate’s degree in computer science, Engineering Technology, Instrumentation & Controls

Bachelor's in Engineering

Tools

SAP

Kepware

Wireshark

Patch Manager

ServiceNow

Panorama

Tenable.IO

VMware

ESXi

Job description

Business Introduction

We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it’s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply.

We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.

Position Summary

You will provide daily automation and controls support of value stream production equipment and processes in coordination with the area maintenance team. Contribute toward the successful implementation of small and large capital equipment projects by providing technical support to engineering teams in the execution phases of installation, commissioning, and validation. Manage and assume all responsibilities for the implementation of small equipment and process improvement projects targeted to improve failure rate and overall equipment efficiency. Support assessment and capabilities development of engineering technicians in coordination with maintenance supervisor.

Responsibilities

• Provide daily on the floor production support to value stream areas experiencing engineering/automation or instrumentation and controls equipment issues or failure.
• Work with maintenance, engineering and production staff in developing and implementing a variety of equipment improvements, primarily in the areas of OEE, reliability engineering, safety, or process
• and/or quality improvements.
• Work with maintenance staff in continuously evaluating corrective, preventative and predictive maintenance strategies on production equipment and systems by participation in continuous
• improvement projects.
• Develop technical documentation including e-pips, Change Control Request, technical specifications, training documents, etc as directed by maintenance supervisor.
• Provide mentoring and support to maintenance staff as required.
• Support capability development of engineering techs (ET) by participating is skills assessments and training sessions.

Basic Qualifications

• Associate’s degree in computer science, Engineering Technology, Instrumentation & Controls, or equivalent years of experience.
• 5+ years of industrial engineering/automation experience including knowledge of instrumentation, control systems, PLC’s, HMI’s, pneumatic, electrical, electronic, and mechanical systems.

Preferred Qualifications

• Technical expertise in P&ID nomenclature, instrumentation and electrical wiring diagrams.
• Proficient in SAP (work orders, history, maintenance plans).
• Good knowledge of cGMPs, and experience in an FDA regulated environment.
• Excellent written and oral communication skills.
• Bachelor's in science in Engineering
• Experience within Mechanical, Electrical, Chemical, Civil/Structural, Instrumentation & Controls
• Technical knowledge of this the technology and ability to problem solve.
• Works well on team, flexibility, time management, task prioritization, Strong communication skills, self-motivated
• Ability to learn quickly, think creatively and apply new skills given rapid change in technology
• Knowledge of Industrial communication protocols (Modbus, Ethernet/IP, DeviceNet, ControlNet, BACnet, OPC UC, etc.)
• Experience w/ Software(s): Kepware, Wireshark, Patch Manger, Service Now, Panorama, Tenable.IO, VM Ware, ESXi Host Manag. and familiar w/ Nutanix or other hyperconverged environments
• Experience administering Windows Active Directory, Network Services (IP, DHCP, DNS and WINS), group management
• Experience with serialization systems; experience with MES solutions; experience with laboratory automation; experience with databases.
• Experience working in a regulated / GMP environment
• Experience working onsite with local teams and remotely with global teams
• Knowledge of Industrial Cybersecurity Standards
• Available for On-Call as required

Work Arrangement

This role is on-site at a GSK manufacturing facility in the United States. You will regularly work on the production floor and may occasionally support off-hour commissioning or urgent troubleshooting.

About the Zebulon Site at GSK

GSK’s Zebulon site is a global supplier of Respiratory and Solid Dose medicines to patients around the globe and the largest GSK Pharmaceutical secondary manufacturing site in North America. The site is located less than 30 minutes from downtown Raleigh, Wendell, Knightdale, Rocky Mount, Wilson, and Wake Forest.

Key differentiators about GSK and Zebulon

• Our commitment to inclusion is seen as a critical advantage of ours
• Our focus on cultivating a positive work environment that cares for our employees
• Demonstrated opportunities for continued career growth driven by individual ambition
• Leaders that care about their teams and growth of both individuals and the company
• A priority focus on Safety and Quality
• Clean and GMP compliant work environment
• Onsite cafeteria
• Onsite gym
• Temperature-controlled climate
• Licensed, onsite Health & Wellness clinic

What we offer

You will join a team that values inclusion, respect, and continuous learning. You will have opportunities to grow technical skills and take part in meaningful projects that support supply and patient safety. We welcome people from all backgrounds and encourage you to apply if this role aligns with your experience and career goals.

Ready to bring your automation skills to a team that makes a real difference? We’d love to hear from you.

#Globalsupplychain

Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - [e-mail]

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/