Equipment Engineer (MDPI)

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 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.

About the role

You will serve as the MDPI Equipment Engineer, providing mechanical and automation expertise to support safe, reliable manufacturing. You will work closely with Production, Engineering, Maintenance, Quality, Facilities, Automation and EHS to deliver continuous capital projects and day-to-day production support. This role offers chances to grow technically, lead projects, and contribute to a mission that unites science, technology and talent to get ahead of disease together.

Responsibilities

• Provide hands-on mechanical, instrumentation and controls troubleshooting on production equipment and peripheral systems.
• Lead design, installation, commissioning, qualification and continuous improvement activities for equipment and automation.
• Partner with cross-functional teams and external contractors to deliver projects on time, within scope and compliant with regulations.
• Support investigations, root cause analysis and corrective actions for equipment and process issues.
• Mentor technicians and junior engineers, share best practice, and support capability development.
• Contribute to equipment lifecycle documentation including FAT, SAT, commissioning records and validation deliverables.

Requirements

We are seeking professionals with the following required skills and qualifications:

• Bachelor’s degree and 5+ years' experience in mechanical, electrical, automation, chemical engineering or related technical discipline; or equivalent practical experience supporting production equipment, automation or controls in a Pharma or Medical Devices regulated manufacturing environment.
• AAS degree in Technical field (e.g. Industrial Automation, Electronics, Robotics) and 10+ years' experience supporting production equipment, automation or controls in a Pharma or Medical Devices regulated manufacturing environment.
• Experience with mechanical and automation troubleshooting on production equipment.
• Experience delivering equipment projects, installations or upgrades from design to handover.

Preferred Qualifications

• Experience in pharmaceutical, biologics or other highly regulated industries.
• Knowledge of automation systems such as PLC, HMI, SCADA and MES and familiarity with related wiring, networking and instrumentation.
• Understanding of qualification and validation activities including FAT, SAT, commissioning and testing.
• Experience with computer system validation principles and regulatory requirements relevant to manufacturing.
• Experience managing contractors, vendors and project budgets.
• Strong written and verbal skills, with experience preparing technical documentation and reports.
• Ability to work with cross-functional teams and communicate clearly with technical and non-technical colleagues.
• Willingness to work on the shop floor and provide practical, timely support to production.

About the site

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.

• Commitment to inclusion as a critical advantage.
• Focus on cultivating a positive work environment that cares for employees.
• Opportunities for continued career growth driven by individual ambition.
• Leaders that care about their teams and growth of both individuals and the company.
• Priority focus on Safety and Quality.
• Clean and GMP compliant work environment.
• Onsite cafeteria and gym.
• Temperature-controlled climate.
• Licensed, onsite Health & Wellness clinic.

Benefits

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

Skills

• Asset Life Cycle Management
• Data Integrity
• Digital Fluency
• GxP Regulations
• Lean Management
• Manufacturing Technologies
• Pharmaceutical Manufacturing
• Problem Solving
• Risk Awareness
• Standards Compliance

Work arrangement: This position is on-site in the United States. Hybrid or remote work is not available for this role.