Gsk

Gsk

Equipment Engineer (MDPI)

USA - North Carolina - Zebulon

Sponsorship not specifiedDetected 1 day ago
Supply ChainProcurementHRRoboticsPLCGMPMedical DevicesCommunicationProblem SolvingSCADAGxP

About the role

  • These responsibilities include some of the following: Provide hands-on mechanical, instrumentation and controls troubleshooting on production equipment and peripheral systems.
  • Contribute to equipment lifecycle documentation including FAT, SAT, commissioning records and validation deliverables.
  • Work arrangement This position is on-site in the United States.

Responsibilities

  • This role will provide YOU the opportunity to lead key activities to progress YOUR career.
  • 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.
  • Experience delivering equipment projects, installations or upgrades from design to handover.
  • 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.
  • Business Introduction We manufacture and supply reliable, high-quality medicines and vaccines to meet patients' needs and drive our performance.
  • Position Summary You will serve as the MDPI Equipment Engineer, providing mechanical and automation expertise to support safe, reliable manufacturing.

Requirements

  • Experience with mechanical and automation troubleshooting on production equipment.

Nice to have

  • 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 managing contractors, vendors and project budgets.
  • Ability to work with cross-functional teams and communicate clearly with technical and non-technical colleagues.
  • About the Zebulon 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.
  • Experience with computer system validation principles and regulatory requirements relevant to manufacturing.

Skills

  • Strong written and verbal skills, with experience preparing technical documentation and reports.

Benefits

  • 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.
  • You will join a team that values clear communication, practical support and continuous learning.

This listing is sourced directly from Gsk's careers page and normalized into a canonical job model.