Equipment Engineer; MDPI
Listed on 2026-07-24
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Engineering
Automation & Mechatronics Engineer, Validation Engineer, Quality Engineering
Location: Zebulon
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.
Summary
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. We value practical problem solvers who collaborate clearly, act with integrity, and drive improvements that make a real difference to patients.
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.
This role will provide you the opportunity to lead key activities to progress your career. These responsibilities include some of the following:
- 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.
Work arrangement
This position is on‑site in the United States. Hybrid or remote work is not available for this role.
Basic QualificationWe are seeking professionals with the following required skills and qualifications to help us achieve our goals:
- 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
-or- - AAS degree in Technical field (i.e. 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.
If you have the following characteristics, it would be a plus:
- 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…
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