Automation Engineer – DeltaV & MES (Night Shift)

GSK; Upper Merion Township (Montgomery County); On-site; USD 85,000 - 110,000; Full time

Job summary

GSK in the United States seeks an Associate Automation Engineer to provide night‑shift support for process controls and MES in a biopharma manufacturing setting. You will evaluate technology, plan modifications, troubleshoot systems, and support critical operations.

This role offers career progression opportunities and exposure to capital projects. The position requires a Bachelor’s degree and 1+ years in a GMP environment, with preferred engineering or life sciences backgrounds and hands‑on

Qualifications

• Bachelor’s degree required; GMP experience preferred.
• Experience in a GMP environment is required to perform in the role.

Responsibilities

• Provide technical support for process controls and MES during night shifts.
• Evaluate and implement modifications to control systems and MES.
• Troubleshoot process controls and MES issues and provide solutions.
• Lead continuous improvement initiatives and capital projects.
• Maintain operation procedures and documentation for GxP compliance.
• Administer OT environment including servers and networks.
• Communicate technical issues to cross‑functional teams.

Skills

Problem solving

Data integrity

Digital fluency

GxP regulations

Lean management

Pharmaceutical manufacturing

Standards compliance

Risk awareness

Manufacturing technologies

Life Cycle Management

Education

Bachelor’s degree

BS/BA in Engineering, Life Sciences, Biology, Electrical, Chemical, Process or Software Engineering

Tools

DeltaV DCS

Syncade MES

Emerson Syncade

Job description

GSK in the United States seeks an Associate Automation Engineer to provide night‑shift support for process controls and MES in a biopharma manufacturing setting. You will evaluate technology, plan modifications, troubleshoot systems, and support critical operations.

This role offers career progression opportunities and exposure to capital projects. The position requires a Bachelor’s degree and 1+ years in a GMP environment, with preferred engineering or life sciences backgrounds and hands‑on