Posted 1w ago

Senior Process Engineer

@ The Gorilla Glue Company
Sharonville, Ohio, United States
OnsiteFull Time
Responsibilities:Lead commissioning, Define requirements, Coordinate teams
Requirements Summary:Bachelor’s in Engineering; 8-10+ years GMP manufacturing experience in cosmetics/pharma; lead commissioning and startup; cross-functional collaboration; strong documentation and troubleshooting.
Technical Tools Mentioned:GMP, Documentation, QA/QA systems, Process equipment, FAT, SAT
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Job Description

What's in it for you?
Thanks to our commitment to creating a supportive and engaged workplace culture, Gorilla Glue has been recognized as a top place to work for 15 years in a row. We offer competitive compensation packages, comprehensive healthcare benefits, and other perks and incentives to ensure our employees feel valued and supported.

Joining the Gorilla Glue family means being part of a team passionate about building strong brands and promoting a culture of excellence. As an employee, you'll be able to help create high-quality products and build brands that people love. Join us in an inspiring workplace where you can belong, grow, and make a difference! 

 

Summary Description:

The Senior Process Engineer serves as the technical process owner for GMP manufacturing operations, with primary responsibility for defining process requirements, leading equipment commissioning and startups, and ensuring compliant, reliable, and scalable production in a cosmetic manufacturing environment. This role is accountable for startup success of new and modified equipment, from process definition through stabilized production. The Senior Process Engineer is the final technical escalation point during commissioning and early production.

 

What will your day look like?

  • Serve as lead process engineer for new and modified manufacturing processes and equipment in a GMP-regulated cosmetic manufacturing environment.
  • Define process requirements, operating parameters, and functional expectations for manufacturing equipment, including safeguards and interlocks.
  • Make and defend technical decisions under GMP and operational pressure, including when to pause, modify, or stop startup activities to protect product quality and compliance
  • Partner with controls engineers and system integrators by translating process needs into clear functional specifications; no direct PLC/HMI programming responsibility.
  • Lead commissioning, startup, and stabilization activities, coordinating cross-functionally with Operations, Quality, Maintenance, and Controls.
  • Participate in and lead FAT, SAT, dry runs, wet runs, and first production runs, resolving technical issues in real time.
  • Ensure processes and equipment comply with GMP requirements, including documentation, change control, and audit readiness.
  • Develop and maintain process documentation, SOPs, and technical standards.
  • Support validation activities and quality investigations related to new equipment or process changes.
  • Act as a technical mentor and escalation point for complex process issues.
  • Identify opportunities to improve process robustness, reliability, and compliance; continuous improvement experience is a plus but not the primary focus.
  • All other duties as assigned.