Senior Process Engineer | Noblesville, IN | $105K–$110K + 5% Bonus A leading highly regulated manufacturing organization is hiring a Senior Process Engineer to support sterile pharmaceutical manufacturing in Noblesville, IN. This role will focus on process optimization, equipment reliability, troubleshooting, and new product/process implementation within a highly regulated cGMP environment.
Responsibilities:
  • Lead process improvement, reliability, and troubleshooting initiatives
  • Investigate root causes and implement CAPAs and corrective actions
  • Develop change controls, technical documentation, protocols, and reports
  • Support new product launches, process transfers, and new manufacturing equipment
  • Partner cross-functionally with Manufacturing, Quality, R&D, Validation, and Project Management
  • Establish and improve process KPIs and manufacturing efficiency
Requirements:
  • Bachelor’s degree in Engineering; Mechanical preferred 5+ years of engineering experience in pharmaceutical, biologics, medical device, food, or other highly regulated manufacturing
  • Experience with cGMPs, validation, quality systems, and document control
  • Strong root cause analysis and process improvement experience
  • Experience with CAPAs, deviations, change controls, and technical documentation
  • Pharmaceutical packaging, automated inspection, or vial labeling experience is a plus
  • Lean/Six Sigma experience preferred
  • Up to 10% travel
Benefits:
  • $105K–$110K base + 5% bonus
  • Direct-hire position
  • Benefits begin Day 1Medical, dental, and vision 401(k)PTO, including 20 days in the first full year4 floating holidays + 9 paid holidays
  • Monday–Friday, 8:00 AM–5:00 PM

Also on the board Same function, level within a rung

Level

Lead

Location

Noblesville, IN

Occupation

Manufacturing Engineers

Industry

Pharmaceutical Preparation Manufacturing

Posted

3 days ago

Apply for this role →