Manufacturing Engineer

Manufacturing Engineer Katalyst Healthcares & Life Sciences - 4.0 Indianapolis, IN Job Details Contract 1 day ago Qualifications HVAC system design and layout Bachelor's degree in mechanical engineering CAD software Preventative hardware maintenance Bachelor's degree in industrial engineering Chemical Engineering HVAC system maintenance Technical documentation Pharmaceutical regulatory compliance Engineering Equipment installation Mechanical Engineering Safety standards in production GMP Piping and instrumentation diagrams (P&IDs) Technical support Industrial equipment troubleshooting Bachelor's degree in engineering Energy efficiency & conservation Continuous improvement Industrial Engineering Pharmaceutical plant experience Bachelor's degree in chemical engineering Pneumatic systems Manufacturing Commissioning phase involvement Root cause analysis Design of mechanical systems Senior level Cross-functional collaboration

Full Job Description Job Summary:

We are seeking a Manufacturing Engineer to support pharmaceutical manufacturing operations in Indianapolis, IN. The ideal candidate will be responsible for designing, troubleshooting, optimizing, and maintaining critical utility systems such as HVAC, chilled water, steam, compressed air, and process gases. This role requires collaboration with cross-functional teams to ensure reliable, compliant, and energy-efficient facility operations within a GMP/cGMP-regulated pharmaceutical environment.

Roles & Responsibilities:

Design, troubleshoot, optimize, and maintain utility systems including HVAC, chilled water, steam, compressed air, and process gases. Support pharmaceutical manufacturing facilities by ensuring reliable and energy-efficient utility operations. Develop and review P&IDs, engineering calculations, and equipment specifications. Provide technical support during project design, installation, commissioning, qualification, and startup activities. Conduct root-cause analysis and implement corrective and preventive maintenance solutions. Collaborate with operations, maintenance, engineering, and project teams to minimize downtime and improve system performance. Ensure compliance with c

GMP, FDA/EMA

regulations, safety standards, and engineering best practices. Support equipment troubleshooting, maintenance planning, and continuous improvement initiatives. Utilize AutoCAD for engineering drawings and documentation updates.

Experience:

Experience in the pharmaceutical or life sciences industry required Hands-on experience working in GMP/cGMP-regulated environments Strong background in utility systems and/or facilities engineering Experience with commissioning, qualification, troubleshooting, and maintenance activities Proficiency in AutoCAD and engineering documentation

Mid/Junior Level:

2-7 years of relevant experience

Senior Level:

8+ years of relevant experience

Education:

Bachelor's degree in Mechanical Engineering, Chemical Engineering, Industrial Engineering, or related engineering discipline preferred