Process Engineer

Karwell Technologies

Bloomington, IN

JOB DETAILS
SKILLS
Biotech and Pharmaceutical, Continuous Improvement, Corporate Policies, Corrective Action, Cross-Functional, Data Analysis, Engineering, Equipment Validation, FDA (Food and Drug Administration), GMP (Good Manufacturing Practices), Identify Issues, Lean Manufacturing, Maintain Compliance, Manufacturing, Manufacturing Engineering, Manufacturing Operations, Manufacturing Process Engineering, Medical Equipment, Operational Support, Operations, Operations Processes, Performance Metrics, Problem Solving Skills, Process Development, Process Engineering, Process Improvement, Process Validation, Product/Service Launch, Regulatory Compliance, Risk Analysis, Root Cause Analysis, Technical Support, Technical Writing
LOCATION
Bloomington, IN
POSTED
11 days ago
Job Description:
The Process Engineer II supports manufacturing operations by optimizing production processes, implementing process improvements, and ensuring compliance with quality and regulatory standards. This role partners closely with Operations, Quality, Maintenance, and Engineering teams to improve efficiency and product reliability.
Roles & Responsibilities:
  • Support daily manufacturing operations and troubleshoot process issues.
  • Analyze production data to identify process improvement opportunities.
  • Develop and update manufacturing procedures and work instructions.
  • Lead process validation and equipment qualification activities.
  • Collaborate with Quality on deviation investigations and CAPAs.
  • Monitor KPIs and recommend corrective actions.
  • Support technology transfer and new product introductions.
  • Participate in risk assessments and continuous improvement initiatives.
  • Ensure compliance with GMP, FDA, and company policies.
  • Provide technical support to manufacturing personnel.

Requirements:

  • 3 5 years of manufacturing or process engineering experience.
  • Experience in pharmaceutical, biotechnology, or medical device industries.
  • Knowledge of Lean Manufacturing principles.
  • Experience with process validation activities.
  • Bachelor's Degree in Chemical, Mechanical, Industrial, or Manufacturing Engineering.

Mandatory Skills / Competencies:

  • GMP Compliance
  • Process Validation
  • Root Cause Analysis
  • CAPA
  • Technical Documentation
  • Data Analysis
  • Cross-functional Collaboration
  • Problem Solving

About the Company

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Karwell Technologies