Process Engineer

Katalyst CRO; Bloomington (IN); On-site; USD 90,000 - 120,000; Full time

Job summary

Katalyst CRO in Bloomington, IN is seeking a Process Engineer II to optimize production processes and implement improvements across Operations, Quality, Maintenance, and Engineering.

The role focuses on process validation, GMP compliance, and data-driven decision making to enhance efficiency and product reliability. Candidates should have a manufacturing/engineering background and experience in pharma/biotech/medical devices.

Qualifications

• 35 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.

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.

Skills

GMP Compliance

Process Validation

Root Cause Analysis

CAPA

Technical Documentation

Data Analysis

Cross-functional Collaboration

Problem Solving

Education

Bachelor's Degree in Chemical, Mechanical, Industrial, or Manufacturing Engineering

Job description

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

• 35 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