Manufacturing Engineer

JCW Group; Denver (CO); On-site; USD 90,000 - 120,000; Full time

Job summary

JCW Group is seeking a Manufacturing Engineer II for our Denver, CO site. This technical leadership role provides on-floor engineering support during aseptic manufacturing operations and drives investigations to resolve manufacturing issues.

You will partner cross-functionally to implement process improvements, monitor real-time performance, and ensure inspection-ready documentation. A Bachelor’s degree in Chemical Engineering or a related field plus 3+ years in pharma/biotech is required.

Qualifications

• Bachelor's degree in Chemical Engineering or other scientific discipline.
• 3+ years of experience in pharmaceutical/biotech process development, manufacturing, or MS&T support.
• 2+ years of experience in aseptic operations.
• Experience leading root cause investigations, CAPAs, and change controls in a regulated environment.
• Ability to monitor and troubleshoot aseptic operations and process performance in real time.
• Strong technical writing skills for inspection-ready reports and documentation.

Responsibilities

• Provide on-floor engineering support during aseptic manufacturing operations.
• Lead root cause investigations and CAPA execution.
• Partner cross-functionally to implement process improvements.
• Monitor process performance in real time and troubleshoot operations.

Skills

Root cause investigations

CAPA management

Change controls

Technical writing

Cross-functional collaboration

Education

Bachelor's degree in Chemical Engineering or related field

Job description

Intro

A commercial pharmaceutical manufacturer specializing in aseptic injectables is hiring a Manufacturing Engineer II.

This is a technical leadership role providing on-floor engineering support during aseptic manufacturing operations, driving investigations, and partnering cross-functionally on process improvements.

You should apply if you have:

• Bachelor's degree in Chemical Engineering or other scientific discipline
• 3+ years of experience in pharmaceutical/biotech process development, manufacturing, or MS&T support
• 2+ years of experience in aseptic operations
• Experience leading root cause investigations, CAPAs, and change controls in a regulated environment
• Ability to monitor and troubleshoot aseptic operations and process performance in real time
• Strong technical writing skills for inspection-ready reports and documentation