Senior Process Engineer, Manufacturing - GMP & CQV

Elanco Tiergesundheit AG; Elwood (KS); On-site; USD 110,000 - 140,000; Full time

Benefits offered by this job

Relocation packages

Parental leave (8 weeks)

Employee Resource Groups

Annual bonus opportunity

401(k) matching

Job summary

Elanco Elwood, Kansas is seeking a Sr. Process Engineer to provide on-floor engineering support for manufacturing processes and equipment. You will drive root-cause analysis, CAPA implementation, and CQV activities for capital projects while ensuring compliance with regulatory commitments and Elanco standards.

The role requires a Bachelor’s in science or engineering and 10 years in pharma/biotech or related regulated industries, with strong analytical and cross-functional collaboration skills.

Qualifications

• Bachelor’s degree in science or engineering required.
• 10 years of experience in pharmaceutical/biotech or related regulated industry.
• Strong analytical thinking and technical problem solving; ability to prioritize and deliver results in cross‑functional teams.

Responsibilities

• Provide engineering solutions for process and equipment issues with on-floor support for root cause analysis and CAPA implementation.
• Ensure equipment and processes comply with regulatory commitments, cGMPs, and Elanco standards.
• Use performance and capacity analysis to identify and implement improvements that optimize system performance.
• Support local and major capital projects including CQV activities.
• Create and revise technical documentation such as URS, P&IDs, and PFDs.

Skills

Analytical thinking

Technical problem solving

Cross-functional collaboration

Minimal supervision

Education

Bachelor’s degree in science or engineering

Tools

SAP

AutoCAD

Veeva Vault

RCI

FMEA

QRM tools

Job description

Elanco Elwood, Kansas is seeking a Sr. Process Engineer to provide on-floor engineering support for manufacturing processes and equipment. You will drive root-cause analysis, CAPA implementation, and CQV activities for capital projects while ensuring compliance with regulatory commitments and Elanco standards.

The role requires a Bachelor’s in science or engineering and 10 years in pharma/biotech or related regulated industries, with strong analytical and cross-functional collaboration skills.