Pharma Manufacturing Process Engineer - Optimization

Scorpion Therapeutics

Elwood (KS)

On-site

USD 85,000 - 115,000

Full time

14 days+

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Benefits offered by this job

Relocation packages
8-week parental leave
9 Employee Resource Groups
annual bonus
6% 401K matching

Job summary

Scorpion Therapeutics is seeking a Manufacturing Process Engineer to provide on-floor process and equipment support, drive CAPA, and ensure cGMP compliance at our Elwood, KS site. You will lead capital projects from design to validation and develop critical documentation to support quality and regulatory needs.

The role requires a Bachelor's in chemical/biological engineering, pharma/biotech experience, and strong cross-functional collaboration.

Qualifications

  • Bachelor's degree in Chemical, Biological, or related engineering.
  • Experience in pharmaceutical, biotechnology, or related industry.
  • Self-motivated team player with ability to prioritize and deliver with minimal supervision; working knowledge of cGMP.

Responsibilities

  • Provide technical and on-floor support for process and equipment, including troubleshooting and CAPA.
  • Ensure equipment qualification and regulatory compliance; oversee interventions and changes via change control.
  • Drive process optimization through data analysis to monitor performance and identify improvements.
  • Lead lifecycle of capital projects including design, development, execution, commissioning, qualification, and validation.
  • Develop and manage technical documentation and risk mitigation with cross-functional collaboration.

Skills

Process engineering
CAPA
Root cause analysis
Documentation
Cross-functional collaboration

Education

Bachelor's degree in Chemical, Biological, or related engineering

Tools

SAP EAM
ERP
AutoCAD
Veeva Vault
AVEVA PI
Seeq
Meridian

Job description

Scorpion Therapeutics is seeking a Manufacturing Process Engineer to provide on-floor process and equipment support, drive CAPA, and ensure cGMP compliance at our Elwood, KS site. You will lead capital projects from design to validation and develop critical documentation to support quality and regulatory needs.

The role requires a Bachelor's in chemical/biological engineering, pharma/biotech experience, and strong cross-functional collaboration.

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