On-site Biologics Mfg Associate III - Process Automation

Scorpion Therapeutics

Redmond (WA)

On-site

USD 85,000 - 110,000

Full time

14 days+
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Job summary

Just Evotec Biologics is seeking a Manufacturing Associate III to optimize biologics manufacturing processes in Redmond, Washington. The role focuses on evaluating new technologies, developing design documents, and integrating equipment into automation systems.

Collaboration with vendors on validation and ongoing maintenance supports lifecycle planning. The position requires a BS in engineering or sciences (or MS) with 2+ years in pharma/biotech manufacturing, and strong knowledge of cGMP,

Qualifications

  • BS in engineering, sciences, or related field with 2+ years pharma/biotech manufacturing or MS degree.
  • Solid knowledge of cGMP and biologics processing; experience with single-use systems.
  • Experience with automation, process development, and CQV.

Responsibilities

  • Optimize biologics manufacturing processes.
  • Evaluate new technologies and develop design documents.
  • Integrate equipment into automation systems.
  • Collaborate with vendors on validation and lifecycle planning.
  • Support equipment maintenance and lifecycle planning.
  • Partner with site and global teams on process improvement and technology implementation.
  • Contribute to quality investigations.

Skills

cGMP knowledge
Biologics processing
Single-use systems
Automation (DeltaV)
Process development
CQV

Education

BS in engineering/sciences or related field
MS degree

Tools

DeltaV automation

Job description

Just Evotec Biologics is seeking a Manufacturing Associate III to optimize biologics manufacturing processes in Redmond, Washington. The role focuses on evaluating new technologies, developing design documents, and integrating equipment into automation systems.

Collaboration with vendors on validation and ongoing maintenance supports lifecycle planning. The position requires a BS in engineering or sciences (or MS) with 2+ years in pharma/biotech manufacturing, and strong knowledge of cGMP,

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