Manufacturing Associate III - Cell Culture, Site based, Redmond, WA

Evotec; Redmond (WA); On-site; USD 85,000 - 110,000; Full time

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

Role: Manufacturing Associate III in cell culture at Just Evotec Biologics

Focuses on optimizing biologics manufacturing processes. Responsibilities include evaluating new technologies, developing design documents, integrating equipment into automation systems, working with vendors on validation, and supporting equipment maintenance and lifecycle planning. Collaborates with site and global teams on process improvement, technology implementation, and quality investigations.

Requirements: BS in engineering, sciences, or related field with 2+ years in pharma/biotech manufacturing or MS degree; solid knowledge of cGMP, biologics processing, and single-use systems; experience with automation (DeltaV preferred), process development, and CQV.

High-value biopharma specifics: biologics (monoclonal antibodies), cGMP environment, biologics manufacturing, focus on process technology and automation, validation, and continuous manufacturing experience.

Work setup: on-site in Redmond, WA, with shift from Sunday-Wednesday 7am-6pm; no travel specified.