Process Engineer II, Biotech MSAT | Innovation & Growth

Evotec WD; Redmond (WA); On-site; USD 83,000 - 86,250; Full time

Benefits offered by this job

Medical, Dental and Vision

401k company match

Paid time off

Job summary

Just Evotec Biologics in Redmond, WA is seeking a Process Engineer II to join the Global MSAT team. You will help design, develop, and support new equipment and technologies for the manufacturing network, with a focus on process optimization and regulatory readiness.

The role requires 2–5 years in pharma/biotech or an MS degree, strong knowledge of cGMP, and experience with single-use systems. Collaboration across sites and client projects is expected.

Qualifications

• BS in engineering, sciences, or related life science engineering.
• 2–5 years in Pharmaceuticals/Biotech or life sciences, or MS degree.
• Knowledge of cGMP and biologics/pharmaceutical regulatory requirements.
• Understanding of monoclonal antibody processing at manufacturing scale or development.
• Experience with single-use disposable systems.
• Ability to work independently and in cross-functional teams.

Responsibilities

• Evaluate new and existing technologies to increase efficiency and throughput.
• Develop design documents and platform process specifications.
• Assist with integrating equipment into DCS in the manufacturing suite.
• Evaluate single-use technologies and design manifolds/assemblies.
• Coordinate with vendors on data packages and validation.
• Support procurement and implementation of new technologies.
• Develop SOPs, guidelines, and training for processing equipment.
• Lead equipment maintenance and lifecycle planning with MSAT teams.
• Assist in audits and regulatory inspections, and support site operations.

Skills

cGMP knowledge

Data analysis

Cross-functional teamwork

Process equipment

Education

Bachelor's degree in engineering or life sciences

Tools

DeltaV automation

Job description

Just Evotec Biologics in Redmond, WA is seeking a Process Engineer II to join the Global MSAT team. You will help design, develop, and support new equipment and technologies for the manufacturing network, with a focus on process optimization and regulatory readiness.

The role requires 2–5 years in pharma/biotech or an MS degree, strong knowledge of cGMP, and experience with single-use systems. Collaboration across sites and client projects is expected.