Process Engineer III, Global MSAT

Evotec

Process Engineer III at Just-Evotec Biologics leading technology design and implementation for manufacturing efficiency. Collaborating with stakeholders to enhance biopharmaceutical production processes.

Posted 5/30/2026full-timeRedmond • Washington • 🇺🇸 United StatesMid-LevelSenior💰 $92,400 - $126,500 per yearWebsite

About the role

Key responsibilities & impact

Work with key stakeholders and vendors to evaluate new technologies for implantation into the manufacturing process to increase efficiency and facility throughput.
Develop design documents (user requirement specifications, software functional specifications) based on platform process requirements and validation commissioning and qualification protocols
Collaborate with the automation team on design and development of the Distribute Control System (DCS) with the manufacturing suite.
Support technical evaluations of the facility utility requirements.
Lead evaluation of single-use technologies and design single-use manifolds and assemblies.
Work with vendors to develop data and validation packages supporting technologies.
Facilitate procurement and implementation of approved new technologies.
Develop business processes, guidelines, SOPs, and training for processing equipment and technologies .
Lead the development equipment maintenance & life cycle plans.
Lead non-conformance/deviation investigations and provide process impact evaluations of equipment/technology issues.
Lead technical exchanges problems and solutions throughout the manufacturing network.
Participate in internal and external audits/inspections.

Requirements

What you’ll need

BS in engineering, sciences, or related life science engineering
5+ years of relevant experience in Pharmaceutical, Biotech, or Life Sciences industries, or MS with 2+ years of experience.
Considered a subject matter expert in biopharmaceutical manufacturing single-use processing equipment and technologies
Experienced in leading technology implementation and validation activities for clinical and commercial manufacturing readiness
Working knowledge of cGMP manufacturing and regulatory regulations and requirements for biologics/pharmaceuticals.
Solid understanding of monoclonal antibody processing either at manufacturing scale or in process development
Experience working with single-use disposable manufacturing systems.
Demonstrated ability to work independently and collaboratively on cross-functional teams.
Working knowledge of manufacturing process equipment and automation systems.
Candidate must focus on quality, attention to detail, and effective task/time management and organizational skills.
Ability to organize, analyze/interpret, and effectively communicate process data.
Excellent oral and written communication skills.

Benefits

Comp & perks

discretionary annual bonus
comprehensive benefits to include Medical, Dental and Vision
short-term and long-term disability
company paid basic life insurance
401k company match
flexible work
generous paid time off
paid holiday
wellness and transportation benefits

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

design documentsuser requirement specificationssoftware functional specificationssingle-use technologiessingle-use manifoldsdata validation packagesequipment maintenancelife cycle planscGMP manufacturingmonoclonal antibody processing

Soft Skills

collaborationleadershipattention to detailtask managementorganizational skillsindependent workcross-functional teamworkcommunication skillsproblem-solvinganalytical skills

Certifications

BS in engineeringMS in engineering or related life sciences