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Process Engineer III
EvotecProcess Engineer III responsible for equipment design and procurement at Just Evotec Biologics. Collaborating with diverse teams to enhance manufacturing processes and technologies.
Posted 5/15/2026full-timeRedmond • Washington • 🇺🇸 United StatesMid-LevelSenior💰 $92,400 - $126,500 per yearWebsite
About the role
Key responsibilities & impact- Lead the design, development and procurement of new equipment and technologies for the Just-Evotec manufacturing network
- Evaluate new technologies for implementation into the manufacturing process to increase efficiency and facility throughput
- Develop design documents based on platform process requirements and validation commissioning and qualification protocols
- Collaborate with the automation team on design and development of the Distributed Control System (DCS)
- 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 and paid holiday
- wellness and transportation benefits
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
design developmentprocurementvalidation commissioningsingle-use technologiesdata validation packagesequipment maintenancenon-conformance investigationsprocess impact evaluationsmanufacturing process equipmentautomation systems
Soft Skills
collaborationindependent workcross-functional teamworkquality focusattention to detailtask managementorganizational skillsdata analysiseffective communicationproblem-solving
Certifications
BS in engineeringMS in engineering or related field