Materials Process Engineer I/II – Manufacturing Technical Operations

Evotec

Materials Process Engineer II at Just-Evotec Biologics supporting design, development, and procurement of single-use technologies. Collaborating with stakeholders to enhance manufacturing quality and efficiency.

Posted 7/28/2026full-timeRedmond • Washington • 🇺🇸 United StatesJuniorMid-Level💰 $80,000 - $92,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in cGMP manufacturing and regulatory compliance for biologics and pharmaceuticals, with a strong focus on single-use manufacturing systems and monoclonal antibody processing. Capable of effectively communicating technical data and collaborating with cross-functional teams to enhance manufacturing efficiency.

Highest-signal resume keywords

BS In EngineeringCGMP Manufacturing KnowledgeSingle-Use Disposable Manufacturing SystemsMonoclonal Antibody ProcessingProcess Impact Evaluation

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Qualification Document CreationTechnical Report WritingData AnalysisValidation CommissioningProcess Equipment UnderstandingAutoclave Systems KnowledgeManufacturing Process EvaluationTechnical Problem Solving

Soft Skills

Attention To DetailEffective CommunicationOrganizational SkillsTeam CollaborationIndependent Work

Industry Keywords

Pharmaceutical IndustryBiotech IndustryLife SciencesRegulatory RegulationsManufacturing Throughput

About the role

Key responsibilities & impact

Work with key stakeholders to evaluate new and existing technologies components to increase efficiency and facility throughput.
Create qualification documents based on platform process requirements and validation commissioning and qualification protocols.
Create assessment, test and technical reports to determine the feasibility and justification for creating the component or using the instrumentation.
Assist projects lead to evaluate the fit, form and function of the client process within the JEB manufacturing processing platform.
Work with Process Engineers on designing and manufacturing single-use bags and flow paths on new and existing equipment.
Work with vendors to develop data and validation packages supporting technologies.
Facilitate procurement and implementation of approved single-use technologies.
Lead the development single-use expiry & life cycle plans.
Partner with Site MSAT Manufacturing Technology & Science teams on global and site objectives.
Participate in non-conformance/deviation investigation and provide process impact evaluations of single-use issues .
Participate in exchange of technical 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
2-5 years of relevant experience in Pharmaceutical, Biotech, or Life Sciences industries, or an MS degree
Working knowledge of cGMP manufacturing and regulatory regulations and requirements for biologics/pharmaceuticals
Solid understanding of monoclonal antibody processing at manufacturing scale and associated process equipment and manufacturing
Experience working with single-use disposable manufacturing systems
Demonstrated ability to work independently and collaboratively on cross-functional teams.
Working knowledge of large-scale autoclave systems
Candidate must focus on quality, attention to detail, and effective task/time management organizational skills.
Ability to organize, analyze/interpret, and effectively communicate investigation data.
Good interpersonal, team, and collaborative skills are a must.
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