Process Engineer III, Global MSAT

Evotec WD; Redmond (WA); On-site; USD 92,400 - 126,500; Full time

Benefits offered by this job

Discretionary annual bonus

Comprehensive benefits

401(k) company match

Flexible work

Generous paid time off

Job summary

Evotec WD in Redmond is seeking a Process Engineer III to lead the design, development, and procurement of new technologies within the manufacturing network. You will collaborate with key stakeholders to enhance manufacturing efficiency and guide regulatory submissions.

The ideal candidate will have over 5 years of experience in the biopharmaceutical sector and a solid understanding of single-use processing equipment. We offer competitive salaries and comprehensive benefits including bonuses, healthcare, and paid time off.

Qualifications

• 5+ years of relevant experience in Pharmaceutical, Biotech, or Life Sciences industries.
• Experience leading technology implementation and validation activities.
• Solid understanding of monoclonal antibody processing.

Responsibilities

• Lead design and procurement of new equipment.
• Develop design documents and process guidelines.
• Support technical evaluations of facility utility requirements.

Skills

Single-use processing equipment expertise

Project management

cGMP knowledge

Technical problem-solving

Excellent communication skills

Education

BS in engineering or sciences

MS with 2+ years of experience

Tools

DeltaV automation

Distribute Control System (DCS)

Job description

Job Title: Process Engineer III

Location: Redmond, WA

Reports To: Director, Global MSAT

About Us

Just‑Evotec Biologics is a forward‑thinking team in the biopharmaceutical sector that thrives on challenging the status quo and driving innovation through curiosity.

The Role

As a Process Engineer III, you will lead the design, development, and procurement of new equipment and technologies within the Just‑Evotec manufacturing network, working closely with stakeholders. You will lead technology testing, develop validation documentation, provide technical support to MSAT and Manufacturing Operations, and guide regulatory submissions and inspections.

What You’ll Do

• 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 of 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.

Who You Are

• BS in engineering, sciences, or related life science engineering or MS with 2+ years of experience.
• 5+ years of relevant experience in Pharmaceutical, Biotech, or Life Sciences industries.
• Subject matter expert in biopharmaceutical manufacturing single‑use processing equipment and technologies.
• Experience 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.

Additional Preferred Qualifications

• Experience with continuous manufacturing processes.
• Leading newer engineers and using DeltaV automation.
• Participation in global teams, Center of Excellence, etc.
• Applies knowledge and expertise to solve complex technical problems.
• Proficiency developing and executing commissioning/qualification (CQV) plans and protocols.
• Ability to work independently and in project teams; may lead projects within functional area expertise at Just‑Evotec Biologics.

Why Join Us

Growth opportunities, inclusive culture, innovative projects, and a culture that encourages curiosity.

Base Pay Range

$92,400 to $126,500 at commencement of employment. Additional total rewards include discretionary annual bonus, comprehensive benefits (Medical, Dental, Vision), short‑term and long‑term disability, company‑paid basic life insurance, 401(k) company match, flexible work, generous paid time off and paid holiday, wellness and transportation benefits.

EEO Statement

Evotec (US) Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.