Process Engineer II

Job Title

Upstream Process Engineer II

Redmond, WA

Site MSAT

We are looking for a passionate and curious Upstream Process Engineer II to join our team. In this role, you’ll drive impactful bioreactor and cell culture improvements, collaborate with bright minds, and explore uncharted territories. The role reports to the Upstream Senior Manager for Site MSAT and supports upstream processing for multiple clinical‑scale cGMP manufacturing trains.

• Represent Site MSAT on project teams as technical subject matter expert (SME) and interface with Global MSAT, Operations, and Quality functions.
• Develop process understanding and expertise.
• Author, review, and own process‑related documentation (technical documents, test protocols, batch records, process descriptions, SOPs, etc.).
• Lead change controls, including managing change implementation as the assigned change agent.
• Partner with Manufacturing to develop high‑quality batch records, robust processes, and innovative technology solutions.
• Utilize technical skills and process knowledge to participate and/or lead investigations related to process/New product implementation.
• Collaborate with impacted groups to drive implementation of CAPAs from approval to closure and effectiveness check.
• Participate in quality and technical risk assessment activities.
• Support technology transfer or new production introduction activities.
• Monitor and report on process performance data analysis.
• Partner with Validation and Quality groups in supporting equipment onboarding activities and periodic review programs as process owners.
• Provide 24/7 on‑call support during production.
• Apply Operational Excellence principles to lead continuous improvement for upstream process improvements.

• Bachelor’s degree in Engineering with 2–4 years of pharmaceutical/biotech experience, or a master’s degree in Engineering with >1 year of experience.
• Experience supporting process transfer / technology transfer projects and teams in the biopharmaceutical industry; commercial manufacturing campaign support is a plus.
• Solid understanding of upstream processing, including hands‑on experience in single‑use bioreactor operations and perfusion technology at manufacturing scale or in process development of biologics.
• Solid understanding of GMP concepts and quality systems necessary to support manufacturing and new product introduction activities.
• Working knowledge of manufacturing process equipment and automation systems.
• Ability to organize, analyze/interpret, and effectively communicate process data.
• Strong focus on quality, attention to detail, and effective task/time management and organizational skills.
• Good interpersonal, team, and collaborative skills.
• Excellent verbal and written communication skills in English; ability to interface with all levels of the organization.

• Ability to navigate regulatory CMC documents.
• Experience with DeltaV for process control.
• Experience supporting late‑stage manufacturing, technical transfer and process validation studies.
• Experience in supporting audits and inspections by health authorities, clients and other external auditors as a presenter or audit support staff.

The base pay range for this position at commencement of employment is expected to be $86,250 to $90,000. Base salary may vary depending on skills, experience, and market value. Additional total rewards include discretionary annual bonus and comprehensive benefits:
Medical, Dental and Vision, short‑term and long‑term disability, company‑paid basic life insurance, 401(k) company match, flexible work, paid time off, paid holiday, wellness and transportation benefits.

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.