Process Engineer II
Evotec
June 27, 2026
On-site
Redmond, WA
Operations
Roles And Responsibilities:
- Represent Site MSAT on project teams as technical SME; interface with Global MSAT, Operations, and Quality.
- Develop process understanding and expertise.
- Author, review, and own process documentation (technical documents, test protocols, batch records, process descriptions, SOPs).
- Author, review, and lead change controls; manage change implementation as assigned change agent.
- Partner with Manufacturing to develop high-quality batch records, robust processes, and technology solutions.
- Participate and/or lead investigations for process/new product implementation; drive CAPA implementation from approval through closure and effectiveness check.
- Participate in quality and technical risk assessments.
- Support technology transfer and new production introduction.
- Monitor and report process performance data analysis.
- Partner with Validation and Quality on equipment onboarding and periodic review programs as process owners.
- Provide 24/7 on-call support during production.
- Apply Operational Excellence principles to lead continuous improvement.
Position Requirements:
- BS in Engineering with 2–4 years pharma/biotech experience, or MS in Engineering with 1+ year experience.
- Experience supporting process/technology transfer (commercial campaign support is a plus).
- Solid upstream processing knowledge; hands-on single-use bioreactor operations and perfusion technology (manufacturing scale or process development).
- Solid GMP and quality systems knowledge for manufacturing/new product introduction.
- Working knowledge of manufacturing process equipment and automation systems.
- Ability to organize, analyze/interpret, and communicate process data.
- Strong quality focus and attention to detail; effective time/task management.
- Interpersonal and collaborative skills.
- Excellent English verbal/written communication; interface with all organizational levels.
Additional Preferred Qualifications:
- Ability to navigate regulatory CMC documents.
- DeltaV experience.
- Late-stage manufacturing, technical transfer, and process validation study experience.
- Audit/inspection support experience as presenter or support staff.
Benefits (as stated): Base pay range $86,250–$90,000; discretionary annual bonus; Medical/Dental/Vision; short- and long-term disability; basic life insurance; 401k match; flexible work; paid time off and paid holidays; wellness and transportation benefits.
- Represent Site MSAT on project teams as technical SME; interface with Global MSAT, Operations, and Quality.
- Develop process understanding and expertise.
- Author, review, and own process documentation (technical documents, test protocols, batch records, process descriptions, SOPs).
- Author, review, and lead change controls; manage change implementation as assigned change agent.
- Partner with Manufacturing to develop high-quality batch records, robust processes, and technology solutions.
- Participate and/or lead investigations for process/new product implementation; drive CAPA implementation from approval through closure and effectiveness check.
- Participate in quality and technical risk assessments.
- Support technology transfer and new production introduction.
- Monitor and report process performance data analysis.
- Partner with Validation and Quality on equipment onboarding and periodic review programs as process owners.
- Provide 24/7 on-call support during production.
- Apply Operational Excellence principles to lead continuous improvement.
Position Requirements:
- BS in Engineering with 2–4 years pharma/biotech experience, or MS in Engineering with 1+ year experience.
- Experience supporting process/technology transfer (commercial campaign support is a plus).
- Solid upstream processing knowledge; hands-on single-use bioreactor operations and perfusion technology (manufacturing scale or process development).
- Solid GMP and quality systems knowledge for manufacturing/new product introduction.
- Working knowledge of manufacturing process equipment and automation systems.
- Ability to organize, analyze/interpret, and communicate process data.
- Strong quality focus and attention to detail; effective time/task management.
- Interpersonal and collaborative skills.
- Excellent English verbal/written communication; interface with all organizational levels.
Additional Preferred Qualifications:
- Ability to navigate regulatory CMC documents.
- DeltaV experience.
- Late-stage manufacturing, technical transfer, and process validation study experience.
- Audit/inspection support experience as presenter or support staff.
Benefits (as stated): Base pay range $86,250–$90,000; discretionary annual bonus; Medical/Dental/Vision; short- and long-term disability; basic life insurance; 401k match; flexible work; paid time off and paid holidays; wellness and transportation benefits.