Evotec
Overview
Job Title:
Senior Scientist I, Purification Process Development Location:
Seattle, WA Reports to:
Principal Scientist, Purification Process Development About Us At Just-Evotec, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what’s possible. We\u2019re on a mission to create a place where curiosity isn\u2019t just encouraged, it’s celebrated. Are you someone who asks questions, seeks answers, and isn\u2019t afraid to go deeper? #BeCureious with us and see where your curiosity can take you! Role
We’re looking for a passionate and curious Senior Scientist I to join our team. In this role, you’ll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories. You’ll have the freedom to ask hard questions, think outside the box, and find creative solutions that push us forward. This role supports personal growth and team success. Responsibilities
Leading a diverse group of scientists encompassing all aspects of purification process development, characterization, and validation, as well as technology transfer to cGMP manufacturing for hybrid and continuous processes. Serving as an internal technical resource for cGMP manufacturing and Process Design, and as a SME for external clients and partners for purification processes (small scale models, process transfer, and scale up), including authoring CMC regulatory sections. Serving as a functional area lead for platform or complex client early-stage (FIH) and late-stage Process Characterization (PC) projects as well as technology development projects. Serving as a Project Team Lead within the process development organization to execute on client projects involving multiple functional areas for platform, early-stage (FIH) projects. Clearly and effectively communicating scientific information, experimental plans, and data to internal project teams, senior management, external clients, vendors, and technology development collaborators. Independently designing, executing, and analyzing statistically designed experiments (DOE). Authoring SOPs, reports, and slides that summarize, organize, and interpret experimental results with review by appropriate team members. Training, mentoring, and supervising staff and interns. Driving technology development for process intensification and continuous manufacturing to reduce manufacturing costs and footprint through improvements in culture productivity, product quality, and data management. Supporting the management of staff, capital resources, and planning within the department. Other tasks as assigned. Qualifications
BS/MS in Engineering, Biochemistry, Biology, or related field with 8+ years of experience or Ph.D. in Engineering, Biochemistry, Biology, or related field with 3+ years of experience. Expertise in purification technology and process development, transfer to cGMP manufacturing plants, and authoring CMC sections of regulatory filings. Experience with commercial process development, process characterization, and validation. Expertise in design of experiments (DOE) and statistical analysis. Experience in training, mentoring, and supervising team members as well as leading development teams for external client projects and collaborations and internal technology development initiatives. Experience with high throughput process development systems is a plus. Additional Qualifications
Experience analyzing data in tools such as JMP, R, or Python. General understanding of cell biology, fluid dynamics, and protein chemistry as well as knowledge in other functional areas (upstream and analytical sciences). Experience working in a cGMP or clean room setting (non-GMP but knowledge of GMP is helpful for process/tech transfer activities). Why Join Us
Growth Opportunities: We’re committed to continuous learning and development through professional courses, mentorship, or new projects. Flexible Work Environment: Hybrid work options in many locations. Inclusive Culture: We value diversity and curiosity. Innovative Projects: Work on cutting-edge initiatives in an environment where curiosity drives success. A Place for Big Ideas: We encourage and welcome ideas. Equal Opportunity Employer: 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.
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Job Title:
Senior Scientist I, Purification Process Development Location:
Seattle, WA Reports to:
Principal Scientist, Purification Process Development About Us At Just-Evotec, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what’s possible. We\u2019re on a mission to create a place where curiosity isn\u2019t just encouraged, it’s celebrated. Are you someone who asks questions, seeks answers, and isn\u2019t afraid to go deeper? #BeCureious with us and see where your curiosity can take you! Role
We’re looking for a passionate and curious Senior Scientist I to join our team. In this role, you’ll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories. You’ll have the freedom to ask hard questions, think outside the box, and find creative solutions that push us forward. This role supports personal growth and team success. Responsibilities
Leading a diverse group of scientists encompassing all aspects of purification process development, characterization, and validation, as well as technology transfer to cGMP manufacturing for hybrid and continuous processes. Serving as an internal technical resource for cGMP manufacturing and Process Design, and as a SME for external clients and partners for purification processes (small scale models, process transfer, and scale up), including authoring CMC regulatory sections. Serving as a functional area lead for platform or complex client early-stage (FIH) and late-stage Process Characterization (PC) projects as well as technology development projects. Serving as a Project Team Lead within the process development organization to execute on client projects involving multiple functional areas for platform, early-stage (FIH) projects. Clearly and effectively communicating scientific information, experimental plans, and data to internal project teams, senior management, external clients, vendors, and technology development collaborators. Independently designing, executing, and analyzing statistically designed experiments (DOE). Authoring SOPs, reports, and slides that summarize, organize, and interpret experimental results with review by appropriate team members. Training, mentoring, and supervising staff and interns. Driving technology development for process intensification and continuous manufacturing to reduce manufacturing costs and footprint through improvements in culture productivity, product quality, and data management. Supporting the management of staff, capital resources, and planning within the department. Other tasks as assigned. Qualifications
BS/MS in Engineering, Biochemistry, Biology, or related field with 8+ years of experience or Ph.D. in Engineering, Biochemistry, Biology, or related field with 3+ years of experience. Expertise in purification technology and process development, transfer to cGMP manufacturing plants, and authoring CMC sections of regulatory filings. Experience with commercial process development, process characterization, and validation. Expertise in design of experiments (DOE) and statistical analysis. Experience in training, mentoring, and supervising team members as well as leading development teams for external client projects and collaborations and internal technology development initiatives. Experience with high throughput process development systems is a plus. Additional Qualifications
Experience analyzing data in tools such as JMP, R, or Python. General understanding of cell biology, fluid dynamics, and protein chemistry as well as knowledge in other functional areas (upstream and analytical sciences). Experience working in a cGMP or clean room setting (non-GMP but knowledge of GMP is helpful for process/tech transfer activities). Why Join Us
Growth Opportunities: We’re committed to continuous learning and development through professional courses, mentorship, or new projects. Flexible Work Environment: Hybrid work options in many locations. Inclusive Culture: We value diversity and curiosity. Innovative Projects: Work on cutting-edge initiatives in an environment where curiosity drives success. A Place for Big Ideas: We encourage and welcome ideas. Equal Opportunity Employer: 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.
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