Downstream Process Development, Engineer II

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use .  I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Join Takeda as a Downstream Process Development, Engineer II.  As an early-career professional, you handle problems of limited scope and complexity, adhering to established policies and procedures. Your decision-making is within a defined scope, using standardized methods to analyze situations and data. You are developing knowledge of basic principles, theories, and concepts, and beginning to apply industry practices and standards. Typically, this role requires some relevant experience, with contributions mostly related to task-specific activities. Your primary contacts are with your immediate team, and you work under moderate direction and close supervision, following specific, detailed instructions. About the role: The Downstream Process Development, Engineer II is responsible for supporting downstream biotherapeutics process development through hands-on purification and recovery development experiments. This individual contributor role supports process development across multiple scales, from micro scale through bench and pilot scale, and contributes to both early-stage and late-stage programs. You will work in teams with more senior process engineers to collaboratively execute larger experiments, while also working closely with process development team members to generate data, maintain accurate records, and contribute to the development and optimization of downstream processes. How you will contribute: • Execute chromatography, harvest operations, ultrafiltration and diafiltration (UF/DF), and viral clearance experiments with additional potential support of bioconjugation. • Support downstream process development across micro scale, bench scale, and pilot scale studies • Help maintain laboratory equipment and support routine readiness of instruments used in process development work • Work with more senior process engineers to collaboratively plan and execute larger experiments and study activities • Document experimental work in electronic laboratory notebooks and maintain clear, complete, and timely records • Perform basic data analysis to review trends, compare conditions, and support study conclusions • Prepare technical summaries, study updates, and other written materials to share results and findings • Follow established laboratory and process development procedures, including quality and safety requirements • Contribute to continuous improvement efforts by identifying ways to improve workflows, data capture, and experimental execution • Assist with small projects or specific project tasks under close supervision What you bring to Takeda: • Associate degree with 2+ years of relevant experience, or bachelor’s degree with relevant experience, in chemical engineering, chemistry, biochemistry, biotechnology, or a related field • Experience with chromatography, harvest, ultrafiltration and diafiltration, and viral clearance steps • Comfort with emerging digital tools and openness to AI-enabled processes that support data analysis, documentation, and workflow improvement. • Experience with basic bioprocess control systems • Experience using electronic laboratory notebooks for study documentation/data entry • Ability to perform basic data analysis and present results clearly in written form • Familiarity with technical writing for laboratory reports or development documents • Understanding of laboratory practices, process development methods, and quality requirements • Ability to follow detailed procedures, maintain accurate records, and work under close supervision • Some relevant experience in process development, protein purification, or a related laboratory setting Important Considerations: At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product. In this role, you may: Work in a controlled environment requiring special gowning and wear protective clothing over the head, face, hands, feet and body. This may include additional hearing protection for loud areas. Need to remove all make-up, jewelry, contact lenses, nail polish and/or artificial fingernails while in the manufacturing environment. Work in a cold, wet environment. Work multiple shifts, including weekends, or be asked to work supplemental hours, as necessary. Work around chemicals such as alcohol, acids, buffers and Celite that may require respiratory protection. More about us: At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work. Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. #GMSGQ  #ZR1  #LI-MA1 Takeda Compensation and Benefits Summary We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.   For Location: Lexington, MA U.S. Base Salary Range: $71,800.00 - $112,860.00 The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for