Position Summary: The PD Scientist I will apply scientific principles to design and execute laboratory studies for unit operation development and optimization. They are expected to develop a working knowledge of the downstream functional area with strong aptitude in one or more operations, including chromatography and tangential flow filtration. The Scientist I will also author and review technical documents including protocols and reports, commensurate with PD compliance and quality standards. This role encompasses process development duties as well as supporting technology transfer activities in preparation for cGMP production. Finally, the PD Scientist I is responsible for maintaining training compliance, according to site expectations. This is a salaried, exempt position, with the expectation to cover shift work as needed to fully support ongoing laboratory activities and organizational need. Position Responsibilities: * Designs and conducts laboratory experiments in support of downstream/drug substance process development including preparing solutions, running downstream unit operations (chromatography, tangential flow filtration, clarification, normal filtration, etc.), sampling and executing basic analysis of process samples (concentration, pH, conductivity, etc.). * Observes and analyzes data resulting from executed experiments; leads identification and troubleshooting of unexpected results. * Compiles data and drafting of technical documents. Generates and may lead client presentation development, presents to clients and may serve as technical SME for functional area on team. * Documents procedures, observations, and results in laboratory notebooks and responsible for maintaining training compliance, according to site expectation. Reviews documentation and records as assigned. * Conceptualizes, proposes and executes the evaluation, development and implementation of new downstream technologies leading to process improvements and efficiency of operation in support of downstream process development and manufacturing activities. * Contributes to general lab maintenance and operation excellence initiatives in accordance with internal guidance. Assures proper labeling, handling, and storage of all chemicals used in the area; assures proper labeling and disposition of hazardous waste in satellite areas; adheres to all safety requirements and follows safe procedures, and attends all required safety and health training, including handling hazardous waste. * Exercises judgment within defined procedures and practices to determine appropriate action. Recommends when it's appropriate to deviate from defined procedures. Reacts to change productively and handles other essential tasks as assigned. Minimum Requirements: Scientist I requires a B.S. degree in biotechnology or related (or equivalent training) with 8+ years experience, a M.S. degree with 6+ years experience or Ph.D. Salary Range: $90,925 - $125,022 Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidate's qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, 401K matching with 100% vesting in 60 days and employee recognition programs. About KBI: KBI Biopharma, Inc., a JSR Life Sciences company, is a global contract development and manufacturing organization (CDMO) providing fully integrated and accelerated drug development and biologics manufacturing services to life science companies. KBI supports its 500+ customers in advancing more than 160 drug candidates from preclinical and clinical stages to market, including the manufacture of ten commercial products. Recognized for quality manufacturing, KBI delivers robust process development and cGMP manufacturing services across its six global locations in the USA and Europe. For more information, visit www.kbibiopharma.com. KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must inform KBI Biopharma of their vaccination status and must submit their vaccination status. All vaccinated employees are required to provide proof of their COVID-19 vaccination, with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization. KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply. I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary. I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.