In Process Research Associate

Position Summary We are seeking an In-Process Support Associate with a strong protein chemistry background to perform cGMP in-process analytical support. These services include in-process and release testing for drug substances manufactured internally. The In-Process Support Associate will be trained to execute analytical test methods and their corresponding analytical techniques, complete data analysis and/or perform data integrity review of STAT samples which support manufacturing operations, and when time permits, execute QC testing for Release and in-process samples. This position will primarily work 1st shift hours, but night, weekend, and holiday work will sometimes be required. Off‑shift coverage is assigned to team members as needed on a rotating basis. Position Responsibilities Performs testing on in‑process or drug substance/drug product using bio‑analytical techniques such as HPLC, UV‑Vis and simple compendial testing. Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals. Makes detailed observations and carries out elementary data analysis. Understands experiments, conducts troubleshooting analysis, and maintains knowledge of instrumentation. Documents work (Notebook and Worksheet) upkeep and writes clearly. Maintains familiarity with current scientific literature and professional expertise. Assures proper labeling, handling, and storage of all chemicals used in the area, ensures proper labeling and disposition of hazardous waste in the satellite area, adheres to all safety requirements, follows safety procedures, and attends all required safety and health training, including hazardous waste handling. Responds to changes productively and handles other essential tasks as assigned. Position Requirements BS in a scientific discipline or equivalent. Experience in QC analysis of proteins, antibodies, peptides, or vaccines is a plus but not required. Excellent verbal and written communication skills. Experience working in a cGMP environment preferred. Pay Range Pay Range: $19.23/hour – $26.44/hour Pay range is provided based on current averages and expectations. The pay rate and job title for this opening will be based on the selected candidate’s qualifications and experience and may be outside this range. KBI offers a robust total rewards strategy that includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, 401(k) matching with 100% vesting upon hire, 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 Equal Employment Opportunity KBI is a proud EEO/AA employer dedicated to building a diverse and inclusive workforce. We believe that innovation thrives in an environment where all voices are heard and valued. We actively seek individuals from all backgrounds—regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability, or veteran status—and strongly encourage all qualified candidates to apply and bring their unique perspectives to our team. #J-18808-Ljbffr NCBiotech