Scientist I

Summary

Perform contract, analytical, and development services, including formulation, analytical development programs for monoclonal antibodies, recombinant proteins, viruses, nanoparticles, and peptides. Apply biophysical, biochemical and biopharmaceutical principles and techniques to develop protein formulations (liquid or lyophilized). Experience with bio-analytical techniques such as HPLC, SDS-CGE, IEF, Fluorescence, biophysical characterization techniques on proteins, and other techniques applicable to monitor physical and chemical stability of the proteins. Design new experimental plans to answer critical research questions for a wide variety of bio therapeutics. Produce high quality documentation suitable for publication and regulatory requirements. Managing cost and time constraints in meeting committed targets and schedules. Act as spokesperson on development programs and interact positively and productively with clients. Advise management on program status. Responsible for training of lower-level associates.

Job description

Requirements

• PhD degree or equivalent in Biophysics, Biochemistry, Biology, Chemistry, Physics or related field of study
• Bachelor's degree or equivalent in Biophysics, Biochemistry, Biology, Chemistry, Physics or related field of study and 5 years of progressive experience in biopharmaceutical science, in lieu of PhD degree or equivalent
• Biophysical and protein characterization techniques, including SV-AUC, CD, DSC, FTIR, HPLC, UV-Vis, and Fluorimetry
• Designing and executing complex experiments to meet a client's needs
• Presenting complex biophysical and biochemical data and results to clients
• Scientific writing, including standard operating procedures, method development reports, method qualification protocols, method qualification reports, and detailed electronic laboratory notebook entries
• Troubleshooting instrumentation and process issues
• Working with instrumentation vendors and internal lab operations for procurement, site preparation, and repair and maintenance of lab equipment and instrumentation
• Quantitatively analyzing complex data by using data analysis software or by developing data analysis methods
• Experience using lab equipment, including SV-AUC, CD, DSC, FTIR, HPLC, UV-Vis, Fluorimetry, gravimetric scales, pH meters, desktop centrifuges, and UV Spectroscopy

Benefits

• Medical Insurance
• Dental Insurance
• Vision Insurance
• 401(k) With Company Match
• Paid Time Off
• Paid Holidays

Company overview

KBI Biopharma is an award-winning global contract development and manufacturing organization (CDMO) that provides fully integrated, accelerated drug development and biologics manufacturing services to pharmaceutical and biotechnology companies worldwide. Founded in 1996 and now part of JSR Life Sciences, KBI has established itself as a next-generation CDMO specializing in complex biologics. The company serves over 500 client partners and has supported the advancement of more than 160 drug candidates from preclinical stages to market, including the manufacture of ten commercial products. KBI's comprehensive service portfolio includes cell line development, process development, analytical services, formulation development, and clinical and commercial cGMP manufacturing for both mammalian and microbial programs. With strategically located facilities across the United States and Europe, KBI leverages world-class analytical capabilities and proprietary platforms like SUREtechnology™ and PUREplatform™ to deliver personalized, accelerated solutions for biopharmaceutical development. The company is recognized for its scientific excellence, quality manufacturing, and commitment to helping clients bring innovative medicines to patients faster.