Associate Scientist – CMC R&D

Kashiv BioSciences, LLC • Piscataway, NJ

1d • Onsite

About The Position

CMC R&D is seeking candidates interested in contributing to a burgeoning field that has the potential to help millions of patients. As a growing company, Kashiv BioSciences offers real development opportunities for candidates excited to take on responsibility, make an immediate impact, and help us achieve our vision. As part of a close-knit team, you’ll have the opportunity to work in a unique, high-science industry while expanding your career.

Requirements

• Minimum B.S. degree in Analytical Chemistry, Biophysical/biochemical sciences, pharmaceutical sciences with 6-8 years industry experience
• Or Master’s degree in Analytical Chemistry, Biophysical/biochemical sciences, pharmaceutical sciences with 6-8 years industry experience
• Or Ph.D. in Biochemistry, Biotechnology, Biology with 0-2 years’ experience
• Experience with a wide variety of analytical technologies such as peptide mapping, HPLC, UPLC SEC, HIC, IEX at a minimum
• Experience in method development, as well as method qualification/verification/validation in a GLP/GMP environment
• Excellent communication and technical writing skills
• Ability to multitask technical responsibilities in a fast-paced, dynamic environment is required
• Proficiency with the following software is required: Microsoft Word, Excel, PowerPoint, and Outlook.

Nice To Haves

• Experience with Empower and/or ChemStation HPLC software programs is desired.
• Experience with any or all of the following is considered advantageous: spectroscopy (UV-Vis, CD, and fluorescence), mass spectrometry, DOE software, strong knowledge of statistics.

Responsibilities

• Develop, qualify, and validate methods for protein analysis on HPLC/UPLC, capillary systems, and equivalent analytical instruments, and plate-based assays using different readers, using literature references and scientific principles.
• Ensure adherence to highest quality and efficiency standards in laboratory operations (cGLP, cGMP)
• Develop, optimize, and validate new chromatography methods
• Document laboratory work in notebooks and appropriate systems in accordance with GLP systems and internal SOPs, following compliance.
• Write and review technical documents such as study protocols, reports, SOPs, experiment summaries test method, etc.
• Foster morale and teamwork
• Performs other functions as required or assigned
• Complies with all company policies and standards

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Ph.D. or professional degree