Associate Scientist – CMC R&D

Reposted 5 Days Ago
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Piscataway, NJ, USA
In-Office
Senior level
Biotech • Pharmaceutical
The Role
Develop, optimize, qualify, and validate protein analytical methods (HPLC/UPLC, capillary systems, plate assays) under GLP/GMP. Document experiments, write technical reports and SOPs, and support lab operations in a controlled cleanroom environment, ensuring compliance and team collaboration.
Summary Generated by Built In

Description

  

Position Summary

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. 

Essential Duties & 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

Requirements

  

Position Requirements and Qualifications

Education:

  • 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

Special Skills: 

  • 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.
  • 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. 

Work Environment & Physical Demands:

General work environment and physical demands as required to successfully perform the essential functions of this job. Ability to work flexible hours as needed. Ability to work under pressure and meet deadlines. Some travel may be involved.

General Work Environment:

  • Laboratory and controlled cleanroom space.
  • Cleanroom gowning required.

Noise:

  • Standard noise levels expected with laboratory and manufacturing equipment.

Standing/Lifting:

  • Extended periods of standing and walking while working in the manufacturing areas
  • Must be able to lift 15 lbs.

Visual:

  • No special requirements

Stress:

  • High-paced, demanding environment to meet manufacturing schedules

Travel:

  • Travel not expected.

Supervisory Responsibility, if any: No

This position description is not a complete list of all responsibilities, duties, or skills required for the job and is subject to review and change at any time, with or without notice, in accordance with the needs of the organization.

Kashiv BioSciences, LLC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, or genetics. In addition to federal law requirements, Kashiv BioSciences, LLC complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Skills Required

  • B.S. in Analytical Chemistry, Biophysical/biochemical sciences, or pharmaceutical sciences with 6-8 years industry experience; OR Master's in same with 6-8 years; OR Ph.D. in Biochemistry/Biotechnology/Biology with 0-2 years experience
  • Experience with analytical technologies: peptide mapping, HPLC, UPLC, SEC, HIC, IEX
  • Experience in method development and method qualification/verification/validation in a GLP/GMP environment
  • Document laboratory work and write/review technical documents (protocols, reports, SOPs)
  • Proficiency with Microsoft Word, Excel, PowerPoint, and Outlook
  • Excellent communication and technical writing skills
  • Ability to multitask technical responsibilities in a fast-paced, dynamic environment
  • Ability to work in laboratory and controlled cleanroom space (cleanroom gowning required)
  • Ability to lift 15 lbs
  • Experience with Empower and/or ChemStation HPLC software programs
  • Experience with spectroscopy (UV-Vis, CD, fluorescence), mass spectrometry, DOE software, and strong knowledge of statistics
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The Company
HQ: Piscataway, NJ
600 Employees
Year Founded: 2010

What We Do

Kashiv BioSciences is a fully-integrated biopharmaceutical company with global R&D, clinical, manufacturing, regulatory, and IP capabilities, focusing on developing and manufacturing biosimilars and complex peptide medicines to improve access to important therapies.

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