Intern, Research and Development

Exela Pharma SciencesLenoir, NC
4hOnsite

About The Position

Exela Pharma Sciences, LLC., seeks a Summer Intern, API Synthesis to join our team in Lenoir, NC. The Summer Intern, API Synthesis will be responsible in process development to support ongoing API Synthesis projects and in process testing (Using TLC, HPLC etc.) with some supervision. The incumbent will also generate test results and review technical documents that support the API synthesis. The individual will also be responsible for managing his/her activities with efficient time management to maximize productivity. This position supports the ongoing process development of pharmaceutical products in compliance with local procedures, corporate policies, and the regulatory requirements of the U.S. Food and Drug Administration. Priority consideration will be given to candidates who are in their final year of study or have recently completed their degree.

Requirements

  • Pursuing a Bachelor's Degree in Chemistry or an Associate Degree in scientific discipline required
  • Currently in final year of undergraduate/graduate program, and/or
  • Recently completed degree (within the past year)
  • Excellent attention to detail and working knowledge of FDA Regulations/Guidance’s, Good Laboratory Practices.
  • Excellent verbal and written communication, organization, time-management, display sound judgment, problem-solving, interpersonal skills.

Responsibilities

  • Develop and validate process for various API Synthesis with some supervision.
  • Draft and review technical documents supporting API process development such as process validation protocols and reports.
  • Perform analytical testing as needed to support product development.
  • Perform analytical testing of samples supporting incoming raw materials.
  • Utilize analytical instrumentation such as FTIR, HPLC, GC, wet chemistry techniques, UV/VIS, KF, and LCMS and have a scientific understanding of these techniques.
  • Help in cleaning the API clean room as needed.
  • Perform all activities in compliance with cGLP/cGMP requirements.
  • Assume other responsibilities as assigned by area management.
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