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Teva Scientist Drug Product Development 
United States, Pennsylvania, East Bradford Township 
98767686

25.06.2024

This position is located out of West Chester, PA and the person hired is required to be onsite 5 days a week

How you’ll spend your day
  • Design and execute the experiments based on QbD principles, evaluate quality of the data and work on ways to improve data analysis and presentation formats.
  • Represent DPD for selected project in cross functional project management teams, as needed.
  • Effectively collaborate with different CMC functions as well as other non-technical teams in Teva to facilitate routine operations.
  • Design and execute formulation and process development studies.
  • Perform routine analytical tests. Generate and organize data in compliance with regulatory guidance and applicable policies.
  • Author protocols, reports, technical documents and other relevant regulatory filings documents including IND/IMPD and marketing applications, as needed.
  • Assist in the set-up and maintenance of research labs including ownership of instrumentation, authorize instrument working instructions and serve as subject matter expert for the related analytical technologies.
  • Support manufacturing technology transfer, as appropriate.

Minimum Requirements:

  • MS or BS in pharmaceutical sciences, biochemistry, chemical engineering or other related discipline with 4+ or 8+, respectively, years relevant experience, Ph.D. in a similar discipline with 0-4 years relevant experience.
  • Minimum 3 years hands-on experience in biologic product development and analytical testing using biophysical and biochemical, characterization methods, such as general appearance, opalescence, osmolality, MFI, HIAC, viscosity, HPLC, DLS, DSC, and CD spectroscopies.
  • Excellent planning, verbal and written communication skills.

Preferred Qualifications:

  • Formulation and/or process development experience including the analysis or characterization of proteins required.
  • Experience in application of a statistical software (eg. JMP), or implementation of QbD elements.
  • Highly motivated individual, with ability to work in a team environment and build productive relationships within or across departments.
  • Ability to troubleshoot and determine creative solutions to achieve better processes.
  • Experience in GMPs, biopharmaceutical industry and/or writing of regulatory submission documents.
  • Proficient in Microsoft Office Suite of Programs.

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