Analytical Scientist - Dissolution & Method Dev

Teva

Florida

On-site

USD 65,000 - 90,000

Full time

14 days+

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Benefits offered by this job

Health Insurance
401(k) with employer match
Paid Time Off
Life and Disability Insurance

Job summary

Teva Pharmaceuticals is seeking an Analytical Scientist to join the Analytical Research & Development team in New York. You will support analytical characterization and dissolution testing of oral solid dosage forms and related drug substances, contributing to method development and data interpretation under scientific guidance.

The role involves executing analytical methods, maintaining records, and ensuring compliance with cGMP and data integrity standards, while developing proficiency in

Qualifications

  • Bachelor’s or master’s degree in chemistry, biochemistry, pharmaceutical sciences, or a related scientific discipline.
  • Bachelor’s degree with at least three (3) years of relevant pharmaceutical or biopharmaceutical experience, or a master’s degree with relevant laboratory experience.
  • Foundational knowledge of analytical chemistry, pharmaceutical analysis, and basic principles relevant to oral solid dosage forms.
  • Ability to analyze and interpret experimental data, identify trends, and communicate scientifically sound conclusions.
  • Ability to organize and prioritize multiple laboratory activities, work independently within assigned responsibilities, and collaborate effectively in a team environment.
  • Effective written and verbal communication skills, with strong attention to detail, scientific accuracy, and documentation quality.
  • Working knowledge of Microsoft Office applications, including Word, Excel, and PowerPoint.

Responsibilities

  • Perform dissolution testing and analytical characterization of drug substances and drug products, with emphasis on oral solid dosage forms.
  • Execute dissolution and related analytical method-development, optimization, feasibility, and troubleshooting studies using approved study plans or protocols, as applicable.
  • Conduct analytical testing using HPLC, UV-Vis spectroscopy, dissolution instrumentation, and other relevant laboratory technologies.
  • Execute laboratory experiments under appropriate scientific guidance and evaluate the effects of formulation, material, and manufacturing-process variables on product performance.
  • Analyze, interpret, trend, and summarize experimental data; prepare clear tables, figures, presentations, and basic scientifically justified conclusions.
  • Maintain complete, accurate, attributable, and contemporaneous laboratory records, including notebooks, worksheets, electronic data, and supporting documentation.
  • Support data review and the investigation and resolution of method, instrument, or testing issues; document observations and elevate concerns appropriately.
  • Perform routine instrument checks and support instrument maintenance, as assigned.
  • Conduct laboratory work safely and in accordance with applicable procedures, cGMP requirements, data-integrity principles, and environmental, health, and safety standards.
  • Develop proficiency in relevant scientific principles, analytical techniques, laboratory software, and regulatory expectations through training and practical application.

Skills

Analytical chemistry
Data interpretation
Documentation
Microsoft Office
Laboratory teamwork

Education

Bachelor’s or Master’s degree in chemistry/biochemistry/pharmaceutical sciences

Tools

HPLC
UV-Vis spectroscopy
Dissolution instrumentation
cGMP awareness

Job description

Teva Pharmaceuticals is seeking an Analytical Scientist to join the Analytical Research & Development team in New York. You will support analytical characterization and dissolution testing of oral solid dosage forms and related drug substances, contributing to method development and data interpretation under scientific guidance.

The role involves executing analytical methods, maintaining records, and ensuring compliance with cGMP and data integrity standards, while developing proficiency in

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