About The Position

Develop and optimize formulations for oral solid dosage forms (tablets, capsules, and modified release products). Conducting pre-formulation studies, excipient compatibility assessments, and dissolution profiling. Supporting analytical method development and validation for assay, dissolution, and stability- indicating methods. Design and execute stability studies as per ICH guidelines to establish product shelf life. Perform troubleshooting of formulation and analytical issues during development and scale-up. Collaborate with manufacturing and quality teams for pilot-scale and commercial-scale technology transfer. Prepare technical reports, development documents, and regulatory submission support (ANDA/CTD). Ensure strict adherence to cGMP, GLP, and regulatory requirements throughout the development process.

Requirements

  • Master’s degree in Pharmacy or Chemistry or Pharmaceutics, or related field.
  • 12 months of experience in the position or in a related position.

Responsibilities

  • Develop and optimize formulations for oral solid dosage forms (tablets, capsules, and modified release products).
  • Conduct pre-formulation studies, excipient compatibility assessments, and dissolution profiling.
  • Support analytical method development and validation for assay, dissolution, and stability-indicating methods.
  • Design and execute stability studies as per ICH guidelines to establish product shelf life.
  • Perform troubleshooting of formulation and analytical issues during development and scale-up.
  • Collaborate with manufacturing and quality teams for pilot-scale and commercial-scale technology transfer.
  • Prepare technical reports, development documents, and regulatory submission support (ANDA/CTD).
  • Ensure strict adherence to cGMP, GLP, and regulatory requirements throughout the development process.
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