About The Position

The Senior Scientist, MS&T, is responsible for contributing to research and development activities across the product lifecycle—from pre-formulation through product development to successful commercialization. This role contributes to the scientific and technical aspect of designing robust formulations, optimizing manufacturing processes, and ensuring seamless technology transfer.

Requirements

  • Bachelors Degree (BA/BS) in chemistry or other relevant Pharmaceutical Sciences - Required
  • 8 years or more experience in the pharmaceutical development demonstrating the application of scientific principles (with Bachelor's Degree)
  • In depth knowledge of pharmaceutical chemistry and understanding of pharmaceutics in developing complex dosage forms and drug delivery systems
  • Knowledge of Pharmaceutical process validation techniques, product lifecycle management
  • Knowledge of critical aspects of BE studies and application in the oral solid dosage forms

Nice To Haves

  • Master Degree (MS/MA) in chemistry or other relevant Pharmaceutical Sciences - Preferred
  • Ph. D. in chemistry or other relevant Pharmaceutical Sciences - Preferred
  • 6 years or more experience in the pharmaceutical development demonstrating the application of scientific principles (with Master's Degree)
  • less than one year experience in the pharmaceutical development demonstrating the application of scientific principles (with Ph.D.)

Responsibilities

  • Collaborate in the design and development of a range of pharmaceutical dosage forms, including modified-release and immediate-release oral solids and powders for suspension, contributing to cross-functional team efforts.
  • Apply a deep understanding of formulation science, material properties, and pharmacokinetics to ensure robust product performance.
  • Guide formulation strategies that align with therapeutic goals, regulatory expectations, and commercial feasibility.
  • Write and critically review process performance qualification (PPQ) protocols and reports, cleaning verification and validation protocols, and other technical study plans required throughout the product lifecycle.
  • Ensure all documentation meets regulatory standards and supports a state of control in manufacturing processes.
  • Collaborate with Quality Assurance and Validation teams to ensure seamless execution and compliance.
  • Implement timely execution of projects starting with the selection of raw materials, packaging components, formulation strategy, scientific development and process scale up.
  • Draft comprehensive technical reports and project presentations that clearly communicate development progress, scientific rationale, and outcomes.
  • Collaborate closely with Analytical Development, Regulatory Affairs, and Manufacturing teams to align on project goals, resolve challenges, and meet submission timelines.
  • Evaluate analytical data to inform formulation decisions and ensure product quality.
  • Provide mentorship and technical guidance to junior scientists in experimental design, data interpretation, and troubleshooting.
  • Foster a collaborative and innovative lab environment that encourages scientific curiosity and continuous learning.
  • Apply scientific creativity and critical thinking to solve complex formulation and process development problems.
  • Leverage literature, prior knowledge, and experimental data to propose and implement effective solutions.
  • Contribute to the preparation of regulatory documents such as ANDA submissions, ensuring clarity, accuracy, and scientific justification.
  • Provide technical support for both commercial and non-commercial manufacturing operations.
  • Troubleshoot formulation and process-related issues, identify root causes, and implement corrective actions.
  • Recommend process improvements to enhance efficiency, yield, and product quality, contributing to continuous improvement initiatives across the organization.
  • Other duties as assigned.

Benefits

  • health and insurance benefits
  • 401(k) matching contribution
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