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Curricular Internship - Drug Formulation Development (Pharmaceutical Writing)

On-site in Coim·Added 6 days ago (last checked 22 Oct)

Bluepharma

5 open roles

Our summary

Work mode
On-site, Coim

This job advert was originally written in Portuguese.

The role

Main Responsibilities

  • Participate in the definition and scientific justification of critical product parameters, including excipient selection, physicochemical properties of the drug, dissolution profile, and compatibility, developing well-founded scientific rationales;
  • Participate in the review and improvement of product development risk assessments, so that they may be integrated into regulatory dossiers;
  • Build and update technical databases, ensuring traceability and consistency of scientific information;
  • Assist in the preparation of technical and scientific documentation (reports and protocols) related to Formulation Development.

Requirements

  • Master's Integrated/Bachelor's student in Pharmaceutical Sciences, Pharmaceutical Technology;
  • Interest in Quality by Design (QbD) methodologies and in risk assessment tools applied to pharmaceutical development;
  • Ability for critical analysis and synthesis of scientific information;
  • Proficiency in the English Language;
  • IT knowledge from a user perspective.

About Bluepharma

Industry
Pharmaceuticals
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