Primary Responsibility

- Support oral solid dosage formulation development and pharmaceutical process development activities.

General Duties And Responsibilities

- Provide technical support to formulators during R&D; activities (e.g., literature reviews, equipment setup and cleaning, manufacturing, packaging, and physical testing of R&D; batches).

- Support technical and quality activities within the GMP pilot plant.

- Source laboratory consumables, equipment, and accessories, and provide purchasing recommendations.

- Perform other related duties as required.

Specific Duties And Responsibilities

- Characterize active pharmaceutical ingredients (APIs) using XRPD, DSC, TGA, DVS, particle size distribution (PSD), density, flowability, compression testing, and other analytical techniques.

- Develop formulations and manufacturing processes.





- Select dosage forms (tablets, capsules, sachets), inactive ingredients (excipients), manufacturing processes, and packaging configurations.

- Analyze formulations, including weight variation, hardness, friability, disintegration, API polymorphic form assessment, moisture content determination (LOD), and other physical tests.

- Conduct stability studies.

- Prepare prototype formulations for pharmacokinetic studies in animal models.

- Prepare technical reports.

Qualifications And Skills

- B.Sc. in Pharmaceutical Sciences, Master’s degree in Drug Development, or equivalent relevant work experience.

Reporting To

- Immediate Supervisor: To be determined.

📌 Formulation Assistant (Laval)
🏢 Corealis Pharma
📍 Laval