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.
Apply now Each role is integral to advancing OSD solutions and offers a unique chance to contribute to meaningful, industry-leading work.
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📌 Formulation & Process Development Assistant (Quebec City)
🏢 Corealis Pharma
📍 Quebec City