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Added 2 mins ago
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Corealis Pharma Inc.

Formulation Assistant

Laval, QC, Canada

Full-time

Apply About employer

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Job details

Job type: Full-time
Apply by: Oct 31, 2026
Posting language: English
Posted: Aug 7, 2026

Original job description

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.

Apply About employer

More about this job

Responsibilities

Support oral solid dosage formulation and pharmaceutical process development, including R&D batch preparation, GMP pilot plant activities, and sourcing laboratory supplies. Characterize APIs, develop and test formulations and manufacturing processes, conduct stability studies, prepare prototypes for animal pharmacokinetic studies, and write technical reports.

Requirements

The role requires a B.Sc. in Pharmaceutical Sciences, a master’s degree in Drug Development, or equivalent relevant work experience. It calls for practical capability in pharmaceutical formulation development, API characterization, physical testing, and GMP pilot plant support.

Skills

Formulation Development
Pharmaceutical Process Development
Active Pharmaceutical Ingredient Characterization
XRPD
DSC
TGA
DVS
Particle Size Distribution
Density and Flowability Testing
Compression Testing
Dosage Form Selection
Excipient Selection
GMP Pilot Plant Support
Physical Testing
Stability Studies
Technical Report Writing

Visa sponsorship

Not detected in the job text

Keywords

Oral Solid Dosage
Formulation Development
Pharmaceutical Process Development
Active Pharmaceutical Ingredients
XRPD
DSC
TGA
DVS
Particle Size Distribution
Density
Flowability
Compression Testing
Tablets
Capsules
Sachets
Excipients
GMP
Pilot Plant
Weight Variation
Hardness
Friability
Disintegration
Polymorphic Form Assessment
Loss on Drying
Stability Studies
Pharmacokinetic Studies
Animal Models
Technical Reports
Packaging
R&D

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