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Corealis Pharma Inc.

Analytical Techician

Laval, QC, Canada

Job type: Full-time
Apply by: Oct 3, 2026

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At a glance

Automatically prepared from the listing. Check the original description for the full requirements.

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Responsibilities

Perform pharmaceutical product development analyses using techniques like HPLC and titration while ensuring compliance with GMP and SOPs. Maintain laboratory documentation, manage reagent inventory, and conduct off-spec research.

Requirements

Requires a Diploma of Collegiate studies and 3 years of related work experience. Candidates must be bilingual in English and French with proficiency in MS Office 365.

Experience

2 to 5 years

Education

associate degree

Working hours

40 hours per week

Work arrangement

On-site

Skills

HPLC
Sample Preparation
Titration
Dissolution
Stability Analysis
Physical Characterisation
GMP
SOP
MS Office 365
Bilingual English/French

Visa sponsorship

Not detected in the job text

Keywords

Pharmaceutical Manufacturing
HPLC
Titration
Dissolution
Stability Analyses
API
GMP
SOP
Analytical Chemistry
Laboratory Maintenance
Off-spec Research
Pharmaceutical Development
MS Office 365

Original job description

Tasks And Responsibilities

Carrying out analyses relating to pharmaceutical product development work using various analytical techniques and equipment.
This may include, but is not limited to
HPLC
Sample preparation
Titration
Dissolution
Stability analyses
Physical characterisation of API, intermediates, and finished products
Conducting off-spec research
Respect the safety and hygiene rules of the laboratory;
Master the different analytical methods and techniques, and the operation of the equipment;
Respect deadlines and priorities;
Maintain all relevant documentation of their activities;
Respect the SOPs and GMPs relating to their work;
Actively participate in all required analytical investigations;
Monitor and carry out inventory of reagents, standards and chromatographic columns as required.
Ensure general maintenance of the laboratory.
Carry out analyses according to instructions, transcribe data into relevant reports, evaluate data against R & D / GMP criteria with guidance from supervisor.
Perform all related duties.

Qualifications

Diploma of Collegiate studies
3 years of prior work experience in a related field
Bilingual (English, French)
Computer skills (MS Office 365)

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