Analytical Techician

Corealis Pharma Inc.; Laval (administrative region); On-site; CAD 42,000 - 65,000; Full time

Job summary

Corealis Pharma Inc. seeks a laboratory analyst to perform analyses for pharmaceutical product development using HPLC, titration, and dissolution techniques. You will ensure GMP compliance, maintain documentation, and manage laboratory inventory under supervision.

The role requires a Diploma of Collegiate studies, 3 years of related experience, and bilingual English/French, with strong MS Office skills. This is a full-time on-site position located in Laval, Quebec, Canada.

Qualifications

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

Responsibilities

• Carry out analyses relating to pharmaceutical product development work using various analytical techniques and equipment.
• Carry out analyses according to instructions, transcribe data into relevant reports, evaluate data against R & D / GMP criteria with guidance from supervisor.
• Monitor and carry out inventory of reagents, standards and chromatographic columns as required.
• Ensure general maintenance of the laboratory.
• Maintain all relevant documentation of activities and respect SOPs and GMPs.

Skills

Bilingual English/French

Computer skills

Education

Diploma of Collegiate studies

Tools

HPLC

Titration

Dissolution

Stability analyses

Job description

• Carrying out analyses relating to pharmaceutical product development work using various analytical techniques and equipment.
• This may include, but is not limited to
• HPLC
• 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.

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)