Analytical Laboratory Technician

COREALIS Pharma Inc.; Laval (administrative region); On-site; CAD 45,000 - 55,000; Full time

Benefits offered by this job

Extended health care

Life insurance

Paid time off

Employer-matched RRSP

Job summary

COREALIS Pharma Inc. is seeking an analytical laboratory professional in Laval to perform analyses across pharmaceutical development activities.

You will work with HPLC, titration, dissolution and stability testing, ensuring accurate documentation and compliance with GMP/SOPs. The candidate should have a DEC in a related field, at least 3 years of lab experience, and be fluent in English and French, with proficiency in Microsoft Office 365.

Qualifications

• DEC in Chemistry, Biochemistry, Laboratory Technology, Pharmaceutical Sciences, or related field.
• Minimum of 3 years of experience in a related laboratory environment.
• Bilingual English and French.
• Proficient in Microsoft Office 365.

Responsibilities

• Perform analyses using analytical techniques and laboratory instrumentation as described (HPLC, titration, dissolution, stability).
• Adhere to SOPs, GMP, health and safety procedures, and maintain documentation.
• Meet established timelines and priorities; document results accurately.
• Monitor inventories of reagents, reference standards, and columns; ensure lab is organized and maintained.
• Participate in analytical investigations and evaluate data under supervisor guidance.
• Perform other related duties as assigned.

Skills

Bilingual English/French

Microsoft Office 365

Education

DEC in Chemistry or related field

Tools

HPLC

Titration

Dissolution testing

Stability testing

Job description

Perform analyses related to pharmaceutical product development activities using a variety of analytical techniques and laboratory instrumentation. This includes, but is not limited to:

• High Performance Liquid Chromatography (HPLC)
• Titration
• Dissolution testing
• Stability testing
• Physical characterization of APIs, intermediates, and finished products
• Out-of-Specification (OOS) investigations

The successful candidate will also:

• Adhere to laboratory health, safety, and hygiene procedures;
• Demonstrate proficiency in analytical methods, laboratory techniques, and the operation of analytical instruments;
• Meet established timelines and priorities;
• Maintain accurate and up-to-date documentation related to laboratory activities;
• Comply with Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP);
• Actively participate in analytical investigations as required;
• Monitor and maintain inventories of reagents, reference standards, and chromatographic columns;
• Ensure the general upkeep and organization of the laboratory;
• Perform analyses according to approved procedures, accurately document results in laboratory reports, and evaluate data against R&D and GMP acceptance criteria under the guidance of the supervisor;
• Perform other related duties as assigned.

Qualifications

• Diploma of Collegial Studies (DEC) in Chemistry, Biochemistry, Laboratory Technology, Pharmaceutical Sciences, or a related field;
• Minimum of 3 years of experience in a related laboratory environment;
• Bilingual (English and French);
• Proficient in Microsoft Office 365.

Job Type

Full-time, Permanent

Starting at $50,000 per year

Benefits

• Extended health care
• Life insurance
• Paid time off
• Employer-matched Registered Retirement Savings Plan (RRSP)

Location Requirements

Commute or Relocation

Must be able to reliably commute to Laval, Québec, or relocate before starting employment (required).

Education

Diploma of Collegial Studies (DEC) (preferred)

Experience

Laboratory experience: 3 years (preferred)

Work Location

On-site