Senior Research Analyst

Corealis Pharma Inc.; Laval (administrative region); On-site; CAD 100,000 - 140,000; Full time

Job summary

Corealis Pharma Inc. in Laval invites a Senior Research Analyst to lead analytical development and support GMP laboratory operations for drug product development. You will plan, validate methods, analyze data, and ensure compliance while mentoring analysts and technicians.

The role requires a MSc in Chemistry or related field, 5+ years in pharmaceutical analytics, strong GMP knowledge, and experience with CDS, LIMS, ELN. In-person work location expected.

Qualifications

• MSc in Chemistry, Pharmaceutical Sciences, or related field is required.
• 5+ years of experience in analytical development in the pharmaceutical industry.
• Strong knowledge of GMP, method validation, and stability programs.
• Experience with chromatography systems and laboratory software (CDS, LIMS, ELN).
• Strong leadership, organization, and problem-solving skills.

Responsibilities

• Develop and validate analytical methods for drug products.
• Plan and execute analytical activities aligned with project timelines; analyze data and provide insights.
• Manage GMP stability studies and investigate OOS/OOT results.
• Oversee daily lab activities and documentation; ensure GMP, safety, and data integrity compliance.
• Support analytical equipment, CDS, and stability systems (e.g., SLIM, ELN, LIMS).
• Train and mentor analysts and technicians.

Skills

Leadership

Organization

Problem-solving

Education

MSc in Chemistry, Pharmaceutical Sciences, or related field

Tools

Chromatography systems

CDS

LIMS

ELN

Job description

Position Overview

We are seeking a Senior Research Analyst to lead analytical development and support GMP laboratory operations. This role combines scientific expertise, project leadership, and team mentorship to ensure high-quality, compliant analytical results that support drug product development.

Key Responsibilities

• Development and validation of analytical methods for drug products.
• Plan and execute analytical activities aligned with project timelines. Analyze data and provide actionable insights.
• Manage GMP stability studies and investigate OOS/OOT results.
• Oversee daily lab activities and documentation. Ensure compliance with GMP, safety, and data integrity standards.
• Support analytical equipment, CDS, and stability systems (e.g., SLIM, ELN, LIMS).
• Train and mentor analysts and technicians.

Qualifications

• MSc in Chemistry, Pharmaceutical Sciences, or related field
• 5+ years in analytical development in the pharmaceutical industry
• Strong knowledge of GMP, method validation, and stability programs
• Experience with chromatography systems and laboratory software (CDS, LIMS, ELN)
• Strong leadership, organization, and problem-solving skills

Work Location: In person