Back to results

Senior Research Analyst – Analytical Development

  • Laval, QC, Canada

Full-time

Applications open in a new tab.

Job details

Job type
Full-time
Apply by
Posting language
English
Posted

Original 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
More about this job

Responsibilities

Develop and validate analytical methods, plan and execute project-aligned analytical activities, analyze results, and manage GMP stability studies and OOS/OOT investigations. Oversee laboratory operations and documentation, maintain compliance and analytical systems, and train and mentor analysts and technicians.

Requirements

An MSc in Chemistry, Pharmaceutical Sciences, or a related field and at least five years of pharmaceutical-industry experience in analytical development are required. Candidates should have strong knowledge of GMP, method validation, and stability programs, experience with chromatography and laboratory software, and strong leadership, organizational, and problem-solving skills.

Skills

  • Analytical Method Development
  • Method Validation
  • GMP Compliance
  • Stability Studies
  • Chromatography
  • Data Analysis
  • OOS/OOT Investigations
  • Laboratory Operations
  • Data Integrity
  • CDS
  • LIMS
  • ELN
  • Project Leadership
  • Team Mentorship
  • Problem-Solving

Visa sponsorship

Not detected in the job text

Categories

  • Science & Research
  • Manufacturing
  • Management & Leadership
  • Healthcare

Keywords

  • Analytical Development
  • Drug Products
  • Analytical Method Development
  • Method Validation
  • GMP
  • Stability Studies
  • OOS/OOT Investigations
  • Chromatography
  • CDS
  • LIMS
  • ELN
  • SLIM
  • Data Integrity
  • Laboratory Operations
  • Pharmaceutical Manufacturing
  • Project Timelines
  • Data Analysis
  • Laboratory Documentation
  • Safety Compliance
  • Team Mentorship

Report this job