Senior Research Analyst
- Laval, QC, Canada
Full-time
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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
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.
- 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 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 laboratory staff.
Requirements
Requires an MSc in Chemistry, Pharmaceutical Sciences, or a related field, along with at least five years of pharmaceutical analytical development experience. Candidates should have strong knowledge of GMP, method validation, stability programs, chromatography systems, and laboratory software, as well as 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
- Project Planning
- Team Leadership
- Training and Mentoring
- CDS
- LIMS
- ELN
- Problem-Solving
Visa sponsorship
Not detected in the job text
Categories
- Science & Research
- Manufacturing
- Management & Leadership
- Data & Analytics
Keywords
- Analytical Development
- Drug Products
- Analytical Method Development
- Method Validation
- Good Manufacturing Practice
- GMP
- Stability Studies
- OOS Investigations
- OOT Investigations
- Chromatography
- CDS
- LIMS
- ELN
- SLIM
- Data Integrity
- Laboratory Operations
- Analytical Equipment
- Pharmaceutical Manufacturing
- Project Timelines
- Data Analysis
- Laboratory Documentation
- Safety Compliance
- Team Mentorship