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Senior Research Analyst – Analytical Development
- Laval, QC, Canada
Full-time
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Job details
- Job type
- Full-time
- Closing date
- Posting language
- English
- Posted
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Archived listing. The details below describe a past opening.
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
The role focuses on leading analytical development and supporting GMP laboratory operations to ensure high-quality drug product results. Key duties include validating analytical methods, managing stability studies, and mentoring laboratory staff.
Requirements
Candidates must hold an MSc in Chemistry or Pharmaceutical Sciences with over 5 years of experience in pharmaceutical analytical development. Proficiency in GMP standards, chromatography systems, and laboratory software like LIMS and ELN is required.
Skills
- Analytical Method Development
- Method Validation
- GMP Compliance
- Stability Studies
- Chromatography
- LIMS
- ELN
- CDS
- OOS/OOT Investigation
- Project Leadership
- Team Mentorship
- Data Integrity
Visa sponsorship
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Categories
- Science & Research
- Manufacturing
- Healthcare
- Management & Leadership
- Engineering
Keywords
- Analytical Development
- GMP
- Method Validation
- Stability Programs
- Chromatography
- CDS
- LIMS
- ELN
- SLIM
- OOS
- OOT
- Pharmaceutical Manufacturing
- Data Integrity
- Drug Product Development
- Laboratory Operations