Project Leader, Bioanalytical

Location: Laval, Quebec

Position Type: Permanent | Full-Time

Work Arrangement: On-site

Schedule: 36.25 hours/week | Monday to Friday (Daytime)

About the Opportunity

Groom & Associates is currently partnering with a well-established and growing bioanalytical laboratory to recruit an experienced Project Leader, Bioanalytical

This opportunity is ideal for a scientific professional who enjoys ensuring the integrity, quality, and compliance of bioanalytical data within a GLP-regulated environment. Working alongside experienced scientific leadership, you will play a key role in reviewing bioanalytical data generated from clinical and non-clinical studies while contributing to the delivery of high-quality results for pharmaceutical and biotechnology clients.

This position also offers excellent long-term career growth within a collaborative scientific environment.

Key Responsibilities

- Perform comprehensive review of raw and processed bioanalytical data generated using LC-MS/MS.
- Review chromatograms, analytical sequences, calibration curves, quality controls, and study sample results.
- Review method validation data and sample analysis for both clinical and non-clinical studies.
- Verify data accuracy, integrity, completeness, and compliance with applicable regulatory requirements.
- Ensure all activities are conducted in accordance with Good Laboratory Practices (GLP), Standard Operating Procedures (SOPs), FDA, EMA, and other applicable guidelines.
- Prepare, review, and finalize analytical reports and supporting scientific documentation.
- Identify discrepancies, investigate data issues, and collaborate with laboratory personnel to resolve findings.
- Communicate with clients regarding project progress and scientific deliverables when required.




- Work closely with Scientific Leadership, Principal Investigators, Operations, and Quality Assurance to ensure project timelines and quality expectations are achieved.
- Participate in continuous improvement initiatives to optimize laboratory processes and data quality.

Qualifications

- DEC or Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Life Sciences, or another related scientific discipline.
- Minimum of two (2) years of full time experience as a Bioanalytical Data Reviewer/Bioanalytical Scientist within a GLP-regulated laboratory.
- Strong understanding of LC-MS/MS bioanalysis and bioanalytical workflows.
- Experience reviewing chromatographic data, analytical reports, method validations, and regulated laboratory documentation.
- Working knowledge of bioanalytical extraction techniques including:
- Solid Phase Extraction (SPE)
- Liquid-Liquid Extraction (LLE)
- Protein Precipitation
- Thorough understanding of GLP regulations and familiarity with FDA and EMA guidance.
- Experience preparing and reviewing scientific and technical reports.
- Excellent analytical thinking, attention to detail, and organizational skills.
- Ability to manage multiple priorities while maintaining exceptional quality standards.
- Strong communication and collaboration skills.

Preferred Background

Experience gained within pharmaceutical, CRO, or bioanalytical laboratories specializing in regulated LC-MS/MS bioanalysis.

What Our Client Offers

- Permanent full-time opportunity
- Competitive compensation based on experience
- Comprehensive group benefits program
- Employer-matched retirement savings plan
- Paid personal and sick days
- Supportive and cooperative scientific environment
- Long-term career development opportunities
- Free parking and convenient access to public transportation

📌 Project Leader, Bioanalytical (Laval)
🏢 Groom u0026 Associés / Associates
📍 Laval