LC-MS/MS Bioanalysis Data Reviewer

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LC-MS/MS Bioanalysis Data Reviewer

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 LC-MS/MS Bioanalysis Data Reviewer.

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 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.
• Bilingualism (French and English) is considered an asset.

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 collaborative scientific environment
• Long-term career development opportunities
• Free parking and convenient access to public transportation