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