LC-MS​/MS Bioanalysis Data Reviewer

LC-MS/MS Bioanalysis Data Reviewer

LC-MS/MS Bioanalysis Data Reviewer

Location:

Laval, Quebec
Position Type:
Permanent | Full-Time
Work Arrangement:
On-site

Schedule:

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:
o Solid Phase Extraction (SPE)
o Liquid-Liquid Extraction (LLE)
o 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 collaborative scientific environment

• Long-term career development opportunities

• Free parking and convenient access to public transportation

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