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Altasciences

QC Reviewer (BSD)

Laval, QC, Canada

Full-time

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Job details

Job type: Full-time
Apply by: Dec 3, 2026
Experience: Experience in the medical and/or pharmaceutical fields with typically 3 years of experience in data review and quality control field.
Posting language: English
Posted: Nov 3, 2026

Original job description

About The Role

The QC Reviewer (BSD) is responsible to perform the quality control for data generated and work conducted in the laboratory.

What You'll Do Here

Ensures that all batch related documentation is completed accurately and in a timely manner by the analysts and that all procedures are respected as per the company’s SOPs.
Based on training QC reviewer can draft study documents for BPI review such as Memo to File, SOP/Protocol/Study Plan deviations., perform quality control batch review by performing multi-batch trend analysis, and compile study documentation,
Based on training, provide report and/or final results within study timelines and ensure any deviation, exception or events are reflected as appropriate and assure that all analysis conducted are reported and accurate for the review of the Bioanalytical Principal Investigator .
Based on training, responsible for daily in process quality control for batches ongoing in the lab.
Raises any flags to line manager regarding any quality issue or trends observed and is part of addressing these issues in an appropriate manner.
Supports responses to QA reports.
Monitors the quality within the laboratory according to GLP, regulatory agencies requirements and internal SOPs.
Supports and mentors analysts in the daily laboratory documentation procedures and processes.
Can participate in basic training of laboratory staff.
Could be assigned to ensure that the verification of laboratory instruments is performed as required by the internal procedures.
Could be assigned to ensure harmonization of techniques, process and documentation between analysts in the laboratory.
May be required to participate in laboratory inspections: executes and reports deviations and any health and safety concerns.
As assigned, assist for planning sample analysis by maintaining timeline and scheduling commitments.
Stays up to date on new SOPs, procedures, and techniques via training sessions, team meetings and internal communication avenues and observes all company guidelines and policies.
Respecting Health and Safety standards in terms of personal protection, laboratory maintenance, and work procedures.

What You'll Need To Succeed

College degree and/or University degree in Chemistry, Biochemistry or Immunology or equivalent field.
Pertinent experience may be considered in lieu.
Experience in the medical and/or pharmaceutical fields with typically 3 years of experience in data review and quality control field.
Must understand general SOPs and have knowledge of GLP regulations.
Proven organizational skills
Excellent attention to details with respect to sample preparation procedures and raw data handling.
Strong communication and leadership skills.
Ability to work cross functionally.
Good MS Office skills.

Altasciences Strives To Provide a French Work Environment For Its Employees In Quebec. Altasciences Has Taken All Reasonable Measures To Avoid Imposing The Above Language Requirement. This Requirement Is Essential For The Position Of QC Reviewer (BSD) In Particular, But Without Limitation, For The Following Reason(s)

The requirement to have study protocols read and documented in English as required by industry regulatory agencies

What We Offer

Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.

Altasciences' Benefits Package Includes

Health/Dental/Vision Insurance Plans
401(k)/RRSP with Employer Match
Paid Vacation and Holidays
Paid Sick and Bereavement Leave
Employee Assistance & Telehealth Programs

Altasciences' Incentive Programs Include

Training & Development Programs
Employee Referral Bonus Program
Annual Performance Review

Apply About employer

More about this job

Responsibilities

Review laboratory data, batch records, and study documentation for accuracy, completeness, and compliance with GLP, regulatory requirements, and internal SOPs. Support analysts through mentoring and training, identify and address quality issues, and help maintain study timelines and laboratory processes.

Requirements

A college or university degree in Chemistry, Biochemistry, Immunology, or an equivalent field is required, although relevant experience may substitute. The role typically requires three years of experience in data review and quality control, knowledge of SOPs and GLP, strong organizational and communication skills, attention to detail, cross-functional collaboration, and Microsoft Office proficiency.

Skills

Quality Control
Data Review
Batch Documentation Review
Multi-Batch Trend Analysis
Good Laboratory Practice (GLP)
Standard Operating Procedures (SOPs)
Regulatory Compliance
Raw Data Handling
Sample Preparation
Study Documentation
Deviation Management
Laboratory Instrument Verification
Analyst Mentoring
Organizational Skills
Attention to Detail
Microsoft Office

Benefits

Health Insurance
Dental Insurance
Vision Insurance
401(k)/RRSP With Employer Match
Paid Vacation
Paid Holidays
Paid Sick Leave
Bereavement Leave
Employee Assistance Program
Telehealth Programs
Training and Development Programs
Employee Referral Bonus Program
Annual Performance Review

Visa sponsorship

Not detected in the job text

Keywords

Quality Control
Bioanalytical Laboratory
Data Review
Batch Review
Multi-Batch Trend Analysis
Good Laboratory Practice (GLP)
Standard Operating Procedures (SOPs)
Regulatory Compliance
Study Protocols
Study Plans
Study Documentation
Memo to File
Deviations
Raw Data
Sample Preparation
Laboratory Instruments
Instrument Verification
Quality Assurance Reports
Health and Safety
Analyst Training
Laboratory Inspections
Timeline Planning
Microsoft Office
Chemistry
Biochemistry
Immunology

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