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Added 14 mins ago
TT
10. SEO Client Success Advocate
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- Full-time
Since 1997 Online Marketing Team and Website Marketing Experts Global & Local Digital Marketing Services Website Design + Web Development Company
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Land Stewardship Manager
Government of Manitoba
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- Full-time
Reporting to the Section Manager of the Habitat & Endangered Species Section, the incumbent is responsible for the leadership, development and management of the Land Stewardship Unit…
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M
Manager, National Tax Services
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- Full-time
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Added 14 mins ago
V
Maintenance Manager
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- Full-time
…technical team, the operation is entering an exciting stage of development, creating an opportunity for a Maintenance & Asset Manager to play a key role in building and leading its…
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RG
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Project Manager – Engineering
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Contribute to the firm's growth and business development efforts;
Added 43 mins ago
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Project Manager – Engineering
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Contribute to the firm's growth and business development efforts;
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Registered Nurse (Full Time) | CVH - CVH Emergency
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CO
Job ID #32266: Manager, Vacant Unit Tax & General Revenue
City of Hamilton
Hamilton, ON
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Job ID #32267: Manager, Provincial Offences
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Hamilton, ON
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Job ID #31786: Health, Safety & Wellness Specialist
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Added 1 hour ago
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Manager, Chapter Operational Excellence
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Branch Manager
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Manager, Internal Controls
Husky Technologies
Bolton, ON
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Working with Internal Audit and the global Finance and Operations teams, the Manager, Internal Controls will play a critical role in Husky’s global financial reporting. This includes the…
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OI
HCA Program Manager
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Vancouver, BC
- $85,000 to $100,000 CAD / year
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Senior Advisor, Program Governance
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Montreal, QC
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Working closely with the Commercial Financing Transformation Program Manager (Pillar 5), pillar leaders, initiative owners and delivery teams, you contribute to the operation and evolution…
Added 1 hour ago
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Marketing Associate Intern, Severe Asthma & Nasal Polyps - Mississauga or Montreal
GSK
Hamilton, ON · Mississauga, ON · Oakville, ON · Toronto, ON · Montreal, QC
- $31,980 to $79,950 CAD / year
- Full-time
We combine the science of the immune system with advanced technologies, enhanced by targeted business development and world-class partnerships, to develop new medicines and vaccines that…

Altasciences

QC Reviewer, LBA

Laval, QC, Canada

Full-time

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Job details

Job type: Full-time
Experience: Minimum of 2 years of experience in the medical and/or pharmaceutical fields
Posting language: English
Posted: Aug 31, 2026

Original job description

About The Role

Le/la Réviseur(se) contrôle qualité, LBA est chargé(e) d'effectuer les contrôles de qualité des données générées et des travaux réalisés au sein du laboratoire afin de garantir leur exactitude, leur conformité et le respect des normes applicables.

What You’ll Do Here

Ensure that all batch-related documentation is completed accurately and on time by the analysts, and that all procedures are followed in accordance with the company’s standard operating procedures (SOPs)
Conduct daily in-process quality control for batches currently being processed in the laboratory
Provide support in responding to quality assurance reports
Monitor quality within the laboratory in accordance with Good Laboratory Practice (GLP), regulatory requirements, and internal Standard Operating Procedures (SOPs)
Guide and supervise analysts in the laboratory’s daily documentation procedures and processes
Ensure that laboratory instrument calibration is performed in accordance with internal procedures.
Ensure consistency in techniques, processes, and documentation among laboratory analysts.
Report quality issues or trends to the line manager and participate in resolving them.
May be required to participate in laboratory inspections: identify and report nonconformities as well as any health and safety issues.
Based on their training, be able to draft study documents for review by the bioanalytical manager (BPI), such as notes for inclusion in the file, reports on deviations from standard operating procedures (SOPs), the protocol, or the study plan; perform quality control on batches by conducting trend analyses across multiple batches; and compile study documentation
Depending on their training, be able to provide reports and/or final results within the study’s specified deadlines, ensure that any deviations, exceptions, or events are properly documented, and ensure that all analyses performed are recorded and accurate for review by the principal investigator in bioanalysis
Contribute to the planning of sample analysis by meeting deadlines and honoring scheduling commitments.
Stay informed about standard operating procedures (SOPs), procedures, and techniques through training sessions, team meetings, and internal communication channels, and comply with all company guidelines and policies
Comply with health and safety standards regarding personal protective equipment, laboratory maintenance, and work procedures

What You’ll Need to Succeed

College degree in Chemistry, Biochemistry or Immunology or equivalent field.
Minimum of 2 years of experience in the medical and/or pharmaceutical fields
MS Word, Excel, Outlook and Power Point
Ability to read and interpret technical documents and industry specific manuals.
Ability to write advanced reports and correspondence.
Ability to speak effectively before groups of employees of the organization.
Bilingual proficiency in French may be required, depending on location.
Excellent verbal and written communication skills.
Well developed interpersonal skills are required.
Personal/professional integrity and proven discretion in handling confidential information.
Ability to develop strong trusting relationships in order to gain support and achieve results.
Capable of managing multiple conflicting priorities.
Must be self-directed, motivated, and have a willingness to take the initiative to identify and anticipate client needs and make recommendations for implementation.

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, LBA 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

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More about this job

Responsibilities

The QC Reviewer is responsible for performing quality control on laboratory data and documentation to ensure accuracy, compliance with GLP, and adherence to standard operating procedures. They also supervise analysts, monitor laboratory processes, and participate in resolving quality issues or nonconformities.

Requirements

Candidates must hold a college degree in Chemistry, Biochemistry, Immunology, or a related field. A minimum of 2 years of experience in medical or pharmaceutical environments is required, along with proficiency in Microsoft Office and strong technical documentation skills.

Skills

Quality control
Batch documentation
GLP compliance
Technical writing
Data analysis
Trend analysis
Bioanalytical documentation
Regulatory compliance
Standard operating procedures
Communication
Interpersonal skills
Confidentiality
Time management
Problem solving
Laboratory safety

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

Visa sponsorship

Not detected in the job text

Keywords

QC Reviewer
LBA
Quality Control
Laboratory
GLP
SOP
Bioanalytical
Chemistry
Biochemistry
Immunology
Batch documentation
Calibration
Regulatory requirements
Trend analysis
Protocol
Study plan
Nonconformities
Health and safety
Pharmaceutical
Medical
Data integrity
Compliance
Documentation
Sample analysis
Microsoft Office

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