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Altasciences

Integrated CRO for early-phase drug development

QC Reviewer - BSD

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeLaval, QC, CanadaNo salary listedIn-person

About the Job

Requirements

  • A college or university degree in Chemistry, Biochemistry, Immunology, or an equivalent field; pertinent experience may be considered in lieu.
  • Typically three years of experience in data review and quality control in the medical or pharmaceutical fields.
  • Understanding of general standard operating procedures and knowledge of Good Laboratory Practice regulations.
  • Organizational skills.
  • Attention to detail in sample preparation procedures and raw data handling.
  • Communication and leadership skills.
  • Ability to work cross-functionally.
  • Microsoft Office skills.
  • Ability to read and document study protocols in English.

Responsibilities

  • Ensure analysts complete batch-related documentation accurately and on time and follow company standard operating procedures.
  • Based on training, draft study documents for Bioanalytical Principal Investigator review, including Memo to File and standard operating procedure, protocol, or study plan deviations; perform quality control batch review through multi-batch trend analysis; and compile study documentation.
  • Based on training, provide reports and/or final results within study timelines, reflect deviations, exceptions, or events appropriately, and ensure analyses are reported accurately for Bioanalytical Principal Investigator review.
  • Based on training, perform daily in-process quality control for batches ongoing in the laboratory.
  • Raise quality issues or observed trends to the line manager and participate in addressing them appropriately.
  • Support responses to Quality Assurance reports.
  • Monitor laboratory quality according to Good Laboratory Practice, regulatory agency requirements, and internal standard operating procedures.
  • Support and mentor analysts in daily laboratory documentation procedures and processes.
  • Participate in basic training of laboratory staff.
  • As assigned, ensure verification of laboratory instruments according to internal procedures.
  • As assigned, ensure harmonization of techniques, processes, and documentation among laboratory analysts.
  • Participate in laboratory inspections as required, and execute and report deviations and health and safety concerns.
  • Assist with planning sample analysis by maintaining timelines and scheduling commitments, as assigned.
  • Keep up to date on new standard operating procedures, procedures, and techniques through training sessions, team meetings, and internal communications, and observe company guidelines and policies.
  • Follow health and safety standards for personal protection, laboratory maintenance, and work procedures.

About the Company

Altasciences

Integrated CRO for early-phase drug development

Altasciences provides integrated early-stage drug development services, covering preclinical testing, early clinical trials, and contract manufacturing. It functions as a single, in-house CRO that coordinates discovery support, safety testing, clinical research, and manufacturing to streamline a program from start to early proof of concept. The company differentiates itself by offering an end-to-end, one-stop path rather than requiring clients to contract multiple vendors. Its goal is to help innovator programs move quickly and efficiently through early development to speed up decision making and progression to later-stage trials.

Company size
1,001-5,000
Company stage
Early VC
Total funding
$6.7M
Headquarters
Laval, Canada
Founded
1976

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