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Altasciences

Integrated CRO for early-phase drug development

QC Reviewer - Flow Cytometry

Regulatory & Quality (Life Sciences)Posted on Nov 13
Full-timeLaval, QC, CanadaNo salary listedIn-person

About the Job

Requirements

  • A college degree in Chemistry, Biochemistry, Immunology, or an equivalent field is required.
  • At least 2 years of experience in the medical and/or pharmaceutical fields is required.
  • Proficiency with Microsoft Word, Excel, Outlook, and PowerPoint is required.
  • Ability to read and interpret technical documents and industry-specific manuals is required.
  • Ability to write advanced reports and correspondence is required.
  • Ability to speak effectively before groups of employees is required.
  • Bilingual proficiency in French may be required, depending on location.
  • Ability to handle confidential information with integrity and discretion is required.
  • Ability to develop trusting relationships to gain support and achieve results is required.
  • Ability to manage multiple conflicting priorities is required.
  • Ability to work independently, take initiative, identify and anticipate client needs, and make implementation recommendations is required.

Responsibilities

  • Ensure analysts complete batch-related documentation accurately and on time and follow company standard operating procedures.
  • Perform daily in-process quality control for batches ongoing in the laboratory.
  • 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.
  • Ensure laboratory instruments are verified as required by internal procedures.
  • Harmonize techniques, processes, and documentation between laboratory analysts.
  • Escalate quality issues or trends to the line manager and participate in resolving them.
  • Participate in laboratory inspections as assigned, including executing and reporting deviations and health and safety concerns.
  • Based on training, draft study documents for Bioanalytical Principal Investigator review, such as memoranda to file and standard operating procedure, protocol, or study plan deviations; perform quality control batch reviews through multi-batch trend analysis; and compile study documentation.
  • Based on training, provide reports and/or final results within study timelines, ensure deviations, exceptions, or events are appropriately reflected, and ensure analyses are accurately reported for Bioanalytical Principal Investigator review.
  • Assist in planning sample analysis by maintaining timelines and scheduling commitments.
  • Stay current on standard operating procedures, procedures, and techniques through training sessions, team meetings, and internal communications, and follow 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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