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Altasciences

Integrated CRO for early-phase drug development

QC Reviewer - Sample Management

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

About the Job

Requirements

  • A high school diploma or higher in health sciences, or equivalent, and at least 3 years of experience.
  • In-depth knowledge of FDA good laboratory practice, good clinical practice, and TPD regulations.
  • Bilingual fluency in French and English; fluency in English is essential for documenting study protocols, designs, and clinical research documents required by industry regulatory agencies.
  • Strong knowledge of good laboratory practice and good clinical practice.
  • Excellent organizational skills and written and oral communication skills.
  • Strong leadership, decision-making, and problem-solving skills.
  • Customer-oriented approach.
  • Proficiency with Access, Outlook, Microsoft Office, and Watson.

Responsibilities

  • Perform 100% quality control review of documentation generated by the Sample Management team.
  • Maintain responsibility for quality within the Sample Management team.
  • Develop, execute, and write reports for audits within the team.
  • Complete additional information forms as necessary to ensure documentation is accurate and complete.
  • Complete documentation necessary to track deviations and non-conformance reports within the team.
  • Respond to quality assurance citations.
  • Archive documentation.
  • Write, revise, and/or review standard operating procedures for sample management and glass washing.
  • Write, revise, and/or update training materials.
  • Keep abreast of relevant regulatory developments in the industry.
  • Perform work in accordance with applicable standard operating procedures, good clinical practice, and good laboratory practice, and adhere to company guidelines and policies.
  • Keep abreast of new standard operating procedures, procedures, and techniques through training sessions, meetings, and internal communications.

Desired Qualifications

  • Experience in the medical or pharmaceutical field.

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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