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Altasciences

Integrated CRO for early-phase drug development

Technician 1 - Sample Management

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeLaval, QC, CanadaIn-person

About the Job

Requirements

  • A Diploma of College Studies (DEC) in health sciences, laboratory technology, or a related field is required; a bachelor's degree is an asset.
  • At least 6 months of work experience is required.
  • Knowledge of FDA-GLP, GCP, and TPD regulations is an asset.
  • Experience in the medical or pharmaceutical field is an asset.
  • Experience with Watson LIMS and Microsoft Office applications, including Excel, Outlook, PowerPoint, and Word.
  • Ability to read and interpret technical documents and industry-specific manuals.
  • Ability to write correspondence.
  • Ability to speak effectively with groups of employees in the organization.
  • Bilingual proficiency in French may be required, depending on location; the role requires protocols to be read and documented in English as required by industry regulatory agencies.
  • Strong organizational and interpersonal skills, attention to detail, a customer-focused approach, and ability to work effectively in a team environment.

Responsibilities

  • Conduct sample management activities, including sample and material inventory, service requests, disposal, and shipment.
  • Support the organization and maintenance of storage areas and ensure accurate handling and tracking of samples in accordance with established procedures and regulatory requirements.
  • Execute transactions in LIMS and electronic inventory systems for all sample movements.
  • Ensure proper storage conditions and accurate locations for samples and study materials.
  • Generate and maintain study material and inventory reports.
  • Handle Containment Level 2 (CL2) and cytotoxic study materials in accordance with safety procedures.
  • Maintain accurate and compliant laboratory documentation.
  • Contribute to process improvements within sample management operations.
  • Ensure all work complies with SOPs, GxP standards, and company policies.
  • Receive, inventory, and label study samples.
  • Conduct service requests and preparation of analytical samples, study samples, and biological matrices.
  • Inventory new analytical material.
  • Store and service reference standard material.
  • Conduct sample disposal and prepare samples for shipment.
  • Assemble and scan samples for long-term storage.
  • Prepare samples in boxes for shipment; assemble and prepare samples for shipment.
  • Perform inventory, system updates, and basic tracking of critical reagents and/or study materials.
  • Receive, inventory, label, and dispose of critical reagents and/or study materials.
  • Fulfill service requests for critical reagents and/or study materials.
  • Assemble and prepare critical reagents and study materials for shipment.

Desired Qualifications

  • Knowledge of FDA-GLP, GCP, and TPD regulations.
  • Experience in the medical or pharmaceutical field.
  • A bachelor's degree.

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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