Sample Management Technician

**Sample Management Technician**

**Summary**

Reporting to the Sample Reception Manager, the Sample Management Technician is responsible for receiving, logging, inventorying and labeling, samples as well as reagents and materials in compliance with laboratory standards, safety protocols, and quality assurance requirements.

**Responsibilities**

**More specifically, you will participate in the following**

• Perform the reception, inventory, labeling and storage of samples and study reagents.
• Accurately log the information into the laboratory information management system (LIMS).
• Maintain proper storage conditions for the samples and reagents (e.g., refrigeration, freezing).
• Confirm proper delivery conditions or communicate any discrepancy or shipment non-conformity to designated individuals.
• Ensure the chain of custody is correctly maintained.
• Prepare the shipments of samples and study reagents to send to clinical sites, sponsors, or collaborators.
• Prepare, document and execute the destruction of samples
• Manage storage space for the various storage temperatures (from ambient to cryogenic).
• Perform tasks and maintain documentation as per appropriate SOP and applicable GLP regulations and GCLP guidelines.

**Education**

• High School or College degree. Science-related qualifications are an asset.

**Main Requirements**

• Experience in a similar role or laboratory environment is an asset.
• Strong attention to detail and accuracy as well as commitment to achieving good quality work.
• Excellent time management and organizational skills.
• Ability to work under pressure in a fast-paced and changing environment to meet operational deadlines.
• Effective interpersonal and communication abilities.
• Excellent record keeping skills.
• Ability to work autonomously as well as part of a team.
• Positive and professional attitude.
• Problem solving skills and good sense of initiative.
• Knowledge and understanding of French, oral and written, and English, oral and written.
• Proficiency with MS Office suite, especially Excel.
• Experience with LIMS is an asset.
• Experience in working in a GLP/GCLP environment is an asset.
• Knowledge of IATA regulations is an asset.
• Availability to work on some statutory holidays and occasionally work longer hours, depending on operational needs.
• Capability to lift loads weighing up to 25kg.

**Work Schedule**

• Tuesday to Saturday (weekdays are 11:00 AM to 7:00 PM, and weekend days are 9:00 AM to 5:00 PM). **Note that a shift premium will be applied.**

**Benefits**

**We offer a wide range of benefits including**

• Competitive Wages
• Vacation and Personal Days
• Comprehensive Group Insurance Plans
• RRSP Contribution with Employer Matching
• Employee Annual Incentive Plan (EAIP)
• Dialogue Telemedicine Service and Employee Assistance Program (EAP)
• OPUS & Cie Contribution
• Parking Reimbursement
• Referral Program
• Career Advancement Opportunities

**About CellCarta**

CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The Company operates globally with facilities located in Canada, USA, Belgium, Australia, and China.

Joining CellCarta means working with dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world

**Join us as we make an impact on patient therapy**

yzrG1QYgHm