QC Reviewer, Sample Management (12-month contract)

Altasciences Company Inc ยท Laval, Quebec ยท First seen 2026-10-29

Apply on company site View on the company's hiring page (altasciences.wd1.myworkdayjobs.com)

Posted by Altasciences Company Inc on the hiring system it uses for its careers page; applications go straight to the company.

Can I apply?

  • Full-time
  • On-site
  • Work permit not stated
From the posting
employment types
ATS employment type: full_time
workplace
ATS workplace type: onsite
locations
ATS location: Laval, Quebec

Job description

About the role The Quality Control Reviewer, Sample Management Department, is responsible for the quality control review of documentation related to the Sample Management team. He/she also conducts audits within the team to ensure that quality standards are met. He/she participates in the drafting and/or revision of standard operating procedures for sample management and glass washing.

What you'll be doing here

- Perform 100% quality control on documentation generated by the sample management team.

- Responsible for quality within the sample management team.

- Perform audits within the team: develop, execute and write reports.

- Completes 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 QA 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 all work in accordance with applicable SOPs, GCPs and GLPs and adhere to all company guidelines and policies.

- Keep abreast of new SOPs, procedures and techniques through training sessions, meetings and internal communications.

What you need to succeed

- You have a high school diploma or higher in health sciences or equivalent with at least 3 years' experience.

- You must have in-depth knowledge of FDA-GLP, GCP and TPD regulations.

- Experience in the medical or pharmaceutical field is an asset.

- Excellent management, organizational, communication (written and oral) and interpersonal skills.

- Strong GLP/GCP focus.

- Detail-oriented.

- Strong leadership, decision-making and problem-solving skills.

- Customer oriented.

- Must be bilingual (French and English).

- Software: Access, Outlook, MS-Office, Watson.

Altasciences strives to provide a French working environment for its employees in Quebec. Although as part of its francization program has taken all reasonable steps to avoid imposing the above-mentioned requirement. Fluency in English is an essential requirement for the position of QC Reviewer, Sample Management including, but not limited to, for the following reasons:

- The requirement to have study protocols, designs and clinical research documents written and documented in English as required by industry regulatory agencies.

What we offer Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.

Altasciences' incentive programs include:

- Training and development programs

- Employee orientation bonus program

- Annual performance reviews

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