QC Reviewer, Sample Management at Altasciences
Laval, QC, Canada -
Full Time


Start Date

Immediate

Expiry Date

30 Oct, 25

Salary

0.0

Posted On

30 Jul, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Regulatory Agencies, Sample Management, English

Industry

Pharmaceuticals

Description

YOUR NEW COMPANY!

At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you’re a recent college graduate or seeking your next career opportunity, it’s time to discover your future at Altasciences.
We are better together and together We Are Altasciences.

Responsibilities

The QC Reviewer, Sample Management, is responsible for overseeing activities for all sample management general activities:

  • Perform the quality control review of the documentation related to the Sample Management team.
  • Perform audits within the team to ensure that quality standards are respected
  • Assist in reviewing SOPs pertaining to Sample Management department
  • Coaching and training of new employees

    What You’ll Do Here

  • Performs 100% QC review on documentation generated by the Sample Management groups and follow-up with technical staff.

  • To conduct all work in compliance with applicable SOPs, GCPs, GLPs, and observe all company guidelines and policies.
  • Stay up to date on new SOPs, procedures, and techniques via training sessions, team meetings and internal communication avenues.
  • Perform QC review of information and transactions recorded in LIMS
  • To write and review memo to files in support of raw data for supplementary information.
  • Initiate deviation (DTS) and assist follow-up, ensure closure and determine root cause
  • Report on discrepancies, enter discrepancies in tracker and ensure follow-up
  • Create and update training documents related to Quality Control within Sample Management
  • Training of new technicians for GDP and QCs
  • Follow-up of corrections to be performed by analyst and/or technician
  • Archiving documentation
  • Participate and support process improvement
  • Perform any other duties as required
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