QC Reviewer (LBA) - Flow Cytometry at Altasciences
Laval, QC, Canada -
Full Time


Start Date

Immediate

Expiry Date

17 May, 25

Salary

0.0

Posted On

17 Feb, 25

Experience

3 year(s) or above

Remote Job

No

Telecommute

No

Sponsor Visa

No

Skills

Good communication skills

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

ABOUT THE ROLE

The QC Reviewer (LBA) - Flow Cytometry is responsible to perform the quality control for data generated and work conducted in the laboratory.

WHAT YOU’LL DO HERE

  • Ensures that all batch related documentation is completed accurately and in a timely manner by the analysts and that all procedures are respected as per the company’s SOPs.
  • Raises any flags to line manager regarding any quality issue or trends observed and is part of addressing these issues in an appropriate manner.
  • Supports responses to QA reports.
  • Monitors the quality within the laboratory according to GLP, regulatory agencies requirements and internal SOPs.
  • Supports and mentors analysts in the daily laboratory documentation procedures and processes.
  • Can participate in basic training of laboratory staff.
  • Could be assigned to ensure that the verification of laboratory instruments is performed as required by the internal procedures.
  • Could be assigned to ensure harmonization of techniques, process and documentation between analysts in the laboratory.
  • May be required to participate in laboratory inspections: executes and reports deviations and any health and safety concerns.
  • As assigned, assist for planning sample analysis by maintaining timeline and scheduling commitments.
  • Stays up to date on new SOPs, procedures, and techniques via training sessions, team meetings and internal communication avenues and observes all company guidelines and policies.
  • Respecting Health and Safety standards in terms of personal protection, laboratory maintenance, and work procedures.

Based on training QC reviewer can

  • Draft study documents for BPI review such as Memo to File, SOP/Protocol/Study Plan deviations, perform quality control batch review by performing multi-batch trend analysis, compile study documentation.
  • Provide report and/or final results within study timelines and ensure any deviation, exception or events are reflected as appropriate and assure that all analysis conducted are reported and accurate for the review of the Bioanalytical Principal Investigator.
  • Responsible for daily in process quality control for batches ongoing in the lab.
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