QC Reviewer (BSD)

CareAbout; Laval; On-site; CAD 65,000 - 85,000; Full time

Benefits offered by this job

Health/Dental/Vision Insurance Plans

RRSP/401(k) Employer Match

Paid Vacation and Holidays

Paid Sick and Bereavement Leave

Employee Assistance & Telehealth

Job summary

Altasciences seeks a QC Reviewer to perform comprehensive quality control of data generated in the laboratory. You ensure batch-related documentation is complete, verify SOP adherence, and draft or review study documents as needed, enabling timely review by the Bioanalytical Principal Investigator.

The role includes daily in-process QC, flagging quality issues, supporting QA responses, mentoring analysts, and participating in inspections.

Qualifications

• Experience in medical/pharmaceutical fields with 3 years data review and quality control.
• Understand SOPs and GLP regulations.
• Proven organizational skills and attention to detail.
• Strong communication and leadership abilities.
• Ability to work cross-functionally and with MS Office.

Responsibilities

• Ensures batch-related documentation is completed accurately and timely per SOPs.
• Drafts study documents for QA review and performs multi-batch trend analysis.
• Provides reports within study timelines and records deviations appropriately.
• Manages daily in-process quality control for batches in the lab.
• Raises flags about quality issues to line manager and helps address them.
• Supports QA responses and monitors GLP-compliance in the lab.
• Mentors analysts in daily documentation procedures and processes.
• Participates in basic training of laboratory staff.
• Ensures verification of laboratory instruments as required.
• Aids harmonization of techniques and documentation across analysts.
• Participates in laboratory inspections and reports deviations/health-safety concerns.
• Assists planning sample analysis by maintaining timelines and commitments.
• Stays updated on SOPs and procedures through training and meetings.

Job description

About The Role

The QC Reviewer (BSD) 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.
• 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, and compile study documentation,
• Based on training, 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 .
• Based on training, responsible for daily in process quality control for batches ongoing in the lab.
• 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.

What You’ll Need to Succeed

• College degree and/or University degree in Chemistry, Biochemistry or Immunology or equivalent field.
• Pertinent experience may be considered in lieu.
• Experience in the medical and/or pharmaceutical fields with typically 3 years of experience in data review and quality control field.
• Must understand general SOPs and have knowledge of GLP regulations.
• Proven organizational skills
• Excellent attention to details with respect to sample preparation procedures and raw data handling.
• Strong communication and leadership skills.
• Ability to work cross functionally.
• Good MS Office skills.

Altasciences strives to provide a French work environment for its employees in Quebec. Altasciences has taken all reasonable measures to avoid imposing the above language requirement. This requirement is essential for the position of QC Reviewer (BSD) in particular, but without limitation, for the following reason(s):

• The requirement to have study protocols read 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’ Benefits Package Includes:

• Health/Dental/Vision Insurance Plans
• 401(k)/RRSP with Employer Match
• Paid Vacation and Holidays
• Paid Sick and Bereavement Leave
• Employee Assistance & Telehealth Programs

Altasciences’ Incentive Programs Include:

• Training & Development Programs
• Employee Referral Bonus Program
• Annual Performance Review

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