QC Reviewer (BSD)
- Laval, QC, Canada
Full-time
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Job details
- Job type
- Full-time
- Experience
- Experience in the medical and/or pharmaceutical fields with typically 3 years of experience in data review and quality control field.
- Posting language
- English
- Posted
Original 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
More about this job
Responsibilities
The QC Reviewer is responsible for performing quality control on laboratory data and ensuring all batch documentation adheres to company SOPs and GLP regulations. They also support analysts, monitor laboratory quality, and assist in the reporting of final study results.
Requirements
Candidates must hold a college or university degree in Chemistry, Biochemistry, Immunology, or a related field. A minimum of 3 years of experience in data review and quality control within the medical or pharmaceutical industry is required.
Skills
- Quality Control
- Data Review
- GLP Regulations
- SOP Compliance
- Laboratory Documentation
- Batch Analysis
- Trend Analysis
- Sample Preparation
- Raw Data Handling
- Communication
- Leadership
- MS Office
- Laboratory Maintenance
- Regulatory Compliance
- Mentoring
Benefits
- Health Insurance
- Dental Insurance
- Vision Insurance
- 401(k)
- RRSP
- Employer Match
- Paid Vacation
- Paid Holidays
- Paid Sick Leave
- Bereavement Leave
- Employee Assistance Program
- Telehealth Programs
- Training & Development Programs
- Employee Referral Bonus Program
- Annual Performance Review
Visa sponsorship
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Categories
- Science & Research
- Healthcare
- Manufacturing
Keywords
- QC Reviewer
- Laboratory
- GLP
- SOP
- Bioanalytical
- Chemistry
- Biochemistry
- Immunology
- Data Review
- Quality Control
- Batch Analysis
- Regulatory Agencies
- Sample Preparation
- Raw Data
- MS Office
- Pharmaceutical
- Medical
- Documentation
- Compliance
- Trend Analysis
- Laboratory Instruments
- Health and Safety