QC Reviewer (BSD)
- Laval, QC, Canada
Full-time
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Job details
- Job type
- Full-time
- Apply by
- 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
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.
- 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.
- The requirement to have study protocols read and documented in English as required by industry regulatory agencies
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
- Training & Development Programs
- Employee Referral Bonus Program
- Annual Performance Review
More about this job
Responsibilities
Review laboratory data, batch records, and study documentation for accuracy, completeness, and compliance with GLP, regulatory requirements, and internal SOPs. Support analysts through mentoring and training, identify and address quality issues, and help maintain study timelines and laboratory processes.
Requirements
A college or university degree in Chemistry, Biochemistry, Immunology, or an equivalent field is required, although relevant experience may substitute. The role typically requires three years of experience in data review and quality control, knowledge of SOPs and GLP, strong organizational and communication skills, attention to detail, cross-functional collaboration, and Microsoft Office proficiency.
Skills
- Quality Control
- Data Review
- Batch Documentation Review
- Multi-Batch Trend Analysis
- Good Laboratory Practice (GLP)
- Standard Operating Procedures (SOPs)
- Regulatory Compliance
- Raw Data Handling
- Sample Preparation
- Study Documentation
- Deviation Management
- Laboratory Instrument Verification
- Analyst Mentoring
- Organizational Skills
- Attention to Detail
- Microsoft Office
Benefits
- Health Insurance
- Dental Insurance
- Vision Insurance
- 401(k)/RRSP With Employer Match
- Paid Vacation
- Paid Holidays
- Paid Sick Leave
- Bereavement Leave
- Employee Assistance Program
- Telehealth Programs
- Training and Development Programs
- Employee Referral Bonus Program
- Annual Performance Review
Visa sponsorship
Not detected in the job text
Categories
- Science & Research
- Healthcare
- Management & Leadership
- Security & Safety
Keywords
- Quality Control
- Bioanalytical Laboratory
- Data Review
- Batch Review
- Multi-Batch Trend Analysis
- Good Laboratory Practice (GLP)
- Standard Operating Procedures (SOPs)
- Regulatory Compliance
- Study Protocols
- Study Plans
- Study Documentation
- Memo to File
- Deviations
- Raw Data
- Sample Preparation
- Laboratory Instruments
- Instrument Verification
- Quality Assurance Reports
- Health and Safety
- Analyst Training
- Laboratory Inspections
- Timeline Planning
- Microsoft Office
- Chemistry
- Biochemistry
- Immunology