QC Reviewer (BSD)
Laval, QC · On-site
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 ...
Laval, QC · On-site
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 ...
Laval, QC · On-site
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 ...
Ensure that all batch-related documentation is completed accurately and on time by the analysts ... This requirement is essential for the position of QC Reviewer, LBA in particular, but without ...
Ensure that all batch-related documentation is completed accurately and on time by the analysts ... This requirement is essential for the position of QC Reviewer, LBA in particular, but without ...
Ensure consistency in specification structure, terminology, performance criteria, and document quality across all disciplines. * Define specification development workflows, review cycles, approval ...
Ensure consistency in specification structure, terminology, performance criteria, and document quality across all disciplines. * Define specification development workflows, review cycles, approval ...
The role focuses on process assurance, compliance assessment, documentation reviews, lifecycle traceability, and quality governance. It does not include software development, source code review ...
The role focuses on process assurance, compliance assessment, documentation reviews, lifecycle traceability, and quality governance. It does not include software development, source code review ...
Saint-bruno, QC · On-site
The role focuses on process assurance, compliance assessment, documentation reviews, lifecycle traceability, and quality governance. It does not include software development, source code review ...
Saint-bruno, QC · On-site
The role focuses on process assurance, compliance assessment, documentation reviews, lifecycle traceability, and quality governance. It does not include software development, source code review ...
In addition to performing all core TMF review and quality control activities, the TMF Document Coordinator II independently leads TMF activities for Investigator‑Initiated Studies (IIS) and ...
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In addition to performing all core TMF review and quality control activities, the TMF Document Coordinator II independently leads TMF activities for Investigator‑Initiated Studies (IIS) and ...
At KPMG, the quality and precision of our deliverables contribute directly to the trust clients ... Prepare files for translation, linguistic review, or client delivery. * Import, structure, and ...
At KPMG, the quality and precision of our deliverables contribute directly to the trust clients ... Prepare files for translation, linguistic review, or client delivery. * Import, structure, and ...
Review the batch record and the batch record reconciliation from beginning to end of the ... Meticulously document in -process checks, results of inspection, and any deviations from approved ...
Review the batch record and the batch record reconciliation from beginning to end of the ... Meticulously document in -process checks, results of inspection, and any deviations from approved ...
Montreal, QC · On-site
Perform document quality control review when requested. Assist with writing or review of relevant training materials or work instructions as needed. Clinical Research/Academic Writing Support * Lead ...
Montreal, QC · On-site
Perform document quality control review when requested. Assist with writing or review of relevant training materials or work instructions as needed. Clinical Research/Academic Writing Support * Lead ...
Lead quality system programs (i.e. calibration, maintenance, training, CAPA, complaints, non-conformances, supplier quality, management review, operational qualifications, document control, change ...
Lead quality system programs (i.e. calibration, maintenance, training, CAPA, complaints, non-conformances, supplier quality, management review, operational qualifications, document control, change ...
$40K - $55K/yr
Ensure QA documentation is complete, accurate and maintained according to Good Documentation Practices * Review, organize and file records related to quality activities * Support compliance ...
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$40K - $55K/yr
Ensure QA documentation is complete, accurate and maintained according to Good Documentation Practices * Review, organize and file records related to quality activities * Support compliance ...
Montreal, QC · On-site
The QA Inspector is responsible for inspecting incoming materials, inspecting and testing Final ... Document the inspection results and thoroughly review documentation. To maximize the effectiveness ...
Montreal, QC · On-site
The QA Inspector is responsible for inspecting incoming materials, inspecting and testing Final ... Document the inspection results and thoroughly review documentation. To maximize the effectiveness ...
Reviews quality documentation for conformance with N299.2 and ISO 9001:2015 requirements, providing interpretation where necessary * Ensures all quality documentation is compiled, approved for use ...
Reviews quality documentation for conformance with N299.2 and ISO 9001:2015 requirements, providing interpretation where necessary * Ensures all quality documentation is compiled, approved for use ...
Montreal, QC · Hybrid
... quality and coverage Support product launches by ensuring documentation is ready and aligned with ... Pay equity reviews, inclusive policies, and a Women's Employee Resource Group offering networking ...
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Montreal, QC · Hybrid
... quality and coverage Support product launches by ensuring documentation is ready and aligned with ... Pay equity reviews, inclusive policies, and a Women's Employee Resource Group offering networking ...
Montreal, QC · On-site
Ensures the quality control documentation is compiled, reviewed, approved for use, and completed * Documents, and reports on quality issues * Quality interface/liaison with owner, owner ...
Montreal, QC · On-site
Ensures the quality control documentation is compiled, reviewed, approved for use, and completed * Documents, and reports on quality issues * Quality interface/liaison with owner, owner ...
Identify, document, and segregate nonconforming materials and products * Initiate and support ... Support Material Review Board (MRB) activities as required * Assist with incoming quality issues ...
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Identify, document, and segregate nonconforming materials and products * Initiate and support ... Support Material Review Board (MRB) activities as required * Assist with incoming quality issues ...
Brossard, QC · On-site
Through careful inspections, accurate documentation, and strong collaboration with production teams ... Participate in internal audits and process reviews. * Help maintain clean, organized, and compliant ...
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Brossard, QC · On-site
Through careful inspections, accurate documentation, and strong collaboration with production teams ... Participate in internal audits and process reviews. * Help maintain clean, organized, and compliant ...
Support internal and external ISO audits by providing documentation and inspection evidence. * Support contract review activities related to quality requirements. * Perform minor mechanical assembly ...
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Support internal and external ISO audits by providing documentation and inspection evidence. * Support contract review activities related to quality requirements. * Perform minor mechanical assembly ...
As a Global GMP Quality Auditor at Novartis, you will play a critical role in ensuring compliance ... Document audit observations, prepare reports, and communicate findings to stakeholders. Review and ...
As a Global GMP Quality Auditor at Novartis, you will play a critical role in ensuring compliance ... Document audit observations, prepare reports, and communicate findings to stakeholders. Review and ...
Performing quality control of own work, seeking clarification when necessary, and reviewing work of ... Documenting, logging, tracking and responding to calls, emails, voicemail and drop-bys for document ...
Performing quality control of own work, seeking clarification when necessary, and reviewing work of ... Documenting, logging, tracking and responding to calls, emails, voicemail and drop-bys for document ...
| Aspect | Document Quality Reviewer | Data Entry Clerk |
|---|---|---|
| Primary Role | Review and ensure accuracy of documents for quality and compliance | Input and update data into systems accurately |
| Skills Needed | Attention to detail, knowledge of document standards, quality assurance | Typing speed, accuracy, basic computer skills |
| Work Environment | Office, remote, quality assurance teams | Office, data processing centers, remote |
| Certifications | Often requires familiarity with document standards, quality control | None typically required, basic computer skills suffice |
The main difference is that Document Quality Reviewers focus on evaluating and ensuring the quality of documents, while Data Entry Clerks primarily input data into systems. Both roles require attention to detail, but the Reviewer emphasizes quality assurance, whereas the Clerk emphasizes data accuracy and speed.

Laval, QC • On-site
Full-time
Medical, Dental, Vision, Retirement, PTO
Re-posted 15 days ago
7.6
Based on 17 frontline employees who took The Breakroom Quiz
About The Role
The QC reviewer 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 working environment for its employees in Quebec. Although as part of its francization program has taken all reasonable steps to avoid imposing the above-mentioned requirement. Fluency in English is an essential requirement for the position of QC reviewer including, but not limited to, for the following reasons:
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
Get the full story on Breakroom
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Scientific research and development services
1,001 - 5,000 Employees
Overland Park, KS, US