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Posted 5 days ago

QC Reviewer (BSD)

@ Altasciences Company Inc

Laval, Quebec

On-siteFull-time3+ years experience
Apply now
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Overview

Altasciences Company Inc is hiring a full-time QC Reviewer (BSD) to perform quality control on laboratory data and work. The role covers batch documentation review, GLP compliance monitoring, study document drafting and mentoring of analysts. The posting states an essential English-language requirement tied to study protocols read under industry regulatory agencies.

Responsibilities:

  • Réviser les dossiers de lots et les données pour la conformité aux SOP
  • Rédiger des documents d'étude et des rapports de déviation
  • Surveiller la qualité selon les BPL et les exigences réglementaires
  • Soutenir et encadrer les analystes dans la documentation
  • Participer aux inspections de laboratoire et à la formation du personnel

Requirements summary:

  • Diplôme universitaire en chimie, biochimie, immunologie ou domaine équivalent
  • Environ 3 ans d'expérience en révision de données et contrôle qualité
  • Connaissance des SOP et de la réglementation BPL
  • Excellente attention aux détails et organisation
  • Solides habiletés de communication et de leadership
  • Bonne maîtrise de la suite MS Office

Tools & skills

Source and dates

Employer career site / ATS feed · workday

Employer posting date
2026-11-02
First seen by our source
2026-11-03
Source record updated
2026-11-03

These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.

Job details

SeniorityMid level
DepartmentQuality assurance
Experience3+ years
Hours per week40 (estimated)
Travelair: none · ground: none
Work settingLaboratory, Office
PositionSitting and standing
Physical demandsphysical low · computer high
LanguagesEnglish, French
EducationBachelor’s degree (required)
Fields of studyChemistry, Biochemistry, Immunology
Perks mentionedGenerous paid time off, Retirement plan, Performance bonus, Wellness, Paid training

Summary and details written by AI from the posting; the employer’s posting is the authority.

Altasciences Company Inc

Saved company profile

Historical company information from a saved The Jobs API profile (LinkedIn/Crunchbase fields). It is not live-verified; figures may have changed. Missing values remain unknown.

Quicker go/no-go decisions with integrated preclinical, clinical, bioanalytical, manufacturing, and CRO services.

Full company description

Outsourcing made easy with a one-stop solution to early-phase drug development. We are an integrated drug development solution company, offering pharmaceutical and biotechnology companies a proven, flexible approach that removes the need for multiple service providers during the early stages of drug development. Whether for one study or an end-to-end program, we help you reach critical decision-making milestones sooner by improving speed and ease from lead candidate selection to clinical proof of concept, and beyond. When partnering with Altasciences, you can experience up to 40% in time savings thanks to our integrated, one-stop solution offering. We strive to create a true partnership with our clients, our partners, and our colleagues that enables a mutually supporting relationship built on a combination of excellent science and solid communication. Helping sponsors get better drugs to the people who need them, faster, for over 30 years. Our full-service offering is always tailored to your specific research needs: - Preclinical research - Clinical pharmacology - Drug formulation - Manufacturing and analytical services - Bioanalysis - Program management - Medical writing - Biostatics - Data management - And so much more!

LinkedIn followers
43,874
People associated on LinkedIn
1,911
Reported office locations
  • 575 Boulevard Armand-Frappier, Laval, Quebec H7V 4B3, CA
  • 1200 Avenue Beaumont, Montreal, Quebec H3P 3P1, CA
  • 10103 Metcalf Ave, Overland Park, Kansas 66212, US
  • 6605 Merrill Creek Pkwy, Everett, Washington 98203, US
  • 1510 Delp Dr, Harleysville, Pennsylvania 19438, US
  • 5630 Cerritos Ave, Cypress, California 90630, US
  • 130 Discovery Dr, Scott, Pennsylvania 18447, US
  • 562 State Road DD, Auxvasse, Missouri 65231, US
Business categories
  • Health Care
  • Medical Device
  • Wellness
  • Biotechnology
  • Medical
Other recorded names
  • CareAbout
  • Altasciences
Specialties
  • Clinical Research
  • Clinical Trials
  • Phase I-II
  • Human Abuse Liability & Abuse Potential
  • Early Cardiac Safety & TQT
  • Biosimilars
  • Bioanalytical Laboratory
  • Analytical Services
  • Toxicology Study
  • CDMO
  • Safety Pharmacology
  • Preclinical Study
  • GLP / Non-GLP Study
  • IND-Enabling
  • NDA Submission
  • LCMS and LBA
  • Small and Large Molecule Bioanalysis
  • Research Support Services
  • Medical Writing
  • Clinical Project Management
  • and Pharmaceutical Manufacturing
Profile identifies a recruitment agency
No
Reported total investment
0

Currency and observation date were not supplied; this is not a current valuation or a funding round.

Outsourcing made easy with a one-stop solution to early-phase drug development. We are an integrated drug development solution company, offering pharmaceutical and biotechnology companies a proven, flexible approach that removes the need for multiple service providers during the early stages of drug development. Whether for one study or an end-to-end program, we help you reach critical decision-making milestones…

FieldValue
IndustryResearch Services
Company size1,001-5,000 employees
HeadquartersLaval, Quebec
Organization typePrivately Held
Year founded1995
SpecialtiesClinical ResearchClinical TrialsPhase I-IIHuman Abuse Liability & Abuse PotentialEarly Cardiac Safety & TQTBiosimilarsBioanalytical LaboratoryAnalytical ServicesToxicology StudyCDMO
Open jobs on Jobsy28
LinkedInView page
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

#LI-MB1


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