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QC Reviewer, Flow Cytometry

@ Altasciences Company Inc

Laval, Quebec

On-siteFull-time2+ years experience
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Overview

Altasciences Company Inc is hiring a full-time QC Reviewer for Flow Cytometry to check laboratory data, documentation and batch quality against SOPs, GLP and regulatory requirements. The role also mentors analysts and supports QA report responses. The posting requires a college degree in Chemistry, Biochemistry or Immunology or equivalent, and at least 2 years of medical or pharmaceutical experience.

Responsibilities:

  • Vérifier la documentation des lots et le respect des SOP
  • Effectuer le contrôle qualité quotidien des lots en cours
  • Surveiller la qualité selon les BPL et les exigences réglementaires
  • Soutenir et encadrer les analystes dans leurs procédures
  • Signaler les problèmes et tendances de qualité au gestionnaire

Requirements summary:

  • Diplôme collégial en chimie, biochimie, immunologie ou domaine équivalent
  • Minimum de 2 ans d'expérience en milieu médical ou pharmaceutique
  • Maîtrise de Word, Excel, Outlook et PowerPoint
  • Excellentes communications écrites et verbales
  • Capacité à gérer plusieurs priorités concurrentes
  • Français bilingue possiblement requis selon l'emplacement
Source and dates

Employer career site / ATS feed · workday

Employer posting date
2026-11-12
First seen by our source
2026-11-13
Source record updated
2026-11-13

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

Job details

SeniorityEntry level
DepartmentQuality assurance
Experience2+ years
Hours per week40 (estimated)
Travelair: none · ground: none
Work settingLaboratory
PositionSitting and standing
Physical demandsphysical low · computer high
LanguagesEnglish, French
EducationCollege diploma (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
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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 Jobsy29
LinkedInView page
Job description

About The Role

The QC Reviewer, Flow Cytometry is responsible for performing the quality control reviews of data generated and work conducted in the laboratory to ensure accuracy, compliance, and adhere to applicable standards.


What You'll Do Here

  • Ensure 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
  • Perform daily in process quality control for batches ongoing in the laboratory
  • Support responses to QA reports
  • Monitor the quality within the laboratory according to GLP, regulatory agencies requirements and internal SOPs
  • Support and mentor analysts in the daily laboratory documentation procedures and process
  • Ensure verification of laboratory instruments is performed as required by the internal procedures
  • Ensure harmonization of techniques, process and documentation between analysts in the laboratory
  • Escalate quality issues or trends to the line manager and participate in their resolution
  • May be assigned to participate in laboratory inspection: execute and report deviations and any health and safety concerns
  • Based on training, can draft study documents for BPI review such as Memo to File, SOP/Protocol/Study Plan deviations. and perform quality control batch review by performing multi-batch trend analysis, and compile study documentation
  • Based on training, can 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
  • Assist in planning sample analysis by maintaining timeline and scheduling commitments.
  • Stay up to date with SOPs, procedures, and techniques via training sessions, team meetings and internal communication avenues and observe all company guidelines and policies
  • Adhere to Health and Safety standards in terms of personal protection, laboratory maintenance, and work procedures

What You'll Need to Succeed

  • College degree in Chemistry, Biochemistry or Immunology or equivalent field.
  • Minimum of 2 years of experience in the medical and/or pharmaceutical fields
  • MS Word, Excel, Outlook and Power Point
  • Ability to read and interpret technical documents and industry specific manuals.
  • Ability to write advanced reports and correspondence.
  • Ability to speak effectively before groups of employees of the organization.
  • Bilingual proficiency in French may be required, depending on location.
  • Excellent verbal and written communication skills.
  • Well developed interpersonal skills are required.
  • Personal/professional integrity and proven discretion in handling confidential information.
  • Ability to develop strong trusting relationships in order to gain support and achieve results.
  • Capable of managing multiple conflicting priorities.
  • Must be self-directed, motivated, and have a willingness to take the initiative to identify and anticipate client needs and make recommendations for implementation.

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, Flow Cytometry 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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