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Publié il y a 8 jours

QC Reviewer (BSD)

@ Altasciences Company Inc

Laval, Québec

Sur placeTemps plein3+ ans d’expérience
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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.

Responsabilités :

  • 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

Résumé des exigences :

  • 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

Outils et compétences

Source et dates

Site carrière / système de candidatures · workday

Date publiée par l’employeur
2026-11-02
Première détection par notre source
2026-11-03
Mise à jour du dossier source
2026-11-03

Ces dates décrivent le dossier source, pas une vérification en direct du recrutement. Consultez l’offre originale.

Détails du poste

NiveauIntermédiaire
DomaineAssurance qualité
Expérience3 an(s) et plus
Heures par semaine40 (estimé)
Déplacementsavion : aucun · route : aucun
Milieu de travailLaboratoire, Bureau
PositionAssis et debout
Exigences physiquesphysique faible · ordinateur élevé
LanguesEnglish, French
FormationBaccalauréat (exigé)
Domaines d’étudesChemistry, Biochemistry, Immunology
Avantages mentionnésCongés payés généreux, Régime de retraite, Prime de rendement, Mieux-être, Formation payée

Résumé et détails rédigés par l’IA à partir de l’offre; l’offre de l’employeur fait foi.

Altasciences Company Inc

Profil d’entreprise sauvegardé

Renseignements historiques provenant d’un profil The Jobs API sauvegardé (champs LinkedIn/Crunchbase). Ils ne sont pas vérifiés en temps réel; les chiffres peuvent avoir changé. Les valeurs manquantes restent inconnues.

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

Description complète de l’entreprise

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!

Abonnés LinkedIn
43 874
Personnes associées sur LinkedIn
1 911
Bureaux déclarés
  • 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
Catégories d’activité
  • Health Care
  • Medical Device
  • Wellness
  • Biotechnology
  • Medical
Autres noms enregistrés
  • CareAbout
  • Altasciences
Spécialités
  • 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
Le profil indique une agence de recrutement
Non
Investissement total déclaré
0

La devise et la date d’observation ne sont pas fournies; ce n’est ni une valorisation actuelle ni une ronde de financement.

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…

ChampValeur
SecteurResearch Services
Taille1,001-5,000 employees
Siège socialLaval, Quebec
Type d’organisationPrivately Held
Fondée en1995
SpécialitésClinical ResearchClinical TrialsPhase I-IIHuman Abuse Liability & Abuse PotentialEarly Cardiac Safety & TQTBiosimilarsBioanalytical LaboratoryAnalytical ServicesToxicology StudyCDMO
Offres sur Jobsy29
LinkedInVoir la page
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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