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Publié il y a 16 jours

QC Reviewer, Sample Management (12-month contract)

@ Altasciences Company Inc

Laval, Québec

Sur placeTemps plein3+ ans d’expérience
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Altasciences Company Inc is hiring a QC Reviewer for its Sample Management department on a 12-month contract. The role performs 100% quality control review of sample management documentation, runs team audits, and helps write and revise SOPs for sample management and glass washing. The work requires bilingual French and English and knowledge of FDA-GLP, GCP and TPD regulations.

Responsabilités :

  • Effectuer un contrôle qualité à 100 % de la documentation de gestion des échantillons
  • Réaliser des audits internes, rédiger les rapports
  • Rédiger et réviser les procédures opérationnelles normalisées
  • Suivre les écarts et les non-conformités
  • Répondre aux citations de l'AQ

Résumé des exigences :

  • Diplôme d'études secondaires ou plus en sciences de la santé, ou équivalent, avec au moins 3 ans d'expérience
  • Connaissance approfondie des règlements FDA-GLP, GCP et TPD
  • Expérience dans le domaine médical ou pharmaceutique un atout
  • Bilinguisme français et anglais obligatoire
  • Forte orientation GLP/GCP et sens du détail

Outils et compétences

Source et dates

Site carrière / système de candidatures · workday

Date publiée par l’employeur
2026-10-26
Première détection par notre source
2026-10-27
Mise à jour du dossier source
2026-11-09

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

Détails du poste

NiveauIntermédiaire
DomaineProfessions paramédicales
Expérience3 an(s) et plus
Heures par semaine40 (estimé)
Déplacementsavion : aucun · route : aucun
Milieu de travailLaboratoire, Bureau
PositionSurtout assis
Exigences physiquesphysique faible · ordinateur élevé
LanguesEnglish, French
FormationSecondaire (DES) (exigé)
Domaines d’étudeshealth sciences
Avantages mentionnésPrime de rendement, 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 Quality Control Reviewer, Sample Management Department, is responsible for the quality control review of documentation related to the Sample Management team. He/she also conducts audits within the team to ensure that quality standards are met. He/she participates in the drafting and/or revision of standard operating procedures for sample management and glass washing.


What you'll be doing here

  • Perform 100% quality control on documentation generated by the sample management team.
  • Responsible for quality within the sample management team.
  • Perform audits within the team: develop, execute and write reports.
  • Completes additional information forms as necessary to ensure documentation is accurate and complete.
  • Complete documentation necessary to track deviations and non-conformance reports within the team.
  • Respond to QA citations.
  • Archive documentation.
  • Write, revise and/or review standard operating procedures for sample management and glass washing.
  • Write, revise and/or update training materials.
  • Keep abreast of relevant regulatory developments in the industry.
  • Perform all work in accordance with applicable SOPs, GCPs and GLPs and adhere to all company guidelines and policies.
  • Keep abreast of new SOPs, procedures and techniques through training sessions, meetings and internal communications.

What you need to succeed

  • You have a high school diploma or higher in health sciences or equivalent with at least 3 years' experience.
  • You must have in-depth knowledge of FDA-GLP, GCP and TPD regulations.
  • Experience in the medical or pharmaceutical field is an asset.
  • Excellent management, organizational, communication (written and oral) and interpersonal skills.
  • Strong GLP/GCP focus.
  • Detail-oriented.
  • Strong leadership, decision-making and problem-solving skills.
  • Customer oriented.
  • Must be bilingual (French and English).
  • Software: Access, Outlook, MS-Office, Watson.

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, Sample Management including, but not limited to, for the following reasons:

  • The requirement to have study protocols, designs and clinical research documents written 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' incentive programs include:

  • Training and development programs
  • Employee orientation bonus program
  • Annual performance reviews

#LI-MB1


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