Associé(e) principal(e) en qualité, Marque privée/ Senior Quality Associate, Private Label (contrat 18 Mois)
Saint-Laurent, Canada Job ID JR0147253 Category Quality Assurance, Information Technology Post Date May. 22, 2026McKesson, l’une des 10 premières entreprises du classement Fortune Global 500, touche à pratiquement tous les aspects des soins de santé et s’emploie à faire une réelle différence. Nous sommes reconnus pour notre capacité à offrir un savoir, des produits et des services qui rendent les soins de qualité plus accessibles et plus abordables. Chez nous, la santé, le bonheur et le bien-être de nos gens et des personnes que nous desservons sont prioritaires—et nous tiennent à cœur.
Ce que tu fais chez McKesson a de l’importance. Nous favorisons une culture où tu peux t’épanouir et avoir un impact, et où tu es encouragé à proposer de nouvelles idées. Ensemble, nous façonnons l’avenir de la santé pour nos patients, nos communautés et nos équipes. Si tu souhaites dès aujourd’hui contribuer à la santé de demain, nous aimerions avoir de tes nouvelles.
McKesson is an impact-driven, Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights, products, and services that make quality care more accessible and affordable. Here, we focus on the health, happiness, and well-being of you and those we serve – we care.
What you do at McKesson matters. We foster a culture where you can grow, make an impact, and are empowered to bring new ideas. Together, we thrive as we shape the future of health for patients, our communities, and our people. If you want to be part of tomorrow’s health today, we want to hear from you.
Sommaire du poste:
Relevant au Chef principale Qualité, Marque privée, l’Associé(e) principal(e), Qualité – Marque privée est responsable de soutenir divers processus tels que la relâche de produits, le lancement de nouveaux produits, ainsi que d’autres activités connexes.
Ce rôle joue un rôle clé dans le maintien de l’intégrité des opérations de marques privées de McKesson, notamment en contribuant à la revue de la documentation des lots, à la gestion des activités de contrôle des changements et au soutien des analyses confirmatoires. De plus, le poste contribue aux initiatives d’amélioration continue et collabore avec les équipes internes ainsi qu’avec les partenaires externes afin d’atteindre et de maintenir les objectifs qualité.
Responsabilités spécifiques
Enregistrer la documentation de lots reçue dans le système de gestion de la qualité et faire la pré-revue.
Recevoir et examiner la documentation de lots afin d’assurer la conformité aux exigences réglementaires et internes de qualité produit, incluant notamment :
Certificat d’analyse
Certificat de conformité (fabrication et conditionnement)
Déviations et enquêtes
Participer au processus de contrôle des changements pour les relâches, incluant l’initiation de DCR et les tâches associées.
Soutenir les processus de tests confirmatoires (création des demandes d’analyse, suivi des résultats).
Collaborer aux revues complètes de dossier des lots lorsque requis.
Créer, évaluer et mettre à jour les documents liés aux DMF dans le système de gestion de la qualité.
Soutenir le processus de lancement de nouveaux produits au besoin.
Soutenir les demandes APQR et de stabilité auprès des fournisseurs et assurer les suivis selon le calendrier.
Rédiger, formater, réviser, traduire et mettre à jour les SOPs, instructions de travail, formulaires et documents contrôlés.
Gérer la documentation dans MasterControl (standardisation des gabarits, contrôle documentaire, archivage).
Collaborer avec les partenaires et fabricants pour aligner les priorités.
Animer les réunions fournisseurs
Préparer les ordres du jour
Documenter les comptes rendus
Soutenir les activités liées à la libération.
Contribuer à la préparation des inspections de Santé Canada et corporatives; diriger ou soutenir des projets spéciaux au besoin.
Participer aux audits internes et externes.
Contribuer aux initiatives d’amélioration continue.
Effectuer toute autre tâche connexe.
Responsabilités générales
Assurer la conformité aux exigences de formation GMP.
Travailler avec un encadrement modéré dans son domaine d’expertise.
Recevoir occasionnellement des directives sur des aspects qualité spécifiques et suivre les procédures établies.
Fournir du support aux projets et mandats au besoin.
Contribuer aux initiatives d’amélioration continue.
Collaborer efficacement avec les équipes internes et partenaires externes.
Exigences clés du poste
Formation
Baccalauréat en sciences de la santé, ou expérience équivalente
Minimum de 3 ans d’expérience en pharma/opérations/fabrication
Bonne connaissance des lignes directrices pertinentes.
Compétences techniques et comportementales
Bilingue (français et anglais, oral et écrit)
Excellentes compétences en communication
Expérience avec un système électronique de gestion de la qualité
Maîtrise de la suite Microsoft (Outlook, Word, Excel, PowerPoint).
Compétences en gestion / aptitudes
Rigueur et souci du détail
Capacité à travailler sous pression
Excellentes compétences interpersonnelles et rédactionnelles
Forte capacité d’organisation et gestion du temps (multi‑projets)
Esprit d’équipe et collaboration
Capacité à coordonner des activités transversales
Engagement envers l’amélioration continue.
Le/la titulaire de ce poste aura à soutenir de façon quotidienne des clients internes et/ou externes à l’extérieur du Québec et/ou aux États-Unis. Par conséquent, ce poste requiert une maîtrise de l’anglais à l’écrit et à l’oral. Veuillez noter que le nombre de postes dont les tâches requièrent une connaissance de la langue anglaise a été restreint dans la mesure du possible.
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Job Summary:
Reporting to the Senior Quality Manager, Private Label, the Senior Quality Associate, Private Label, will be responsible for supporting various processes such as Release, New Product Launch and others.
The Senior Quality Associate will play an important role in supporting the integrity of McKesson’s private label operations by contributing to batch documentation review, managing change control activities, and supporting confirmatory testing. Additionally, the position contributes to continuous improvement initiatives and collaborates with internal teams and external partners to achieve and maintain quality objectives.
Specific Responsibilities
Record received batch documentation in the Quality Management System (QMS) and perform the initial review.
Receive and review batch documentation to ensure compliance with regulatory and internal product quality requirements, including but not limited to:
Certificates of Analysis
Certificates of Compliance (manufacturing and packaging)
Deviations and investigations
Participate in the change control process for batch releases, including the initiation of DCRs and associated tasks.
Support confirmatory testing processes (creation of analysis requests and follow‑up on results).
Collaborate on full batch record reviews as required.
Create, review, and update Drug Master File (DMF)‑related documents within the Quality Management System.
Support new product launch activities as needed.
Support APQR and stability requests with suppliers and ensure follow‑up in accordance with established timelines.
Draft, format, review, translate, and update SOPs, work instructions, forms, and controlled documents.
Manage documentation in MasterControl (template standardization, document control, and archiving).
Collaborate with partners and manufacturers to align priorities.
Facilitate supplier meetings, including:
Preparing agendas
Documenting meeting minutes
Support activities related to batch release.
Contribute to the preparation of Health Canada and corporate inspections; lead or support special projects as required.
Participate in internal and external audits.
Contribute to continuous improvement initiatives.
Perform any other related duties.
General Responsibilities
Ensure compliance with GMP training requirements.
Work with moderate supervision within area of expertise.
Receive occasional guidance on specific quality matters and follow established procedures.
Provide support to projects and assignments as needed.
Contribute to continuous improvement initiatives.
Collaborate effectively with internal teams and external partners.
Key Job Requirements
Education
Bachelor’s degree in Health Sciences or equivalent experience.
Minimum of 3 years of experience in pharmaceutical, operations, or manufacturing environments.
Strong knowledge of applicable regulatory guidelines.
Technical and Behavioral Skills
Bilingual (French and English), both written and spoken.
Excellent communication skills.
Experience with an electronic Quality Management System (eQMS).
Proficiency in Microsoft Office (Outlook, Word, Excel, PowerPoint).
Management / Professional Competencies
Strong attention to detail and rigor.
Ability to work under pressure.
Excellent interpersonal and written communication skills.
Strong organizational and time‑management skills (ability to manage multiple projects).
Team‑oriented with a collaborative mindset.
Ability to coordinate cross‑functional activities.
Commitment to continuous improvement.
The incumbent of this position will provide daily support to internal and/or external clients outside Quebec and/or in the United States. Therefore, he/she must be proficient in spoken and written English. Please note that the number of positions requiring English language skills has been limited where possible.
#LI-JT2
We are proud to offer a competitive compensation package at McKesson as part of our Total Rewards. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. The pay range shown below is aligned with McKesson's pay philosophy, and pay will always be compliant with any applicable regulations. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered. For more information regarding benefits at McKesson, please click here.
Notre échelle salariale de base pour ce poste
Our Base Pay Range for this position
$63,100 - $105,100McKesson has become aware of online recruiting-related scams in which individuals who are not affiliated with or authorized by McKesson are using McKesson’s (or affiliated entities, like CoverMyMeds or RxCrossroads) name in fraudulent emails, job postings or social media messages. In light of these scams, please bear the following in mind:
McKesson Talent Advisors will never solicit money or credit card information in connection with a McKesson job application.
McKesson Talent Advisors do not communicate with candidates via online chatrooms or using email accounts such as Gmail or Hotmail. Note that McKesson does rely on a virtual assistant (Gia) for certain recruiting-related communications with candidates.
McKesson job postings are posted on our career site: careers.mckesson.com.
McKesson is an Equal Opportunity Employer
McKesson provides equal employment opportunities to applicants and employees, without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, age, genetic information, or any other legally protected category. For additional information on McKesson’s full Equal Employment Opportunity policies, visit our Equal Employment Opportunity page.
McKesson is committed to being an Equal Employment Opportunity Employer and offers opportunities to all job seekers including job seekers with disabilities. If you need a reasonable accommodation to assist with your job search or application for employment, please contact us by sending an email to (United States) Disability_Accommodation@McKesson.com or (Canada) Accessibility@mckesson.ca. Resumes or CVs submitted to this email box will not be accepted.
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McKesson has become aware of online recruiting-related scams in which individuals who are not affiliated with or authorized by McKesson are using McKesson’s (or affiliated entities, like CoverMyMeds or RxCrossroads) name in fraudulent emails, job postings or social media messages. In light of these scams, please bear the following in mind:
- McKesson Talent Advisors will never solicit money or credit card information in connection with a McKesson job application.
- McKesson Talent Advisors do not communicate with candidates via online chatrooms or using email accounts such as Gmail or Hotmail. Note that McKesson does rely on a virtual assistant (Gia) for certain recruiting-related communications with candidates.
- McKesson job postings are posted on our career site: careers.mckesson.com
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