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Génome Québec

Responsable qualité et accréditation / Quality and Accreditation Lead

Montreal, QC, Canada

Full-time

Apply on LinkedIn About employer

Applications open in a new tab.

Job details

Job type: Full-time
Apply by: Nov 13, 2026
Posting language: English · French
Posted: Oct 14, 2026

Original job description

English section of this bilingual listing.

At Génome Québec, we believe genomics has the power to address some of society’s greatest challenges, from health and the environment to agriculture and innovation. For more than 25 years, we have supported leading-edge research and helped establish Québec as a leader in genomics.

We are seeking a professional recognized for their expertise in quality and accreditation to support the continued development of the Centre of Expertise and Services (CES) and uphold the highest quality standards. This is a two-year contract.

If you enjoy tackling complex challenges, serving as a resource on quality matters, helping teams interpret standards, and contributing to the achievement and maintenance of recognized accreditations, this position is for you.

What you will do

Accreditation and compliance

Lead efforts to obtain, maintain, and renew accreditations, particularly ISO 15189 and ISO/IEC 17025, as well as any new accreditation required as activities and needs evolve.
Coordinate accreditation assessments and serve as the primary contact for assessment bodies.
Advise and support teams in interpreting and applying the requirements of standards.
Serve as a resource on standards, frameworks, and accreditation requirements.

Quality management system

Develop, implement, maintain, and evolve the QMS.
Oversee document control, change management, risk management, deviations, and nonconformities.
Coordinate internal audits, corrective and preventive actions, and management reviews.
Develop and monitor performance indicators to ensure the QMS is effective and continually improving.

Support and continuous improvement

Assess existing practices and processes and recommend improvements to support the evolution of CES activities.
Help integrate quality principles into daily operations.
Work with directors, technical leads, team leads, and external consultants to advance quality and accreditation objectives.
Help identify training needs and provide quality-related awareness and support activities.

Compliance and follow-up

Ensure documentation complies with requirements and that current policies, procedures, and guidelines are followed.
Coordinate activities required to obtain and maintain accreditations, including method validation and verification, proficiency testing, and interlaboratory comparisons.
Prepare reports and recommendations on QMS performance, accreditation status, and quality-related risks and issues.

The profile we are looking for

Education and experience

An undergraduate degree in life sciences, laboratory sciences, biology, biochemistry, molecular biology, or a related field, or an equivalent combination of education and experience.
At least three years of experience in quality assurance or quality management in a laboratory setting.
Demonstrated hands-on experience with ISO 15189.
Experience with laboratory quality management systems, audits, and accreditation processes.
Project management experience and a demonstrated ability to coordinate projects involving multiple stakeholders.
Knowledge of method validation and verification, nonconformity management, CAPA, internal audits, and document control.
The following would be assets:
Direct involvement in obtaining initial ISO 15189 accreditation.
Knowledge of or hands-on experience with ISO/IEC 17025.
Knowledge of or experience with other standards, frameworks, or regulatory requirements applicable to laboratories, scientific activities, or CES services.
Experience in genomics, molecular biology, or molecular diagnostics.
Knowledge of next-generation sequencing (NGS), genotyping, or bioinformatics pipelines.
Training or certification in quality auditing.

Skills and abilities

Proficiency in spoken and written French and English (the person in this role must be able to understand specialized documents and system interfaces in English and communicate with suppliers and technical support teams, most of whom are English-speaking).
Thoroughness and attention to detail.
Analytical thinking and a proactive approach to problem-solving.
A methodical, structured approach focused on achieving results.
Excellent ability to manage priorities, deadlines, and multiple projects.
Team spirit and a collaborative approach.

Why choose Génome Québec?

Because your work will have a real impact. By joining our team, you will help raise awareness of scientific advances shaping the future of Québec and beyond.

Please send us your résumé and cover letter by October 15, 2026.

Read the full bilingual original

Chez Génome Québec, nous croyons que la génomique a le pouvoir de relever certains des plus grands défis de notre société. Depuis plus de 25 ans, nous soutenons la recherche de pointe et contribuons à faire du Québec un chef de file en génomique.

Nous sommes à la recherche d’une personne reconnue pour son expertise en qualité et en accréditation afin de soutenir l’évolution des activités du Centre d’expertise et de services (CES) et le maintien des plus hauts standards de qualité pour un contrat de deux (2) ans.

Si vous aimez relever des défis complexes, agir comme référence en matière de qualité, accompagner les équipes dans l’interprétation des exigences normatives et contribuer à l’obtention et au maintien d’accréditations reconnues, ce poste est pour vous.

Ce que vous ferez

Accréditation et conformité

Piloter les démarches d’obtention, de maintien et de renouvellement des accréditations, notamment les normes ISO 15189 et ISO/IEC 17025, ainsi que toute nouvelle accréditation requise en fonction de l'évolution des activités et des besoins.
Coordonner les activités liées aux évaluations d’accréditation et agir comme principal point de contact auprès des organismes d’évaluation.
Conseiller et accompagner les équipes dans l’interprétation et l’application des exigences normatives.
Agir comme personne-ressource pour les questions liées aux normes, référentiels et exigences d’accréditation.

Système de gestion de la qualité

Développer, implanter, maintenir et faire évoluer le système de management de la qualité (SMQ).
Assurer la gestion documentaire, la gestion des changements, des risques, des écarts et des non-conformités.
Coordonner les audits internes, les actions correctives et préventives ainsi que les revues de direction.
Développer et suivre les indicateurs de performance afin d’assurer l’efficacité et l’amélioration continue du SMQ.

Accompagnement et amélioration continue

Évaluer les pratiques et processus en place et recommander les améliorations nécessaires afin de soutenir l’évolution des activités du CES.
Favoriser l’intégration des principes de qualité dans les opérations quotidiennes.
Collaborer avec les directions, les responsables techniques, les chef(fe)s d’équipe et les consultants externes afin de soutenir les objectifs qualité et d’accréditation.
Participer à la définition des besoins de formation et offrir des activités de sensibilisation et d’accompagnement en matière de qualité.

Conformité et suivi

Assurer la conformité de la documentation et veiller à l’application des politiques, procédures et directives.
Coordonner les activités requises pour l’obtention et le maintien des accréditations, notamment les validations et vérifications de méthodes, les essais d’aptitude et les comparaisons inter laboratoires.
Produire les rapports et recommandations relatifs à la performance du SMQ, à l’état des accréditations ainsi qu’aux risques et enjeux qualité.

Le profil que nous recherchons

Formation et expérience

Diplôme universitaire de premier cycle en sciences de la vie, sciences de laboratoire, biologie, biochimie, biologie moléculaire ou dans un domaine connexe, ou combinaison de formation et d’expérience jugée équivalente.
Minimum de trois (3) ans d’expérience en assurance ou gestion de la qualité dans un environnement de laboratoire.
Expérience pratique démontrée avec la norme ISO 15189.
Expérience avec les systèmes de gestion de la qualité en laboratoire, les audits et les processus d’accréditation.
Expérience en gestion de projet et capacité démontrée à coordonner des projets impliquant plusieurs parties prenantes.
Connaissance des processus de validation/vérification des méthodes, gestion des non-conformités, CAPA, audits internes et gestion documentaire.
Les éléments suivants seraient considérés comme des atouts :
Expérience ayant contribué directement à l’obtention initiale d’une accréditation ISO 15189.
Connaissance ou expérience pratique de la norme ISO/IEC 17025.
Connaissance ou expérience avec d'autres normes, référentiels ou cadres réglementaires applicables aux laboratoires, aux activités scientifiques ou aux services du CES.
Expérience en génomique, biologie moléculaire ou diagnostic moléculaire.
Connaissance des technologies de séquençage de nouvelle génération (NGS), du génotypage ou des pipelines bio-informatiques.
Formation ou certification en audit qualité.

Compétences recherchées

Maîtrise du français et de l’anglais, parlé et écrit (la personne en poste doit être en mesure de comprendre des documents spécialisés et des interfaces en anglais, et d’échanger avec des fournisseurs et le support technique des compagnies pour la plupart anglophones).
Rigueur et souci du détail.
Esprit d’analyse et capacité à résoudre les problèmes de façon proactive.
Approche méthodique et structurée favorisant l’atteinte des résultats.
Excellente gestion des priorités, des échéanciers et de projets multiples.
Esprit d'équipe et approche collaborative.

Pourquoi choisir Génome Québec?

Parce que votre travail aura une portée réelle. En rejoignant notre équipe, vous contribuerez à faire connaître des avancées scientifiques qui façonnent l’avenir du Québec et d’ailleurs.

Faites-nous parvenir votre curriculum vitae et votre lettre de motivation au plus tard le 15 octobre 2026.

*************************************************************************************************

What you will do

Accreditation and compliance

Lead efforts to obtain, maintain, and renew accreditations, particularly ISO 15189 and ISO/IEC 17025, as well as any new accreditation required as activities and needs evolve.
Coordinate accreditation assessments and serve as the primary contact for assessment bodies.
Advise and support teams in interpreting and applying the requirements of standards.
Serve as a resource on standards, frameworks, and accreditation requirements.

Quality management system

Develop, implement, maintain, and evolve the QMS.
Oversee document control, change management, risk management, deviations, and nonconformities.
Coordinate internal audits, corrective and preventive actions, and management reviews.
Develop and monitor performance indicators to ensure the QMS is effective and continually improving.

Support and continuous improvement

Assess existing practices and processes and recommend improvements to support the evolution of CES activities.
Help integrate quality principles into daily operations.
Work with directors, technical leads, team leads, and external consultants to advance quality and accreditation objectives.
Help identify training needs and provide quality-related awareness and support activities.

Compliance and follow-up

Ensure documentation complies with requirements and that current policies, procedures, and guidelines are followed.
Coordinate activities required to obtain and maintain accreditations, including method validation and verification, proficiency testing, and interlaboratory comparisons.
Prepare reports and recommendations on QMS performance, accreditation status, and quality-related risks and issues.

The profile we are looking for

Education and experience

An undergraduate degree in life sciences, laboratory sciences, biology, biochemistry, molecular biology, or a related field, or an equivalent combination of education and experience.
At least three years of experience in quality assurance or quality management in a laboratory setting.
Demonstrated hands-on experience with ISO 15189.
Experience with laboratory quality management systems, audits, and accreditation processes.
Project management experience and a demonstrated ability to coordinate projects involving multiple stakeholders.
Knowledge of method validation and verification, nonconformity management, CAPA, internal audits, and document control.
The following would be assets:
Direct involvement in obtaining initial ISO 15189 accreditation.
Knowledge of or hands-on experience with ISO/IEC 17025.
Knowledge of or experience with other standards, frameworks, or regulatory requirements applicable to laboratories, scientific activities, or CES services.
Experience in genomics, molecular biology, or molecular diagnostics.
Knowledge of next-generation sequencing (NGS), genotyping, or bioinformatics pipelines.
Training or certification in quality auditing.

Skills and abilities

Proficiency in spoken and written French and English (the person in this role must be able to understand specialized documents and system interfaces in English and communicate with suppliers and technical support teams, most of whom are English-speaking).
Thoroughness and attention to detail.
Analytical thinking and a proactive approach to problem-solving.
A methodical, structured approach focused on achieving results.
Excellent ability to manage priorities, deadlines, and multiple projects.
Team spirit and a collaborative approach.

Why choose Génome Québec?

Because your work will have a real impact. By joining our team, you will help raise awareness of scientific advances shaping the future of Québec and beyond.

Please send us your résumé and cover letter by October 15, 2026.

Apply on LinkedIn About employer

More about this job

Responsibilities

Lead accreditation activities, including obtaining, maintaining, and renewing accreditations, and develop and oversee the laboratory quality management system. Coordinate audits, corrective actions, method validation and verification, compliance monitoring, training, and continuous improvement, while reporting on system performance and quality risks.

Requirements

Requires an undergraduate degree in life sciences, laboratory sciences, or a related field (or equivalent education and experience), at least three years of laboratory quality experience, and hands-on experience with ISO 15189. Candidates should also have experience with laboratory quality systems, audits, accreditation, project coordination, method validation and verification, nonconformities, CAPA, and document control; spoken and written French and English are required.

Skills

Quality Management
Accreditation
ISO 15189
ISO/IEC 17025
Quality Management Systems
Internal Auditing
Corrective and Preventive Actions
Document Control
Risk Management
Nonconformity Management
Method Validation and Verification
Project Management
Continuous Improvement
Proficiency Testing
French and English Communication
Stakeholder Collaboration

Visa sponsorship

Not detected in the job text

Keywords

ISO 15189
ISO/IEC 17025
Accreditation
Quality Assurance
Quality Management System
Laboratory Quality Management
Document Control
Change Management
Risk Management
Nonconformity Management
Corrective and Preventive Actions
CAPA
Internal Audits
Management Reviews
Method Validation
Method Verification
Proficiency Testing
Interlaboratory Comparisons
Performance Indicators
Continuous Improvement
Project Management
Genomics
Molecular Biology
Molecular Diagnostics
Next-Generation Sequencing
NGS
Genotyping
Bioinformatics Pipelines
Quality Auditing
French and English

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