Responsable Qualité du site, Fabrication et Approvisionnement Canada - Site Quality Head, Canada Manufacturing and Supply (Laval)

Responsable Qualité du site, Fabrication et Approvisionnement Canada - Site Quality Head, Canada Manufacturing and Supply (Laval)

05 Oct
|
Moderna
|
Laval

05 Oct

Moderna

Laval

The Role: The Site Quality Head, Canada Manufacturing & Supply is a senior quality leader accountable for end-to-end quality oversight of Moderna’s Canada operations.

This role provides strategic and operational leadership to ensure robust, compliant, and inspection-ready quality systems that support commercial and clinical manufacturing across internal sites and external partners.

As the senior quality authority for the Laval site and Canada Commercial organization, this leader ensures that quality policies, systems, and practices are effectively implemented, maintained, and continuously improved in alignment with global quality strategy and regulatory expectations.

The position serves as a key member of site and enterprise leadership teams, acting as the primary quality representative to global regulators and health authorities, and fostering a strong, visible culture of quality on the manufacturing floor and across external manufacturing networks.

The role is instrumental in enabling growth, innovation, and operational excellence by ensuring quality systems are scalable, resilient, and aligned with Moderna’s long-term business and patient commitments.

Here’s What You’ll Do: Provide direct oversight of the Laval Quality organization, External DP CMO and Country Quality operation for Canada Quality Assurance organization.

Establish and effectively lead a dedicated organization responsible for supporting Drug Substance and Drug Product Commercial and Clinical manufacturing operations.

Ensure the quality policy and objectives are understood, implemented, and maintained at all levels of the Laval site.

Ensure quality systems, processes, specifications, and SOPs are appropriate for the manufacture, testing, release, and distribution of product for the Laval site and consistent with the global quality strategy, and all relevant regulatory requirements.

Implement and ensure full comprehension and adherence to quality policies, procedures, and training across the site, with an emphasis on contamination control and compliance with GMP.

Ensure personnel in the Canada Manufacturing and Commercial organizations follow Good Documentation Practices and Data Integrity requirements to ensure data, documentation, and records are completed and maintained for use by the business and available to support audits or inspections.

Ensure personnel in the Canada Manufacturing and Commercial organizations are properly trained and complete training in assigned learning plans according to the defined timing and prescribed requalification cadence.

Monitor key quality system metrics, process indicators, and overall health of the cGMP Quality Management System (QMS) at the Laval site and External Manufacturing organization to proactively identify and address quality systems or product issues and ensure its continuing stability, effectiveness, and improvement.

Responsible for Quality Management Review (QMR) and assure that there are no significant interruptions to the business due to quality or compliance issues.

Ensure all deviations from established procedures are appropriately documented and investigated by the Quality Unit.

Ensure processes and materials are appropriately qualified and validated to align with the phase of the production program.

Ensure appropriate maintenance and a state of qualification is maintained for equipment and facilities.

Manage and maintain the Laval site and Commercial Office self-inspection program.

Ensure a consistent Quality Assurance presence on the manufacturing floor, fostering a culture of quality and compliance.

Engage in detailed reviews and approvals of cGMP documentation, such as Change Management, Deviation Management, and Batch Records, aligning them with global processes.

For external manufacturing, this includes Person-in-Plant programs.

Ensure robust and timely processes for Batch Disposition, contributing to the efficiency and reliability of our manufacturing operations.

Identify and assign appropriate deputies to support business in times of absence.

Build, coach, and lead a high-performing quality organization aligned with Moderna’s values, quality objectives, and strategic goals.

Set clear goals, objectives, and expectations for team members and actively monitor execution to ensure alignment with business priorities.

Provide guidance and direction to employees in line with organizational strategies, fostering clarity and accountability.

Inspire and motivate team members to reach their full potential, recognizing and celebrating high performance.

Establish succession plans and employee development plans to build long-term capability and organizational resilience.

Foster a positive, inclusive, and high-trust work culture that promotes collaboration, innovation, and continuous improvement.

Act as a role model for Moderna’s Quality Culture and Mindsets, leading by example and upholding the highest ethical and compliance standards.

Serve as the senior quality representative on Site Leadership Teams,



responsible for quality culture and compliance performance.

Interface directly with health authorities (FDA, EMA, Health Canada, etc.) during inspections and regulatory communications.

Ensure sites are inspection-ready and aligned with Moderna’s global standards.

Support site-level execution of product technology transfers, new product introductions, and continued process verification (CPV).

Drive cross-functional project planning, governance, and risk management efforts.

Collaborate with internal and external stakeholders to deliver manufacturing and quality milestones.

Provide strategic support for Global Quality transformation initiatives, aligning objectives, scope, and outcomes with broader Quality and enterprise priorities.

Serve as a senior cross-functional integrator, partnering with Global Quality, site leaders, Manufacturing, Digital, and other stakeholders to drive alignment and decision-making across regions.

Lead organizational change and stakeholder engagement at the director level, influencing leaders and teams to adopt new processes, capabilities, and ways of working.

Establish mechanisms to measure impact, sustainability, and value realization, transitioning outcomes and ownership to steady-state Quality teams at project completion.

Additional duties may be assigned as needed.

Here’s What You’ll Need (Basic Qualifications): Education: Bachelor’s / Master’s Degree.

Experience: BS or equivalent and 12+ years of experience, or a Master’s level degree and 8+ years of experience in the pharmaceutical/biotech industry.

Demonstrated aptitude or ability to learn in order to gain a strong understanding of GMP regulations The position requires proficiency in both French and English due to interactions with teams, partners, and tools located outside Quebec Our Working Model As we build our company, we have always believed that an in-person culture is critical to our success.

This role is 100% onsite, reflecting the importance of being physically present to support the work, collaborate closely with colleagues, and contribute to our site-based operations.

Working onsite enables real-time collaboration, solid team connections, direct mentorship, and the hands-on partnership needed to deliver our mission.

Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.

Moderna is a smoke-free, alcohol-free, and drug-free work environment.

As part of Moderna’s commitment to build a sustainable workforce, a minimum of 2 years of work authorization is required for this role.

As part of Moderna’s commitment to workplace safety and in compliance with Health Canada requirements, pre-hire and periodic medical evaluations are required for this role. Rémunération et avantages sociaux Chez Moderna, nous croyons que lorsque vous vous sentez au mieux de votre forme, vous pouvez donner le meilleur de vous-même. C’est pourquoi nos avantages sociaux mondiaux et nos ressources en matière de bien-être sont conçus pour vous soutenir – au travail, à la maison et partout entre les deux.

Des soins de santé de premier ordre, ainsi que des programmes d'avantages volontaires adaptés à vos besoins spécifiques Une approche holistique du bien-être, avec un accès à des services de remise en forme, de pleine conscience et de soutien en santé mentale Des avantages pour la construction familiale, y compris un soutien en matière de fertilité, d’adoption et de gestation pour autrui Des congés généreux, incluant les vacances, les jours fériés, les journées de bénévolat, les congés sabbatiques, les journées mondiales de ressourcement, ainsi qu'une fermeture discrétionnaire en fin d’année Des solutions d’épargne et d’investissement pour vous aider à planifier votre avenir Des avantages et extras spécifiques à chaque lieu Les avantages offerts peuvent varier en fonction de la nature de votre emploi chez Moderna et du pays dans lequel vous travaillez La fourchette salariale pour ce poste est de $185,250.00 - $204,750.00.

Cette fourchette représente le salaire de base minimal et maximal que nous prévoyons offrir pour ce poste selon notre structure de rémunération actuelle.

Le salaire de base réellement offert à chaque employé est déterminé avec diligence, en tenant compte de facteurs tels que l’expérience pertinente, les compétences, les qualifications, la formation, le rendement et les besoins de l’entreprise.





Nous révisons régulièrement les fourchettes salariales et la rémunération individuelle afin d’assurer notre compétitivité par rapport au marché externe et de maintenir l’équité interne, conformément aux principes de rémunération et de transparence salariale de l’entreprise.

La personne retenue pourrait être admissible à une prime annuelle discrétionnaire, à d’autres formes de rémunération incitative ou à une attribution de titres de participation, sous réserve des critères d’admissibilité applicables aux régimes en vigueur et du rendement individuel.

Veuillez noter que ces renseignements sont fournis à des fins de transparence et de conformité réglementaire.

Ils ne constituent pas un engagement contractuel ni une garantie d’un taux de rémunération précis. À propos de Moderna Depuis notre fondation en 2010, nous aspirons à bâtir la principale plateforme technologique d’ARNm, l’infrastructure pour réinventer la manière dont les médicaments sont créés et distribués, ainsi qu’une équipe de calibre mondial.

Nous croyons qu’il est important d’offrir à nos employés une plateforme pour transformer la médecine et une opportunité de changer le monde.

En vivant notre mission, nos valeurs et nos façons de penser chaque jour, nos employés sont le moteur de notre progrès scientifique et de notre culture.

Ensemble, nous créons une culture d’inclusion et bâtissons une organisation qui se soucie profondément de ses patients, de ses employés, de l’environnement et des communautés.

Nous sommes fiers d’avoir été reconnus comme un des meilleurs employeurs biopharmaceutiques par Science Magazine , un des meilleurs milieux de travail pour les innovateurs par Fast Company , et un excellent lieu de travail aux États-Unis.

Si vous souhaitez faire une différence et rejoindre une équipe qui transforme l’avenir de la médecine, nous vous invitons à visiter pour en savoir plus sur nos possibilités actuelles.

Moderna est un lieu où chacun peut évoluer.

Si vous répondez aux qualifications de base du poste et que vous êtes enthousiaste à l’idée de contribuer à notre mission chaque jour, veuillez postuler! Moderna s’engage à offrir l’égalité d’accès à l’emploi et à ne pratiquer aucune discrimination envers ses employés ou les candidats qualifiés, sans égard à la race, à la couleur, au sexe, à l’identité ou l’expression de genre, à l’âge, à la religion, à l’origine nationale, à l’ascendance ou à la citoyenneté, à l’ethnie, à un handicap, au statut militaire ou de vétéran protégé, aux informations génétiques, à l’orientation sexuelle, à l’état civil ou familial, ou à toute autre caractéristique personnelle protégée par la loi en vigueur.

Nous étudions les candidatures qualifiées, peu importe les antécédents judiciaires, conformément aux exigences légales.

Nous nous concentrons sur l’attraction, la rétention, le développement et la progression de nos employés.

En cultivant un milieu de travail qui valorise les expériences, les origines et les idées diversifiées, nous créons un environnement où chaque employé peut donner le meilleur de lui-même. ------------------------------------------------------------------------------------------------------------------------------------------------------ Pay & Benefits At Moderna, we believe that when you feel your best, you can do your best work.

That’s why our global benefits and well-being resources are designed to support you—at work, at home, and everywhere in between.

Competitive healthcare, plus voluntary benefit programs to support your unique needs A holistic approach to well-being with access to fitness, mindfulness, and mental health support Family building benefits, including fertility, adoption, and surrogacy support Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown Savings and investments to help you plan for the future Location-specific perks and extras The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.

The salary range for this role is $185,250.00 - $204,750.00.

This range reflects the minimum and maximum base pay we expect to pay for this position based on our current compensation structure.

The actual base pay offered to each employee is determined with due diligence, taking into account factors such as relevant experience, skills, qualifications, education, performance, and business requirements.

We regularly review pay ranges and individual compensation to ensure competitiveness with the external market and to maintain internal equity in alignment with our company’s compensation and pay-transparency principles.

The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or an equity award, subject to applicable plan eligibility criteria and individual performance.

Please note that this information is provided for transparency and compliance purposes.

It does not constitute a contractual commitment or guarantee of a specific rate of pay.

📌 Responsable Qualité du site, Fabrication et Approvisionnement Canada - Site Quality Head, Canada Manufacturing and Supply (Laval)
🏢 Moderna
📍 Laval

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