Job Title

Overview (Franais) Le poste Rejoindre Moderna, c'est saisir une occasion unique de participer un projet avant-gardiste qui rvolutionne la mdecine avec la technologie de l'ARNm. Notre portefeuille vari comprend plusieurs programmes de dveloppement ciblant diverses maladies. En tant que membre de notre quipe, vous contribuerez une organisation en pleine expansion, collaborant avec des collgues hors pair et des partenaires stratgiques travers le monde, tout en apportant votre pierre l'difice des initiatives de sant globales. Chez Moderna, notre dvouement repousser les limites de la technologie des mdicaments ARNm promet une carrire stimulante et enrichissante, offrant la chance d'impacter significativement la vie des patients de par le monde. Laval, le partenariat stratgique de longue dure entre Moderna et le gouvernement canadien est en train de rvolutionner la prparation et la ractivit du pays face aux pandmies. Notre prochaine installation de production de vaccins ARNm, la pointe de la technologie, jouera un rle central en garantissant un accs rapide aux vaccins pour les virus respiratoires, sous rserve de l'approbation de Sant Canada. En investissant dans le dveloppement des comptences locales et en encourageant les collaborations en recherche et dveloppement, nous renforons la position du Canada en tant que leader mondial dans le domaine de l'ARNm. Rejoignez-nous dans notre engagement btir un avenir robuste dans le domaine de la biotechnologie et de l'innovation dans les soins de sant. Le/la Directeur(trice) Associ(e), Conformit du site, Canada, jouera un rle de leadership stratgique dans limplantation et la gestion du Systme de gestion de la qualit (SGQ) de Moderna sur notre site de fabrication Laval. Cette personne assurera la conformit du site aux exigences rglementaires mondiales et locales en mettant en place des processus robustes, en maintenant un tat constant de prparation aux inspections, et en dveloppant une culture proactive de qualit. Relevant de la direction qualit du site, ce rle collaborera avec les quipes Qualit, Fabrication et Conformit mondiale tout en dirigeant une quipe ddie Laval. Le poste offre galement lopportunit de travailler avec des outils numriques de pointe, incluant des solutions bases sur lIA gnrative pour soutenir lanalyse de conformit, la gestion des donnes qualit, et loptimisation des processus numriques. Ce que vous ferez Vos principales responsabilits seront : Mettre en uvre le SGQ de Moderna sur le site de Laval conformment au Manuel Qualit global et aux politiques de lentreprise. Piloter lamlioration continue du SGQ selon lvolution des exigences rglementaires, des normes industrielles et des donnes de conformit. Assurer un leadership transversal en tant quexpert(e) en conformit GxP, et agir comme propritaire des processus lis aux Dviations, Changements, Plaintes, Escalades, Comits d'examen des matriaux, Revues qualit, et aux rapports aux autorits rglementaires. Superviser les processus lis la Gestion des risques qualit, la Documentation, la Formation, lIntgrit des donnes et aux systmes numriques associs (e.g., eQMS, LMS, LIMS, ERP). Maintenir un tat permanent de prparation aux inspections rglementaires, y compris la gestion des audits internes et des inspections dautorits de sant. Diriger des forums qualit (Revue de direction qualit, Conseil qualit, Comit de revue des dviations, etc.) et remonter les enjeux au leadership du site. Appliquer des outils de rsolution structure de problmes (5 Pourquoi, arbre de dfaillance, diagramme dIshikawa, AMDEC) pour renforcer la qualit produit et la performance du SGQ. Reprsenter le site dans les Conseils mondiaux de conformit et assurer le dploiement local conforme des initiatives SGQ globales. Collaborer avec les quipes Digital et Qualit globale pour concevoir des processus efficients intgrant des outils dIA gnrative. Dvelopper une culture qualit sur le site travers la formation, le coaching, et lapproche bien du premier coup. Vos responsabilits comprendront galement : Diriger et encadrer une quipe de professionnels de la conformit base Laval. tre responsable des interactions avec les inspecteurs rglementaires (salle de front), tout en grant la logistique en salle arrire (tri des demandes, prparation des experts, documentation, briefings). Piloter le Programme dauto-inspection du site. Assurer ladoption et le dploiement efficace de solutions numriques avances incluant des outils bass sur lIA pour la surveillance de conformit, la prparation aux audits et lapprentissage digital. laborer des plans de relve et de dveloppement pour les rles critiques de conformit sur le site. Les mindsets cls de Moderna ncessaires pour russir dans ce rle : Nous agissons en tant que propritaires. Les solutions que nous construisons vont au-del de toute description de poste. Dans ce rle, vous incarnerez une posture de leadership intgral en assurant la gouvernance du SGQ de Laval avec une vision long terme et une grande rigueur. Vous reprsenterez lengagement qualit de Moderna travers vos dcisions et vos actions. Nous numrisons partout o cest possible, en utilisant la puissance du code pour maximiser notre impact sur les patients. Ce mindset est essentiel alors que vous serez au cur de la transformation numrique du systme de qualit. Vous serez un catalyseur dans ladoption de technologies modernes, notamment lIA gnrative, pour optimiser la conformit, la gestion des donnes et la formation. Ce dont vous aurez besoin (Qualifications de base) Diplme de baccalaurat (en sciences ou en ingnierie de prfrence) avec un minimum de 8 ans dexprience applique en qualit pharmaceutique/biologique. Solide comprhension des systmes de qualit pharmaceutiques et conformit GMP/GxP dans un environnement de fabrication commerciale. Exprience en soutien ou en gestion dinspections des autorits de sant (ex. : Sant Canada, FDA, EMA/PIC/S). Dans le cadre de lengagement de Moderna pour btir une main-duvre durable, une autorisation de travail minimale de 2 ans est requise pour ce poste. Ce que vous apporterez lquipe (Qualifications prfres) Diplme avanc (M.Sc., PharmD, MBA) ou certifications supplmentaires (ASQ CQA/CQE, auditeur principal, Six Sigma/Lean). Exprience en leadership dans les domaines de la conformit de site ou de rseau, des systmes qualit, ou des oprations AQ, incluant la gestion dquipe et linfluence interfonctionnelle sans autorit. Expertise des rglements et normes mondiaux relatifs aux produits biologiques/fabrication strile : ICH Q10/Q9/Q7, EU Annexe 1, PIC/S, 21 CFR 210/211/600, 21 CFR Partie 11/Annexe 11, et les lignes directrices de Sant Canada (GUI). Exprience dmontre dans la gestion dinspections (porte-parole en salle de front, responsable en salle arrire), incluant la planification de la prparation, les storyboards, lencadrement des experts, la gestion des enjeux, et le contrle quotidien des inspections. Exprience pratique de la gestion dlments cls du SGQ (Dviations/CAPA, Contrle des changements, Plaintes/Rappels, Gestion des fournisseurs, Revue de gestion, Notifications la direction) et des indicateurs de performance associs. Leadership dmontr en matire dintgrit des donnes (ALCOA+) et conformit des systmes informatiss (CSV/GAMP 5); exprience avec les plateformes qualit numriques (ex. : Veeva/TrackWise, SAP/Oracle, LIMS, LMS, eDoc). Exprience en traitement aseptique/injectables striles, produits biologiques, vaccins ou plateformes ARNm; comprhension de la stratgie de contrle de contamination et de la classification des salles blanches. Solide comptence en gestion des risques et gouvernance (QRM, AMDEC, registres de risques) avec une capacit bien prioriser et escalader. Esprit damlioration continue; matrise de la conception dindicateurs, des tableaux de bord, et de lanalyse des tendances pour surveiller la sant du SGQ et guider les dcisions. Matrise du franais et de langlais fortement prfre, avec dexcellentes comptences en communication crite et orale, et une forte prsence excutive. Capacit naviguer les attentes de Sant Canada au Qubec et les interfaces avec les autorits rglementaires internationales; exprience dans des environnements de reconnaissance mutuelle/PIC/S un atout. Historique de dveloppement des talents, de cration dquipes performantes et de promotion dune culture de qualit et de responsabilisation. Franais et Anglais (EN) The Role Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization, working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience, with the potential to make a significant impact on patients' lives worldwide. In Laval, Moderna's long-term strategic partnership with the Canadian Government is revolutionizing the nation's pandemic preparedness and response capabilities. Our upcoming state-of-the-art mRNA vaccine manufacturing facility will play a pivotal role in ensuring rapid access to vaccines for respiratory viruses, contingent on Health Canada's approval. By investing in local talent development and fostering research and development collaborations, we're cementing Canada's position as a global center of mRNA excellence. Join us as we build a resilient future in biotechnology and healthcare innovation. The Associate Director, Site Compliance, Canada will play a critical leadership role in shaping and delivering Modernas Quality Management System (QMS) at our Laval manufacturing facility. This role ensures the sites compliance with global and local regulatory requirements through strong governance, continuous improvement, and a proactive culture of inspection readiness. Reporting to site Quality leadership, you will act as a strategic partner across Quality, Manufacturing, and Global Compliance functions, guiding internal teams through GxP compliance expectations while directly managing a team of quality professionals in Laval. With direct engagement in enterprise-level QMS initiatives and digital transformation projects, you will also be well positioned to interact with Generative AI tools being introduced to enhance compliance analytics, quality data management, and digital process optimization. Heres What Youll Do Your key responsibilities will be: Lead the implementation of Modernas QMS at the Laval site, ensuring alignment with the global Quality Manual, policies, and procedures. Drive continuous QMS improvement based on evolving regulatory expectations, industry standards, and compliance data. Provide cross-functional leadership as a subject matter expert (SME) for GxP compliance and act as site process owner for core QMS elements, including Deviation Management, Change Control, Complaints, Notifications to Management, MRBs, Quality Reviews, and Health Authority reporting. Oversee compliance processes in Quality Risk Management, Documentation, Training, and Data Integrity; ensure digital systems (e.g., eQMS, LMS, LIMS, ERP) are adopted and governed effectively. Maintain a proactive state of inspection readiness, including management of internal audits and Health Authority inspections. Lead forums such as Quality Management Review, Quality Council, and Deviation Review Board to assess performance and escalate risks as needed. Drive compliance excellence through structured problem solving (e.g., 5 Whys, fault tree, fishbone, FMEA) to improve product quality and performance. Represent Laval on Global Compliance Councils and lead compliant implementation of global QMS initiatives at site level. Partner with Digital and Global Quality teams to co-design efficient, AI-enhanced digital processes that streamline compliance activities. Build site quality culture by coaching teams on quality behaviors, right-first-time execution, and data integrity. Your responsibilities will also include: Leading and developing a high-performing compliance team based in Laval. Facilitating Health Authority inspections with excellence managing front room communications and running the back room (triage, SME prep, document control, and briefings). Owning the sites Self-Inspection Program and ensuring alignment with Modernas inspection readiness standards. Driving adoption of advanced tools, including Generative AI solutions for predictive compliance insights, audit readiness, and digital learning integration. Supporting succession planning and development pathways for critical compliance roles within the Laval Quality team. The key Moderna Mindsets youll need to succeed in the role: We behave like owners. The solutions were building go beyond any job description. In this role, youll own critical aspects of compliance and inspection readiness, treating the Laval sites QMS with the accountability and foresight required to uphold Modernas quality promise. Your influence will extend across departments and global stakeholders. We digitize everywhere possible using the power of code to maximize our impact on patients. This mindset is essential as you help drive adoption of AI-driven compliance tools and data systems (e.g., eQMS, LIMS). You'll champion digital process transformation while maintaining full regulatory compliance. Heres What Youll Need (Basic Qualifications) Bachelors degree (Sciences or Engineering preferred) with 8+ years of applied pharmaceutical/biologics quality experience. Demonstrated depth in Pharmaceutical Quality Systems and GMP/GxP compliance within commercial manufacturing environments. Experience supporting or hosting Health Authority inspections (e.g., Health Canada, FDA, EMA/PIC/S). As part of Modernas commitment to build a sustainable workforce, a minimum of 2 years of work authorization is required for this role. Heres What Youll Bring to the Table (Preferred Qualifications) Advanced degree (MSc, PharmD, MBA) or additional certification (ASQ CQA/CQE, Lead Auditor, Six Sigma/Lean). Leadership experience in site or network compliance, quality systems, or QA operations, including people leadership and crossfunctional influence without authority. Expertise with global regulations and standards relevant to biologics/sterile manufacturing: ICH Q10/Q9/Q7, EU Annex 1, PIC/S, 21 CFR 210/211/600 series, 21 CFR Part 11/Annex 11, and Health Canada GUI guidance. Proven inspection leadership (frontroom spokesperson, backroom lead) with strong readiness planning, storyboards, SME coaching, issue management, and daily inspection control rooms. Handson ownership of core QMS elements (Deviation/CAPA, Change Control, Complaints/Recall, Supplier Management, QMR, Notifications to Management) and associated KPIs. Demonstrated data integrity leadership (ALCOA+) and computerized system compliance (CSV/GAMP 5); experience with digital quality platforms (e.g., Veeva/TrackWise, SAP/Oracle, LIMS, LMS, eDoc). Experience in aseptic processing/sterile injectables, biologics, vaccines, or mRNA platforms; working knowledge of contamination control strategy and cleanroom classification. Strong risk management and governance (QRM, FMEA, risk registers) with ability to prioritize and escalate effectively. Continuous improvement mindset; skilled in metrics design, dashboards, and trend analysis to monitor QMS health and drive decisions. Bilingual French/English strongly preferred, exceptional written and verbal communication with executive presence. Ability to navigate Health Canada expectations in Qubec and global regulator interfaces; experience with mutual recognition/PIC/S settings a plus. Track record of talent development, building highperforming teams, and shaping a culture of quality and accountability. Franais et Anglais The Role (EN) Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization, working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience, with the potential to make a significant impact on patients' lives worldwide. In Laval, Moderna's long-term strategic partnership with the Canadian Government is revolutionizing the nation's pandemic preparedness and response capabilities. Our upcoming state-of-the-art mRNA vaccine manufacturing facility will play a pivotal role in ensuring rapid access to vaccines for respiratory viruses, contingent on Health Canada's approval. By investing in local talent development and fostering research and development collaborations, we're cementing Canada's position as a global center of mRNA excellence. Join us as we build a resilient future in biotechnology and healthcare innovation. The Associate Director, Site Compliance, Canada will play a critical leadership role in shaping and delivering Modernas Quality Management System (QMS) at our Laval manufacturing facility. This role ensures the sites compliance with global and local regulatory requirements through strong governance, continuous improvement, and a proactive culture of inspection readiness. Reporting to site Quality leadership, you will act as a strategic partner across Quality, Manufacturing, and Global Compliance functions, guiding internal teams through GxP compliance expectations while directly managing a team of quality professionals in Laval. With direct engagement in enterprise-level QMS initiatives and digital transformation projects, you will also be well positioned to interact with Generative AI tools being introduced to enhance compliance analytics, quality data management, and digital process optimization. Heres What Youll Do Your key responsibilities will be: Lead the implementation of Modernas QMS at the Laval site, ensuring alignment with the global Quality Manual, policies, and procedures. Drive continuous QMS improvement based on evolving regulatory expectations, industry standards, and compliance data. Provide cross-functional leadership as a subject matter expert (SME) for GxP compliance and act as site process owner for core QMS elements, including Deviation Management, Change Control, Complaints, Notifications to Management, MRBs, Quality Reviews, and Health Authority reporting. Oversee compliance processes in Quality Risk Management, Documentation, Training, and Data Integrity; ensure digital systems (e.g., eQMS, LMS, LIMS, ERP) are adopted and governed effectively. Maintain a proactive state of inspection readiness, including management of internal audits and Health Authority inspections. Lead forums such as Quality Management Review, Quality Council, and Deviation Review Board to assess performance and escalate risks as needed. Drive compliance excellence through structured problem solving (e.g., 5 Whys, fault tree, fishbone, FMEA) to improve product quality and performance. Represent Laval on Global Compliance Councils and lead compliant implementation of global QMS initiatives at site level. Partner with Digital and Global Quality teams to co-design efficient, AI-enhanced digital processes that streamline compliance activities. Build site quality culture by coaching teams on quality behaviors, right-first-time execution, and data integrity. Your responsibilities will also include: Leading and developing a high-performing compliance team based in Laval. Facilitating Health Authority inspections with excellence managing front room communications and running the back room (triage, SME prep, document control, and briefings). Owning the sites Self-Inspection Program and ensuring alignment with Modernas inspection readiness standards. Driving adoption of advanced tools, including Generative AI solutions for predictive compliance insights, audit readiness, and digital learning integration. Supporting succession planning and development pathways for critical compliance roles within the Laval Quality team. The key Moderna Mindsets youll need to succeed in the role: We behave like owners. The solutions were building go beyond any job description. In this role, youll own critical aspects of compliance and inspection readiness, treating the Laval sites QMS with the accountability and foresight required to uphold Modernas quality promise. Your influence will extend across departments and global stakeholders. We digitize everywhere possible using the power of code to maximize our impact on patients. This mindset is essential as you help drive adoption of AI-driven compliance tools and data systems (e.g., eQMS, LIMS). You'll champion digital process transformation while maintaining full regulatory compliance. Heres What Youll Need (Basic Qualifications) Bachelors degree (Sciences or Engineering preferred) with 8+ years of applied pharmaceutical/biologics quality experience. Demonstrated depth in Pharmaceutical Quality Systems and GMP/GxP compliance within commercial manufacturing environments. Experience supporting or hosting Health Authority inspections (e.g., Health Canada, FDA, EMA/PIC/S). As part of Modernas commitment to build a sustainable workforce, a minimum of 2 years of work authorization is required for this role. Heres What Youll Bring to the Table (Preferred Qualifications) Advanced degree (MSc, PharmD, MBA) or additional certification (ASQ CQA/CQE, Lead Auditor, Six Sigma/Lean). Leadership experience in site or network compliance, quality systems, or QA operations, including people leadership and crossfunctional influence without authority. Expertise with global regulations and standards relevant to biologics/sterile manufacturing: ICH Q10/Q9/Q7, EU Annex 1, PIC/S, 21 CFR 210/211/600 series, 21 CFR Part 11/Annex 11, and Health Canada GUI guidance. Proven inspection leadership (frontroom spokesperson, backroom lead) with strong readiness planning, storyboards, SME coaching, issue management, and daily inspection control rooms. Handson ownership of core QMS elements (Deviation/CAPA, Change Control, Complaints/Recall, Supplier Management, QMR, Notifications to Management) and associated KPIs. Demonstrated data integrity leadership (ALCOA+) and computerized system compliance (CSV/GAMP 5); experience with digital quality platforms (e.g., Veeva/TrackWise, SAP/Oracle, LIMS, LMS, eDoc). Experience in aseptic processing/sterile injectables, biologics, vaccines, or mRNA platforms; working knowledge of contamination control strategy and cleanroom classification. Strong risk management and governance (QRM, FMEA, risk registers) with ability to prioritize and escalate effectively. Continuous improvement mindset; skilled in metrics design, dashboards, and trend analysis to monitor QMS health and drive decisions. Bilingual French/English strongly preferred, exceptional written and verbal communication with executive presence. Ability to navigate Health Canada expectations in Qubec and global regulator interfaces; experience with mutual recognition/PIC/S settings a plus. Track record of talent development, building highperforming teams, and shaping a culture of quality and accountability. Framing in English (EN) The Role Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization, working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience, with the potential to make a significant impact on patients' lives worldwide. In Laval, Moderna's long-term strategic partnership with the Canadian Government is revolutionizing the nation's pandemic preparedness and response capabilities. Our upcoming state-of-the-art mRNA vaccine manufacturing facility will play a pivotal role in ensuring rapid access to vaccines for respiratory viruses, contingent on Health Canada's approval. By investing in local talent development and fostering research and development collaborations, we&aposre cementing Canada's position as a global center of mRNA excellence. Join us as we build a resilient future in biotechnology and healthcare innovation. The Associate Director, Site Compliance, Canada will play a critical leadership role in shaping and delivering Modernas Quality Management System (QMS) at our Laval manufacturing facility. This role ensures the sites compliance with global and local regulatory requirements through strong governance, continuous improvement, and a proactive culture of inspection readiness. Reporting to site Quality leadership, you will act as a strategic partner across Quality, Manufacturing, and Global Compliance functions, guiding internal teams through GxP compliance expectations while directly managing a team of quality professionals in Laval. With direct engagement in enterprise-level QMS initiatives and digital transformation projects, you will also be well positioned to interact with Generative AI tools being introduced to enhance compliance analytics, quality data management, and digital process optimization. Heres What Youll Do (EN) Your key responsibilities will be: Lead the implementation of Modernas QMS at the Laval site, ensuring alignment with the global Quality Manual, policies, and procedures. Drive continuous QMS improvement based on evolving regulatory expectations, industry standards, and compliance data. Provide cross-functional leadership as a subject matter expert (SME) for GxP compliance and act as site process owner for core QMS elements, including Deviation Management, Change Control, Complaints, Notifications to Management, MRBs, Quality Reviews, and Health Authority reporting. Oversee compliance processes in Quality Risk Management, Documentation, Training, and Data Integrity; ensure digital systems (e.g., eQMS, LMS, LIMS, ERP) are adopted and governed effectively. Maintain a proactive state of inspection readiness, including management of internal audits and Health Authority inspections. Lead forums such as Quality Management Review, Quality Council, and Deviation Review Board to assess performance and escalate risks as needed. Drive compliance excellence through structured problem solving (e.g., 5 Whys, fault tree, fishbone, FMEA) to improve product quality and performance. Represent Laval on Global Compliance Councils and lead compliant implementation of global QMS initiatives at site level. Partner with Digital and Global Quality teams to co-design efficient, AI-enhanced digital processes that streamline compliance activities. Build site quality culture by coaching teams on quality behaviors, right-first-time execution, and data integrity. Your responsibilities will also include: Leading and developing a high-performing compliance team based in Laval. Facilitating Health Authority inspections with excellence managing front room communications and running the back room (triage, SME prep, document control, and briefings). Owning the sites Self-Inspection Program and ensuring alignment with Modernas inspection readiness standards. Driving adoption of advanced tools, including Generative AI solutions for predictive compliance insights, audit readiness, and digital learning integration. Supporting succession planning and development pathways for critical compliance roles within the Laval Quality team. The key Moderna Mindsets youll need to succeed in the role: We behave like owners. The solutions were building go beyond any job description. In this role, youll own critical aspects of compliance and inspection readiness, treating the Laval sites QMS with the accountability and foresight required to uphold Modernas quality promise. Your influence will extend across departments and global stakeholders. We digitize everywhere possible using the power of code to maximize our impact on patients. This mindset is essential as you help drive adoption of AI-driven compliance tools and data systems (e.g., eQMS, LIMS). You'll champion digital process transformation while maintaining full regulatory compliance. Expirasyon Les avantages offerts peuvent varier selon la nature de votre emploi chez Moderna et le pays dans lequel vous travaillez. propos de Moderna Depuis notre fondation en 2010, nous aspirons btir la principale plateforme technologique dARNm, linfrastructure pour rinventer comment les mdicaments sont crs et distribus, ainsi quune quipe de calibre mondial. Nous croyons quil est important doffrir nos employs une plateforme pour transformer la mdecine et une opportunit de changer le monde. En vivant notre mission, nos valeurs et nos faons de penser chaque jour, nos employs sont le moteur de notre progrs scientifique et de notre culture. Ensemble, nous crons une culture dinclusion et btissons une organisation qui se soucie profondment de ses patients, de ses employs, de lenvironnement et des communauts. Nous sommes fiers davoir t 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 tats-Unis. En btissant notre entreprise, nous avons toujours cru quune culture en personne est essentielle notre succs. Moderna dfend les avantages importants de la collaboration en prsentiel en adoptant un modle de travail 70/30. Cette structure 70 % au bureau favorise une culture riche en innovation, en travail dquipe et en mentorat direct. Joignez-vous nous pour faonner un monde o chaque interaction est une opportunit dapprendre, de contribuer et davoir un impact significatif. Si vous souhaitez faire une diffrence et rejoindre une quipe qui transforme lavenir de la mdecine, nous vous invitons visiter modernatx.com/careers pour en savoir plus sur nos possibilits actuelles. Moderna est un environnement de travail sans fume, sans alcool et sans drogue. Moderna est un lieu o chacun peut voluer. Si vous rpondez aux qualifications de base du poste et que vous tes enthousiaste lide de contribuer notre mission chaque jour, veuillez postuler! Moderna sengage offrir lgalit daccs lemploi et ne pratiquer aucune discrimination envers ses employs ou les candidats qualifis, sans gard la race, la couleur, au sexe, lidentit ou lexpression de genre, lge, la religion, lorigine nationale, lascendance ou la citoyennet, lethnie, un handicap, au statut militaire ou de vtran protg, aux informations gntiques, lorientation sexuelle, ltat civil ou familial, ou toute autre caractristique personnelle protge par la loi en vigueur. Nous tudions les candidatures qualifies, peu importe les antcdents judiciaires, conformment aux exigences lgales. Nous nous concentrons sur lattraction, la rtention, le dveloppement et la progression de nos employs. En cultivant un milieu de travail qui valorise les expriences, les origines et les ides diversifies, nous crons un environnement o chaque employ peut donner le meilleur de lui-mme. Moderna sengage offrir des mesures dadaptation raisonnables aux candidats qualifis en situation de handicap. Tout candidat ncessitant une mesure dadaptation dans le cadre du processus dembauche et/ou pour exercer les fonctions essentielles du poste pour lequel il postule est invit contacter lquipe responsable des congs et des mesures dadaptation ladresse suivante : . ------------------------------------------------------------------------------------------------------------------------------------------------------ #J-18808-Ljbffr