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Technician - mRNA Vaccines Production - Night Shift


Moderna


Location

Laval, QC | Canada


Job description

The Role:
J oining 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 strategic partnership with the Canadian Government is reshaping 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. We're investing in local talent development and research collaborations, reinforcing Canada's position as a global mRNA excellence center.

Moderna is seeking a qualified Technician for the production of mRNA vaccines at our new manufacturing facility in Laval, Canada. This role involves operating production equipment in compliance with cGMP standards and health and safety regulations. The successful candidate will have excellent technical skills, a scientific mindset, and a commitment to meticulous work. Knowledge of mRNA processes is an asset.

Here’s What You’ll Do:
Within 3 Months, You Will…

Operate equipment and prepare buffer solutions for the manufacturing process.

Manage transcription, filtration, and purification processes using automated and computer-assisted equipment.

Sample for analyses at critical stages of the process and conduct environmental controls.

Apply performance tools in place, working as a team to achieve operational KPIs objectives.

Within 6 Months, You Will…

Clean equipment and manufacturing/preparation areas.

Proactively identify and report compliance and health and safety issues to the supervisor.

Perform basic routine maintenance tasks.

Participate in multiple projects and contribute to continuous improvement in a fast-paced changing environment.

Within 12 Months, You Will:
Work closely with QA peers to complete the necessary documentation for the release of commercial batches on time.

Participate in investigations into quality deviations/health and safety incidents and CAPA tasks.

Demonstrate commitment to Moderna's values and embody these values in the workplace.

Here’s What You’ll Bring to the Table:
3 to 5 years of experience in a GMP manufacturing environment.

Post-secondary degree in pharmaceutical sciences or biotechnology sector .

Ability to collaborate with peers, supervisors and support function teams.

Excellent written and oral communication skills and excellent organizational skills.

Ability to pay attention to details while performing multiple tasks with minimal supervision.

Demonstrated commitment to Moderna's values (Bold, Collaboration, Curiosity and Relentles s) and embody these values in the workplace .

Fluency in French and English in working language.

Le rôle:
Rejoindre Moderna, c'est participer à une équipe pionnière qui révolutionne la médecine avec la technologie de l'ARNm et un large éventail de programmes de développement couvrant diverses maladies. En tant qu'employé, vous ferez partie d'une organisation en croissance continue, travaillant aux côtés de collègues exceptionnels et de partenaires stratégiques dans le monde entier, contribuant aux initiatives de santé mondiale. L'engagement de Moderna à faire avancer la frontière technologique des médicaments à ARNm garantit une expérience de carrière stimulante et gratifiante, avec un impact significatif sur la vie des patients partout dans le monde.

À Laval, le partenariat stratégique de Moderna avec le gouvernement canadien transforme les capacités du pays en matière de préparation et de réponse aux pandémies. Notre future installation de fabrication de vaccins à ARNm de pointe jouera un rôle crucial pour assurer un accès rapide aux vaccins contre les virus respiratoires, sous réserve de l'approbation de Santé Canada. En investissant dans le développement des talents locaux et en favorisant les collaborations en recherche et développement, nous renforçons la position du Canada en tant que centre mondial d'excellence en ARNm.

Moderna recherche un Technicien qualifié pour rejoindre notre unité de production de vaccins à ARNm à notre nouvelle installation de fabrication à Laval, Canada. Ce rôle implique l'opération d'équipements de production conformément aux normes cGMP ainsi qu'aux règlements de santé et de sécurité. Le candidat retenu devra posséder d'excellentes compétences techniques, un esprit scientifique et une capacité d'apprentissage rapide, tout en faisant preuve d'un comportement méticuleux. Une connaissance des processus d'ARNm est un atout.

Voici ce que vous allez faire:
Dans les 3 Mois, Vous Allez…

Opérer l'équipement et préparer les solutions tampons pour le processus de fabrication.

Gérer et contrôler les processus de transcription, de filtration et de purification en utilisant des équipements automatisés et assistés par ordinateur.

Prélever des échantillons pour les analyses à des étapes critiques du processus et effectuer des contrôles environnementaux.

Appliquer les outils de performance en place pour atteindre les objectifs opérationnels KPIs en équipe.

Dans les 6 Mois, Vous Allez…

Nettoyer les équipements et les zones de fabrication/préparation.

Identifier et signaler de manière proactive les problèmes de conformité et de santé et sécurité au superviseur.

Effectuer la maintenance de routine de base (lubrification, vérification mécanique de base, changement de filtre, etc.).

Participer à plusieurs projets et à l'amélioration continue dans un environnement en constante évolution.

Dans les 12 Mois, Vous Allez:
Travailler étroitement avec les pairs QA pour compléter la documentation nécessaire à la libération des lots commerciaux dans les délais.

Participer aux enquêtes sur les écarts de qualité/incidents de santé et sécurité et aux tâches CAPA.

Voici ce que vous apporterez à la table:
3 à 5 ans d'expérience dans un environnement de fabrication BPF.

Diplôme d'étude supérieur (ou post-secondaire) dans le secteur des sciences pharmaceutiques ou des biotechnologies.

Capacité à collaborer de manière fluide avec les pairs, les superviseurs et les équipes de support.

Excellentes compétences en matière de communication écrite et orale et excellent sens de l’organisation

Capacité à prêter attention aux détails tout en exécutant des tâches multiples avec une supervision minimale.

Engagement manifeste en faveur des valeurs de Moderna, à savoir l'audace, la collaboration, la curiosité et l'acharnement, et incarnation de ces valeurs sur le lieu de travail.

Maîtrise du français et de l'anglais en tant que langues de travail.

Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work.

We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:
Quality healthcare and insurance benefits
Lifestyle Spending Accounts to create your own pathway to well-being
Free premium access to fitness, nutrition, and mindfulness classes
Family planning and adoption benefits
Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, and a discretionary year-end shutdown
Educational resources
Savings and investments
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.

About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.

By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.

We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.

If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.

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

Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!

Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.

Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.

Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.

Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at [email protected] . (EEO/AAP Employer) #LI-DS2
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