Technician - Mrna Vaccines Production - Night Shift

3 months ago

Laval, Canada Moderna Full time

We are excited to announce that we are expanding our team and have multiple positions available for this role - join us in shaping the future*

**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.

**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.

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 mínimal 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.
- Nous sommes ravis d'annoncer que nous agrandissons notre équipe et avons plusieurs postes disponibles pour ce rôle - bâtissons l'avenir ensemble*

**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.

**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

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