Operator - Mrna Vaccines Production - Night Shift

3 weeks ago

Laval, Canada Moderna Full time

**The Role**:
The Operator will be expected to demonstrate digital proficiency, being comfortable to work in a highly technological environment where his participation in improvements and innovations will be regularly required.

This will be a night shift position.

**Here’s What You’ll Do**:
**Health and Safety**:
Practice safe work habits, adhere to Moderna’s safety procedures and guidelines

Adhere to gowning procedures and maintain housekeeping of assigned area for compliant and safe working

Participate in incident investigation (RCA) and CAPA tasks

**Compliance and Quality Assurance**:
Responsible for the execution of operations activities following current good manufacturing practices, standard operating procedures, and manufacturing documentation

Closely partner with QA peers for closure of documentation required for timely disposition of commercial batches.

Participate in investigation of deviations (RCA) and CAPA tasks

**Operations and Production**:
Responds rapidly and troubleshoots routine equipment process and digital issues.

Proactively identify and report to Team Lead compliance issue/health and safety issue

Responsible for keeping training records and associated documentation up to date

Perform routine basic maintenance (lubrication, basic mechanical check, filter change) of equipment using hand-tools

Flexibility to work off hours and overtime if needed

**Project and Collaboration**:
These plans will align with corporate goals and commercial demand.

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

Effectively collaborate in a dynamic, cross-functional matrix environment.

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

A College degree with a specialization in Pharmaceutical production technology or equivalent

Ability to collaborate fluidly with peers, teamleads and cross-functional support groups required.

Excellent written, oral communication, and organizational skills required.

Ability to maintain attention to detail while executing multiple tasks with mínimal supervision

Demonstrated commitment to Moderna's values of Bold, Collaborative, Curious, and Relentless, embodying these values in the workplace.

Experience in audit / inspection preparation, understanding Health authority and regulatory guidelines.

**Le rôle**:
L'opérateur devra démontrer une maîtrise du numérique et être à l'aise pour travailler dans un environnement hautement technologique où sa participation aux améliorations et aux innovations sera régulièrement requise.

Ce poste travaillera de nuit.

**Voici ce que vous allez faire**:
**Santé et sécurité**:
Adopter des habitudes de travail sûres et respecter les procédures et directives de Moderna en matière de sécurité.

Respecter les procédures d'habillage et assurer l'ordre et la propreté de la zone assignée pour un travail conforme et sécuritaire.

Participer aux enquêtes sur les incidents (RCA) et aux tâches CAPA.

**Conformité et assurance qualité**:
Responsable de l'exécution des activités opérationnelles conformément aux bonnes pratiques de fabrication, aux procédures opérationnelles normalisées et à la documentation de fabrication en vigueur.

Travailler en étroite collaboration avec les pairs de l'assurance qualité pour compléter la documentation nécessaire à la libération des lots commerciaux dans les délais prévus.

Participer aux enquêtes sur les déviations (RCA) et aux tâches CAPA.

**Opérations et production**:
Réagit rapidement et résout les problèmes de routine liés au processus d'équipement et aux problèmes numériques.

Identifie et signale proactivement au chef d'équipe les problèmes de conformité et de santé-sécurité.

Responsable de la mise à jour de sa formation et de la documentation associée

Effectue les entretiens de routine de base (lubrification, vérification mécanique de base, changement de filtre) des équipements à l'aide d'outils manuels.

Flexibilité pour travailler en dehors des heures de travail et faire des heures supplémentaires si nécessaire

**Projet et collaboration**:
Ces plans s'aligneront sur les objectifs de l'entreprise et la demande commerciale.

Participer à de multiples projets et à l'amélioration continue dans un environnement en évolution rapide.

Collaborer efficacement dans un environnement dynamique et interfonctionnel.

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

Diplôme collégial avec une spécialisation en technologie de production pharmaceutique ou équivalent

Capacité à collaborer de manière fluide et efficace avec les pairs, les chefs d'équipe et les groupes de support interfonctionnels.

Excellentes compétences en matière de communication écrite, communication orale et d'organisation sont requises.

Capacité à prêter attention aux

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