Analyst, Quality Control

5 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**:
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 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 crucial role in ensuring rapid access to vaccines for respiratory viruses. We're dedicated to investing in local talent and fostering research collaborations, strengthening Canada's role as a global mRNA excellence center.

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

Perform routine analytical chemistry and stability testing using techniques such as HPLC, UPLC, GC, UV, Particle Analysis, KF, etc.

Begin HPLC and NaOH plate reader-based assays in support of manufacturing process stat testing.

Maintain cGMP documentation for work performed and assist with general laboratory support activities.

Within 6 Months, You Will

Establish and maintain a safe laboratory working environment, including sample management and equipment maintenance.

Execute responsibilities in compliance with stability program SOPs, including creating, reviewing, and revising stability protocols and reports.

Perform stability set down, stability pull activities, and manage QC lab supplies.

**Within 12 Months, You Will**:
Assist with creating stability schedules for GMP stability drug substances and products, ensuring timely sample distribution to test labs.

Perform trending of stability data, maintain stability tables and charts, and execute stability sample shipments to external labs.

Support review and authoring of stability sections for regulatory submissions, and assist with troubleshooting assay methods and equipment.

**Here’s What You’ll Bring to the Table**:
BA/BSc in Chemistry (preferred) or other relevant scientific discipline.

**Working experience**: at least 5-7 years in quality control laboratory of a pharmaceutical company.

Fluency in French and English as a 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 saisir une occasion unique de faire partie d'une équipe pionnière qui révolutionne la médecine grâce à la technologie de l'ARNm. Notre portefeuille varié comprend plusieurs programmes de développement ciblant diverses maladies. En tant que membre de notre équipe, vous contribuerez à une organisation en pleine expansion, collaborant avec des collègues hors pair et des partenaires stratégiques à travers le monde, tout en apportant votre pierre à l'édifice des initiatives de santé globales. Chez Moderna, notre dévouement à repousser les limites de la technologie des médicaments à ARNm promet une carrière stimulante et enrichissante, offrant la chance d'impacter significativement la vie des patients partout sur la planète.

À Laval, le partenariat stratégique de Moderna avec le gouvernement canadien est en train de transformer les capacités de préparation et de réponse du pays aux pandémies. Notre future installation de production de vaccins à ARNm de pointe jouera un rôle crucial en garantissant un accès rapide aux vaccins pour les virus respiratoires. Nous nous engageons à investir dans le talent local et à encourager les collaborations de recherche, renforçant ainsi le rôle du Canada en tant que centre mondial d'excellence en ARNm.

**Voici ce que vous ferez**:
Dans les premiers 3 mois, vous...

Effectuerez des analyses chimiques et des tests de stabilité standards, utilisant des techniques avancées telles que HPLC, UPLC, GC, UV, analyse de particules et KF.

Initierez des essais HPLC et des analyses via lecteur de plaque NaOH, cruciaux pour les tests de statut des processus de fabrication.

Assurerez la gestion rigoureuse de la documentation cGMP pour toutes les opérations effectuées et contribuerez activement au support général du laboratoire.

Au cours des 6 mois suivants, vous...

Instaurerez et préserverez un environnement de laboratoire sécurisé, incluant la gestion minutieuse des échantillons et la maintenance des équipements.

Organiserez et superviserez les procédures de mise en place et de suivi des tests de stabil

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