Analyst, Quality Control - Chemistry & Stability

at  Moderna

• 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.
Moderna is seeking a Quality Control Analyst specializing in Chemistry & Stability for our manufacturing facility in Laval, Canada. Reporting to the Associate Director of Quality Control, this role will focus on cGMP QC testing, supporting Global GMP stability programs, and maintaining stability databases. The candidate will be responsible for conducting routine analytical chemistry and stability testing, data trending, and statistical analyses.

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.