Analyst, Quality Control - Chemistry & Stability
Apply locations Oxford - England Quality time type Full time posted on Posted 30+ Days Ago job requisition id R15366
*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.
Reporting to the Quality Control Associate Director, the individual in this role will perform cGMP QC testing for QC Chemistry, release, and stability. You will also be responsible for supporting Global GMP stability programs, stability sample set down, pull, and sample shipment/receipt activities. Additionally, the individual in this role will be involved in routinely maintaining stability databases, performing data trending and statistical analyses, creation, revision, review and approval of SOP’s, stability protocols and stability reports in accordance with current GMP, FDA, EU and ICH guidelines and regulations; this individual may support special projects as assigned.
Here’s What You’ll Do:
Your key responsibilities will be:
* Performing routine analytical chemistry & stability testing, including HPLC, UPLC, GC, UV, Particle Analysis by Dynamic Light Scattering, KF, etc.
* Supporting Global GMP stability programs, stability sample set down, pull, and sample shipment/receipt activities.
* Maintaining stability databases, performing data trending and statistical analyses.
* Creating, revising, reviewing, and approving SOPs, stability protocols, and reports in line with GMP, FDA, EU, and ICH guidelines.
Your responsibilities will also include:
* LIMS sample result entry, execution of Electronic Assay Forms in LIMS.
* General laboratory support activities, including reagent preparation, sample management, and equipment maintenance.
* Establishing and maintaining a safe laboratory working environment.
* Supporting and executing stability sample shipments to external labs, and updating in-house stability databases.
The key Moderna Mindsets you’ll need to succeed in the role:
* Pivot Fearlessly: You will navigate through the complexities of QC testing and stability studies, adapting to new challenges and data with agility.
* Pursue Options in Parallel: Your role demands managing multiple stability protocols and analytical methods simultaneously to ensure the most efficient outcomes.
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.
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.
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 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. 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 or adjustments to qualified job applicants with disabilities.
#J-18808-Ljbffr