Scientist, Mass Spectrometry and Critical Reagents

The Role:

The Scientist will be responsible to support the protein quantification and proteomics analysis using Mass spectrometry for PK and PD studies ensuring the timely and efficient management of critical reagents used in the development validation and execution of bioanalytical and molecular assays to support clinical assays at Moderna. The successful candidate will work closely with cross-functional teams for protein analysis qualify critical reagents as well as establish and maintain robust systems for their monitoring tracking and storage. This is in person laboratory based position located in Norwood MA.

Heres What Youll Do:

• Support LC-MS based protein quantification/proteomics assay development validation and sample analysis under regulatory compliance.

• A solid background in modern analytical techniques used in the analysis of mRNA-based therapeutic products is essential.

• Maintain a robust system for the monitoring tracking and storage of critical reagents to ensure their availability and quality. Support reagent characterization to generate CoA documentation.

• Knowledge of peptide/proteins aptamer-antibody based conjugation systems for DNA RNA and Protein/antibodies.

• Maintain a database of Reference standards/reagents including their specifications source usage and expiration dates.

• Conduct regular audits of critical reagent inventory and work with cross-functional teams to manage the procurement and disposition of the reagents.

• Vendor management to ensure the availability and quality of critical reagents.

• Develop and implement policies procedures and training programs to ensure compliance with regulatory requirements and industry best practices.

• Collaborate with cross-functional teams to develop reagent-specific risk assessments and mitigation strategies.

• Monitor industry trends and advancements in critical reagent management and implement the best practices to improve efficiency and effectiveness.

Heres What Youll Need (Basic Qualifications)

• Ph.D. in a scientific field such as chemistry biochemistry or biology with 3 years of experience in Bioanalytical Sciences/regulated bioanalysis. M.S. with at least 7 years of bioanalytical experience will also be considered.

• Strong knowledge of critical reagents management as well as current industry best practices and regulatory requirements.

• Deep understanding of Proteomics/Protein mass spectrometry for PK and biomarker analysis

• Demonstrated ability to work collaboratively with cross-functional teams to achieve shared goals.

• Excellent organizational analytical and problem-solving skills.

• Proven ability to manage multiple projects simultaneously and prioritize tasks in a fast-paced environment.

Heres What Youll Bring to the Table (Preferred Qualifications):

• Experience with the Biophysical Characterization of Biologics (LCMS SDS-PAGE cIEF SPR BLI SEC-HPLC SEC-MALS UV-VIS)

• Experience working in a GLP environment (ELN/LIMS/automation)

• Experience with HRMS and software for protein analysis/characterization

Pay & Benefits

At Moderna we believe that when you feel your best you can do your best work. Thats why our US benefits and global well-being resources are designed to support youat work at home and everywhere in between.

• Best-in-class healthcare coverage plus voluntary benefit programs to support your unique needs

• A holistic approach to well-being with access to fitness mindfulness and mental health support

• Family planning benefits including fertility adoption and surrogacy support

• Generous paid time off including vacation volunteer days sabbatical global recharge days and a discretionary year-end shutdown

• Savings and investment opportunities to help you plan for the future

• Location-specific perks and extras

The successful candidate may be eligible for an annual discretionary bonus other incentive compensation or equity award subject to company plan eligibility criteria and individual performance.

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.

We are proud to have been recognized as a Science Magazine Top Biopharma Employer a Fast Company Best Workplace for Innovators and a Great Place to Work in the U.S.

If you want to make a difference and join a team that is changing the future of medicine we invite you to visit to learn more about our current opportunities.

Our Working Model

As we build our company we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation teamwork and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn contribute and make a meaningful impact.

Moderna is a smoke-free alcohol-free and drug-free work environment.

Equal Opportunities

Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a persons 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 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 an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories consistent with legal requirements.

Accommodations

Were focused on attracting retaining developing and advancing our employees. By cultivating a workplace that values diverse experiences backgrounds and ideas we create an environment where every employee can contribute their best.

Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations team at .

Export Control Notice

This position may involve access to technology or data that is subject to U.S. export control laws including the Export Administration Regulations (EAR). As such employment is contingent upon the applicants ability to access export-controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements only individuals who qualify as U.S. persons (citizens permanent residents asylees or refugees) are eligible for this position. For this role Moderna is unable to sponsor non-U.S. persons to apply for an export control license.

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