The posting
The Role
The Moderna Analytical Technical Operations (ATO) team is seeking a Scientist to lead operational method development and enable the transition of analytical methods from development into robust, scalable, and high-throughput laboratory execution. This is an onsite role based at Moderna’s Technology Center campus in Norwood, MA.
You will serve as a critical scientific interface between Analytical Development and ATO, combining technical expertise in LC/MS, chromatography, microfluidic methods, automation, and high-throughput methodologies with a strong understanding of sample demand, turnaround time, equipment capacity, data flow, and routine execution requirements. You will drive method optimization, technology transfer, troubleshooting, and lifecycle improvements supporting characterization, in-process, release, and stability testing across Moderna programs.
Here’s What You’ll Do
- Lead operational method development focused on robustness, reproducibility, throughput, automation compatibility, data integrity, and long-term sustainability.
- Translate Analytical Development methods into standardized and scalable workflows suitable for routine, high-volume testing environments while preserving scientific intent and required performance.
- Design and execute method studies supporting optimization, performance characterization, comparability, pre-validation, transfer, and operational readiness.
- Provide technical expertise in LC/MS and separation sciences including HPLC/UHPLC, capillary electrophoresis, microfluidic platforms, method execution, data interpretation, and troubleshooting.
- Advance microfluidic analytical methods including LabChip or comparable platforms, to improve speed, sample efficiency, consistency, and scalability.
- Develop automation-ready workflows including sample preparation and analytical methods compatible with liquid handlers, robotic platforms, plate-based execution, and integrated data systems.
- Apply high-throughput principles to optimize batching, instrument utilization, analyst touch time, cycle time, and overall laboratory capacity.
- Serve as a primary scientific interface with Analytical Development by engaging early in method design and communicating operational requirements for volume, run time, controls, standards, equipment, data review, automation, and transferability.
- Lead or support analytical technology transfer including transfer strategy, execution, acceptance criteria, knowledge transfer, training, documentation, and post-transfer monitoring.
- Drive complex technical troubleshooting and investigations involving methods, instrumentation, reagents, samples, data, and workflow interactions using structured root cause analysis and experimental design.
- Partner across Process Development, Formulation Sciences, Quality Control, Digital, Automation, Laboratory Engineering, and external organizations to ensure end-to-end method and technology readiness.
- Create clear technical documentation including protocols, reports, transfer packages, work instructions, risk assessments, and training materials that enable consistent execution.
- Mentor colleagues and strengthen organizational capability in method science, operational development, technology transfer, automation, and data-driven problem solving.
- Drive continuous improvement and method lifecycle management through performance monitoring, modernization, change implementation, and sustainable corrective and preventive actions.
Here’s What You’ll Need (Basic Qualifications)
- Education: PhD in Analytical Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, Molecular Biology, or a related scientific discipline, or a Master’s or Bachelor’s degree with directly applicable industry experience.
- Experience: Demonstrated experience in analytical method development, optimization, transfer, validation or pre-validation, troubleshooting, and lifecycle support.
- LC/MS and chromatography: Hands-on experience with LC/MS and liquid chromatographic techniques, including method performance assessment, data interpretation, and troubleshooting.
- Operational method development: Experience translating scientific method requirements into reliable routine execution while accounting for volume, capacity, scheduling, turnaround time, training, and executional robustness.
- Technical leadership: Demonstrated ability to independently design studies, analyze data, solve complex problems, manage multiple priorities, and influence outcomes across cross-functional teams.
Here’s What You’ll Bring to the Table (Preferred Qualifications)
- Advanced analytical platforms: Experience with microfluidic, capillary electrophoretic, plate-based, or comparable high-throughput analytical technologies, including LabChip or similar platforms.
- Automation and high throughput: Experience designing, implementing, or improving automated or semi-automated laboratory workflows using liquid handlers, robotic systems, integrated workcells, or automated data processing.
- Advanced therapeutic modalities: Experience supporting mRNA, oligonucleotide, gene therapy, biologics, vaccines, lipid nanoparticles, or other advanced therapeutic modalities.
- Method lifecycle and regulated environments: Knowledge of analytical procedure lifecycle management, data integrity, GMP/GLP expectations, and phase-appropriate method control.
- Digital laboratory systems: Experience with LIMS, ELN, chromatography data systems, laboratory scheduling tools, automated data pipelines, or instrument integration.
- External collaboration: Experience partnering with contract laboratories, external development or manufacturing organizations, instrument vendors, or automation providers.
- Ways of working: Strong scientific judgment, technical writing, collaboration, communication, and the ability to translate complex scientific concepts into practical operational solutions.
- Mindset: Proactive, curious, data-driven, and committed to quality, operational excellence, continuous improvement, and Moderna’s mission.
Our Working Model
As we build our company, we have always believed that an in-person culture is critical to our success. This role is 100% onsite, reflecting the importance of being physically present to support the work, collaborate closely with colleagues, and contribute to our site-based operations.
Working onsite enables real-time collaboration, strong team connections, direct mentorship, and the hands-on partnership needed to deliver our mission. 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.
Pay & Benefits
At Moderna, we believe that when you feel your best, you can do your best work. That’s why our benefits and well-being resources are designed to support you—at work, at home, and everywhere in between.
- Competitive healthcare, 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 investments to help you plan for the future
- Location-specific perks and extras
The salary range for this role is $109,200.00 - $174,600.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An individual’s position within the salary range will be based on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs.
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 modernatx.com/careers to learn more about our current opportunities.
Equal Opportunities
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. 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 an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Accommodations
We’re 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 [email protected].
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 applicant’s 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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