Scientist, Analytical Development

The Role

In this role, you will join the Analytical Sciences team within Analytical Development and serve as a scientific lead for the transfer and implementation of analytical methods developed in AD into Analytical Testing Operations (ATO) and Quality Control (QC) laboratories. You will assess method readiness, design and execute phase-appropriate transfer strategies, and work directly with sending and receiving laboratories to ensure methods are scientifically understood, reproducible, operationally robust, and fit for their intended use. Success in this role requires substantial hands-on analytical method development experience, a strong understanding of analytical method performance and failure modes, practical experience executing and troubleshooting method transfers, and a solid grasp of GMP and global regulatory expectations. You will partner closely with AD method developers, APLs, ATO, Analytical Sciences & Technology (AST), QC, Quality, Quantitative Sciences, and Regulatory to build a durable feedback loop between development and routine testing and to improve analytical performance across the network.

Here’s What You’ll Do

• Serve as the Analytical Sciences technical transfer lead for assigned analytical methods moving from Analytical Development into ATO and QC laboratories, driving transfer activities from readiness assessment through execution, troubleshooting, and transfer closeout.

• Perform rigorous method-transfer readiness assessments using development and qualification data, robustness knowledge, method risk assessments, critical method parameters, system suitability, assay controls, reference standards, critical reagents, sample preparation, data processing, and known method limitations.

• Define and execute phase-appropriate transfer strategies, protocols, acceptance criteria, and study designs that reflect the method’s intended use, product-development phase, scientific maturity, and patient/product risk.

• Partner with method-development scientists before formal handoff to improve transferability, including strengthening method robustness, operational ranges, procedural clarity, system suitability and assay controls, critical-material controls, and troubleshooting guidance.

• Apply strong hands-on laboratory expertise during method transfer as needed to reproduce methods, train receiving-laboratory analysts, evaluate analyst/instrument/site effects, and rapidly resolve technical barriers to successful execution.

• Lead scientific troubleshooting and root-cause investigations during transfer and early routine use, designing targeted experiments to distinguish method, sample, reagent, instrument, software, analyst, and laboratory-environment sources of variability and implementing durable corrective actions.

• Ensure development knowledge is translated into complete and usable transfer packages, including scientific rationale, critical steps and parameters, method failure modes, material and reagent requirements, expected performance, data-analysis conventions, and practical troubleshooting guidance.

• Partner with AST, QC, Quality, ATO, and Regulatory to align method qualification, validation, verification, and transfer expectations with ICH Q2(R2), ICH Q14, USP <1224> , applicable GMP requirements, and phase-appropriate principles for clinical development.

• Provide scientific support for deviations, OOS/OOT investigations, change controls, CAPAs, and post-transfer stabilization when method performance or execution issues arise, ensuring that troubleshooting remains grounded in method-development knowledge and scientific rationale.

• Build and improve standardized transfer playbooks, templates, readiness criteria, and best practices across method families, helping establish consistent expectations for transfers into clinical and commercial testing laboratories.

• Monitor transfer outcomes and early method-performance trends, capture lessons learned, and feed findings back to Analytical Development and Analytical Sciences to drive continual method improvement, platform harmonization, and stronger future method designs.

• Author and review transfer protocols and reports, analytical procedures, risk assessments, technical summaries, training materials, change-control documentation, and regulatory-supporting content with a high standard of scientific rigor and data integrity.

Here’s What You’ll Need (Basic Qualifications)

• Ph.D. in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related field with 2+ years of relevant industry experience, or M.S. with 8+ years, or B.S./B.A. with 12+ years of relevant experience in analytical development, analytical sciences, Quality Control, or related pharmaceutical development functions.

Here’s What You’ll Bring to the Table (Preferred Qualifications)

• Strong hands-on analytical method development experience, with demonstrated ability to optimize methods, establish robustness, understand method failure modes, and translate scientific knowledge into reliable routine procedures.

• Direct experience executing multiple analytical method transfers into GMP or GMP-supporting laboratories, with strong preference for candidates who have led transfers across different methods, products, laboratories, or sites.

• Demonstrated expertise troubleshooting difficult analytical method-performance issues during transfer or routine testing and designing scientifically sound experiments to identify root causes and implement sustainable solutions.

• Strong working knowledge of analytical procedure development, qualification, validation, verification, and lifecycle principles, including ICH Q2(R2), ICH Q14, USP <1224> , quality risk management, and data-integrity expectations.

• Solid understanding of phase-appropriate GMP principles and the ability to apply an appropriate level of analytical rigor, documentation, controls, and validation based on clinical phase, intended use, method maturity, and risk.

• Scientific depth in one or more major analytical technology areas such as chromatography/separation science, electrophoresis, spectroscopy, compendial testing, molecular methods, bioassays, or other analytical platforms relevant to biologics, vaccines, nucleic acids, or advanced modalities.

• Experience assessing laboratory-to-laboratory differences in instrumentation, software, reagents, reference standards, sample preparation, environmental conditions, and analyst technique and determining appropriate bridging or mitigation strategies.

• Strong understanding of system suitability, assay controls, critical reagents and materials, reference-standard strategy, statistical assessment of method performance, and the relationship between method robustness and successful transfer.

• Experience supporting deviations, OOS/OOT investigations, change controls, CAPAs, method remediation, or lifecycle changes in a regulated analytical environment.

• Experience working across Analytical Development, QC, Quality, Regulatory, AS&T/MS&T, and/or external testing laboratories, with the ability to translate development science into practical expectations for routine laboratory execution.

• Experience with mRNA, LNP, vaccines, biologics, or other advanced therapeutic modalities is preferred.

• Excellent technical writing, communication, collaboration, and stakeholder-management skills, with the ability to explain complex analytical issues clearly, influence cross-functional decisions, and maintain scientific rigor in a fast-moving environment.

• Self-motivated, highly collaborative, and comfortable combining hands-on technical work with cross-functional leadership, with a desire to make an impact as part of a company that is Bold, Relentless, Curious, and Collaborative.

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 View email address on aiapply.co.

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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