Principal Research Associate, Analytical Development

Moderna Therapeutics; Norwood (MA); On-site; USD 90,000 - 144,000; Full time

Benefits offered by this job

Competitive healthcare

Well-being resources

Family planning benefits

Generous paid time off

Savings and investments

Location-specific perks

Job summary

Moderna Therapeutics in Norwood, MA is seeking an analytical development scientist to advance method development and validation for clinical-stage qualification and commercial readiness.

The role emphasizes cross-functional collaboration with Quality, QC and manufacturing, troubleshooting complex assay issues, and driving continuous improvement in lifecycle management of analytical methods. Strong GMP experience and data interpretation are essential.

Qualifications

• This role requires MS with 5 years or BS with 8 years in biotech/pharma analytical development.
• Strong hands-on experience with analytical methods (HPLC, absorption, molecular biology assays).
• Experience with method transfer to QC or external labs and GMP environmental context.

Responsibilities

• Mitigate risks in method development and validation per ICH Q2/Q14.
• Troubleshoot complex assay results and issues.
• Drive continuous improvement for method transfer and routine operations.
• Ensure robust method development for clinical-stage qualification and commercial validation-readiness.
• Collaborate across Method Development, AST, ATO, QC to align analytical expectations.
• Represent Analytical Development in cross-functional forums with AS&T and QC.
• Ensure methods meet technical, operational, and regulatory requirements.
• Lead investigations and root-cause analyses for performance issues.
• Influence method development and lifecycle improvements based on data.
• Collaborate with Quality and AST on deviations, CAPAs, and change controls.
• Analyze complex datasets to inform performance and variability.
• Author and review protocols, reports, and method lifecycle documents.

Skills

Analytical methods

HPLC

Absorption assays

Molecular biology assays

Method transfer

GMP experience

Cross-functional collaboration

Data interpretation

Communication

Ownership

Education

MS with 5 years' biotech/pharma analytical development experience

Job description

Key Responsibilities

• Proactively mitigate risks related to method development and validation per ICH Q2 and Q14
• Troubleshoot out-of-expectation results
• Articulate continuous improvement opportunities related to method transfer and routine operations
• Ensure robust method development for clinical-stage qualification and commercial validation-readiness
• Serve as a liaison between Method Development, AST, ATO, and QC, ensuring alignment on analytical method expectations, readiness, and performance
• Represent Analytical Development in cross-functional forums with AS&T and QC
• Ensure methods are designed to meet appropriate technical, operational, and regulatory requirements before qualification or validation
• Serve as subject matter expert for investigations and performance issues across development and QC environments, identifying root causes, supporting hypothesis tests, and implementing solutions
• Influence method development, assay optimization and continuous improvement efforts based on operational feedback, robustness requirements, and lifecycle needs
• Collaborate with Quality and AST teams to support deviation investigations, CAPAs, and change controls related to analytical methods
• Analyze and interpret complex datasets to inform performance, variability, and comparability
• Author and review technical documentation including protocols, reports, method lifecycle documents

What You’ll Bring to the Table

• MS with 5 years or BS with 8 years of biotech or pharmaceutical industry experience in analytical development
• Strong hands-on experience with analytical methods, such as HPLC, Absorption, and Molecular Biology assays
• Demonstrated experience with analytical method transfer to QC or external laboratories
• Proven ability to troubleshoot complex assay issues and lead investigations in a GMP or late-stage development environment
• Understanding of CQA frameworks, assay lifecycle management, and regulatory expectations
• Experience working cross-functionally with Quality, QC, and/or manufacturing organizations
• Strong analytical thinking and ability to interpret data to drive decisions and improvements
• Excellent communication skills with the ability to translate technical concepts across functions
• Ability to manage multiple priorities in a fast-paced, highly collaborative environment
• Self-motivated, proactive, and comfortable operating with a high degree of ownership

This position is site-based, requiring you to be at Moderna’s site full-time. This position is not eligible for remote work. At Moderna, we are focused on delivering on our mission by enabling talent to thrive. For this role, we are currently unable to offer immigration sponsorship. Candidates must already hold work authorization in US and be able to maintain that status without the need for future sponsorship.

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 $89,900.00 - $143,800.00. 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 [e-mail].

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.

Our Mission and Vision

At Moderna we are pioneering the development of a new class of drugs made of messenger RNA (mRNA). This novel drug platform builds on the discovery that modified mRNA can direct the body’s cellular machinery to produce nearly any protein of interest, from native proteins to antibodies and other entirely novel protein constructs that can have therapeutic activity inside and outside of cells. We have a clear mission to propel the field of mRNA science forward and deliver new medicines to patients and a unique vision for how to achieve this mission.

Our Mission: To deliver on the promise of transformative messenger RNA (mRNA) science to bring new medicines to patients.

Our Vision: To unlock the potential of mRNA by establishing an ecosystem of teams and partners that will work together to develop the broadest possible array of drugs, across diverse therapeutic areas and routes of administration, for serious diseases that are not treatable today.

Third Party Staffing Agencies

Moderna does not accept unsolicited resumes from any source other than directly from candidates. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. Unsolicited resumes sent to Moderna from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Moderna and do not obligate Moderna to pay fees if we hire from those resumes.