Scientist, Analytical Sciences and Technology, Chemistry

Moderna; Norwood (KY); On-site; USD 109,000 - 175,000; Full time

Job summary

Moderna seeks an experienced analytical chemistry leader to oversee method transfer, validation, troubleshooting, investigations, and continuous improvement for chemistry-based analytical methods. You will partner with QC, QA, Regulatory Affairs, and CMOs to ensure robust, inspection-ready analytical performance across a global network.

The role emphasizes HPLC/UPLC, compendial methods, data analysis, CAPA development, and documentation to support GMP manufacturing and regulatory submissions.

Qualifications

• Bachelor’s degree or higher in Analytical Chemistry or related field with 5+ years of industry experience.
• Experience supporting analytical method transfer, qualification, validation, verification, or lifecycle management in GMP environments.
• Experience authoring technical documents (protocols, reports, SOPs) and working knowledge of GMP data integrity.

Responsibilities

• Lead chemistry-focused analytical method transfers, validations, verifications, and comparability assessments across internal/external labs.
• Provide expertise for chromatography-based methods performance monitoring and lifecycle management.
• Collaborate cross-functionally to support investigations, CAPAs, and regulatory readiness.

Skills

Analytical chemistry

HPLC/UPLC

Method transfer

Troubleshooting

Data review

Education

BS in Chemistry

MS in Analytical Chemistry

PhD in Analytical Chemistry

Tools

HPLC systems

Analytical instrumentation

Job description

Moderna is seeking an Individual that will provide technical leadership and execution support for analytical method lifecycle management across commercial and late‑stage development programs. This role will be responsible for method transfer, validation, troubleshooting, investigations, and continuous improvement activities supporting Quality Control laboratories, manufacturing operations, and external testing partners with a focus on chemistry‑based analytical methods.

The Candidate will serve as a key technical resource across the analytical network, collaborating with Quality Control, Quality Assurance, Regulatory Affairs, Manufacturing Sciences, and Contract Manufacturing Organizations (CMOs) to ensure robust analytical performance, compliance, and inspection readiness.

The successful candidate will leverage scientific expertise to support product lifecycle management, drive technical solutions, and ensure reliable execution of analytical testing strategies.

Here’s What You’ll Do

• Lead and support chemistry‑focused analytical method transfers, validations, verifications, and comparability assessments across internal and external laboratories, with emphasis on HPLC/UPLC, compendial methods, and other chemistry‑based analytical techniques.
• Provide technical expertise for chemistry and compendial method performance monitoring, troubleshooting, and lifecycle management activities.
• Evaluate chemistry analytical method suitability and identify opportunities for continuous improvement.

Technical Support & Troubleshooting

• Serve as a subject matter expert for chemistry‑based analytical methods and instrumentation, with particular emphasis on HPLC/UPLC and chromatographic techniques, and compendial testing.
• Lead and support troubleshooting of analytical issues impacting laboratory operations, manufacturing, and product disposition.
• Collaborate cross‑functionally to identify root causes and implement effective corrective actions.

Investigations & Data Review

• Support laboratory investigations, out‑of‑specification (OOS), out‑of‑trend (OOT), and atypical result assessments.
• Perform scientific data analysis to identify trends, risks, and opportunities for process improvement.
• Contribute to development and implementation of CAPAs to address analytical and operational issues.

Documentation & Compliance

• Author, review, and approve technical documents including protocols, reports, methods, specifications, and standard operating procedures (SOPs).
• Ensure documentation is accurate, compliant, and inspection‑ready.
• Support regulatory submissions, health authority inspections, and internal audits as required.

QC Network & External Partner Support

• Collaborate with QC laboratories and external testing partners to ensure successful method implementation and execution.
• Provide technical oversight and support for analytical activities conducted at CMOs and contract testing laboratories.
• Support network harmonization efforts and best‑practice sharing across sites.

Data Trending & Continuous Improvement

• Analyze analytical performance metrics and trending data to drive informed decision‑making.
• Support development and implementation of process improvements that enhance efficiency, compliance, and robustness.
• Support assessment and implementation of new or revised compendial requirements, including USP and other applicable global pharmacopeial requirements, and evaluate potential impacts to analytical methods, specifications, and testing strategies
• Contribute to digital and data‑driven initiatives supporting analytical operations.

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

• Bachelor’s degree in Analytical Chemistry, Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering, or related scientific discipline with 5+ years of relevant industry experience; OR
• Master’s degree in Analytical Chemistry, Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering, or related scientific discipline with 3+ years of relevant industry experience; OR
• PhD in Analytical Chemistry, Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering, or related scientific discipline with 0–2 years of relevant industry experience.
• Experience supporting analytical method transfer, qualification, validation, verification, or lifecycle management activities in a GMP‑regulated pharmaceutical, biotechnology, biologics, or vaccine environment.
• Experience authoring and reviewing technical documents, including protocols, reports, specifications, test methods, investigations, and standard operating procedures (SOPs).
• Working knowledge of GMP regulations, data integrity principles, and pharmaceutical quality systems.
• Experience supporting laboratory investigations, including out‑of‑specification (OOS), out‑of‑trend (OOT), deviation, or atypical result assessments.
• Demonstrated ability to analyze scientific data, identify trends, and apply scientific judgment to solve technical problems.
• Experience working effectively in cross‑functional teams with Quality Control, Quality Assurance, Manufacturing, Regulatory Affairs, and/or external partners.

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

• Strong hands‑on analytical chemistry experience, with demonstrated technical proficiency in HPLC/UPLC and chromatographic method execution, troubleshooting, and data interpretation; experience with additional analytical techniques and compendial methods is preferred.
• Demonstrated ability to independently troubleshoot analytical methods and instrumentation, evaluate unexpected or atypical results, develop scientifically sound hypotheses, and drive technical issues through resolution.
• Strong understanding of analytical method validation, transfer, qualification, verification, and lifecycle management principles, including application of risk‑based and phase‑appropriate strategies.
• Knowledge of applicable regulatory and compendial expectations, including ICH, USP, FDA, EMA, and other global health authority requirements.
• Experience leading or substantially contributing to investigations, CAPAs, deviation management, change controls, or analytical troubleshooting activities.
• Demonstrated technical ownership and independent problem‑solving, with the ability to design and execute experiments, interpret complex analytical data, draw scientifically supported conclusions, and recommend next steps.
• Experience supporting analytical control strategies, method readiness, product lifecycle changes, regulatory filing activities, or commercial manufacturing support.
• Ability to communicate complex technical topics clearly to cross‑functional stakeholders, including Quality, Manufacturing, Regulatory, Technical Development, and senior leadership audiences.
• Demonstrated ability to prioritize and independently drive technical work in a fast‑paced, matrixed environment while collaborating effectively across functions.

Competency

• Scientific problem solving and critical thinking
• Technical leadership and collaboration
• Strong data analysis and interpretation skills
• Effective communication and stakeholder management
• Attention to detail and commitment to quality
• Ability to manage multiple priorities in a fast‑paced 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.

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.