Senior Engineer II, Applied Technologies

The Role

Joining Moderna offers the unique opportunity to be part of a pioneering team thats revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases.

As an employee youll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide contributing to global health initiatives.

Modernas commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients lives worldwide.

This high-impact individual contributor role will lead the strategy and deployment of Process Analytical Technology (PAT) across Modernas mRNA drug substance and drug product platforms. You will architect and implement cutting-edge inline online and at-line analytical tools that unlock real-time monitoring and data-driven control from early-stage development through GMP manufacturing. Working across functional boundaries you will build the digital and analytical backbone of next-generation bioprocessing. This is a unique opportunity to operate at the intersection of automation advanced analytics and mRNA science and to shape how Moderna integrates Generative AI tools and intelligent control systems into its manufacturing future.

Heres What Youll Do

Your key responsibilities will be:

• Lead the end-to-end PAT and control strategy ensuring cross-platform consistency and alignment with Modernas digital and automation roadmaps.

• Design deploy and maintain a diverse suite of spectroscopic chromatographic and sensor technologies (e.g. Raman FTIR UPLC rapid sterility pH/DO micro sensors).

• Develop chemometric models and real-time dashboards linking process parameters with critical quality attributes.

• Serve as a technical lead on integration of PAT tools into Modernas digital ecosystem including data lakes electronic batch records (eBR) and advanced process control layers.

• Author and lead technology transfer packages to internal GMP sites and external partners ensuring seamless comparability and calibration approaches.

Your responsibilities will also include:

• Collaborate closely with analytical development MS&T process automation digital engineering quality and regulatory teams to ensure PAT solutions are seamlessly manufacturable and inspection-ready.

• Drive continuous improvement initiatives that reduce cycle times enhance right-first-time metrics and improve overall process robustness.

• Mentor staff and champion a scientific culture of curiosity innovation and excellence.

• Translate complex analytical and regulatory requirements into integrated solutions aligned with Modernas next-gen manufacturing platforms.

• Travel up to 10% supporting deployment at domestic and international manufacturing sites.

The key Moderna Mindsets youll need to succeed in the role:

• We digitize everywhere possible using the power of code to maximize our impact on patients. In this role youll be instrumental in embedding real-time PAT data into Modernas digital infrastructure laying the groundwork for automated insights and AI-driven decisions across the manufacturing network.

• We push past possible to be the best version of Moderna. Youll be expected to pioneer forward-thinking PAT strategies challenge conventional approaches and set new benchmarks for what real-time analytics can deliver in a fully digital biotech environment.

Heres What Youll Need (Basic Qualifications)

• Ph.D. in Chemical/Biomedical Engineering Analytical Chemistry or related discipline with 2years OR M.S. with 8years OR B.S. with 10years of relevant industrial experience.

• Hands-on experience developing and implementing PAT tools in biopharmaceutical or advanced therapy manufacturing environments including sensor specification installation and data modelling and technology transfer.

• Proficient in multivariate data analysis/chemometrics tools (SIMCA Unscrambler Python R) and integration with process automation systems manufacturing data platforms and communication protocols (e.g. DeltaV SynTQ PI AF OPC UA).

• Strong understanding of Design of Experiment (DoE) cGMP Quality by Design principles and process validation fundamentals.

• This position is site-based requiring you to be at Modernas site full-time. This position is not eligible for remote work.

Heres What Youll Bring to the Table (Preferred Qualifications)

• Demonstrated authorship of CMC regulatory submissions (IND IMPD BLA/MAA) and participation in health authority interactions related to PAT packages real-time release testing and continuous manufacturing.

• Experience with life cycle management including GMP compliance and training.

• Familiarity with expedited regulatory pathways EU GMP Annex1 ATMP/CGT guidances and relevant ICH (e.g. Q8 Q9 Q10 Q12 Q13).

• Expertise with mRNA lipid nanoparticle formulation or other nucleic acid-based modalities.

• Experience deploying PAT for personalized or small batch therapeutics.

• Lean/Six Sigma Green Belt (or higher) and a track record of driving efficiency improvements in GMP settings.

• Exceptional communication skills and a collaborative mindset focused on patient impact.

• A desire to make an impact as part of a high-growth transformational company that is Bold Relentless Curious and Collaborative.

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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