Engineer III, Process Development

The Role

Moderna is working to develop first-in-class messenger RNA (mRNA) based medicines. We are seeking a highly skilled and motivated Individual to join Modernas Technical Development organization in Norwood MA.

In this role you will support the development of manufacturing processes for Modernas mRNA-based medicines to enable clinical and commercial supply with a focus on process understanding and process control strategy definition and the transfer of established RNA production processes into fully integrated automated next-generation manufacturing systems. The ideal candidate will combine deep expertise in RNA manufacturing with a systems-level mindset enabling the design and implementation of next-generation equipment and end-to-end production workflows. The individual will act as a subject matter expert (SME) collaborating with cross-functional teams in R&D MS&T and Manufacturing to apply standardized design practices and deliver innovative solutions aligned with Modernas engineering and quality standards.

Heres What Youll Do

• Serve as a technical SME for RNA manufacturing processes (e.g. IVT purification) and translate processes into detailed functional and technical requirements for automated systems.

• Participate in the development of process flow diagrams (PFDs) P&IDs User Requirement Specifications (URS) and Functional Requirement Specifications (FRS) for Drug Substance of manufacturing systems.

• Support the design scale-up and implementation of modular and small-scale process skids in alignment with GxP requirements and Modernas global standards.

• Partner with engineering automation and equipment vendors to design novel manufacturing platforms that enable closed and continuous operations that meet performance safety regulatory and data integrity requirements.

• Contribute to Clean-In-Place (CIP) system design and optimization focusing on process safety efficiency and reliability.

• Contribute to technical reviews design evaluations and standardization initiatives under Modernas Technical Authority governance model.

• Ensure compliance with GxP/GMP regulations and Modernas quality and documentation systems.

• Support global site startup activities via tech transfer process investigations and provide person-in-plant support may require domestic or international travel (up to 15% of working time).

Heres What Youll Need (Basic Qualifications)

• BS or MS in chemical engineering biological engineering chemistry biochemistry or closely related field
• BS with 5 years or MS with 2 years of relevant industry experience in bioprocess development pharmaceutical development or closely related area
• Hands-on experience with chromatography ultrafiltration normal flow filtration and/or development of innovative unit operations or experience in nucleic acid drug development (DNA RNA oligonucleotides) and/or nanoparticle delivery.
• Experience in designing executing and analyzing scientific experiments
• Proven ability to support process design and equipment specification in a regulated manufacturing setting.

Heres What Youll Bring to the Table (Preferred Qualifications)

• Experience in technology transfer and optimization of manufacturing processes.
• Familiarity with bioprocess skid design automation and process analytical technologies (PAT).
• Experience supporting or leading cross-functional technical projects.
• Exposure to personalized medicine or individualized manufacturing processes
• Certifications/Training:GxP/GMP compliance training.
• Strong understanding of FDA EMA and ICH regulations.
• Strong communication and collaboration skills across functional teams and organizational levels.
• Demonstrated ability to manage multiple technical priorities within a fast-paced matrixed environment.
• Proven problem-solving and analytical skills to identify and resolve complex technical issues.
• Commitment to data integrity safety and quality excellence in all work activities.

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

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 .

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