What are the responsibilities and job description for the CQV Engineer III position at Moderna?
The Role
Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.
Moderna is strengthening its presence in Marlborough, Massachusetts, a key hub for research, development, and technical operations. Our Marlborough campus advances our mRNA platform from discovery through clinical development, turning promising science into real world solutions. We welcome talent committed to innovation and improving health outcomes worldwide.
In this role, you will lead commissioning, qualification, and validation (CQV) activities to ensure facilities, utilities, equipment, systems (FUSE), and analytical instruments remain in a qualified and compliant state within a cGMP manufacturing environment.
You will provide technical leadership, drive validation strategy, and serve as a subject matter expert across cross-functional and capital projects.
This is a U.S.-based individual contributor role with a full-time, 5 days onsite expectation in Marlborough, MA, and approximately 5% travel to Norwood, ensuring strong on-the-floor presence and direct engagement with manufacturing and technical operations teams.
Here’s What You’ll Do
Here’s What You’ll Bring to the Table (Preferred Qualifications):
“We behave like owners. The solutions we’re building go beyond any job description.”
“We digitize everywhere possible using the power of code to maximize our impact on patients.”
Pay & Benefits
At Moderna, we believe that when you feel your best, you can do your best work. That’s why our US benefits and global well-being resources are designed to support you—at work, at home, and everywhere in between.
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.
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 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 leavesandaccommodations@modernatx.com.
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.
Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.
Moderna is strengthening its presence in Marlborough, Massachusetts, a key hub for research, development, and technical operations. Our Marlborough campus advances our mRNA platform from discovery through clinical development, turning promising science into real world solutions. We welcome talent committed to innovation and improving health outcomes worldwide.
In this role, you will lead commissioning, qualification, and validation (CQV) activities to ensure facilities, utilities, equipment, systems (FUSE), and analytical instruments remain in a qualified and compliant state within a cGMP manufacturing environment.
You will provide technical leadership, drive validation strategy, and serve as a subject matter expert across cross-functional and capital projects.
This is a U.S.-based individual contributor role with a full-time, 5 days onsite expectation in Marlborough, MA, and approximately 5% travel to Norwood, ensuring strong on-the-floor presence and direct engagement with manufacturing and technical operations teams.
Here’s What You’ll Do
- Lead commissioning, qualification, and validation (CQV) activities for facilities, utilities, equipment, systems (FUSE), and analytical instruments.
- Develop and execute validation strategies for complex systems and capital projects.
- Author and approve lifecycle validation documentation including risk assessments, IQ/OQ/PQ protocols, and summary reports.
- Lead deviation investigations, perform root cause analysis, and drive CAPA development and implementation.
- Perform and approve change control impact assessments and implementation plans to maintain validated state.
- Serve as a subject matter expert (SME) during internal and external regulatory inspections.
- Drive continuous improvement initiatives within the CQV program to enhance compliance and operational efficiency.
- Influence validation strategy and site compliance decisions through strong technical expertise.
- Lead complex or high-risk validation projects with minimal oversight.
- Provide technical mentorship to junior CQV engineers and contribute to department-level improvements.
- Independently resolve complex technical and compliance issues in alignment with validation lifecycle principles and regulatory requirements.
- Apply advanced technical writing and documentation review skills to ensure high-quality, inspection-ready deliverables.
- Collaborate cross-functionally to remove barriers, accelerate project execution, and strengthen validation excellence.
- Leverage digital tools and data-driven approaches — including exposure to advanced analytics and emerging generative AI technologies — to modernize validation practices and maximize patient impact.
- Bachelor of Science in Engineering (Chemical or Mechanical preferred; other scientific disciplines considered).
- 5 years of experience in biopharmaceutical validation, CQV, engineering, or related cGMP manufacturing roles.
- Strong understanding of validation lifecycle principles and global regulatory requirements.
- Demonstrated ability to lead complex validation efforts and capital projects.
- Advanced technical writing and documentation review skills.
- Proven ability to independently resolve complex technical and compliance issues.
- Strong cross-functional leadership and communication skills.
Here’s What You’ll Bring to the Table (Preferred Qualifications):
- Operate independently with minimal oversight.
- Lead complex or high-risk validation projects.
- Influence validation strategy and site compliance decisions.
- Mentor junior engineers and contribute to department-level improvements.
“We behave like owners. The solutions we’re building go beyond any job description.”
“We digitize everywhere possible using the power of code to maximize our impact on patients.”
Pay & Benefits
At Moderna, we believe that when you feel your best, you can do your best work. That’s why our US benefits and global well-being resources are designed to support you—at 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 modernatx.com/careers 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 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 leavesandaccommodations@modernatx.com.
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.
Salary : $89,900 - $143,800