Technician III, Process/Utility Maintenance

BioSpace; Marlborough (MA); On-site; USD 63,000 - 101,000; Full time

Benefits offered by this job

Healthcare coverage

Well-being programs

Family planning benefits

Generous paid time off

Retirement savings

Job summary

Moderna is seeking an on-site Maintenance Technician for 1st shift at our Marlborough GMP facility. You will independently maintain, troubleshoot, and optimize complex equipment, ensuring regulatory compliance and operational continuity.

Working at the intersection of engineering and digital systems, you will engage with data-driven maintenance and Generative AI-enabled insights to enhance reliability and performance. This hands-on role is not remote.

Qualifications

• High school diploma or GED; technical cert or associate degree preferred; min 5 years related experience.
• Site-based role; not eligible for remote work.
• US work authorization without sponsorship; no immigration sponsorship available.

Responsibilities

• Perform preventive and corrective maintenance across GMP manufacturing systems.
• Diagnose, troubleshoot, and resolve issues on critical process equipment in real time.
• Document maintenance activities in MAXIMO with accuracy and data integrity.
• Support calibration, validation, and commissioning activities for lifecycle management.
• Provide first-line technical support for production-critical systems and escalate as needed.
• Oversee and perform repairs with autonomy, prioritizing minimal disruption to operations.

Skills

Maintenance expertise

Troubleshooting

GMP knowledge

Communication skills

Education

Maintenance certification

Tools

MAXIMO CMMS

Job description

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, home to a state-of-the-art GMP facility supporting individualized therapy (INT) clinical-to-commercial manufacturing. Our Marlborough campus provides end-to-end capabilities - from buffer preparation through drug substance and drug product manufacturing - leveraging automation, robotics, and digital tools to enable robust, scalable operations across our mRNA portfolio.

In this role, you will serve as a critical on-site technical expert supporting 1st shift manufacturing operations within a GMP environment.

You will independently maintain, troubleshoot, and optimize complex facility and process equipment, ensuring operational continuity and regulatory compliance.

Working at the intersection of engineering, digital systems, and advanced manufacturing, you will also engage with evolving technologies—including data-driven maintenance and Generative AI-enabled insights—to enhance equipment reliability and performance.

Here’s What You’ll Do

• Independently perform preventive and corrective maintenance across manufacturing, utility, and facility systems in a GMP pharmaceutical environment.
• Diagnose, troubleshoot, and resolve issues on critical process equipment in real time to minimize downtime and ensure continuity of operations.
• Execute and document maintenance activities within Maximo, ensuring accuracy, compliance, and data integrity.
• Support equipment calibration, validation, and commissioning activities, contributing to lifecycle management and regulatory readiness.
• Provide first-line technical support for production- critical systems, resolving issues directly and escalating complex challenges when required.
• Oversee and perform repairs and maintenance tasks with a high degree of autonomy and technical judgment.
• Coordinate and prioritize maintenance activities to ensure timely execution with minimal disruption to manufacturing operations.
• Develop, refine, and implement maintenance procedures and protocols to enhance system performance, reliability, and longevity.
• Monitor and manage maintenance inventory, ensuring availability of critical spare parts, tools, and supplies.
• Train and mentor junior technicians, fostering technical capability, adherence to GMP standards, and a strong safety culture.
• Ensure full compliance with safety regulations and proactively promote a culture of safety and accountability across all maintenance activities.
• Operate fully on-site as part of a hands-on, 1st shift team supporting continuous manufacturing operations (this role is not eligible for remote work).
• Take on additional responsibilities as required to support site operations and evolving business needs.

The key Moderna Mindsets you’ll need to succeed in the role:

"We act with urgency; Action today compounds the lives saved tomorrow."

"We behave like owners. The solutions we’re building go beyond any job description."

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

• High school diploma or GED required; Technical Certification or Associate’s Degree in Mechanical, Electrical, or Industrial Maintenance is preferred, with a minimum of 5 years of related experience.
• 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.

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

• Military training equivalent of above is acceptable.
• Previous experience in a cGMP environment is a plus.
• Familiarity with documentation practices used in a GMP environment is preferred.
• Experience documenting work in a CMMS (MAXIMO) preferable.
• Strong troubleshooting and problem-solving skills, with the ability to analyze complex issues and develop effective solutions.
• Proficient in reading and interpreting technical manuals, blueprints, and schematics.
• Excellent communication and interpersonal skills, with the ability to effectively communicate technical information to team members and stakeholders.
• Physical stamina and ability to perform manual labor.
• In-depth knowledge of various facility systems, including electrical, plumbing, HVAC, carpentry, and general maintenance.
• A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.

Pay & Benefits

• 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 salary range for this role is $63,200.00 - $100,900.00. 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.

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.

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

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.