Technician III, Process/Utility Maintenance

Initial Therapeutics, Inc.; Marlborough (MA); On-site; USD 63,200 - 100,900; Full time

Benefits offered by this job

Best-in-class healthcare coverage

Generous paid time off

Fitness and mental health support

Job summary

Initial Therapeutics, Inc. is seeking a skilled technician in Marlborough, Massachusetts to provide on-site support for 1st shift manufacturing operations. The ideal candidate should have a high school diploma or GED with at least 5 years of related experience in a GMP environment.

This role focuses on maintaining and optimizing equipment, ensuring compliance with safety regulations. The position offers competitive pay and benefits, including best-in-class healthcare and generous paid time off.

Qualifications

• Minimum of 5 years of related experience in a GMP environment.
• Proficient in reading and interpreting technical manuals and schematics.

Responsibilities

• Perform preventive and corrective maintenance in a GMP setting.
• Diagnose and resolve issues to ensure operational continuity.
• Support equipment calibration and validation activities.

Skills

Troubleshooting

Problem-solving

Communication

Technical manual interpretation

Physical stamina

Education

High school diploma or GED

Technical certification or Associate’s degree

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 the 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

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.

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.

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].

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!

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.

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