Manufacturing Associate I

Initial Therapeutics, Inc.; Norwood (MA); On-site; USD 54,000 - 86,000; Full time

Benefits offered by this job

Competitive healthcare

Well-being resources

Generous paid time off

Location-specific perks

Job summary

Moderna is seeking a Manufacturing Associate I in Drug Substance Operations in Norwood, MA. You will perform hands-on manufacturing tasks in a GMP environment, focusing on precision, documentation, and teamwork to produce mRNA drug substance.

The role emphasizes adherence to procedures, cleanroom discipline, and continuous improvement as you support aseptic processing, formulation, and filling activities. Onsite collaboration and a strong quality culture are essential.

Qualifications

• Bachelor’s degree in a STEM field with 0-1 years of relevant industry experience or Associate’s degree with 2-4 years relevant industry experience or High school diploma with more than 4 years of relevant industry experience
• Experience in manufacturing, operations, biopharma, life sciences, or other regulated or technical environments is helpful. An interest in a structured digital-forward advanced biomanufacturing environment is important.

Responsibilities

• Execute manufacturing operations by following approved procedures, batch records, and work instructions in a GMP-regulated environment
• Perform cleanroom operations with discipline, attention to detail, and a strong focus on consistency
• Support drug substance manufacturing activities including aseptic processing, formulation, filtration, mixing, filling, and dispensing
• Follow all safety procedures, waste handling requirements, and environmental guidelines
• Complete required training on time and maintain qualifications as needed for gowning and assigned operations
• Work closely with teammates and cross-functional partners, communicate clearly, escalated issues early, and help support smooth execution across the operation

Skills

Attention to detail

Disciplined execution

Focused in structured environment

Team mindset

Learn technical processes

Judgment and accountability

Cleanroom experience

Continuous improvement

Escalation of issues

Education

Bachelor’s degree in STEM

Associate’s degree + 2–4 years experience

High school diploma + 4+ years experience

Tools

SAP

Veeva

DeltaV

Syncade

LIMS

CMMS

Job description

The Role

This is a hands‑on manufacturing role for someone who takes pride in doing important work with precision, consistency, and care.

As a Manufacturing Associate I in Drug Substance Operations, you will be part of the team responsible for producing mRNA drug substance in a highly controlled, regulated GMP environment. The work is technical, disciplined, and team driven. It calls for people who can stay focused, follow through, and bring a high standard to routine execution every day.

This role is a strong fit for someone who wants to build real operating capability in an environment where details matter, preparation matters, and the attention put into the quality of your work has a direct impact on our patients. You do not need to know everything on day one, but you do need to bring the mindset to learn quickly, stay curious, work carefully, and take ownership for doing the work the right way. This is a role for someone who is driven to learn, committed to the team, and accountable for delivering the work with care and precision.

Here’s What You’ll Do:

• Execute manufacturing operations by following approved procedures, batch records, and work instructions in a GMP-regulated environment

• Perform cleanroom operations with discipline, attention to detail, and a strong focus on consistency

• Support drug substance manufacturing activities including aseptic processing, formulation, filtration, mixing, filling, and dispensing

• Work within Moderna’s human performance model for error prevention, carrying out tasks with focus and accountability for accurate execution

• Complete documentation in real time using good documentation practices and data integrity standards

• Maintain the cleanliness, control, and readiness of the production area

• Use manufacturing systems and equipment such as SAP, Veeva, DeltaV, Syncade, LIMS, and CMMS as required

• Build a practical understanding of the equipment, process flow, and digital systems that support manufacturing so you can recognize issues, respond appropriately, and continue to develop and execute technical judgment

• Follow all safety procedures, waste handling requirements, and environmental guidelines

• Complete required training on time and maintain qualifications as needed for gowning and assigned operations

• Work closely with teammates and cross‑functional partners, communicate clearly, escalated issues early, and help support smooth execution across the operation

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

• Bachelor’s degree in a STEM field with 0-1 years of relevant industry experience or Associate’s degree with 2-4 years relevant industry experience or High school diploma with more than 4 years of relevant industry experience

• Experience in manufacturing, operations, biopharma, life sciences, or other regulated or technical environments is helpful. An interest in a structured digital‑forward advanced biomanufacturing environment is important.

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

• Strong attention to detail

• A disciplined and consistent approach to execution

• The ability to stay focused in a structured environment

• A team‑first mindset and willingness to support shared goals

• The ability to learn technical processes and apply them reliably

• Good judgment, professionalism, and accountability

• Comfort working in a cleanroom environment and following defined procedures closely

• A mindset of continuous improvement and a willingness to keep raising the bar

• The confidence to speak up early, escalated issues appropriately, and help maintain a strong quality and compliance culture

Our Working Model

As we build our company, we have always believed that an in‑person culture is critical to our success. This role is 100% onsite, reflecting the importance of being physically present to support the work, collaborate closely with colleagues, and contribute to our site‑based operations.

Working onsite enables real‑time collaboration, strong team connections, direct mentorship, and the hands‑on partnership needed to deliver our mission. 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.

Pay & Benefits

At Moderna, we believe that when you feel your best, you can do your best work. That’s why our benefits and well‑being resources are designed to support you—at work, at home, and everywhere in between.

• Competitive healthcare, 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 investments to help you plan for the future
• Location‑specific perks and extras

The salary range for this role is $53,500.00 - $85,600.00. 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.

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.

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 [e-mail].

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.