Manufacturing Associate II, Process Development

Biopharma Careers; Norwood (KY); On-site; USD 63,000 - 101,000; Full time

Benefits offered by this job

Healthcare

Well-being programs

Family planning benefits

Generous PTO

Savings & investments

Location-specific perks

Job summary

Moderna is seeking a Manufacturing Associate II for Lipid Nanoparticle and Drug Product pilot-scale production at the Norwood, MA site. The role requires a BS/BA in a related field with 0–2 years of experience and involves hands-on bioprocess work in a fast-paced setting.

You will perform established unit operations, ensure documentation integrity, and support continuous improvement initiatives. Successful candidates will demonstrate strong communication, meticulous attention to detail, and a

Qualifications

• This position requires a BS/BA in Chemistry, Systems, Biomedical or Chemical Engineering or closely related field.
• Demonstrated success in bioprocess development, technical problem solving, and technology transfer is essential.
• Hands-on tangential flow filtration experience is preferred.
• Excellent written and oral communication skills are expected.

Responsibilities

• Execute Lipid Nanoparticle and Drug Product unit operations per approved procedures; lead processes after training.
• Prepare materials, buffers, equipment, and work areas for successful manufacturing execution.
• Follow Good Laboratory Practices and Good Documentation Practices with accurate material tracking.
• Operate, clean, and maintain pilot-scale equipment and maintain clean, safe work areas.
• Identify and communicate issues with clear context across processes and safety.
• Support troubleshooting with accurate observations and process understanding.
• Assist onboarding, peer training, continuous improvement, and operational excellence activities.

Skills

Bioprocess development

Technical problem solving

Technology transfer

Tangential flow filtration

Multi-tasking

Written and oral communication

Education

BS/BA in Chemistry, Systems, Biomedical or Chemical Engineering

Job description

The Role:

The Pilot Scale Operations team is seeking a highly motivated full-time Manufacturing Associate II to support Formulations (Lipid Nanoparticle and Drug Product) pilot-scale production Moderna’s Norwood, MA site. This role will support established Lipid Nanoparticle, and/or Drug Product manufacturing processes in a fast-paced technical development environment. A successful candidate will have hands‑on experience in a biotechnology manufacturing, development, quality, or laboratory environment and will be able to execute procedures with independence, attention to detail, and strong documentation discipline. Once trained and qualified, this individual may lead established manufacturing process executions with appropriate support and oversight. This role requires strong communication, safe work habits, operational ownership, and a collaborative mindset to support daily manufacturing execution, troubleshooting, continuous improvement, and team readiness.

Here’s What You’ll Do:

• Execute established Lipid Nanoparticle, and/or Drug Product unit operations according to approved procedures and laboratory expectations. Lead established processes once trained and qualified.
• Prepare materials, buffers, equipment, and work areas to support successful manufacturing execution.
• Practice Good Laboratory Practices, Good Documentation Practices, and accurate material tracking.
• Operate, clean, and maintain laboratory and pilot-scale equipment; maintain work areas in accordance with safety and 5S expectations.
• Identify and communicate process, equipment, material, documentation, or safety issues with clear context.
• Support troubleshooting by providing accurate observations, execution details, and process understanding.
• Support onboarding, peer training, continuous improvement, and operational excellence activities as appropriate.

Here’s What You’ll Bring to the Table:

• BS/BA (required) in Chemistry, Systems, Biomedical or Chemical Engineering, or closely related field with 0-2 years related experience
• Demonstrated success in bioprocess development, technical problem solving, and technology transfer are essential
• Hands- on experience with tangential flow filtration experience is preferred
• Ability to multi-task in relentless pursuit of successful outcomes
• Exceptional written and oral communication

This position is site-based, requiring you to be at Moderna’s site full-time. This position is not eligible for remote work.

Pay & Benefits

• 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 $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.

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.

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 [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.