Specialist, DNA Manufacturing Support

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 Norwood, Massachusetts, a cornerstone of our manufacturing and operational excellence. Our Norwood campus translates mRNA science into scalable impact, supporting the global delivery of our medicines. We welcome talent ready to drive innovation and make a meaningful difference for patients worldwide.

You'll provide hands-on GMP manufacturing and technical support for DNA plasmid production, helping enable the mRNA vaccines and therapeutics at the heart of Moderna's platform.

Working closely with Manufacturing, MS&T, Quality, Supply Chain, Facilities, Digital, and other site partners, you'll help ensure safe, compliant, and efficient execution of plasmid fermentation and purification operations while supporting investigations, change controls, manufacturing readiness, and continuous improvement.

As an individual contributor, you'll combine working knowledge of GMP processes, bioprocess equipment, documentation, quality systems, and data integrity with strong cross-functional execution-completing assigned work with quality and timeliness, escalating issues appropriately, and helping strengthen how DNA manufacturing operates at Norwood.

Here's What You'll Do

• Support DNA operations directly on the manufacturing floor, providing hands-on assistance, gathering and communicating process information, escalating emerging issues, and helping ensure plasmid fermentation and purification activities are executed safely, efficiently, and in compliance with GMP requirements.
• Facilitate cross-functional meetings across Manufacturing, MS&T, Quality, Facilities, Digital, Supply Chain, and other partner functions. Communicate complex technical and operational information clearly and influence senior stakeholders to build alignment around high-impact manufacturing initiatives.
• Draft and revise assigned GMP documentation, including batch records, standard operating procedures, electronic work instructions, forms, and job aids, ensuring changes progress through the appropriate review and approval processes.
• Support investigations, change controls, and CAPAs by gathering relevant manufacturing and process information, obtaining stakeholder input, drafting implementation details, completing assigned actions, and tracking deliverables through closure in accordance with established quality-system requirements.
• Complete required training within established timelines and, as assigned, support the training of colleagues on revised documentation, routine manufacturing practices, and updated ways of working.
• Participate in Lean, Six Sigma, and broader process-improvement activities focused on advancing safety, quality, compliance, cycle time, yield, and cost performance. Take ownership of discrete actions and deliverables within larger continuous-improvement initiatives.
• Support technology transfer and manufacturing readiness activities, including bill of material readiness, equipment start-up, commissioning, validation, and other assigned Manufacturing support activities required to prepare processes and equipment for GMP execution.
• Partner across Manufacturing, MS&T, Quality, Facilities, Digital, Supply Chain, and other site functions to troubleshoot and resolve routine operational issues and ensure assigned manufacturing and technical deliverables are completed on time and to the expected standard.
• Support audit and inspection readiness by maintaining complete and accurate GMP documentation, completing assigned readiness actions, gathering requested information, and providing that information through appropriate channels.
• Represent Manufacturing during internal audits and health-authority inspections, helping provide clear, accurate, and appropriately documented information regarding manufacturing processes, practices, and execution.
• Consistently follow site expectations for safety, GMP, gowning, documentation, and data integrity, promptly escalating any safety, quality, operational, or compliance concerns through the appropriate channels.
• Apply working knowledge of GMP manufacturing processes, documentation requirements, quality systems, and bioprocess equipment to support reliable day-to-day operations while completing assigned work with quality, accuracy, and timeliness and contributing to broader team objectives within established procedures and guidance.
• Look for opportunities to use Moderna's digital capabilities and gain exposure to Generative AI-enabled tools where appropriate, helping simplify information workflows, accelerate learning, and support more efficient manufacturing execution while maintaining applicable GMP, quality, and data-integrity requirements.

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

• "We act with dynamic range, driving strategy and execution at the same time at every step."
• "We behave like owners. The solutions we're building go beyond any job description."

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

• B.S. in Chemical/Biochemical Engineering, Biotechnology, or related science and 1-3 years' experience in biotechnology cGMP manufacturing/quality/development (or M.S. and 0-2 years).
• In-depth knowledge of FDA, EMA, and ICH cGMP guidelines.
• 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.

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 $74,000.00 - $118,400.00. 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.