Moderna, Inc.

Specialist, Quality Control

Moderna, Inc.$74K — $118K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor’s degree in a relevant scientific discipline, preferably Analytical Chemistry or Chemistry
  • 5 years of laboratory experience with a focus on analytical chemistry
  • Strong understanding of GxP regulations (GMP, GLP, GCP, GDP) or ability to learn

Responsibilities

  • Perform routine QC analytical chemistry testing including HPLC, GC, and UV
  • Support method acquisition, qualification, and re-qualification protocols
  • Troubleshoot methods and equipment
  • Conduct data entry and support trending and analysis
  • Perform general laboratory support activities such as reagent preparation and equipment maintenance
  • Author and revise laboratory procedures and reports
  • Enter sample results into LIMS and execute electronic assay forms

Benefits

  • Competitive healthcare with voluntary benefit programs
  • Holistic well-being approach including fitness, mindfulness, and mental health support
  • Family planning benefits including fertility, adoption, and surrogacy support
  • Generous paid time off for vacations and sabbaticals
  • Savings and investments support
  • Location-specific perks and extras
Full Job Description

The Role

Moderna is seeking a Quality Control Chemistry Specialist based at their Norwood, MA site. The individual in this role will focus on Release, Stability and In Process data review and reporting for clinical and commercial products. This role may support special projects as needed.

Here’s What You’ll Do:

  • Perform routine QC analytical chemistry testing including HPLC, GC, UV, Particle Analysis and Dynamic Light Scattering, etc.

  • Support execution of method acquisition, qualification, re-qualification protocols

  • Supports Troubleshooting of methods and equipment

  • Perform data entry and supports trending and analysis

  • Performs general laboratory support activities including reagent preparation, sample management, equipment maintenance, lab housekeeping etc.

  • Supports authoring and revision of equipment, method and other laboratory procedures and reports

  • LIMS sample result entry, execution of electronic assay forms

  • Perform STAT testing in support to manufacturing process testing as needed, may require shift flexibility

  • Stability program support

  • Complete and maintain cGMP documentation for work performed.

  • Support authoring quality systems records such as deviations, change controls, CAPAs

  • Establish and maintain a safety, laboratory working environment

  • Follow all relevant GxP regulations guidelines, and company policies to ensure compliance with regulatory and internal requirements

  • Execute tasks precisely as defined in internal guiding documents including but not limited to standard operation procedures (SOPs) and work instructions

  • Follow Good Documentation Practices and Data Integrity requirements to ensure data, documentation, and records are completed and maintained for use by the business and available to support audits or inspections

  • Complete training in assigned required learning plan according to the defined timing and the prescribed requalification cadence.

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

  • Minimum education required: Bachelor’s degree in a relevant scientific discipline, preferred in Analytical Chemistry, or Chemistry

  • Minimum experience required: 5 years in a laboratory setting with focus in analytical chemistry

  • Demonstrated aptitude or ability to learn to gain a strong understanding of GxP regulations (specify GMP.GLP, GCP, GDP or other applicable standards)

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 $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.

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 to learn more about our current opportunities. 


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