Moderna, Inc.

Associate II, Quality Control

Moderna, Inc.$63K — $100K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • BA/BS in relevant scientific discipline
  • 2 years of laboratory experience
  • Ability to learn GxP regulations
  • Demonstrated analytical chemistry skills
  • Experience with data entry and documentation in lab settings
  • Familiarity with cGMP standards

Responsibilities

  • Perform routine analytical chemistry testing including HPLC, UPLC, and GC
  • Support special projects as assigned
  • Troubleshoot assay methods and equipment
  • Perform data entry and support trending
  • Manage laboratory supplies and general support tasks
  • Write and revise SOPs, protocols, and reports
  • Execute tasks in accordance with GxP regulations

Benefits

  • Competitive healthcare and voluntary benefits
  • Access to fitness, mindfulness, and mental health support
  • Family planning benefits including fertility and adoption support
  • Generous paid time off including sabbaticals and recharge days
  • Savings and investments to help plan for the future
  • Location-specific perks and extras
Full Job Description

The Role:

Moderna is seeking a Quality Control Chemistry Associate II based at their Norwood, MA site.  The individual in this role will perform cGMP QC Chemistry testing for QC Chemistry, release, stability and in process samples. This role may support special projects as needed. This role will be working on the 2nd shift Sunday through Thursday.

Here’s What You’ll Do:

  • Performs routine analytical chemistry testing including HPLC, UPLC, GC, UV, Particle Analysis and Dynamic Light Scattering, KF, etc.

  • Supports special projects as assigned.

  • May assist with Troubleshoots assay methods and equipment.

  • Performs data entry and supports trending.

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

  • Supports authoring of SOPs, protocols and reports.

  • LIMS (LabVantage) sample result entry, execution of Electronic Assay Forms in LIMS

  • Perform HPLC (AEX) and NaOH plate reader-based assays in support of manufacturing process stat testing as needed

  • Stability program support.

  • Support more junior staff with data review, training, and troubleshooting.

  • Managing/stocking of QC lab supplies

  • Write/revise SOPs, protocols and reports.

  • Complete and maintain cGMP documentation for work performed.

  • Participate in authoring quality systems records such as investigations, deviations, change controls, CAPAs

  • Establish and maintain a safe 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 operating 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):

  • Education: BA/BS in relevant scientific discipline

  • Experience: 2 years of Laboratory experience.

  • Demonstrated aptitude or ability to learn to gain a strong understanding of GxP regulations.

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 $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.

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