Quality Control & Raw Materials Associate I

Moderna Therapeutics

Norwood (MA)

On-site

USD 54,000 - 86,000

Full time

3 days ago
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Benefits offered by this job

Competitive healthcare
Paid time off and global recharge days
Location-specific perks

Job summary

Moderna seeks a Quality Control Raw Materials Associate I at its Norwood, MA site to support GMP manufacturing through QC RM activities and potential special projects. This is a first shift, Monday–Friday.

The role includes sampling, shipping, testing (pH, conductivity, TruScan RM spectroscopy, appearance, and dimensional verification), and LIMS data logging. You will inspect materials and retain samples, release consumables, and maintain cGMP documentation while upholding a safe, compliant lab

Qualifications

  • BS in a relevant scientific discipline.
  • 0-2 years with BS or 3+ years in GMP QC laboratory setting.
  • Demonstrated aptitude or ability to learn GxP Regulations and work in a team.

Responsibilities

  • Requesting, sampling, and shipping of raw materials.
  • Sample coordination across internal/external labs.
  • Supporting domestic and international sample shipments.
  • Testing support for pH, conductivity, TruScan RM spectroscopy, appearance, and dimensional verification.
  • Inspecting retain samples of products and raw materials.
  • Logging results in LIMS (LabVantage) and data entry.
  • Inspecting and releasing raw materials and consumables.
  • Maintain clean room gowning and aseptic techniques.
  • Stocking/stock management for QC lab supplies; routine lab cleaning.
  • Complete cGMP documentation and ensure data integrity and compliant records.
  • Maintain safe laboratory working environment.
  • Follow SOPs and internal guides for all tasks.
  • Complete required training on schedule.

Skills

GxP Regulations
Teamwork
Attention to detail

Education

BS in a relevant scientific discipline

Tools

LIMS (LabVantage)

Job description

Moderna seeks a Quality Control Raw Materials Associate I at its Norwood, MA site to support GMP manufacturing through QC RM activities and potential special projects. This is a first shift, Monday–Friday.

The role includes sampling, shipping, testing (pH, conductivity, TruScan RM spectroscopy, appearance, and dimensional verification), and LIMS data logging. You will inspect materials and retain samples, release consumables, and maintain cGMP documentation while upholding a safe, compliant lab

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