GMP Stability QC Analyst – Analytical Chemistry

Moderna; Oxford; On-site; GBP 55,000 - 80,000; Full time

Job summary

Moderna is establishing a leading research, development, and manufacturing facility at Harwell to support onshore mRNA vaccine production for respiratory diseases in the UK. At Moderna's Harwell site, you will play a critical role in ensuring the quality, integrity, and stability of materials and products supporting our manufacturing operations.

Reporting to the Associate Director, Quality Control, you will combine hands-on analytical chemistry expertise with coordination of GMP stability

Qualifications

• Experience performing cGMP-quality control testing for materials and products.
• Proficient with HPLC/UPLC, GC, UV, DLS, KF analyses.
• Knowledge of GMP stability protocols and regulatory guidelines.

Responsibilities

• Deliver high-quality analytical chemistry and stability testing for raw materials to product release.
• Support manufacturing process testing with HPLC AEX and plate-reader assays.
• Coordinate GMP stability studies for drug substance and drug product.
• Manage stability samples from labeling to storage and disposal.
• Maintain LIMS data entry, electronic forms, and stability databases.
• Perform data trending and statistical analyses on stability results.

Skills

Analytical chemistry

Stability testing

Data analysis

LIMS experience

Tools

HPLC/UPLC

KF analysis

LIMS

AEX

Job description

Moderna is establishing a leading research, development, and manufacturing facility at Harwell to support onshore mRNA vaccine production for respiratory diseases in the UK. At Moderna's Harwell site, you will play a critical role in ensuring the quality, integrity, and stability of materials and products supporting our manufacturing operations.

Reporting to the Associate Director, Quality Control, you will combine hands-on analytical chemistry expertise with coordination of GMP stability