QC Microbiology Analyst: Environmental Monitoring (GMP)

Moderna Therapeutics; Oxford; Hybrid; GBP 38,000 - 52,000; Full time

Benefits offered by this job

Healthcare

Family building benefits

Generous paid time off

Sabbatical

Global recharge days

Job summary

Moderna Therapeutics in Oxford, England, seeks an Analyst in Quality Control Microbiology to perform routine environmental monitoring and water sampling at the GMP facility. The role supports microbiological testing for GMP materials and products, contributing to method transfers and validation activities.

You will work within a cross-functional team, ensuring data integrity and compliance with regulatory requirements, with onsite collaboration as part of a dedicated manufacturing site.

Qualifications

• BSc in a relevant scientific discipline with minimum 2 years Quality Control experience in a cGMP environment.
• Hands-on experience of microbiology testing techniques and analyses (e.g. Vitek, Bioburden, Sterility, Endotoxin).
• Working knowledge of FDA, EU, ICH guidelines and regulations.

Responsibilities

• Perform routine environmental monitoring and water sampling in a GMP facility.
• Execute GMP QC microbiology methods focusing on Sterility, Bioburden, Endotoxin and related assays.
• Support testing for release, stability, and method verification/validation samples.
• Collaborate on method transfers and participate in validation activities.
• Prepare and maintain quality systems records (deviations, CAPAs, investigations).

Skills

Microbiology testing

cGMP knowledge

Investigations

Cross-functional collaboration

Prioritization

Education

BSc in a relevant scientific discipline

Tools

Vitek

Isolator Technology

Job description

Moderna Therapeutics in Oxford, England, seeks an Analyst in Quality Control Microbiology to perform routine environmental monitoring and water sampling at the GMP facility. The role supports microbiological testing for GMP materials and products, contributing to method transfers and validation activities.

You will work within a cross-functional team, ensuring data integrity and compliance with regulatory requirements, with onsite collaboration as part of a dedicated manufacturing site.