QC Microbiology Scientist - cGMP for mRNA Medicines

Moderna Therapeutics; Madrid; Presencial; EUR 42.000 - 62.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Competitive healthcare

Voluntary benefit programs

Well-being resources

Family building benefits

Generous paid time off

Descripción de la vacante

Moderna Therapeutics is expanding its Madrid analytical centre and seeks a QC Microbiology professional to support testing and release of mRNA medicines. You will perform cGMP microbiology testing, endotoxin and sterility assessments, and environmental monitoring for release and stability.

You will assist with Method Qualification, data integrity, CAPA investigations, and document control in a fast-paced, cross-functional team environment.

Formación

• Technical qualification (FP) or degree in Biology, Biochemistry, or other relevant scientific discipline with at least 2 years’ experience.
• Hands-on experience with growth promotion, endotoxin and sterility testing within QC microbiology labs.
• Working knowledge of FDA/EU/I CH guidelines and data integrity practices.

Responsabilidades

• Perform cGMP QC microbiology testing with focus on Endotoxin, Sterility, Environmental Monitoring for release and stability.
• Support Method Qualification and Acquisition activities as required.
• Execute GMP QC Microbiology testing including Sterility and Endotoxin testing and Micro sequencing.
• Maintain accurate cGMP documentation and GDP/Data Integrity compliance.
• Collaborate in CAPA investigations and non-conforming results.

Conocimientos

QC Microbiology

Endotoxin testing

Sterility testing

Growth promotion

Environmental monitoring

Educación

Biology/Biochemistry degree or Technical qualification (FP)

Herramientas

LabVantage LIMS

Descripción del empleo

Moderna Therapeutics is expanding its Madrid analytical centre and seeks a QC Microbiology professional to support testing and release of mRNA medicines. You will perform cGMP microbiology testing, endotoxin and sterility assessments, and environmental monitoring for release and stability.

You will assist with Method Qualification, data integrity, CAPA investigations, and document control in a fast-paced, cross-functional team environment.