QC Microbiology Specialist — cGMP & Sterility Testing

Moderna; Madrid; Presencial; EUR 42.000 - 64.000; Jornada completa

Descripción de la vacante

Moderna Madrid hosts a Quality Control Microbiology role focused on cGMP testing, including endotoxin and sterility assessments, to support release and stability programs. The role is an individual contributor in a collaborative lab setting, with opportunities to engage in digital systems and continuous improvement.

You will work in a fast-paced environment, performing data entry, participating in investigations, and maintaining rigorous GDP/data integrity practices while adhering to GxP

Formación

• Education: degree in Biology/Biochemistry or equivalent with at least 2 years’ experience.
• 2+ years’ experience in QC laboratory of a pharmaceutical company preferred.
• Hands-on endotoxin, sterility testing in QC micro laboratories.
• Working knowledge of FDA/EU/ICH guidelines preferred.
• Able to collaborate in a cross-functional environment.
• Working proficiency in English required.

Responsabilidades

• Perform cGMP QC microbiology testing focusing on endotoxin, sterility, and environmental monitoring for release and stability.
• Support method qualification and acquisition activities as required.
• Execute GMP QC microbiology testing including sterility/endotoxin testing and sequencing.
• Support testing of drug substances/products and generate data for release/stability programs.
• Perform data entry and data trending in applicable electronic systems.
• Execute electronic assay forms and results in LabVantage LIMS.
• Provide stability program support.
• Maintain QC lab inventory and supplies.
• Troubleshoot assay methods and equipment; assist investigations and CAPAs.

Conocimientos

Growth promotion

Endotoxin testing

Sterility testing

Data entry

English proficiency

Educación

Biology or Biochemistry degree

Technical qualification (FP/Ciclo Superior)

Herramientas

LabVantage LIMS

Descripción del empleo

Moderna Madrid hosts a Quality Control Microbiology role focused on cGMP testing, including endotoxin and sterility assessments, to support release and stability programs. The role is an individual contributor in a collaborative lab setting, with opportunities to engage in digital systems and continuous improvement.

You will work in a fast-paced environment, performing data entry, participating in investigations, and maintaining rigorous GDP/data integrity practices while adhering to GxP