GMP QC Technician – Analytical & Cell Assays

Valneva SE; Wien; Hybrid; EUR 33,000 - 40,000; Full time

Benefits offered by this job

Work Life Balance

Financial perks

Health & Wellbeing

Job summary

Valneva, a global biotech company in Austria, seeks a Technical Assistant (m/f/d) to join the Quality Control team in a GMP-regulated environment. You will support scientific teams through efficient coordination and administration.

The role requires experience with HPLC, ELISA, qPCR and cell-based assays, fluency in English, and strong documentation skills. You will work in a collaborative, international setting with flat hierarchies and regular events.

Qualifications

• HTL/technical degree or higher in a scientific field.
• Experience with analytical methods: HPLC, ELISA, qPCR.
• GMP-regulated lab experience is a plus.
• Strong documentation skills and attention to detail.
• Ability to work independently and in a team.
• Fluent written/spoken English.
• Proficiency in MS Office.

Responsibilities

• Examination of release and stability samples using analytical methods.
• Ensuring SOP compliance and reviewing data.
• Documenting, reporting and reviewing results timely.
• Cultivation of eukaryotic cells and cell-based assays.
• Preparation, revision and review of GMP documents.
• Active participation in laboratory investigations including documentation.
• Maintaining and supervising laboratory equipment, including qualification, cleaning, calibration and maintenance.

Skills

HPLC

ELISA

qPCR

Cell-based assays

GMP environment

MS Office

Documentation

Communication

Team player

English fluency

Education

HTL/Technical degree or Bachelor/Master in science

Tools

MS Office

Job description

Valneva, a global biotech company in Austria, seeks a Technical Assistant (m/f/d) to join the Quality Control team in a GMP-regulated environment. You will support scientific teams through efficient coordination and administration.

The role requires experience with HPLC, ELISA, qPCR and cell-based assays, fluency in English, and strong documentation skills. You will work in a collaborative, international setting with flat hierarchies and regular events.