QC Technical Assistant - GMP Lab & Data Support

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

Benefits offered by this job

Work Life Balance

Lunch vouchers

Office Massages

Job summary

Valneva in Vienna is seeking a Technical Assistant (m/f/d) to join our Quality Control team. The role supports analytical testing and documentation in a GMP-regulated environment and coordinates scientific activities.

You will work with methods such as ELISA, HPLC and cell-based assays, maintain equipment, review SOPs, and prepare GMP documents. Fluent English and strong organization are essential, with a collaborative, detail-oriented approach encouraged by a global biotech company.

Qualifications

• HTL/technical degree or higher in a relevant science field.
• Experience with HPLC, ELISA, qPCR and cell-based assays.
• GMP-regulated laboratory experience is a plus.
• Detail-oriented with strong documentation skills.
• Fluent written and spoken English; MS Office proficiency.

Responsibilities

• Examination of release and stability samples using various analytical methods.
• Ensure SOP compliance and review analytical data.
• Document, report and review results accurately and timely.
• Cultivation of eukaryotic cells and cell-based assays.
• Prepare, revise and review GMP-relevant documents.
• Participate in laboratory investigations with proper documentation.
• Oversee laboratory equipment including qualification, cleaning, calibration and maintenance

Skills

Analytical methods

HPLC

ELISA

qPCR

Cell-based assays

MS Office

Fluent English

Team player

Independent work

Education

HTL/Technical degree in science

Tools

Laboratory equipment maintenance

Job description

Valneva in Vienna is seeking a Technical Assistant (m/f/d) to join our Quality Control team. The role supports analytical testing and documentation in a GMP-regulated environment and coordinates scientific activities.

You will work with methods such as ELISA, HPLC and cell-based assays, maintain equipment, review SOPs, and prepare GMP documents. Fluent English and strong organization are essential, with a collaborative, detail-oriented approach encouraged by a global biotech company.