GMP QC Technician — Lab Support & Analysis

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

Benefits offered by this job

Flexitime

Bonus & Lunch vouchers

Wellbeing program

Job summary

Valneva, a global biotech company, is seeking a Technical Assistant (m/f/d) to join our Quality Control team in Vienna. This role suits a highly organized individual who thrives in a GMP environment and supports scientific teams through efficient coordination and administration.

Responsibilities include analysis of release and stability samples using methods like HPLC, ELISA, qPCR, and cell-based assays, ensuring SOP compliance, and maintaining documentation.

Qualifications

• HTL/BTA/CTA or equivalent degree in a scientific field.
• Experience with HPLC, ELISA, qPCR or cell-based assays.
• GMP environment experience or willingness to work under BSL-3.
• Excellent documentation and communication skills.
• Fluent English and MS Office proficiency.
• Independent yet collaborative work style.

Responsibilities

• Examination of release and stability samples using analytical methods (ELISA, HPLC, UV/VIS, cell-based assays).
• 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 (SOPs, deviations, changes).
• Participate in laboratory investigations with documentation.
• Maintain responsibility for laboratory equipment including qualification, cleaning, calibration, and maintenance.

Skills

English fluency

Organizational skills

Education

HTL/BTA/CTA or science degree

Tools

HPLC

ELISA

qPCR

Cell-based assays

Job description

Valneva, a global biotech company, is seeking a Technical Assistant (m/f/d) to join our Quality Control team in Vienna. This role suits a highly organized individual who thrives in a GMP environment and supports scientific teams through efficient coordination and administration.

Responsibilities include analysis of release and stability samples using methods like HPLC, ELISA, qPCR, and cell-based assays, ensuring SOP compliance, and maintaining documentation.