Auf einen Blick
- Aufgaben: Join us in examining vaccine samples and ensuring compliance with quality standards.
- Arbeitgeber: Be part of a leading specialty vaccine company making a global health impact.
- Mitarbeitervorteile: Enjoy flexitime, performance bonuses, lunch vouchers, and access to LinkedIn Learning.
- Warum dieser Job: Work in a diverse team with innovative projects in a fast-paced international environment.
- GewĂĽnschte Qualifikationen: Bring your scientific degree and lab experience; teamwork and communication skills are key.
- Andere Informationen: Opportunity to work under BSL-3 conditions and contribute to groundbreaking vaccine development.
Das voraussichtliche Gehalt liegt zwischen 34000 - 48000 € pro Jahr.
We are a specialty vaccine company that develops, manufactures, and commercializes prophylactic vaccines for infectious diseases addressing unmet medical needs. We have leveraged our expertise and capabilities both to commercialize three vaccines, including the world’s first and only chikungunya vaccine, and to rapidly advance a broad range of vaccine candidates into and through the clinic, including candidates against Lyme disease and Zika.
With operations in Austria, Canada, France, Sweden, the United Kingdom, and the U.S., we are committed to making a positive impact on global public health. Together, we are a global Company which is open to people of all backgrounds. Our diverse and inclusive workforce makes Valneva a great place to work.
Responsibilities
- Examination of release and stability samples for market products using various analytical methods (ELISA, HPLC, UV/VIS spectrophotometry, cell-based assays, ICP-OES etc.)
- Ensuring compliance with SOPs and review of analytical data
- Cultivation of eukaryotic cells and performance of cell-based assays
- Preparation, revision and review of GMP-relevant documents (e.g. standard operating procedures, deviations, changes, etc.)
- Active participation in laboratory investigations including documentation
- Taking responsibility for laboratory equipment including its qualification and supervision of regular cleaning, calibration and maintenance
Qualifications
- HTL, Bachelor or Master Degree in a relevant scientific field with working experience in a GxP-regulated environment
- Experience in laboratory settings with excellent laboratory skills (cell culture, immunological assays) is preferred
- Experience with maintenance and upkeep of laboratory equipment and willingness to work under BSL-3 conditions as a plus
- Experience in developing SOPs and GMP/GDP documentation (nice-to-have)
- Detail oriented work style and excellent communication skills
- Team player with strong interpersonal skills and excellent command of English (spoken and written)
- Ability to work on various projects in a fast-growing, international environment
Benefits
- Open, appreciative company culture with innovative spirit and attractive assignments
- International surrounding with flat hierarchies
- Good team spirit in a strong and highly motivated team
- Wide range of benefits like flexitime, compensation days, performance-related bonus, lunch vouchers, child care center (“Kindergarten”), company events, myClubs and full access to LinkedIn Learning, …
Due to legal reasons we are obliged to disclose the minimum salary for this position, which is € 34.000,00 gross per year based on full-time employment. However our salaries are market oriented and in line with your qualifications and experience.
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Technical Assistant Quality Control (m/f/d) Arbeitgeber: Valneva

Kontaktperson:
Valneva HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Technical Assistant Quality Control (m/f/d)
✨Tip Number 1
Familiarize yourself with the specific analytical methods mentioned in the job description, such as ELISA and HPLC. Having hands-on experience or knowledge about these techniques will give you an edge during the interview.
✨Tip Number 2
Highlight any previous experience you have in a GxP-regulated environment. Be prepared to discuss how you ensured compliance with SOPs and how you handled documentation in your past roles.
✨Tip Number 3
Showcase your teamwork and communication skills. Since this role requires collaboration in a fast-growing international environment, be ready to share examples of how you've successfully worked in teams.
✨Tip Number 4
Research Valneva's current projects and their impact on global public health. Being knowledgeable about the company's mission and recent developments will demonstrate your genuine interest in the position.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Technical Assistant Quality Control (m/f/d)
Tipps für deine Bewerbung 🫡
Understand the Company: Familiarize yourself with Valneva's mission and values. Highlight your alignment with their commitment to global public health and innovation in vaccine development.
Tailor Your CV: Customize your CV to emphasize relevant experience in laboratory settings, particularly in GxP-regulated environments. Include specific analytical methods you are proficient in, such as ELISA or HPLC.
Craft a Strong Cover Letter: Write a compelling cover letter that showcases your detail-oriented work style and excellent communication skills. Mention your ability to work in a team and your willingness to adapt to fast-paced environments.
Highlight Relevant Skills: In your application, clearly outline your laboratory skills, experience with SOPs, and any familiarity with GMP/GDP documentation. This will demonstrate your readiness for the responsibilities of the role.
Wie du dich auf ein Vorstellungsgespräch bei Valneva vorbereitest
✨Know Your Analytical Methods
Familiarize yourself with the analytical methods mentioned in the job description, such as ELISA, HPLC, and UV/VIS spectrophotometry. Be prepared to discuss your experience with these techniques and how you've applied them in previous roles.
✨Emphasize Compliance and Documentation Skills
Highlight your understanding of SOPs and GMP documentation. Share specific examples of how you've ensured compliance in past positions, and be ready to discuss any experience you have in preparing or reviewing GMP-relevant documents.
✨Showcase Your Teamwork and Communication Skills
Since the role requires strong interpersonal skills, think of examples where you've successfully collaborated with a team. Be ready to discuss how you communicate effectively in a diverse environment and how you handle conflicts or challenges within a team.
✨Prepare for Questions on Laboratory Equipment Maintenance
Be prepared to talk about your experience with laboratory equipment maintenance and your willingness to work under BSL-3 conditions. Discuss any relevant experiences you have with equipment qualification, cleaning, calibration, and maintenance.