Analyst in the Quality Control Department (all genders)

TN Austria; Wien; Vor Ort; EUR 40 000 - 60 000; Vollzeit

Zusammenfassung

Ein etabliertes Unternehmen sucht einen Analysten für die Qualitätskontrolle in Wien. In dieser spannenden Rolle sind Sie verantwortlich für die Durchführung analytischer Tests und die Dokumentation gemäß GMP-Standards. Sie werden Teil eines internationalen Teams und erhalten umfassende Schulungen, um Ihre Fähigkeiten zu entwickeln. Diese Position bietet Ihnen die Möglichkeit, in einer dynamischen Umgebung zu arbeiten und Ihre Karriere in der pharmazeutischen Industrie voranzutreiben. Wenn Sie eine Leidenschaft für Qualitätssicherung haben und in einem globalen Unternehmen arbeiten möchten, ist dies die perfekte Gelegenheit für Sie.

Leistungen

Internationale Karrierechancen

Technische und persönliche Weiterbildung

Flexible Arbeitszeiten

Onboarding-Trainings

Qualifikationen

• Abgeschlossenes Studium oder Ausbildung als Labortechniker.
• Erfahrung in einem GMP-Umfeld und Kenntnisse in HPLC.

Aufgaben

• Durchführung analytischer Aktivitäten im GMP-Labor.
• Überprüfung von Daten und Dokumentation gemäß GMP-Standards.

Kenntnisse

Analytische Fähigkeiten

Teamarbeit

Flexibilität

Kommunikationsfähigkeiten

Englischkenntnisse

Deutschkenntnisse

Motivation

Ausbildung

Wissenschaftliches Studium

Ausbildung als Labortechniker

Tools

HPLC

Empower Software

Jobbeschreibung

Analyst in the Quality Control Department (all genders), Vienna

Client:

Eurofins

Location:

Vienna

Job Category:

Other

EU work permit required:

Yes

Job Reference:

409b0b52e6c5

Job Views:

4

Posted:

20.03.2025

Expiry Date:

04.05.2025

Job Description:

Job Description

For one of our teams based in Vienna, we are currently looking for an Analyst (all genders) in the Quality Control department. In this exciting and interesting role, your responsibilities would include, but are not limited to:

• Performing various analytical activities in the quality control (GMP) laboratory. This includes, among other things, the testing of active ingredients, raw material and bulk products in accordance with specified pharmacopoeia or internal methods.
• Carrying out analyses using HPLC and HPLC-Dissolution, as well as various wet chemical analyses.
• Troubleshooting and participation in investigations.
• Review data generated by other analysts.
• Analysis and documentation according to GMP and internal quality standards.

Qualifications

For this versatile and challenging position we are looking for personalities with:

• Completed scientific studies or apprenticeship as a laboratory technician, CTA, etc.
• Knowledge of HPLC, dissolution and Empower software would be an advantage
• First experiences in a GMP environment
• Very good written and spoken English, German would be an advantage
• Independent, careful and responsible way of working
• Ability to communicate and work in a team
• High motivation, ability to work under pressure, flexibility and reliability
• High level of commitment and enthusiasm

Additional Information

We are offering you an interesting position within a truly global company and international team. After several onboarding trainings, to make sure you have the experience you need, you will be working independently in our team.

• Limited 1 year, full time contract with Eurofins PSS
• Interesting international as well as national career opportunities
• Different trainings focused on technical experiences as well as soft skills
• Deviating from the collective agreement weekly working hours of 38 instead of 40

If this position could be of interest to you or if you have any questions regarding this position please feel free to reach out to Dhivi Sanghi, PSS Talent Attraction Specialist Germany and Austria.

The collective agreement minimum salary (employment group (Vewendungsgruppe) III) for this position is at least 2369,18 €. Due to the responsibilities and the challenging tasks and with appropriate qualifications, there will be an appropriate overpayment.