Laborant in der Qualitätskontrolle (m/w/d) - Schwerpunkt Methodenetablierung

At Elanco (NYSE: ELAN) – it all starts with animals!

As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.

At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.

At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.

We believe that diversity is the driving force behind innovation, creativity, and overall business success.

Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.

Making animals’ lives better makes life better – join our team today!

Your role: Laboratory Assistant in Quality Control (m/f/d)

The position is initially limited to 2 years.

In this technically demanding role, you will be largely responsible for the practical implementation and maintenance of our analytical test procedures.

Your focus will be on ensuring robust analysis in accordance with international standards directly in the laboratory.

Your Responsibilities:


* Wide-ranging analysis: You will apply chromatographic (HPLC, GC) and wet chemical methods to ensure precise quality control, maintaining data integrity through GMP-compliant documentation and modern laboratory standards (e.g., 5S).


* Pharmacopoeia compliance: You will independently establish and verify analytical methods according to applicable monographs (e.g.

EP, USP) and carry out verifications in regulatory revisions.


* Method optimization & CAPA management: You will experimentally investigate and optimize analytical procedures in the context of deviations and CAPA measures to sustainably increase methodological robustness.


* Conducting validation studies: You will carry out method validations and verifications for new products and feedstocks practically on the device and strictly comply with GMP requirements.


* Securing method transfer (APVs): You will develop "best practices" for analytics and record them in supplementary audit regulations (APVs) to ensure consistent application of the methods across the team.

What You Need to Succeed (minimum qualifications):


* Education: You have completed training as a chemical laboratory assistant (m/f/d), CTA (m/f/d) or a comparable qualification and 2+ years relevant professional experience in pharmaceutical quality control.



* Expertise: You have in-depth, field-tested knowledge in instrumental analysis (HPLC, GC, spectroscopy) as well as in the application of international pharmacopoeia (EP, USP).


* Languages: Fluent German and good English skills for working with international pharmacopoeia.

What Will Give You a Competitive Edge (Preferred Qualifications)


* Methodological competence: Experience in the practical processin...