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Scientist; M​/F​/D) focus Method Validation, Method Development and Analytical Transfers

in 80331, München, Bayern, Deutschland
Unternehmen: Eurofins
Vollzeit position
Verfasst am 2026-09-13
Berufliche Spezialisierung:
  • Wissenschaft
    Pharmazeutische Wissenschaften, Analytische Chemie
Gehalts-/Lohnspanne oder Branchenbenchmark: 50000 - 70000 EUR pro Jahr EUR 50000.00 70000.00 YEAR
Stellenbeschreibung
Stellenbezeichnung: Scientist (M/F/D) with a focus on Method Validation, Method Development and Analytical Transfers

Eurofins Scientific is an international life sciences company that provides a unique range of analytical testing services to clients across multiple industries. The Group is a world leader in food, environment, pharmaceutical and cosmetics product testing, Agro Sciences CRO services, genomics, discovery pharmacology, forensics, CDMO, advanced material sciences, and clinical diagnostics.

Eurofins PSS Insourcing Solutions® is a global, award‑winning in sourcing solution that places skilled teams directly at client sites, managing operations seamlessly and eliminating complexities. We deliver a long‑term service commitment that brings Eurofins expertise, cGMP compliance and advanced methodologies to client facilities.

Job Description

In this dynamic and impactful role you will support analytical activities within an international pharmaceutical project located near Munich. Your main responsibilities include:

  • Supporting project and resource planning for all analytical activities in close collaboration with the local Project Lead and team.
  • Coordinating, executing, and documenting method transfers, development, validation, and verification of complex analytical methods (e.g., HPLC, AAS, KF) both internally and with external laboratories.
  • Performing analytical testing and preparing protocols and reports in accordance with GMP requirements and internal quality standards.
  • Reviewing and assessing existing methods for practicality, compliance with EU and US GMP validation requirements, and regulatory status; executing further method development and validation as needed.
  • Troubleshooting method‑related and instrument‑specific issues, with access to a global expert network across multiple laboratories.
  • Identifying opportunities for method improvements, modernization, and enhanced robustness.
  • Reviewing and verifying laboratory records, plans, and notes from other projects and preparing procedural documents.
  • Preparing analytical documentation to support regulatory submissions.
  • Supporting multiple analytical transfer activities simultaneously.
Qualifications

We are looking for a candidate who:

  • has a degree in Chemical Engineering, Analytical Chemistry, or completed training as a Chemical Laboratory Technician (or equivalent qualification);
  • has at least 2 years of professional experience in applying, interpreting, and validating pharmaceutical analytical methods under GMP (e.g., chromatography, spectroscopy, physicochemical testing);
  • is proficient with analytical software in a GMP environment, ideally Waters Empower;
  • has an independent, structured, and proactive working style with the ability to set priorities and meet timelines;
  • demonstrates excellent teamwork and communication skills, strong persuasive abilities, and assertiveness;
  • has a very good command of German and English, both written and spoken;
  • exhibits high proactivity, flexibility, and resilience in a dynamic project environment.
Additional Information

We offer you an engaging position within a truly global company. After onboarding trainings, you will work independently within our team. Benefits include:

  • Unlimited full‑time contract with Eurofins PSS;
  • Interesting international and national career opportunities;
  • A comprehensive catalogue of trainings focused on technical, leadership, and management skills;
  • Dynamic international environment with strong growth and development opportunities.
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