Eurofins

GMP Project Coordinator - Pharma

Stellenbeschreibung:

Overview

In this role you will lead pharma analytics projects within a global CRO network, coordinating analytical development, method validation, and related services under GMP. You will work with internal labs, clients, and partners to plan, execute, and optimize projects, ensuring data integrity and audit readiness. You’ll map projects in LIMS and contribute to continuous improvement in quality and efficiency. This is an opportunity to influence cross-functional delivery in a fast-paced, compliance-driven environment.

Leistungen / Benefits
  • Flexible working hours
  • Partial remote work
  • Professional development: training and mobility within Eurofins
  • International exposure across global projects
  • Modern workplace and tools, including LIMS-driven processes
  • Competitive compensation and benefits
Verantwortungsbereiche
  • End-to-end project leadership for Pharma Analytics across Analytical Development, Method Validation, Dissolution, Chromatography, Particle Testing, Stability Storage, and subcontracted services
  • Project planning and timeline management: define plans, track milestones, manage POs, risks and forecasts, report status to stakeholders
  • Technical coordination: review customer requests and create work packages and proposals
  • GMP compliance: ensure correct execution of analytical work per GMP; contribute to audit readiness and continuous improvement
  • LIMS configuration: map and configure projects in LIMS and support data integrity best practices
  • Stakeholder management: coordinate interfaces between internal labs, clients, and external partners; support new project acquisition
  • Quality system contributions: author and maintain SOPs and GMP documentation; support audits
  • Process optimization: identify and implement efficiency, quality, and throughput improvements
Zentrale Anforderungen
  • Degree in life sciences or completed vocational training in pharmaceutical/chemical field with 3+ years in a regulated environment (ISO 17025, GLP, ideally GMP)
  • Hands-on experience in pharmaceutical QC and/or analytical development
  • Strong customer orientation with clear, confident communication (written & verbal)
  • Very good IT literacy and Office skills; LIMS experience is a plus
  • Demonstrated project management capability
  • Excellent organizational, prioritization, and problem-solving skills in dynamic settings
  • High sense of responsibility, reliability, and team spirit
  • Language: very good German, good English
  • customer orientation
  • clear communication
  • team spirit
  • LIMS configuration
  • GMP/compliance knowledge
  • Analytical development
NOTE / HINWEIS:
EnglishEN: Please refer to Fuchsjobs for the source of your application
DeutschDE: Bitte erwähne Fuchsjobs, als Quelle Deiner Bewerbung

Stelleninformationen

  • Veröffentlichungsdatum:

    14 Sep 2026
  • Standort:

    Konstanz

    Einsatzort:

    Gelsenkirchen, Deutschland
  • Typ:

    Vollzeit
  • Arbeitsmodell:

    Vor Ort
  • Kategorie:

  • Erfahrung:

    2+ years
  • Arbeitsverhältnis:

    Angestellt

KI Suchagent

AI job search

Möchtest über ähnliche Jobs informiert werden? Dann beauftrage jetzt den Fuchsjobs KI Suchagenten!