GMP Project Coordinator - Pharma
On-site · Konstanz, Baden-Wurttemberg, Germany
Job Summary
End-to-end project leadership for Pharma Analytics: Analytical Development & Method validation, Dissolution, Chromatography, Particle Testing, Stability Storage, and related subcontracted services within the Eurofins Group. Includes project planning, timeline management, reviewing technical requests, GMP execution, LIMS configuration, and coordination between internal labs, clients, and external partners. Contributes to SOPs and GMP documentation, audits, and continuous improvement; identifies and implements process improvements to increase efficiency, quality, and throughput. Requires a degree in life sciences (pharmacy, chemistry, biology) or completed vocational training in a pharmaceutical/chemical field with 3+ years in a regulated environment; hands-on QC/analytical development experience; strong customer orientation; excellent IT literacy; LIMS experience is a plus; demonstrated project management ability; strong organization and problem-solving skills; fluent German and English.
Required Qualifications
- Degree in life sciences (pharmacy, chemistry, biology) or completed vocational training in a pharmaceutical or chemical field
- 3+ years of relevant professional experience 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 skills, prioritization, and problem-solving in dynamic settings
- High sense of responsibility, reliability, and team spirit
- Language: very good German, good English
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