GMP Specialist | GMP Spezialist (m/w/d)
Randstad Professional
Job Summary
This role involves supporting pharmaceutical production and clinical trial supply operations within a strictly regulated GMP environment in Ingelheim. As a GMP Specialist, your day-to-day responsibilities will include preparing packaging documentation, creating and applying labels for clinical samples, and managing warehouse logistics, including goods receipt and dispatch. You will also play a key role in equipment qualification within the GMP manufacturing area and execute precise packaging activities. This position is ideal for a detail-oriented professional with a background in pharmaceutical manufacturing who enjoys a mix of administrative documentation and hands-on operational tasks. The role is particularly attractive due to its long-term perspective with a global leader in the pharmaceutical industry, offering a structured environment, competitive benefits, and significant opportunities for professional development through specialized e-learning platforms.
Required Skills
Education
Completed vocational training as a Pharmaceutical Technician (Pharmakant) or a comparable qualification.
Experience
- Professional experience working within a GMP-regulated environment
- Experience in pharmaceutical packaging and labeling activities
- Experience in warehouse logistics, specifically handling goods receipt and dispatch
- Experience in preparing technical documentation and equipment qualification
Languages
Additional
- Location: Ingelheim; Full-time, permanent contract; Requires a self-independent working style and high level of conscientiousness.
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