GMP Specialist | GMP Spezialist (m/w/d)

Randstad Professional

Ingelheim am Rhein, Rheinland-Pfalz, Deutschland
Published Feb 10, 2026
Full-time
Permanent

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

German (Fluent)

Additional

  • Location: Ingelheim; Full-time, permanent contract; Requires a self-independent working style and high level of conscientiousness.