Biotechnologist / Biologist / IRT Specialist | Biotechnologe (m/w/d) Biologe (m/w/d) IRT Specialist (m/w/d)

agento PersonalManagement GmbH

Biberach an der Riß, Baden-Württemberg, Deutschland
Published Feb 18, 2026
Full-time
Permanent

Job Summary

This role involves serving as an Interactive Response Technology (IRT) Specialist within a leading global pharmaceutical company in Biberach. You will independently lead all activities related to the evaluation, planning, conceptual implementation, and maintenance of study-specific IRT concepts. As a key representative in cross-functional project teams, you will ensure that technical implementations of clinical study designs comply with drug safety and patient protection standards. Day-to-day responsibilities include managing the software development lifecycle of IRT systems, overseeing computer system validation of cloud-based platforms, and ensuring adherence to international GMP and GCP guidelines. This position is particularly attractive due to its hybrid work model (2-3 days remote), a highly competitive salary of approximately €68,000 per annum from day one, and the opportunity to work for a top-tier employer with excellent long-term permanent takeover prospects.

Required Skills

Education

Master's degree in Natural Sciences (Biology, Biotechnology, or related) or a Bachelor's degree with significant professional experience.

Experience

  • Several years of professional experience in a related scientific field with a Master's degree, or extensive experience with a Bachelor's degree.
  • Professional experience in the field of Quality Assurance or IRT systems.
  • Proven knowledge of technical aspects and functions of IRT systems.
  • Experience with global activities regarding investigational medicinal products and clinical study design.
  • Demonstrated experience working within GMP/GCP regulatory frameworks in the pharmaceutical industry.

Languages

English (Fluent)

Additional

  • Location: Biberach. Hybrid work model available (2-3 days remote). Candidates must be able to work under GMP and GCP guidelines as well as US and EU international regulations.