Galenic Development Assistant | Entwicklungsassistent Galenik (m/w/i)

MEDICE Arzneimittel Pütter GmbH & Co. KG

Iserlohn, Nordrhein-Westfalen, Deutschland
Published Jul 30, 2025
Full-time
Fixed-term

Job Summary

This role involves supporting the development of pharmaceutical formulations, specifically focusing on galenic preparations. The assistant will be responsible for planning, manufacturing, and in-process control of experimental batches, as well as developing formulations and processes for solid, semi-solid, liquid, and sterile dosage forms. Key tasks include transferring products and processes from development to production scale, optimizing existing procedures, and managing technology transfers. The ideal candidate will have a background as a pharmaceutical technician (Pharmakant), pharmaceutical-technical assistant (PTA), or medical assistant (MFA), possess strong organizational skills, and be proficient in MS Office. This position offers an opportunity to contribute to meaningful work in a family-oriented, future-focused company with a strong emphasis on individual development and workplace security.

Required Skills

Education

Completed vocational training as a Pharmaceutical Technician (Pharmakant), Pharmaceutical-Technical Assistant (PTA), Medical Assistant (MFA), or an alternative relevant educational background

Experience

  • Experience in planning, manufacturing, and in-process control of experimental batches
  • Experience with formulation and process development of various dosage forms
  • Experience in product and process transfer from development to production scale
  • Experience in process optimization of approved products
  • Experience with technology transfers (insourcing, outsourcing)
  • Experience in organizing and conducting process validation studies
  • Experience in preparing and evaluating data, creating work instructions, and manufacturing documentation
  • Experience in preparing risk analyses, development, and validation plans/reports
  • Experience supporting GMP-compliant manufacturing of clinical trial products
  • Experience in coordinating change control processes

Languages

German (Fluent)English (Basic)

Additional

  • The position is initially limited to 2 years.