Process Development Specialist for Sterile Dosage Forms | Mitarbeiter für die Prozessentwicklung steriler Arzneiformen (m/w/d)

Vetter Pharma-Fertigung GmbH & Co. KG

Ravensburg, Württemberg, Baden-Württemberg, Deutschland
Published Feb 17, 2026
Full-time
Permanent

Job Summary

This role involves the development and practical implementation of process steps for sterile pharmaceutical filling and packaging. As a key member of the development team, you will be responsible for designing and procuring product-contact equipment, determining specific process parameters, and conducting experimental series and simulations within development laboratories. You will play a vital role in bridging the gap between lab-scale development and commercial production by supporting the implementation of new technologies and overseeing GMP batches. The position is highly interdisciplinary, requiring collaboration with various expert teams to optimize existing commercial processes and handle quality investigations. This is an attractive opportunity to work for a global leader in the pharmaceutical service industry, contributing to life-saving treatments for conditions such as Multiple Sclerosis and cancer within a modern, family-owned corporate environment that offers extensive professional development and comprehensive employee benefits.

Required Skills

Education

Completed scientific or technical vocational training with an advanced additional qualification, or a university degree (Master's or Diploma) in a natural science field.

Experience

  • Several years of professional experience in the manufacture and development of parenteral dosage forms at both production and laboratory scales
  • Proven experience in managing complex technical workflows and production processes
  • Experience in the design and procurement of product-contact equipment
  • Professional background in conducting and documenting experimental series according to regulatory guidelines
  • Experience working within interdisciplinary teams for process optimization and change management

Languages

English (Fluent)

Additional

  • Must be able to work in a full-time, permanent capacity. Requires the ability to work in a GMP-regulated environment and handle product-specific equipment.