Scientist / Process Developer Parenterals | Scientist / Prozessentwickler Parenteralia &

Brunel GmbH NL Mannheim

Nordrhein-Westfalen, Deutschland
Published May 5, 2026
Full-time
Permanent

Job Summary

In this role, you will be responsible for the planning, execution, and analysis of experiments focused on developing manufacturing processes for parenteral pharmaceuticals, including vials, syringes, cartridges, and lyophilized products. You will oversee technical batch manufacturing and support the transfer of these processes to commercial production sites, ensuring optimization and efficiency. A key aspect of the position involves taking technical responsibility for specific process development areas, balancing scientific rigor with regulatory and economic requirements. You will also manage laboratory equipment, conduct user training, and ensure all work is documented according to GMP/GSP standards for regulatory submissions. This position is ideal for a detail-oriented scientist who enjoys collaborative project work and wants to contribute to innovative pharmaceutical solutions within a professional engineering service environment. You will be supported by a culture that values professional growth, continuous training, and long-term career development.

Required Skills

Education

Completed degree in a scientific field (e.g., Pharmacy, Biotechnology, Chemistry, or Process Engineering).

Experience

  • Professional experience in the development of pharmaceutical manufacturing processes
  • Specific experience with parenteral dosage forms
  • Proven experience in scientific documentation and standard software applications
  • Practical experience in cGMP-regulated environments

Languages

German (Intermediate)English (Intermediate)

Additional

  • Must comply with all applicable safety and occupational health guidelines. Ability to present and represent scientific results internally and externally.