Bioprocess Engineer | cGMP Manufacturing | Process Optimization & Training
A global organization focused on high-quality pharmaceutical and biotechnological production. The company emphasizes compliance with cGMP guidelines, continuous process improvement, and cross‑functional collaboration to optimize production efficiency and maintain high standards of quality and safety.
Key Responsibilities
* Execute production campaigns in compliance with cGMP guidelines.
* Create and review risk analyses and implement resulting measures.
* Ensure batch execution, evaluate test results, troubleshoot production equipment, and provide solution proposals.
* Maintain complete process and GMP documentation, preserving process know‑how.
* Identify continuous improvement opportunities for processes, equipment, and workflows in collaboration with R&D and project teams.
* Train staff on assigned products and support cross‑project training initiatives.
Qualifications
* Bachelor’s or Master’s degree in Biotechnology, Life Science, Chemical Engineering, or related field.
* Professional experience in pharmaceutical or biotechnological production, preferably in Operations.
* Fluent in German and English.
* Strong understanding of GMP regulations.
* Excellent team, leadership, and communication skills.
* Structured, cross‑functional, and focused working style.
* Well‑organized, open to new ideas and suggestions.
Additional Advantage
* Experience in Operations and knowledge of TrackWise.
* German preferred, English acceptable if German is not possible.
Department: Manufacturing / Bioprocess Engineering
Contact: Miguel Gomes – m.gomes@panda-int.com or +31 20 20 44 502
Seniority level
Mid‑Senior level
Employment type
Contract
Industry
Pharmaceutical Manufacturing
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