R&D Scientist – Plasma Protein Processes (Temporary)

Octapharma Austria

Wien

On-site

EUR 44,000 - 53,000

Part time

3 days ago
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Benefits offered by this job

Company restaurant & meal subsidy
Training & further education
Health promotion
Parking spaces
Company events

Job summary

Octapharma Pharmazeutika Produktionsges.m.b.H. in Wien seeks a temporary R&D professional to develop and optimize production processes for plasma proteins and to establish analytical methods for process and product characterization.

You will collaborate with CROs, universities and internal production, QC and regulatory teams, plan and document GMP‑compliant experiments, and support inquiries while preparing technical reports and mentoring lab staff.

Qualifications

  • Completed degree in natural science (Master or PhD).
  • Experience in protein purification and analytical method development.
  • Knowledge of protein labeling is a plus.
  • Experience in blood plasma/diagnostic industry is a plus.
  • Strong communication and project management skills.
  • Fluent German and proficient English (spoken and written).

Responsibilities

  • Develop and optimize production processes for plasma proteins.
  • Establish analytical test methods for process and product characterization.
  • Collaborate with CROs, universities and internal interfaces.
  • Plan, execute, and GMP‑compliant document laboratory experiments.
  • Support regulatory and customer inquiries.
  • Prepare technical and scientific documents and present results.
  • Provide technical guidance to laboratory technicians.

Skills

Protein purification
Analytical methods
Lab supervision
LIMS
GMP
German language
English language
Microsoft 365

Education

Master or PhD in natural sciences

Tools

LIMS
Microsoft 365

Job description

Octapharma Pharmazeutika Produktionsges.m.b.H. in Wien seeks a temporary R&D professional to develop and optimize production processes for plasma proteins and to establish analytical methods for process and product characterization.

You will collaborate with CROs, universities and internal production, QC and regulatory teams, plan and document GMP‑compliant experiments, and support inquiries while preparing technical reports and mentoring lab staff.

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