Role Overview:

Supports USP, DSP, and IPC operations through equipment handling, calibration, material readiness, sample management, and GMP‑compliant activities to ensure safe and efficient manufacturing processes.

Tasks :

• Conduct Single‑Use Assembly checks.

• Execute column buffer exchange activities.

• Perform harvest filter deinstallation.

• Operate autoclaves (loading, cycle execution, unloading)

• Complete material checklists and ensure consumable availability.

• Notify BPE of missing chemicals or discrepancies.

• Conduct ethanol aliquotation under GMP and safety guidelines

• Support dispensing activities

• Perform inoculation area and room cleaning (GMP‑compliant).

• Execute buffer drainage with DSP teams.

• Deliver samples to QC/IPC and other areas.

• Complete accurate GMP documentation.

• Follow safety, quality, and environmental procedures.

Qualification:

• Apprenticeship/technical diploma in Chemical Engineering, Biotechnology, Lab Technology, or Pharmaceutical/Production Technology.

• Solid understanding of GMP and cleanroom operations.

• Ability to follow SOPs and batch records in English.

• 1–3 years in pharma/biotech/chemical manufacturing (USP or DSP preferred).

• Cleanroom experience (Grade C/D or higher).

• Hands‑on experience with any of the following:

• Bioreactors

• Media/buffer prep

• Chromatography systems

• UF/DF

• Autoclaves/sterilization

• GMP documentation and deviation reporting experience is an advantage

• Fluency in English or German, both preferred

Requirements: