Specialist in GMP Manufacturing Regulations / Production Documentation (m/f/d)

This job offer is no longer available.

Switzerland |

Temporary Employment

Responsibilities:

• Creation and refinement of manufacturing specifications, SOPs, and risk analyses

• Collaboration on the optimization of documentation standards and templates

• Close collaboration with production, chemists, and technical teams directly on the shop floor

Qualifications:

• Background in chemistry

• Understanding of production processes

• Very good command of German and English

Reference number: 17624

Industry: Pharmaceutical Industry

Project start: ASAP

Duration: 9 months

Employment type: Temporary Employment

Contact

Eva Joy Schmidt

e.schmidt@aristo-group.ch

+41 44 274 39 00

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Munich

Zurich

Vienna

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