Hobson Prior are currently looking for a GMP Consultant to join a brilliant pharmaceutical corporation on a contract basis located in Munich. Our client is focused on offering novel products and services internationally.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

• For this role, you will plan risk analysis such as process risk analysis.
• Produce validation papers such as cleaning validation, sterilisation of equipment, semi-automatic inspection, etc.
• You will execute training courses on the SOPs.
• May be responsible for one day a week for project management for the start-up phase such as production of GMP-pertinent papers.
• Any other assigned duties.

Requirements:

• Familiarity with the production of sterile pharmaceuticals, preferably in aseptic archiving and lyophilisation.
• Know-how of EU and US GMP guidelines, including Annex 1.
• Acquaintance with generating SOPs, risk analysis and qualification and validation documents.
• Fluency in the German language.
• Computer literacy in MS Office.
• Possess an accurate and effective way of operating.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.