i-Pharm Consulting

QA Manager GCP (m/f) Switzerland

05 Dec 2018
19 Dec 2018
Contract Type
QA Manager GCP (m/f) in Switzerland

We are currently looking for a QA Manager GCP (f/m) that holds a master’s degree with 5 years of experience in clinical trials and QA. In this role you will work 100% office based at our client’s site in Switzerland. Here, you will mainly focus on ensuring the compliance of regulatory, ethical and good clinical practices requirements as well as training and managing the audits.

Language Requirements: Fluency in English, German and French are a plus.

Employment Type: Permanent

Salary: Competitive basic salary with pension scheme


* Support development of QDs for the Quality Assurance function.
* Support and coordinate training for the staff in GCP, QA and Risk management.
* Support management in Audits and Quality control reviews.
* Support risk management plans for clinical activities.


* Strong knowledge of clinical Research.
* Experienced in regulatory requirements (GxP).
* Minimum 4 years of relevant experience.
* Ability to work independently.
* Advanced post graduate degree or graduate degree.
* Fluency in written and spoken English other languages are a plus.

For further information please do not hesitate to contact Mario Becerra, Recruitment Consultant at I-Pharm Consulting +41 (0) 61 588 02 03. Please send your application documents to:


If this role doesn’t apply to you, feel free to contact Mario for further discussion on other career opportunities. In case you know someone in your network that could be interested, feel free to provide him/her with Mario’s contact details and he will be at their disposal.

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