QA Manager (M/F)




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Kennziffer der Stelle



Operations — Engineering



Mindestanforderungen Erfahrungsniveau

5 bis 10 Jahre


Valais, Schweiz



Location: VISP

Contract: Permanent with AKKA Switzerland

Starting date: June 2021

Languages: English Mandatory and German minimal basics is a plus.

Prerequisite: (Eligible to work in Switzerland)


The Role:

The QA Manager work in close collaboration with different quality and operations functions in order to ensure cGMP-compliant manufacturing activities and documentation

Tasks and Responsibilities:

- Review of completed batch and / or cleaning logs, including data such as device printouts, temperature charts, test procedures, raw QC data and logbooks, to ensure that cGMP manufacturing activities have been performed and documented in accordance with approved written procedures

- Support Improvement and EBR implementation initiatives

- Collect and evaluate on a regular basis KPI data

- You are responsible for the QA Qualification of equipment, facilities and utilities

- You are responsible for operational QA follow-up during the production or distribution of the goods

- You will support in handling complaints, change controls, deviations, CAPA, etc..


Your Profile:

- Bachelor, Master degree or PhD in Biology, Chemistry, Biotechnology, Life Science or other related field

- Knows the concept of deviation management and documentation

- Understands the TrackWise, SAP, LIMS, and Microsoft Office systems

- 7 years’ work experience in a pharmaceutical environment

- Very good GMP knowledge 


What working at AKKA has to offer:

- A steady follow-up and career guidance.

- A large network of collaborators across the world.

- Several learning platforms and access to trainings.

- Compelling challenges for prestigious and international clients.

- Several dedicated events gathering all the collaborators and promoting corporate culture.


For more information, please contact me at

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