This position is within the Quality organization at the Neuchâtel facility and is intended for the Quality Assurance department.
Within this position, QA Expert is responsible for compliance and quality oversight related to activities throughout the manufacturing and release process of bulk drug substance (BDS).
The QA Expert is the representative for both routine GMP (Good Manufacturing Practices) activities as well as for all improvement projects for the site. He / she must ensure the quality of information reported within the various systems and documentation with respect to current guidelines, compliance and regulatory requirements.
Participation in GMP zone audits as well as internal and external regulatory inspection is an integral part of his / her activities. The QA expert is accountable for the promotion of continuous improvement and involved related initiatives.
The QA Expert has to understand and apply company guidelines and commitments policy, take care of its own safety, report risk situations and improvement opportunities to supervisory personnel.
The job holder can act as back up of other QA Experts and QA Manager / Supervisor as requested.
Contact : Alba Jansa
Whatsapp Business : +41 76 811 63 99
albajansa(at)