This position is within the Quality organization at the Neuchâtel facility and is intended for the Quality Assurance department.
Within this position, the 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 inspections is an integral part of his/her activities. The QA Expert is accountable for the promotion of continuous improvement and involved in related initiatives.
The QA Expert has to understand and apply company guidelines and commitments policy, take care of their own safety, and report risk situations and improvement opportunities to supervisory personnel.
The job holder can act as a backup for other QA Experts and QA Manager/Supervisor as requested.
Contact
Alba Jansa
Whatsapp Business: +41 76 811 63 99
Seniority level
* Entry level
Employment type
* Full-time
Job function
* Quality Assurance
* Industries: Professional Services
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