Quality Auditor

At nemensis ag, we connected thousands of applicants with their dream jobs and gave them the opportunity to develop or re-enter the job market. For our client, an international company in Lucerne, we are in search for an Quality Auditor (f/m/d).
- **
Employment type: Temporary via nemensis ag, 100%**:

- ** Duration: 03.01.2023 - 31.12.2023 (option for extension)**:

- ** Salary: CHF 7'500 - 8'800. / month gross**

**Your role**:
Key collaborator working closely with site personnel and Clinical Supply QMS Redesign Team to ensure successful implementation of new QMS by assisting with project-specific tasks, including but not limited to, project management, document management, documentation review, technical editing, meeting coordination and facilitation, training, onboarding, and other administrative tasks.

**Your responsibilities**:

- Work on Complaint Investigations.
- Perform documentation review and technical editing to ensure consistency (e.g. language, formatting, etc. ) within the Redesign Team and across the Clinical Supply network.
- Serve as communication channel between global network site personnel.
- Assist with site metrics collection / reporting and sharing of success stories / achievements.
- Support development of the learning strategy for new and revised QMS topics, including access to LMS content and generation of reports, creation of training materials and communication of training requirements.
- Being responsible for project management activities, optimization of communication strategy and change management strategy.
- Management of document lifecycle (new or existing documents) and review/approval workflows.
- Maintain electronic repository / communication mechanism (e.g. QMS SharePoint Site, Microsoft Teams).
- Serve as a change agent helping the Clinical Supply QMS Redesign Team drive culture change.

**Your profile**:

- Bachelor's Degree in an appropriate scientific or business field of study or longtime education in this area.
- Minimum of five (3-5) years' experience in the Pharmaceutical or equivalent industry.
- Strong technical knowledge, skills and experience in project and documentation management.
- Excellent verbal and written communication skills as well as presentation skills.
- Experience in Microsoft tools such as Outlook, Word, Excel, PowerPoint, SharePoint, Teams and Project is strongly recommended.
- Experience directly related to the development of Quality Standards and core requirements for Market Supply and / or Clinical Supply.
- Experience directly related to Quality Assurance, Quality Control, GMP regulations or pharmaceutical regulations.
- Language English C1 and German B2, written and spoken.

For further questions please contact:
Nicolas Gerster

+41 61 205 98 69