Quality Systems Specialist - Documentation
応募 後で応募 求人ID R0176493 掲載日 03/20/2026 Location:Neuchâtel, SwitzerlandBy clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description
About the role:
The Quality Compliance and Systems II role focuses on ensuring the quality of processes and product outputs. This position is responsible for defining activities, processes, and standards to meet quality requirements, auditing and monitoring processes, and reporting on deviations and defects. This role supports Takeda's mission by maintaining high-quality standards and ensuring compliance with regulatory requirements.
How you will contribute:
- Define and specify activities, processes, and standards to fulfill quality requirements
- Audit and monitor the quality of processes or outputs against defined standards
- Conduct product integrity testing to ensure compliance with quality requirements
- Report on process deviations and defects
- Apply basic analytical methods and operational processes following standard operating procedures
- Communicate with immediate team, focusing on clear and simple information exchange
What you bring to Takeda:
- Proficiency in using electronic document management systems (e.g., Veeva Vault).
- Proficiency in French and English (minimum B2 level or equivalent).
- Proficiency in Microsoft Office tools, including Word, Excel, Power Point and SharePoint.
- Minimum 2 years of experience in the (bio)pharmaceutical industry, ideally in a multinational company.
- Familiarity with GMP and regulatory guidelines (e.g., FDA, EMA, ICH).
- Good understanding of Good Data and Documentation Practices (GDDP) and Data Integrity principles.
- Knowledge of document version control, document workflows, and archiving.
- Awareness of audit and inspection readiness requirements.