Responsibilities
As QA Manager, you will be responsible for updating and maintaining the Quality Management System of DICE.
Tasks include:
- Internal training
- Internal audits
- Organization of vendor audits
- Preparation and facilitation of audits executed by DICE customers
- Preparation and facilitation of inspections by competent authorities
- QMS updates to comply with regulatory guidelines
- QMS updates to reflect organizational needs at DICE
Requirements
Education:
Experience:
- Experience in QA in a pharmaceutical company or CRO
- Experience with clinical studies, especially with biometric activities
Skills:
- In-depth knowledge of ICH-GCP
- In-depth knowledge of laws, guidelines, and industry standards
- Excellent verbal and written skills in English - knowledge of Dutch or French a plus
- Good knowledge of MS Office (especially Word, Excel, PowerPoint, Visio)
- Excellent organizational and time management skills
- Excellent communication and problem-solving skills
- Educational skills to train fellow team members
Key competencies
- Flexibility to engage in a variety of tasks
- Able to work independently
- Able to work in a rapidly growing and dynamic environment
- Eagerness to learn and continuously develop
- Stress resistant
- Eye for detail
- Team spirit
- Integrity and trustworthiness