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:

• Master's degree

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