DPDS Quality Assurance Consultant

at  CAPGEMINI ENGINEERING

QUALIFICATIONS:

• Master’s degree in Pharmaceutical Sciences, or equivalent through experience
• Profound knowledge and experience in use of pharmacopeia and compendia, especially at handling revisions and nonconformities
• Working knowledge of operational facets of drug production, as well as QC and regulatory
• Independent working skills and self-starter mindset. Willingness to go out and find issues and their root causes, without strict guidance
• Strong planning and tracking skills, well organized and capable of handling multiple projects with respect to priorities and resources
• Excellent organization, communication skills in a team setting
• Understanding of regulatory guidelines for quality
• Flexible and adapt quickly to constantly evolving business needs
• Good written and verbal communication skills in English next to being fluent in Dutch or French
• Practical experience in industry and knowledge of GMP regulations are an asset
• “Can do” mentality and taking full ownership of your work

RESPONSIBILITIES:

• Interacts with the team to identify current issues, blocking points, inefficiencies, and delays
• Proactively searches out stakeholders and experts, proposes solutions, and drives implementation of new and/or improved procedures
• Leads and participates in meetings as appropriate to support team goals
• Coordinates globally as the projects often span offices and time zones
• Participates in trainings and continuous improvement initiatives
• Ensures compliance with all relevant regulations, GMP and safety
• Interprets the regulatory guidelines for quality and EHS and ensures their compliance