Senior Consultant Regulatory Affairs

QbD Group offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, Biotech and Medical Devices/IVD.

Requirements

• University degree in life science
• Sound knowledge of European/UK/US pharmaceutical regulations and guidelines
• Significant regulatory affairs experience
• Excellent written and verbal communication skills
• Proven negotiation skills
• Good organizational skills and analytical mindset
• Ability to work in an international environment

Benefits

• Attractive and competitive salary package
• Job security
• Lasting, meaningful connections
• Continuous journey of learning and development
• Global success story
• Award-winning company
• Community where people grow, laugh, build, and contribute