Regulatory Affairs Post-Approval Associate-Europe - DEMO Global Services Center

Regulatory Affairs Associate position available at Demo SA in Hyderabad, India. Responsibilities include post-marketing regulatory submissions for Europe and other global markets. The ideal candidate has a degree in Pharmacy and 3+ years of experience in Regulatory Affairs/CMP within a Pharmaceutical organization.

Requirements

• Bachelor or Master Degree in Pharmacy
• 3+ years of experience in Regulatory Affairs / CMC within a Pharmaceutical organization
• Knowledge of CMC and global regulatory guidelines for Sterile and oral solid/liquid dosage form
• Strong organization skills, multi-tasking and able to meet deadlines
• Effective communication and relationship management
• Ability to work under pressure, resilience

Benefits

• Competitive salary
• Continuous specialized training
• Career development
• Friendly working environment