Regulatory Affairs Associate II

Roles & Responsibilities:
• Provide regulatory support for European Market Regulatory Affairs (RA) activities
• Coordinate, prioritize, and monitor assigned regulatory tasks and submissions
• Prepare and maintain regulatory documentation as per internal work instructions
• Maintain regulatory IT systems and ensure documentation compliance
• Communicate with Teva units across European markets, third parties, and Health Authorities
• Develop and maintain expertise in European regulatory requirements
• Monitor updates in regulatory legislation and guidelines
• Support and guide junior team members
• Complete assigned trainings within defined timelines
• Participate in team meetings and provide activity updates to management
• Perform additional departmental and ad-hoc tasks as directed by senior RA staff

Qualification:
• Master’s in Pharmacy (M.Pharm)
• OR Master’s in Science / Life Sciences
• Equivalent university degree with relevant regulatory exposure

Experience:
• 4–6 years of experience in the pharmaceutical industry
• Experience in Regulatory Affairs preferred
• Candidates from R&D, Development, or QA with regulatory documentation experience may be considered
• Experience handling regulatory documentation for European markets

Skills:
• Strong understanding of European regulatory frameworks and guidelines
• Knowledge of regulatory documentation and submission processes
• Good coordination and task management skills
• Strong written and verbal communication skills
• Ability to work cross-functionally with international stakeholders
• Familiarity with regulatory IT systems
• Analytical thinking and problem-solving ability

About the Organization:
Teva Pharmaceuticals is a global biopharmaceutical leader with a strong generics business and innovative portfolio in neuroscience and immunology. Operating worldwide, Teva focuses on delivering high-quality medicines while fostering an inclusive culture that supports professional growth and global healthcare advancement.