Regulatory Affairs Manager Job Opportunity
This role is an excellent chance to take on a challenging position in regulatory affairs, working closely with the global team to ensure timely and effective submissions of operational registration and life-cycle management projects.
The successful candidate will be responsible for leading and executing assigned projects, promoting high-quality regulatory best practices, and collaborating with cross-functional teams to achieve corporate objectives.
To be considered for this position, candidates should have a strong background in human pharmaceutical regulatory experience, with a focus on lifecycle maintenance of marketed products in Europe and emerging markets.
Additional requirements include project management experience, excellent communication skills, and the ability to write and prepare relevant CTD documents to support submissions.
Key Responsibilities:
- Lead assigned operational registration and life-cycle management projects
- Promote high-quality regulatory best practices
- Collaborate with cross-functional teams to achieve corporate objectives
Qualifications & Experience:
- Human pharmaceutical regulatory experience, focusing on lifecycle maintenance of marketed products in Europe and emerging markets
- Project management experience
- Excellent communication skills
- Ability to write and prepare relevant CTD documents to support submissions
We offer:
- A dynamic and collaborative work environment
- Opportunities for professional growth and development
- A competitive compensation package
How to Apply:
Please submit your CV to [insert contact information]