Global Regulatory Affairs Manager – CMC
1 month ago
About the Role:
We are seeking a highly skilled Global Regulatory Affairs Manager to join our CMC department. As a key member of our team, you will be responsible for ensuring the regulatory compliance of our pharmaceutical products throughout their lifecycle.
Key Responsibilities:
- Develop and implement regulatory strategies for CMC activities, ensuring compliance with global regulations and guidelines.
- Collaborate with cross-functional teams to ensure timely and effective regulatory submissions and approvals.
- Provide expert advice on CMC regulatory matters, including risk management and scientific advice.
- Participate in the development and optimization of departmental and working processes.
- Stay up-to-date with changing regulatory requirements and ensure that our products remain compliant.
Requirements:
- Minimum 5 years of experience in global regulatory affairs, preferably in CMC activities.
- M.Sc. in a life science or pharmacy.
- Excellent communication and negotiation skills, with the ability to work effectively with stakeholders at all levels.
- Strong analytical and problem-solving skills, with the ability to interpret complex regulatory requirements.
- Experience with IT systems, including MS Office.
What We Offer:
As a Global Regulatory Affairs Manager at Ferring Pharmaceuticals, you will have the opportunity to work in a dynamic and innovative environment, collaborating with a talented team of professionals. We offer a competitive salary and benefits package, as well as opportunities for career development and growth.
Location:
Ferring Denmark
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