Regulatory Affairs Specialist
3 weeks ago
About the Role
We are seeking a highly skilled Regulatory Affairs Consultant to join our team at Parexel.
As a Regulatory Affairs Consultant, you will be responsible for handling the life cycle management of approved drug products, including tablets, syrups, and parenterals.
You will lead and contribute to the planning, preparation, and delivery of regulatory maintenance submissions from a global and regional perspective.
Key Responsibilities:
- 8+ years' experience in handling life cycle management of approved drug products.
- Good understanding of regulatory framework, including regional trends, for various types of applications and procedures.
- Lead and/or contribute to the planning, preparation, and delivery of regulatory maintenance submissions.
- Working knowledge of EU/US regulatory procedures, including post-approval requirements.
- Experience in handling CMC-related health authority queries.
- Liaise closely with cross-functional members with aligned product responsibilities.
- Develop, execute, and maintain submission delivery plans and proactively provide status updates to stakeholders.
- To prepare, review, and submit safety variations to Health Authorities and perform post-approval CMC-related updates.
- Prior working experience in Regulatory Information Management Systems like Veeva Vault is desirable.
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