
Regulatory Document Specialist
2 weeks ago
Job Description:
We are seeking a seasoned professional to manage the preparation and submission of regulatory documents in eCTD format using Veeva Vault.
This role involves compiling, formatting, and publishing regulatory documents according to global health authority requirements.
The successful candidate will ensure compliance with regulatory guidelines and internal processes, perform quality control checks on eCTD submissions, and collaborate with cross-functional teams to gather and manage content.
Required Skills & Qualifications:
- Strong experience in Veeva Vault eCTD Publishing is mandatory.
- Familiarity with global regulatory requirements is essential.
- Hands-on experience in preparing eCTD sequences and publishing ready dossiers is desirable.
- Attention to detail with strong organizational skills is required.
- Good communication skills to collaborate with multiple stakeholders are necessary.
- Prior experience in Life Sciences / Pharma regulatory publishing is highly valued.
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