
Veeva eCTD Publishing Professional
1 week ago
Key Responsibilities:
- Manage and publish regulatory documents in eCTD format using Veeva Vault.
- Compile and format submissions according to global health authority requirements.
- Ensure compliance with regulatory guidelines (FDA, EMA) and internal processes.
- Perform quality checks of eCTD submissions, including file structure, hyperlinks, and metadata.
- Collaborate with cross-functional teams to gather and manage content.
- Track submission timelines and deliverables to meet regulatory deadlines.
Required Skills & Qualifications:
- Strong experience in Veeva Vault eCTD Publishing.
- Knowledge of global regulatory requirements.
- Hands-on experience in preparing eCTD sequences and publishing ready dossiers.
- Attention to detail with strong organizational skills.
- Good communication skills to collaborate with multiple stakeholders.
- Prior experience in Life Sciences / Pharma regulatory publishing is mandatory.
Benefits:
This role offers the opportunity to work on complex projects, develop new skills, and contribute to the success of the organization.
What We Offer:
A dynamic and supportive work environment, opportunities for professional growth, and a competitive compensation package.
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