Veeva ETCD BLA Publisher

- Prepare and manage BLA (Biologics License Application) submissions in eCTD format using Veeva Vault eCTD Publishing.- Hands-on experience with Docubridge and Lorenz Validator for regulatory submissions.- Strong background in Regulatory Publishing with knowledge of global regulatory requirements (FDA, EMA).- Experience in Life Sciences / Pharma regulatory...

Prepare and manage BLA (Biologics License Application) submissions in eCTD format using Veeva Vault eCTD Publishing.Hands-on experience with Docubridge and Lorenz Validator for regulatory submissions.Strong background in Regulatory Publishing with knowledge of global regulatory requirements (FDA, EMA).Experience in Life Sciences / Pharma regulatory...

Prepare and manage BLA (Biologics License Application) submissions in eCTD format using Veeva Vault eCTD Publishing . Hands-on experience with Docubridge and Lorenz Validator for regulatory submissions. Strong background in Regulatory Publishing with knowledge of global regulatory requirements (FDA, EMA) . Experience in Life Sciences / Pharma regulatory...

Prepare and manage BLA (Biologics License Application) submissions in eCTD format using Veeva Vault eCTD Publishing.Hands-on experience with Docubridge and Lorenz Validator for regulatory submissions.Strong background in Regulatory Publishing with knowledge of global regulatory requirements (FDA, EMA).Experience in Life Sciences / Pharma regulatory...

Prepare and manage BLA (Biologics License Application) submissions in eCTD format using Veeva Vault eCTD Publishing.Hands-on experience with Docubridge and Lorenz Validator for regulatory submissions.Strong background in Regulatory Publishing with knowledge of global regulatory requirements (FDA, EMA).Experience in Life Sciences / Pharma regulatory...

We are seeking a passionate and detail-oriented Veeva eCTD BLA Publisher to support global regulatory submissions for biologics and BLA products. The ideal candidate will have hands-on experience with Veeva Vault eCTD Publishing , strong knowledge of FDA and EMA guidelines , and a proven track record of compiling, formatting, and dispatching high-quality...

- Prepare and manage BLA (Biologics License Application) submissions in eCTD format using Veeva Vault eCTD Publishing. - Hands-on experience with Docubridge and Lorenz Validator for regulatory submissions. - Strong background in Regulatory Publishing with knowledge of global regulatory requirements (FDA, EMA). - Experience in Life Sciences / Pharma...

Job Title Life Sciences Regulatory Affairs RA Associate - Publishing Job Summary We are looking for a skilled and experienced Regulatory Affairs Associate - Publishing to join our Life Sciences Practice The ideal candidate will support global regulatory submission activities by managing electronic publishing document-level and submission-level ...

Associate III - Business Analysis Regulatory Affairs - Life Sciences Publishing Role Summary The Associate III - Business Analyst Regulatory Affairs - Publishing plays a crucial role in supporting regulatory operations within the life sciences industry This role involves understanding stakeholder needs gathering and analyzing requirements and...

**India - Hyderabad** **JOB ID**: R-218809 **ADDITIONAL LOCATIONS**: - India - Hyderabad **WORK LOCATION TYPE**: On Site **DATE POSTED**: Jul. 01, 2025 **CATEGORY**: Regulatory **ABOUT AMGEN** Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover,...