M Pharm Jobs at Sun Pharma | Apply Now for Junior Submission Publisher Role
Are you looking for a rewarding career opportunity in regulatory operations? Sun Pharmaceutical Industries Ltd is hiring a Junior Submission Publisher in Mumbai, Gurugram, or Vadodara. This role offers the chance to contribute to global regulatory submissions while growing your expertise in eCTD, NeeS formats, and global health authority requirements. Join a company that empowers you to create your own sunshine and thrive in a collaborative environment.
About Sun Pharma
At Sun Pharmaceutical Industries Ltd, we are committed to helping you “Create your own sunshine” by fostering a culture of growth, ownership, and collaboration. Here, you’ll find opportunities to become Better every day, take charge of your professional journey, and thrive together in a supportive environment.
Job Details
- Position: Junior Submission Publisher
- Location: Mumbai (preferred) / Gurugram / Vadodara
- Qualifications: M.Pharm (Pharmaceutics / Regulatory Affairs / Pharmaceutical Sciences)
- Experience: 3–5+ years in regulatory publishing.
- Knowledge: Understanding of CTD/eCTD structure and submission requirements.
- Tools: Familiarity with Lorenz DocuBridge, Extedo, Liquent, or similar.
- Skills: Strong attention to detail, MS Office & Adobe Acrobat proficiency, effective communication, and ability to work under tight deadlines.
Position Summary
The Junior Submission Publisher will play a key role in compiling, formatting, publishing, and validating regulatory submissions in both eCTD and non-eCTD formats. This role provides global exposure, supporting submissions for agencies such as the US FDA, EMA, Health Canada, MHRA, and more.
Key Responsibilities
- Assist in publishing regulatory submissions (NDA, ANDA, BLA, MAA, variations, supplements, IND, DMF, etc.) in eCTD and NeeS formats.
- Support the preparation of submission-ready documents compliant with global health authority standards.
- Perform document formatting, bookmarking, and hyperlinking as per agency requirements.
- Execute validation checks using publishing tools to ensure error-free submissions.
- Assist with the timely delivery of submissions to agencies through electronic gateways (ESG for FDA, CESP for EMA, etc.).
- Maintain archival and version control of submission packages.
- Collaborate with regulatory operations leads, submission managers, and medical writers for smooth workflows.
- Troubleshoot and resolve technical issues in submission files.
- Stay updated with evolving eCTD specifications, guidance, and tools.
Why Join Sun Pharma?
Your success and well-being matter to us. At Sun Pharma, you’ll benefit from professional development opportunities, a supportive community, and a culture built on collaboration and innovation. Join us to make a lasting impact and build a brighter future together.
Disclaimer
This job description outlines the general nature and scope of the role. Responsibilities may evolve as required, with comparable duties assigned in line with experience and organizational needs.
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