
Senior Submission Publisher
20 hours ago
Job Description Title: Senior Submission Publisher Business Unit: Regulatory Operations Global Regulatory & Business Continuity Innovative Medicines Job Grade G10 / Manager Location : Mumbai (preferred) / Gurgaon / Baroda Key Responsibilities At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine As you enter the Sun Pharma world, you'll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other's journeys. Job Purpose The Senior Submission Publisher will lead and oversee the planning, preparation, publishing, and dispatch of regulatory submissions in eCTD and non-eCTD formats to global health authorities. This role not only ensures submission compliance and quality but also provides leadership in workload management, publishing strategy, and adoption of new tools and technologies to streamline the submission process. Key Responsibilities Core Publishing - Oversee end-to-end publishing activities for major and minor submissions (NDA, ANDA, BLA, MAA, IND, DMF, variations, renewals, supplements). - Ensure compliance with global health authority requirements (FDA, EMA, Health Canada, MHRA, TGA, WHO, etc.). - Perform document formatting, hyperlinking, bookmarking, and validation using industry-standard publishing tools. - Ensure on-time dispatch of submission packages via electronic gateways (e.g., ESG, CESP, MHRA portal). Quality & Compliance - Conduct quality reviews of submissions prepared by junior publishers, ensuring adherence to specifications and eliminating validation errors. - Maintain submission archives, version control, and audit-ready documentation. - Implement best practices and continuous process improvements to strengthen publishing quality and compliance. Workload & Team Support - Manage daily workload distribution within the publishing team to meet timelines. - Provide guidance and technical support to junior publishers and new team members. - Act as the first point of contact for troubleshooting complex publishing issues. Metrics & Process Improvement - Generate and track submission metrics (cycle times, on-time delivery, volume, quality compliance) for management review. - Identify opportunities for process optimization and automation within publishing workflows. - Support development and refinement of Standard Operating Procedures (SOPs) and work instructions. Technology & Innovation - Participate in testing, validation, and implementation of publishing tools version upgrades. - Provide feedback to IT and system vendors in enhancing publishing tool functionality. - Stay updated on emerging regulatory publishing trends, specifications, and technologies. Qualifications & Skills - Master's degree in Pharmacy (M.Pharm) or Life Sciences (preferred). - 610 years of hands-on regulatory publishing experience in eCTD and non-eCTD formats. - Expertise in CTD/eCTD structure, regional specifications, and global submission requirements. - Proficiency with industry-leading publishing tools (Lorenz, Liquent, Extedo, Veeva Vault, Amplexor etc.) and validation tools. - Strong attention to detail, organizational skills, and ability to manage multiple priorities. - Good leadership and team mentoring skills. - Excellent written and verbal communication skills. - Experience in metrics generation, process improvement, and tool implementation preferred. - Experience in RIMS Implementation, Regulatory Data Management and Governance will be an added advantage. Travel Estimate Low Job Requirements Educational Qualification Master's degree in Pharmacy (M.Pharm) or Life Sciences Experience 8+ years of hands-on regulatory publishing experience in eCTD and non-eCTD formats. Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let's create a brighter future together Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).
-
Junior Submission Publisher
20 hours ago
Gurugram, India SUN PHARMA Full timeJob Description Title: Junior Submission Publisher Business Unit: Regulatory Operations Global Regulatory & Business Continuity Innovative Medicines Job Grade Senior Executive / G11B Location : Mumbai (preferred) / Gurugram / Vadodara Key Responsibilities At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you...
-
Junior Submission Publisher
7 days ago
Gurugram, India SUN PHARMA Full timeTitle: Junior Submission Publisher Business Unit: Regulatory Operations – Global Regulatory & Business Continuity – Innovative Medicines Job Grade Senior Executive / G11B Location : Mumbai (preferred) / Gurugram / Vadodara Key Responsibilities At Sun Pharma, we commit to helping you “Create your own sunshine ”— by fostering an...
-
Junior Submission Publisher
3 weeks ago
Gurugram, India Sun Pharmaceutical Industries, Inc. Full timeTitle: Junior Submission Publisher Date: Sep 15, 2025 Location: Gurgaon - R&D Company: Sun Pharmaceutical Industries Ltd Title: Junior Submission Publisher Business Unit: Regulatory Operations – Global Regulatory & Business Continuity – Innovative Medicines Job Grade Senior Executive / G11B Location : Mumbai (preferred) / Gurugram / Vadodara Key...
-
Junior Submission Publisher
3 weeks ago
Gurugram, India SUN PHARMA Full time*Title: *Junior Submission Publisher *Business Unit: *Regulatory Operations – Global Regulatory & Business Continuity – Innovative Medicines Job GradeSenior Executive / G11B Location :Mumbai (preferred) / Gurugram / Vadodara *Key Responsibilities At Sun Pharma, we commit to helping you "Create your own sunshine *"— by fostering an environment where you...
-
Regulatory Submission Publisher
2 days ago
Madurai, Tamil Nadu, India, Tamil Nadu Aurolab Full timePurpose: Regulatory Submission Publisher will be responsible for assisting in the compilation, formatting, publishing, and validation of regulatory submissions in eCTD and non-eCTD formats. The role will provide exposure to global regulatory submission requirements for agencies such as US FDA, EMA, Health Canada, MHRA, and others.Responsibilities:• Assist...
-
BLA Regulatory Publishing Specialist
2 days ago
India vueverse. Full timeKey Responsibilities: Prepare and manage BLA (Biologics License Application) submissions in eCTD format using Veeva Vault eCTD Publishing . Compile, format, and publish regulatory documents according to global health authority requirements. Ensure compliance with regulatory guidelines (FDA, EMA) and internal processes. Perform QC of eCTD submissions,...
-
India vueverse. Full timeKey Responsibilities:Prepare and manage BLA (Biologics License Application) submissions in eCTD format using Veeva Vault eCTD Publishing.Compile, format, and publish regulatory documents according to global health authority requirements.Ensure compliance with regulatory guidelines (FDA, EMA) and internal processes.Perform QC of eCTD submissions, including...
-
india, IN vueverse. Full timeKey Responsibilities:Prepare and manage BLA (Biologics License Application) submissions in eCTD format using Veeva Vault eCTD Publishing.Compile, format, and publish regulatory documents according to global health authority requirements.Ensure compliance with regulatory guidelines (FDA, EMA) and internal processes.Perform QC of eCTD submissions, including...
-
India vueverse. Full timeKey Responsibilities: - Prepare and manage BLA (Biologics License Application) submissions in eCTD format using Veeva Vault eCTD Publishing. - Compile, format, and publish regulatory documents according to global health authority requirements. - Ensure compliance with regulatory guidelines (FDA, EMA) and internal processes. - Perform QC of eCTD submissions,...
-
Publisher Account Manager
5 days ago
Gurugram, India Taboola Full timeJob Description Realize your potential by joining the leading performance-driven advertising company! As a Publisher Account Manager on the Partnerships team in our Gurgaon Office, you'll play a vital role in strengthening and scaling relationships with premium publishers in the Indian market. You'll lead the implementation and optimization of the Taboola...