Consultant – Regulatory Publishing at Biocon Biologics, Bengaluru
A rare opportunity among Biocon Regulatory Publishing Jobs has emerged at Biocon Biologics for a Consultant in Regulatory Affairs/Regulatory Publishing in Bengaluru. Candidates with 1–2 years of experience in eCTD, NeeS, and document-level publishing are encouraged to explore this opportunity.
About Biocon Biologics
Biocon Biologics is a leading global biopharmaceutical company based in Bengaluru, India. The organization focuses on the development of innovative biologics and biosimilars, aiming to provide affordable healthcare solutions across the globe. With a commitment to excellence in research and development, Biocon Biologics operates in the highly regulated pharmaceutical sector, ensuring compliance with international standards.
Job Details:
Position: Consultant – Regulatory Affairs / Regulatory Publishing
Location: Bengaluru
Experience: 1–2 years
Employment Type: Entry/Contract
Biocon Regulatory Publishing Jobs: Job Description
In this Biocon Regulatory Publishing Jobs opportunity, the Consultant will be responsible for regulatory publishing activities, including the preparation and submission of eCTD and NeeS documents. The role requires knowledge of lifecycle variations, amendments, renewals, and proficiency in tools such as Lorenz DocuBridge and ISI Toolbox. The successful candidate will ensure document-level publishing meets regulatory requirements and timelines.
Key Responsibilities
- Prepare and publish regulatory submissions in eCTD format.
- Manage lifecycle variations, amendments, and renewals of documents.
- Utilize tools such as Lorenz DocuBridge and ISI Toolbox.
- Ensure compliance with regulatory standards and guidelines.
- Collaborate with cross-functional teams to gather necessary documentation.
- Review and validate submissions for accuracy and completeness.
- Maintain up-to-date knowledge of regulatory requirements.
- Assist in the training of junior staff on regulatory publishing processes.
Eligibility Criteria
- 1–2 years of experience in regulatory affairs or publishing.
- Familiarity with eCTD, NeeS, and related regulatory frameworks.
- Strong attention to detail and organizational skills.
- Ability to work under tight deadlines and manage multiple projects.
Required Skills
- Proficiency in eCTD and NeeS submissions.
- Experience with Lorenz DocuBridge and ISI Toolbox.
- Knowledge of regulatory guidelines and compliance.
- Strong communication and teamwork abilities.
- Analytical skills for document review and validation.
How to Apply
Interested candidates can apply through the official LinkedIn job posting: CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE.
Conclusion
This opportunity at Biocon Biologics presents a unique chance for qualified candidates to advance their careers in regulatory affairs and publishing. For candidates considering Biocon Regulatory Publishing Jobs, interested individuals are encouraged to apply before the deadline to ensure their consideration for this role.
