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📢 Biological E. Limited is hiring for Antigen Manufacturing – Drug Substance 🧬💉🔬

Biological E. Limited is hiring for Regulatory Affairs – CTD Authoring Specialist – Bio

🏢 Biological E. Limited, a leading biopharmaceutical company committed to advancing vaccine innovation and making quality vaccines accessible and affordable, invites experienced professionals to join its Vaccine Business!

⚙️ Key Responsibilities:

🧫 Execution of Upstream & Downstream Manufacturing Batches.
⏱️ Ensure timely batch execution and adherence to GMP guidelines.
🧪 Monitor manufacturing processes to meet product specifications.
🏭 Routine monitoring of equipment, facilities & utilities.
📋 Ensure quality, compliance and smooth production operations.

🎯 Key Skills Required:

🧫 Upstream Processing
🔬 Downstream Processing
🧪 Cell Culture
♨️ Autoclave
📑 Production – QMS
✅ GMP Compliance

🎓 Qualifications: B.Sc. / M.Sc. (Life Sciences), Diploma or ITI, as applicable.
🚀Experience: 2–9 Years of Relevant Experience
🕒 Work Requirement: Willingness to work in rotational shifts.

📩 Ready to be part of our journey?

📧 Share your updated CV at: vaishnavi.neemkar@biologicale.com

📌 Email Subject: Application for Antigen Manufacturing

🌟 Join Biological E. Limited – Creating a Healthier Tomorrow Through Vaccines!

🔁 Share this opportunity with your network!

Biological E. Limited is hiring for Regulatory Affairs – CTD Authoring Specialist – Bio

🏢 Biological E. Limited – Vaccine Business is looking for experienced and passionate professionals to join our team and contribute to advancing global vaccine innovation and regulatory excellence. 💉

🎯 About the Role:

🧬 Hands-on experience in CTD dossier authoring for Biologics / Vaccines.
📑 Expertise in preparation, authoring and review of regulatory documents.
📚 Strong understanding of CTD/eCTD formats and regulatory submission requirements.
💉 Experience in biologics and/or vaccine regulatory documentation.
🔍 Ability to review technical documents and ensure accuracy, consistency and compliance.
🌐 Understanding of regulatory guidelines and global submission standards.

🎓 Preferred Background: Regulatory Affairs | Biologics | Vaccines | CTD/eCTD Authoring

🌍 Relevant Experience: 5 –10 Years

📩 Interested?

📄 Share your updated CV with Vaishnavi.Neemkar@biologicale.com and take the next step in your professional journey!

🚀 Be part of Biological E. Limited – Advancing Vaccine Innovation, Protecting Lives!

🔄 Know someone who fits this role? Tag them or share this opportunity with your network! 🤝