Technical Writer Job

🚀 Ready to Write the Future of Cell Therapy? Join Us as a Technical Writer - CMC Regulatory Submissions! 🚀 📍 Location: New Brunswick, NJ

What you’ll be doing: ✨ Crafting top-notch CMC documentation that drives regulatory strategy from early-stage development all the way through registrational filings ✨ Leading submission kick-offs like a pro-managing timelines, deliverables, and cross-functional magic ✨ Collaborating with brilliant experts in Process Development, Analytical Development, Quality, and more teamwork makes the dream work! ✨ Keeping our dossiers sharp, compliant, and ready to impress Health Authorities worldwide ✨ Mentoring future stars and driving improvements to keep us ahead of the game

Who you are: 🎓 A Biology or related discipline grad (bonus points for advanced degrees!) 🧬 A biotech or pharma pro with 2+ years navigating the product development lifecycle 📑 A regulatory writing wizard, especially in cell therapy CMC and eCTD formatting ✍️ A meticulous writer/editor with an eagle eye for detail and a passion for precision 📅 An organizational individual who juggles multiple priorities without breaking a sweat

❗ Important Notice for Third-Party Vendors ❗ Third-party vendors, PLEASE DO NOT APPROACH. The selected consultant will be our employee on our payroll, and we are not engaging in C2C arrangements with third-party vendors.

📩 How to Apply: 👉DM us for inquiries or to apply directly. 👉Email your updated resume to hr@theveritashealthcare.net if you’re interested.