Calling all regulatory experts and quality management professionals! Are you ready to make a significant impact in the medical device industry? Oyster Medisafe is looking for a detail-oriented Executive to join their Quality Assurance & Regulatory Affairs team in Hyderabad!
🏢 Company: Oyster Medisafe Pvt. Ltd.
📍 Location: Hyderabad, India
💼 Position: Executive – Quality Assurance & Regulatory Affairs
Your Mission: 🎯
- Be the guardian of regulatory compliance and quality standards
- Manage digital documentation with precision
- Ensure our medical devices meet the highest global standards
Key Responsibilities Will Include: 📋
- 🔒 Ensuring compliance with ISO 13485 and CE marking
- 📄 Digital document management and control
- 🏆 Implementing and maintaining GMP quality systems
- 🤝 Liaising with drug authorities and regulatory bodies
- 🕵️ Preparing and supporting internal and external audits
- 📚 Training staff on quality and regulatory best practices
Ideal Candidate Profile: 💡
- 🎓 Bachelor’s degree in Bio Engineering, Life Sciences, or related field
- 🌟 3-5 years experience in quality and regulatory affairs
- 🏅 Preferred: Internal auditor certification in ISO 13485
- 🧠 Deep understanding of medical device regulations
- 📝 Exceptional documentation and communication skills
What We Offer: ✨
- Dynamic and innovative work environment
- Opportunity to shape quality standards
- Professional growth and development
- Cutting-edge medical device industry exposure
Quick Apply: 🚀 Interested? Click here: https://jobs.bbraun.com/job/Executive-Quality-Assurance-&-Regulatory-Affairs/1278-en_US
