Sandoz is a global leader in generic and biosimilar medicines, committed to providing high-quality, affordable healthcare solutions. In 2024 alone, Sandoz delivered over 900 million patient treatments across 100+ countries. With continuous investments in innovation, production, and partnerships, Sandoz is shaping the future of sustainable medicine.
The company fosters an inclusive, collaborative work culture that encourages professional growth and diversity. If you are looking for a dynamic career in the pharmaceutical industry, Sandoz offers exciting opportunities to make a real impact.
Job Openings at Sandoz, Telangana
1. Regulatory Affairs Specialist (Documentation)
Job Description
- Ensures controlled documentation systems, record retention, and compliance with regulatory requirements.
- Manages global regulatory submission projects and supports regulatory strategy.
- Maintains technical and non-technical documentation change systems.
- Coordinates regulatory dossiers and ensures adherence to documentation standards.
- Reports adverse events/complaints within 24 hours (if applicable).
Key Responsibilities
- Manage medium to small global submission projects.
- Provide regulatory intelligence for product development and maintenance.
- Support global regulatory systems and processes.
- Collaborate with cross-functional teams and external stakeholders.
Skills Required
✅ Clinical Study Reports
✅ Data Analysis
✅ Documentation Management
✅ Lifesciences
✅ Operational Excellence
✅ Regulatory Compliance
Experience & Qualifications
- Experience: 3-5 years in Regulatory Affairs, Pharma Documentation, or Compliance.
- Education: Bachelor’s/Master’s in Pharmacy, Life Sciences, or related field.
- Preferred Skills: Cross-cultural collaboration, project management.
Estimated Salary
- ₹6 – 10 LPA (Based on experience and industry standards)
2. Sr. Associate – RA Documentation
Job Description
- Ensures controlled documentation and compliance with regulatory standards.
- Supports record retention and electronic documentation processes.
- Follows established policies and assists in regulatory submissions.
- Reports technical complaints/adverse events (if applicable).
Key Responsibilities
- Learn and apply basic regulatory principles.
- Work under supervision on routine documentation tasks.
- Maintain data integrity and compliance with SOPs.
Skills Required
✅ Data Analysis
✅ Documentation Management
✅ Operational Excellence
Experience & Qualifications
- Experience: 2 – 7 years in pharma documentation or regulatory support.
- Education: Bachelor’s in Pharmacy, Biotechnology, or Life Sciences.
Estimated Salary
- ₹7 – 9 LPA (Based on experience)
Why Join Sandoz?
✔ Global Impact – Work on life-saving medicines reaching millions.
✔ Career Growth – Agile work environment with learning opportunities.
✔ Inclusive Culture – Diversity-driven workplace.
✔ Hybrid Work Model – Flexible work arrangements.
How to Apply?
Application Link Regulatory Affairs Specialist (Documentation)
