Looking to build a career in Regulatory Affairs, Documentation Management, and Pharmaceutical Operations? Sandoz, a global leader in generic and biosimilar medicines, is hiring for the position of Regulatory Affairs Associate – Documentation in Telangana, India.
This is an excellent opportunity for pharmacy and life sciences professionals seeking experience in regulatory documentation, compliance management, data analysis, and operational excellence within a globally recognized pharmaceutical company.
About Sandoz
Sandoz is a global leader in high-quality generic and biosimilar medicines, providing more than 900 million patient treatments annually across over 100 countries. The company is committed to improving access to affordable healthcare and pioneering access for patients worldwide.
Job Details
| Particulars | Details |
|---|---|
| Position | Regulatory Affairs Associate – Documentation |
| Company | Sandoz |
| Location | Telangana, India |
| Employment Type | Full-Time |
| Department | Regulatory Affairs |
| Job ID | REQ-10029275 |
| Posted On | June 2026 |
Key Responsibilities
As a Regulatory Affairs Associate – Documentation, you will:
- Maintain controlled documentation systems and record retention processes.
- Ensure compliance with regulatory requirements and company policies.
- Support documentation change control activities.
- Classify, maintain, and archive technical and non-technical records.
- Interpret and enforce documentation formatting standards and SOPs.
- Coordinate regulatory dossier documentation and submissions.
- Analyze and evaluate data for regulatory purposes.
- Prepare information summaries and documentation reports.
- Maintain product-related documentation and information databases.
- Collaborate with internal stakeholders and cross-functional teams.
- Report technical complaints, adverse events, and special case scenarios related to Sandoz products within 24 hours of receipt.
- Support distribution of marketing samples where applicable.
Required Qualifications
Educational Qualification
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or a related discipline.
Skills Required
- Documentation Management
- Regulatory Documentation
- Data Analysis
- Operational Excellence
- Compliance Management
- Cross-Functional Collaboration
- Stakeholder Management
- Record Retention Management
Experience
- Experience in documentation, pharmaceutical operations, or regulatory affairs is preferred.
- Exposure to cross-cultural and global working environments will be an advantage.
Desired Competencies
Candidates should demonstrate:
- Strong attention to detail
- Excellent organizational skills
- Analytical thinking abilities
- Effective communication skills
- Ability to follow established procedures
- Team collaboration mindset
Why Join Sandoz?
Working at Sandoz offers:
- Global pharmaceutical industry exposure
- Career growth in Regulatory Affairs
- Collaborative and inclusive work culture
- Learning opportunities across international teams
- Exposure to biosimilars and generic medicines
- Professional development and training programs
- Opportunity to contribute to patient access initiatives worldwide
Salary Information
Based on industry benchmarks for Regulatory Affairs Associate positions in Telangana, the expected salary range is:
₹4.5 LPA – ₹8.5 LPA
Actual compensation may vary depending on qualifications, experience, and company policies.
How to Apply
