Regulatory Affairs Associate – Operations Coordinator Position at Sandoz in Hyderabad
A rare chance has emerged for aspiring professionals exploring Sandoz careers, as Sandoz seeks a Regulatory Affairs Associate – Operations Coordinator in Telangana (Hyderabad), India. This full-time position offers flexible hybrid work arrangements and focuses on supporting Regulatory Affairs for the Australia and New Zealand (ANZ) market. The application deadline is 16 October 2026.
About the Company
Sandoz is a global leader in generic pharmaceuticals and biosimilars, dedicated to providing high-quality, accessible medicines. As a division of Novartis, Sandoz operates in various markets worldwide, including Australia and New Zealand. The company is committed to innovation and excellence in the pharmaceutical sector, ensuring that patients have access to essential medications.
Job Details:
- Position: Regulatory Affairs Associate – Operations Coordinator
- Location: Telangana (Hyderabad), India
- Reference Number: REQ-10032267
- Employment Type: Full-time, flexible-hybrid
- Posted on: 8 October 2026
- Application Deadline: 16 October 2026
Sandoz Careers: Job Description
The Regulatory Affairs Associate – Operations Coordinator will provide operational and administrative support to the Regulatory Affairs team. This Sandoz careers role includes supporting the Director of Scientific Affairs with meetings, reports, and projects; monitoring regulatory correspondence; managing health authority portal access and system administration; handling invoices, purchase orders, and vendor reconciliation; procuring reference listed drug samples with global vendors; maintaining regulatory records and archiving; and tracking ANZ submissions, approvals, and post-approval commitments.
Key Responsibilities
- Support the Director of Scientific Affairs with various administrative tasks.
- Monitor and manage regulatory correspondence.
- Oversee health authority portal access and system administration.
- Handle invoices, purchase orders, and vendor reconciliation.
- Procure RLD samples with global vendors.
- Maintain regulatory databases and RIM tracking.
- Track ANZ submissions, approvals, and post-approval commitments.
Eligibility Criteria
- Graduate with experience in the pharmaceutical industry.
- Minimum of 2 years of industry experience desired.
- Strong attention to detail and thorough document preparation.
- Proficiency in English.
How to Apply
Interested candidates can apply through the official Sandoz Workday posting using the reference number REQ-10032267. For more information, visit Sandoz Careers.
Why Join Sandoz
Joining Sandoz offers a unique opportunity to be part of a leading organization in the pharmaceutical industry, where innovation and patient care are at the forefront. Employees benefit from a collaborative work environment that encourages professional growth and development while contributing to the accessibility of essential medicines worldwide.
CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE
Qualified candidates pursuing Sandoz careers are encouraged to seize this opportunity and apply before the deadline of 16 October 2026. This role promises to be a pivotal step in advancing a career in the pharmaceutical sector.
