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
- Ensuresย controlled documentation systems, record retention, and compliance withย regulatory requirements.
- Managesย global regulatory submission projectsย and supports regulatory strategy.
- Maintainsย technical and non-technical documentationย change systems.
- Coordinatesย regulatory dossiersย and ensures adherence to documentation standards.
- Reportsย adverse events/complaintsย within 24 hours (if applicable).
Key Responsibilities
- Manageย medium to small global submission projects.
- Provideย regulatory intelligenceย for product development and maintenance.
- Supportย global regulatory systemsย and processes.
- Collaborate withย cross-functional teamsย and external stakeholders.
Skills Required
โ
Clinical Study Reports
โ
Data Analysis
โ
Documentation Management
โ
Lifesciences
โ
Operational Excellence
โ
Regulatory Compliance
Experience & Qualifications
- Experience:ย 3-5 years inย Regulatory Affairs, Pharma Documentation, or Compliance.
- Education:ย Bachelorโs/Masterโs inย Pharmacy, Life Sciences, or related field.
- Preferred Skills:ย Cross-cultural collaboration, project management.
Estimated Salary
- โน6 – 10 LPAย (Based on experience and industry standards)
2. Sr. Associate – RA Documentation
Job Description
- Ensuresย controlled documentationย and compliance withย regulatory standards.
- Supportsย record retentionย and electronic documentation processes.
- Followsย established policiesย and assists in regulatory submissions.
- Reportsย technical complaints/adverse eventsย (if applicable).
Key Responsibilities
- Learn and applyย basic regulatory principles.
- Work under supervision onย routine documentation tasks.
- Maintainย data integrityย and compliance with SOPs.
Skills Required
โ
Data Analysis
โ
Documentation Management
โ
Operational Excellence
Experience & Qualifications
- Experience:ย 2 – 7 years inย pharma documentation or regulatory support.
- Education:ย Bachelorโs inย Pharmacy, Biotechnology, or Life Sciences.
Estimated Salary
- โน7 – 9 LPAย (Based on experience)
Why Join Sandoz?
โ Global Impact โ Work on life-saving medicines reaching millions.
โ Career Growth โ Agile work environment with learning opportunities.
โ Inclusive Culture โ Diversity-driven workplace.
โ Hybrid Work Model โ Flexible work arrangements.
How to Apply?
Application Link Regulatory Affairs Specialist (Documentation)
Application Link Sr. Associate – RA Documentation