Global pharmaceutical leader Sandoz has announced an exciting opportunity for Analyst – Safety Label Change (SLC) at its Telangana (Hyderabad) location. This role is ideal for professionals with 2–5 years of experience in Pharmacovigilance, Regulatory Affairs, Labeling Operations, Quality Operations, Artwork Operations, Supply Chain, or Pharmaceutical Operations.

Candidates with a background in B.Pharm, M.Pharm, Pharm.D, Life Sciences, Biotechnology, or related disciplines and strong analytical skills can apply. The position offers exposure to global stakeholders, safety labeling governance, KPI tracking, compliance management, and operational excellence within one of the world’s leading generic and biosimilar pharmaceutical companies.

Job Overview

Key Responsibilities

The selected candidate will be responsible for:

• Monitor Safety Label Change implementation milestones across global markets.
• Track KPIs and ensure timely execution of safety-related labeling changes.
• Coordinate with Regulatory Affairs, Pharmacovigilance, Packaging Sites, Quality Assurance, Supply Chain, and Patient Safety teams.
• Identify compliance risks, implementation delays, and process gaps.
• Support CAPA implementation and deviation management.
• Prepare management reports, dashboards, and KPI presentations.
• Maintain documentation, trackers, and governance records.
• Support internal audits and regulatory inspections.
• Ensure compliance with GMP, GxP, SOPs, and quality standards.
• Participate in continuous improvement and operational excellence initiatives.
• Perform advanced data analysis using Microsoft Excel.
• Maintain large datasets related to safety labeling compliance.

Eligibility Criteria

Applicants should possess:

• Graduate or Postgraduate degree in:
  • B.Pharm
  • M.Pharm
  • Pharm.D
  • Life Sciences
  • Biotechnology
  • Related healthcare discipline

Experience required:

• 2–5 years in one or more of the following:
  • Safety Label Change
  • Pharmacovigilance
  • Regulatory Affairs
  • Labeling Operations
  • Artwork Operations
  • Pharmaceutical Operations
  • Quality Operations
  • Supply Chain

Required Skills

Candidates should demonstrate expertise in:

• Pharmacovigilance processes
• Safety Label Change management
• Regulatory Affairs
• GMP and GxP compliance
• CAPA implementation
• Quality Systems
• Cross-functional stakeholder management
• Project coordination
• Data analysis
• Dashboard reporting
• Advanced Microsoft Excel
• Pivot Tables
• XLOOKUP / VLOOKUP
• Data Validation
• Power Query (preferred)
• VBA/Macros (preferred)

Why Join Sandoz?

Working with Sandoz offers several advantages:

• Opportunity to work with one of the world’s largest generic and biosimilar pharmaceutical companies.
• Global exposure through collaboration with international teams.
• Hybrid and flexible work culture.
• Career growth in Pharmacovigilance and Regulatory Operations.
• Exposure to global quality and compliance systems.
• Continuous learning and operational excellence initiatives.
• Inclusive, collaborative, and innovation-driven workplace.

How to Apply

Application Link