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Sandoz Hiring Medical Safety Specialist

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Sandoz

B.Pharm, M.Pharm, Pharm.D, MBBS, MD, M.Sc Life Sciences, Other relevant healthcare and life sciences qualifications

Telangana

Experience in PV

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Sandoz, a global leader in generic and biosimilar medicines, is hiring for the position of Medical Safety Specialist in Telangana, India. This is an excellent opportunity for professionals with experience in pharmacovigilance, drug safety, clinical research, and regulatory compliance to work with one of the world’s leading pharmaceutical companies.

As a Medical Safety Specialist at Sandoz, you will contribute to drug safety surveillance, safety signal detection, risk management activities, and regulatory safety documentation throughout the product lifecycle.

About Sandoz

Sandoz is a pioneering provider of sustainable generic and biosimilar medicines, delivering over 900 million patient treatments across more than 100 countries. The company continues to invest in innovation, development capabilities, manufacturing sites, and strategic partnerships to expand access to affordable, high-quality medicines worldwide.


Job Details

  • Position: Medical Safety Specialist
  • Company: Sandoz
  • Location: Telangana, India
  • Job Type: Full-Time
  • Job ID: REQ-10029375
  • Application Deadline: June 25, 2026
  • Department: Medical Safety and Pharmacovigilance

Key Responsibilities

The selected candidate will:

  • Support medical safety delivery activities and co-author safety documents.
  • Provide safety input for regulatory and clinical documents.
  • Monitor product safety profiles through literature review and medical case evaluations.
  • Assist in signal detection and risk management activities.
  • Prepare responses for Health Authority queries and assessment reports.
  • Provide safety support for new indication submissions and regulatory filings.
  • Evaluate and prepare safety deliverables as assigned.
  • Manage local safety deviations and compliance activities.
  • Respond to internal and external safety-related requests.
  • Act as a Subject Matter Expert (SME) and mentor junior team members.
  • Collaborate with cross-functional teams to ensure pharmacovigilance compliance.

Required Skills and Qualifications

Candidates with educational backgrounds in the following disciplines may be suitable:

  • B.Pharm
  • M.Pharm
  • Pharm.D
  • MBBS
  • MD
  • M.Sc Life Sciences
  • Other relevant healthcare and life sciences qualifications

Essential Skills

  • Pharmacovigilance and Drug Safety
  • Clinical Research and Clinical Trials
  • Literature Review and Medical Evaluation
  • Regulatory Compliance
  • Safety Science and Risk Assessment
  • Medical Records Management
  • Operations Management and Execution
  • Project Management
  • Cross-functional Collaboration
  • Crisis Management and Decision-Making

Why Join Sandoz?

Sandoz offers an agile and collaborative work environment where employees can make a meaningful impact on global healthcare.

Benefits of Working at Sandoz

  • Opportunity to work with a global pharmaceutical leader
  • Exposure to end-to-end pharmacovigilance and medical safety operations
  • Career growth in drug safety and regulatory sciences
  • Flexible and inclusive workplace culture
  • Learning and development opportunities
  • Participation in innovative generic and biosimilar medicine programs

How to Apply

Application Link

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