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Azurity Pharmaceuticals Hiring Associate, Drug Safety in PV

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Azurity Pharmaceuticals is inviting applications for the position of Associate, Drug Safety – Quality, Standards & Training at its Hyderabad location. This pharmacovigilance job is ideal for candidates with 1–3 years of experience in drug safety, quality systems, compliance, or training coordination within pharmaceutical, biotech, or regulated healthcare environments.

The role offers an opportunity to contribute to global pharmacovigilance operations by supporting quality systems, inspection readiness, SOP management, and training activities. Candidates with a background in life sciences and an understanding of pharmacovigilance regulations are encouraged to apply.

About Azurity Pharmaceuticals

Azurity Pharmaceuticals is a privately held specialty pharmaceutical company focused on developing innovative medicines for underserved patient populations. The company provides high-quality medications across therapeutic areas including cardiovascular, neurology, endocrinology, gastroenterology, institutional, and orphan diseases. Azurity’s patient-centric portfolio has positively impacted millions of patients worldwide.

Job Details

  • Position: Associate, Drug Safety – Quality, Standards & Training
  • Company: Azurity Pharmaceuticals
  • Location: Hyderabad, India
  • Job Type: Full-Time
  • Department: Global Drug Safety – Quality, Standards & Training
  • Experience Required: 1–3 Years
  • Education: Bachelor’s Degree in Life Sciences, Healthcare, Quality, Training, or related fields

Key Responsibilities

As an Associate, Drug Safety – Quality, Standards & Training, you will:

  • Support maintenance and administration of Drug Safety SOPs, work instructions, and standards.
  • Coordinate document updates, version control, and SOP management activities.
  • Support onboarding and periodic pharmacovigilance training programs.
  • Track training completion and maintain training compliance records.
  • Prepare documentation for regulatory inspections and pharmacovigilance audits.
  • Maintain inspection-ready quality and training documentation.
  • Collaborate with Drug Safety Operations, Compliance, Regulatory Affairs, Quality, and Clinical teams.
  • Coordinate quality and training communications within the Drug Safety function.
  • Support global drug safety initiatives requiring standardized processes and training implementation.

Eligibility Criteria

Candidates should possess:

Educational Qualifications

  • Bachelor’s Degree in:
    • Pharmacy (B.Pharm)
    • Life Sciences
    • Healthcare
    • Quality Management
    • Training and Development
    • Related disciplines

Experience Requirements

  • 1–3 years of experience in:
    • Pharmacovigilance
    • Drug Safety Operations
    • Quality Systems
    • Compliance Management
    • Training Coordination
    • Pharmaceutical or Biotechnology industries

Preferred Skills

  • Understanding of pharmacovigilance regulations and quality systems
  • SOP and document management experience
  • Training coordination and compliance tracking
  • Strong communication and organizational abilities
  • Inspection and audit readiness support experience
  • Cross-functional collaboration skills

Why Join Azurity Pharmaceuticals?

Working at Azurity Pharmaceuticals offers:

  • Opportunity to work in a global pharmacovigilance environment
  • Exposure to quality systems and regulatory compliance processes
  • Experience in SOP management and pharmacovigilance inspections
  • Career growth in Drug Safety Compliance and Quality Assurance
  • Collaborative and inclusive workplace culture
  • Opportunity to contribute to patient-centric pharmaceutical innovation

How to Apply

Application Link

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