Azurity Pharmaceuticals is inviting applications for the position of Associate, Drug Safety – Quality, Standards & Training at its Hyderabad location. This pharmacovigilance job offers an excellent opportunity for professionals with 1–3 years of experience in drug safety, PV compliance, SOP management, or quality systems within the pharmaceutical industry.
Azurity Pharmaceuticals is a specialty pharmaceutical company focused on patient-centric medicines for underserved patient populations. The company operates across therapeutic areas such as cardiovascular, neurology, endocrinology, gastroenterology, institutional care, and orphan diseases.
The Associate Drug Safety role supports global pharmacovigilance quality systems, training programs, SOP documentation, and regulatory inspection readiness. Candidates interested in pharmacovigilance jobs in Hyderabad and drug safety compliance roles in pharma companies should consider applying.
Job Details
Company: Azurity Pharmaceuticals
Position: Associate, Drug Safety – Quality, Standards & Training
Location: Hyderabad, India
Experience: 1–3 Years
Industry: Pharmaceutical / Pharmacovigilance
Department: Global Drug Safety / PV Compliance
Key Responsibilities
The Drug Safety Associate – Quality & Training will support the global pharmacovigilance quality framework and inspection readiness.
Key responsibilities include:
- Support maintenance and administration of Drug Safety SOPs, work instructions, and standards
- Manage document control, version updates, and SOP lifecycle processes
- Coordinate Drug Safety training programs, including onboarding and refresher training
- Track training completion metrics and compliance reports
- Maintain training documentation and PV compliance records
- Assist in regulatory inspection readiness and audit preparation
- Organize and maintain inspection-ready pharmacovigilance documentation
- Collaborate with Drug Safety Operations, Quality, Compliance, Regulatory Affairs, and Clinical teams
- Support global drug safety initiatives and standardized PV processes
- Coordinate quality and training communications within the Drug Safety department
Required Qualifications
Education
- Bachelor’s degree in Life Sciences, Pharmacy, Healthcare, Quality, or related field
Experience
- 1–3 years experience in pharmacovigilance, drug safety, quality systems, or compliance
- Experience supporting SOP management or training coordination preferred
Skills
Candidates should have knowledge of:
- Pharmacovigilance systems and processes
- Global PV regulatory requirements
- Quality systems in regulated pharmaceutical environments
- SOP documentation and training management
- Audit and inspection readiness support
Strong communication, documentation, and organizational skills are required.
Why Work at Azurity Pharmaceuticals
Azurity Pharmaceuticals offers a patient-focused work culture and strong innovation pipeline.
Key benefits include:
- Opportunity to work in global pharmacovigilance operations
- Exposure to drug safety compliance, quality systems, and PV audits
- Collaborative work environment with cross-functional teams
- Experience supporting global regulatory inspections
- Career growth in pharmacovigilance and drug safety operations
How to Apply
