Drug Safety Associate Job at Azurity Pharmaceuticals
Looking for a Drug Safety Associate Job with a global pharmaceutical company? Azurity Pharmaceuticals Careers has opened an excellent opportunity for an Associate, Drug Safety – Quality, Standards & Training in Hyderabad, India. This role is ideal for professionals with experience in pharmacovigilance, quality, compliance, or drug safety who are looking to build a rewarding career in Medical Jobs in India. Join a patient-focused organization committed to innovation, quality, and improving healthcare outcomes.
About Azurity Pharmaceuticals:
Azurity Pharmaceuticals is a privately held specialty pharmaceutical company dedicated to developing innovative medicines for underserved patient populations. The company focuses on delivering accessible, high-quality therapies across cardiovascular, neurology, endocrinology, gastrointestinal, institutional, and orphan disease segments. With an expanding commercial portfolio and a strong late-stage pipeline, Azurity continues to improve the lives of millions of patients worldwide.
Driven by science, quality, and patient care, Azurity fosters an inclusive workplace where innovation and collaboration thrive. Employees work in a dynamic environment that encourages professional development, continuous learning, and excellence in pharmaceutical research, compliance, and patient safety.
Job Details:
- Job Title: Associate, Drug Safety – Quality, Standards & Training
- Location: Hyderabad, India
- Department: Global Drug Safety
- Employment Type: Full-Time
Key Responsibilities:
- Support the maintenance and administration of Drug Safety SOPs, work instructions, and quality standards.
- Coordinate onboarding and periodic Drug Safety training programs.
- Maintain training records and monitor compliance metrics.
- Assist in regulatory inspection readiness and pharmacovigilance audits.
- Organize and maintain inspection-ready documentation.
- Collaborate with Drug Safety Operations, Compliance, Regulatory Affairs, Quality, and Clinical teams.
- Coordinate quality and training communications across the Drug Safety function.
- Support continuous improvement initiatives and standardized drug safety processes.
- Ensure documentation follows global pharmacovigilance regulations and company policies.
Educational Qualification for this Drug Safety Associate Job:
Candidates should possess:
- Bachelor’s degree in Healthcare or a related discipline.
Experience Required:
Applicants should have:
- 1–3 years of experience in pharmacovigilance, quality, compliance, training, or related pharmaceutical roles.
- Experience supporting quality systems, SOP documentation, or training coordination is preferred.
- Good understanding of pharmacovigilance regulations and quality management systems.
Required Skills for this Drug Safety Associate Job:
- Knowledge of pharmacovigilance and drug safety processes.
- Understanding of quality systems and SOP management.
- Regulatory compliance awareness.
- Documentation and record management skills.
- Strong communication and coordination abilities.
- Excellent organizational and time management skills.
- Ability to collaborate with cross-functional teams.
- Attention to detail and commitment to quality.
- Inspection and audit readiness knowledge.
- Continuous improvement mindset.
