If you’ve been searching for high-growth clinical research jobs with a global pharmaceutical leader, this opportunity at AstraZeneca is designed for you. The company is hiring a Patient Safety QA Advisor in Bangalore to strengthen its global patient safety, compliance, and pharmacovigilance operations. For professionals aiming to build long-term AstraZeneca careers in quality, safety, and scientific excellence, this is a golden chance.
- Title: Patient Safety QA Advisor, Patient Safety (PS)
- Location: Bengaluru, Karnataka, India
- Job ID: R-240905
ABOUT THE COMPANY:
AstraZeneca is one of the world’s leading science-driven biopharmaceutical companies committed to delivering life-changing medicines. With a bold ambition to impact 200 million patients and launch 20 new medicines by 2030, AstraZeneca fosters innovation, collaboration, and continuous learning. The GBS R&D Services team is expanding to support global research, patient safety, and pharmacovigilance functions — making it an ideal place for candidates seeking advancement in clinical research jobs.
JOB OVERVIEW:
This role supports AstraZeneca’s global patient safety operations through quality assurance, risk management, compliance monitoring, and inspection readiness. You will work closely with cross-functional teams across R&D, patient safety, regulatory, and quality systems to ensure adherence to global and regional safety regulations. This is a high-impact global role well-suited for professionals aiming for advanced pharmacovigilance jobs or clinical research jobs within multinational organizations.
- Work Mode: Hybrid (3 days onsite, 2 days remote)
- Work Hours: 9 am–6 pm IST / 2 pm–11 pm IST
- Experience Required: 3–7 years
EDUCATIONAL REQUIREMENTS:
- Bachelor’s degree in Life Sciences or equivalent
- 2–3 years of experience in GxP Quality Assurance
- Experience with Veeva Vault QMS (mandatory)
KEY RESPONSIBILITIES:
- Maintain & enhance the Patient Safety Quality Management System (QMS)
- Manage controlled documents (SOPs, WIs) and training curricula
- Lead change management, quality metrics, and compliance monitoring
- Support audits, inspections, internal assessments, and risk-based QA
- Run deviation handling, RCA, CAPA planning, monitoring & effectiveness
- Partner with cross-functional teams for global safety compliance
- Enhance inspection readiness with continuous improvement initiatives
- Contribute to global patient safety processes, tools, and data governance
- Ensure adherence to global and regional pharmacovigilance regulations
SKILLS REQUIRED:
- Strong foundation in Quality Assurance and GxP systems
- Proficiency in Veeva Vault QMS, audits, and SOP lifecycle management
- Knowledge of global patient safety and pharmacovigilance regulations
- Excellent communication, documentation, and analytical abilities
- Ability to work cross-functionally and manage multiple priorities
If you’re passionate about improving patient safety on a global scale and building a fulfilling career in clinical research jobs, this AstraZeneca opportunity is an excellent stepping stone. Join a mission-driven team transforming healthcare through science, quality, compliance, and innovation.
