Amgen Associate Job Opening, BSc & MSc Life Sciences Apply Online
PC Triage and Intake Associate
India – Hyderabad
JOB ID: R-205446
LOCATION: India – Hyderabad
WORK LOCATION TYPE: On Site
DATE POSTED: Feb. 02, 2025
CATEGORY: Information Systems
Job Summary
The PC Triage and Intake Associate is responsible for global triage of Product Complaints and ensuring proper Adverse Events and/or Other Safety Findings are captured. Ensures to capture the patient outcome because of the reported event. This position ensures compliance with global and local procedural documents and local implementation of Amgen Corporate, Patient Safety, and Quality objectives, policies, processes, and procedures.
Key Activities
- Work within the Quality Management System framework, including all applicable training and controlled documentation governing Pharmacovigilance processes.
- Ensure triage of initial data entry (book-in) of new PC, AE, and OSF cases is complete.
- Perform the initial book-in activities and append additional information or documents to the case as they are received in the global intake system.
- Ensure compliance with global and local procedural documents and local implementation of Amgen Corporate, Patient Safety, and Quality objectives, policies, processes, and procedures.
- Support performance-emphasized culture.
- Ensure quality of PC, AE, and OSF records.
- Implement Standard Operating Procedure requirements for the triage process.
What We Expect of You
We are all different, yet we all use our unique contributions to serve patients.
Education & Experience (Basic):
- Master’s degree and 3 years of Drug Safety or Life Sciences experience OR
- Bachelor’s degree and 5 years of Drug Safety or Life Sciences experience
Education & Experience (Preferred):
- Pharmacovigilance or Quality experience in biotech, pharmaceutical, or medical device industry
- Bachelor’s Degree in a health-care subject area or scientific field
- Previous experience with a corporate intake system or safety database
- Ability to successfully manage workload to strict timelines
- Familiarity with basic project management tools
- Demonstrated ability to consistently deliver on-time and high-quality results
- Ability to operate in a matrixed or team environment
- Understanding of the applicable global regulatory requirements (Good Manufacturing Practices, Good Pharmacovigilance Practices)
Editor’s Note: Amgen Associate Job Opening, BSc & MSc Life Sciences Apply Online. Please ensure you are subscribed to the Biotecnika Times Newsletter and our YouTube channel to be notified of the latest industry news. Follow us on social media like Twitter, Telegram, Facebo
