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Senior Associate, Research And Development (R&D) Quality Compliance

0-2 years
Not Disclosed
10 Nov. 6, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Position: Senior Associate, Research and Development (R&D) Quality Compliance
Location: Hyderabad, India
Job ID: R-225413
Category: Quality
Work Location Type: On-Site
Date Posted: October 31, 2025


Job Overview

The Senior Associate, R&D Quality Compliance supports the R&D Quality (RDQ) Compliance Managers in maintaining quality oversight, audit and inspection readiness, and process improvement within the General Medicine team. The role involves ensuring compliance with regulatory requirements, supporting CAPA management, and driving operational excellence through AI-enabled data analytics and reporting.


Key Responsibilities

Quality Management & Compliance

  • Input audit responses into the Quality Management System (QMS).

  • Enter site inspection data into the Inspection Management System.

  • Work with deviation owners to ensure timely CAPA development and closure, including submission of objective evidence within defined timelines.

  • Prepare and submit documentation to the Potentially Reportable Serious Breach Committee within required timeframes.

Collaboration & Communication

  • Partner with Clinical Study Teams to facilitate effective communication as directed by the RDQ Compliance Manager.

  • Maintain and update the General Medicine SharePoint site and Teams channels.

  • Support inspection readiness activities under RDQ Compliance Manager supervision.

Metrics & Reporting

  • Prepare weekly metric reports for the General Medicine team, covering deviations, CAPAs, serious breaches, audit, and inspection findings.

  • Highlight overdue items and collaborate with compliance managers to ensure timely resolution.

  • Work with the data quality analytics team to assess and optimize report effectiveness.

Meetings & Documentation

  • Facilitate General Medicine team meetings, including agenda creation and presentation preparation.

  • Maintain decision and action logs; follow up with owners for timely completion.

  • Manage Q&A logs and ensure traceability of discussions and resolutions.

AI and Process Improvement

  • Leverage Artificial Intelligence (AI) tools and technologies to streamline workflows, automate processes, and support data-driven decision-making.

  • Identify opportunities to apply AI for operational efficiency and continuous improvement initiatives.

  • Support development of lessons learned and best practices documentation.

Cross-Functional Collaboration

  • Collaborate with other Amgen R&D Quality functions to ensure consistency and best practice sharing.

  • Provide quality oversight of small clinical programs under guidance of the RDQ Compliance Manager.


Skills & Competencies

  • Strong understanding of clinical research quality systems and regulatory compliance processes.

  • Experience in CAPA management, deviation tracking, and inspection readiness.

  • Data-driven mindset with ability to leverage AI tools for analytics and automation.

  • Excellent organizational, documentation, and communication skills.

  • Proficiency in Microsoft SharePoint, Teams, and reporting tools.


Reporting To

R&D Quality (RDQ) Compliance Manager