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**Senior Associate – R&D Quality Compliance

5-10 years
Not Disclosed
10 Nov. 24, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

**Senior Associate – R&D Quality Compliance (On-Site)

Location: Hyderabad, India**

Experience Required:
Bachelor’s or Master’s degree with 5–10 years of professional experience in Quality, R&D Quality Compliance, Clinical Research, or Pharmaceutical/ Biotech Operations.


About the Role

Amgen is seeking a Senior Associate, Research and Development (R&D) Quality Compliance to support global R&D Quality (RDQ) operations and compliance oversight across clinical programs. This on-site position, based in Hyderabad, India, plays a critical role in ensuring adherence to global regulatory standards, inspection readiness, timely CAPA management, and high-quality documentation workflows across clinical and quality teams.

The role collaborates closely with RDQ Compliance Managers, Clinical Study Teams, and data analytics teams to support compliance reporting, deviation management, oversight activities, and quality system optimization.


Key Responsibilities

  • Enter audit responses into the Quality Management System (QMS) accurately and within defined timelines.

  • Upload and maintain site inspection data in the Inspection Management System.

  • Collaborate with deviation and CAPA owners to ensure timely development, submission of objective evidence, and closure of corrective actions.

  • Prepare and submit documentation for the Potentially Reportable Serious Breach Committee as required.

  • Support communication with Clinical Study Teams as directed by RDQ Compliance Managers.

  • Create weekly General Medicine metric reports, including open deviations, CAPAs, serious breaches, and audit/inspection findings.

  • Highlight overdue compliance items and coordinate follow-up for timely resolution.

  • Partner with RDQ Compliance Managers and Data Quality Analytics teams to evaluate reporting effectiveness and drive optimization.

  • Facilitate General Medicine team meetings, including agenda creation, presentation preparation, and maintenance of Decision & Action logs.

  • Manage Q&A logs and ensure follow-up with responsible stakeholders.

  • Support inspection readiness activities under supervision of RDQ Compliance Managers.

  • Provide quality oversight for small clinical programs, ensuring compliance with SOPs and regulatory expectations.

  • Apply artificial intelligence (AI) tools to automate workflows, improve operational efficiency, and support data-driven decision-making.

  • Assist in developing lessons learned, best practices, and continuous improvement documentation.

  • Collaborate with cross-functional R&D Quality teams as required.

  • Maintain and update General Medicine SharePoint sites and Teams channels.


Required Skills & Qualifications

  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or related field.

  • 5–10 years of work experience in R&D Quality, Clinical Quality, Pharmacovigilance Quality, or Quality Compliance in the pharmaceutical or biotechnology sector.

  • Strong understanding of clinical research operations, deviation management, and CAPA processes.

  • Proficiency in QMS tools and inspection management platforms.

  • Experience preparing compliance reports and quality metrics.

  • Knowledge of regulatory frameworks including GCP and applicable global guidelines.

  • Demonstrated ability to use AI-driven tools for workflow automation and operational enhancement.

  • Strong communication, documentation, and stakeholder coordination skills.

  • Ability to manage multiple priorities and maintain high accuracy under pressure.

  • Experience working with SharePoint, MS Teams, and Microsoft Office Suite.


Preferred Skills

  • Experience supporting audits, inspections, and inspection readiness activities.

  • Familiarity with clinical operations in multinational environments.

  • Ability to interpret quality metrics and optimize reporting structures.

  • Strong organizational skills and capability to manage cross-functional communication.


Job Details

Job ID: R-225413
Category: Quality
Work Location Type: On-Site
City: Hyderabad, India
Additional Locations: Hyderabad, India