Manager, C&Q Document Preparation (Drug Product) at Amgen - ScoutJobs - The AI-curated global job board
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Amgen
Posted 24 days ago

Manager, C&Q Document Preparation (Drug Product)

AmgenManager, C&Q Document Preparation (Drug Product)

Requirements

Bachelor's or Master's in Engineering or Life Sciences, 5–9 years GMP commissioning or qualification experience, Experience in pharmaceutical or biotechnology industry, Knowledge of risk-based qualification methodologies, Experience leading technical teams

Skills

GMP

About the role

Responsibilities

  • Lead a blended team of employees and contingent workers in the preparation and delivery of compliant C&Q documentation.
  • Oversee the development of qualification protocols, reports, risk assessments, and traceability matrices.
  • Partner with Engineering, Validation, Quality, and Manufacturing teams to ensure documentation aligns with project timelines and operational readiness.
  • Execute C&Q documentation using established Center of Excellence (CoE) standards and templates to ensure consistency and compliance.
  • Monitor documentation progress, identify potential risks, and drive timely resolution of issues.
  • Maintain inspection-ready documentation to support regulatory inspections and internal audits.
  • Provide leadership, coaching, and professional development to team members.

Requirements

  • Bachelor's or Master's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or a related technical field.
  • 5–9 years of experience in GMP commissioning, qualification, validation, or technical operations within the pharmaceutical or biotechnology industry.
  • Proven experience leading technical teams, including full-time employees and outsourced resources.
  • Strong understanding of risk-based qualification methodologies and lifecycle validation approaches.
  • Experience preparing or overseeing qualification documentation such as protocols, reports, and risk assessments.
  • Deep knowledge of GMP documentation practices, data integrity, and inspection readiness.

Preferred Qualifications

  • Experience working within a Commissioning & Qualification Center of Excellence (CoE) model.
  • Familiarity with Drug Product manufacturing systems, packaging systems, facilities, and utilities.
  • Experience supporting global Engineering capital projects in a regulated environment.
  • Exposure to continuous improvement initiatives focused on documentation quality and operational efficiency.

About the Company

Amgen harnesses the best of biology and technology to fight the world’s toughest diseases and make people’s lives easier, fuller, and longer. A biotechnology pioneer since 1980, Amgen discovers, develops, manufactures, and delivers innovative medicines to help millions of patients worldwide.

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Manager, C&Q Document Preparation (Drug Product)

Amgen · Hyderabad

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