C&Q Document Preparation Support (Drug Product)

Amgen Technology; Hyderabad; On-site; INR 1,400,000 - 2,200,000; Full time

Job summary

Amgen Technology in Hyderabad seeks a Senior Associate specializing in Commissioning Qualification to support CQ lifecycle documentation across engineering projects and GMP systems. You will partner with Engineering, Validation, Quality, Manufacturing, Facilities, Automation, and Project teams to deliver compliant, inspection-ready CQ documents.

The role focuses on preparing qualification documentation for drug substance, product, packaging, and facilities utilities, with emphasis on quality and

Qualifications

• Experience in GMP commissioning, qualification, or validation is preferred.
• Experience authoring CQ lifecycle documents including protocols and reports.
• Understanding of lifecycle documentation and data integrity practices.

Responsibilities

• Prepare and revise commissioning and qualification lifecycle documentation for projects.
• Author qualification protocols, reports, risk assessments, matrices, and test scripts.
• Coordinate review cycles and incorporate comments to final documents.
• Ensure documents are accurate, complete, compliant, and inspection-ready.
• Collaborate with Engineering, Validation, Quality, Manufacturing, Facilities, and Projects.
• Track deliverables and support execution against schedules and milestones.
• Maintain document organization and version control within quality systems.
• Support audit and inspection readiness activities as required.
• Contribute to continuous improvement of documentation quality and efficiency.

Skills

GMP commissioning

CQ lifecycle documentation

Technical writing

Cross-functional collaboration

Regulatory readiness

Inspections readiness

Documentation control

Project coordination

Quality systems

Job description

About the Role

Amgen is seeking a Senior Associate specializing in Commissioning Qualification (CQ) to join the Engineering CQ Center of Excellence (CoE). In this role, you will support the preparation, coordination, and delivery of commissioning and qualification lifecycle documentation supporting engineering projects and GMP manufacturing systems across Amgen operations.

The Senior Associate will partner closely with Engineering, Validation, Quality, Manufacturing, Facilities, Automation, and Project teams to develop compliant, inspection-ready documentation that supports commissioning, qualification, and operational readiness activities. This role plays an important part in ensuring documentation quality, consistency, and alignment with established CQ standards, procedures, and regulatory expectations.

This position may support one or more areas including Drug Substance, Drug Product, Finished Drug Product Packaging, or Facilities Utilities.

Roles Responsibilities

• Prepare and revise commissioning and qualification lifecycle documentation supporting Engineering projects and systems
• Author qualification protocols, reports, risk assessments, traceability matrices, test scripts, and related CQ documentation
• Support document development activities using approved templates, standards, and CoE procedures
• Coordinate technical review cycles and incorporate comments and revisions into final documents
• Ensure documentation is accurate, complete, compliant, and inspection-ready
• Partner with Engineering, Validation, Quality, Manufacturing, Facilities, and Project teams to gather technical information
• Track assigned deliverables and support execution against project schedules and milestones
• Maintain document organization and version control within applicable quality systems
• Support audit and inspection readiness activities as required
• Contribute to continuous improvement initiatives focused on documentation quality, consistency, and efficiency

Area-Specific Experience Preferred

• Experience supporting commissioning and qualification activities for drug product manufacturing systems
• Familiarity with formulation, compounding, filling, lyophilization, and aseptic processing equipment
• Understanding of sterile manufacturing practices, contamination control strategies, and cleanroom operations preferred
• Experience preparing qualification documentation supporting aseptic processing systems and manufacturing operations
• Familiarity with process equipment qualification including mixers, filling lines, isolators, and autoclaves preferred
• Experience supporting startup or qualification activities for sterile manufacturing capital projects preferred

Preferred / Good to Have Qualifications Skills

• Experience in GMP commissioning, qualification, validation, or technical operations
• Experience authoring CQ lifecycle documentation including qualification protocols and reports
• Familiarity with risk-based qualification methodologies and lifecycle validation approaches
• Knowledge of GMP documentation practices and data integrity requirements
• Experience working in a fast-paced capital project or startup environment preferred
• Strong written and verbal communication skills
• Strong organizational skills and attention to detail
• Experience working in cross-functional project teams

Key Competencies

• Technical Writing and Documentation Excellence
• Attention to Detail and Quality Focus
• Cross-Functional Collaboration
• Planning and Execution
• Problem Solving and Analytical Thinking
• Continuous Improvement Mindset
• Communication and Stakeholder Partnership