Telangana Author Jobs – 134 Open Jobs Today

C&Q Document Preparation Support (Drug Product)
Amgen —Hyderabad, Telangana
- Organisational skills
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Consumer Safety Science Scientist
Haleon —Hyderabad, Telangana
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Customer Centric Engineer (APAC Market)
Workato —Hyderabad, Telangana
- Computer Science
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Quick apply
Sr. Specialist, IT Validation Services
Bristol-Myers Squibb —Hyderabad, Telangana
- Email
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SAP FICO BRM
Luxoft —Hyderabad, Telangana
- English
- Banking
Analyst IT
Mattel —Hyderabad, Telangana
- Full-time
- Azure
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- System design
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Sr. Business Analyst
Micron —Hyderabad, Telangana
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Engineer III - Quality Engg & AI
Anblicks —Hyderabad, Telangana
- Azure
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Document Controller
Enviri Global Service Centre —Hyderabad, Telangana
- Full-time
- English
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Senior Consultant
Virtusa —Hyderabad District, Telangana
- Remote
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Senior Security Engineer (Intake - Hyderabad, India)
Yext —Hyderabad, Telangana
- Email
- Azure
- AWS
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Sr. Associate Pharamocovigilance Operations
Amgen —Hyderabad, Telangana
- In-person
Consultant Trainee
Pulsus Group —Hyderabad, Telangana
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Asset & Wealth Management - Margin Engineering - Vice President - Hyderabad
Goldman Sachs —Hyderabad, Telangana
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Principal Software Engineer
Keka Technologies Pvt. Ltd —Hyderabad, Telangana
- Full-time
- Computer Science
- Master's degree
- Bachelor's degree
Quick apply
Business Process Architect
Accenture —Hyderabad, Telangana
- Full-time
- Bachelor's degree
- Leadership
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1d
CUSTOMER SERVICE/HELP DESK
UnyKloud —Hyderabad, Telangana
- Email
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Forward Deployed Engineer
Workato —Hyderabad, Telangana
- Computer Science
- Salesforce
- English
Quick apply
Strategic Solutions Architect - Retail / CPG
Saaki Argus & Averil Consulting —Hyderabad, Telangana
- Microsoft Powerpoint
- Microsoft Word
- English
Quick apply
Manager
Jeevan —Hyderabad, Telangana
- Medicine
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C&Q Document Preparation Support (Drug Product)

Amgen -
Hyderabad, Telangana

Apply Now

Job details

8 days ago

Qualifications

Organisational skills
Manufacturing
Communication skills

Full job description

India - Hyderabad

JOB ID: R-248238 LOCATION: India - Hyderabad WORK LOCATION TYPE: On Site DATE POSTED: Jun. 30, 2026 CATEGORY: Engineering

About the Role

Amgen is seeking a Senior Associate specializing in Commissioning & Qualification (C&Q) to join the Engineering C&Q 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 C&Q 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 C&Q 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 C&Q 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

Apply Now

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author jobs in telangana

C&Q Document Preparation Support (Drug Product)

Consumer Safety Science Scientist

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Manager

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