Telangana Author Jobs – 135 Open Jobs Today

C&Q Document Preparation Support (Drug Substance)
Amgen —Hyderabad, Telangana
- Master's degree
- Bachelor's degree
- Organisational skills
On Job Trainee
Pulsus Group —Hyderabad, Telangana
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Automation Tester
Resolver —Hyderabad, Telangana
- Full-time
- Java
- JavaScript
- Agile
- Health insurance
- Life insurance
Customer Success Engineer (Tier 2)
Ideagen —Hyderabad, Telangana
- Part-time
- Azure
- Software troubleshooting
- SQL
Prof, Controlled Doc Mgmt
サイネオス・ヘルス —Madhapur, Hyderabad, Telangana
- Travel
Data Engineer, Global Procurement Technology
ADCI HYD 13 SEZ —Hyderabad, Telangana
- Full-time
- Java
- Databases
- SQL
8d
Editorial Assistant (Females/Freshers only)
Gavin Publishers and Conferences —Somajiguda, Hyderabad, Telangana
- ₹15,000 - ₹25,000 a month
- Full-time
- B.Sc
- Microsoft Office
- Master's degree
Quick apply
Technical Solutions Consultant, PDM-PLM
Google —Hyderabad, Telangana
- Full-time
- Computer Science
- Engineering
- System design
Senior Software Engineer
Zuddl —Hyderabad, Telangana
- System design
- Java
- JavaScript
Quick apply
13d
Product Manager, Manufacturing Execution & Batch Lifecycle
ValGenesis —Hyderabad, Telangana
- Full-time
- Computer science
- Doctoral degree
- B.Sc
Quick apply
Specialist Stability
Amgen —Hyderabad, Telangana
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Senior Specialist ITVS Digital Validation
Bristol-Myers Squibb —Hyderabad, Telangana
- Email
- Hybrid work
- Computer Science
- English
- Databases
2d
Sr Analyst IT
Mattel —Hyderabad, Telangana
- Full-time
- Oracle
- Computer Science
- Master's degree
Quick apply
C&Q Document Preparation Support (Finished Drug Product)
Amgen —Hyderabad, Telangana
- Organisational skills
- In-person
- Manufacturing
9d
SQA Engineer IV
Brightstar Lottery —Hyderabad, Telangana
- APIs
- AI
- Python
8d
Principal Product Analyst
Amgen —Hyderabad, Telangana
- Azure
- DevOps
- Public speaking
Lead Software Engineer
HealthEdge —Hyderabad, Telangana
- Full-time
- Azure
- Computer Science
- Databases
Senior IBM DOM Developer – Supply chain DTC
Mattel —Hyderabad, Telangana
- Full-time
- Hybrid work
- Azure
- Computer Science
- System design
Quick apply
Consultant - Nutritionist
Yoganta —Hyderabad, Telangana
- Full-time
- Research
- Presentation skills
- Bachelor's degree
Associate Director, Triage and Medical Review
Regeneron —Hyderabad, Telangana
- Medicine
- Databases
- Bachelor's degree
- Health insurance
- Paid time off

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C&Q Document Preparation Support (Drug Substance)

Amgen -
Hyderabad, Telangana

Apply Now

Job details

Qualifications

Master's degree
Bachelor's degree
Organisational skills
IT
Manufacturing
Communication skills

Full job description

India - Hyderabad

JOB ID: R-245881 LOCATION: India - Hyderabad WORK LOCATION TYPE: On Site DATE POSTED: Jun. 10, 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 biotechnology manufacturing systems including upstream and downstream processing equipment
Familiarity with bioprocess equipment such as bioreactors, chromatography skids, filtration systems, centrifuges, and process support systems
Experience supporting CIP/SIP systems and clean process equipment qualification activities
Understanding of GMP documentation requirements related to biologics manufacturing operations
Familiarity with single-use technologies and hybrid manufacturing systems preferred
Experience supporting startup, commissioning, or qualification activities for biotechnology 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

Basic Qualifications and Experience:

Bachelor’s or Master’s degree in a relevant field (e.g., Computer Science, Engineering or equivalent).
5–9 years of work experience in Information Technology, Information Systems, or a related field
Experience in the global pharmaceutical industry preferred.

EQUAL OPPORTUNITY STATEMENT
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Apply Now

Refine Your Search

author jobs in telangana

C&Q Document Preparation Support (Drug Substance)

On Job Trainee

Automation Tester

Customer Success Engineer (Tier 2)

Prof, Controlled Doc Mgmt

Data Engineer, Global Procurement Technology

Editorial Assistant (Females/Freshers only)

Technical Solutions Consultant, PDM-PLM

Senior Software Engineer

Product Manager, Manufacturing Execution & Batch Lifecycle

Specialist Stability

Senior Specialist ITVS Digital Validation

Sr Analyst IT

C&Q Document Preparation Support (Finished Drug Product)

SQA Engineer IV

Principal Product Analyst

Lead Software Engineer

Senior IBM DOM Developer – Supply chain DTC

Consultant - Nutritionist

Associate Director, Triage and Medical Review

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