Telangana Author Jobs – 133 Open Jobs Today

Associate Product Quality - Data Verification
Amgen —Hyderabad, Telangana
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
4d
Manager-Analytical & Data Verification
Amgen —Hyderabad, Telangana
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Global Clinical Development Manager
Sandoz —Telangana
- Full-time
- Medicine
- Management
- Research
Senior Functional Tester - Hybris QA
EPAM Systems, Inc. —Hyderabad, Telangana
- Health insurance
- Paid time off
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Lead AI Product Manager
hirezy.ai —Hyderabad, Telangana
- ₹8,00,000 - ₹20,00,000 a year
- Full-time
- Hybrid work
- Salesforce
- Databases
- Analysis skills
Quick apply
9d
QA Engineer
WPP Production —Hyderabad, Telangana
- Hybrid work
- Computer Science
- Bachelor's degree
- Communication skills
- Flexible schedule
Quick apply
Test Engineer
QualiZeal —Hyderabad, Telangana
- Full-time
- Java
- SQL
- Analysis skills
Model Validation Analyst- Python/R
Verisk —Hyderabad, Telangana
- Full-time
- Microsoft Excel
- Databases
- SQL
Sr Microbiologist
AVEVA DRUG DELIVERY SYSTEMS INC —Kukatpally, Hyderabad, Telangana
- Weekend availability
- Microsoft Word
- Microsoft Excel
- Microsoft Access
Lead Developer (C# .Net and C++)
Hyland —Hyderabad, Telangana
- Full-time
- Hybrid work
- Master's degree
- C++
- JavaScript
AI Tools and Governance - Lead Engineer
WSA APAC —Hyderabad, Telangana
- Azure
- Master's degree
- Software development
Quick apply
Lead II - Software Testing - playwright
UST —Hyderabad, Telangana
- Weekend availability
- Google Suite
- Computer Science
- DevOps
Quick apply
EDITORS/PROOFREADERS
BSP Books —Hyderabad, Telangana
- Microsoft Word
- English
- Microsoft Office
Assistant Managing Editor
Pulsus Group —Hyderabad, Telangana
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
AWS Database Migration Architect
EPAM Systems, Inc. —Hyderabad, Telangana
- English
- AWS
- Health insurance
- Paid time off
Senior Associate Medical Data Reviewer
Amgen —Hyderabad, Telangana
- Nursing
- Medicine
- Data analysis skills
Senior Specialist, External Data Acquisition and Delivery
Regeneron —Hyderabad, Telangana
- Oracle
- Bachelor's degree
- Communication skills
- Health insurance
- Paid time off
G&P - Government & Public Services - Specialist Design - Graphic Designer - Hyderabad
Deloitte —Hyderabad, Telangana
- Microsoft Office
- Bachelor's degree
- Leadership
13d
Associate Director – Joint Process Team (JPT) Leader, Dry External Manufacturing
Eli Lilly —Hyderabad, Telangana
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
7d
Bioinformatics Scientist
Amgen —Hyderabad, Telangana
- Doctoral degree
- Research
- Java

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Associate Product Quality - Data Verification

Amgen -
Hyderabad, Telangana

Apply Now

Job details

4 days ago

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Microsoft Office
Master's degree
Bachelor's degree
Communication skills
FDA regulations

Full job description

India - Hyderabad

JOB ID: R-248502 LOCATION: India - Hyderabad WORK LOCATION TYPE: On Site DATE POSTED: Jul. 03, 2026 CATEGORY: Quality

ABOUT AMGEN

Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today.

ABOUT THE ROLE

Role Description:

The Associate Quality Compliance is an individual contributor role that plays a vital part in supporting Product Quality Teams (PQTs). This role ensures adherence to Amgen’s compliance practices for late-stage and commercial products by reviewing critical data and documents to confirm accuracy, integrity, and regulatory readiness.

Through diligent verification, navigation of GMP-compliant systems, and close collaboration across global teams, you will help ensure Amgen continues to deliver products of the highest quality and safety.

Roles & Responsibilities:

Execute transactions in GMP computer-based systems (e.g., Veeva, LIMS).
Review and verify data in technical documents within GMP Quality systems.
Navigate GMP systems (Spotfire, Veeva, SampleManager LIMS) to identify and validate data sources.
Manage time-sensitive compliance activities across multiple teams and projects independently.
Collaborate with document authors across sites and time zones to support project milestones.
Provide guidance and feedback to authors of GMP documents to ensure compliance and accuracy.

Basic Qualifications and Experience:

Bachelor's/Master’s degree with minimum of 3 years of pharmaceutical industry or directly related experience

Functional Skills:

Must-Have Skills:

General knowledge of GMP principles and pharmaceutical industry standards for Quality
Strong organization skills with high attention to detail
Ability to meet deadlines and deliver high-quality results using GMP systems
Excellent written and verbal communication skills

Good-to-Have Skills:

Knowledge of FDA and ICH regulations
Experience working in cross-functional, virtual teams across time zones
Familiarity with GMP applications such as Veeva, Spotfire, SampleManager LIMS
Proficiency in MS Office (Word, Excel, PowerPoint, Teams)

Soft Skills:

Strong initiative and self-motivation
Team-oriented mindset with focus on achieving shared goals
Ability to work effectively in diverse, global, virtual environments

What Success Looks Like

In this role, success will be demonstrated by:

Timely and accurate completion of document reviews and compliance activities
Proactive collaboration with cross-functional teams to meet project timelines
Effective use of GMP systems to maintain compliance and data integrity

Growth & Development

Amgen invests in employee growth. In this role, you will receive structured training on GMP systems and mentoring to develop your compliance expertise.

EQUAL OPPORTUNITY STATEMENT

Amgen is an Equal Opportunity employer. We will consider all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We are committed to providing reasonable accommodation for individuals with disabilities during the application and interview process, in performing essential job functions, and in accessing employment benefits. Please contact us to request accommodation.

Apply Now

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Associate Product Quality - Data Verification

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