Telangana Author Jobs – 134 Open Jobs Today

Sr Associate Product Quality - Analytical
Amgen —Hyderabad, Telangana
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
6d
Executive - DQA
Piramal Pharma Limited —Digwal, Telangana
- Full-time
- Master's degree
- APIs
2d
Assistant Managing Editor
Pulsus Group —Hyderabad, Telangana
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
C&Q Document Preparation Support (Drug Product)
Amgen —Hyderabad, Telangana
- Organisational skills
- In-person
- Manufacturing
9d
EDITORS/PROOFREADERS
BSP Books —Hyderabad, Telangana
- Microsoft Word
- English
- Microsoft Office
Specialist Stability
Amgen —Hyderabad, Telangana
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Business Process Architect
Accenture —Hyderabad, Telangana
- Full-time
- Bachelor's degree
- Leadership
- Communication skills
2d
Senior Manager Medical Review
Regeneron —Hyderabad, Telangana
- Medicine
- Bachelor's degree
- AI
- Health insurance
- Paid time off
Technical Writer
AVEVA DRUG DELIVERY SYSTEMS INC —Kukatpally, Hyderabad, Telangana
- ₹25 - ₹30 an hour
- Writing skills
- Project management
- Bachelor's degree
Strategic Solutions Architect - Retail / CPG
Saaki Argus & Averil Consulting —Hyderabad, Telangana
- Microsoft Powerpoint
- Microsoft Word
- English
Quick apply
Internal Job Posting-Software Engineer - III
FactSet Research Systems —Hyderabad, Telangana
- Full-time
- Computer Science
- System design
- Java
10h
Epidemiology Analyst
Amgen —Hyderabad, Telangana
- Medicine
- Doctoral degree
- Research
Quality & Validation Lead
Opella Healthcare Group —Hyderabad, Telangana
- Full-time
- Computer Science
- Engineering
- Master's degree
10d
C&Q Document Preparation Support (Facilities & Utilities)
Amgen —Hyderabad, Telangana
- HVAC
- Organisational skills
- In-person
Staff engineer , ASIC AMS Verification
Micron —Hyderabad, Telangana
- B.Sc
- Master's degree
- Bachelor's degree
9d
Sub Editor
VSIL —Hyderabad, Telangana
- ₹1,00,000 - ₹3,00,000 a year
- Email
- Writing skills
- English
- Microsoft Office
.NET Engineer with AI Assisted Development Tools
Rinf.tech —Hyderabad, Telangana
- Full-time
- AI
Product Owner
Kensium —Hyderabad, Telangana
- Full-time
- Azure
- Salesforce
- DevOps
Automation Tester
Resolver —Hyderabad, Telangana
- Full-time
- Java
- JavaScript
- Agile
- Health insurance
- Life insurance
Senior Revenue Cycle Specialist - Work From Home
ClinicMind —Hyderabad, Telangana
- Remote
- Microsoft Excel
- English
- Finance
- Work from home
Quick apply

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Sr Associate Product Quality - Analytical

Amgen -
Hyderabad, Telangana

Apply Now

Job details

6 days ago

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Lean
Process improvement
Biotechnology
Microsoft Office
Master's degree
Assembly
Data management
Continuous improvement
Technical writing
Quality systems
Manufacturing
Communication skills
FDA regulations

Full job description

India - Hyderabad

JOB ID: R-248656 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:

This role is an individual contributor role that provides critical support to Product Quality Teams (PQTs) for late-stage clinical and commercial products. In this role, you will serve as a primary author of technical and regulatory reports, manage GMP data within compliant systems, and help ensure accuracy, completeness, and compliance across global submissions.

You will also play an integral role in maintaining Amgen’s electronic databases and mapping tools, supporting continuous improvement initiatives, and providing peer training as needed. This role requires strong expertise in GMP compliance, technical writing, and cross-functional collaboration to drive high-quality outcomes under tight timelines.

Roles & Responsibilities:

Navigate and execute transactions in GMP systems (Empower, LIMS, Veeva, Spotfire).
Work closely with in the product Quality organization to drive standardization of data, and chromatographic overlay activities.
Author and maintain GMP technical reports supporting regulatory filings within quality systems (e.g., Veeva).
Collate, review, verify, and archive GMP data for late-stage clinical and commercial products.
Ensure accuracy and completeness of product data with high attention to detail.
Collaborate across global teams and time zones, effectively communicating findings and project updates.

Basic Qualifications

Master’s degree with minimum 6 years of Pharmaceutical/Biotechnology experience in Quality, Operations, Scientific, or Manufacturing fields

Functional Skills:

Must-Have Skills:

Strong understanding of GMP requirements, US FDA, and ICH regulations
Proven technical expertise in Chromatographic techniques /software and overlays
Expertise in GMP systems (Veeva, Empower, LIMS, Spotfire)
Strong data management, analytical, and problem-solving skills
Experience supporting cross-functional teams in matrixed, global environments
Proficiency in MS Office (Word, Excel, PowerPoint, Teams)
Excellent written and verbal communication across all levels of the organization
Continuous improvement mindset with experience applying lean practices

Good-to-Have Skills:

Knowledge of stability data management and annual product review
Experience in assembling annual product reviews
Experience in business process improvement and electronic data tool development

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 with minimal supervision

What Success Looks Like

Timely and accurate delivery of technical and regulatory reports
Effective collaboration across global teams to meet project milestones
Proactive improvements to data management processes and quality systems
Contribution to team knowledge through peer training and mentorship

Growth & Development

This role offers opportunities to build advanced expertise in GMP compliance, regulatory authorship, and quality systems.

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

Refine Your Search

author jobs in telangana

Sr Associate Product Quality - Analytical

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Assistant Managing Editor

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