Telangana Author Jobs – 133 Open Jobs Today

Manager-Analytical & Data Verification
Amgen —Hyderabad, Telangana
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Global Regulatory Writing – Senior Manager
Amgen —Hyderabad, Telangana
- Doctoral degree
- Word processing
- Writing skills
Senior Software Engineer(Java, Restapi)-FIP Data Layer
FactSet Research Systems —Hyderabad, Telangana
- Full-time
- Computer Science
- System design
- Java
- Paid time off
Research Scientist - Generative AI & Foundation Models
YAL —Kothaguda, Telangana
- Doctoral degree
- Computer Science
- Research
Quick apply
Applied Scientist II, Sheriff Team- Payroll tech
ADCI HYD 13 SEZ —Hyderabad, Telangana
- Full-time
- Doctoral degree
- Customer service
- Research
Associate Specialist, Tester
MSD —Hyderabad, Telangana
- Full-time
- Azure
- Computer Science
- Java
16h
Manager, C&Q Document Preparation (Manufacturing Support)
Amgen —Hyderabad, Telangana
- Master's degree
- Bachelor's degree
- Organisational skills
Principal Threat Research Lead
Microsoft —Hyderabad, Telangana
- Full-time
- Azure
- Research
- Master's degree
13d
Specialist IS Engineer - System Implementation & Development
Amgen —Hyderabad, Telangana
- Azure
- Computer Science
- Public speaking
Senior Model Validation Analyst II(Python/R)
Verisk —Hyderabad, Telangana
- Full-time
- SQL
- AWS
- Bachelor's degree
Executive - DQA
Piramal Pharma Limited —Digwal, Telangana
- Full-time
- Master's degree
- APIs
2d
Product Manager, Manufacturing Execution & Batch Lifecycle
ValGenesis —Hyderabad, Telangana
- Full-time
- Computer science
- Doctoral degree
- B.Sc
Quick apply
Technical Solutions Consultant, PDM-PLM
Google —Hyderabad, Telangana
- Full-time
- Computer Science
- Engineering
- System design
Principal Product Manager Technical, Associate Experience
ADCI HYD 13 SEZ —Hyderabad, Telangana
- Full-time
- Customer service
- Bachelor's degree
6d
Specialist Stability
Amgen —Hyderabad, Telangana
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Data Engineer, Global Procurement Technology
ADCI HYD 13 SEZ —Hyderabad, Telangana
- Full-time
- Java
- Databases
- SQL
8d
Senior Product Manager, FinOps
ADCI HYD 13 SEZ —Hyderabad, Telangana
- Full-time
- Computer Science
- Engineering
- Master's degree
2d
Customer Success Engineer (Tier 2)
Ideagen —Hyderabad, Telangana
- Part-time
- Azure
- Software troubleshooting
- SQL
Business Systems Analyst
Zeta Global —Hyderabad, Telangana
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Office
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

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Manager-Analytical & Data Verification

Amgen -
Hyderabad, Telangana

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Job details

Qualifications

Microsoft Powerpoint
Microsoft Word
Biochemistry
Microsoft Excel
Microsoft Outlook
Public speaking
Microsoft Office
Master's degree
Quality assurance
Data management
Chemistry
Quality systems
Manufacturing
Communication skills

Full job description

India - Hyderabad

JOB ID: R-245903 LOCATION: India - Hyderabad WORK LOCATION TYPE: On Site DATE POSTED: Jun. 09, 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 Stability function is part of the Amgen Product Quality organization, providing governance and management of lean, harmonized, and compliant Stability data packages for all of Amgen’s products. In this team-based role, Manager Stability will collaborate with Product Quality Teams (PQTs), supporting specialist teams, and Global stability teams to ensure the design, management, maintenance, and data analysis of a product’s stability program support GMP compliance and meet the Market Authorization commitments. In this management role you will provide critical support to PQTs through management of activities and staff supporting different programs for late-stage clinical and commercial products.

In this team-oriented manager role, you will serve as a subject matter expert of GMP data management strategy, directly adding to the success of PQTs by ensuring support for the product Quality strategies. In this role, you will be working closely with diverse functional groups including Supply Chain, Manufacturing, Global CMC Statistics, External Supplier Quality, Quality Control, Regulatory, Quality Assurance, external providers, and other departments on a variety of activities. Such activities include managing data standardization activities, Chromatographic overlays, data verification and, where warranted, investigations, regulatory submissions and support for inspections across the Amgen manufacturing and testing network.

Roles & Responsibilities:

Directly supervise Quality staff supporting Product Quality Teams and activities enabling regulatory submissions
Adeptly manage staff training and independently coordinate staff assignments supporting time-sensitive activities across multiple teams
Author, revise, review, and approve technical documents in GMP Quality systems, including but not limited to data reports, Standard Operating Procedures, and Work Instructions
Work closely with the global Product Quality organization to drive standardization of data, Chromatographic overlays and data verification activities
Lead continuous improvement projects that may be global or local in scope
Own, manage, and participate in deviations, CAPAs, and cross functional investigations
Communicate and collaborate with cross-functional teams across multiple sites and time zones to coordinate stability study starts and sample requests
Participate in audits and inspections across multiple sites
Mentor and train staff, as required

Basic Qualifications and Experience:

Master's degree in chemistry, biochemistry, biology, or a related pharmaceutical sciences field and above 10 years of Quality, Operations, Scientific experience.

Functional Skills:

Must-Have Skills:

Experience and expertise in managing teams and motivating staff to deliver high quality results and adhere to project timelines using digital GMP Quality systems
Demonstrated proficiency and knowledge in biologics manufacturing processes including analytical methods, cGMP, and international regulatory expectations
Demonstrated proficiency is oral and written communication of complex information
Ability to build and maintain cross-functional relationships and strong partnerships through written and verbal communication skills
Exceptional attention to detail and accuracy in all deliverables
Strong scientific data management and organization skills
Expertise with chromatography systems, Laboratory Information Management Systems
Expertise in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) and virtual collaboration tools (e.g., MS Teams)
Effective communication, critical thinking and problem solving

Good-to-Have Skills:

Experience working virtually on a cross-functional team in a matrix environment across multiple time zones
Expertise in computer applications such as Veeva, Spotfire, SHINY
Expertise in MS Office (Word, Excel, PowerPoint, MS Teams)

Soft Skills:

Analytical and problem-solving skills
Ability to work effectively with global, virtual teams
High degree of initiative and self-motivation
Ability to manage multiple priorities successfully, react quickly to address urgent requests and meet challenging timelines
Team-oriented, with a focus on achieving team goals
Strong presentation and public speaking skills

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 an accommodation.

Apply Now

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author jobs in telangana

Manager-Analytical & Data Verification

Global Regulatory Writing – Senior Manager

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