Telangana Author Jobs – 136 Open Jobs Today

Manager-Analytical & Data Verification
Amgen —Hyderabad, Telangana
- Microsoft Powerpoint
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- Microsoft Excel
Senior Associate Medical Data Reviewer
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FactSet Research Systems —Hyderabad, Telangana
- Full-time
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React Developer with .Net
Verisk —Hyderabad, Telangana
- Full-time
- Azure
- Computer Science
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Senior Validation Engineer
Amgen —Hyderabad, Telangana
- Public speaking
- Master's degree
- Analysis skills
IT&D Manager, Demand Planning
Reckitt —Hyderabad, Telangana
- Project management
- Agile
- Analytics
- Health insurance
Software Dev Engineer II , Last Mile Delivery Prdct&Tech
ADCI HYD 13 SEZ —Hyderabad, Telangana
- Full-time
- Computer Science
- Bachelor's degree
- Software development
12d
Senior Security Analyst - Compliance
TriNet —Hyderabad, Telangana
- Computer Science
- Microsoft Office
- Finance
- Health insurance
Senior Software Engineer/Applied AI Scientist
The Hartford —Hyderabad, Telangana
- Full-time
- Azure
- Databases
- SQL
Sub Editor
VSIL —Hyderabad, Telangana
- ₹1,00,000 - ₹3,00,000 a year
- Email
- Writing skills
- English
- Microsoft Office
Senior Staff Engineer – StoreWeb Modernization
TJX Companies —Hyderabad, Telangana
- Full-time
- Azure
- SQL
- APIs
Data Engineer
Accenture —Hyderabad, Telangana
- Full-time
- Azure
- SQL
- AWS
Technical Writer
AVEVA DRUG DELIVERY SYSTEMS INC —Kukatpally, Hyderabad, Telangana
- ₹25 - ₹30 an hour
- Writing skills
- Project management
- Bachelor's degree
Staff Software Engineer/Data Scientist
The Hartford —Hyderabad, Telangana
- Full-time
- Azure
- Databases
- SQL
Translational Data Management, Automation, & AI Engineer
Amgen —Hyderabad, Telangana
- Full-time
- Doctoral degree
- AWS
- Bachelor's degree
6d
Sr Associate Biostatistics
Amgen —Hyderabad, Telangana
- Doctoral degree
- English
- Master's degree
Senior Engineer, Software Dev
GCC India —Hyderabad, Telangana
- Full-time
- Azure
- SQL
- AWS
Librarian
Pallavi International School, Sagar Road, Chintapally Guda, Hyderabad —Bongulur, Telangana
- From ₹20,000 a month
- Full-time
- Research
- Master's degree
- Bachelor's degree
- Health insurance
Quick apply
14d
Senior Software Engineer - AI I
Thomson Reuters —Hyderabad, Telangana
- Full-time
- Hybrid work
- Azure
- APIs
- AI
- Work from home
C&Q Document Preparation Support (Facilities & Utilities)
Amgen —Hyderabad, Telangana
- HVAC
- Organisational skills
- In-person

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Manager-Analytical & Data Verification

Amgen -
Hyderabad, Telangana

Apply Now

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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