Content Factory Integration Manager, Global MedInfo

Takeda; Bengaluru; Hybrid; INR 1,500,000 - 2,500,000; Full time

Benefits offered by this job

Annual bonus

Hybrid work

Healthcare insurance

Life insurance

Employee assistance

Learning platforms

Diversity & inclusion

Internet & mobile reimbursements

Employee referral program

Parental leaves

Job summary

Takeda in Bengaluru, India, invites applications for a Medical Information content role within our Innovation Capability Center. You will act as the primary interface for GMI requests, translating needs into briefs and coordinating development of standard responses and FAQs.

You will identify reuse opportunities, manage content lifecycles, and coordinate production with the Content Factory Medical Information liaison, ensuring accuracy and adherence to briefs throughout the review process.

Qualifications

• Over 5–8 years of relevant experience; at least 3 years in biopharma Medical Information, Medical Writing, or content operations.
• Education in Medical/science fields required.
• Fluent English; additional languages advantageous.

Responsibilities

• Serve as the enterprise single entry point for Global Medical Information content requests.
• Translate GMI requirements into briefs and coordinate development of standard response documents and FAQs.
• Identify reuse opportunities and support local adaptation and content lifecycle management.
• Coordinate production briefs and source packages for Content Factory Medical Information liaison.
• Ensure draft outputs reflect the approved brief before quality control and review.

Skills

MI content

Content briefs

Stakeholder Mgmt

AI-enabled tools

Attention to detail

Content workflows

Education

Medical/science degree

Tools

Content repositories

Version control

Job description

Job Description

Job Posting Description

The Future Begins Here

At Takeda, we are leading digital evolution and global transformation. By building innovative solutions and future-ready capabilities, we are meeting the need of patients, our people, and the planet.

Bengaluru, the city, which is India’s epicenter of Innovation, has been selected to be home to Takeda’s recently launched Innovation Capability Center. We invite you to join our digital transformation journey. In this role, you will have the opportunity to boost your skills and become the heart of an innovative engine that is contributing to global impact and improvement.

Role Objectives :

• Serve as the enterprise single entry point for Global Medical Information content requests and the primary interface with the designated Content Factory Medical Information liaison
• Translate GMI requirements into clear briefs and coordinate the development of standard response documents, FAQs and related Medical Information content
• Proactively identify reuse opportunities, challenging unnecessary duplication and supporting appropriate local adaptation and content lifecycle management

Key Responsibilities :

Request Intake & Brief Development

• Receive requests from Global Medical Information teams for new, updated or localized content
• Meet with GMI teams to understand the purpose, audience, scope, format, timing, source materials and required review pathway
• Route requests to the appropriate reuse, update, localization or net-new development pathway in line with Global Medical Information standards

Content Reuse & Prioritization

• Assess requests against existing approved assets and planned content and determine whether to reuse, adapt, combine or progress net-new content within agreed guardrails
• Identify duplicative requests and promote reuse of globally developed content while recognizing valid market-specific needs
• Monitor overall content lifecycle needs based on inputs from the Global Medical Information teams

Content Factory Integration

• Prepare and maintain clear production briefs and approved source packages for the Content Factory Medical Information liaison
• Coordinate Content Factory questions, timelines, delivery status, dependencies and required revisions
• Confirm that draft outputs reflect the approved brief before routing them to quality control and formal Global Medical Information review

Qualifications :

Experience: More than 5- 8 years of relevant professional experience, including at least 3 years within the biopharmaceutical industry experience in Medical Information, Medical Writing, scientific content development, and content operations required. Experience in vendor management and/or vendor coordination is preferred.

Technical skills:

• Understanding of Medical Information content and standard response-document workflows
• Ability to translate inquiry and content needs into structured production briefs
• Knowledge of balanced, factual and non-promotional Medical Information principles
• Familiarity with content repositories, metadata, version control and review workflows
• Strong coordination, stakeholder management and issue-resolution capabilities
• Experience working with AI-enabled tools
• Attention to detail

Education: A Medical, scientific, pharmacy, nursing, life sciences, Medical communications or related degree is required

Languages: Fluent English required; additional languages advantageous

BENEFITS:

t is our priority to provide competitive compensation and a benefit package that bridges your personal life with your professional career. Amongst our benefits are:

• Competitive Salary + Performance Annual Bonus
• Flexible work environment, including hybrid working
• Comprehensive Healthcare Insurance Plans for self, spouse, and children
• Group Term Life Insurance and Group Accident Insurance programs
• Employee Assistance Program
• Broad Variety of learning platforms
• Diversity, Equity, and Inclusion Programs
• Reimbursements – Home Internet & Mobile Phone
• Employee Referral Program
• Leaves – Paternity Leave (4 Weeks) , Maternity Leave (up to 26 weeks), Bereavement Leave (5 calendar days)

Locations

IND - Bengaluru

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time