PHARMAFull time
Group Lead – Content Approval Excellence & Content Operations
By Admin · Medical & Scientific Writing
HYDERABAD (IN)ONSITEPOSTED: 11/4/2026
PHARMAFull time
HIRING ORGANIZATIONSANOFIPharmaceuticals / Biotechnology

ROLE OVERVIEW
Sanofi is hiring a Group Lead for Content Approval Excellence and Content Operations in Hyderabad. The role leads Scientific Communications content operations, approval quality and scalable workflow delivery across the content lifecycle.
ROLE DEFINITION & RESPONSIBILITIES
- •Lead the Scientific Communications operations team and capabilities model, serving as domain expert and strategic partner to function leadership.
- •Design and govern an end-to-end content operating framework from brief through creation, review, approval and completion, with clear roles, decision rights and handoffs.
- •Set service levels and delivery governance, remove duplicate handoffs and administrative burden, and scale operating practices across therapeutic areas and content types.
- •Own a risk-based Scientific Communications quality management framework, including content standards, quality-at-source controls, qualification pathways and role-specific control responsibilities.
- •Run independent monitoring and sampling of content and workflow records, define issue taxonomy and escalation triggers, and lead root-cause analysis with corrective and preventive actions.
- •Act as business champion for content workflow requirements in Veeva and related systems, identifying automation and system-enabled quality controls with Digital/IT and Analytics.
- •Oversee vendor operations for payments and copyrights, including compliant payment processes for print and shipment of Scientific Communications materials with procurement and finance.
- •Lead operational excellence, capacity planning, demand management, business continuity planning and standardization of processes, templates and tools across Scientific Communications and Medical Information.
REQUIRED VERIFIED SKILLS
Scientific Communications operations
Medical Information
Content lifecycle and workflow governance
Veeva content systems
Quality management and quality-at-source controls
Independent monitoring and root-cause analysis
Corrective and preventive actions
Vendor payments and copyrights management
Capacity planning and demand management
Business continuity planning
Process standardization
Project management
Stakeholder engagement
Coaching and mentoring
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
ORGANIZATION CONTEXT & CULTURE
Sanofi operates a Global Hub in India that centralises processes and activities for Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. The hub supports Medical, HEVA and Commercial organisations globally.
TEAM SIZE: Approximately 90,000 employees
INDUSTRY: Pharmaceuticals / Biotechnology
APPLICATION ADVISORY
Highlight experience in Scientific Communications or Medical Information content operations, Veeva workflow requirements, quality management frameworks and independent monitoring or root-cause analysis. Also show exposure to vendor payment and copyright processes, capacity planning and cross-functional work with Digital, Analytics, procurement and finance.
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