Sanofi is hiring for three positions in its Research and Development (R&D) and Clinical Supply Chain operations in Hyderabad. The openings are Associate Global Supply Study Support (AGSSS), Global Supply Study Support (GSSS), and Global Supply Support Team Leader.

These full-time opportunities focus on clinical trial supply management, investigational medicinal product (IMP) distribution, inventory reconciliation, regulatory compliance, documentation, and clinical supply chain operations. Candidates with experience in pharmaceutical production, supply chain, quality, clinical trials, or clinical operations can review the eligibility criteria for each position.

Sanofi Recruitment 2026: Job Details

Sanofi Job Openings in Hyderabad

1. Associate Global Supply Study Support (AGSSS)

Job Requisition ID: R2874845
Experience Required: 3–5 years

The Associate Global Supply Study Support position focuses on operational support for clinical trial supply activities. The role assists Clinical Supply Chain Study Leaders in managing investigational products, tracking shipments, maintaining inventory records, and ensuring accurate documentation throughout clinical studies.

Key Responsibilities

• Create and manage depot transfers in Interactive Response Technology (IRT) and maintain the Inventory Product Stock Management (IPSM) tracker.
• Manage the destruction of expired investigational medicinal products (IMPs) and auxiliary medicinal products (AxMPs).
• Monitor IRT interface failures and alert the Clinical Supply Chain Study Leader.
• Record clinical supply plans in Sanofi’s supply management tools.
• Perform global study reconciliation and follow up on discrepancies with relevant stakeholders.
• Upload, file, and archive IMP-related documents in the electronic Trial Master File (eTMF).
• Monitor product stock levels and alert the study leader about potential shortages.
• Track shipments and prepare required customs and country-specific documentation.
• Support preparation for regulatory inspections.

2. Global Supply Study Support (GSSS)

Job Requisition ID: R2874848
Experience Required: 6–8 years

The Global Supply Study Support role involves managing clinical supply processes and providing advanced operational expertise. In addition to performing the responsibilities covered by the associate-level position, the role includes coaching colleagues, conducting quality checks, supporting issue resolution, and contributing to process improvement.

Key Responsibilities

• Manage depot transfers, inventory tracking, expired product destruction, and clinical supply reconciliation.
• Monitor IRT interfaces and maintain accurate supply plans in Sanofi’s clinical supply tools.
• Support shipment tracking, stock monitoring, and preparation of mandatory shipping documentation.
• Maintain IMP-related records and support regulatory inspection readiness.
• Coach new team members and conduct peer reviews to promote compliant, right-first-time execution.
• Act as a subject matter expert or key user for assigned processes.
• Develop and maintain technical notes, FAQs, lessons learned, and process documentation.
• Identify opportunities for process standardization, improvement, and automation.
• Assess operational risks, resolve issues, and coordinate with global study stakeholders.

3. Global Supply Support Team Leader

Job Requisition ID: R2874827
Experience Required: 7+ years, including at least 2 years in people management or team coordination

The Global Supply Support Team Leader leads a team supporting centralized clinical supply chain activities. The position involves team development, operational planning, stakeholder coordination, performance monitoring, and continuous improvement across relevant supply support functions.

Key Responsibilities

• Lead, coach, train, and develop team members while supporting onboarding and career development.
• Manage workload distribution, resource allocation, and operational priorities.
• Align team objectives with organizational goals and clinical study timelines.
• Monitor performance metrics, project trends, risks, and operational status.
• Coordinate with Clinical Supply Chain Operations (CSCO), Global Quality Operations (GQO), and Chemistry, Manufacturing and Controls (CMC).
• Identify operational issues and implement process improvements and corrective actions.
• Oversee relevant Global Supply Study Support activities, including inventory tracking, reconciliation, shipment documentation, and supply planning.
• Support Investigational Product Services activities, including temperature excursions, import licences, and distribution-related requirements.
• Provide backup support for temperature excursion management and ensure compliance with GxP requirements.
• Oversee applicable documentation, system training, external resource onboarding, and product receipt and transfer activities.

Eligibility and Educational Qualifications

Associate Global Supply Study Support (AGSSS)

• Bachelor’s degree required; an advanced degree is preferred.
• 3–5 years of operational experience in pharmaceutical production, supply chain, quality, and/or clinical trials.
• Basic knowledge of clinical development and investigational product management.
• Understanding of Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and GxP requirements.

Global Supply Study Support (GSSS)

• Bachelor’s degree required; an advanced degree is preferred.
• 6–8 years of operational experience in pharmaceutical production, supply chain, quality, and/or clinical trials.
• Demonstrated mastery of associate-level responsibilities and related tools and processes.
• Knowledge of clinical trial supply management, regulatory requirements, and investigational product lifecycle activities.

Global Supply Support Team Leader

• B.Sc. in Life Sciences or an equivalent qualification.
• At least 7 years of experience in the pharmaceutical or CRO industry in clinical operations or clinical development.
• At least 2 years of people management or team coordination experience.
• GMP certification.
• Project management experience.
• Quality experience and knowledge of GxP regulations are advantageous.

Required Skills

Across these Sanofi clinical supply chain vacancies, relevant skills include:

• Clinical trial design, protocols, randomization, dosing regimens, and cohort management.
• Investigational medicinal product management, including shelf life, depot management, distribution, reconciliation, and destruction.
• Knowledge of GCP, GMP, and applicable GxP requirements.
• Experience with clinical supply systems, ERP, IRT, document management tools, and Veeva applications.
• Proficiency in Microsoft Office applications, including Word, Excel, SharePoint, and Power BI.
• Strong organizational, documentation, communication, and stakeholder management skills.
• Ability to manage concurrent tasks, meet deadlines, and work in global, multicultural teams.
• Problem-solving, adaptability, and a methodical approach to operational challenges.

For the Global Supply Support Team Leader role, additional emphasis is placed on people leadership, workload management, project planning, performance monitoring, and continuous improvement.

Application Details