About the role

Aplyr's Quick Take

This role is about leading a team focused on supply chain management for clinical trials, ensuring compliance with regulatory standards and managing budgets. You'll be responsible for project execution, stakeholder coordination, and mentoring team members, making it a mix of management and technical oversight.

Good fit

Ideal candidates have significant experience in supply chain management, particularly in pharmaceuticals or clinical trials. A collaborative working style and strong leadership skills will help you thrive in this role.

Worth noting

The job requires a blend of technical and managerial skills, and the emphasis on compliance and regulatory standards suggests a high-stakes environment. The role is office-based in Hyderabad, which may not suit those looking for remote work options.

Job Description Summary

This is a universal job description meant to capture some of the primary duties of this role that are common across functions or divisions. It is not intended to represent all of the specific responsibilities of the position -Management TrackLead and manage the Engineering, Logistics and Safety Experts team inthe Local Supply Center to ensure deliveries of intermediates anddrug substance, maintaining compliance with internal and externalregulatory and quality standards(GMP and HSE) and budget targets.Responsible for maintenance and investment budgets and long terminvestment plan for DSS.TRD Representative for Engineering for Rhinetal Valley. -Scientific / Technical TrackHas operational end to end responsibility for assigned supply activities. Leads and manages complex and demanding projects and global network activities and participates in cross-functional teams. Accountable for performance improvement initiatives. -Produces, packages and manufactures drugs to be used in clinical trials. Responsible for distribution, warehousing, transportation, packaging, randomization, blinding, and labeling of material for clinical trials in conformity with guidelines of the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH), Good Clinical Practice (GCP), and Good Manufacturing Practice (GMP). -To oversee clinical supply on holistic global trials level, proactively negotiates and communicates clinical supply plan/timeline to internal and external customers and partners.

Job Description

Major Accountabilities

Lead and drive end-to-end project execution, ensuring milestones, quality, timelines, and budget adherence.
Represent the unit in cross-functional/global teams and ensure effective stakeholder coordination.
Establish and maintain governance processes to ensure compliance with Novartis and regulatory standards.
Drive strategic planning and execution in partnership with Unit Head to meet current and future business needs.
Manage resources effectively, including allocation, constraints handling, and cost optimization initiatives.
Mentor and coach team members globally, supporting capability building in technical and leadership areas.
Lead SOP development/review and ensure adherence to quality, compliance, and continuous improvement standards.
Act as a facilitator/mediator in complex situations, driving issue resolution, risk mitigation, and process improvements.

Minimum Requirements

Proven experience in leading cross-functional projects and driving execution in a matrix/global environment.
Strong exposure to stakeholder management and organizational representation at senior levels.
Demonstrated people leadership and mentoring experience, including coaching and team development.
Experience in project/program management, supply chain, or clinical operations within regulated industries.
Solid understanding of compliance, quality standards (e.g., GMP), and continuous improvement frameworks.

Skills Desired

Continual Improvement Process, Master Data, Material Requirements Planning (Mrp), Materials Management, People Management, Production Planning, Supplier Relationship Management (Srm), Supply-Chain Management, Supply Chain Planning, Technical Requirements, Waterfall Model, Wms (Warehouse Management Systems)

Skills & Tags

Aplyr's read

Novartis is a Swiss-based global healthcare leader, known for its focus on innovative medicines and commitment to addressing patient needs through diverse roles.
Synthesized from recent postings & public sources

What's promising

•Novartis invests heavily in research and development, driving innovation in pharmaceuticals.
•The company offers a wide range of global career opportunities across various fields.
•Strong focus on cutting-edge therapies, including gene therapy and AI-driven solutions.

What to watch

•Regulatory challenges can impact the speed of drug approval and market entry.
•High competition in the pharmaceutical industry requires constant innovation to maintain market position.
•Complex organizational structure may slow decision-making processes.

Why Novartis

•Novartis has a robust pipeline of innovative medicines, setting it apart in the healthcare sector.
•The company emphasizes a diverse and inclusive workplace culture across its global operations.
•Novartis is a leader in digital transformation within pharmaceuticals, integrating AI and data science.

Aplyr’s read is generated by AI from public sources. Was it useful?

About Novartis

Novartis

novartis.com

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Novartis is a global healthcare company based in Switzerland that provides solutions to address the evolving needs of patients worldwide. It focuses on innovative medicines, generics, and eye care.