Colombia

Director, Integrated Risk Management Lead (Villamaría)

Director, Integrated Risk Management Lead (Villamaría)
Descripción
We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.Our Team, Your Impact

The Risk Management Leader for External Manufacturing at Empresa confidencial is responsible for establishing and executing a proactive, end-to-end risk management framework across Teva’s integral CDMO/CMO network supporting generics, complex generics, biosimilars, specialty medicines, and sterile/aseptic operations.

The role ensures the resilience, compliance, and continuity of Teva’s external supply by driving structured risk assessment, quantification, mitigation strategies, early-warning detection, and governance processes.Location This role can be based in Bulgaria (Sofia), Croatia (Zagreb) or India. How You’ll Spend Your Day 1. Teva External Manufacturing Risk Strategy & Governance

Develop the right ExM integrated risk framework which needs to align with existing frameworks in TGO / other functions Implement, and maintain ExM standardized integrated risk management framework Lead risk governance processes and escalation pathways. Ensure full ExM risk map is established, regularly updated and mitigations are carried out by operational units and functions as planned. Measure effectiveness of the framework on an on-going basis through improvement rate of CSL, reduction of crisis situations, and maturity assessments of the organization.

2. Supply Continuity & Operational Risk

Identify and quantify risks impacting supply reliability.

3. GMP, Quality & Compliance Risk

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