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Director, integrated risk management lead

Port Talbot
Teva Pharmaceuticals
Risk manager
€80,000 a year
Posted: 2h ago
Offer description

The Risk Management Leader for External Manufacturing at Teva Pharmaceuticals is responsible for establishing and executing a proactive, end-to-end risk management framework across Teva's global 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.


Responsibilities

* Develop the right ExM integrated risk framework which aligns with existing frameworks in TGO and 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 ongoing basis through improvement rate of CSL, reduction of crisis situations, and maturity assessments of the organization.
* Identify and quantify risks impacting supply reliability.
* Partner with Teva Quality to integrate GMP and regulatory risks.
* Ensure financial, geopolitical (including healthcare policy evolution), and corporate stability of CMOs are included in the overall risk assessment methodology.
* Ensure financial, contractual and supply risks related to unexpected evolution of demand are also well included in the overall risk assessment methodology.
* Implement digital dashboards, analytics, and predictive tools.
* Integrate risk data with Teva supply chain/quality systems.
* Train Teva ExM teams on risk methodologies.
* Promote transparency and proactive risk mitigation.
* Lead cross‑operational units collaboration and standardization.


Qualifications

* Bachelor's degree in Engineering, Life Sciences, Chemistry, Supply Chain, or related.
* Certification in risk management desirable.
* 10+ years pharmaceutical/biopharma experience.
* 5+ years experience with risk frameworks in global networks.
* Experience with external manufacturing networks and associated challenges.
* Experience with digital risk tools.
* Consulting experience in risk management highly desirable.


Capabilities & Behaviors

* Highly organized and structured.
* Analytical and structured problem-solving.
* Executive communication and influencing.
* Collaboration, adaptability, and resilience.
* Patient-focused decision-making.
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