Jobid=3197050965
Overview
In this role you will lead Teva’s external manufacturing network to ensure reliable patient supply, product quality, and compliant, cost-effective operations. You’ll steer a cross-functional virtual plant team and serve as the primary operations interface with partner sites. You’ll drive governance, risk mitigation, and continuous improvement across manufacturing, quality, regulatory and supply chain. This is a strategic leadership position with impact on enterprise-critical products and long-term supplier value. You’ll work in a high-performance, collaborative culture that values growth and innovation.
Arbeidsvoorwaarden / Benefits
- generous annual leave
- reward plans
- flexible working schedules
- tailored health support
- Twist career development platform
- internal growth opportunities
Verantwoordelijkheden
- Coordinate end-to-end operations with external partners to secure patient supply, tech transfer, validation, regulatory approvals, and lifecycle changes
- Establish governance, metrics and management reviews across internal and external stakeholders
- Communicate priorities and performance outcomes to align cross-functional teams
- Identify and mitigate supplier and business risks with proactive contingency plans
- Resolve manufacturing delivery issues and partner-related challenges
- Collaborate with MSAT for process capability, control strategy, ROB, and COGS improvement
- Ensure ongoing cGMP compliance, inspection readiness, and quality governance with QA/Regulatory
- Sponsor investigations and cross-site technical improvements; manage manufacturing readiness
- Promote safety, health and environmental policy adherence in operations
- Drive Lean, digital manufacturing and standardization across external partners
- Build executive-level relationships with suppliers to enhance reliability and value creation
- Coach and develop cross-functional team members; manage projects and major initiatives
- Support capacity, capital planning, and major external manufacturing projects for compliance and growth
- Lead due diligence input on capacity and supplier network decisions
- Contribute to supplier strategy and contract development to ensure supply continuity
- Collaborate in License and Supply Agreement development to embed external manufacturing oversight
Belangrijkste vereisten
- 15+ years in biologics manufacturing/related roles
- 10+ years leadership in biologics manufacturing and external CDMO management
- Bachelor in Engineering (Master/MBA preferred)
- Strong knowledge of cGMP, tech transfer, process validation, quality systems, product lifecycle
- Experience with regulatory filings, inspections, and launches
- Financial acumen including COGS, S&OP/IBP, capital investment
- Proven cross-functional leadership and stakeholder influence across global matrix organizations
- Strong change management and continuous improvement track record
- Willingness to travel 25%
- collaboration
- influence and relationship-building
- communication
- cGMP
- technology transfer
- process validation
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