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Director global engineering - sterile & bio

Castleford
Teva Pharmaceuticals
Global engineering
Posted: 21 October
Offer description

The opportunity

Technology SME Leader for Sterile and Bio production

The Engineer will provide the overall subject matter expertise on a TGO level, on a cluster level and on a site level as needed.

Scope of SME support may include – Standardization processes, Compliance GAP CAP, Reliability improvements, Machine, Facility and Process design and PS, RA processes.

The BP will lead the GE interface with global and local functions - MS&T, EHS&S, R&D, OPEX, Finance, Procurement, Cluster lead and any other related function as needed.

How you’ll spend your day

BP scope through the above site processes and monitoring framework, focus but not limited to:

1. CAPEX – LRP, AOP, routines, financial performance, KPIs management.
2. PRODEX – Planning and management of three Eng. Related budgets – Energy, Maintenance, Consumables.
3. GMI – Saving initiatives planning and projects execution.
4. People – agile organization, risk management, community building.

Your experience and qualifications

5. BS. Degree in Engineering (Mechanical/Electrical/Chemical/Industrial)
6. MBA Degree - Advantage
7. At least 10 years’ experience in Aseptic/Sterile technologies.
8. Complex manufacturing (Respiratory, patches, etc.) – nice to have
9. Experience in sterile and bio - must have
10. Coordinating initiatives in a complex global environment.
11. Equipment Reliability and understanding of OPEX principles.
12. Excellent understanding of Aseptic/Sterile equipment industry standards and major OEM players.
13. Understanding trends in equipment technology across the pharma industry.
14. Large, complex, multi-level organizational interface experience.
15. Global, multinational experience.

Languages:

16. Fluent in English. Additional languages advantage.

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