Global Serialization Associate Director

Vertex Pharmaceuticals Incorporated

$164,100 - $246,100; bonus + equity eligible; comp...
Hybrid - eligible to work remotely up to two days per week or on-site five days per week with ad hoc flexibility.
Serialization process design
Track and trace implementation
Sop development and maintenance
Vertex Pharmaceuticals is seeking a Global Serialization Associate Director to oversee the design, implementation, and maintenance of global serialization processes. The role requires extensive experience in project management within the pharmaceutical industry, focusing on new product launches and operational issues, with a strong emphasis on communication and relationship-building

Job Summary

  • The Serialization Associate Director contributes to the design, implementation and maintenance of global serialization / track and trace at Vertex.
  • This role independently manages multiple projects or phase(s) of a larger project related to serialization and master data management and builds relationships with internal and external stakeholders.
  • Vertex offers inclusive market-leading benefits to meet employees' needs, including generous paid time off, educational assistance, and a 401(k).

Matching Summary

Match Score: 85

Vertex Pharmaceuticals is seeking a Global Serialization Associate Director to oversee the design, implementation, and maintenance of global serialization processes. The role requires extensive experience in project management within the pharmaceutical industry, focusing on new product launches and operational issues, with a strong emphasis on communication and relationship-building.

Salary

$164,100 - $246,100; Bonus and equity eligible; Comprehensive benefits package

Skills & Requirements

Must-have

  • Serialization process design
  • Track and trace implementation
  • SOP development and maintenance
  • Operational issue troubleshooting
  • Global product launch support
  • Master data management
  • Change control management

Nice-to-have

  • Cross-departmental collaboration
  • Building stakeholder relationships
  • Sound judgment in problem-solving
  • Continuous process improvement

Key Requirements

  • 8 years of relevant experience
  • Bachelor's degree in relevant discipline
  • PMP certification preferred
  • Experience with software systems validation
  • Knowledge of FDA cGxP and 21 CFR Part 11

Work Rights

Not specified

Tailored Resume

Cover Letter