Engineering Associate Director—Aseptic Filling & Validation

Jubilant HollisterStier CMO

Spokane (WA)

Vor Ort

USD 142.000 - 227.000

Vollzeit

vor 5 Stunden
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

FSA/HSA beginning day one
Life Insurance
AD&D Insurance
Disability Insurance
Employee Assistance Program

Zusammenfassung

Jubilant HollisterStier in Spokane seeks an Engineering Associate Director to lead a team of 10-15 technical engineers, directing design, installation, qualification and continuous improvement of aseptic filling equipment for liquid and lyophilized products.

This role ensures compliance with cGMP and regulatory standards, while collaborating with Manufacturing, Quality and Validation teams to meet process needs and timelines.

Qualifikationen

  • 12+ years in pharmaceutical engineering with at least 3 years in aseptic filling equipment projects.
  • 5 years managing technical personnel.
  • Proven track record of on-time equipment design, installation, and qualification under cGMP.
  • Strong knowledge of aseptic processing, isolator technology, and lyophilization.

Aufgaben

  • Manage end-to-end engineering projects for aseptic filling systems, isolators, lyophilizers, and related equipment.
  • Develop and maintain project timelines, budgets, and resource plans.
  • Lead IQ/OQ/PQ activities in alignment with validation protocols and regulatory standards.

Kenntnisse

Project management
Leadership
Communication
Problem solving
Cross-functional collaboration

Ausbildung

BS in Mechanical Engineering

Tools

SAP
Microsoft Office
CAD software

Jobbeschreibung

Jubilant HollisterStier in Spokane seeks an Engineering Associate Director to lead a team of 10-15 technical engineers, directing design, installation, qualification and continuous improvement of aseptic filling equipment for liquid and lyophilized products.

This role ensures compliance with cGMP and regulatory standards, while collaborating with Manufacturing, Quality and Validation teams to meet process needs and timelines.

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