Associate Director, Quality Assurance

Lonza Group

Bend, Oregon, USA
Not specified; not specified; medical, dental, vis...
Not specified (relocation assistance available)
10 years pharmaceutical industry experience
5 years cdmo environment experience
5 years supervisory management experience
Lonza Group is seeking an Associate Director of Quality Assurance in Bend, Oregon, to lead a high-performing QA team focused on compliance within pharmaceutical development and manufacturing. The role requires extensive industry experience and supervisory skills, with a strong emphasis on regulatory compliance and quality systems

Job Summary

  • This role involves leading a high-performing QA team to ensure compliance across pharmaceutical development and manufacturing.
  • The position requires overseeing deviation management, CAPA processes, and supporting internal and external regulatory inspections.
  • Lonza offers relocation assistance for eligible candidates along with medical, dental, vision insurance and performance-based compensation.

Matching Summary

Match Score: 85

Lonza Group is seeking an Associate Director of Quality Assurance in Bend, Oregon, to lead a high-performing QA team focused on compliance within pharmaceutical development and manufacturing. The role requires extensive industry experience and supervisory skills, with a strong emphasis on regulatory compliance and quality systems.

Salary

Not specified; Not specified; Medical, dental, vision insurance included

Skills & Requirements

Must-have

  • 10 years pharmaceutical industry experience
  • 5 years CDMO environment experience
  • 5 years supervisory management experience
  • FDA audit hosting and management
  • GMP production and document lifecycle control

Nice-to-have

  • Agile career and dynamic working culture
  • Strong communication and presentation skills
  • Ability to manage multiple projects and deadlines
  • Training development and curriculum management skills

Key Requirements

  • Bachelor's degree or equivalent experience
  • Commercial experience in pharmaceutical industry
  • Experience hosting FDA audits
  • 5 years of supervisory or management experience

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter