Validation Team Leader

Pfizer Venezuela S.A

Middleton, US
Base: $82,700.00 - $137,900.00; bonus/equity: 10.0...
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Validation master plans
Cgmp requirements
Cross-functional collaboration
** Pfizer Venezuela S.A is seeking a Validation Team Leader for its Middleton, US site. The role involves leading the validation team to ensure compliance with regulatory standards while fostering continuous improvement and collaboration across departments. **

Job Summary

  • Lead the Middleton Site validation team to deliver compliant, effective, and sustainable validation programs, enabling successful execution of cleaning, equipment, and process validations.
  • Serve as the site validation subject matter expert, providing technical and strategic oversight to ensure all validation activities comply with cGMP requirements, internal SOPs, and site Validation Master Plans.
  • Partner closely with Site Leadership, Quality, Engineering, Production, and network stakeholders to identify, prioritize, and implement improvements that strengthen validation capabilities and drive long-term site performance.

Matching Summary

Match Score: 75

** Pfizer Venezuela S.A is seeking a Validation Team Leader for its Middleton, US site. The role involves leading the validation team to ensure compliance with regulatory standards while fostering continuous improvement and collaboration across departments. **

Salary

Base: $82,700.00 - $137,900.00; Bonus/Equity: 10.0% of base salary; Benefits: Comprehensive benefits package including 401(k) plan, paid time off, and health benefits

Skills & Requirements

Must-have

  • Validation Master Plans
  • cGMP requirements
  • cross-functional collaboration
  • process validations
  • equipment validations
  • cleaning validations

Nice-to-have

  • continuous improvement initiatives
  • strategic oversight
  • fostering accountability
  • driving innovation

Key Requirements

  • Bachelor's degree with at least 2 years of experience
  • Master's degree with 0+ years of experience
  • Associate's degree with 6 years of experience
  • High school diploma with 8 years of relevant experience
  • Manufacturing experience in pharmaceutical GMP environment
  • Project execution experience
  • Mentoring and training experience

Work Rights

Permanent work authorization in the United States

Tailored Resume

Cover Letter