Validation Team Leader

Pfizer Com Ec

Middleton, United States
Base: $82,700.00 - $137,900.00; bonus/equity: 10.0...
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Validation master plans
Cgmp requirements
Cross-functional initiatives
** Pfizer is seeking a Validation Team Leader for its Middleton site, responsible for leading validation programs that ensure compliance with regulatory standards in a pharmaceutical manufacturing environment. The ideal candidate will possess strong technical expertise in validation, project management experience, and a collaborative mindset to drive continuous improvement. **

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.
  • The annual base salary for this position ranges from $82,700.00 to $137,900.00, with eligibility for a bonus target of 10.0% of base salary and comprehensive benefits.

Matching Summary

Match Score: 75

** Pfizer is seeking a Validation Team Leader for its Middleton site, responsible for leading validation programs that ensure compliance with regulatory standards in a pharmaceutical manufacturing environment. The ideal candidate will possess strong technical expertise in validation, project management experience, and a collaborative mindset to drive continuous improvement. **

Salary

Base: $82,700.00 - $137,900.00; Bonus/Equity: 10.0% bonus target; Benefits: Comprehensive benefits package

Skills & Requirements

Must-have

  • Validation Master Plans
  • cGMP requirements
  • cross-functional initiatives
  • process validation
  • equipment validation
  • cleaning validation

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
  • Project execution experience
  • Mentoring and training experience

Work Rights

Permanent work authorization in the United States

Tailored Resume

Cover Letter