QA Manager – Infant Formula Quality & Release

Perrigouk

Eau Claire, Northern (WI, KY)

Hybrid

USD 110,000 - 140,000

Full time

33 hours ago
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Benefits offered by this job

Competitive compensation
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Forbes Best Employers 2024

Job summary

Perrigo is seeking a Quality Assurance Manager to ensure infant formula products meet FDA regulations and company standards. You will lead daily QA operations and collaborate with Manufacturing, Laboratory, Engineering, and Warehouse teams to uphold product safety and quality.

This role drives continuous improvement and decisive quality release decisions. The role requires a Bachelor's degree in a scientific or technical field, five years in a regulated setting, and strong knowledge of cGMP and

Qualifications

  • Bachelor’s degree in a scientific or technical field required.
  • Five years’ experience in a regulated manufacturing environment preferred (infant formula, food, or pharma).
  • Strong understanding of cGMP, FDA regulations and quality systems.
  • Excellent communication, problem solving, and decision-making skills.

Responsibilities

  • Oversee QA activities for infant formula production and product release.
  • Review batch records and maintain quality systems oversight.
  • Lead internal audits and support FDA, customer, and corporate audits.
  • Review and approve SOPs, change controls, validation documents, and critical records.
  • Train, mentor, and lead QA staff to foster a strong quality culture.

Skills

QA leadership
Regulatory compliance
Quality systems
Problem solving
Communication

Education

Bachelor's degree in a scientific or technical field

Job description

Perrigo is seeking a Quality Assurance Manager to ensure infant formula products meet FDA regulations and company standards. You will lead daily QA operations and collaborate with Manufacturing, Laboratory, Engineering, and Warehouse teams to uphold product safety and quality.

This role drives continuous improvement and decisive quality release decisions. The role requires a Bachelor's degree in a scientific or technical field, five years in a regulated setting, and strong knowledge of cGMP and

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