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Quality Assurance Manager

Job in Eau Claire, Eau Claire County, Wisconsin, 54701, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-07-09
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers
Salary/Wage Range or Industry Benchmark: 75000 - 95000 USD Yearly USD 75000.00 95000.00 YEAR
Job Description & How to Apply Below

Responsibilities

  • Manage, enforce, and analyze Quality Assurance trends and verification activities.
  • Ensure robust root cause investigations for deviations and product non-conformance; outline and implement CAPA.
  • Lead timely completion of deviation reports.
  • Analyze data for pre-requisite programs (environmental monitoring, pest control, foreign body prevention) to reduce adverse findings and improve food safety.
  • Support internal assessments and provide production floor support to assure quality system performance; report effectiveness and propose improvements.
  • Provide coaching presence to ensure compliance with factory procedures and practices.
  • Ensure implementation and compliance to Quality Monitoring Schemes, cGMPs, and pre-requisite programs; ensure products meet internal/external standards.
  • Drive improvement projects using cross-functional feedback to reduce deviations/non-conformances.
  • Oversee GMP auditing program execution and other verification activities; ensure QA procedures and appropriate record maintenance.
  • Support Continuous Improvement and Quality Management System compliance; identify non-conformances and coordinate Quality/Food Safety risk analysis.
Experience / Qualifications
  • Bachelor’s degree (Engineering, Food Science, Chemistry, Microbiology) or equivalent food manufacturing quality experience.
  • 2+ years direct leadership experience.
  • Experience with pre-requisite programs, deviation report writing, and CAPA management.
  • Working knowledge of environmental monitoring.
  • Experience in a highly regulated manufacturing environment.
  • Working knowledge of cGMPs and FDA requirements.
  • Supervisory experience with a coaching mindset.
Skills
  • Excellent written/oral communication.
  • Knowledge of Microsoft Suite.
  • Working knowledge of pathogens and environmental monitoring.
  • Ability to prioritize/multi-task in a fast-paced environment.
  • People development, problem-solving, quick accurate decisions, and ability to lead cross-functional teams.
Benefits
  • Competitive compensation; benefits for you and your family; career development opportunities; “Total Rewards” (link referenced in posting).
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