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Baxter International

Global provider of medical care products

Quality Associate 1

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeCleveland, MS, USA

About the Job

Requirements

  • A bachelor's degree in Microbiology, Biology, Chemistry, or Engineering is required.
  • Good knowledge of quality systems and procedures.
  • Ability to make independent decisions regarding product conformance and handle issues as they arise.
  • Ability to communicate effectively in written and verbal form.
  • Ability to manage and prioritize multiple tasks and projects.
  • Ability to perform tasks independently with minimum supervision.
  • Ability to sit, stand, and/or walk for long periods of time; reach above the shoulder; bend or stoop; and meet the visual acuity requirements documented in Baxter Cleveland Human Resources Procedure 1.04.
  • Knowledge of plant and department environmental health and safety regulations and compliance with those regulations.
  • Applicants must be authorized to work for any employer in the United States.

Responsibilities

  • Provide quality supervisory oversight for the Solution areas.
  • Implement, maintain, and improve quality systems, processes, and procedures in the Solution departments.
  • Manage and support area technicians, assuring a teamwork environment.
  • Oversee training and cross-training of technicians.
  • Train and integrate new associates.
  • Support process validation, process capability, and process control studies for assigned areas.
  • Perform customer complaint investigations, including defect and failure analysis, on products as required.
  • Conduct nonconformance investigations and implement corrective actions for product or process defects or failures.
  • Trend key quality performance metrics for the Solution departments.
  • Communicate shift activities and occurrences clearly and in an organized manner to appropriate personnel.
  • Interface with other plant functions and global functions.
  • Support quality and manufacturing projects using Lean, problem-solving, process-control, and project-management tools to achieve and sustain operational excellence.
  • Maintain working knowledge of plant systems, processes, procedures, documentation, and products.
  • Evaluate changes to systems and ensure they are appropriately assessed and executed in accordance with Baxter procedures.
  • Benchmark new technologies and methodologies for facility use.
  • Travel as needed to perform duties.
  • Occasionally carry out duties of the Quality Manager as needed.
  • Perform other duties and responsibilities as determined by supervision or management.
  • Interview, hire, and train employees; plan, assign, and direct work; appraise performance; reward and discipline employees; and resolve problems.

Desired Qualifications

  • Experience in FDA manufacturing is preferred.
  • Six Sigma Green Belt Certification or an industry-standard equivalent is preferred.
  • Lean Manufacturing skills and experience are preferred.

About the Company

Baxter International

Global provider of medical care products

Baxter International develops and manufactures medical products and equipment for hospitals and blood banks. Its products include sterile IV solutions and blood storage containers; innovations like the Transfuso-Vac extended blood shelf life, and a plastic blood bag helped shape modern blood banking. The company differs from competitors through a long track record of sterile manufacturing, blood-storage innovations, and strategic mergers that broaden its product portfolio. Its goal is to provide reliable, safe medical products that support patient care and hospital operations worldwide.

Company size
10,001+
Company stage
IPO
Headquarters
Deerfield, IL
Founded
1931

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