Quality Assurance Coordinator

1 week ago

Louisville, Kentucky, United States Zeochem LLC Full time
Quality Systems Coordinator Job Description

Zeochem LLC is seeking a highly skilled Quality Systems Coordinator to oversee the quality assurance program for its chemical manufacturing facility located in Louisville, KY.

Key Responsibilities:
  • Maintain and implement quality assurance processes and procedures for site quality systems
  • Lead local Quality Improvement Team (QIT) meetings and implement local Continuous Improvement Process program
  • Draft quality assurance policies and procedures, interpret and implement quality assurance standards and procedures, and evaluate adequacy of quality assurance standards
  • Document internal audits and other quality assurance activities, investigate customer complaints and non-conformance issues, and ensure customer resolution
  • Maintain Safety Data Sheet system and monitor for compliance to all applicable regulations for adsorbent product lines
  • Analyze data to identify areas for improvement in the quality system, develop, recommend, and monitor corrective and preventive actions, and prepare reports to communicate outcomes of quality activities
  • Identify training needs and organize training interventions to meet quality standards, coordinate and support on-site audits conducted by external providers, and evaluate audit findings and implement appropriate corrective actions
  • Monitor risk management activities, responsible for document management systems, including contracts, and assure ongoing compliance with quality and industry regulatory requirements
Requirements:
  • Bachelor's degree preferred
  • 5+ years' experience in Quality Assurance
  • Certified ISO auditor preferred
  • Certifications including Quality Auditor, Quality Engineer, Quality Improvement Associate, or Six Sigma preferred
  • Quality inspection, auditing, and testing experience, strong computer skills including Microsoft Office, QA applications and databases
  • Proven experience managing projects and ability to meet deadlines, strong written, communications, and interpersonal relationship skills, and ability to present data and presentations across multiple levels
  • Strong Organization Skills, experience with implementation of corrective action programs, molecular Sieve or industry related experience desired, knowledge of tools, concepts, and methodologies of QA, and knowledge of relevant regulatory requirements
Physical Demands:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this job, the employee is regularly required to stand; walk; sit; use hands to finger, handle, or feel; reach with hands and arms; talk or hear; and taste or smell. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision.

Work Environment:

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts, fumes or airborne particles, and toxic or caustic chemicals. The noise level in the work environment is usually quiet.

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