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Cretex Companies

Diversified industrial conglomerate with manufacturing

Quality Systems Engineer

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeBrooklyn Park, MN, USA

About the Job

Requirements

  • A bachelor's degree in Computer Science, Software Engineering, Programming, or a related STEM certified program.
  • At least five years of experience working with quality management systems in a regulated environment, including ISO 13485, EUMDR, or FDA requirements.
  • Knowledge of quality systems, regulatory requirements, and industry standards.
  • Academic experience with business intelligence software tools.
  • Proficiency with Microsoft Outlook, Word, Excel, PowerPoint, and Publisher.
  • Ability to work in a manufacturing environment.
  • Ability to travel up to 15%.

Responsibilities

  • Identify, develop, and maintain quality management system programs that promote quality awareness and ensure compliance with company policies and procedures, including engineering and document changes, corrective and preventive action, standards library administration, internal audit management, customer audit management, regulatory audit management, and quality system and regulatory training management.
  • Lead internal, external, and supplier audits, including preparation, execution, reporting, and follow-up.
  • Manage the internal audit program, from selecting and training the internal audit group through implementing effective corrective actions.
  • Assist in defining and continuously improving quality system business processes that comply with ISO 9001, ISO 13485, and/or FDA Quality System Regulation requirements.
  • Participate in internal audits associated with ISO 9001, ISO 13485, and/or FDA Quality System Regulation standards.
  • Write and revise technical procedure and policy content within the scope of the quality system.
  • Analyze data and identify improvement opportunities.
  • Support audit activities, including closing audit findings, creating finding reports, and collaborating to determine appropriate corrective and preventive actions.
  • Implement, monitor, lead, and assist corrective and preventive actions resulting from second-party, third-party, and internal audits.
  • Contribute technically to business intelligence reporting and dashboard design and validation, enterprise business workflow design and administration, and quality system business-process automation through software-based systems.
  • Ensure business systems are supported, maintained, and functioning according to defined requirements.
  • Support and comply with the company quality system, ISO standards, and medical device requirements.
  • Read, understand, and follow work instructions and standard work.
  • Participate in required company meetings.
  • Maintain an organized work area using 5S.
  • Participate in the Operational Excellence Program.
  • Complete other assigned work duties.

About the Company

Cretex Companies

Diversified industrial conglomerate with manufacturing

Cretex Companies designs, manufactures, and supplies products across medical devices, materials, and engineered components through its divisions like Cretex Medical, Cretex Materials, and Cretex Specialty Products. Its products use specialized engineering and manufacturing to create components for healthcare, industrial, and consumer applications, often supporting customers from design through production. The company differentiates itself with a century-long history, a commitment to honesty and integrity, a diversified, vertically integrated portfolio, and a strong financial position that supports long-term planning. Its goal is to provide meaningful work for employees while delivering reliable products and services to customers today and building lasting growth.

Company size
51-200
Company stage
Not listed
Total funding
Not listed
Headquarters
Elk River, MN
Founded
1917

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