C

Cretex Companies

Diversified industrial conglomerate with manufacturing

Quality Systems Specialist

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

About the Job

Requirements

  • A bachelor's degree in a related field or equivalent relevant experience.
  • Three years of experience working with quality management systems.
  • Experience with ISO 13485:2016 and FDA requirements.
  • Lead Auditor Certification.
  • Ability to achieve short- and long-term business results.
  • Ability to prioritize work and manage multiple tasks.
  • Ability to follow through on commitments and hold team members accountable.
  • Ability to produce work that meets customer requirements.
  • Focus on operational excellence.
  • Project management skills.
  • Proficiency in Microsoft Office, including Outlook, Word, Excel, PowerPoint, and Publisher.
  • Clear and effective verbal and written communication skills.
  • Attention to detail.
  • Organizational skills.
  • Ability to work in a fast-paced team environment.
  • Ability to work in a manufacturing environment.
  • Ability to travel up to 15%.

Responsibilities

  • Assist or lead second- and third-party audits, including audit preparation, execution, reporting, and follow-up activities.
  • Manage or lead internal audits, including implementation of effective corrective actions.
  • Perform process and product audits to identify gaps and deficiencies, and implement process improvement initiatives using lean techniques.
  • Assist in maintaining a Global Quality System model that scales with organizational growth.
  • Implement, monitor, lead, and assist Corrective and Preventive Actions (CAPAs) resulting from second-party, third-party, and internal audits.
  • Assist in maintaining relevant quality management system training programs to promote quality awareness and ensure compliance with company policies and procedures.
  • Partner with quality and operations to implement quality system improvements.
  • Support and comply with the company Quality System, ISO, and medical device requirements.
  • Read, understand, and follow work instructions and standard work.
  • Partner with other business segments, including sales and marketing, customer service, engineering, quality, and finance.
  • Understand customer needs and the core business markets served.
  • Ensure business systems are implemented, maintained, and functioning properly.
  • Participate in required company meetings.
  • Maintain an organized work area using 5S.
  • Participate in the Operational Excellence Program.
  • Complete other work duties as assigned.

Desired Qualifications

  • Quality systems experience in a manufacturing setting.
  • Continuing education, including participation in local chapters, associations, or organizations.

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

Recently Posted Jobs

Explore more opportunities at Cretex Companies

See more jobs