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Cook Group

Medical devices for minimally invasive care

Quality Engineering Specialist - Quality Engineering

Validation, Compliance & Quality SystemsPosted on Nov 9
Full-timeEllettsville, IN, USANo salary listedIn-person

About the Job

Requirements

  • One to two years of Quality Assurance or relevant experience.
  • Knowledge of medical device regulations, including pertinent standards.
  • Computer literacy and proficiency.
  • Ability to understand and comply with FDA 21 CFR 820, ISO 13485, and other applicable regulatory requirements.
  • Ability to adhere to safety requirements and maintain regular, punctual attendance.
  • Ability to maintain company quality and quantity standards.
  • Effective communication skills and ability to work collaboratively and independently with minimal supervision.
  • Ability to remain calm and receptive in fast-paced situations.

Responsibilities

  • Drive project improvement initiatives with minimal oversight.
  • Monitor and report project progress, delays, and completions, involving management at appropriate times.
  • Investigate quality issues.
  • Communicate with other departments to identify and troubleshoot project issues.
  • Provide feedback to management on areas for improvement from a systems and personnel standpoint.
  • Monitor and maintain processes critical to the CMLLC Quality Management System.
  • Participate in internal and external quality assessments and audits.
  • Independently produce, organize, and maintain documents or systems critical to the department.
  • Lead short-term, long-term, or system-forward projects.
  • Organize and participate in quality projects.
  • Maintain all training requirements for the position while seeking opportunities for continuous development and growth.
  • Adhere to the Quality Management System and its processes to meet FDA 21 CFR 820, ISO 13485, and other applicable regulatory requirements.
  • Work and interact effectively and professionally with others throughout various levels of the global organization.

Desired Qualifications

  • Experience in statistical and analytical reasoning.
  • CQA or similar certification.
  • A bachelor's degree in a technical field or equivalent experience.
  • Knowledge of Cook quality systems, associated documentation, and product lines.

About the Company

Cook Group

Medical devices for minimally invasive care

Cook Group manufactures medical devices focused on minimally invasive procedures. Its Cook Medical division develops and produces a broad portfolio—over 16,000 products—across cardiology, urology, gastroenterology, endoscopy, and vascular care. The company sells to hospitals and clinics worldwide, operating a B2B model in about 135 countries, with a European footprint centered in Ireland. As a family-owned business led by Carl Cook, it aims to support clinicians with reliable technologies and clinical support to expand alternatives to open surgery.

Company size
5,001-10,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Paris, France
Founded
1963

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