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Cook Group

Medical devices for minimally invasive care

Quality and Regulatory Specialist

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timePoway, CA, USA$38 - $42 /hr

About the Job

Requirements

  • An associate degree in Quality, Engineering Technology, Manufacturing Technology, Industrial Technology, Science, or a related field is required; relevant manufacturing quality experience may substitute for the degree.
  • At least three years of experience in a manufacturing or quality environment.
  • Working knowledge of quality systems and quality principles.
  • General understanding of customer complaints, corrective and preventive action (CAPA), root cause investigation, auditing, document control, calibration, and validation.
  • Proficiency with Microsoft Word, Excel, PowerPoint, and Outlook.
  • Ability to lift up to 10 pounds and perform light physical effort, including regularly sitting or standing, reaching, and moving about the facility.
  • Ability to use task-dependent personal safety equipment, which may include safety goggles, ear protection, a full-face shield, an apron, arm guards, rubber boots, and gloves.

Responsibilities

  • Review customer complaints and return authorization requests to determine appropriate handling and escalation, communicate with customers and internal stakeholders, and coordinate complaint activities through closure.
  • Coordinate investigations, corrective actions, responses, and supporting documentation; track progress, commitments, and due dates to support timely resolution.
  • Support root cause investigations and continuous improvement activities.
  • Review customer surveys, quality agreements, and regulatory requests to determine appropriate handling, required information, and escalation needs.
  • Prepare responses within established guidelines and coordinate input from internal stakeholders to support timely and accurate customer communications.
  • Coordinate production part approval processes (PPAPs), first article documentation, certifications, and related customer submissions.
  • Maintain and review customer quality and regulatory records to support compliance and customer requirements.
  • Coordinate Quality Management System review activities, including management reviews and quality meetings; gather information from multiple departments and track action items and commitments through completion.
  • Maintain controlled quality records and coordinate document review and approval activities.
  • Coordinate internal, customer, and certification audits; review supporting documentation, work with process owners to address audit requests, and track findings and corrective actions through closure.
  • Schedule, coordinate, and document calibration activities with internal and external parties; review calibration status and track overdue activities to ensure equipment remains in calibration.
  • Support validation, investigation, risk assessment, and quality improvement projects.
  • Review drawings, specifications, and quality data to support assigned activities.
  • Develop technical expertise in company products, materials, manufacturing processes, and quality systems.
  • Provide backup support for designated Quality Engineer responsibilities as experience and training permit.
  • Provide backup inspection support during absences, workload fluctuations, or investigations.
  • Maintain working knowledge of inspection methods and quality requirements.

Desired Qualifications

  • Approachability and inquisitiveness, and the ability to relate well to people with varied backgrounds.
  • Good written and spoken communication skills.
  • Ability to thrive in a fast-paced environment while managing multiple projects and assignments simultaneously.

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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