Quality Systems Specialist II

Posted 7 Days Ago
Be an Early Applicant
Avondale, PA, USA
In-Office
Mid level
Healthtech • Manufacturing
The Role
Lead and conduct complaint investigations, return material evaluations, root cause analyses, and CAPA activities. Perform risk assessments, trend analysis, and cross-functional coordination to implement corrective actions and improve the Quality Management System. Mentor junior staff and support continuous improvement initiatives.
Summary Generated by Built In

The Quality Systems Specialist II independently conducts complaint investigations, return material evaluations, root cause analysis activities, and corrective and preventive action processes to support the effectiveness of the Quality Management System.

This role serves as a primary investigator for routine to moderately complex quality issues and works cross-functionally to identify root causes, evaluate risk, implement corrective actions, and improve organizational performance.

The Quality Systems Specialist II applies risk-based decision making and structured problem-solving methodologies to ensure quality issues are effectively addressed and opportunities for improvement are identified.

Essential Responsibilities

Complaint, Investigation & CAPA Management

  • Lead complaint evaluations and investigations.
  • Conduct return material evaluations and associated investigations.
  • Facilitate root cause analysis activities.
  • Develop corrective and preventive action recommendations.
  • Evaluate investigation effectiveness and closure readiness.
  • Ensure investigations are timely, thorough, evidence-based, and compliant.

Risk Assessment & Decision Support

  • Perform risk assessments associated with complaints, investigations, and quality issues.
  • Support stakeholders in evaluating quality-related risks.
  • Facilitate balanced decision-making based on available evidence.
  • Escalate significant issues appropriately.

Trend Analysis & Continuous Improvement

  • Analyze complaint, investigation, and CAPA data for emerging trends.
  • Identify systemic issues requiring additional investigation or action.
  • Recommend process improvements based on quality system performance.
  • Support management system effectiveness initiatives.

 Cross-Functional Leadership

  • Coordinate investigations involving multiple departments.
  • Facilitate investigation meetings and action planning activities.
  • Partner with Engineering, Manufacturing, Regulatory Affairs, Customer Care, and other stakeholders.
  • Serve as a resource regarding investigation methodologies and quality system processes.

Coaching & Mentorship

  • Provide guidance to Quality Systems Specialist I personnel.
  • Support development of investigation and problem-solving skills within the organization.
  • Share best practices and lessons learned.

Knowledge, Skills & Abilities

Required

  • Strong understanding of complaint handling and investigation processes.
  • Strong root cause analysis and problem-solving skills.
  • Ability to independently manage multiple investigations.
  • Strong analytical and decision-making capabilities.
  • Effective facilitation and communication skills.
  • Ability to influence stakeholders without direct authority.

Preferred

  • Experience with risk management methodologies.
  • Experience facilitating cross-functional investigations.
  • Experience in medical device or regulated industries.

Education & Experience

Required

  • Bachelor's degree or equivalent experience in Quality, Engineering, Manufacturing, Life Sciences, Business, or related discipline.
  • Minimum 3 years of relevant experience.

Preferred

  • ASQ certification or equivalent professional credentials.
  • Medical device or other regulated industry experience.

Medical, Dental, and Vision coverage starts on Day One! 
Free life insurance, short and long-term disability insurance, Telehealth Appointments, and Employee Assistance Program. Immediate vesting of 401(k) matching. Generous PTO and 11 Paid Holidays a year.  And, most importantly...truly meaningful work!

Would you like to make a difference in the lives of cancer patients and their families? We design and manufacture radiation oncology medical devices to ensure more accurate, comfortable treatment for cancer patients.  CQ Medical is the global market leader in patient positioning.  As an innovative medical device company, we focus on discovering, developing, and distributing technology-driven solutions to improve outcomes for radiotherapy patient positioning.

We are continuing to grow and expand our products.   Join us and earn a Paycheck with a Purpose.   www.cqmedical.com

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

Skills Required

  • Bachelor's degree or equivalent experience in Quality, Engineering, Manufacturing, Life Sciences, Business, or related discipline
  • Minimum 3 years of relevant experience
  • Strong understanding of complaint handling and investigation processes
  • Strong root cause analysis and problem-solving skills
  • Ability to independently manage multiple investigations
  • Strong analytical and decision-making capabilities
  • Effective facilitation and communication skills
  • Ability to influence stakeholders without direct authority
  • Experience with risk management methodologies
  • Experience facilitating cross-functional investigations
  • Experience in medical device or regulated industries
  • ASQ certification or equivalent professional credentials
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The Company
HQ: Orange City, IA
137 Employees
Year Founded: 1982

What We Do

CQ Medical is the global leader in patient radiotherapy positioning and healthcare innovations that advance human care. Our products uniquely combine medical technology with empathy for the patient. To our way of thinking, that’s the better way to achieve better outcomes.

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