Spec Clinical Product Surveillance

Under general supervision, the Clinical Product Surveillance Specialist is responsible for independently using knowledge of clinical workflows and product use when investigating post-market complaints and providing clinical resource support to internal and external customers. This role acts as a patient safety advocate and participates in various cross-functional activities that include, but are not limited to Complaint Handling, Risk Management, Design Quality, and Regulatory Compliance, to support product safety and efficacy and recommend improvements and/or corrections as needed.

• Identify and investigate domestic and international post‑market complaints with a potential safety issue and elevate complaints for further investigations as needed.
• Ensure adverse event reports (i.e. MDRs, ICSSRS) are processed, prepared, and submitted to the FDA within regulation timelines.
• Process FDA reportable post‑market complaints and assist in coordinating international adverse event reporting with local health authorities or authorized representatives.
• Collaborate with team members and act as a clinical resource for internal and external customers.
• Ensure communications are created and issued to internal and external customers.
• Review customer responses for technical and clinical accuracy as related to Medline products.
• Provide clinical insight, evaluation, and resolution during post‑market, risk management, and design development/modifications processes for new and existing Medline products.
• Participate in the analysis of safety and risk data within areas of responsibility and identify actionable findings, trends, or product safety issues that require further investigations.
• Assess clinical, health, and safety risks during Health Hazard Evaluations, product recall or field action determinations, and acceptance of product as‑is.
• Ensure compliance with applicable post‑market regulations for areas of responsibility and participate in regulatory audits, regulatory body communications, and/or additional information requests as applicable.
• Participate in process improvements and Corrective and Preventative Actions (CAPAs).
• Participate in the development and maintenance of processes/procedures associated with Adverse Event Reporting, Risk Management, and Standard Operating Procedures (SOPs) associated with Clinical Risk Evaluation.
• Facilitate clinical safety meetings and conduct trainings related to post‑market surveillance, clinical use, product risk, and SOP requirements.
• Maintain active Registered Nurse (RN) licensure and good standing with state or other governing licensure body.

• Education:
  
  Bachelor's Degree in Nursing (BSN)
• Certification / Licensure:
  Actively licensed as an RN to administer healthcare and in good standing with state or other governing licensure body.
• Work Experience:
  
  least 5 years of patient care experience OR a BSN with 4 years or less of patient care experience and 2 years of experience in a similar role.
• Knowledge / Skills / Abilities:
  Knowledge of quality improvement and patient safety.
• Knowledge / Skills / Abilities:
  Understanding of clinical standards, processes, and workflows.
• Knowledge / Skills / Abilities:
  Familiarity with medical devices and pharmaceuticals related to patient safety.
• Knowledge / Skills / Abilities:
  Ability to assess clinical outcomes, analyze data, and present findings to various audiences.
• Knowledge / Skills / Abilities:
  Proficiency in Microsoft Office (Outlook, Teams, Excel, Word, PowerPoint).
• Knowledge / Skills / Abilities:
  Strong work ethic and proactive approach to responsibilities.
• Knowledge / Skills / Abilities:
  Customer-focused with a results-oriented mindset.
• Knowledge / Skills / Abilities:
  Ability to make sound…