Post Market Surveillance Specialist at Intuitive in Sunnyvale, California

Posted in Other 10 days ago.





Job Description:

Company Description

At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints.



As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a difference. For more than 25 years, we have worked with hospitals and care teams around the world to help solve some of healthcare's hardest challenges and advance what is possible.



Intuitive has been built by the efforts of great people from diverse backgrounds. We believe great ideas can come from anywhere. We strive to foster an inclusive culture built around diversity of thought and mutual respect. We lead with inclusion and empower our team members to do their best work as their most authentic selves.



Passionate people who want to make a difference drive our culture. Our team members are grounded in integrity, have a strong capacity to learn, the energy to get things done, and bring diverse, real world experiences to help us think in new ways. We actively invest in our team members to support their long-term growth so they can continue to advance our mission and achieve their highest potential.



Join a team committed to taking big leaps forward for a global community of healthcare professionals and their patients. Together, let's advance the world of minimally invasive care.

Job Description




Primary Function of Position:



The Regulatory Post Market Surveillance Specialist investigates customer complaints, makes an initial reporting decision, provides failure analysis letters, and ensures completeness and consistency of complaint and related documentation.




Roles and Responsibilities:




This position has responsibility and authority for:



  • Investigating complaints daily:

    • Perform the preliminary classification of complaints and escalate complaints that require additional review.

    • Perform Failure Analysis investigation review and escalate complaints that require additional review.

    • File Malfunction MDR Reports as identified

    • Escalate Adverse Event or Incident reports to Level IV Analysts as identified

    • Evaluate documentation for completeness and consistency, and assign additional actions as necessary to close the complaint file.

    • Approve final complaint file for closure after all applicable actions are completed.

    • Manage complaint workload to required backlog goals.

    • Review and analyze lot documentation (DHRs) to determine if there are any anomalies that maybe related to reported product failures.



  • Escalate complaints to the Regulatory Post Market Surveillance Manager or Lead when new failure modes are encountered

  • Escalate complaints to the Post Market Investigation (PMI) group as required

  • Evaluate complaints for reporting requirements in accordance with company procedures and Regulatory requirements.

  • Interface with Customer Service and hospitals to gather additional information required for complaint investigation, including retrieval of RMA

  • Create customer response letters

  • Provide peer review and feedback of complaints and reports

  • Participate in new hire training and continuous Regulatory Compliance training as required

  • Participate in process improvement activities to continuously improve process effectiveness

  • Execute on projects as required

  • Perform other duties as directed


Qualifications




Skills and Job Requirements:





Education - Minimum Undergraduate degree in engineering, life science, or equivalent



Experience -Minimum 2+ years of experience in medical device field, with experience or exposure in the following areas:


· Knowledge and understanding with Medical Device Complaint files and quality record documentation


· Knowledge and understanding of Regulatory reporting requirements for Medical Devices (US FDA requirements, EU MDD requirements, etc.)


· General technical and or clinical medical device knowledge



Skills: The following skills are required for this position:



  • Demonstrate strong written and verbal communication skills

  • Strong computer skills (Excel, Word, PowerPoint, database)

  • Efficient independent worker with ability to focus

  • Attention to detail

  • Demonstrate cross functional communication skills in email and in person

  • Excellent organizational and analytical skills

  • Ability to handle and manage workload independently

  • Prioritize numerous activities in a rapid paced environment

  • Contribute to team oriented tasks

  • Strong analytical skills

  • Strong interpersonal and decision making skills.




Competency / Training: The following competencies are essential for this position:



  • General understanding of Regulatory reporting requirements for Medical Devices and complaint system and process requirements.

  • General understanding of quality records requirements and how they apply to complaint files.


Able to make decisions quickly using information at hand and evaluate the need to obtain clarification and direction when necessary


Additional Information

Due to the nature of our business and the role, please note that Intuitive and/or your customer(s) may require that you show current proof of vaccination against certain diseases including COVID-19. Details can vary by role.


Intuitive is an Equal Employment Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees, and prohibit discrimination and harassment of any type, without regard to race, sex, pregnancy, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, genetic information or any other status protected under federal, state, or local applicable laws.


We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws.



Shift : Day



Travel : None

Travel Requirements:None Shift:Day
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