Entry Level Post Market Surveillance Medical Device Jobs

... Complaints, Medical Device Reporting, Adverse Event Reporting, Corrections and Removals (Recall ... Post Market Surveillance processes for products and ensure effective execution into the Quality ...

... Complaints, Medical Device Reporting, Adverse Event Reporting, Corrections and Removals (Recall ... Post Market Surveillance processes for products and ensure effective execution into the Quality ...

... Complaints, Medical Device Reporting, Adverse Event Reporting, Corrections and Removals (Recall ... Post Market Surveillance processes for products and ensure effective execution into the Quality ...

Experience submitting Medical Device Reports (MDRs) and/or adverse event reports to regulatory agencies. * Experience with post-market surveillance activities in accordance with IVDR regulations ...

Assists with the preparing and submitting post market surveillance reporting including but not limited to Medical Device Reports and Adverse Events to the FDA within regulatory timeframes. * Assists ...

Preferred * 1 year of post-market surveillance, quality, regulatory affairs, clinical, or related experience within a regulated industry. * Experience within the medical device industry. * Prior ...

The Product Surveillance Analyst supports post-market surveillance activities through the ... Experience in the medical device, pharmaceutical, biotechnology, or regulated manufacturing ...

Support medical device surveillance and post-market vigilance activities. * Maintain knowledge of new products, regulations, and reporting requirements. * Support continuous improvement of complaint ...

... Entry-level medical device safety and complaint investigation role responsible for intake ... Vigilance & Post-Market Surveillance * Complaint Investigation * Adverse Event Reporting (ADE)

The Data Engineer Lead - PMS & QA leads data analysis, visualization, and reporting of Medical Device performance and Post Market Surveillance activities within the PMS team as well as the broader QA ...

Supervises Post-Market Surveillance Specialists by interviewing, training, evaluating job ... Knowledge of medical product/device use. COMPETENCIES * Interpersonal skills * Written and verbal ...

... Post Market Surveillance processes for Integer under the direction, instruction and guidance from ... medical device or other regulated industry experience preferred). Specialized Knowledge: * While ...

This role also supports Post-Market Surveillance (PMS) activities and works closely with cross ... Make reportability determinations and submit Medical Device Reports (MDRs) as required. * Conduct ...

The Regulatory Post Market Surveillance Specialist investigates customer complaints, makes an ... Knowledge and understanding with Medical Device Complaint files and quality record documentation ...

Experience with complaint handling, adverse event reporting, post-market surveillance, or quality systems. * Knowledge of FDA Medical Device Reporting requirements (21 CFR Part 803), complaint ...

Experience with complaint handling, adverse event reporting, post-market surveillance, or quality systems. * Knowledge of FDA Medical Device Reporting requirements (21 CFR Part 803), complaint ...

Supervises Post-Market Surveillance Specialists by interviewing, training, evaluating job ... Knowledge of medical product/device use. COMPETENCIES * Interpersonal skills * Written and verbal ...

... Post Market Surveillance processes for Integer under the direction, instruction and guidance from ... medical device or other regulated industry experience preferred). Specialized Knowledge: * While ...

... Post Market Surveillance processes for Integer under the direction, instruction and guidance from ... medical device or other regulated industry experience preferred). Specialized Knowledge: * While ...

... Post Market Surveillance activities and other governmental inspections as directed. 9. Performs ... COMPETENCIES • Global medical device adverse event reporting, such as MDR, MPR, TGA, and ...