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Regulatory Affairs Intelligence Project Manager

Job in 33038, San Daniele del Friuli, Friuli-Venezia Giulia, Italy
Listing for: Enovis Corp
Full Time position
Listed on 2026-01-13
Job specializations:
  • Management
    Healthcare Management
  • Healthcare
    Healthcare Management
Job Description & How to Apply Below
Location: San Daniele del Friuli

Regulatory Affairs Intelligence Project Manager page is loaded## Regulatory Affairs Intelligence Project Manager locations:
San Daniele del Friuli, Friuli Venezia-Giulia, Italytime type:
Full time posted on:
Posted Todayjob requisition :
R0031630
** Chi siamo
**** ENOVIS
* * Enovis Corporation (NYSE: ENOV) è un'azienda in crescita nel settore delle tecnologie mediche orientata all'innovazione e dedicata allo sviluppo di soluzioni clinicamente differenziate che migliorano in modo misurabile i risultati dei pazienti e trasformano i flussi di lavoro. Grazie a una cultura del miglioramento continuo, al talento globale e all'innovazione, l'ampia gamma di prodotti, servizi e tecnologie integrate dell'azienda alimenta stili di vita attivi in ortopedia e non solo.

Per ulteriori informazioni su Enovis, visitare il sito  
** Who We Are
**** ABOUT ENOVIS
** Enovis Corporation (NYSE: ENOV) is an innovation-driven medical technology growth company dedicated to developing clinically differentiated solutions that generate measurably better patient outcomes and transform workflows. Powered by a culture of continuous improvement, global talent and innovation, the Company’s extensive range of products, services and integrated technologies fuels active lifestyles in orthopedics and beyond. For more information about Enovis, please visit .
** Di cosa ti occuperai | What You'll Do
** At Enovis we sweat the little things. We embrace collaboration with our partners and patients, and we glory in the grind of scientific excellence — with the goal of transforming medical technology as we know it.

Because that’s how we change the lives of patients for the better. And that’s how we create better together.

As a key member, employees will play an integral part in helping Enovis drive the medical technology industry forward through transforming patient care and creating better patient outcomes.
** Job Title**:

Regulatory Affairs Intelligence Project Manager
** Reports To**:

VP RA, Recon and/or Dir/ Sr. Dir. RA
*
* Location:

** San Daniele del Friuli (UD) - Italy
** Business Unit(s) Description**:

Recon Corporate
** Job Title/High Level Position Summary**:  This Regulatory Affairs (RA) Intelligence Project Manager is responsible for developing, facilitating and overseeing the process for managing standards and regulations impacting Recon business units (BUs). This role will establish and maintain a process by which the business remains compliant to external influences (medical device standards and regulations) through pro-active monitoring and critical assessments, orchestrate subject matter experts (SME) to determine, document and implement necessary changes to the QMS/processes/practices within impacted BUs.

This role must communicate changes in regulatory/standards environments affecting the development, approval, and lifecycle management of Enovis Recon medical devices.
*
* Essential Duties and Responsibilities:

*** Primarily responsible for the establishment and maintenance of a process which will ensure Recon BUs remain in steady compliance to external influences. This process must comprehensively evaluate the impact of Regulations and Standards developments on Enovis’s current and future medical devices (pipeline and established marketed products).
* Monitor, react and interpret global regulatory developments, guidance documents, and policy changes from agencies such as FDA, EU MDR, TGA, Health Canada, ANVISA and other international regulators.
* Convene relevant SMEs to analyze the impact of regulation and standards & make interpretations of how best to comply to both statutory requirements as well as consensus Standards developments (such as ISO, EN or standards issued by ANSI, ASTM, ASME, etc.)
* Collaborate with SMEs to document gap analyses and implement required changes with the QMS to ensure Enovis current and future medical device products remain compliant to state-of-the-art requirements.
* Broaden awareness of external impacts to the global business.
* Analyze and synthesize the Regulatory Intelligence for reporting during periodic business reviews.
* Provide strategic regulatory guidance during all phases of product development,…
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