Informazioni su Mozarc Medical

La visione di Mozarc Medical è quella di reimmaginare il futuro della tecnologia olistica per la salute dei reni.

Fondata nel 2023 grazie agli investimenti paritari di DaVita, fornitore leader di servizi per la cura dei reni, e di Medtronic, una delle più grandi aziende di dispositivi medici al mondo, Mozarc Medical offre un'esperienza di start-up unica ed entusiasmante, sostenuta dal supporto di due leader di lunga data del settore e del mercato.

Guidati dalla nostra missione e dai nostri valori, mettiamo i nostri pazienti al centro di tutto ciò che facciamo.

I nostri dipendenti svolgono un ruolo fondamentale nello sviluppo di soluzioni tecnologiche che arricchiscono la vita dei pazienti e creano progressi significativi nel trattamento delle malattie renali.

Trovate il vostro scopo e la vostra passione in Mozarc Medical.

You will be an individual contributor in the Quality Management System Team for the electronic management of the documentation of new products in development.

A Day in the Life

Responsibilities may also include the following and other duties may be assigned.

• Analyzes proposed changes of product design to determine effect on overall product and system.
• Coordinates modification records for management control.
• Establishes change orders and prepares for change authorization and documentation by company and subcontractor.
• Prepares reports of change effect on overall product.
• Reviews and analyzes released engineering change data and coordinates changes with engineering, quality, support, manufacturing, and engineering data control activities.
• Ensures that customer requirements are implemented and reviews change accounting activity to ensure compliance with configuration management policies.
• Effectively manage the end to end change lifecycle and identify process improvements where possible.
• Identification and allocation of relevant change approvals
• Conducting & verifying post implementation reviews, investigating issues arising out of change implementation
• Participate in internal & customer end to end user groups to improve the efficiency of future deliveries and business processes
• Drive continuous improvements to the quality and efficiency of the change management process
• Ensure operational teams adhere to Medtronic quality standards

Must Haves

• Bachelor's degree in engineering, science or technical discipline
• 2+ years of configuration assurance administration experience in the medical device industry or automotive industry using PLM system
• Fluent in English
• PC skills, MS Office (Word, Excel, Power Point)

Nice to Haves

• 2+ years of supplier quality engineering experience in the medical device industry delivering dialysis products
• Knowledge of Agile System
• SAP knowledge
• Experience of transfer from paper based production to electronical system
• Autonomy: Established and productive individual contributor. Works independently with general supervision on larger, moderately complex projects / assignments.
• Innovation and Complexity: Problems and issues faced are general, and may require understanding of broader set of issues or other job areas but typically are not complex. Makes adjustments or recommends enhancements in systems and processes to solve problems or improve effectiveness of job area.
• Communication and Influence: Communicates primarily and frequently with internal contacts. External interactions are less complex or problem solving in nature. Contacts others to share information, status, needs and issues in order to inform, gain input, and support decisionmaking

Why Work with Us?

Working here is highly rewarding - we have the privilege of helping kidney patients experience greater freedom, improved outcomes and a renewed passion for life.

It's essential our team members feel valued, supported and empowered too.

That's why we provide a comprehensive total rewards package and opportunities to grow, develop and give back to the communities where we live and work - helping you reach your potential and enjoy a career full of life-changing possibilities.

Physical Job Requirements

The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job.

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

For Office Roles:
While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers.

Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.

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