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Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose.
Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege.
Our Sales teams help to deliver Reckitt's purpose by building shared success with our customers, making access to the highest quality hygiene, wellness, and nourishment possible in-stores and online.
Within Sales, we're focused on achieving outperformance across all of our channels, operating in highly competitive categories. This focus results in a dynamic, fast paced environment where cross functional teams are encouraged to collaborate to achieve success.
We have around 10,000 sales people across the world, within market roles and ranging in areas like Field Sales, Key Accounts, Trade Marketing and Category Development.
About the role
Working with customers in the medical and pharmaceutical fields, youll take ownership for your own area of the business. Managing your own territory, youll design and implement medical marketing strategies. Youll build trust and relationships. Youll educate doctors, medical and pharmaceutical specialists to understand the benefits of our products. Ultimately helping to improve the lives of millions of patients.
Your responsibilities
Responsibility for a defined customer line in the southern region
Responsibility for meeting sales targets
Treatment of the availability and visibility of products on the shelf

The Regulatory Affairs Specialist provides regulatory guidance for business unit product lines. The Regulatory Affairs Specialist works directly with cross functional teams to support global product market clearances .

Your role:
Act as the Regulatory Affairs representative for CT/AMI products, supporting regulatory activities such as labeling, marketing, technical documentation, global registrations, and regulatory design change assessments within the product Development Life Cycle.
Provide regulatory guidance to cross-functional teams throughout all design control phases for new products and major/minor changes.
Coordinate and prepare document packages to support global submissions and regulatory activities.
Support regulatory audits and compliance activities.
Serve as the local regulatory liaison between markets and the BIU site.
Maintain Product Shipment Authorization for CT/AMI product lines, ensuring compliance with localization and licensing requirements

we are looking for a Regulatory Affairs Specialist
What you will be doing:

Provide regulatory support to the Development and Post marketing activities related to INSIGHTEC products.
Preparation and maintenance of regulatory submissions and registrations of INSIGHTEC products in relevant markets.
Review complex reports, validations, etc. for scientific merit and regulatory appropriateness; Provide technical review of data or reports that will be incorporated into regulatory submissions to assure scientific rigor, accuracy, and clarity of presentation
Preparation and maintenance of annual renewals of Establishment Registrations, Device Listing, and other pertinent regulatory licenses.
Review of customer complaints to determine reportability according to regulatory requirements and execution of reporting per determination.
Provide ongoing regulatory support and assessments to different QMS related processes (e.g. MRB, CAPA, Contract review)
Actively participate in the evaluation of changes to the INSIGHTECs QMS documents and device design/process for impact on pending or existing registrations
Provide support for all external/internal audits at HQ and globally, as needed
Advise project teams on premarket regulatory requirements, labeling requirements and/or other compliance issues.
Work closely with various other INSIGHTEC teams (e.g. R&D, Operations, Quality, Marketing) both locally and around the world, to provide regulatory inputs as needed.
Monitor and advise the organization of upcoming or new guidance, regulations, agency/industry initiatives, etc. to ensure ongoing regulatory compliance
Attend other regulatory related needs, as required
Working according to Insightec Quality Policy, relevant Quality Procedures & Standards, and privacy & safety rules.

we are looking for a Software Student (as an outsource employee)
What you will be doing

You will be taking part of developing the heart of the SW in Insightec products
You will experience in software development Python & C/C++.
Examine full development of project including DevOps processes
Be part of developing for a top medical company with high impact on people day life
Experience in working with hardware/Embedded systems (eg. Raspberry pi, Arduino)
Communicative, self-motivated, and self-learning.
Working according to Insightec Quality Policy, relevant Quality Procedures & Standards, and privacy & safety rules.
Work in an Agile environment