Regulatory Affairs

5 days ago

المملكة العربية السعودية, Saudi Arabia Radiometer Full time

**The family of Diagnostics companies at Danaher work with conviction that every moment matters and realize that behind every test is a patient, waiting for an answer that could change their life. Our 23,000 team members, across 6 operating companies globally, proudly push the boundaries of **what’s** possible in safeguarding patient health and improving diagnostic confidence. We develop tools and technologies that set the standard for innovation and impact wherever health care happens—from a family physician’s office to leading trauma hospitals and laboratories. Our teams collaborate in an inclusive environment as we connect our people, processes, and **expertise**, focused on the world’s biggest health challenges such as cardiac disease, infectious disease, and cancer. At **DH Diagnostics**,** **you’ll** thrive and quickly see the impact of your contribution.**:
**In this role, you will have the opportunity to**:

- ** Identifies information sources and resources for local regulations.**:

- ** Collects and coordinates information on regulatory requirements for in vitro diagnostic devices, quality, preclinical and clinical data to meet applicable regulations.**:

- ** Assist in device registration activities - agency communication; registration requirements; participation in submission document preparation.**:

- ** Maintain files on local, regional, and global regulatory intelligence and other related information.**:

- ** Generate regulatory reports to communicate local registration activities.**:

- ** Establish and review Regulatory Affairs priorities as they relate to department and company goals and objectives.**:

- ** Get along with RSA regulatory leaders and peers to expedite approval of pending registrations.**:

- ** Interact with departments to generate protocols and reports that require in-country testing data for registration purposes.**:

- ** Maintain a "focused vitality" as the need arises by specific events.**:

- ** Recognize problems, including situations that include ambiguity, by actively reviewing and analyzing internal and external factors.**:

- ** Prepare written reports, PowerPoint presentations, and documents for distribution within work unit and regions.**:

- ** Provide training and coordinate with department personnel from regulatory, quality, and manufacturing sites, Sales, and Marketing.**:

- ** Organizes and maintain RA files such as Responsibilities Matrix, Certificates from Notified Bodies, and other RA related material. Ensures that existing approvals and documentation are maintained.**:
**The essential requirements of the job include**:

- ** Good organizational skills with attention to detail and accuracy.**:

- ** Ability to work independently in a fast-paced environment with flexibility to manage changing priorities.**:

- ** Able to demonstrate a broad experience of manufacturing processes and equipment.**:

- ** Able to confidently deal with ambiguous issues and provide input towards suitable actions.**:

- ** Demonstrated excellence in communicating and presenting complex information to technical and non-technical partners.**:

- ** Proven ability to manage and prioritize multiple projects. Highly motivated, takes initiative, follow through, and complete projects in a professional and timely manner.**:

- ** IVD product experience is highly preferred.**:

- ** Prior knowledge of different databases like SAP, Sales Force, Tarius, Track wise etc. including Agile documentation system is a bonus.**:

- ** Understands Regulatory Affairs concepts and should be familiar with **regulations/guidelines** governing development of diagnostic products.**:

- ** Excellent oral and written communication and presentation skills. Proficient in Microsoft Word, Excel, PowerPoint, Outlook, and Adobe Acrobat.**:

- ** Bachelor’s degree with 7 years of related work experience.**:
**we believe in designing a better, more sustainable workforce**. **We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to **providing** enriching careers, no matter the work arrangement**. **This position is eligible for a hybrid work arrangement in which you can work part-time at the Company location **identified** above and part-time remotely from your home**. **Additional** information about this hybrid** **work arrangement will be provided by your interview team**.**:
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

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