Regulatory Affairs Manager, Hospital Patient

Job TitleRegulatory Affairs Manager, Hospital Patient Monitoring METAJob DescriptionJob title:Main point of contact between BU, Market and Local Business Team for product registration preparation and renewals.You are responsible for Create regulatory awareness level as determined within the organization. Supports implementation of simplified yet robust...

In our line of work, life isn't a given - it's the ultimate goal. When life takes an unexpected turn, our technology and solutions enable caregivers to make informed diagnostic decisions to improve patient care. This is our shared purpose at Radiometer and what unites all +4000 of us - no matter our roles or where in the world we're located. Creating...

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our...

**Regulatory Affairs Manager**: - **Job Summary** Tasks and Responsibilities - contributing to the organization’s strategic plan and annual plans, in areas such as quality and risk management, regarding registration matters; - writing and periodically updating drug regulatory affairs (DRA)-related local SOPs; - reviewing draft registration files and...

About Dexcom Founded in 1999, Dexcom, Inc. (NASDAQ: DXCM), develops and markets Continuous Glucose Monitoring (CGM) systems for ambulatory use by people with diabetes and by healthcare providers for the treatment of people with diabetes. The company is the leader in transforming diabetes care and management by providing CGM technology to help patients and...

Regulatory Affairs Manager:- Job SummaryTasks and Responsibilities- contributing to the organization's strategic plan and annual plans, in areas such as quality and risk management, regarding registration matters;- writing and periodically updating drug regulatory affairs (DRA)-related local SOPs;- reviewing draft registration files and submitting new and...

In our line of work, life isn’t a given - it’s the ultimate goal. When life takes an unexpected turn, our technology and solutions enable caregivers to make informed diagnostic decisions to improve patient care. This is our shared purpose at Radiometer and what unites all +4000 of us - no matter our roles or where in the world we’re located. Creating...

About DexcomFounded in 1999, Dexcom, Inc (NASDAQ: DXCM), develops and markets Continuous Glucose Monitoring (CGM) systems for ambulatory use by people with diabetes and by healthcare providers for the treatment of people with diabetes. The company is the leader in transforming diabetes care and management by providing CGM technology to help patients and...

About AbbottAbbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future, anticipating changes in medical science and technology.Working at AbbottAt Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life.You will...

**About Abbott** Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. **Working at Abbott** At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full...

REGULATORY AFFAIRS EXPERIENCED Coordinate with project lead and stakeholders to assess and define projects scope, requirements and timelines for proper planning and execution. Act as a point of contact and communicate project status with countries. Coordinate with Logistics/ Supply Chain/ Labeling teams and manufacturing site to obtain valid artworks and...

We are looking to hire Regulatory Affairs Specialist to be a part of our Regulatory Affairs team.Requirements:2-3 years' experience in pharmaceuticals registration is mandatoryFood Supplements and medical devices are added benefit.Aware of SFDA Requirements and regulation.Excellent organizational and presentation skills.Proactive and Punctual.Location:...

Regulatory Affairs Coordinator - Tamheer Program:Remote Eligible: HybridOnsite Location(s): Riyadh, SAWork Location : Riyadh, Saudi ArabiaKey Responsibilities: Give support on regulatoryrelated issues associated with compliance and achieving the business plan. Will be introduced to product registration planning and prioritization for his/her respective...

To coordinate regulatory activities throughout the regulatory life cycle by carrying out project specific tasks related to writing and collecting submission documents from cross functional departments to ensure an efficient preparation of submissions that comply with latest regulations and within the defined timelines. **Description**: Follows all relevant...

**Kinetic** has partnered with a leading **Pharmaceutical** company who are hiring a **Deputy Regulatory Affairs Manager** to be based in **Riyadh**.** **Key aspects of the role include**: - Develop and implement regulatory strategies to ensure timely and successful product registrations and approvals. - Prepare, and execute regulatory operational plans...

**Regulatory Affairs Specialist, KSA**: - Work mode: Hybrid- Onsite Location(s): Riyadh, SA**Additional Locations**: N/A **Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance** At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing...

**About Johnson & Johnson**: For our Local Operating Company in Saudi Arabia, we are currently recruiting for a Regulatory Affairs Expert to be based in our Riyadh office. In this role you will be leading our Regulatory activities across the region, as well as support a team based across the KSA and Gulf cluster. This role is an excellent opportunity for...

Regulatory Affairs Supervisor| Riyadh, Saudi Arabia **The Company**: An aggressive expansion program together with acquisitions in new vertical markets have created an exciting opportunity to join a dynamic multinational team dedicated to furthering growth plans for the group. **About the Role**: The Regulatory Affairs Supervisor is responsible to...

**Kinetic** has partnered with a multinational **Pharmaceutical** company who are hiring a **Regulatory Affairs Officer** to be based in **Riyadh**.** *** **_Please note that due to Saudization, only Saudi Nationals can be considered for this role._** *** **The main responsibilities will include but not limited to**: - Track and follow up with the...

**About Zahrawi Group**: Zahrawi Group is a leading company in the GCC Healthcare Industry with its presence in UAE, KSA, Qatar, Bahrain, & Oman markets. The company supplies and distributes high-quality products and services to Hospitals, Clinics, Laboratories, & Analytical Industries. **job Brief**: The incumbent is responsible for all Product...