Regulatory affairs specialist

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...

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...

Hello. We're Haleon. A new world-leading consumer health company. Shaped by all who join us. Together, we're improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands - including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum - through a unique combination of deep human...

This role is based in Riyadh, Saudi ArabiaOverviewResponsible for regulatory affairs activities to assist in regulatorysubmission, annual reports, registrations and listings. Assurecompliance with applicable medical device regulations per jurisdiction,guidance and standards. Assist in creation and maintenance ofregulatory files.Job ResponsibilitiesWrite,...

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...

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...

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...

You must first log in before applying to jobs. The Regulatory Affairs Supervisor is responsible for preparing registration dossiers for new products, line extensions, and new indications. They will also be responsible for maintaining the license of existing registered products by managing all regulatory activities throughout the product lifecycle.Main...

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...

About Zahrawi GroupZahrawi 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 highquality products and services to Hospitals Clinics Laboratories & Analytical Industries. job Brief The incumbent is responsible for all Product Classification/Manufacturing...

Job Description Purpose**: The incumbent will work in close collaboration with GCC Regulatory and commercial organizations, International Growth markets (IGM), Development, Chemistry, Manufacturing and Control (CMC) Regional contacts as well as relevant global, regional and local stakeholders.He/she will lead local regulatory activities in KSA to ensure...

Reg Affairs - P4: Work mode: Hybrid Onsite Location(s): Riyadh, SAAdditional Locations: N/ADiversity - Innovation - Caring - Global Collaboration - Winning Spirit - High PerformanceAt Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most...

Job TitleRegulatory Affairs ManagerAbout 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...

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...

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...

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...

Role Purpose:To validate artworks and product advertisements and ensure they follow the SFDA and GSO standards and to keep quality certificates updated as required.Key Accountabilities: Lead the process of validation artworks (Marketing, R&D &Agency) Reviewing and validating product artwork from Quality, Regulatory and R&D perspective Tracking the artwork...

Role Purpose:To validate artworks and product advertisements and ensure they follow the SFDA and GSO standards and to keep quality certificates updated as required.Key Accountabilities:Lead the process of validation artworks (Marketing, R&D &Agency)Reviewing and validating product artwork from Quality, Regulatory and R&D perspectiveTracking the artwork...