![Haleon](https://media.trabajo.org/img/noimg.jpg)
Regulatory Affairs Specialist
2 weeks ago
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 understanding and trusted science.
What's more, we're achieving it in a company that we're in control of. In an environment that we're co-creating. And a culture that's uniquely ours. Care to join us. It isn't a question.
With category leading brands such as Sensodyne, Voltaren and Centrum, built on trusted science and human understanding, and combined with our passion, knowledge and expertise, we're uniquely placed to do this and to grow a strong, successful business.
About the role
Regulatory Affairs Specialist will be responsible to maintain and keep the life cycle of the products of the company valid and accurate at SFDA systems, such as eSDR and GHAD.
Key responsibilities- Prepare the file as eCTD for new registration submission at eSDR.- Prepare and review the artwork (leaflet, outer pack, and label).- Reviewing the initial documentation and ensure its compliance with regulations for OTC, food supplements and Medical Device.- Keeping the internal company systems e,g Veeva and champs accurate and most updated.
Essential- Bachelor degree- 2-5 years' experience in Regulatory Affairs in pharmaceutical company.
Preferred- Experience in food product registration.- Experience in medical device registration.
Please save a copy of the job description, as this may be helpful to refer to once the advert closes.
At Haleon we embrace our diverse workforce by creating an inclusive environment that celebrates our unique perspectives, generates curiosity to create unmatched understanding of each other, and promotes fair and equitable outcomes for everyone.
We're striving to create a climate where we celebrate our diversity in all forms by treating each other with respect, listening to different viewpoints, supporting our communities, and creating a workplace where your authentic self belongs and thrives.
We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.
At Haleon we embrace our diverse workforce by creating an inclusive environment that celebrates our unique perspectives, generates curiosity to create unmatched understanding of each other, and promotes fair and equitable outcomes for everyone.
We're striving to create a climate where we celebrate our diversity in all forms by treating each other with respect, listening to different viewpoints, supporting our communities, and creating a workplace where your authentic self belongs and thrives.
We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.Haleon is an Equal Opportunity Employer.
All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, Haleon may be required to capture and report expenses Haleon incurs, on your behalf, in the event you are afforded an interview for employment.
This capture of applicable transfers of value is necessary to ensure Haleon's compliance to all federal and state US Transparency requirements.
-
Regulatory affairs specialist
2 weeks ago
Riyadh, Ar Riyāḑ, Saudi Arabia Alewan Full timeWe 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
2 weeks ago
Riyadh, Ar Riyāḑ, Saudi Arabia Radiometer Full timeIn 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...
-
Regional Regulatory Affairs Specialist
2 weeks ago
Riyadh, Ar Riyāḑ, Saudi Arabia Dexcom Full timeAbout 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...
-
Regulatory Affairs Specialist Middle East
2 weeks ago
Riyadh, Ar Riyāḑ, Saudi Arabia Abbott Laboratories Full timeAbout 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 Executive
2 weeks ago
Riyadh, Ar Riyāḑ, Saudi Arabia Aramed Full timeREGULATORY 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...
-
Regulatory Affairs Specialist
2 weeks ago
Riyadh, Ar Riyāḑ, Saudi Arabia Genesis Executive Full timeThis 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
2 weeks ago
Riyadh, Ar Riyāḑ, Saudi Arabia Boston Scientific Corporation Full timeRegulatory 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
2 weeks ago
Riyadh, Ar Riyāḑ, Saudi Arabia Al Safa Pharmaceutical Store Full timeRegulatory 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...
-
Regulatory Affairs Lead
2 weeks ago
Riyadh, Ar Riyāḑ, Saudi Arabia Johnson & Johnson Full timeAbout 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
2 weeks ago
Riyadh, Ar Riyāḑ, Saudi Arabia MS Pharma Injectable Full timeYou 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...
-
Regulatory Affairs Executive/specialist
2 weeks ago
Riyadh, Ar Riyāḑ, Saudi Arabia Zahrawi Medical Full timeAbout 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...
-
Regulatory Affairs ExecutiveSpecialist
2 weeks ago
Riyadh, Ar Riyāḑ, Saudi Arabia Precision Hire Solution Full timeAbout 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...
-
Senior Regulatory Affairs Manager
2 weeks ago
Riyadh, Ar Riyāḑ, Saudi Arabia Biogen Full timeJob 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
2 weeks ago
Riyadh, Ar Riyāḑ, Saudi Arabia Boston Scientific Corporation Full timeReg 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...
-
Regulatory Affairs Manager
2 weeks ago
Riyadh, Ar Riyāḑ, Saudi Arabia Abbott Laboratories Full timeJob 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...
-
Regulatory Affairs Specialist
2 weeks ago
Riyadh, Ar Riyāḑ, Saudi Arabia Cepheid Full timeIdentifies 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...
-
Riyadh, Ar Riyāḑ, Saudi Arabia Philips Full timeJob 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...
-
Riyadh, Ar Riyāḑ, Saudi Arabia Philips Full timeJob 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...
-
Regulatory Affairs Specialist
2 weeks ago
Riyadh, Ar Riyāḑ, Saudi Arabia Al Safi-Danone Co. Full timeRole 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...
-
Regulatory Affairs Specialist
2 weeks ago
Riyadh, Ar Riyāḑ, Saudi Arabia Al Safi-Danone Co. Full timeRole 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...