Regulatory Affairs Specialist

6 months ago


Riyadh, Saudi Arabia Boston Scientific Corporation Full time

**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 employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing - whatever your ambitions.

As an Regulatory Affairs Specialist, you will be responsible of supporting the regulatory submission and provide input on regulatory-related issues associated with compliance and achieving the business plan for assigned countries, in Middle East.
- Key Responsibilities:_
- Prioritize and plan on product registration for his/her respective product lines.
- Maintain an active knowledge of the status of pending approvals /submissions, and shepherd registrations through the approval process.
- Provide the management team with regular updates on product registration.
- Ensure product registrations files are reviewed and renewed as required.
- Supports tender operations by timely supply of accurate regulatory documents.
- Establish and maintain a good working relationship with regional RA peers to gain positive & timely support for document preparation.
- Ensures to meet additional Regulatory project requirements support if assigned and when needed.
- Required Skills and Qualifications:_
- BS in Scientific discipline/engineering preferred
- Has the at least 2 to 3 years’ experience in Regulatory environment
- Knowledge and experience of local regulations and standards.
- Must highly have organization skills / and can manage multitask in very competitive environment.

**Requisition ID**:573157

**Job Segment**:Regulatory Affairs, Compliance, Law, Engineer, Supply, Legal, Engineering, Operations



  • Riyadh, Saudi Arabia Alcon Full time

    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...


  • Riyadh, Saudi Arabia Dexcom Full time

    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...


  • Riyadh, Saudi Arabia Haleon Full time

    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...

  • Regulatory Affairs

    6 months ago


    Riyadh, Saudi Arabia Radiometer Full time

    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...


  • Riyadh, Saudi Arabia Al Safa Pharmaceutical Store Full time

    **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...


  • Riyadh, Saudi Arabia Hikma Pharmaceuticals PLC Full time

    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...


  • Riyadh, Saudi Arabia Almarai Full time

    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...


  • Riyadh, Saudi Arabia Johnson & Johnson Full time

    **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...


  • Riyadh, Saudi Arabia Kinetic Full time

    **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...


  • Riyadh, Saudi Arabia IBM Full time

    Introduction At IBM, work is more than a job - it's a calling: To build. To design. To code. To consult. To think along with clients and sell. To make markets. To invent. To collaborate. Not just to do something better, but to attempt things you've never thought possible. Are you ready to lead in this new era of technology and solve some of the world's most...


  • Riyadh, Saudi Arabia Kinetic Full time

    **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...


  • Riyadh, Saudi Arabia Cepheid Full time

    **In this role, the associate**: - Identify information sources and resources for local regulations. - Serve as RA lead on global Market Expansion registrations for simple to medium complicated projects for initial product approvals and renewals, for assays, instruments or software, in global regions outside US and EU to ensure OTD product launches. - Be...


  • Riyadh, Saudi Arabia Philips Full time

    **Job Title**: Regulatory Affairs Manager, Hospital Patient Monitoring META **Job 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...

  • Reg Affairs

    6 months ago


    Riyadh, Saudi Arabia Boston Scientific Corporation Full time

    **Reg Affairs - P4**: - 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 employees,...


  • Riyadh, Saudi Arabia Danone Full time

    About the job Danone MENA is looking for a talented **Regulatory affairs executive** to be based in **Riyadh, Saudi Arabia**, like you! In the context of Specialized Nutrition MENA, you will be responsible for managing regulatory submissions within the pharmaceutical industry. This involves preparing and submitting documents to regulatory Manager, ensuring...


  • Riyadh, Saudi Arabia Biogen Full time

    **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...


  • Riyadh, Saudi Arabia Al Safi-Danone Co.Ltd. Full time

    **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 -...


  • Riyadh, Saudi Arabia Microsoft Full time

    Microsoft’s mission is to empower every person and every organization on the planet to achieve more. As employees we come together with a growth mindset, innovate to empower others, and collaborate to realize our shared goals. Each day we build on our values of respect, integrity, and accountability to create a culture of inclusion where everyone can...


  • Riyadh, Saudi Arabia Jamjoom pharma Full time

    Jamjoom Pharma has in a very short span of time emerged, as one of the leading pharmaceutical companies in the Afrasia region. The geographical focus of the company is on countries in the Middle East, Africa, and CIS regions. Strategic focus on selected therapeutic categories has contributed to the rapid growth, market acceptance, and overall success of the...


  • Riyadh, Saudi Arabia Amgen Full time

    **Regional Specific Activities** - Ensure regulatory submissions are made on time and meet Amgen’s corporate and local regulatory requirements. - Contribute to and execute the filing plan for their country where applicable - Review source text for country labeling - Review promotion and non-promotion materials - Disseminate relevant information to team(s)...