Regulatory Affairs Hub Strategy Manager

**JOB INFORMATION** **JOB SUMMARY** Summarize the primary purpose & key accountabilities of the job. - Handle related regulatory strategies for allocated Products, and ensure communication/clarity of regulatory timelines and strategy. - Single point of contact for global/product strategists, and In-Country Regulatory Team on regional issues to facilitate the...

Identifying Job Information_ JOB TITLE: _Title reflected Pfizer Org Chart_) Regional Regulatory Affairs strategist Manger REPORTS TO: _Manager Title_) Regional Hub Team Lead DIVISION/BUSINESS LINE: Global Product Development (GPD) VERSION DATE: 01-Feb-2019 SUB DIVISION: Global Regulatory Affairs (GRA) DEPARTMENT NAME: Regional Regulatory...

**Position title**: Manager, Regulatory Affairs, International **Introduction/Purpose** (provide a brief explanation of the purpose of the position) The Manager, Regulatory Affairs International supports ambitious geographical expansion plans. The position will support registration of existing portfolio products into new territories and to register...

**Job Purpose**: To implement regulatory strategies and direct planned submissions by providing guidance to project teams in a fast paced, complex environment to achieve well-timed submissions and clearances/approvals while complying with standards and latest regulations **Strategy** - Participates in the development of the departmental strategy in line...

**Position **Summary**: **The Head of Regulatory Affairs JENA **will be responsible for leading regulatory affairs activities in the cluster for the Janssen portfolio and support the local GPH regulatory team (limited support) as required striving for convergence in ways of working. The JENA cluster comprises Egypt, Libya, Sudan, Ethiopia, and any new...

About the job Director, Regulatory Affairs **Purpose of the job** Managing the regulatory affairs, overseeing the industry practices & ensure all government regulations being met to support the current and future strategic plans of Orange. **Duties and responsibilities** - Ensure coordination and enrichment of the company's strategic plan. - Provide...

The Regulatory Affairs Specialist is responsible for coordinating various regulatory affairs activities including but not limited to; products submissions, renewals and updates by coordinating between plants and agents and continuously communicating with all parties involved (including governmental and official authorities) to ensure timely submission and...

**Job Description**: **Are You Ready to Make It Happen at Mondelēz International?** **Join our Mission to Lead the Future of Snacking. Make It With Pride.** You execute the regulatory affairs strategy for your respective category or categories and geographical area using your technical and regulatory knowledge. You ensure our policies, regulatory programs...

As a Regulatory Affairs Executive, you will be responsible for the day-to-day monitoring of the company’s regulatory activities to ensure compliance with all regulations. You will be a key member of our regulatory affairs team, which is responsible for the company’s regulatory processes and reporting of the regulatory activities. **Responsibilities** -...

**Main purpose**: Manage Regulatory Affairs for AbbVie Egypt/Libya Region **Main Responsibilities**: REGULATORY AFFAIRS Advance Pipeline/Marketed Product Support: Submissions, Renewals & Approvals: - Keep abreast of emerging legislation, local or international, related to registration and pharmacovigilance and highlight the potential impact on the...

**Description**: Regulatory Affairs Officer is responsible for performing Regulatory activities to maintain product registrations, product licenses and relevant life cycle management activities within the defined timelines and in full compliance with the legislations and regulations. **Duties & Responsibilities**: - Obtain marketing authorizations and...

One of the leading FMCGs companies is looking to hire a Regulatory Affairs Head! Key Responsibilities: - You will be managing Quality QPD, IMPD, and HSE - As Regulatory Affairs Head, your stakeholders will be EMPA, HACCAP, ISO and other Food related associations. - You will be responsible for labelling on both levels locally and globally. - Managing the...

**Job Summary**: Interacting and communicating with regulatory organizations and authorities to expedite drug registration in addition to reviewing the preparation of registration documents and ensuring the unambiguousity of the content for all submitted documents as well as following up on changing regulations in order to maintain the license of already...

**Purpose**: Regulatory Affairs Supervisor is responsible for performing Regulatory activities to maintain product registrations, product licenses and relevant life cycle management activities within the defined timelines and in full compliance with the legislations and regulations. **Responsibilities**: - Secure obtaining marketing authorizations of new...

**MultiCare** is a well-established Pharmaceutical Company with diversified scope in both manufacturing and marketing of pharmaceutical products, supplements, cosmetics and medical devices. **MultiCare** has +22 years of prominent existence in the local market and has almost +66 products marketed and more to come through the pipelines. **MultiCare **Egypt...

**Position Summary**: - Support in Regulatory Affairs and Quality operations in the affiliate, in collaboration with the affiliate RA Manager and Quality Lead; including maintaining an appropriate Quality Management System. - Provide Regulatory Affairs and Quality Operations support to the local affiliate to help the market(s) achieve their revenue and...

RAY one of the leading contract research organizations in Egypt and the Middle East is hiring: Freelancer Regulatory Affairs Manger to be based in Egypt. - 3 years experience in regulatory affairs in middle east. Awareness of local and international regulations, guidelines and regulatory requirements. - Ability to communicate quickly and actively with the...

Ensures a controlled documentation system, record retention, and information services including electronic records retention processes in accordance with regulatory requirements. Ensures compliance to the requirements from regulatory agencies. Maintains the technical and non-technical documentation change system. Assures procedures are in place to classify...

**Position Summary** Accountable for the achievement of the local affiliate, Cluster and Corporate objectives, in collaboration with the affiliate RA Manager to support in RA Egypt affiliate and Levant region, and provide Regulatory Affairs support to the local affiliate to help the market(s) achieve their revenue and growth targets: - Obtain new product...

**MultiCare **Egypt for Pharmaceutical Industries is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, gender identity or expression, age disability, or other characteristics protected by prevailing regulations, practice or customs/traditions. **MultiCare** is a...