Purpose of consultancyThe purpose of the Roster of Experts (ROE) is to provide trusted technical, scientific, regulatory, leadership, and management support to the AVAREF Secretariat, which will, in turn, support the development of comprehensive regulations for clinical trials, procedures for review of Clinical Trials Applications and dossiers for registration of vaccines, bio-therapeutics, pharm...
Purpose of consultancy The purpose of the Roster of Experts (ROE) is to provide trusted technical, scientific, regulatory, leadership, and management support to the AVAREF Secretariat, which will, in turn, support the development of comprehensive regulations for clinical trials, procedures for review of Clinical Trials Applications and dossiers for registration of vaccines, bio-therapeutics, phar...
The World Health Organization is a specialized agency of the United Nations that is concerned with international public health. It was established on 7 April 1948, headquartered in Geneva, Switzerland. Purpose of consultancy The purpose of the Roster of Experts (ROE) is to provide trusted technical, scientific, regulatory, leadership, and management support to the AVAREF Secretariat, which will, ...
BIOPHARMA Limited is active in the creation of a networking following a spirit of globalization of trade. Our main focus is to provide a wide range of high quality pharmaceutical products to our valued customers. Our full range of dosage form includes Oral, Tablets, Capsules, Lotions, Gels, Ointments & creams are manufactured in facilities to conform the WHO CGMP norms, in compliance with the str...
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Job Summary The Regulatory Affairs Manager role focuses on ensuring regulatory compliance for products in East African markets, both before and after approval. This includes compiling product dossiers for registering any other necessary information, also providing regulatory advice for business planning, and promptly communicating regulatory changes and impact to the organization. The role involv...
No Relocation Assistance Offered # 159102 - Nairobi, Nairobi Municipality, Kenya Who We Are Colgate-Palmolive Company is a caring, innovative growth company that is reimagining a healthier future for all people, their pets and our planet. Focused on Oral Care, Personal Care, Home Care and Pet Nutrition, we sell our products in more than 200 countries and territories under brands such as Colgate, ...
Legal Jobs In Kenya.Brief Job Description: Ensure that the company s products comply with the regulations in the Countries where they are distributed.Timely compilation and submission of registration dossiers for Kenya and other countries per required format and guidelines.Keep up to date with national and international legislation, guidelines, and customer practices.Collect, collate, and evaluat...
Ensures timely compilation of product registration dossiers/notification, using ZenGRC an internal tool for loading documentation requests. Ensures proactive compliance of Colgate products with all applicable regulations across the East Africa Region.Supports Technology and other internal stakeholders by delivering regulatory assessments.Keeps abreasts on latest regulatory developments in East Af...
Job Description What you ll do? As the successful candidate, you will have an opportunity to work with a passionate team of individuals dedicated to accelerating access to life-changing & innovative medicines for our patients. In addition, gain exposure and network to Health Authority regulatory framework across the various SSA countries within the African Cluster. Prepare regulatory submissions ...
AstraZeneca is a global, science-led biopharmaceutical company that spans the discovery, development, manufacturing, distribution and worldwide commercialisation of primary care and speciality care medicines. We believe the best way we can help patients is to focus on breakthrough science in order to uncover disease mechanisms and develop novel, targeted therapies that interact with them. This is...
AstraZeneca is a global, science-led biopharmaceutical company that spans the discovery, development, manufacturing, distribution and worldwide commercialisation of primary care and speciality care medicines. We believe the best way we can help patients is to focus on breakthrough science in order to uncover disease mechanisms and develop novel, targeted therapies that interact with them. This is...
Genedrift is a leading consultancy and solutions provider for compliance and risk services for the Life Science industry, for Regulatory Affairs and Pharmacovigilance We ve been making the to-market process faster and smarter, covering Drugs, Medical Devices, Cosmetics and Food Supplements Responsibilities Review of labels following local HA guidelines and advise customers on the best compliance ...
Develop, implement, and review legal policies and procedures to ensure that they are in accordance with the existing legislation;Monitor compliance with legal and statutory requirements of the organisation as well as market participants as per SRO requirements;Conduct regular compliance reviews and audits to identify areas of noncompliance and implement corrective actions as needed;Prepare and su...
Job Description JOB PURPOSE Find your purpose at Unilever. You will lead innovations, big and small, that will make our business win and grow. You will learn from brilliant business leaders and colleagues in a truly global and diverse culture to ultimately become a better you. If you are You will be the Regulatory Affairs Manager for East Africa cross Business groups in EA region and Personal car...
JOB PURPOSE Find your purpose at Unilever. You will lead innovations, big and small, that will make our business win and grow. You will learn from brilliant business leaders and colleagues in a truly global and diverse culture to ultimately become a better you. If you are You will be the Regulatory Affairs Manager for East Africa cross Business groups in EA region and Personal care Africa lead fo...
Job SummaryThe Regulatory Affairs Manager role focuses on ensuring regulatory compliance for products in East African markets, both before and after approval. This includes compiling product dossiers for registering any other necessary information, also providing regulatory advice for business planning, and promptly communicating regulatory changes and impact to the organization. The role involve...
On any day, 2 billion people use Unilever products to look good, feel good and get more out of life giving us a unique opportunity to build a brighter future. Great products from our range of more than 400 brands give us a unique place in the lives of people all over the world JOB PURPOSE Find your purpose at Unilever. You will lead innovations, big and small, that will make our business win and ...
Regulatory Affairs ManagerReporting to the Chief Legal and Regulatory Affairs Officer (CLRO), this role will ensure that the organization operates within its legal framework and complies with all relevant regulations. The role will work with the CLRO to ensure market participants operate within the set rules of the Exchange in accordance with the Exchange's Self-Regulatory Organization (SRO) mand...
SummaryReporting to the Chief Legal and Regulatory Affairs Officer (CLRO), this role will ensure that the organization operates within its legal framework and complies with all relevant regulations. The role will work with the CLRO to ensure market participants operate within the set rules of the Exchange in accordance with the Exchange's Self-Regulatory Organization (SRO) mandate. The Regulatory...
EABX Plc is a regional market organiser established to consolidate the fixed income and money markets in a transparent, responsible and transformative way. EABX Plc is a strategic financial market infrastructure organisation that is positioned to provide market integration through seamless flow of executions from pre-trade to post-trade Summary Reporting to the Chief Legal and Regulatory Affairs ...
Regulatory Affairs Manager
Review of labels following local HA guidelines and advise customers on the best compliance practices. Perform high-quality CMC review of technical documentation i.e. CTD Modules, Medical Data Packages, SmPCs, PIs, PILs, and Labelling documents, for filings with HA. Attend Pre-Submission meetings with the HA and prepare post-meeting package/minutes for internal, client, and HA records. Assist in t...
BD is one of the largest global medical technology companies in the world and is advancing the world of healthTM by improving medical discovery, diagnostics and the delivery of care. The company supports the heroes on the frontlines of healthcare by developing innovative technology, services and solutions that help advance both clinical therapy for patients and clinical process for healthcare pro...
In our endeavour to transform leadership in Africa in the 21st Century, Strathmore Business School (SBS) has taken the responsibility of influencing leadership of public and private sectors in the continent. This we believe is our overarching mission at SBS; Service to Society through the development of international executive business management and leadership programs. Since its inception in 20...
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