Regulatory affairs in pharmaceuticals

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...

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...

No Relocation Assistance Offered# 159102 - Nairobi, Nairobi Municipality, KenyaJob 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 c...

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, ...

As the Regulatory Affairs Specialist EAST AFRICA , you will be responsible for obtaining and maintaining regulatory approvals and in meeting of in country regulations for IVD's so to ensure Abbott products are compliant to meet appropriate in country regulations for all business units under Abbott Rapid Diagnostics for the region assigned.What You'll DoProduct registrationsSupports the preparatio...

PRODUCT REGISTRATIONSSupports the preparation and timely completion of submission of registrations for in vitro diagnostic devices (assays, instruments, software) to meet project and business needs for ARDX division for different business units - ID, CM and Tox for the assigned region.Participation on cross functional project teams to provide the required input that enables strategic guidance to ...

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...

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 ...

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...

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 ...

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...

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 ...

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...

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...

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...

Regulatory Affairs Specialist at Becton, Dickinson and Company (BD)

Ferring Pharmaceuticals is a research-driven, biopharmaceutical company devoted to identifying, developing and marketing innovative products in the fields of reproductive health, urology, gastroenterology, endocrinology and orthopaedics Your day at Ferring Visit Doctors, Pharmacists and Hospitals in order to inform on products according to the marketing strategy and with the frequency and number ...

Your day at FerringVisit Doctors, Pharmacists and Hospitals in order to inform on products according to the marketing strategy and with the frequency and number of impacts approved for each segment of doctor.Build up and maintain a relationship with these stakeholders. Assist to Scientific congresses determined by the company.Classification of doctors and other stakeholders of the area according ...