electric regulatory commission

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 Do Product registrations Supports the prepara...

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 ...

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...

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...

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, ...

The Insurance Regulatory Authority of Kenya (IRA) is the sole authority charged with regulation and supervision of the insurance industry within the Republic of Kenya. It ensures compliance by insurance/reinsurance companies, protects consumers and promotes a high degree of security for policyholders. REF: MI/11 Purpose The position is responsible for coordinating the supervision of insurance int...

The Insurance Regulatory Authority of Kenya (IRA) is the sole authority charged with regulation and supervision of the insurance industry within the Republic of Kenya. It ensures compliance by insurance/reinsurance companies, protects consumers and promotes a high degree of security for policyholders. REF: SMS/01 Job Purpose The position is responsible for ensuring efficient registration and exit...

The Insurance Regulatory Authority of Kenya (IRA) is the sole authority charged with regulation and supervision of the insurance industry within the Republic of Kenya. It ensures compliance by insurance/reinsurance companies, protects consumers and promotes a high degree of security for policyholders. REF: MICT/08 Purpose The position is responsible for developing and implementing strategy, polic...

The Insurance Regulatory Authority of Kenya (IRA) is the sole authority charged with regulation and supervision of the insurance industry within the Republic of Kenya. It ensures compliance by insurance/reinsurance companies, protects consumers and promotes a high degree of security for policyholders. REF: MS/03 Job purpose To ensure efficient registration and exit from the market of insurers and...

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...

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...

Job Overview: Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines. Prepare site regulatory documents, revie...

Job Description Job Overview: Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines. Prepare site regulatory ...

Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary.Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.Prepare site regulatory documents, reviewing for complet...

IQVIA, formerly Quintiles and IMS Health, Inc.,is an American multinational company serving the combined industries of health information technology and clinical research. It is a provider of biopharmaceutical development and commercial outsourcing services, focused primarily on Phase I-IV clinical trials and associated laboratory and analytical services, including consulting services. It has a n...

Regulatory and Start Up Specialist IQVIA RSUWork from any location Must speak Dutch and EnglishJoin us on our exciting journey!IQVIA Clinical Functional Services Partnerships (FSP) business is unique. Our teams are dedicated to a single sponsor partner, where the common goal is quality delivery for our customers. We set ourselves apart with collaboration and face to face contact both at start up ...

Regulatory Manager at Airtel

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...

The Insurance Regulatory Authority of Kenya (IRA) is the sole authority charged with regulation and supervision of the insurance industry within the Republic of Kenya. It ensures compliance by insurance/reinsurance companies, protects consumers and promotes a high degree of security for policyholders. REF: MF/10 Purpose The position is responsible for implementing strategies aimed at prudent mana...

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 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...

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...

Job Overview:Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary.Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.Prepare site regulatory documents, reviewin...