Eduardo Edgar Soares

Indústria

Indústria

Educação

IU - International University of Applied Sciences

ISCTEM - Instituto Superior de Ciencias e Tecnologia de Mocambique

Technical Director and Owner

Farmácia Malene, Matola

As the Technical Director and Owner of a Pharmacy, responsibilities include overseeing daily pharmacy operations, ensuring compliance with regulatory standards, managing inventory, and supervising staff. Experience involves ensuring the accurate dispensing of medications, maintaining patient safety, implementing quality control procedures, managing customer relations, and staying updated on pharmaceutical advancements and regulations to provide highquality services

GENERAL MANAGER (FOUNDER)

DE. GROUP, LDA.

As the Founder and General Manager of a Logistics Company , responsibilities include developing business strategies, overseeing daily operations, managing supply chain and distribution, securing client contracts, and ensuring customer satisfaction. Experience involves optimizing logistics processes, managing finances, leading teams, ensuring regulatory compliance, and driving company growth through strategic planning and effective problemsolving in the logistics sector.

LQPPV - Local Qualified Person for Pharmacovigilance for Mozambique and Angola

HALEON PLC.

As the Local Qualified Person Responsible for Pharmacovigilance (QPPV), key responsibilities include overseeing the pharmacovigilance system, ensuring compliance with local and international safety regulations, and managing adverse event reporting. Experience involves monitoring and assessing safety data, preparing safety reports (e.g., PSURs), coordinating risk management strategies, and maintaining communication with regulatory authorities to ensure timely and accurate safety reporting

TECHNICAL DIRECTOR, QPPV & QA RESPONSIBLE

MISTOLIN MOÇAMBIQUE, LDA

As the Responsible Pharmacist in a factory, key responsibilities include ensuring compliance with pharmacovigilance by monitoring and reporting adverse events, managing safety data, and maintaining regulatory compliance. In Quality Assurance, duties involve overseeing GMP compliance, conducting internal audits, managing documentation, and implementing corrective actions to ensure product safety, quality, and adherence to regulatory standards.

QPPV and QA Responsible & Member of the Board of Advisors

Medis Farmacêutica, Lda. (Grupo Azevedos)

In pharmacovigilance, responsibilities include monitoring adverse events, risk assessments, and ensuring compliance with regulations. Experience involves safety data analysis and collaboration with authorities. In quality assurance, tasks include ensuring GMP compliance, audits, and documentation control. In supply chain, responsibilities involve managing inventory, logistics, and optimizing distribution. In regulatory affairs, duties include preparing submissions and advising on product approvals. In advisory boards, responsibilities involve organizing expert meetings, gathering insights, and aligning strategies with regulatory requirements to inform decisionmaking across departments.