Executive (Pharmacovigilance), SMD

Job Description

Title: Executive (Pharmacovigilance), SMD

Company Name: Healthcare Pharmaceuticals Ltd.

Vacancy: --

Age: At least 26 years

Job Location: Dhaka

Salary: --

Experience:

• At most 1 year
• The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies

B. Pharm/MBBS from any reputed university or medical college.

• At most 1 year
• The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies

• Age At least 26 years

• 6 months-1 year experience in Pharmacovigilance field of any reputed pharmaceuticals company.

• Strong understanding of pharmacovigilance principles, drug safety regulations, and ICH/GVP guidelines.

• Strong organizational and record-management skills, ability to work independently as well as collaboratively in a cross-functional team.

• Ability to coordinate with regulatory authorities, healthcare professionals, and business partners when required.

Healthcare Pharmaceuticals Ltd. is one of the leading pharmaceutical companies in Bangladesh, certified by the international pharmaceutical regulatory authorities like EU GMP, TGA (Australia), NPRA (Malaysia), MCAZ (Zimbabwe), TFDA (Tanzania) etc. We at HPL believe that Patient safety is one of our core business principles. The aim of Pharmacovigilance is to promote public health by identifying, evaluating and minimizing safety issues in all possible ways that may have arisen from the use of our products. We are looking for candidates who are interested to join our team for the mentioned position:

Job function: Pharmacovigilance

Location: Head Office

Job Responsibilities:

• Ensure timely reporting, documentation, and follow-up of all Adverse Events (AEs) and Product Complaints (PCs) in compliance with HPL SOPs, Good Pharmacovigilance Practices (GVP), and DGDA requirements.

• Identify, investigate, document, and escalate pharmacovigilance and quality compliance issues, including the implementation and monitoring of Corrective and Preventive Actions (CAPA).

• Prepare, review, revise, implement, and conduct training on relevant Pharmacovigilance (PhV) SOPs, guidelines, and regulatory requirements.

• Conduct quarterly quality control (QC) of Individual Case Safety Reports (ICSRS), PSUR and RMPs in the HPL Safety Database and prepare comprehensive QC reports.

• Coordinate and support pharmacovigilance audits of external partners and perform other related duties and responsibilities.