Pharmacovigilance Executive/ Senior Executive

Job Description

Title: Pharmacovigilance Executive/ Senior Executive

Company Name: Everest Pharmaceuticals Ltd.

Vacancy: --

Age: Na

Job Location: Dhaka

Salary: --

Experience:

Published: 2025-07-17

Application Deadline: 2025-07-24

Education:

• Bachelor of Medicine and Bachelor of Surgery(MBBS)

MBBS (Having BMDC reg.) / M. Pharm ("A" Grade Pharmacist reg. from PCB) from a reputed medical college or University respectively

• Experienced candidates with the same field will get preference

• Fresher`s are encouraged to apply

• Age preferably below 32 years (as per local industry norms)

• Strong knowledge of pharmacovigilance guidelines (ICH, WHO, DGDA)

• Proficient in Microsoft Office Suite (Word, Excel, PowerPoint)

• Excellent verbal and written communication skills in English and Bangla

• Good scientific writing and analytical skills

• Strong presentation and reporting abilities

• Team-oriented, with a proactive and responsible mindset

• Female candidates are encouraged to apply

Everest Pharmaceuticals Ltd. is a new era`s dynamic & innovation driven pharmaceutical company in Bangladesh. With its clear objective of acquiring pre-eminent technologies & skills, Everest has already attracted some of the sharpest minds in high-tech and beyond who thrive to seek opportunities to do their best effort. Our brand essence is being encoded in our business DNA with striving for innovative healthcare solutions to care generation to generation safeguarded with affordable & best quality products to improve the lives of patients around the world.

Employees at Everest challenge to conquer the highest standards and accomplishments through launching many innovative generics which are First-Time-In-The World & also numerous high demanded products which are First-Time-In-Bangladesh. Our values determine how we work together in congenial professional environment and our business acumen is integral part to drive for success. As a part of our strategic vision to expand the business horizon, we are looking for vibrant and dynamic candidates who are willing to change, grow & transform their lives.

Key Responsibilities

• Collect, review, and analyze Adverse Event (AE) reports from patients, healthcare providers, and company representatives

• Maintain an up-to-date Pharmacovigilance System Master File (PSMF) in compliance with DGDA and global regulations

• Communicate with regulatory authorities (e.g., DGDA) regarding ADR monitoring, safety reporting, and risk minimization plans

• Train internal staff and field force on identification, documentation, and reporting of adverse events

• Perform literature screening for local and international safety data and report findings

• Prepare periodic safety update reports (PSURs) and signal detection summaries for internal and external submission

• Assist in the development of SOPs, protocols, and internal safety audit documents

• Support cross-functional teams with medical/scientific safety insights as needed

Competitive salary package

• Festival & Profit bonus

• Earned Leave Encashment

• Medical & health support

• Mobile handset & Transport facilities

• Group Life Insurance

• Provident fund & Gratuity

• Special Allowances