Executive/Sr. Executive - Pharmacovigilance
Mega We Care Perú - Mega Lifesciences PTY Perú SAC.
Date: 5 days ago
City: Thāne, Maharashtra
Contract type: Full time
Are you a highly responsible person?
Do you have a knack of knowing what’s important?
Do you have a knack of knowing how to partner with people?
Mega Lifesciences is looking for an Executive/Sr. Executive Pharmacovigilance to work closely with Assistant Manager - Pharmacovigilance in a fast-paced environment that will offer ample opportunities to learn and expand your experience and expertise.
Job Summary
As an Executive/Sr. Executive – Pharmacovigilance, your key tasks are as below:
Applications are invited from the potential candidates who meet the following criteria:
The ideal candidate must have hands-on experience in ICSR case processing, literature search, and authoring or supporting aggregate reports (PSURs, PBRERs, RMPs, AddCos). The incumbent must possess strong knowledge of global pharmacovigilance regulations, coupled with exceptional attention to detail and proficiency in scientific writing. The role requires the ability to prioritize and manage multiple deliverables within committed timelines, along with strong communication, problem-solving, and collaboration skills—particularly in working with global affiliates and cross-functional teams.
If you are eager to make the most of this opportunity, kindly fill in the details in respective fields and submit your application for the position.
For any further clarification and information related to the position, you may please contact +91 22 4141 7923 (Ms. Pradnya).
Do you have a knack of knowing what’s important?
Do you have a knack of knowing how to partner with people?
Mega Lifesciences is looking for an Executive/Sr. Executive Pharmacovigilance to work closely with Assistant Manager - Pharmacovigilance in a fast-paced environment that will offer ample opportunities to learn and expand your experience and expertise.
Job Summary
As an Executive/Sr. Executive – Pharmacovigilance, your key tasks are as below:
- Authoring aggregate safety reports including PSURs, PBRERs, RMPs, and AddCos
- Performing data entry and management of ICSRs in the global safety database
- Conducting literature searches for individual and periodic safety reports
- Ensuring compliance with internal SOPs and global regulatory requirements
- Coordinating with global pharmacovigilance affiliate
Applications are invited from the potential candidates who meet the following criteria:
- Bachelor’s Degree or Master’s Degree in Pharmacy
- Minimum 2 - 4 years of experience in pharmacovigilance, with a strong focus on authoring aggregate reports (PSUR, PBRER, RMP, AddCo)
- Hands-on experience in ICSR case processing, literature review, safety signal identification
- Familiarity with regulatory requirements and compliance standards (ICH, GVP, FDA, EMA, local PV regulations)
The ideal candidate must have hands-on experience in ICSR case processing, literature search, and authoring or supporting aggregate reports (PSURs, PBRERs, RMPs, AddCos). The incumbent must possess strong knowledge of global pharmacovigilance regulations, coupled with exceptional attention to detail and proficiency in scientific writing. The role requires the ability to prioritize and manage multiple deliverables within committed timelines, along with strong communication, problem-solving, and collaboration skills—particularly in working with global affiliates and cross-functional teams.
If you are eager to make the most of this opportunity, kindly fill in the details in respective fields and submit your application for the position.
For any further clarification and information related to the position, you may please contact +91 22 4141 7923 (Ms. Pradnya).
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