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Pharmacovigilance Specialists Jobs in Hyderabad at Medifodil

Pharmacovigilance Specialists Jobs in Hyderabad at Medifodil for ICSR, Aggregate Reports and PV QA roles. Apply via email today.

Are you an experienced pharmacovigilance professional looking to advance your career in Hyderabad? A growing drug safety organization is expanding its Pharmacovigilance (PV) division and inviting applications from skilled candidates with 4–6 years of relevant industry experience. If you have hands-on exposure to ICSR processing, aggregate reporting, or PV Quality Assurance, this opportunity offers strong professional growth in a compliance-focused work environment. Pharmacovigilance Specialists Jobs in Hyderabad


Company Overview

Medifodil Smart Pharma Solutions is an emerging pharmaceutical service organization specializing in pharmacovigilance, regulatory support, and safety compliance services. The company works with global regulatory frameworks and focuses on maintaining high-quality standards in drug safety monitoring and reporting. Pharmacovigilance Specialists Jobs in Hyderabad

With an expanding presence in Hyderabad, Medifodil aims to strengthen its PV operations by onboarding experienced professionals who can contribute to global safety reporting requirements and regulatory compliance programs.


Job Location & Employment Type

  • Location: Kukatpally, Hyderabad, Telangana
  • Work Mode: Onsite
  • Department: Pharmacovigilance
  • Experience Required: 4–6 Years
  • Position Level: Senior Executive / Specialist
  • Employment Type: Full-Time

Immediate joiners will be given preference during the hiring process.


Open Positions / Department Details

The company is currently recruiting for multiple roles within its Pharmacovigilance department: Pharmacovigilance Specialists Jobs in Hyderabad

  1. PV ICSR Specialist
  2. Aggregate Reports Specialist
  3. PV Quality Assurance (QA) Professional

Each role focuses on critical aspects of global drug safety monitoring and regulatory reporting.


Key Roles & Responsibilities

1. PV ICSR Specialist

Professionals in this role will manage individual case safety reports (ICSRs) in compliance with international regulatory standards.

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Key responsibilities include:

  • Handling end-to-end case processing from intake to submission.
  • Performing follow-up activities to ensure completeness of safety data.
  • Supporting medical review and preparing accurate case narratives.
  • Coding adverse events and products using MedDRA.
  • Conducting case quality checks before regulatory submission.
  • Ensuring adherence to global reporting timelines for agencies such as FDA, EMA, and MHRA.
  • Maintaining accurate safety database entries.

This role is ideal for candidates experienced in safety databases such as Argus or ARISg. Pharmacovigilance Specialists Jobs in Hyderabad


2. Aggregate Reports Specialist

This position focuses on periodic safety reporting and benefit–risk evaluation.

Key responsibilities include:

  • Assisting in the preparation and review of PSUR, PBRER, and DSUR documents.
  • Compiling and analyzing safety data from multiple sources.
  • Supporting benefit–risk assessment and safety signal detection activities.
  • Performing trend analysis and interpreting cumulative safety data.
  • Ensuring submission of aggregate reports within global regulatory timelines.
  • Collaborating with cross-functional regulatory and medical teams.

Candidates with regulatory writing experience and strong analytical skills will find this role particularly rewarding. Pharmacovigilance Specialists Jobs in Hyderabad


3. PV Quality Assurance (QA)

This role supports pharmacovigilance system compliance and quality oversight.

Key responsibilities include:

  • Assisting in implementation and maintenance of PV SOPs.
  • Performing quality checks on safety cases and reports.
  • Supporting internal audits and inspection readiness activities.
  • Tracking CAPA (Corrective and Preventive Actions) implementation.
  • Ensuring compliance with global pharmacovigilance guidelines.
  • Maintaining documentation aligned with regulatory standards.

This position is suitable for candidates with prior exposure to PV audits, compliance monitoring, and regulatory inspections. Pharmacovigilance Specialists Jobs in Hyderabad

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Eligibility Criteria

Education

  • B.Pharm
  • M.Pharm
  • Pharm.D
  • B.Sc / M.Sc in Life Sciences or related disciplines

Candidates from pharmacy or life sciences backgrounds with relevant PV experience will be considered.


Experience

  • Minimum 4–6 years of hands-on pharmacovigilance experience.
  • Practical exposure to ICSR processing, aggregate reporting, or PV QA.
  • Experience working in global regulatory environments.

Skills Required

  • Strong understanding of global pharmacovigilance regulations including ICH guidelines, GVP modules, FDA and EMA requirements.
  • Experience with safety databases such as Argus or ARISg preferred.
  • Good knowledge of MedDRA coding and medical terminology.
  • Excellent analytical and documentation abilities.
  • Strong written and verbal communication skills.
  • Ability to work in a quality-driven and compliance-focused environment.
  • Capability to meet strict regulatory timelines.

Pharmacovigilance Specialists Jobs in Hyderabad


Salary & Benefits

Compensation will be offered as per company norms and based on candidate experience. Employees will benefit from: Pharmacovigilance Specialists Jobs in Hyderabad

  • Exposure to global pharmacovigilance processes.
  • Career advancement at Senior Executive / Specialist level.
  • Opportunity to work in a growing safety-focused organization.
  • Skill enhancement in regulatory compliance and reporting.

Selection Process

The hiring process may involve:

  1. Resume screening and shortlisting.
  2. Technical interview focusing on pharmacovigilance knowledge.
  3. Assessment of database handling and regulatory understanding.
  4. Final HR discussion.

Only shortlisted candidates will be contacted.


How to Apply

Interested and eligible candidates should send their updated resume to:

careers@medifodil.com

Subject Line Format:
Application – Position Name – (Experience)

Example:
Application – PV ICSR – 5 Years

Candidates are advised to clearly mention their current experience and preferred role in the subject line for faster processing.

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Important Dates

  • Application Deadline: Not specified (Apply at the earliest)

Why Apply for This Pharmacovigilance Job?

This opportunity allows experienced pharmacovigilance professionals to expand their expertise in a structured and compliance-oriented work environment. Candidates will gain exposure to: Pharmacovigilance Specialists Jobs in Hyderabad

  • End-to-end ICSR lifecycle management.
  • Advanced aggregate safety reporting practices.
  • Global regulatory frameworks and inspection readiness.
  • Quality assurance systems in pharmacovigilance.
  • Career growth in senior-level PV roles.

For professionals aiming to strengthen their regulatory knowledge and safety reporting expertise, this role offers long-term development prospects in Hyderabad’s growing pharmaceutical services sector.


Important Note / Disclaimer

IndiaPharmaJobs.in is an independent job information platform dedicated to sharing verified pharma and life sciences job updates. We are not directly affiliated with Medifodil Smart Pharma Solutions or any organization mentioned above. Candidates should verify all job-related information through official company communication channels before applying. We do not charge any fee for job postings or applications. Pharmacovigilance Specialists Jobs in Hyderabad


Interested candidates meeting the eligibility criteria are encouraged to apply immediately and take the next step in their pharmacovigilance career. Pharmacovigilance Specialists Jobs in Hyderabad

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