Vizen Life Sciences hiring multiple Pharmacovigilance roles
- PV Vacancies for Experienced Candidates – Vizen Life Sciences
- Company Overview
- Job Role & Responsibilities
- Open Positions & Key Responsibilities
- Eligibility / Qualifications
- Mandatory Requirements
- Role-Specific Qualifications
- Relevant Educational Background
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Is pharmacovigilance experience mandatory?
- Are freshers eligible for these roles?
- Can medical doctors apply for these positions?
- How do I apply for these vacancies?
- Are these permanent positions?
- Summary Table
PV Vacancies for Experienced Candidates – Vizen Life Sciences
Vizen Life Sciences hiring multiple Pharmacovigilance roles. PV experience mandatory. Apply via email. India location.
Vizen Life Sciences is expanding its Pharmacovigilance and Drug Safety operations and is inviting applications from experienced PV professionals across multiple specialized roles. These opportunities are designed for candidates with hands-on pharmacovigilance experience who want to work in a regulated, compliance-driven environment supporting global drug safety and post-marketing surveillance activities.
Company Overview
Vizen Life Sciences is a growing life sciences organization focused on delivering pharmacovigilance, drug safety, and regulatory-compliant healthcare solutions. The company supports pharmaceutical and biotechnology organizations with end-to-end PV services, including case processing, signal management, aggregate reporting, and safety training.
With a strong emphasis on regulatory compliance, data accuracy, and patient safety, Vizen Life Sciences plays an important role in strengthening global drug safety systems. The organization follows international guidelines such as ICH, GVP, and FDA regulations, ensuring high-quality pharmacovigilance deliverables for its clients.
Job Role & Responsibilities
Vizen Life Sciences is hiring for multiple Pharmacovigilance and Drug Safety positions. All roles require prior hands-on PV experience and a strong understanding of global drug safety processes.
Open Positions & Key Responsibilities
PSUR Specialist (Experience: 3–5 Years)
- Preparation and review of Periodic Safety Update Reports (PSURs)
- Data analysis, literature review, and benefit-risk evaluation
- Compliance with global regulatory submission timelines
- Coordination with internal safety and regulatory teams
Drug Safety Associate (Experience: 2–8 Years)
- End-to-end case processing and safety data management
- Adverse event intake, triage, and narrative writing
- MedDRA and WHO-Drug coding
- Compliance with GVP and SOP requirements
Pharmacovigilance Trainer (Experience: 8–12 Years)
- Design and delivery of PV training programs
- Mentoring PV teams on regulatory requirements
- Development of training materials and SOP guidance
- Audit readiness and quality improvement initiatives
Drug Safety Physician (MBBS / BDS + 2 Years PV Experience)
- Medical review of Individual Case Safety Reports (ICSRs)
- Clinical evaluation of adverse events and causality assessment
- Signal detection support and benefit-risk assessment
- Collaboration with global safety physicians and regulatory teams
Signal Management / Drafting / Reviewer (Experience: 3–7 Years)
- Signal detection, validation, and management activities
- Preparation and review of signal evaluation reports
- Literature review and safety data analysis
- Support regulatory submissions and risk management plans
These roles directly contribute to patient safety, regulatory compliance, and effective post-marketing surveillance of pharmaceutical products.
Eligibility / Qualifications
Mandatory Requirements
- Pharmacovigilance experience is mandatory for all roles
- Strong understanding of global PV regulations and guidelines
- Excellent documentation and communication skills
- Ability to work in a compliance-driven environment
Role-Specific Qualifications
- Drug Safety Physician: MBBS or BDS with minimum 2 years of pharmacovigilance experience
- Other PV Roles: Relevant life sciences or pharmacy background with required experience
Relevant Educational Background
B.Pharmacy, M.Pharmacy, Pharm.D, MBBS, BDS, B.Sc Life Sciences, M.Sc Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research, Pharmacology
Location & Salary
- Job Location: India (details as per role and interview discussion)
- Employment Type: Full-time, Permanent
- Salary: As per industry standards and experience
Compensation is competitive and aligned with current pharmacovigilance and drug safety market benchmarks.
Application Process
Interested and eligible candidates are requested to submit their updated CVs via email:
Candidates are advised to mention the position applied for clearly in the email subject line to ensure faster shortlisting.
Frequently Asked Questions (FAQs)
Is pharmacovigilance experience mandatory?
Yes. Pharmacovigilance experience is mandatory for all listed positions.
Are freshers eligible for these roles?
No. These roles are open only to experienced pharmacovigilance professionals.
Can medical doctors apply for these positions?
Yes. MBBS or BDS candidates with relevant PV experience can apply for the Drug Safety Physician role.
How do I apply for these vacancies?
You can apply by emailing your updated CV to careers@vizenlifesciences.com.
Are these permanent positions?
Yes. All roles are full-time and permanent.
Summary Table
| Category | Details |
|---|---|
| Company | Vizen Life Sciences |
| Vacancies | PSUR Specialist, Drug Safety Associate, PV Trainer, Drug Safety Physician, Signal Management / Reviewer |
| Required Education | B.Pharmacy, M.Pharmacy, Pharm.D, MBBS, BDS, Life Sciences, Biotechnology, Microbiology, Biochemistry |
| Experience | 2 to 12 years (role-specific) |
To apply for this job email your details to careers@vizenlifesciences.com
