Pharmacovigilance Professionals Wanted – Vizen Life Sciences | 0–8 Years

Vizen Life Sciences Hiring Pharmacovigilance Professionals for Drug Safety, Medical Review & Global Submissions

Vizen Life Sciences has announced multiple hiring openings for experienced pharmacovigilance professionals across drug safety, global submissions, medical review, MICC, and quality review functions. The company is actively recruiting candidates with expertise in pharmacovigilance operations, Argus database management, medical review processes, and regulatory safety documentation.

This latest pharmacovigilance recruitment drive is attracting candidates searching for drug safety associate jobs, pharmacovigilance vacancies in India, global submissions careers, medical review openings, safety database jobs, and regulatory affairs opportunities in the pharmaceutical industry.

Company Overview

Vizen Life Sciences is a growing healthcare and life sciences organization focused on delivering pharmacovigilance, regulatory compliance, drug safety, and medical review services to the pharmaceutical and healthcare industry.

The company supports pharmaceutical safety operations aligned with:

• Global pharmacovigilance regulations
• Drug safety monitoring
• Regulatory submissions
• Safety data management
• Medical review processes
• Clinical safety documentation
• Adverse event reporting standards
• Pharmacovigilance compliance systems

With increasing global regulatory focus on patient safety and adverse event monitoring, pharmacovigilance services continue to witness strong hiring demand across pharmaceutical companies, CROs, and healthcare organizations.

Professionals working at Vizen Life Sciences gain exposure to:

• Global safety reporting systems
• Regulatory submission processes
• Safety database operations
• Medical review workflows
• Pharmacovigilance audits
• Quality review procedures
• International drug safety guidelines

The company offers excellent career opportunities for pharmacy and healthcare professionals aiming to build long-term careers in drug safety and regulatory compliance.

Job Role & Responsibilities

Open Positions

Vizen Life Sciences is hiring for the following pharmacovigilance roles:

• Drug Safety Associate
• Global Submissions Professional
• Quality Review Specialist
• MICC Professional
• Medical Review Associate

Experience Requirements

Drug Safety Associate

• Experience: 1 to 8 years

Global Submissions

• Experience: Above 5 years

Quality Review

• Experience: Above 4 years

MICC

• Experience: 2 to 6 years

Medical Review (MBBS/MD)

• Experience: 0 to 5 years

Primary Keyword

Pharmacovigilance Jobs in India

Core Responsibilities

Selected candidates will work in pharmaceutical safety and regulatory operations.

Drug Safety Operations

Candidates applying for Drug Safety Associate roles will handle:

• Adverse event case processing
• Individual case safety reports (ICSR)
• Safety narrative preparation
• Pharmacovigilance documentation
• Case triage activities
• Safety database management
• Regulatory compliance activities

Professionals should possess strong understanding of pharmacovigilance guidelines and global drug safety standards.

Global Submissions Activities

Candidates in Global Submissions roles will be responsible for:

• Regulatory submission tracking
• Safety report submissions
• Global health authority coordination
• Submission compliance checks
• Regulatory documentation management
• Safety reporting timelines

Experience in international pharmacovigilance submission systems will provide an added advantage.

Quality Review Responsibilities

Quality Review professionals will work on:

• Safety case quality checks
• Pharmacovigilance audit support
• Data accuracy verification
• Regulatory compliance review
• SOP adherence monitoring
• Quality assurance procedures

Candidates must have strong attention to detail and knowledge of pharmacovigilance quality standards.

MICC Operations

Professionals working in MICC functions may handle:

• Medical information case coordination
• Drug safety communication
• Query management
• Pharmacovigilance coordination activities
• Case follow-up procedures

Strong communication and documentation skills are essential.

Medical Review Activities

Medical Review candidates will support:

• Medical assessment of safety cases
• Clinical review of adverse events
• Causality assessment
• Safety signal evaluation
• Patient safety analysis
• Medical validation activities

MBBS and MD professionals with pharmacovigilance interest or experience are eligible for these roles.

Eligibility / Qualifications

Educational Qualification

Candidates with the following educational backgrounds can apply:

• B.Pharm
• M.Pharm
• Pharm.D
• MBBS
• MD

Mandatory Requirements

The company has clearly mentioned the following mandatory requirements:

• Pharmacovigilance experience is mandatory
• Experience on Argus Database

Argus Safety Database expertise is considered highly valuable in the global pharmacovigilance industry.

Location & Salary

Job Location

The exact location has not been officially mentioned in the recruitment advertisement. Candidates can confirm work location details directly with the HR team during the application process.

Estimated Salary Range

Based on current pharmacovigilance industry standards:

• Drug Safety Associate: ₹4 LPA to ₹10 LPA
• Global Submissions: ₹8 LPA to ₹16 LPA
• Quality Review: ₹6 LPA to ₹14 LPA
• MICC Roles: ₹5 LPA to ₹11 LPA
• Medical Review: ₹8 LPA to ₹18 LPA

Salary packages generally depend on:

• Pharmacovigilance experience
• Safety database expertise
• Regulatory knowledge
• Medical qualifications
• Global submission exposure
• Communication skills

Professionals with Argus Safety Database expertise often receive higher compensation due to industry demand.

Application Process

Interested candidates can apply by submitting their updated resumes through email.

Email Application

Candidates should send:

• Updated CV/Resume
• Current CTC details
• Notice period information
• Relevant pharmacovigilance experience
• Argus database exposure details

Official Email ID

careers@vizenlifesciences.com

Candidates are advised to mention the applied role in the email subject line for faster shortlisting.

FAQs

1. Which company is hiring for these pharmacovigilance roles?

Vizen Life Sciences is hiring for multiple pharmacovigilance positions.

2. What qualifications are eligible for these openings?

Candidates with B.Pharm, M.Pharm, Pharm.D, MBBS, and MD qualifications can apply.

3. Is pharmacovigilance experience mandatory?

Yes. The company has clearly stated that pharmacovigilance experience is mandatory.

4. Is Argus database experience required?

Yes. Experience on Argus Safety Database is mandatory.

5. Which roles are currently open?

Openings are available for Drug Safety Associate, Global Submissions, Quality Review, MICC, and Medical Review.

6. How can candidates apply?

Candidates can send their updated CV to careers@vizenlifesciences.com.

Summary Table

Company	Vizen Life Sciences
Department Vacancies	Drug Safety, Global Submissions, Quality Review, MICC, Medical Review
Qualification	B.Pharm, M.Pharm, Pharm.D, MBBS, MD
Experience	0–8 Years depending on role
Location	Not Officially Mentioned