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Vizen Life Sciences Hiring AGM PVQA | 10–15 Yrs Exp.
Vizen Life Sciences hiring AGM in Pharmacovigilance Quality Assurance. Apply with B.Pharm, M.Pharm, or Pharm.D and 10–15 yrs PVQA experience.
Vizen Life Sciences is inviting senior-level professionals for the role of Assistant General Manager (AGM) – Pharmacovigilance Quality Assurance (PVQA). This is an exciting opportunity for experienced pharma professionals to lead PVQA functions, including QMS management, audit readiness, and SOP compliance, within a global service-driven environment.
Company Overview
Vizen Life Sciences is a leading pharmaceutical services organization committed to excellence in drug safety, pharmacovigilance, and quality compliance. The company partners with global pharma and biotech clients to ensure regulatory adherence and patient safety. At Vizen, employees benefit from working in a collaborative, innovation-driven environment that emphasizes growth, compliance, and high-quality service delivery.
Job Role & Responsibilities
As an AGM – Pharmacovigilance Quality Assurance, you will:
- Lead the PVQA team responsible for Quality Management Systems (QMS).
- Oversee SOP development, periodic quality reviews, and compliance checks.
- Manage internal and external audits, ensuring regulatory readiness.
- Monitor and review aggregate reports, ICSR (Individual Case Safety Reports), and periodic reports.
- Conduct team training and ensure PV operations meet global regulatory standards.
- Coordinate with clients and stakeholders, ensuring transparent communication and compliance delivery.
- Drive continuous improvement initiatives across PVQA processes.
Eligibility / Qualifications
- Education: B.Pharm, M.Pharm, Pharm.D.
- Experience: 10–15 years in Pharmacovigilance Quality Assurance.
- Required Skills:
- Strong knowledge of PV systems, QMS, and global compliance.
- Proven people management and leadership skills.
- Experience in pharma and service organizations.
- Excellent communication, client handling, and presentation abilities.
Relevant Courses: B.Pharm, M.Pharm (Pharmaceutical Analysis, Pharmacovigilance, Quality Assurance), Pharm.D.
Location & Salary
- Job Location: Not explicitly mentioned (applicants may confirm during application).
- Salary: Attractive package based on experience and qualifications.
Application Process
Interested candidates can apply directly by contacting:
- Contact Person: Praveen Kumar, General Manager HR
- Phone: +91 800 810 2515
- Email: plotti@vizenlifesciences.com
Apply before 23rd August 2025 to secure your opportunity with Vizen Life Sciences.
FAQs
Q1: What experience level is required?
10–15 years of PVQA experience in pharma and service organizations.
Q2: What is the role of AGM – PVQA?
To lead teams handling SOPs, QMS, audits, ICSR, aggregate report reviews, and PV compliance.
Q3: Which qualifications are accepted?
B.Pharm, M.Pharm, Pharm.D.
Q4: What skills are important for this role?
Leadership, PV compliance expertise, communication, client handling, and audit readiness.
Q5: How can I apply?
Send your CV to plotti@vizenlifesciences.com or call the HR contact.
Why Join Vizen Life Sciences?
- Opportunity to lead Pharmacovigilance Quality Assurance in a global setting.
- Exposure to regulatory-driven PV systems and client projects.
- Career growth in leadership and compliance management.
- Collaborative culture with emphasis on continuous improvement.
- Competitive salary and benefits.
Quick Summary Table
| Category | Details |
|---|---|
| Company | Vizen Life Sciences |
| Vacancies | AGM – Pharmacovigilance Quality Assurance (PVQA) |
| Required Education | B.Pharm, M.Pharm, Pharm.D |
| Experience | 10–15 years in PVQA |
| Location | Not specified (to be confirmed) |
| Application Email | plotti@vizenlifesciences.com |
| Contact Number | +91 800 810 2515 |
Vizen Life Sciences Hiring AGM PVQA
