Navitas Life Sciences is inviting applications for the position of QPPV Office Expert / Senior Drug Safety Associate (Senior DSA) within its Pharmacovigilance division. This opportunity is ideal for experienced Pharmacovigilance professionals with expertise in QPPV office operations, safety compliance, regulatory intelligence, PSMF management, and global drug safety activities.
Candidates with 4–8 years of Pharmacovigilance experience and strong knowledge of post-marketing safety surveillance, clinical trial safety reporting, and regulatory compliance are encouraged to apply.
Job Details
| Particulars | Details |
|---|---|
| Position | QPPV Office Expert / Senior DSA |
| Company | Navitas Life Sciences |
| Experience | 4–8 Years |
| Department | Pharmacovigilance |
| Employment Type | Full-Time |
| Location | India |
| Industry | Life Sciences / Drug Safety / Pharmacovigilance |
Key Responsibilities
As a QPPV Office Expert / Senior DSA, you will be responsible for:
- Acting as the national Pharmacovigilance point of contact for assigned markets.
- Leading Pharmacovigilance coordination and communication activities.
- Serving as the primary liaison for all PV-related matters.
- Collaborating with regulatory authorities and regulatory stakeholders.
- Managing Local Contact Persons (LCPs) across multiple countries.
- Supporting global and local Pharmacovigilance compliance activities.
- Handling Pharmacovigilance System Master File (PSMF) drafting and maintenance.
- Ensuring ongoing PSMF compliance and inspection readiness.
- Managing post-marketing safety surveillance activities.
- Supporting clinical trial safety reporting requirements.
- Driving regulatory intelligence and safety updates across global markets.
- Ensuring compliance with global Pharmacovigilance regulations and company procedures.
Required Qualifications
To be considered for this Pharmacovigilance job, candidates should possess:
Educational Qualification
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Medicine, Biotechnology, Nursing, or related healthcare disciplines.
Experience
- 4–8 years of relevant Pharmacovigilance experience.
- Experience in QPPV office activities and Drug Safety operations.
- Hands-on experience with PSMF management and maintenance.
- Exposure to global Pharmacovigilance regulations.
- Experience working with regulatory authorities and health agencies.
Preferred Skills
- Strong understanding of Pharmacovigilance systems and processes.
- Knowledge of Clinical Trial Safety Reporting.
- Expertise in Post-Marketing Surveillance activities.
- Regulatory Intelligence and compliance management experience.
- Excellent communication and stakeholder management skills.
- Ability to coordinate with cross-functional global teams.
- Experience managing Local Contact Persons (LCPs) in multiple countries.
Why Join Navitas Life Sciences?
Joining Navitas Life Sciences provides an opportunity to:
- Work in a global Pharmacovigilance environment.
- Gain exposure to international regulatory requirements.
- Collaborate with experienced Drug Safety professionals.
- Participate in strategic QPPV office operations.
- Contribute to patient safety and regulatory compliance initiatives.
- Advance your career in Pharmacovigilance and Drug Safety.
How to Apply
Interested candidates can share their updated CV at:
Email: Recruitment.Bangalore@navitaslifesciences.com
Applicants should mention “QPPV Office Expert / Senior DSA Application” in the email subject line for faster processing.
