Qinecsa Solutions Hiring Experienced Pharmacovigilance Professionals

Immediate Openings for B Pharm / M Pharm / Pharm D in Pharmacovigilance – Qinecsa Solutions | Mysore & Bangalore

Pharmacovigilance job for B Pharm, M Pharm, Pharm D graduates with 1+ year experience at Qinecsa Solutions in Mysore or Bangalore. Immediate joiners preferred.

Drug Safety Job Opportunities for B Pharm, M Pharm, Pharm D Graduates at Qinecsa Solutions

If you’re a qualified healthcare professional passionate about drug safety and eager to grow in a high-impact role, Qinecsa Solutions invites you to apply! We are actively hiring experienced Drug Safety Associates for our Pharmacovigilance division. These full-time roles are perfect for those with a minimum of 1 year of hands-on pharmacovigilance experience and are open to immediate joiners.

Currently operating remotely, Qinecsa’s work culture is flexible, with opportunities to work from either the Mysore or Bangalore office as needed. This makes it a fantastic opportunity for professionals in Karnataka seeking both stability and career growth in a top-tier global organization.

Why Choose Qinecsa Solutions?

Trusted Global Pharma Partner

Qinecsa Solutions is a renowned name in the field of pharmacovigilance and regulatory solutions, offering end-to-end safety and compliance services to leading pharmaceutical clients worldwide.

Competitive Advantages:

• Remote work flexibility
• Opportunity to work from two strategic hubs: Mysore and Bangalore
• Association with a global leader in drug safety and compliance
• Ideal platform for healthcare professionals to advance their pharmacovigilance careers

Who Can Apply?

Minimum Eligibility Criteria:

• Educational Background: B Pharm, M Pharm, Pharm D (Registered Healthcare Professionals)
• Experience Required: At least 1 year of experience in pharmacovigilance
• Joining Timeline: Immediate joiners will be given preference

Job Responsibilities:

Key Areas of Work:

• Case processing and narrative writing
• Triaging, data entry, and medical review support
• Ensuring compliance with regulatory timelines and data integrity
• Collaborating with cross-functional teams for safety data analysis

This role requires attention to detail, familiarity with pharmacovigilance databases, and understanding of global regulatory requirements.

How to Apply?

To be considered for this role, please send your updated CV to: 📧 roopa.shree@Qinecsa.com

Important: Mention your notice period clearly in the subject line to speed up the review process.

Due to a high volume of applications, only candidates meeting the job criteria will be contacted.

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