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Consultant – Quality Assurance & Pharmacovigilance Specialist
Ividata Life Sciences. Manage customer and product complaints .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in pharmacovigilance and clinical development, with a strong focus on managing customer complaints, conducting quality checks, and coordinating communications across teams. Proficient in data management and regulatory surveillance, ensuring compliance and effective monitoring of performance indicators.
Highest-signal resume keywords
PharmacovigilanceClinical Trials ExperienceData ManagementRegulatory SurveillanceDoctor of Pharmacy (PharmD)
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Batch TrackingDocument AnonymizationQuality ChecksSafety Data ReconciliationPerformance Monitoring
Soft Skills
Attention to DetailOrganizational SkillsAnalytical SkillsTeam SpiritAdaptability
Tools & Technologies
DatabasesReporting Tools
Industry Keywords
Product Quality Review (PQR)Local SignalsStandard Operating ProceduresPharmacovigilance CasesCRO Experience
About the role
Key responsibilities & impact- Manage customer and product complaints
- Ensure batch tracking and contribute to the affiliate Product Quality Review (PQR)
- Lead the monitoring and management of subcontractors
- Participate in the affiliate’s global quality activities
- Collect, document, enter, and follow up on local pharmacovigilance cases in databases
- Perform document anonymization, quality checks, and safety data reconciliation
- Contribute to the detection of local signals and the updating of standard operating procedures
- Coordinate communications with local and global teams and external partners
- Monitor performance indicators, reporting tools, and regulatory/literature surveillance related to local activities
- Conducting audits independently is not required for this position
Requirements
What you’ll need- Doctor of Pharmacy (PharmD) degree or an advanced scientific degree (Master’s level) in pharmacovigilance or clinical development
- Junior to mid-level profile
- Successful initial experience in pharmacovigilance, including clinical trials or CRO experience, is accepted
- Attention to detail, strong organizational and prioritization skills
- Autonomy, analytical skills, and reporting capabilities
- Team spirit and excellent adaptability
- Professional fluency in English, both written and spoken
Benefits
Comp & perks- Stimulating and collaborative environment
- High-impact assignments
- Hybrid working arrangement with remote-work opportunities
- Work alongside passionate experts
- Involvement across the full product life cycle
- Constantly evolving environment where ideas and expertise have a real impact