Consultant – Pharmacovigilance and Quality Assurance Lead

Ividata Life Sciences

. Deploy and lead the Quality policy across the French subsidiary, in compliance with regulatory requirements and Group procedures .

Posted 9/21/2026full-timeParis • FranceSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in pharmacovigilance and quality management systems, ensuring compliance with regulatory requirements while leading continuous improvement initiatives. Proficient in risk analysis, project management, and team leadership within the pharmaceutical industry.

Highest-signal resume keywords

Pharmacy DegreePharmacovigilance ExperienceQuality Management Systems KnowledgeRegulatory Compliance ExpertiseTeam Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

PharmacovigilanceQuality AssuranceRisk AnalysisProject ManagementContinuous ImprovementAudit ProcessesISO 9001 KnowledgeSafety Signal DetectionRegulatory RequirementsHealthcare Product Knowledge

Soft Skills

Excellent CommunicationMediation SkillsNegotiation SkillsProactive AttitudeAccountability

Certifications & Qualifications

Registration with the French National Order of Pharmacists

Industry Keywords

Pharmaceutical IndustryQuality Management SystemPharmacovigilance RegulationsHealth Authorities CoordinationQuality Incidents Management

About the role

Key responsibilities & impact

Deploy and lead the Quality policy across the French subsidiary, in compliance with regulatory requirements and Group procedures
Lead the quality management system and contribute to the continuous improvement of internal processes and practices
Oversee the pharmacovigilance and safety surveillance system in accordance with regulatory requirements and local and international procedures
Serve as the Local Safety Officer (LSO) and the person responsible for pharmacovigilance for the subsidiary
Oversee the maintenance and updating of pharmacovigilance reference documentation
Contribute to safety signal detection and assessment activities
Monitor regulatory developments and assess their impact on the subsidiary’s activities
Coordinate interactions with health authorities and healthcare professionals on product safety matters
Oversee the management of quality incidents, complaints, audits, and inspections, as well as the follow-up of corrective and preventive actions
Provide pharmacovigilance, quality, and risk management expertise to the company’s various functions
Contribute to the collection, assessment, and follow-up of safety data generated through the company’s various programs and activities
Escalate safety signals to the relevant stakeholders and contribute to defining action plans
Manage and develop a Quality and Safety Surveillance team
Support change, set priorities, and contribute to the evolution of methods and processes within the assigned scope
Collaborate with pharmaceutical and biotechnology clients on high-value-added projects

Requirements

What you’ll need

Pharmacy degree
Registration with the French National Order of Pharmacists
Significant experience in pharmacovigilance and/or quality assurance within the pharmaceutical industry
Strong knowledge of pharmaceutical and pharmacovigilance regulations
Knowledge of requirements applicable to healthcare products
Knowledge of quality management systems
Experience with audit and inspection processes
Knowledge of ISO 9001 is preferred
Strong skills in risk analysis, project management, and continuous improvement
Experience managing teams and coordinating cross-functional activities
Excellent communication, mediation, and negotiation skills
Rigorous, autonomous, proactive, and accountable
Fluent in French and English

Benefits

Comp & perks

Hybrid working with the possibility of remote work
Stimulating, collaborative, and constantly evolving environment
High-impact assignments at the forefront of healthcare innovation
Support from passionate experts
Opportunities to contribute to continuous improvement and skills development