Regulatory Affairs IVDR - Contractor (North Africa)
IQVIA · Algeria +1 more
RegulatoryFull-timeCompany career page
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Role summary
IQVIA seeks an experienced Regulatory Affairs contractor to support IVDR transition projects and product registrations across North Africa. The role involves managing regulatory submissions, change control activities, and compliance initiatives within the medical diagnostics sector, requiring cross-functional collaboration across the EMEA region.
What they're looking for
- Minimum 2 years regulatory affairs experience in medical devices, preferably in vitro diagnostics
- Knowledge of medical diagnostics industry and regulatory environments in North Africa
- Experience with regulatory submissions, registrations, and change management
- Strong project management and stakeholder engagement capabilities
- Fluent English; French language proficiency advantageous
- Working knowledge of local Ministry of Health regulations and industry standards
- Currently based in Algeria, Morocco, or Tunisia
What you'll be doing
- Develop and execute regulatory submission plans for IVDR transition projects across EU region
- Coordinate with cross-functional teams on regulatory initiatives and change control projects
- Support product registrations and amendments to existing regulatory approvals
- Maintain regulatory databases, track submission status, and report milestones via KPIs
- Monitor regulatory developments and conduct impact assessments for stakeholder communication
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.