Senior Commercial Quality Assurance Specialist - French Speaking - 12 Month Contract

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Regulatory Affairs Specialist – Africa (French Speaking) 12 Month Contract

About Danaher Diagnostics

At Danaher, we are dedicated to advancing science and technology to improve human health. Our Diagnostics businesses provide innovative diagnostic solutions that help healthcare professionals make faster, more accurate decisions and improve patient outcomes.

We are looking for a Regulatory Affairs Specialist – Africa (French Speaking) to support regulatory submissions, product registrations and market expansion activities across African markets.

Regulatory Submissions & Product Registrations

Prepare and manage regulatory submissions for African countries, including initial registrations, renewals, variations and responses to additional information requests from regulatory authorities.

Support market expansion registrations for diagnostic assays, instruments and software, including medium- to high-complexity projects.

Coordinate with local regulatory representatives and health authorities to facilitate product registrations and approvals.

Ensure timely delivery of regulatory activities to support product launches and business priorities.

Maintain accurate regulatory documentation, product approvals, registration records and relevant certificates, including Certificates of Free Sale (CFS).

Regulatory Compliance & Cross-Functional Collaboration

Collaborate with global and regional Regulatory Affairs teams, Quality, Manufacturing, Sales and Marketing to support regulatory activities.

Conduct regulatory change assessments for product design, manufacturing, labeling, packaging and other relevant changes.

Support compliance with applicable regulatory requirements across African markets.

Work closely with global regulatory stakeholders to resolve registration challenges and accelerate pending approvals.

Regulatory Strategy & Market Expansion

Support the development and execution of regulatory registration plans aligned with business priorities.

Identify applicable product classifications, registration pathways and country-specific regulatory requirements.

Gather and share regulatory intelligence, including changes in regulatory requirements across African markets.

Provide regulatory input to new product development and market expansion initiatives.

Support regulatory project planning, including milestones, deliverables and timelines.

Reporting & Documentation

Maintain organized and accurate regulatory submission files, correspondence, approvals and certificates.

Monitor registration progress, key performance indicators (KPIs) and on-time delivery of regulatory deliverables.

Identify regulatory risks, submission delays and opportunities for process improvement.

Apply continuous improvement principles to enhance regulatory processes and efficiency.

Qualifications & Experience

Bachelor's degree in Pharmacy, Biomedical Science, Life Sciences, Biotechnology, Chemistry or a related scientific discipline.

Previous experience in Regulatory Affairs within medical devices, in-vitro diagnostics (IVD), healthcare or life sciences.

Hands-on experience preparing regulatory submissions, product registrations, renewals and regulatory responses.

Knowledge of regulatory requirements and registration processes across African countries, particularly Francophone African markets.

Familiarity with medical device and IVD regulatory frameworks and international standards.