Regulatory Affairs Specialist

Job Description

1. Regulatory Strategy & Planning

• Develop and implement regional regulatory strategies for biosimilar product registrations in the Middle East, North Africa, CIS, and Non-EEA countries.

• Ensure alignment with global regulatory strategy and business priorities.

• Conduct regulatory risk assessment and provide mitigation strategies during planning and execution.

2. Dossier Preparation & Submission

• Oversee the preparation, review, and submission of high-quality dossiers (CTD/eCTD format) for new marketing authorizations, renewals, and variations. • Coordinate with CMC, non-clinical, clinical, and labeling teams to gather required documentation. • Ensure submission timelines are met as per business needs and agency expectations. 3. Agency Engagement & Partner Coordination

• Act as the primary point of contact for Health Authorities in these regions. • Lead technical and administrative discussions with regulatory agencies to facilitate approvals. • Collaborate with regional distributors/partners for local submissions and regulatory intelligence. 4. Lifecycle Management

• Manage post-approval changes (variations), renewals, labelling updates, and compliance reporting.

• Ensure timely implementation of changes across the region.

• Maintain up-to-date regulatory documentation and databases. 5. Compliance & Intelligence

• Monitor and interpret regional regulatory guidelines, regulations, and policies relevant to biosimilars.

• Provide periodic update on impact and compliance to regulatory head.

• Support regulatory inspections as needed. 6. Cross-functional Collaboration

• Work with QA, QC, SCM, PM, Clinical, Commercial, and BD teams to align regulatory priorities.

• Support business development activities, due diligence, and partnership evaluations for the region.

Qualifications & Experience:

• Bachelor's or Master's degree in Pharmacy, Life Sciences, or related field; Regulatory certification is a plus.

• Experience in regulatory affairs in the pharmaceutical/biotech industry, experience in biosimilars is preferred.

• Strong understanding of regulatory pathways for biosimilars (clinical and analytical similarity requirements) and ICH guidelines.

• Experience with regulatory submissions in MENA and CIS countries is mandatory.

Familiarity with SFDA, EMA reliance procedures, and dossier localization requirements.

RequiredSkills & Competencies:

• Strong project management and organizational skills.

• Excellent written and verbal communication skills. • Strategic thinking with attention to detail. • Proactive, collaborative, and culturally aware. • Ability to manage multiple priorities in a fast-paced environment.