Key Responsibility
• Lead innovative product development initiatives.
• Manage and author high-impact scientific publications.
• Provide clinical support for Post-Market Clinical Follow-up (PMCF) studies.
• Conduct comprehensive literature reviews.
• Apply strong analytical skills to complex research and regulatory projects.
• Understand and ensure compliance with biocompatibility requirements for diverse medical devices.
Qualification
• Doctorate (PhD) in Pharmaceutics, Pharmaceutical Chemistry, Biotechnology, or related specialization.
• Proven experience in pharmaceutical or biotechnological product development.
• Track record of successful publications.
• Expertise in clinical study support, literature search, and data analysis.
