Manager​/Sr. Manager, Regulatory Affairs

Position: Manager / Sr. Manager, Regulatory Affairs

Location: Doha, Qatar

Job : 666

# of Openings: 1

Akura Medical, a Shifamed portfolio company, is advancing a differentiated platform for the treatment of venous thromboembolism (VTE), which affects up to 900,000 Americans each year. The company recently received US IDE approval for its QUADRA-PE study evaluating the Katana™ Thrombectomy System in acute pulmonary embolism patients. In parallel, Akura Medical is developing NavIQ™, a software platform that transforms CT angiograms into 3D pulmonary vascular models to enhance visualization, procedural planning, and clot assessment towards better safety, efficacy, and ease of use.

Akura has recently completed a $53 million first close of its Series C financing, led by the Qatar Investment Authority, supporting the launch of a joint venture and a new R&D and manufacturing center in Doha, Qatar.

Founded in 2009 by serial entrepreneur Amr Salahieh, Shifamed LLC is a privately held medical device innovation hub focused on the development of novel medical products to address clinical needs in the rapidly evolving fields of cardiology and ophthalmology.

This Manager / Sr. Manager, Regulatory Affairs will serve as a key member of the cross-functional team, partnering closely with Clinical, Quality, R&D, and Executive Leadership to support U.S. regulatory activities and lead global clinical studies and international market expansion. The ideal candidate brings strong FDA medical device experience combined with hands‑on knowledge of international regulatory pathways, agency interactions, and clinical study support across Europe, the Middle East, and other global markets.

This is a unique opportunity to help shape regulatory strategy for a clinical-stage medical device company as it expands global clinical activities, and prepares for international commercialization.

• Develop and execute global regulatory strategies for Akura Medical's thrombectomy and catheter-based cardiovascular technologies.
• Serve as regulatory lead on cross-functional product development teams from concept through commercialization.
• Provide regulatory guidance on design controls, risk management, verification and validation activities, labeling, and product changes.
• Partner with Quality and R&D teams to ensure compliance with FDA, MDR, ISO 13485, and applicable international requirements.

• Lead preparation, review, and submission of U.S. regulatory filings, including IDE's, 510(k)'s, supplements, and other regulatory submissions as applicable.
• Monitor evolving FDA requirements and assess impact on development and commercialization plans.

• Develop regulatory strategies and market access plans for Europe, the Middle East, and other international markets.
• Support CE Mark and MDR-related activities in partnership with Notified Bodies and external regulatory consultants.
• Lead country-specific registration activities and regulatory submissions across key international markets including Qatar, UAE, Saudi Arabia, and other MENA countries.
• Establish and maintain relationships with regulatory authorities, notified bodies, and international regulatory partners.

• Partner closely with Clinical Affairs to support global clinical studies, including IDE, PMCF, registries, and post-market studies.
• Provide regulatory guidance on protocol development, clinical study design, and regulatory approval pathways.
• Support regulatory submissions associated with clinical trial approvals across multiple countries and regions.
• Participate in investigator meetings, regulatory inspections, audits, and agency interactions.

• Represent the company during interactions with FDA, Notified Bodies, Ministries of Health, and other regulatory authorities.
• Support preparation for regulatory inspections and audits.
• Maintain awareness of evolving global regulatory requirements and communicate potential impacts to leadership.
• Contribute to regulatory…